Hits from PDB |
Structure Title |
EC number |
2DLH | SOLUTION STRUCTURE OF THE SECOND FN3 DOMAIN OF HUMAN RECEPTOR-TYPE TYROSINE-PROTEIN PHOSPHATASE DELTA | 3.1.3.48 |
2DM9 | CRYSTAL STRUCTURE OF PH1978 FROM PYROCOCCUS HORIKOSHII OT3 | 3.6.3.14 |
2DMA | CRYSTAL STRUCTURE OF PH1978 FROM PYROCOCCUS HORIKOSHII OT3 (FORM II) | 3.6.3.14 |
2DN7 | SOLUTION STRUCTURES OF THE 6TH FN3 DOMAIN OF HUMAN RECEPTOR-TYPE TYROSINE-PROTEIN PHOSPHATASE F | 3.1.3.48 |
2DNJ | DNASE I-INDUCED DNA CONFORMATION. 2 ANGSTROMS STRUCTURE OF A DNASE I-OCTAMER COMPLEX | 3.1.21.1 |
2DNR | SOLUTION STRUCTURE OF RNA BINDING DOMAIN IN SYNAPTOJANIN 1 | 3.1.3.36 |
2DO2 | DESIGN OF SPECIFIC INHIBITORS OF PHOSPHOLIPASE A2: CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN A GROUP II CYS 49 PHOSPHOLIPASE A2 AND A DESIGNED PENTAPEPTIDE ALA-LEU-ALA-SER-LYS AT 2.6A RESOLUTION | 3.1.1.4 |
2DOI | THE X-RAY CRYSTALLOGRAPHIC STRUCTURE OF THE ANGIOGENESIS INHIBITOR, ANGIOSTATIN, BOUND TO A PEPTIDE FROM THE GROUP A STREPTOCOCCUS PROTEIN PAM | 3.4.21.7 |
2DOJ | CRYSTAL STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH ADENOSINE AT 2.4 A RESOLUTION | 3.4.21 |
2DOK | CRYSTAL STRUCTURE OF THE PIN DOMAIN OF HUMAN EST1A | 3.1 |
2DOO | THE STRUCTURE OF IMP-1 COMPLEXED WITH THE DETECTING REAGENT (DANSYLC4SH) BY A FLUORESCENT PROBE | 3.5.2.6 |
2DOS | STRUCTURAL BASIS FOR THE RECOGNITION OF LYS48-LINKED POLYUBIQUITIN CHAIN BY THE JOSEPHIN DOMAIN OF ATAXIN-3, A PUTATIVE DEUBIQUITINATING ENZYME | 3.4.22 3.4.19.12 |
2DP4 | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PROTEINASE K AND A HUMAN LACTOFERRIN FRAGMENT AT 2.9 A RESOLUTION | 3.4.21.64 |
2DP6 | CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE IN COMPLEX WITH AP:C CONTAINING DNA | 3.2.2 |
2DP8 | CARBOHYDRATE RECOGNITION BY LACTOFERRIN: CRYSTAL STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH TRISACCHARIDE AT 2.5 A RESOLUTION | 3.4.21 |
2DPX | CRYSTAL STRUCTURE OF HUMAN RAD GTPASE | 3.6.5.2 |
2DPY | CRYSTAL STRUCTURE OF THE FLAGELLAR TYPE III ATPASE FLII | 3.6.3.14 7.1.2.2 |
2DPZ | STRUCTURE OF THE COMPLEX OF PHOSPHOLIPASE A2 WITH N-(4-HYDROXYPHENYL)- ACETAMIDE AT 2.1 A RESOLUTION | 3.1.1.4 |
2DQ6 | CRYSTAL STRUCTURE OF AMINOPEPTIDASE N FROM ESCHERICHIA COLI | 3.4.11.2 |
2DQA | CRYSTAL STRUCTURE OF TAPES JAPONICA LYSOZYME | 3.2.1.17 |
2DQB | CRYSTAL STRUCTURE OF DNTP TRIPHOSPHOHYDROLASE FROM THERMUS THERMOPHILUS HB8, WHICH IS HOMOLOGOUS TO DGTP TRIPHOSPHOHYDROLASE | 3.1.5.1 |
2DQK | CRYSTAL STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH A SPECIFIC LACTOFERRIN PEPTIDE VAL-LEU-LEU-HIS AT 1.93 A RESOLUTION | 3.4.21.64 |
2DQM | CRYSTAL STRUCTURE OF AMINOPEPTIDASE N COMPLEXED WITH BESTATIN | 3.4.11.2 |
2DQS | CRYSTAL STRUCTURE OF THE CALCIUM PUMP WITH AMPPCP IN THE ABSENCE OF CALCIUM | 3.6.3.8 7.2.2.10 |
2DQV | STRUCTURE OF THE C-TERMINAL LOBE OF BOVINE LACTOFERRIN IN COMPLEX WITH GALACTOSE AT 2.7 A RESOLUTION | 3.4.21 |
2DQX | MUTANT BETA-AMYLASE (W55R) FROM SOY BEAN | 3.2.1.2 |
2DQY | CRYSTAL STRUCTURE OF HUMAN CARBOXYLESTERASE IN COMPLEX WITH CHOLATE AND PALMITATE | 3.1.1.1 3.1.1.13 3.1.1.56 |
2DQZ | CRYSTAL STRUCTURE OF HUMAN CARBOXYLESTERASE IN COMPLEX WITH HOMATROPINE, COENZYME A, AND PALMITATE | 3.1.1.1 3.1.1.13 3.1.1.56 |
2DR0 | CRYSTAL STRUCTURE OF HUMAN CARBOXYLESTERASE IN COMPLEX WITH TAUROCHOLATE | 3.1.1.1 3.1.1.13 3.1.1.56 |
2DRO | CRYSTAL STRUCTURE OF REDUCING-END-XYLOSE RELEASING EXO-OLIGOXYLANASE D263C MUTANT | 3.2.1.156 |
2DRQ | CRYSTAL STRUCTURE OF REDUCING-END-XYLOSE RELEASING EXO-OLIGOXYLANASE D263G MUTANT | 3.2.1.156 |
2DRR | CRYSTAL STRUCTURE OF REDUCING-END-XYLOSE RELEASING EXO-OLIGOXYLANASE D263N MUTANT | 3.2.1.156 |
2DRS | CRYSTAL STRUCTURE OF REDUCING-END-XYLOSE RELEASING EXO-OLIGOXYLANASE D263S MUTANT | 3.2.1.156 |
2DS9 | STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH MANNOSE AT 2.8 A RESOLUTION | 3.4.21 |
2DSB | CRYSTAL STRUCTURE OF HUMAN ADP-RIBOSE PYROPHOSPHATASE NUDT5 | 3.6.1.13 3.6.1 3.6.1.58 2.7.7.96 |
2DSC | CRYSTAL STRUCTURE OF HUMAN ADP-RIBOSE PYROPHOSPHATASE NUDT5 IN COMPLEX WITH MAGNESIUM AND ADP-RIBOSE | 3.6.1.13 3.6.1 3.6.1.58 2.7.7.96 |
2DSD | CRYSTAL STRUCTURE OF HUMAN ADP-RIBOSE PYROPHOSPHATASE NUDT5 IN COMPLEX WITH MAGNESIUM AND AMP | 3.6.1.13 3.6.1 3.6.1.58 2.7.7.96 |
2DSF | STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH XYLOSE AT 2.8A RESOLUTION | 3.4.21 |
2DSK | CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HYPERTHERMOPHILIC CHITINASE FROM PYROCOCCUS FURIOSUS | 3.2.1.14 |
2DSN | CRYSTAL STRUCTURE OF T1 LIPASE | 3.1.1.3 |
2DSO | CRYSTAL STRUCTURE OF D138N MUTANT OF DRP35, A 35KDA DRUG RESPONSIVE PROTEIN FROM STAPHYLOCOCCUS AUREUS | 3.1.1.25 3.1.1 |
2DUA | CRYSTAL STRUCTURE OF PHOSPHONOPYRUVATE HYDROLASE COMPLEX WITH OXALATE AND MG++ | 3.11.1.3 |
2DUC | CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE(3CLPRO) | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2DUJ | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PROTEINASE K AND A SYNTHETIC PEPTIDE LEU-LEU-PHE-ASN-ASP AT 1.67 A RESOLUTION | 3.4.21.64 |
2DUK | CRYSTAL STRUCTURE OF MS0616 | 3.6.1.52 3.6.1 |
2DVC | STRUCTURE OF THE BOVINE LACTOFERRIN C-LOBE COMPLEX WITH SUCROSE AT 3.0 A RESOLUTION | 3.4.21 |
2DVN | STRUCTURE OF PH1917 PROTEIN WITH THE COMPLEX OF IMP FROM PYROCOCCUS HORIKOSHII | 3.6.1.66 |
2DVO | STRUCTURE OF PH1917 PROTEIN WITH THE COMPLEX OF ITP FROM PYROCOCCUS HORIKOSHII | 3.6.1.66 |
2DVP | STRUCTURE OF NTPASE FROM PYROCCOUS HORIKOSHII | 3.6.1.66 |
2DW0 | CRYSTAL STRUCTURE OF VAP2 FROM CROTALUS ATROX VENOM (FORM 2-1 CRYSTAL) | 3.4.24 |
2DW1 | CRYSTAL STRUCTURE OF VAP2 FROM CROTALUS ATROX VENOM (FORM 2-2 CRYSTAL) | 3.4.24 |
2DW2 | CRYSTAL STRUCTURE OF VAP2 FROM CROTALUS ATROX VENOM (FORM 2-5 CRYSTAL) | 3.4.24 |
2DW5 | CRYSTAL STRUCTURE OF HUMAN PEPTIDYLARGININE DEIMINASE 4 IN COMPLEX WITH N-ALPHA-BENZOYL-N5-(2-FLUORO-1-IMINOETHYL)-L-ORNITHINE AMIDE | 3.5.3.15 |
2DWA | STRUCTURE OF THE COMPLEX OF LACTOFERRIN C-TERMINAL HALF WITH FUCOSE AT 2.07 A RESOLUTION | 3.4.21 |
2DWH | CRYSTAL STRUCTURE OF N-ACETYLGLUCOSAMINE COMPLEX OF BOVINE LACTOFERRIN C-LOBE AT 2.8 A RESOLUTION | 3.4.21 |
2DWI | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN C-TERMINAL HALF OF BOVINE LACTOFERRIN AND CELLOBIOSE AT 2.2 A RESOLUTION | 3.4.21 |
2DWJ | STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH RAFFINOSE AT 2.3 A RESOLUTION | 3.4.21 |
2DWL | CRYSTAL STRUCTURE OF THE PRIA PROTEIN COMPLEXED WITH OLIGONUCLEOTIDES | 3.6.1 3.6.4 |
2DWM | CRYSTAL STRUCTURE OF THE PRIA PROTEIN COMPLEXED WITH OLIGONUCLEOTIDES | 3.6.1 3.6.4 |
2DWN | CRYSTAL STRUCTURE OF THE PRIA PROTEIN COMPLEXED WITH OLIGONUCLEOTIDES | 3.6.4 |
2DWO | PFKFB3 IN COMPLEX WITH ADP AND PEP | 2.7.1.105 3.1.3.46 |
2DWP | A PSEUDO SUBSTRATE COMPLEX OF 6-PHOSPHOFRUCTO-2-KINASE OF PFKFB | 2.7.1.105 3.1.3.46 |
2DX0 | CRYSTAL STRUCTURE OF THE N-TERMINAL SH2 DOMAIN OF MOUSE PHOSPHOLIPASE C-GAMMA 2 | 3.1.4.11 |
2DXC | RECOMBINANT THIOCYANATE HYDROLASE, FULLY-MATURED FORM | 3.5.5.8 |
2DXL | GLYCEROPHOSPHODIESTERASE FROM ENTEROBACTER AEROGENES | 3.1.4.46 3.1.4.53 |
2DXN | GLYCEROPHOSPHODIESTERASE FROM ENTEROBACTER AEROGENES | 3.1.4.46 3.1.4.53 |
2DXP | CRYSTAL STRUCTURE OF THE COMPLEX OF THE ARCHAEAL SULFOLOBUS PTP-FOLD PHOSPHATASE WITH PHOSPHOPEPTIDES A-(P)Y-R | 3.1.3.48 |
2DXR | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN C-TERMINAL HALF OF BOVINE LACTOFERRIN AND SORBITOL AT 2.85 A RESOLUTION | 3.4.21 |
2DXS | CRYSTAL STRUCTURE OF HCV NS5B RNA POLYMERASE COMPLEXED WITH A TETRACYCLIC INHIBITOR | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2DXY | STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH TREHALOSE AT 2.0 A RESOLUTION | 3.4.21 |
2DY7 | SOLUTION STRUCTURE OF THE FIRST CHROMODOMAIN OF YEAST CHD1 | 3.6.1 3.6.4 |
2DY8 | SOLUTION STRUCTURE OF THE SECOND CHROMODOMAIN OF YEAST CHD1 | 3.6.1 3.6.4 |
2DYN | DYNAMIN (PLECKSTRIN HOMOLOGY DOMAIN) (DYNPH) | 3.6.5.5 |
2DYU | HELICOBACTER PYLORI FORMAMIDASE AMIF CONTAINS A FINE-TUNED CYSTEINE-GLUTAMATE-LYSINE CATALYTIC TRIAD | 3.5.1.49 |
2DYV | HELICOBACTER PYLORI FORMAMIDASE AMIF CONTAINS A FINE-TUNED CYSTEINE-GLUTAMATE-LYSINE CATALYTIC TRIAD | 3.5.1.49 |
2DYX | STRUCTURE OF THE COMPLEX OF LACTOFERRIN C-LOBE WITH MELIBIOSE AT 2.0 A RESOLUTION | 3.4.21 |
2DZY | CRYSTAL STRUCTURE OF N392A MUTANT OF YEAST BLEOMYCIN HYDROLASE | 3.4.22.40 |
2DZZ | CRYSTAL STRUCTURE OF N392V MUTANT OF YEAST BLEOMYCIN HYDROLASE | 3.4.22.40 |
2E00 | CRYSTAL STRUCTURE OF N392L MUTANT OF YEAST BLEOMYCIN HYDROLASE | 3.4.22.40 |
2E01 | CRYSTAL STRUCTURE OF H369A MUTANT OF YEAST BLEOMYCIN HYDROLASE | 3.4.22.40 |
2E02 | CRYSTAL STRUCTURE OF H369L MUTANT OF YEAST BLEOMYCIN HYDROLASE | 3.4.22.40 |
2E03 | CRYSTAL STRUCTURE OF NQ67E MUTANT OF YEAST BLEOMYCIN HYDROLASE | 3.4.22.40 |
2E0L | MUTANT HUMAN RIBONUCLEASE 1 (Q28L, R31L, R32L) | 3.1.27.5 4.6.1.18 |
2E0M | MUTANT HUMAN RIBONUCLEASE 1 (T24L, Q28L, R31L, R32L) | 3.1.27.5 4.6.1.18 |
2E0O | MUTANT HUMAN RIBONUCLEASE 1 (V52L, D53L, N56L, F59L) | 3.1.27.5 4.6.1.18 |
2E0P | THE CRYSTAL STRUCTURE OF CEL44A | 3.2.1.4 3.2.1.151 |
2E0S | CARBOHYDRATE RECOGNITION OF C-TERMINAL HALF OF LACTOFERRIN: CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE WITH RHAMNOSE AT 2.15 A RESOLUTION | 3.4.21 |
2E0T | CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF DUAL SPECIFICITY PHOSPHATASE 26, MS0830 FROM HOMO SAPIENS | 3.1.3.48 3.1.3.16 |
2E0W | T391A PRECURSOR MUTANT PROTEIN OF GAMMA-GLUTAMYLTRANSPEPTIDASE FROM ESCHERICHIA COLI | 2.3.2.2 3.4.19.13 |
2E0X | CRYSTAL STRUCTURE OF GAMMA-GLUTAMYLTRANSPEPTIDASE FROM ESCHERICHIA COLI (MONOCLINIC FORM) | 2.3.2.2 3.4.19.13 |
2E0Y | CRYSTAL STRUCTURE OF THE SAMARIUM DERIVATIVE OF MATURE GAMMA-GLUTAMYLTRANSPEPTIDASE FROM ESCHERICHIA COLI | 2.3.2.2 3.4.19.13 |
2E11 | THE CRYSTAL STRUCTURE OF XC1258 FROM XANTHOMONAS CAMPESTRIS: A CN-HYDROLASE SUPERFAMILY PROTEIN WITH AN ARSENIC ADDUCT IN THE ACTIVE SITE | 3 |
2E1B | CRYSTAL STRUCTURE OF THE ALAX-M TRANS-EDITING ENZYME FROM PYROCOCCUS HORIKOSHII | 6.1.1.7 3.1.1.29 |
2E1E | CRYSTAL STRUCTURE OF THE HRDC DOMAIN OF HUMAN WERNER SYNDROME PROTEIN, WRN | 3.6.1 3.6.4.12 3.1 |
2E1F | CRYSTAL STRUCTURE OF THE HRDC DOMAIN OF HUMAN WERNER SYNDROME PROTEIN, WRN | 3.6.1 3.6.4.12 3.1 |
2E1P | CRYSTAL STRUCTURE OF PRO-TK-SUBTILISIN | 3.4.21.62 3.4.21 |
2E1S | CRYSTAL STRUCTURE OF THE COMPLEX OF C-TERMINAL HALF OF BOVINE LACTOFERRIN AND ARABINOSE AT 2.7 A RESOLUTION | 3.4.21 |
2E1W | CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE COMPLEXED WITH POTENT INHIBITORS | 3.5.4.4 |
2E25 | THE CRYSTAL STRUCTURE OF THE T109S MUTANT OF E. COLI DIHYDROOROTASE COMPLEXED WITH AN INHIBITOR 5-FLUOROOROTATE | 3.5.2.3 |
2E26 | CRYSTAL STRUCTURE OF TWO REPEAT FRAGMENT OF REELIN | 3.4.21 |
2E29 | SOLUTION STRUCTURE OF THE GUCT DOMAIN FROM HUMAN ATP-DEPENDENT RNA HELICASE DDX50, DEAD BOX PROTEIN 50 | 3.6.1 3.6.4.13 |
2E2D | FLEXIBILITY AND VARIABILITY OF TIMP BINDING: X-RAY STRUCTURE OF THE COMPLEX BETWEEN COLLAGENASE-3/MMP-13 AND TIMP-2 | 3.4.24 |
2E2K | HELICOBACTER PYLORI FORMAMIDASE AMIF CONTAINS A FINE-TUNED CYSTEINE-GLUTAMATE-LYSINE CATALYTIC TRIAD | 3.5.1.49 |
2E2L | HELICOBACTER PYLORI FORMAMIDASE AMIF CONTAINS A FINE-TUNED CYSTEINE-GLUTAMATE-LYSINE CATALYTIC TRIAD | 3.5.1.49 |
2E3J | THE CRYSTAL STRUCTURE OF EPOXIDE HYDROLASE B (RV1938) FROM MYCOBACTERIUM TUBERCULOSIS AT 2.1 ANGSTROM | 3.3.2.3 3.3.2.10 |
2E3W | X-RAY STRUCTURE OF NATIVE RNASE A | 3.1.27.5 4.6.1.18 |
2E3X | CRYSTAL STRUCTURE OF RUSSELL'S VIPER VENOM METALLOPROTEINASE | 3.4.24.58 |
2E3Z | CRYSTAL STRUCTURE OF INTRACELLULAR FAMILY 1 BETA-GLUCOSIDASE BGL1A FROM THE BASIDIOMYCETE PHANEROCHAETE CHRYSOSPORIUM IN SUBSTRATE-FREE FORM | 3.2.1.21 |
2E40 | CRYSTAL STRUCTURE OF INTRACELLULAR FAMILY 1 BETA-GLUCOSIDASE BGL1A FROM THE BASIDIOMYCETE PHANEROCHAETE CHRYSOSPORIUM IN COMPLEX WITH GLUCONOLACTONE | 3.2.1.21 |
2E4L | THERMODYNAMIC AND STRUCTURAL ANALYSIS OF THERMOLABILE RNASE HI FROM SHEWANELLA ONEIDENSIS MR-1 | 3.1.26.4 |
2E4T | CRYSTAL STRUCTURE OF CEL44A, GH FAMILY 44 ENDOGLUCANASE FROM CLOSTRIDIUM THERMOCELLUM | 3.2.1.4 3.2.1.151 |
2E52 | CRYSTAL STRUCTURAL ANALYSIS OF HINDIII RESTRICTION ENDONUCLEASE IN COMPLEX WITH COGNATE DNA AT 2.0 ANGSTROM RESOLUTION | 3.1.21.4 |
2E5K | SOLUTION STRUCTURE OF SH3 DOMAIN IN SUPPRESSOR OF T-CELL RECEPTOR SIGNALING 1 | 3.1.3.48 |
2E5T | C-TERMINAL DOMAIN OF EPSILON SUBUNIT OF F1F0-ATP SYNTHASE FROM THE THERMOPHILIC BACILLUS PS3 IN THE PRESENCE OF ATP CONDITION | 3.6.3.14 |
2E5U | C-TERMINAL DOMAIN OF EPSILON SUBUNIT OF F1F0-ATP SYNTHASE FROM THE THERMOPHILIC BACILLUS PS3 | 3.6.3.14 |
2E5X | STRUCTURE OF NUCLEOTIDE TRIPHOSPHATE PYROPHOSPHATASE FROM PYROCOCCUS HORIKOSHII OT3 | 3.6.1.19 3.6.1.66 |
2E5Y | EPSILON SUBUNIT AND ATP COMPLEX OF F1F0-ATP SYNTHASE FROM THE THERMOPHILIC BACILLUS PS3 | 3.6.3.14 |
2E67 | CRYSTAL STRUCTURE OF THE HYPOTHETICAL PROTEIN TTHB029 FROM THERMUS THERMOPHILUS HB8 | 3.5.1 |
2E69 | CRYSTAL STRUCTURE OF THE STATIONARY PHASE SURVIVAL PROTEIN SURE FROM THERMUS THERMOPHILUS HB8 IN COMPLEX WITH SULFATE | 3.1.3.5 |
2E6B | CRYSTAL STRUCTURE OF THE STATIONARY PHASE SURVIVAL PROTEIN SURE FROM THERMUS THERMOPHILUS HB8 IN COMPLEX WITH MAGNESIUM AND TUNGSTATE | 3.1.3.5 |
2E6C | CRYSTAL STRUCTURE OF THE STATIONARY PHASE SURVIVAL PROTEIN SURE FROM THERMUS THERMOPHILUS HB8 COCRYSTALLIZED WITH MANGANESE AND AMP | 3.1.3.5 |
2E6E | CRYSTAL STRUCTURE OF THE STATIONARY PHASE SURVIVAL PROTEIN SURE FROM THERMUS THERMOPHILUS HB8 | 3.1.3.5 |
2E6H | CRYSTAL STRUCTURE OF E37A MUTANT OF THE STATIONARY PHASE SURVIVAL PROTEIN SURE FROM THERMUS THERMOPHILUS HB8 COCRYSTALLIZED WITH MANGANESE AND AMP | 3.1.3.5 |
2E6L | STRUCTURE OF MOUSE WRN EXONUCLEASE DOMAIN | 3.6.1 3.6.4.12 3.1 |
2E6M | STRUCTURE OF MOUSE WERNER EXONUCLEASE DOMAIN | 3.6.1 3.6.4.12 3.1 |
2E6N | SOLUTION STRUCTURE OF THE TUDOR DOMAIN OF STAPHYLOCOCCAL NUCLEASE DOMAIN-CONTAINING PROTEIN 1 | 3.1.31.1 |
2E7V | CRYSTAL STRUCTURE OF SEA DOMAIN OF TRANSMEMBRANE PROTEASE FROM MUS MUSCULUS | 3.4.21 |
2E7Y | HIGH RESOLUTION STRUCTURE OF T. MARITIMA TRNASE Z | 3.1.26.11 |
2E85 | CRYSTAL STRUCTURE OF THE HYDROGENASE 3 MATURATION PROTEASE | 3.4 3.4.23.51 |
2E8I | STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE, D1 MUTANT | 3.5.1.46 |
2E8O | SOLUTION STRUCTURE OF THE N-TERMINAL SAM-DOMAIN OF THE SAM DOMAIN AND HD DOMAIN CONTAINING PROTEIN 1 (DENDRITIC CELL-DERIVED IFNG-INDUCED PROTEIN) (DCIP) (MONOCYTE PROTEIN 5) (MOP-5) | 3.1.5 |
2E8Y | CRYSTAL STRUCTURE OF PULLULANASE TYPE I FROM BACILLUS SUBTILIS STR. 168 | 3.2.1.41 |
2E8Z | CRYSTAL STRUCTURE OF PULLULANASE TYPE I FROM BACILLUS SUBTILIS STR. 168 COMPLEXED WITH ALPHA-CYCLODEXTRIN | 3.2.1.41 |
2E9B | CRYSTAL STRUCTURE OF PULLULANASE TYPE I FROM BACILLUS SUBTILIS STR. 168 COMPLEXED WITH MALTOSE | 3.2.1.41 |
2E9L | CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC NEUTRAL BETA-GLYCOSYLCERAMIDASE (KLOTHO-RELATED PROTE:KLRP) COMPLEX WITH GLUCOSE AND FATTY ACIDS | 3.2.1.21 |
2E9M | CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC NEUTRAL BETA-GLYCOSYLCERAMIDASE (KLOTHO-RELATED PROTE:KLRP) COMPLEX WITH GALACTOSE AND FATTY ACIDS | 3.2.1.21 |
2E9T | FOOT-AND-MOUTH DISEASE VIRUS RNA-POLYMERASE RNA DEPENDENT IN COMPLEX WITH A TEMPLATE-PRIMER RNA AND 5F-UTP | 2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15 |
2E9Z | FOOT-AND-MOUTH DISEASE VIRUS RNA-POLYMERASE IN COMPLEX WITH A TEMPLATE- PRIMER RNA, ATP AND UTP | 2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15 |
2EA1 | CRYSTAL STRUCTURE OF RIBONUCLEASE I FROM ESCHERICHIA COLI COMPLEXED WITH GUANYLYL-2(PRIME),5(PRIME)-GUANOSINE | 3.1.27.6 4.6.1.21 |
2EA2 | H-METAP2 COMPLEXED WITH A773812 | 3.4.11.18 |
2EA3 | CRYSTAL STRUCTURE OF CELLULOMONAS BOGORIENSIS CHYMOTRYPSIN | 3.4.21 |
2EA4 | H-METAP2 COMPLEXED WITH A797859 | 3.4.11.18 |
2EAB | CRYSTAL STRUCTURE OF 1,2-A-L-FUCOSIDASE FROM BIFIDOBACTERIUM BIFIDUM (APO FORM) | 3.2.1.63 |
2EAC | CRYSTAL STRUCTURE OF 1,2-A-L-FUCOSIDASE FROM BIFIDOBACTERIUM BIFIDUM IN COMPLEX WITH DEOXYFUCONOJIRIMYCIN | 3.2.1.63 |
2EAD | CRYSTAL STRUCTURE OF 1,2-A-L-FUCOSIDASE FROM BIFIDOBACTERIUM BIFIDUM IN COMPLEX WITH SUBSTRATE | 3.2.1.63 |
2EAE | CRYSTAL STRUCTURE OF 1,2-A-L-FUCOSIDASE FROM BIFIDOBACTERIUM BIFIDUM IN COMPLEXES WITH PRODUCTS | 3.2.1.63 |
2EAR | P21 CRYSTAL OF THE SR CA2+-ATPASE WITH BOUND TG | 3.6.3.8 7.2.2.10 |
2EAT | CRYSTAL STRUCTURE OF THE SR CA2+-ATPASE WITH BOUND CPA AND TG | 3.6.3.8 7.2.2.10 |
2EAU | CRYSTAL STRUCTURE OF THE SR CA2+-ATPASE WITH BOUND CPA IN THE PRESENCE OF CURCUMIN | 3.6.3.8 7.2.2.10 |
2EB0 | CRYSTAL STRUCTURE OF METHANOCOCCUS JANNASCHII PUTATIVE FAMILY II INORGANIC PYROPHOSPHATASE | 3.6.1.1 |
2EB1 | CRYSTAL STRUCTURE OF THE C-TERMINAL RNASE III DOMAIN OF HUMAN DICER | 3.1.26.3 |
2EBJ | CRYSTAL STRUCTURE OF PYRROLIDONE CARBOXYL PEPTIDASE FROM THERMUS THERMOPHILUS | 3.4.19.3 |
2EBN | CRYSTAL STRUCTURE OF ENDO-BETA-N-ACETYLGLUCOSAMINIDASE F1, AN ALPHA(SLASH)BETA-BARREL ENZYME ADAPTED FOR A COMPLEX SUBSTRATE | 3.2.1.96 |
2EBS | CRYSTAL STRUCTURE ANAALYSIS OF OLIGOXYLOGLUCAN REDUCING-END-SPECIFIC CELLOBIOHYDROLASE (OXG-RCBH) D465N MUTANT COMPLEXED WITH A XYLOGLUCAN HEPTASACCHARIDE | 3.2.1.150 |
2EC0 | RNA-DEPENDENT RNA POLYMERASE OF FOOT-AND-MOUTH DISEASE VIRUS IN COMPLEX WITH A TEMPLATE-PRIMER RNA AND ATP | 2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15 |
2EC9 | CRYSTAL STRUCTURE ANALYSIS OF HUMAN FACTOR VIIA , SOULUBLE TISSUE FACTOR COMPLEXED WITH BCX-3607 | 3.4.21.21 |
2ECF | CRYSTAL STRUCTURE OF DIPEPTIDYL AMINOPEPTIDASE IV FROM STENOTROPHOMONAS MALTOPHILIA | 3.4.14.5 |
2EDA | CRYSTALLOGRAPHIC AND FLUORESCENCE STUDIES OF THE INTERACTION OF HALOALKANE DEHALOGENASE WITH HALIDE IONS: STUDIES WITH HALIDE COMPOUNDS REVEAL A HALIDE BINDING SITE IN THE ACTIVE SITE | 3.8.1.5 |
2EDC | CRYSTALLOGRAPHIC AND FLUORESCENCE STUDIES OF THE INTERACTION OF HALOALKANE DEHALOGENASE WITH HALIDE IONS: STUDIES WITH HALIDE COMPOUNDS REVEAL A HALIDE BINDING SITE IN THE ACTIVE SITE | 3.8.1.5 |
2EDX | SOLUTION STRUCTURES OF THE FN3 DOMAIN OF HUMAN RECEPTOR-TYPE TYROSINE-PROTEIN PHOSPHATASE F | 3.1.3.48 |
2EDY | SOLUTION STRUCTURES OF THE FN3 DOMAIN OF HUMAN RECEPTOR-TYPE TYROSINE-PROTEIN PHOSPHATASE F | 3.1.3.48 |
2EE1 | SOLUTION STRUCTURES OF THE CHROMO DOMAIN OF HUMAN CHROMODOMAIN HELICASE-DNA-BINDING PROTEIN 4 | 3.6.1 3.6.4.12 |
2EE4 | SOLUTION STRUCTURE OF THE RHOGAP DOMAIN FROM HUMAN RHO GTPASE ACTIVATING PROTEIN 5 VARIANT | 3.6.5.2 |
2EE5 | SOLUTION STRUCTURE OF THE N-TERUMINUS EXTENDED RHOGAP DOMAIN FROM HUMAN RHO GTPASE ACTIVATING PROTEIN 5 VARIANT | 3.6.5.2 |
2EEE | SOLUTION STRUCTURE OF THE A1PP DOMAIN FROM HUMAN PROTEIN C6ORF130 | 3.5.1 3.2.2 |
2EEK | CRYSTAL STRUCTURE OF ATLANTIC COD TRYPSIN COMPLEXED WITH BENZAMIDINE | 3.4.21.4 |
2EEP | PROLYL TRIPEPTIDYL AMINOPEPTIDASE COMPLEXED WITH AN INHIBITOR | 3.4.14 3.4.14.12 |
2EEX | CRYSTAL STRUCTURE OF CEL44A, GH FAMILY 44 ENDOGLUCANASE FROM CLOSTRIDIUM THERMOCELLUM | 3.2.1.4 3.2.1.151 |
2EF1 | CRYSTAL STRUCTURE OF THE EXTRACELLULAR DOMAIN OF HUMAN CD38 | 3.2.2.5 3.2.2.6 2.4.99.20 |
2EF4 | CRYSTAL STRUCTURE OF THE ARGINASE FROM THERMUS THERMOPHILUS | 3.5.3.1 |
2EF5 | CRYSTAL STRUCTURE OF THE ARGINASE FROM THERMUS THERMOPHILUS | 3.5.3.1 |
2EG6 | THE CRYSTAL STRUCTURE OF THE LIGAND-FREE DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2EG7 | THE CRYSTAL STRUCTURE OF E. COLI DIHYDROOROTASE COMPLEXED WITH HDDP | 3.5.2.3 |
2EG8 | THE CRYSTAL STRUCTURE OF E. COLI DIHYDROOROTASE COMPLEXED WITH 5-FLUOROOROTIC ACID | 3.5.2.3 |
2EG9 | CRYSTAL STRUCTURE OF THE TRUNCATED EXTRACELLULAR DOMAIN OF MOUSE CD38 | 3.2.2.5 3.2.2.6 2.4.99.20 |
2EGI | CRYSTAL STRUCTURE OF A HYPOTHETICAL PROTEIN(AQ1494) FROM AQUIFEX AEOLICUS | 3.1 |
2EGJ | CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN(AQ1494) FROM AQUIFEX AEOLICUS | 3.1 |
2EGR | CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN(AQ1494) FROM AQUIFEX AEOLICUS | 3.1 |
2EHG | CRYSTAL STRUCTURE OF HYPERTHERMOPHILIC ARCHAEAL RNASE HI | 3.1.26.4 |
2EI6 | FACTOR XA IN COMPLEX WITH THE INHIBITOR (-)-CIS-N1-[(5-CHLOROINDOL-2-YL)CARBONYL]-N2-[(5-METHYL-4,5,6,7-TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL)CARBONYL]-1,2-CYCLOHEXANEDIAMINE | 3.4.21.6 |
2EI7 | FACTOR XA IN COMPLEX WITH THE INHIBITOR TRANS-N1-[(5-CHLOROINDOL-2-YL)CARBONYL]-N2-[(5-METHYL-4,5,6,7-TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL)CARBONYL]-1,2-CYCLOHEXANEDIAMINE | 3.4.21.6 |
2EI8 | FACTOR XA IN COMPLEX WITH THE INHIBITOR (1S,2R,4S)-N1-[(5-CHLOROINDOL-2-YL)CARBONYL]-4-(N,N-DIMETHYLCARBAMOYL)-N2-[(5-METHYL-4,5,6,7-TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL)CARBONYL]-1,2-CYCLOHEXANEDIAMINE | 3.4.21.6 |
2EIP | INORGANIC PYROPHOSPHATASE | 3.6.1.1 |
2EJ1 | CRYSTAL STRUCTURE OF CEL44A, GH FAMILY 44 ENDOGLUCANASE FROM CLOSTRIDIUM THERMOCELLUM | 3.2.1.4 3.2.1.151 |
2EKI | SOLUTION STRUCTURES OF THE TGS DOMAIN OF HUMAN DEVELOPMENTALLY-REGULATED GTP-BINDING PROTEIN 1 | 3.6.5 |
2ENB | CRYSTAL STRUCTURES OF THE BINARY CA2+ AND PDTP COMPLEXES AND THE TERNARY COMPLEX OF THE ASP 21->GLU MUTANT OF STAPHYLOCOCCAL NUCLEASE. IMPLICATIONS FOR CATALYSIS AND LIGAND BINDING | 3.1.31.1 |
2END | CRYSTAL STRUCTURE OF A PYRIMIDINE DIMER SPECIFIC EXCISION REPAIR ENZYME FROM BACTERIOPHAGE T4: REFINEMENT AT 1.45 ANGSTROMS AND X-RAY ANALYSIS OF THE THREE ACTIVE SITE MUTANTS | 3.1.25.1 3.2.2.17 4.2.99.18 |
2ENG | ENDOGLUCANASE V | 3.2.1.4 |
2ENU | MUTANT L121M STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2ENW | MUTANT Y92H STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2ENX | STRUCTURE OF THE FAMILY II INORGANIC PYROPHOSPHATASE FROM STREPTOCOCCUS AGALACTIAE AT 2.8 RESOLUTION | 3.6.1.1 |
2EO0 | CRYSTAL STRUCTURE OF HOLLIDAY JUNCTION RESOLVASE ST1444 | 3.1.22.4 |
2EO7 | CRYSTAL STRUCTURE OF CEL44A, GH FAMILY 44 ENDOGLUCANASE FROM CLOSTRIDIUM THERMOCELLUM | 3.2.1.4 3.2.1.151 |
2EO8 | CRYSTAL STRUCTURE OF A MUTANT PYRROLIDONE CARBOXYL PEPTIDASE (A199P) FROM P. FURIOSUS | 3.4.19.3 |
2EOA | STRUCTURAL STUDY OF PROJECT ID TTHB049 FROM THERMUS THERMOPHILUS HB8 (W85H) | 3.1.3.73 |
2EOB | SOLUTION STRUCTURE OF THE SECOND SH2 DOMAIN FROM RAT PLC GAMMA-2 | 3.1.4.11 |
2EPB | SOLUTION STRUCTURE OF CHROMO DOMAIN 2 IN CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 6 | 3.6.1 3.6.4.12 |
2EPE | CRYSTAL STRUCTURE ANALYSIS OF HEN EGG WHITE LYSOZYME GROWN BY CAPILLARY METHOD | 3.2.1.17 |
2EPK | N-ACETYL-B-D-GLUCOSAMINIDASE (GCNA) FROM STREPTOCOCCUS GORDONII | 3.2.1.52 |
2EPL | N-ACETYL-B-D-GLUCOSAMINIDASE (GCNA) FROM STREPTOCOCCUS GORDONII | 3.2.1.52 |
2EPM | N-ACETYL-B-D-GLUCOASMINIDASE (GCNA) FROM STRETOCOCCUS GORDONII | 3.2.1.52 |
2EPN | N-ACETYL-B-D-GLUCOSAMINIDASE (GCNA) FROM STREPTOCOCCUS GORDONII | 3.2.1.52 |
2EPO | N-ACETYL-B-D-GLUCOSAMINIDASE (GCNA) FROM STREPTOCOCCUS GORDONII | 3.2.1.52 |
2EQD | CRYSTAL STRUCTURE OF CEL44A, GH FAMILY 44 ENDOGLUCANASE FROM CLOSTRIDIUM THERMOCELLUM | 3.2.1.4 3.2.1.151 |
2EQE | SOLUTION STRUCTURE OF THE FOURTH A20-TYPE ZINC FINGER DOMAIN FROM HUMAN TUMOR NECROSIS FACTOR, ALPHA-INDUCED PROTEIN3 | 3 2.3.2 3.4.19.12 |
2EQF | SOLUTION STRUCTURE OF THE 7TH A20-TYPE ZINC FINGER DOMAIN FROM HUMAN TUMOR NECROSIS FACTOR, ALPHA-INDUCED PROTEIN3 | 3 2.3.2 3.4.19.12 |
2EQG | SOLUTION STRUCTURE OF THE FIRST A20-TYPE ZINC FINGER DOMAIN FROM HUMAN TUMOR NECROSIS FACTOR, ALPHA-INDUCED PROTEIN3 | 3 2.3.2 3.4.19.12 |
2EQI | SOLUTION STRUCTURE OF THE SH3 DOMAIN FROM PHOSPHOLIPASE C, GAMMA 2 | 3.1.4.11 |
2EQL | CRYSTALLOGRAPHIC STUDIES OF A CALCIUM BINDING LYSOZYME FROM EQUINE MILK AT 2.5 ANGSTROMS RESOLUTION | 3.2.1.17 |
2EQS | SOLUTION STRUCTURE OF THE S1 RNA BINDING DOMAIN OF HUMAN ATP-DEPENDENT RNA HELICASE DHX8 | 3.6.1 3.6.4.13 |
2ER0 | X-RAY STUDIES OF ASPARTIC PROTEINASE-STATINE INHIBITOR COMPLEXES | 3.4.23.6 3.4.23.22 |
2ER6 | THE STRUCTURE OF A SYNTHETIC PEPSIN INHIBITOR COMPLEXED WITH ENDOTHIAPEPSIN. | 3.4.23.6 3.4.23.22 |
2ER7 | X-RAY ANALYSES OF ASPARTIC PROTEINASES.III. THREE-DIMENSIONAL STRUCTURE OF ENDOTHIAPEPSIN COMPLEXED WITH A TRANSITION-STATE ISOSTERE INHIBITOR OF RENIN AT 1.6 ANGSTROMS RESOLUTION | 3.4.23.6 3.4.23.22 |
2ER9 | X-RAY STUDIES OF ASPARTIC PROTEINASE-STATINE INHIBITOR COMPLEXES. | 3.4.23.6 3.4.23.22 |
2ERO | CRYSTAL STRUCTURE OF VASCULAR APOPTOSIS-INDUCING PROTEIN-1(ORTHORHOMBIC CRYSTAL FORM) | 3.4.24 |
2ERP | CRYSTAL STRUCTURE OF VASCULAR APOPTOSIS-INDUCING PROTEIN-1(INHIBITOR-BOUND FORM) | 3.4.24 |
2ERQ | CRYSTAL STRUCTURE OF VASCULAR APOPTOSIS-INDUCING PROTEIN-1(TETRAGONAL CRYSTAL FORM) | 3.4.24 |
2ERV | CRYSTAL STRUCTURE OF THE OUTER MEMBRANE ENZYME PAGL | 3.1.1.77 |
2ERY | THE CRYSTAL STRUCTURE OF THE RAS RELATED PROTEIN RRAS2 (RRAS2) IN THE GDP BOUND STATE | 3.6.5 |
2ES4 | CRYSTAL STRUCTURE OF THE BURKHOLDERIA GLUMAE LIPASE-SPECIFIC FOLDASE IN COMPLEX WITH ITS COGNATE LIPASE | 3.1.1.3 |
2ESB | CRYSTAL STRUCTURE OF HUMAN DUSP18 | 3.1.3.48 3.1.3.16 |
2EST | CRYSTALLOGRAPHIC STUDY OF THE BINDING OF A TRIFLUOROACETYL DIPEPTIDE ANILIDE INHIBITOR WITH ELASTASE | 3.4.21.36 |
2ETF | CRYSTAL STRUCTURE OF FULL LENGTH BOTULINUM NEUROTOXIN (TYPE B) LIGHT CHAIN | 3.4.24.69 |
2ETJ | CRYSTAL STRUCTURE OF RIBONUCLEASE HII (EC 3.1.26.4) (RNASE HII) (TM0915) FROM THERMOTOGA MARITIMA AT 1.74 A RESOLUTION | 3.1.26.4 |
2ETL | CRYSTAL STRUCTURE OF UBIQUITIN CARBOXY-TERMINAL HYDROLASE L1 (UCH-L1) | 3.4.19.12 6 |
2EUG | CRYSTAL STRUCTURE OF ESCHERICHIA COLI URACIL DNA GLYCOSYLASE AND ITS COMPLEXES WITH URACIL AND GLYCEROL: STRUCTURE AND GLYCOSYLASE MECHANISM REVISITED | 3.2.2.3 3.2.2.27 |
2EVC | CRYSTAL STRUCTURE OF E. COLI. METHIONINE AMINO PEPTIDASE IN COMPLEX WITH 5-(2-(TRIFLUOROMETHYL)PHENYL)FURAN-2-CARBOXYLIC ACID | 3.4.11.18 |
2EVM | CRYSTAL STRUCTURE OF METHIONINE AMINOPEPTIDASE IN COMPLEX WITH 5-(2,5-DICHLOROPHENYL)FURAN-2-CARBOXYLIC ACID | 3.4.11.18 |
2EVO | CRYSTAL STRUCTURE OF METHIONINE AMINO PEPTIDASE IN COMPLEX WITH N-CYCLOPENTYL-N-(THIAZOL-2-YL)OXALAMIDE | 3.4.11.18 |
2EVW | CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH R-CAGED GTP | 3.6.5.2 |
2EW5 | STRUCTURE OF HELICOBACTER PYLORI PEPTIDE DEFORMYLASE IN COMPLEX WITH INHIBITOR | 3.5.1.88 |
2EW7 | CRYSTAL STRUCTURE OF HELICOBACTER PYLORI PEPTIDE DEFORMYLASE | 3.5.1.88 |
2EW9 | SOLUTION STRUCTURE OF APOWLN5-6 | 3.6.3.4 7.2.2.8 |
2EWB | THE CRYSTAL STRUCTURE OF BOVINE LENS LEUCINE AMINOPEPTIDASE IN COMPLEX WITH ZOFENOPRILAT | 3.4.11.1 3.4.13.23 3.4.11.5 |
2EWY | CRYSTAL STRUCTURE OF HUMAN BACE2 IN COMPLEX WITH A HYDROXYETHYLENAMINE TRANSITION-STATE INHIBITOR | 3.4.23.45 |
2EX2 | CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM ESCHERICHIA COLI | 3.4.16.4 3.4.99 3.4.21 |
2EX5 | GROUP I INTRON-ENCODED HOMING ENDONUCLEASE I-CEUI COMPLEXED WITH DNA | 3.1 |
2EX6 | CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM ESCHERICHIA COLI, COMPLEXED WITH AMPICILLIN | 3.4.16.4 3.4.99 3.4.21 |
2EX8 | CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM ESCHERICHIA COLI, COMPLEXED WITH PENICILLIN-G | 3.4.16.4 3.4.99 3.4.21 |
2EX9 | CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM ESCHERICHIA COLI, COMPLEXED WITH PENICILLIN-V | 3.4.16.4 3.4.99 3.4.21 |
2EXA | CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM ESCHERICHIA COLI, COMPLEXED WITH FAROM | 3.4.16.4 3.4.99 3.4.21 |
2EXB | CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM ESCHERICHIA COLI, COMPLEXED WITH FLOMOX | 3.4.16.4 3.4.99 3.4.21 |
2EXH | STRUCTURE OF THE FAMILY43 BETA-XYLOSIDASE FROM GEOBACILLUS STEAROTHERMOPHILUS | 3.2.1.37 |
2EXI | STRUCTURE OF THE FAMILY43 BETA-XYLOSIDASE D15G MUTANT FROM GEOBACILLUS STEAROTHERMOPHILUS | 3.2.1.37 |
2EXJ | STRUCTURE OF THE FAMILY43 BETA-XYLOSIDASE D128G MUTANT FROM GEOBACILLUS STEAROTHERMOPHILUS IN COMPLEX WITH XYLOBIOSE | 3.2.1.37 |
2EXK | STRUCTURE OF THE FAMILY43 BETA-XYLOSIDASE E187G FROM GEOBACILLUS STEAROTHERMOPHILUS IN COMPLEX WITH XYLOBIOSE | 3.2.1.37 |
2EXO | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF THE BETA-1,4-GLYCANASE CEX FROM CELLULOMONAS FIMI | 3.2.1.91 3.2.1.8 |
2EXZ | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T22C | 3.1.31.1 |
2EY1 | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T22V | 3.1.31.1 |
2EY2 | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T41C | 3.1.31.1 |
2EY5 | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T41S | 3.1.31.1 |
2EY6 | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T41V | 3.1.31.1 |
2EYF | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T44V | 3.1.31.1 |
2EYH | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T62S | 3.1.31.1 |
2EYJ | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T62V | 3.1.31.1 |
2EYL | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T82S | 3.1.31.1 |
2EYM | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T120C | 3.1.31.1 |
2EYO | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T120S | 3.1.31.1 |
2EYP | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT T120V | 3.1.31.1 |
2EYQ | CRYSTAL STRUCTURE OF ESCHERICHIA COLI TRANSCRIPTION-REPAIR COUPLING FACTOR | 3.6.4 |
2EZ6 | CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS RNASE III (D44N) COMPLEXED WITH PRODUCT OF DOUBLE-STRANDED RNA PROCESSING | 3.1.26.3 |
2EZH | SOLUTION NMR STRUCTURE OF THE IGAMMA SUBDOMAIN OF THE MU END DNA BINDING DOMAIN OF MU PHAGE TRANSPOSASE, MINIMIZED AVERAGE STRUCTURE | 3.1.22 6.5.1 |
2EZI | SOLUTION NMR STRUCTURE OF THE IGAMMA SUBDOMAIN OF THE MU END DNA BINDING DOMAIN OF MU PHAGE TRANSPOSASE, 30 STRUCTURES | 3.1.22 6.5.1 |
2EZK | SOLUTION NMR STRUCTURE OF THE IBETA SUBDOMAIN OF THE MU END DNA BINDING DOMAIN OF PHAGE MU TRANSPOSASE, REGULARIZED MEAN STRUCTURE | 3.1.22 6.5.1 |
2EZL | SOLUTION NMR STRUCTURE OF THE IBETA SUBDOMAIN OF THE MU END DNA BINDING DOMAIN OF PHAGE MU TRANSPOSASE, 29 STRUCTURES | 3.1.22 6.5.1 |
2F03 | CRYSTAL STRUCTURE OF TETRAMERIC RESTRICTION ENDONUCLEASE SFII IN COMPLEX WITH COGNATE DNA (PARTIAL BOUND FORM) | 3.1.21.4 |
2F0D | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT I92V | 3.1.31.1 |
2F0E | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V23L | 3.1.31.1 |
2F0F | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT L25I | 3.1.31.1 |
2F0G | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66I | 3.1.31.1 |
2F0H | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66L | 3.1.31.1 |
2F0I | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT I72L | 3.1.31.1 |
2F0J | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT I72V | 3.1.31.1 |
2F0K | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V23I/L25I | 3.1.31.1 |
2F0L | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V23L/I72L | 3.1.31.1 |
2F0M | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V23L/I72V | 3.1.31.1 |
2F0N | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT L25I/I72L | 3.1.31.1 |
2F0O | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66I/I72V | 3.1.31.1 |
2F0P | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66I/V99I | 3.1.31.1 |
2F0Q | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66L/I92L | 3.1.31.1 |
2F0S | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66L/I92V | 3.1.31.1 |
2F0T | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66L/V99I | 3.1.31.1 |
2F0U | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V23I/L25I/I72V | 3.1.31.1 |
2F0V | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V23L/V66L/I72L | 3.1.31.1 |
2F0W | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V23I/L25I/V66L/I72L | 3.1.31.1 |
2F0Z | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 IN COMPLEX WITH ZANAMIVIR INHIBITOR | 3.2.1.18 |
2F10 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 IN COMPLEX WITH PERAMIVIR INHIBITOR | 3.2.1.18 |
2F11 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 IN COMPLEX WITH ISOBUTYL ETHER MIMETIC INHIBITOR | 3.2.1.18 |
2F12 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 IN COMPLEX WITH 3- HYDROXYPROPYL ETHER MIMETIC INHIBITOR | 3.2.1.18 |
2F13 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 IN COMPLEX WITH 2',3'- DIHYDROXYPROPYL ETHER MIMETIC INHIBITOR | 3.2.1.18 |
2F18 | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH (2R,3R,4S)-2-({[(1R)-2-HYDROXY-1-PHENYLETHYL]AMINO}METHYL)PYRROLIDINE-3,4-DIOL | 3.2.1.114 |
2F1A | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH (2R,3R,4S)-2-({[(1S)-2-HYDROXY-1-PHENYLETHYL]AMINO}METHYL)PYRROLIDINE-3,4-DIOL | 3.2.1.114 |
2F1B | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH (2R,3R,4S,5R)-2-({[(1R)-2-HYDROXY-1-PHENYLETHYL]AMINO}METHYL)-5-METHYLPYRROLIDINE-3,4-DIOL | 3.2.1.114 |
2F1G | CATHEPSIN S IN COMPLEX WITH NON-COVALENT 2-(BENZOXAZOL-2-YLAMINO)-ACETAMIDE | 3.4.22.27 |
2F1N | STRUCTURE OF CDTB, THE BIOLOGICALLY ACTIVE SUBUNIT OF CYTOLETHAL DISTENDING TOXIN | 3.1 |
2F1W | CRYSTAL STRUCTURE OF THE TRAF-LIKE DOMAIN OF HAUSP/USP7 | 3.1.2.15 3.4.19.12 |
2F1X | CRYSTAL STRUCTURE OF THE TRAF-LIKE DOMAIN OF HAUSP/USP7 BOUND TO A P53 PEPTIDE | 3.4.19.12 |
2F1Y | CRYSTAL STRUCTURE OF THE TRAF-LIKE DOMAIN OF HAUSP/USP7 BOUND TO A MDM2 PEPTIDE | 3.4.19.12 |
2F1Z | CRYSTAL STRUCTURE OF HAUSP | 3.1.2.15 3.4.19.12 |
2F20 | X-RAY CRYSTAL STRUCTURE OF PROTEIN BT_1218 FROM BACTEROIDES THETAIOTAOMICRON. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET BTR8. | 3.4 |
2F24 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 E111Q MUTANT | 3.2.1.18 |
2F25 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 E111Q MUTANT IN COMPLEX WITH DANA INHIBITOR | 3.2.1.18 |
2F26 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 E111Q-Q112E DOUBLE MUTANT | 3.2.1.18 |
2F27 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 E111Q-Q112E DOUBLE MUTANT IN COMPLEX WITH DANA INHIBITOR | 3.2.1.18 |
2F28 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 Q116E MUTANT | 3.2.1.18 |
2F29 | CRYSTAL STRUCTURE OF THE HUMAN SIALIDASE NEU2 Q116E MUTANT IN COMPLEX WITH DANA INHIBITOR | 3.2.1.18 |
2F2G | X-RAY STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT3G16990 | 3.5.1 3.5.99.2 |
2F2N | TRICLINIC HEN EGG LYSOZYME CROSS-LINKED BY GLUTARALDEHYDE | 3.2.1.17 |
2F2O | STRUCTURE OF CALMODULIN BOUND TO A CALCINEURIN PEPTIDE: A NEW WAY OF MAKING AN OLD BINDING MODE | 3.1.3.16 |
2F2P | STRUCTURE OF CALMODULIN BOUND TO A CALCINEURIN PEPTIDE: A NEW WAY OF MAKING AN OLD BINDING MODE | 3.1.3.16 |
2F2Q | HIGH RESOLUTION CRYSTAL STRUCTURE OF T4 LYSOZYME MUTANT L20R63/A LIGANDED TO GUANIDINIUM ION | 3.2.1.17 |
2F30 | TRICLINIC CROSS-LINKED LYSOZYME SOAKED WITH 4.5M UREA | 3.2.1.17 |
2F32 | XRAY CRYSTAL STRUCTURE OF LYSOZYME MUTANT L20/R63A LIGANDED TO ETHYLGUANIDINIUM | 3.2.1.17 |
2F3B | MECHANISM OF DISPLACEMENT OF A CATALYTICALLY ESSENTIAL LOOP FROM THE ACTIVE SITE OF FRUCTOSE-1,6-BISPHOSPHATASE | 3.1.3.11 |
2F3C | CRYSTAL STRUCTURE OF INFESTIN 1, A KAZAL-TYPE SERINEPROTEASE INHIBITOR, IN COMPLEX WITH TRYPSIN | 3.4.21.4 |
2F3D | MECHANISM OF DISPLACEMENT OF A CATALYTICALLY ESSENTIAL LOOP FROM THE ACTIVE SITE OF FRUCTOSE-1,6-BISPHOSPHATASE | 3.1.3.11 |
2F3E | CRYSTAL STRUCTURE OF THE BACE COMPLEX WITH AXQ093, A MACROCYCLIC INHIBITOR | 3.4.23.46 |
2F3F | CRYSTAL STRUCTURE OF THE BACE COMPLEX WITH BDF488, A MACROCYCLIC INHIBITOR | 3.4.23.46 |
2F3K | SUBSTRATE ENVELOPE AND DRUG RESISTANCE: CRYSTAL STRUCTURE OF R01 IN COMPLEX WITH WILD-TYPE HIV-1 PROTEASE | 3.4.23.16 |
2F3V | SOLUTION STRUCTURE OF 1-110 FRAGMENT OF STAPHYLOCOCCAL NUCLEASE WITH V66W MUTATION | 3.1.31.1 |
2F3W | SOLUTION STRUCTURE OF 1-110 FRAGMENT OF STAPHYLOCOCCAL NUCLEASE IN 2M TMAO | 3.1.31.1 |
2F43 | RAT LIVER F1-ATPASE | 3.6.3.14 |
2F47 | XRAY CRYSTAL STRUCTURE OF T4 LYSOZYME MUTANT L20/R63A LIGANDED TO METHYLGUANIDINIUM | 3.2.1.17 |
2F4A | TRICLINIC CROSS-LINKED LYSOZYME SOAKED WITH THIOUREA 1.5M | 3.2.1.17 |
2F4G | TRICLINIC CROSS-LINKED LYSOZYME SOAKED IN BROMOETHANOL 1M | 3.2.1.17 |
2F4M | THE MOUSE PNGASE-HR23 COMPLEX REVEALS A COMPLETE REMODULATION OF THE PROTEIN-PROTEIN INTERFACE COMPARED TO ITS YEAST ORTHOLOGS | 3.5.1.52 |
2F4O | THE MOUSE PNGASE-HR23 COMPLEX REVEALS A COMPLETE REMODULATION OF THE PROTEIN-PROTEIN INTERFACE COMPARED TO ITS YEAST ORTHOLOGS | 3.5.1.52 |
2F4Y | BARNASE CROSS-LINKED WITH GLUTARALDEHYDE | 3.1.27 |
2F55 | TWO HEPATITIS C VIRUS NS3 HELICASE DOMAINS COMPLEXED WITH THE SAME STRAND OF DNA | 3.6.1 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2F56 | BARNASE CROSS-LINKED WITH GLUTARALDEHYDE SOAKED IN 6M UREA | 3.1.27 |
2F5M | CROSS-LINKED BARNASE SOAKED IN BROMO-ETHANOL | 3.1.27 |
2F5N | MUTM CROSSLINKED TO UNDAMAGED DNA SAMPLING A:T BASE PAIR IC1 | 3.2.2.23 4.2.99.18 |
2F5O | MUTM CROSSLINKED TO UNDAMAGED DNA SAMPLING G:C BASE PAIR IC3 | 3.2.2.23 4.2.99.18 |
2F5P | MUTM CROSSLINKED TO UNDAMAGED DNA SAMPLING A:T BASE PAIR IC2 | 3.2.2.23 4.2.99.18 |
2F5Q | CATALYTICALLY INACTIVE (E3Q) MUTM CROSSLINKED TO OXOG:C CONTAINING DNA CC2 | 3.2.2.23 4.2.99.18 |
2F5S | CATALYTICALLY INACTIVE (E3Q) MUTM CROSSLINKED TO OXOG:C CONTAINING DNA CC1 | 3.2.2.23 4.2.99.18 |
2F5W | CROSS-LINKED BARNASE SOAKED IN 3 M THIOUREA | 3.1.27 |
2F61 | CRYSTAL STRUCTURE OF PARTIALLY DEGLYCOSYLATED ACID BETA-GLUCOSIDASE | 3.2.1.45 2.4.1 3.2.1 |
2F6B | STRUCTURAL AND ACTIVE SITE MODIFICATION STUDIES IMPLICATE GLU, TRP AND ARG IN THE ACTIVITY OF XYLANASE FROM ALKALOPHILIC BACILLUS SP. (NCL 87-6-10). | 3.2.1.8 |
2F6D | STRUCTURE OF THE COMPLEX OF A GLUCOAMYLASE FROM SACCHAROMYCOPSIS FIBULIGERA WITH ACARBOSE | 3.2.1.3 |
2F6E | CLOSTRIDIUM DIFFICILE TOXIN A C-TERMINAL FRAGMENT 1 (TCDA-F1) | 3.4.22 2.4.1 |
2F6F | THE STRUCTURE OF THE S295F MUTANT OF HUMAN PTP1B | 3.1.3.48 |
2F6I | CRYSTAL STRUCTURE OF THE CLPP PROTEASE CATALYTIC DOMAIN FROM PLASMODIUM FALCIPARUM | 3.4.21.92 |
2F6T | PROTEIN TYROSINE PHOSPHATASE 1B WITH SULFAMIC ACID INHIBITORS | 3.1.3.48 |
2F6V | PROTEIN TYROSINE PHOSPHATASE 1B WITH SULFAMIC ACID INHIBITORS | 3.1.3.48 |
2F6W | PROTEIN TYROSINE PHOSPHATASE 1B WITH SULFAMIC ACID INHIBITORS | 3.1.3.48 |
2F6Y | PROTEIN TYROSINE PHOSPHATASE 1B WITH SULFAMIC ACID INHIBITORS | 3.1.3.48 |
2F6Z | PROTEIN TYROSINE PHOSPHATASE 1B WITH SULFAMIC ACID INHIBITORS | 3.1.3.48 |
2F70 | PROTEIN TYROSINE PHOSPHATASE 1B WITH SULFAMIC ACID INHIBITORS | 3.1.3.48 |
2F71 | PROTEIN TYROSINE PHOSPHATASE 1B WITH SULFAMIC ACID INHIBITORS | 3.1.3.48 |
2F7D | A MUTANT RABBIT CATHEPSIN K WITH A NITRILE INHIBITOR | 3.4.22.38 |
2F7O | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH MANNOSTATIN A | 3.2.1.114 |
2F7P | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH BENZYL-MANNOSTATIN A | 3.2.1.114 |
2F7Q | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH AMINOCYCLOPENTITETROL | 3.2.1.114 |
2F7R | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH BENZYL-AMINOCYCLOPENTITETROL | 3.2.1.114 |
2F7S | THE CRYSTAL STRUCTURE OF HUMAN RAB27B BOUND TO GDP | 3.6.5.2 |
2F7T | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF MOS1 MARINER TRANSPOSASE | 3.1 |
2F7V | STRUCTURE OF ACETYLCITRULLINE DEACETYLASE COMPLEXED WITH ONE CO | 3.5.1.16 3.5.1 |
2F80 | HIV-1 PROTEASE MUTANT D30N COMPLEXED WITH INHIBITOR TMC114 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2F81 | HIV-1 PROTEASE MUTANT L90M COMPLEXED WITH INHIBITOR TMC114 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2F83 | CRYSTAL STRUCTURE AT 2.9 ANGSTROMS RESOLUTION OF HUMAN PLASMA COAGULATION FACTOR XI ZYMOGEN | 3.4.21.27 |
2F8G | HIV-1 PROTEASE MUTANT I50V COMPLEXED WITH INHIBITOR TMC114 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2F8H | STRUCTURE OF ACETYLCITRULLINE DEACETYLASE FROM XANTHOMONAS CAMPESTRIS IN METAL-FREE FORM | 3.5.1.16 3.5.1 |
2F8Q | AN ALKALI THERMOSTABLE F/10 XYLANASE FROM ALKALOPHILIC BACILLUS SP. NG-27 | 3.2.1.8 |
2F90 | CRYSTAL STRUCTURE OF BISPHOSPHOGLYCERATE MUTASE IN COMPLEX WITH 3-PHOSPHOGLYCERATE AND ALF4- | 5.4.2.4 5.4.2.1 3.1.3.13 5.4.2.11 |
2F91 | 1.2A RESOLUTION STRUCTURE OF A CRAYFISH TRYPSIN COMPLEXED WITH A PEPTIDE INHIBITOR, SGTI | 3.4.21.4 |
2F96 | 2.1 A CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA RNASE T (RIBONUCLEASE T) | 3.1.13 |
2F9B | DISCOVERY OF NOVEL HETEROCYCLIC FACTOR VIIA INHIBITORS | 3.4.21.21 |
2F9L | 3D STRUCTURE OF INACTIVE HUMAN RAB11B GTPASE | 3.6.5.2 |
2F9M | 3D STRUCTURE OF ACTIVE HUMAN RAB11B GTPASE | 3.6.5.2 |
2F9N | CRYSTAL STRUCTURE OF THE RECOMBINANT HUMAN ALPHA I TRYPTASE MUTANT K192Q/D216G IN COMPLEX WITH LEUPEPTIN | 3.4.21.59 |
2F9O | CRYSTAL STRUCTURE OF THE RECOMBINANT HUMAN ALPHA I TRYPTASE MUTANT D216G | 3.4.21.59 |
2F9P | CRYSTAL STRUCTURE OF THE RECOMBINANT HUMAN ALPHA I TRYPTASE MUTANT D216G IN COMPLEX WITH LEUPEPTIN | 3.4.21.59 |
2F9V | HCV NS3 PROTEASE DOMAIN WITH NS4A PEPTIDE AND A KETOAMIDE INHIBITOR WITH P1 AND P2 CYCLOPROPYLALANNINES | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2F9Z | COMPLEX BETWEEN THE CHEMOTAXIS DEAMIDASE CHED AND THE CHEMOTAXIS PHOSPHATASE CHEC FROM THERMOTOGA MARITIMA | 3 |
2FA7 | CRYSTAL STRUCTURE OF THE COMPLEX OF BOVINE LACTOFERRIN C-LOBE WITH A PENTASACCHARIDE AT 2.38 A RESOLUTION | 3.4.21 |
2FAV | CRYSTAL STRUCTURE OF SARS MACRO DOMAIN IN COMPLEX WITH ADP-RIBOSE AT 1.8 A RESOLUTION | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2FBA | GLUCOAMYLASE FROM SACCHAROMYCOPSIS FIBULIGERA AT ATOMIC RESOLUTION | 3.2.1.3 |
2FBB | CRYSTAL STRUCTURE ANALYSIS OF HEXAGONAL LYSOZYME | 3.2.1.17 |
2FBD | THE CRYSTALLOGRAPHIC STRUCTURE OF THE DIGESTIVE LYSOZYME 1 FROM MUSCA DOMESTICA AT 1.90 ANG. | 3.2.1.17 |
2FBL | THE CRYSTAL STRUCTURE OF THE HYPOTHETICAL PROTEIN NE1496 | 3.6.1.25 |
2FBO | CRYSTAL STRUCTURE OF THE TWO TANDEM V-TYPE REGIONS OF VCBP3 (V-REGION-CONTAINING CHITIN BINDING PROTEIN) TO 1.85 A | 3.2.1.14 |
2FBP | STRUCTURE REFINEMENT OF FRUCTOSE-1,6-BISPHOSPHATASE AND ITS FRUCTOSE 2,6-BISPHOSPHATE COMPLEX AT 2.8 ANGSTROMS RESOLUTION | 3.1.3.11 |
2FBT | WRN EXONUCLEASE | 2.7.7 3.6.4.12 3.1 |
2FBV | WRN EXONUCLEASE, MN COMPLEX | 2.7.7 3.6.4.12 3.1 |
2FBX | WRN EXONUCLEASE, MG COMPLEX | 2.7.7 3.6.4.12 3.1 |
2FBY | WRN EXONUCLEASE, EU COMPLEX | 2.7.7 3.6.4.12 3.1 |
2FC0 | WRN EXONUCLEASE, MN DGMP COMPLEX | 2.7.7 3.6.4.12 3.1 |
2FCC | CRYSTAL STRUCTURE OF T4 PYRIMIDINE DIMER GLYCOSYLASE (T4-PDG) COVALENTLY COMPLEXED WITH A DNA SUBSTRATE CONTAINING ABASIC SITE | 3.1.25.1 3.2.2.17 4.2.99.18 |
2FCI | STRUCTURAL BASIS FOR THE REQUIREMENT OF TWO PHOSPHOTYROSINES IN SIGNALING MEDIATED BY SYK TYROSINE KINASE | 3.1.4.11 |
2FCO | CRYSTAL STRUCTURE OF BACILLUS STEAROTHERMOPHILUS PRFA-HOLLIDAY JUNCTION RESOLVASE | 3.1.22.4 |
2FD6 | STRUCTURE OF HUMAN UROKINASE PLASMINOGEN ACTIVATOR IN COMPLEX WITH UROKINASE RECEPTOR AND AN ANTI-UPAR ANTIBODY AT 1.9 A | 3.4.21.73 |
2FDA | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN COAGULATION FACTOR XIA IN COMPLEX WITH ALPHA-KETOTHIAZOLE ARGININE DERIVED LIGAND | 3.4.21.27 |
2FDD | CRYSTAL STRUCTURE OF HIV PROTEASE D545701 BOUND WITH GW0385 | 3.4.23.16 |
2FDE | WILD TYPE HIV PROTEASE BOUND WITH GW0385 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2FDP | CRYSTAL STRUCTURE OF BETA-SECRETASE COMPLEXED WITH AN AMINO-ETHYLENE INHIBITOR | 3.4.23.46 |
2FE1 | CRYSTAL STRUCTURE OF PAE0151 FROM PYROBACULUM AEROPHILUM | 3.1 |
2FE4 | THE CRYSTAL STRUCTURE OF HUMAN NEURONAL RAB6B IN ITS INACTIVE GDP-BOUND FORM | 3.6.1 |
2FE8 | SARS CORONAVIRUS PAPAIN-LIKE PROTEASE: STRUCTURE OF A VIRAL DEUBIQUITINATING ENZYME | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2FEA | CRYSTAL STRUCTURE OF MTNX PHOSPHATASE FROM BACILLUS SUBTILIS AT 2.00 A RESOLUTION | 3.1.3 3.1.3.87 |
2FEB | NMR SOLUTION STRUCTURE, DYNAMICS AND BINDING PROPERTIES OF THE KRINGLE IV TYPE 8 MODULE OF APOLIPOPROTEIN(A) | 3.4.21 |
2FEK | STRUCTURE OF A PROTEIN TYROSINE PHOSPHATASE | 3.1.3.48 |
2FF1 | CRYSTAL STRUCTURE OF TRYPANOSOMA VIVAX NUCLEOSIDE HYDROLASE SOAKED WITH IMMUCILLINH | 3.2.2.1 |
2FF2 | CRYSTAL STRUCTURE OF TRYPANOSOMA VIVAX NUCLEOSIDE HYDROLASE CO-CRYSTALLIZED WITH IMMUCILLINH | 3.2.2.1 |
2FFF | OPEN FORM OF A CLASS A TRANSPEPTIDASE DOMAIN | 2.4.1.129 3.4.16.4 |
2FFI | CRYSTAL STRUCTURE OF PUTATIVE 2-PYRONE-4,6-DICARBOXYLIC ACID HYDROLASE FROM PSEUDOMONAS PUTIDA, NORTHEAST STRUCTURAL GENOMICS TARGET PPR23. | 3.1.1.57 |
2FFJ | CRYSTAL STRUCTURE OF A DUF89 FAMILY PROTEIN (AF1104) FROM ARCHAEOGLOBUS FULGIDUS DSM 4304 AT 2.45 A RESOLUTION | 3.1.3 |
2FFQ | THE CRYSTAL STRUCTURE OF HUMAN NEURONAL RAB6B IN ITS ACTIVE GTPGS-BOUND FORM | 3.6.1 |
2FFY | AMPC BETA-LACTAMASE N289A MUTANT IN COMPLEX WITH A BORONIC ACID DEACYLATION TRANSITION STATE ANALOG COMPOUND SM3 | 3.5.2.6 |
2FFZ | STRUCTURAL STUDIES EXAMINING THE SUBSTRATE SPECIFICITY PROFILES OF PC-PLCBC PROTEIN VARIANTS | 3.1.4.3 |
2FGE | CRYSTAL STRUCTURE OF PRESEQUENCE PROTEASE PREP FROM ARABIDOPSIS THALIANA | 3.4.24 |
2FGL | AN ALKALI THERMOSTABLE F/10 XYLANASE FROM ALKALOPHILIC BACILLUS SP. NG-27 | 3.2.1.8 |
2FGN | STRUCTURAL STUDIES EXAMINING THE SUBSTRATE SPECIFICITY PROFILES OF PC-PLCBC PROTEIN VARIANTS | 3.1.4.3 |
2FGU | X-RAY CRYSTAL STRUCTURE OF HIV-1 PROTEASE T80S VARIANT IN COMPLEX WITH THE INHIBITOR SAQUINAVIR USED TO EXPLORE THE ROLE OF INVARIANT THR80 IN HIV-1 PROTEASE STRUCTURE, FUNCTION, AND VIRAL INFECTIVITY. | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2FGV | X-RAY CRYSTAL STRUCTURE OF HIV-1 PROTEASE T80N VARIANT IN COMPLEX WITH THE INHIBITOR SAQUINAVIR USED TO EXPLORE THE ROLE OF INVARIANT THR80 IN HIV-1 PROTEASE STRUCTURE, FUNCTION, AND VIRAL INFECTIVITY. | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2FGZ | CRYSTAL STRUCTURE ANALYSIS OF APO PULLULANASE FROM KLEBSIELLA PNEUMONIAE | 3.2.1.41 |
2FH6 | CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH GLUCOSE | 3.2.1.41 |
2FH7 | CRYSTAL STRUCTURE OF THE PHOSPHATASE DOMAINS OF HUMAN PTP SIGMA | 3.1.3.48 |
2FH8 | CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH ISOMALTOSE | 3.2.1.41 |
2FHB | CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH MALTOSE | 3.2.1.41 |
2FHF | CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH MALTOTETRAOSE | 3.2.1.41 |
2FHI | SUBSTRATE ANALOG (IB2) COMPLEX WITH THE HIS 96 ASN SUBSTITUTION OF THE FRAGILE HISTIDINE TRIAD PROTEIN, FHIT | 3.6.1.29 |
2FHM | SOLUTION STRUCTURE OF BACILLUS SUBTILIS ACYLPHOSPHATASE | 3.6.1.7 |
2FHR | TRYPANOSOMA RANGELI SIALIDASE IN COMPLEX WITH 2,3- DIFLUOROSIALIC ACID (COVALENT INTERMEDIATE) | 3.2.1.18 |
2FHX | PSEUDOMONAS AERUGINOSA SPM-1 METALLO-BETA-LACTAMASE | 3.5.2.6 |
2FHY | STRUCTURE OF HUMAN LIVER FPBASE COMPLEXED WITH A NOVEL BENZOXAZOLE AS ALLOSTERIC INHIBITOR | 3.1.3.11 |
2FI3 | CRYSTAL STRUCTURE OF A BPTI VARIANT (CYS14->SER, CYS38->SER) IN COMPLEX WITH TRYPSIN | 3.4.21.4 |
2FI4 | CRYSTAL STRUCTURE OF A BPTI VARIANT (CYS14->SER) IN COMPLEX WITH TRYPSIN | 3.4.21.4 |
2FI5 | CRYSTAL STRUCTURE OF A BPTI VARIANT (CYS38->SER) IN COMPLEX WITH TRYPSIN | 3.4.21.4 |
2FIE | STRUCTURE OF HUMAN LIVER FBPASE COMPLEXED WITH POTENT BENZOXAZOLE ALLOSTERIC INHIBITORS | 3.1.3.11 |
2FIR | CRYSTAL STRUCTURE OF DFPR-VIIA/STF | 3.4.21.21 |
2FIT | FHIT (FRAGILE HISTIDINE TRIAD PROTEIN) | 3.6.1.29 |
2FIV | CRYSTAL STRUCTURE OF FELINE IMMUNODEFICIENCY VIRUS PROTEASE COMPLEXED WITH A SUBSTRATE | 3.4.23.16 3.4.23 2.7.7.49 3.1.26.13 3.1.13.2 3.6.1.23 2.7.7 3.1 |
2FIX | STRUCTURE OF HUMAN LIVER FBPASE COMPLEXED WITH POTENT BENZOXAZOLE ALLOSTERIC INHIBITIORS | 3.1.3.11 |
2FJ0 | CRYSTAL STRUCTURE OF JUVENILE HORMONE ESTERASE FROM MANDUCA SEXTA, WITH OTFP COVALENTLY ATTACHED | 3.1.1 |
2FJL | SOLUTION STRUCTURE OF THE SPLIT PH DOMAIN IN PHOSPHOLIPASE C-GAMMA1 | 3.1.4.11 |
2FJM | THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 2 | 3.1.3.48 |
2FJN | THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 2 | 3.1.3.48 |
2FJP | HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 IN COMPLEX WITH AN INHIBITOR | 3.4.14.5 |
2FJU | ACTIVATED RAC1 BOUND TO ITS EFFECTOR PHOSPHOLIPASE C BETA 2 | 3.6.5.2 |
2FJV | RT29 BOUND TO D(CTTAATTCGAATTAAG) IN COMPLEX WITH MMLV RT CATALYTIC FRAGMENT | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2FJW | D(CTTGAATGCATTCAAG) IN COMPLEX WITH MMLV RT CATALYTIC FRAGMENT | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2FJX | RT29 BOUND TO D(CTTGAATGCATTCAAG) IN COMPLEX WITH MMLV RT CATALYTIC FRAGMENT | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2FK6 | CRYSTAL STRUCTURE OF RNASE Z/TRNA(THR) COMPLEX | 3.1.26.11 |
2FKB | CRYSTAL STRUCTURE OF A PUTATIVE ENZYME (POSSIBLE NUDIX HYDROLASE) FROM ESCHERICHIA COLI K12 | 3.6 |
2FKC | CRYSTAL FORM I OF PRE-REACTIVE COMPLEX OF RESTRICTION ENDONUCLEASE HINP1I WITH COGNATE DNA AND CALCIUM ION | 3.1.21.4 |
2FKH | CRYSTAL FORM II OF PRE-REACTIVE COMPLEX OF RESTRICTION ENDONUCLEASE HINP1I WITH COGNATE DNA AND CALCIUM IONS | 3.1.21.4 |
2FL3 | BINARY COMPLEX OF RESTRICTION ENDONUCLEASE HINP1I WITH COGNATE DNA | 3.1.21.4 |
2FLB | DISCOVERY OF A NOVEL HYDROXY PYRAZOLE BASED FACTOR IXA INHIBITOR | 3.4.21.21 |
2FLC | POST-REACTIVE COMPLEX OF RESTRICTION ENDONUCLEASE HINP1I WITH NICKED COGNATE DNA AND MAGNESIUM IONS | 3.1.21.4 |
2FLO | CRYSTAL STRUCTURE OF EXOPOLYPHOSPHATASE (PPX) FROM E. COLI O157:H7 | 3.6.1.11 |
2FLR | NOVEL 5-AZAINDOLE FACTOR VIIA INHIBITORS | 3.4.21.21 |
2FLT | THE X-RAY STRUCTURE OF THE CIS-3-CHLOROACRYLIC ACID DEHALOGENASE CIS-CAAD INACTIVATED WITH (R)-OXIRANE-2-CARBOXYLATE | 3.8.1 |
2FM0 | CRYSTAL STRUCTURE OF PDE4D IN COMPLEX WITH L-869298 | 3.1.4.17 3.1.4.53 |
2FM2 | HCV NS3-4A PROTEASE DOMAIN COMPLEXED WITH A KETOAMIDE INHIBITOR, SCH446211 | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2FM5 | CRYSTAL STRUCTURE OF PDE4D2 IN COMPLEX WITH INHIBITOR L-869299 | 3.1.4.17 3.1.4.53 |
2FM6 | ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (NATIVE FORM) | 3.5.2.6 |
2FMB | EIAV PROTEASE COMPLEXED WITH AN INHIBITOR LP-130 | 3.4.23.16 |
2FMJ | 220-LOOP MUTANT OF STREPTOMYCES GRISEUS TRYPSIN | 3.4.21.4 |
2FN4 | THE CRYSTAL STRUCTURE OF HUMAN RAS-RELATED PROTEIN, RRAS, IN THE GDP-BOUND STATE | 3.6.5 |
2FNS | CRYSTAL STRUCTURE OF WILD-TYPE INACTIVE (D25N) HIV-1 PROTEASE COMPLEXED WITH WILD-TYPE HIV-1 NC-P1 SUBSTRATE. | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2FNT | CRYSTAL STRUCTURE OF A DRUG-RESISTANT (V82A) INACTIVE (D25N) HIV-1 PROTEASE COMPLEXED WITH AP2V VARIANT OF HIV-1 NC-P1 SUBSTRATE. | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2FNX | DESIGN OF SPECIFIC PEPTIDE INHIBITORS OF PHOSPHOLIPASE A2 (PLA2): CRYSTAL STRUCTURE OF THE COMPLEX OF PLA2 WITH A HIGHLY POTENT PEPTIDE VAL-ILE-ALA-LYS AT 2.7A RESOLUTION | 3.1.1.4 |
2FO5 | CRYSTAL STRUCTURE OF RECOMBINANT BARLEY CYSTEINE ENDOPROTEASE B ISOFORM 2 (EP-B2) IN COMPLEX WITH LEUPEPTIN | 3.4.22 |
2FO9 | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 95% ACETONE | 3.4.21.36 |
2FOA | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 40/50/10 % BENZENE | 3.4.21.36 |
2FOB | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 40/50/10 CYCLOHEXANE | 3.4.21.36 |
2FOC | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 55% DIMETHYLFORMAMIDE | 3.4.21.36 |
2FOD | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 80% ETHANOL | 3.4.21.36 |
2FOE | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 80% HEXANE | 3.4.21.36 |
2FOF | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 80% ISOPROPANOL | 3.4.21.36 |
2FOG | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 40% TRIFLUOROETHANOL | 3.4.21.36 |
2FOH | STRUCTURE OF PORCINE PANCREATIC ELASTASE IN 40% TRIFLUOROETHANOL | 3.4.21.36 |
2FOJ | THE CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF HAUSP/USP7 COMPLEXED WITH P53 PEPTIDE 364-367 | 3.1.2.15 3.4.19.12 |
2FOK | STRUCTURE OF RESTRICTION ENDONUCLEASE FOKI | 3.1.21.4 |
2FOM | DENGUE VIRUS NS2B/NS3 PROTEASE | 3.4.21.91 3.6.1.15 3.6.4.13 |
2FOO | THE CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF HAUSP/USP7 COMPLEXED WITH P53 PEPTIDE 359-362 | 3.1.2.15 3.4.19.12 |
2FOP | THE CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF HAUSP/USP7 COMPLEXED WITH MDM2 PEPTIDE 147-150 | 3.1.2.15 3.4.19.12 |
2FOZ | HUMAN ADP-RIBOSYLHYDROLASE 3 | 3.5.1 3.2.1.143 3.2.2 |
2FP0 | HUMAN ADP-RIBOSYLHYDROLASE 3 | 3.5.1 3.2.1.143 3.2.2 |
2FP3 | CRYSTAL STRUCTURE OF THE DROSOPHILA INITIATOR CASPASE DRONC | 3.4.22 |
2FP7 | WEST NILE VIRUS NS2B/NS3PROTEASE IN COMPLEX WITH BZ-NLE-LYS-ARG-ARG-H | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2FPQ | CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE D LIGHT CHAIN | 3.4.24.69 |
2FPR | CRYSTAL STRUCTURE THE N-TERMINAL DOMAIN OF E. COLI HISB. APO MG MODEL. | 3.1.3.15 4.2.1.19 |
2FPS | CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF E.COLI HISB- APO CA MODEL. | 3.1.3.15 4.2.1.19 |
2FPU | CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF E.COLI HISB- COMPLEX WITH HISTIDINOL | 3.1.3.15 4.2.1.19 |
2FPW | CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF E.COLI HISB- PHOSPHOASPARTATE INTERMEDIATE. | 3.1.3.15 4.2.1.19 |
2FPX | CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF E.COLI HISB- SULFATE COMPLEX. | 3.1.3.15 4.2.1.19 |
2FPZ | HUMAN TRYPTASE WITH 2-AMINO BENZIMIDAZOLE | 3.4.21.59 |
2FQ1 | CRYSTAL STRUCTURE OF THE TWO-DOMAIN NON-RIBOSOMAL PEPTIDE SYNTHETASE ENTB CONTAINING ISOCHORISMATE LYASE AND ARYL-CARRIER PROTEIN DOMAINS | 3.3.2.1 6.3.2.14 |
2FQ9 | CATHEPSIN S WITH NITRILE INHIBITOR | 3.4.22.27 |
2FQQ | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (CYS285->ALA, CYS362->ALA, CYS364->ALA, CYS397->ALA) IN COMPLEX WITH 1-METHYL-3-TRIFLUOROMETHYL-1H-THIENO[2,3-C]PYRAZOLE-5-CARBOXYLIC ACID (2-MERCAPTO-ETHYL)-AMIDE | 3.4.22.36 |
2FR5 | CRYSTAL STRUCTURE OF MOUSE CYTIDINE DEAMINASE COMPLEXED WITH TETRAHYDROURIDINE | 3.5.4.5 |
2FR6 | CRYSTAL STRUCTURE OF MOUSE CYTIDINE DEAMINASE COMPLEXED WITH CYTIDINE | 3.5.4.5 |
2FRA | HUMAN CATHEPSIN S WITH CRA-27934, A NITRILE INHIBITOR | 3.4.22.27 |
2FRQ | HUMAN CATHEPSIN S WITH INHIBITOR CRA-26871 | 3.4.22.27 |
2FS2 | STRUCTURE OF THE E. COLI PAAI PROTEIN FROM THE PHYENYLACETIC ACID DEGRADATION OPERON | 3.1.2 |
2FS4 | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C RING | 3.4.23.15 |
2FS8 | HUMAN BETA-TRYPTASE II WITH INHIBITOR CRA-29382 | 3.4.21.59 |
2FS9 | HUMAN BETA TRYPTASE II WITH INHIBITOR CRA-28427 | 3.4.21.59 |
2FT2 | HUMAN CATHEPSIN S WITH INHIBITOR CRA-29728 | 3.4.22.27 |
2FTL | CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH BPTI AT 100K | 3.4.21.4 |
2FTM | CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH THE BPTI VARIANT (TYR35->GLY) | 3.4.21.4 |
2FTW | CRYSTAL STRUCTURE OF DIHYDROPYRIMIDINASE FROM DICTYOSTELIUM DISCOIDEUM | 3.5.2.2 |
2FTY | CRYSTAL STRUCTURE OF DIHYDROPYRIMIDINASE FROM SACCHAROMYCES KLUYVERI | 3.5.2.2 |
2FU6 | ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (APO FORM) | 3.5.2.6 |
2FU7 | ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (CU-SUBSTITUTED FORM) | 3.5.2.6 |
2FU8 | ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (D-CAPTOPRIL COMPLEX) | 3.5.2.6 |
2FU9 | ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (MP2 INHIBITOR COMPLEX) | 3.5.2.6 |
2FUD | HUMAN CATHEPSIN S WITH INHIBITOR CRA-27566 | 3.4.22.27 |
2FUF | CRYSTAL STRUCTURE OF THE SV40 LARGE T ANTIGEN ORIGIN-BINDING DOMAIN | 3.6.4 |
2FUZ | UGL HEXAGONAL CRYSTAL STRUCTURE WITHOUT GLYCINE AND DTT MOLECULES | 3.2.1 3.2.1.179 |
2FV5 | CRYSTAL STRUCTURE OF TACE IN COMPLEX WITH IK682 | 3.4.24.86 |
2FV9 | CRYSTAL STRUCTURE OF TACE IN COMPLEX WITH JMV 390-1 | 3.4.24.86 |
2FVC | CRYSTAL STRUCTURE OF NS5B BK STRAIN (DELTA 24) IN COMPLEX WITH A 3-(1,1-DIOXO-2H-(1,2,4)-BENZOTHIADIAZIN-3-YL)-4-HYDROXY-2(1H)-QUINOLINONE | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2FVH | CRYSTAL STRUCTURE OF RV1848, A UREASE GAMMA SUBUNIT UREA (UREA AMIDOHYDROLASE), FROM MYCOBACTERIUM TUBERCULOSIS | 3.5.1.5 |
2FVK | CRYSTAL STRUCTURE OF DIHYDROPYRIMIDINASE FROM SACCHAROMYCES KLUYVERI IN COMPLEX WITH THE SUBSTRATE DIHYDROURACIL | 3.5.2.2 |
2FVM | CRYSTAL STRUCTURE OF DIHYDROPYRIMIDINASE FROM SACCHAROMYCES KLUYVERI IN COMPLEX WITH THE REACTION PRODUCT N-CARBAMYL-BETA-ALANINE | 3.5.2.2 |
2FVP | A STRUCTURAL STUDY OF THE CA DINUCLEOTIDE STEP IN THE INTEGRASE PROCESSING SITE OF MOLONEY MURINE LEUKEMIA VIRUS | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2FVQ | A STRUCTURAL STUDY OF THE CA DINUCLEOTIDE STEP IN THE INTEGRASE PROCESSING SITE OF MOLONEY MURINE LEUKEMIA VIRUS | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2FVR | A STRUCTURAL STUDY OF THE CA DINUCLEOTIDE STEP IN THE INTEGRASE PROCESSING SITE OF MOLONEY MURINE LEUKEMIA VIRUS | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2FVS | A STRUCTURAL STUDY OF THE CA DINUCLEOTIDE STEP IN THE INTEGRASE PROCESSING SITE OF MOLONEY MURINE LEUKEMIA VIRUS | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2FVV | HUMAN DIPHOSPHOINOSITOL POLYPHOSPHATE PHOSPHOHYDROLASE 1 | 3.6.1.52 3.6.1 |
2FVZ | HUMAN INOSITOL MONOPHOSPHOSPHATASE 2 | 3.1.3.25 |
2FWR | STRUCTURE OF ARCHAEOGLOBUS FULGIDIS XPB | 3.6.4.12 |
2FWW | HUMAN BETA-TRYPTASE II COMPLEXED WITH 4-PIPERIDINEBUTYRATE TO MAKE ACYLENZYME | 3.4.21.59 |
2FX4 | BOVINE TRYPSIN BOUND BY 4-PIPERIDINEBUTYRATE TO MAKE ACYLENZYME COMPLEX | 3.4.21.4 |
2FX5 | PSEUDOMONAS MENDOCINA LIPASE | 3.1.1.3 |
2FX6 | BOVINE TRYPSIN COMPLEXED WITH 2-AMINOBENZAMIDAZOLE | 3.4.21.4 |
2FXD | X-RAY CRYSTAL STRUCTURE OF HIV-1 PROTEASE IRM MUTANT COMPLEXED WITH ATAZANAVIR (BMS-232632) | 3.4.23.16 2.7.7.49 3.1.26.13 |
2FXE | X-RAY CRYSTAL STRUCTURE OF HIV-1 PROTEASE CRM MUTANT COMPLEXED WITH ATAZANAVIR (BMS-232632) | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2FXI | ARSENATE REDUCTASE (ARSC FROM PI258) C10S/C15A DOUBLE MUTANT WITH SULFATE IN ITS ACTIVE SITE | 1.20.4 3.1.3.48 1.20.4.4 |
2FXR | HUMAN BETA TRYPTASE II COMPLEXED WITH ACTIVATED KETONE INHIBITOR CRA-29382 | 3.4.21.59 |
2FXZ | SOLUTION STRUCTURE OF 97-109 SEGMENT OF STAPHYLOCOCCAL NUCLEASE | 3.1.31.1 |
2FYE | MUTANT HUMAN CATHEPSIN S WITH IRREVERSIBLE INHIBITOR CRA-14013 | 3.4.22.27 |
2FYG | CRYSTAL STRUCTURE OF NSP10 FROM SARS CORONAVIRUS | 3.4.19.12 3.4.22 3.4.22.69 |
2FYH | SOLUTION STRUCTURE OF THE 2'-5' RNA LIGASE-LIKE PROTEIN FROM PYROCOCCUS FURIOSUS | 3.1.4.58 |
2FYQ | CRYSTAL STRUCTURE OF THE NORWALK VIRUS PROTEASE | 3.6.1.15 3.4.22.66 2.7.7.48 |
2FYR | CRYSTAL STRUCTURE OF NORWALK VIRUS PROTEASE GROWN IN THE PRESENCE OF AEBSF | 3.6.1.15 3.4.22.66 2.7.7.48 |
2FYV | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH AN AMINO-SALACINOL CARBOXYLATE ANALOG | 3.2.1.114 |
2FZ4 | CRYSTAL STRUCTURE OF THE N-TERMINAL HALF OF ARCHAEOGLOBUS FULGIDUS XPB | 3.6.4.12 |
2FZL | STRUCTURE OF C-TERMINAL DOMAIN OF ARCHAEOGLOBUS FULGIDUS XPB | 3.6.4.12 |
2FZS | CRYSTAL STRUCTURE OF E. COLI CLPP WITH A PEPTIDE CHLOROMETHYL KETONE COVALENTLY BOUND AT THE ACTIVE SITE | 3.4.21.92 |
2FZZ | FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-(3-AMINO-1,2-BENZISOXAZOL-5-YL)-6-(2'-(((3R)-3-HYDROXY-1-PYRROLIDINYL)METHYL)-4-BIPHENYLYL)-3-(TRIFLUOROMETHYL)-1,4,5,6-TETRAHYDRO-7H-PYRAZOLO[3,4-C]PYRIDIN-7-ONE | 3.4.21.6 |
2G00 | FACTOR XA IN COMPLEX WITH THE INHIBITOR 3-(6-(2'-((DIMETHYLAMINO)METHYL)-4-BIPHENYLYL)-7-OXO-3-(TRIFLUOROMETHYL)-4,5,6,7-TETRAHYDRO-1H-PYRAZOLO[3,4-C]PYRIDIN-1-YL)BENZAMIDE | 3.4.21.6 |
2G06 | X-RAY STRUCTURE OF MOUSE PYRIMIDINE 5'-NUCLEOTIDASE TYPE 1, WITH BOUND MAGNESIUM(II) | 3.1.3.5 3.1.3.91 |
2G07 | X-RAY STRUCTURE OF MOUSE PYRIMIDINE 5'-NUCLEOTIDASE TYPE 1, PHOSPHO-ENZYME INTERMEDIATE ANALOG WITH BERYLLIUM FLUORIDE | 3.1.1.5 3.1.3.5 3.1.3.91 |
2G08 | X-RAY STRUCTURE OF MOUSE PYRIMIDINE 5'-NUCLEOTIDASE TYPE 1, PRODUCT-TRANSITION COMPLEX ANALOG WITH ALUMINUM FLUORIDE | 3.1.1.5 3.1.3.5 3.1.3.91 |
2G09 | X-RAY STRUCTURE OF MOUSE PYRIMIDINE 5'-NUCLEOTIDASE TYPE 1, PRODUCT COMPLEX | 3.1.1.5 3.1.3.5 3.1.3.91 |
2G0A | X-RAY STRUCTURE OF MOUSE PYRIMIDINE 5'-NUCLEOTIDASE TYPE 1 WITH LEAD(II) BOUND IN ACTIVE SITE | 3.1.1.5 3.1.3.5 3.1.3.91 |
2G0C | STRUCTURE OF THE RNA BINDING DOMAIN (RESIDUES 404-479) OF THE BACILLUS SUBTILIS YXIN PROTEIN | 3.6.1 3.6.4.13 |
2G0N | THE CRYSTAL STRUCTURE OF THE HUMAN RAC3 IN COMPLEX WITH GDP AND CHLORIDE | 3.6.5.2 |
2G1A | CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE | 3.1.3.2 |
2G1N | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C" RING" | 3.4.23.15 |
2G1O | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C" RING" | 3.4.23.15 |
2G1R | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C RING | 3.4.23.15 |
2G1S | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C RING | 3.4.23.15 |
2G1Y | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C" RING" | 3.4.23.15 |
2G20 | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C RING | 3.4.23.15 |
2G21 | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C" RING" | 3.4.23.15 |
2G22 | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C" RING" | 3.4.23.15 |
2G24 | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C" RING" | 3.4.23.15 |
2G26 | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C" RING" | 3.4.23.15 |
2G27 | KETOPIPERAZINE-BASED RENIN INHIBITORS: OPTIMIZATION OF THE C" RING" | 3.4.23.15 |
2G2N | CRYSTAL STRUCTURE OF E.COLI TRANSTHYRETIN-RELATED PROTEIN WITH BOUND ZN | 3.5.2.17 |
2G2P | CRYSTAL STRUCTURE OF E.COLI TRANSTHYRETIN-RELATED PROTEIN WITH BOUND ZN AND BR | 3.5.2.17 |
2G2U | CRYSTAL STRUCTURE OF THE SHV-1 BETA-LACTAMASE/BETA-LACTAMASE INHIBITOR PROTEIN (BLIP) COMPLEX | 3.5.2.6 |
2G2W | CRYSTAL STRUCTURE OF THE SHV D104K BETA-LACTAMASE/BETA-LACTAMASE INHIBITOR PROTEIN (BLIP) COMPLEX | 3.5.2.6 |
2G3F | CRYSTAL STRUCTURE OF IMIDAZOLONEPROPIONASE COMPLEXED WITH IMIDAZOLE-4-ACETIC ACID SODIUM SALT, A SUBSTRATE HOMOLOGUE | 3.5.2.7 |
2G3I | STRUCTURE OF S.OLIVACEOVIRIDIS XYLANASE Q88A/R275A MUTANT | 3.2.1.8 |
2G3J | STRUCTURE OF S.OLIVACEOVIRIDIS XYLANASE Q88A/R275A MUTANT | 3.2.1.8 |
2G3M | CRYSTAL STRUCTURE OF THE SULFOLOBUS SOLFATARICUS ALPHA-GLUCOSIDASE MALA | 3.2.1.20 |
2G3N | CRYSTAL STRUCTURE OF THE SULFOLOBUS SOLFATARICUS ALPHA-GLUCOSIDASE MALA IN COMPLEX WITH BETA-OCTYL-GLUCOPYRANOSIDE | 3.2.1.20 |
2G43 | STRUCTURE OF THE ZNF UBP DOMAIN FROM DEUBIQUITINATING ENZYME ISOPEPTIDASE T (ISOT) | 3.1.2.15 3.4.19.12 |
2G45 | CO-CRYSTAL STRUCTURE OF ZNF UBP DOMAIN FROM THE DEUBIQUITINATING ENZYME ISOPEPTIDASE T (ISOT) IN COMPLEX WITH UBIQUITIN | 3.1.2.15 3.4.19.12 |
2G47 | CRYSTAL STRUCTURE OF HUMAN INSULIN-DEGRADING ENZYME IN COMPLEX WITH AMYLOID-BETA (1-40) | 3.4.24.56 |
2G48 | CRYSTAL STRUCTURE OF HUMAN INSULIN-DEGRADING ENZYME IN COMPLEX WITH AMYLIN | 3.4.24.56 |
2G49 | CRYSTAL STRUCTURE OF HUMAN INSULIN-DEGRADING ENZYME IN COMPLEX WITH GLUCAGON | 3.4.24.56 |
2G4D | CRYSTAL STRUCTURE OF HUMAN SENP1 MUTANT (C603S) IN COMPLEX WITH SUMO-1 | 3.4.22 |
2G4F | STRUCTURE OF S.OLIVACEOVIRIDIS XYLANASE Q88A/R275A MUTANT | 3.2.1.8 |
2G4K | ANOMALOUS SUBSTRUCTURE OF HUMAN ADP-RIBOSYLHYDROLASE 3 | 3.5.1 3.2.1.143 3.2.2 |
2G4P | ANOMALOUS SUBSTRUCTURE OF LYSOZYME AT PH 4.5 | 3.2.1.17 |
2G4Q | ANOMALOUS SUBSTRUCTURE OF LYSOZYME AT PH 8.0 | 3.2.1.17 |
2G4T | ANOMALOUS SUBSTRUCTURE OF PORCINE PANCREATIC ELASTASE (NA) | 3.4.21.36 |
2G4U | ANOMALOUS SUBSTRUCTURE OF PORCINE PANCREATIC ELASTAASE (CA) | 3.4.21.36 |
2G4V | ANOMALOUS SUBSTRUCTURE OF PROTEINASE K | 3.4.21.64 |
2G4W | ANOMALOUS SUBSTRUCTURE OF RIBONUCLEASE A (C2) | 3.1.27.5 4.6.1.18 |
2G4X | ANOMALOUS SUBSTRUCTURE OD RIBONUCLEASE A (P3221) | 3.1.27.5 4.6.1.18 |
2G4Z | ANOMALOUS SUBSTRUCTURE OF THERMOLYSIN | 3.4.24.27 |
2G51 | ANOMALOUS SUBSTRUCTURE OF TRYPSIN (P1) | 3.4.21.4 |
2G52 | ANOMALOUS SUBSTRUCTURE OF TRYPSIN (P21) | 3.4.21.4 |
2G54 | CRYSTAL STRUCTURE OF ZN-BOUND HUMAN INSULIN-DEGRADING ENZYME IN COMPLEX WITH INSULIN B CHAIN | 3.4.24.56 |
2G55 | ANOMALOUS SUBSTRUCTURE OF TRYPSIN (P3121) | 3.4.21.4 |
2G56 | CRYSTAL STRUCTURE OF HUMAN INSULIN-DEGRADING ENZYME IN COMPLEX WITH INSULIN B CHAIN | 3.4.24.56 |
2G58 | CRYSTAL STRUCTURE OF A COMPLEX OF PHOSPHOLIPASE A2 WITH A DESIGNED PEPTIDE INHIBITOR DEHYDRO-ILE-ALA-ARG-SER AT 0.98 A RESOLUTION | 3.1.1.4 |
2G59 | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PROTEIN TYROSINE PHOSPHATASE FROM HOMO SAPIENS | 3.1.3.48 |
2G5D | CRYSTAL STRUCTURE OF MLTA FROM NEISSERIA GONORRHOEAE MONOCLINIC FORM | 3.2.1 4.2.2 |
2G5N | INDOLE-AMIDINE COMPLEXES WITH BOVINE TRYPSIN | 3.4.21.4 |
2G5P | CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (DPPIV) COMPLEXED WITH CYANOPYRROLIDINE (C5-PRO-PRO) INHIBITOR 21AC | 3.4.14.5 |
2G5T | CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (DPPIV) COMPLEXED WITH CYANOPYRROLIDINE (C5-PRO-PRO) INHIBITOR 21AG | 3.4.14.5 |
2G5V | INDOLE-AMIDINE COMPLEXES WITH BOVINE TRYPSIN | 3.4.21.4 |
2G5X | CRYSTAL STRUCTURE OF LYCHNIN A TYPE 1 RIBOSOME INACTIVATING PROTEIN (RIP) | 3.2.2.22 |
2G63 | CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (DPPIV) COMPLEXED WITH CYANOPYRROLIDINE (C5-PRO-PRO) INHIBITOR 24B | 3.4.14.5 |
2G69 | STRUCTURE OF UNLIGANDED HIV-1 PROTEASE F53L MUTANT | 3.4.23.16 |
2G6D | HUMAN CATHEPSIN S MUTANT WITH VINYL SULFONE INHIBITOR CRA-14009 | 3.4.22.27 |
2G6G | CRYSTAL STRUCTURE OF MLTA FROM NEISSERIA GONORRHOEAE | 3.2.1 4.2.2 |
2G6P | CRYSTAL STRUCTURE OF TRUNCATED (DELTA 1-89) HUMAN METHIONINE AMINOPEPTIDASE TYPE 1 IN COMPLEX WITH PYRIDYL PYRIMIDINE DERIVATIVE | 3.4.11.18 |
2G6V | THE CRYSTAL STRUCTURE OF RIBD FROM ESCHERICHIA COLI | 1.1.1.193 3.5.4.26 |
2G6Z | CRYSTAL STRUCTURE OF HUMAN DUSP5 | 3.1.3.48 3.1.3.16 |
2G7C | CLOSTRIDIUM DIFFICILE TOXIN A FRAGMENT BOUND TO AGAL(1,3)BGAL(1,4)BGLCNAC | 3.4.22 2.4.1 |
2G7E | THE 1.6 A CRYSTAL STRUCTURE OF VIBRIO CHOLERAE EXTRACELLULAR ENDONUCLEASE I | 3.1.21.1 3.1.21 |
2G7F | THE 1.95 A CRYSTAL STRUCTURE OF VIBRIO CHOLERAE EXTRACELLULAR ENDONUCLEASE I | 3.1.21.1 3.1.21 |
2G7K | STRUCTURE OF THE LIGHT CHAIN OF BOTULINUM NEUROTOXIN, SEROTYPE A BOUND TO SMALL MOLECULE INHIBITORS | 3.4.24.69 |
2G7N | STRUCTURE OF THE LIGHT CHAIN OF BOTULINUM NEUROTOXIN SEROTYPE A BOUND TO SMALL MOLECULE INHIBITORS | 3.4.24.69 |
2G7P | STRUCTURE OF THE LIGHT CHAIN OF BOTULINUM NEUROTOXIN SEROTYPE A BOUND TO SMALL MOLECULE INHIBITORS | 3.4.24.69 |
2G7Q | STRUCTURE OF THE LIGHT CHAIN OF BOTULINUM NEUROTOXIN SEROTYPE A BOUND TO SMALL MOLECULE INHIBITORS | 3.4.24.69 |
2G7R | X-RAY STRUCTURE OF THE DEATH DOMAIN OF THE HUMAN MUCOSA ASSOCIATED LYMPHOID TISSUE LYMPHOMA TRANSLOCATION PROTEIN 1 | 3.4.22 |
2G7Y | HUMAN CATHEPSIN S WITH INHIBITOR CRA-16981 | 3.4.22.27 |
2G80 | CRYSTAL STRUCTURE OF UTR4 PROTEIN (UNKNOWN TRANSCRIPT 4 PROTEIN) (YEL038W) FROM SACCHAROMYCES CEREVISIAE AT 2.28 A RESOLUTION | 3.1.3.77 |
2G81 | CRYSTAL STRUCTURE OF THE BOWMAN-BIRK INHIBITOR FROM VIGNA UNGUICULATA SEEDS IN COMPLEX WITH BETA-TRYPSIN AT 1.55 ANGSTRONS RESOLUTION | 3.4.21.4 |
2G8E | CALPAIN 1 PROTEOLYTIC CORE IN COMPLEX WITH SNJ-1715, A CYCLIC HEMIACETAL-TYPE INHIBITOR | 3.4.22.52 |
2G8F | B. HALODURANS RNASE H CATALYTIC DOMAIN E188A MUTANT IN COMPLEX WITH MG2+ AND RNA/DNA HYBRID (NON-P NICK AT THE ACTIVE SITE) | 3.1.26.4 |
2G8H | B. HALODURANS RNASE H CATALYTIC DOMAIN D192N MUTANT IN COMPLEX WITH MG2+ AND RNA/DNA HYBRID (NON-P NICK AT THE ACTIVE SITE) | 3.1.26.4 |
2G8I | B. HALODURANS RNASE H CATALYTIC DOMAIN D192N MUTANT IN COMPLEX WITH MN2+ AND RNA/DNA HYBRID (NON-P NICK AT THE ACTIVE SITE) | 3.1.26.4 |
2G8J | CALPAIN 1 PROTEOLYTIC CORE IN COMPLEX WITH SNJ-1945, A ALPHA-KETOAMIDE-TYPE INHIBITOR. | 3.4.22.52 |
2G8K | B. HALODURANS RNASE H CATALYTIC DOMAIN D192N MUTANT IN COMPLEX WITH CA2+ AND RNA/DNA HYBRID (NON-P NICK AT THE ACTIVE SITE) | 3.1.26.4 |
2G8L | CRYSTAL STRUCTURE OF A DUF89 FAMILY PROTEIN (PH1575) FROM PYROCOCCUS HORIKOSHII AT 2.04 A RESOLUTION | 3.1.3 |
2G8Q | THE CRYSTAL STRUCTURE OF RNASE A FROM MONOCLINIC CRYSTALS AT 100 K | 3.1.27.5 4.6.1.18 |
2G8R | THE CRYSTAL STRUCTURE OF THE RNASE A- 3-N-PIPERIDINE-4-CARBOXYL-3-DEOXY-ARA-URIDINE COMPLEX | 3.1.27.5 4.6.1.18 |
2G8T | INDOLE-AMIDINE COMPLEXES WITH BOVINE TRYPSIN | 3.4.21.4 |
2G8U | B. HALODURANS RNASE H CATALYTIC DOMAIN D132N MUTANT IN COMPLEX WITH MG2+ AND RNA/DNA HYBRID (NON-P NICK AT THE ACTIVE SITE) | 3.1.26.4 |
2G8V | B. HALODURANS RNASE H CATALYTIC DOMAIN E188A MUTANT IN COMPLEX WITH MG2+ AND RNA/DNA HYBRID (REACTION PRODUCT) | 3.1.26.4 |
2G8W | B. HALODURANS RNASE H CATALYTIC DOMAIN E188A MUTANT IN COMPLEX WITH CA2+ AND RNA/DNA HYBRID | 3.1.26.4 |
2G93 | LIGAND RECOGNITION SITE IN C-LOBE OF LACTOFERRIN: CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF BOVINE LACTOFERRIN WITH METHYL ALPHA-D-MANNOPYRANOSIDE AT 1.9 A RESOLUTION | 3.4.21 |
2G94 | CRYSTAL STRUCTURE OF BETA-SECRETASE BOUND TO A POTENT AND HIGHLY SELECTIVE INHIBITOR. | 3.4.23.46 |
2G9D | CRYSTAL STRUCTURE OF SUCCINYLGLUTAMATE DESUCCINYLASE FROM VIBRIO CHOLERAE, NORTHEAST STRUCTURAL GENOMICS TARGET VCR20 | 3.1 3.5.1.96 |
2G9F | CRYSTAL STRUCTURE OF INTEIN-TAGGED MOUSE PNGASE C-TERMINAL DOMAIN | 3.5.1.52 |
2G9G | CRYSTAL STRUCTURE OF HIS-TAGGED MOUSE PNGASE C-TERMINAL DOMAIN | 3.5.1.52 |
2G9N | STRUCTURE OF THE DEAD DOMAIN OF HUMAN EUKARYOTIC INITIATION FACTOR 4A, EIF4A | 3.6.1 3.6.4.13 |
2G9O | SOLUTION STRUCTURE OF THE APO FORM OF THE THIRD METAL-BINDING DOMAIN OF ATP7A PROTEIN (MENKES DISEASE PROTEIN) | 3.6.3.4 7.2.2.8 |
2G9Y | STRUCTURE OF S102T E. COLI ALKALINE PHOSPHATASE IN PRESENCE OF PHOSPHATE AT 2.00 A RESOLUTION | 3.1.3.1 |
2GA2 | H-METAP2 COMPLEXED WITH A193400 | 3.4.11.18 |
2GA3 | STRUCTURE OF S102T E. COLI ALKALINE PHOSPHATASE-PHOSPHATE INTERMEDIATE AT 2.20A RESOLUTION | 3.1.3.1 |
2GA4 | STX2 WITH ADENINE | 3.2.2.22 |
2GA7 | SOLUTION STRUCTURE OF THE COPPER(I) FORM OF THE THIRD METAL-BINDING DOMAIN OF ATP7A PROTEIN (MENKES DISEASE PROTEIN) | 3.6.3.4 7.2.2.8 |
2GAC | T152C MUTANT GLYCOSYLASPARAGINASE FROM FLAVOBACTERIUM MENINGOSEPTICUM | 3.5.1.26 |
2GAE | CRYSTAL STRUCTURE OF MLTA FROM E. COLI | 3.2.1 4.2.2 |
2GAW | WILD TYPE GLYCOSYLASPARAGINASE FROM FLAVOBACTERIUM MENINGOSEPTICUM | 3.5.1.26 |
2GB5 | CRYSTAL STRUCTURE OF NADH PYROPHOSPHATASE (EC 3.6.1.22) (1790429) FROM ESCHERICHIA COLI K12 AT 2.30 A RESOLUTION | 3.6.1.22 3.6.1 |
2GBZ | THE CRYSTAL STRUCTURE OF XC847 FROM XANTHOMONAS CAMPESTRIS: A 3-5 OLIGORIBONUCLEASE OF DNAQ FOLD FAMILY WITH A NOVEL OPPOSINGLY-SHIFTED HELIX | 3.1 |
2GC8 | STRUCTURE OF A PROLINE SULFONAMIDE INHIBITOR BOUND TO HCV NS5B POLYMERASE | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2GCF | SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF THE COPPPER(I) ATPASE PACS IN ITS APO FORM | 3.6.3 7.2.2.8 |
2GCH | REFINED CRYSTAL STRUCTURE OF GAMMA-CHYMOTRYPSIN AT 1.9 ANGSTROMS RESOLUTION | 3.4.21.1 |
2GCT | STRUCTURE OF GAMMA-CHYMOTRYPSIN IN THE RANGE PH 2.0 TO PH 10.5 SUGGESTS THAT GAMMA-CHYMOTRYPSIN IS A COVALENT ACYL-ENZYME ADDUCT AT LOW PH | 3.4.21.1 |
2GCU | X-RAY STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT1G53580 | 3.1.2.6 1.13.11.18 |
2GD4 | CRYSTAL STRUCTURE OF THE ANTITHROMBIN-S195A FACTOR XA-PENTASACCHARIDE COMPLEX | 3.4.21.6 |
2GDD | HUMAN BETA II TRYPTASE WITH INHIBITOR CRA-27592 | 3.4.21.59 |
2GDN | CRYSTAL STRUCTURE OF THE MYCOBACTERIUM TUBERCULOSIS BETA-LACTAMASE | 3.5.2.6 |
2GDT | NMR STRUCTURE OF THE NONSTRUCTURAL PROTEIN 1 (NSP1) FROM THE SARS CORONAVIRUS | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GEF | CRYSTAL STRUCTURE OF A NOVEL VIRAL PROTEASE WITH A SERINE/LYSINE CATALYTIC DYAD MECHANISM | 3.4.21 |
2GEZ | CRYSTAL STRUCTURE OF POTASSIUM-INDEPENDENT PLANT ASPARAGINASE | 3.5.1.1 3.4.19.5 |
2GFH | CRYSTAL STRUCTURE OF A N-ACETYLNEURAMINIC ACID PHOSPHATASE (NANP) FROM MUS MUSCULUS AT 1.90 A RESOLUTION | 3.1.3.29 |
2GFI | CRYSTAL STRUCTURE OF THE PHYTASE FROM D. CASTELLII AT 2.3 A | 3.1.3.8 3.1.3.2 |
2GFJ | CRYSTAL STRUCTURE OF THE ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (INHIBITOR 1) | 3.5.2.6 |
2GFK | CRYSTAL STRUCTURE OF THE ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (INHIBITOR 2) | 3.5.2.6 |
2GFO | STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 8 | 3.1.2.15 3.4.19.12 |
2GFQ | STRUCTURE OF PROTEIN OF UNKNOWN FUNCTION PH0006 FROM PYROCOCCUS HORIKOSHII | 3.1.1.96 |
2GFT | CRYSTAL STRUCTURE OF THE E263A NUCLEOPHILE MUTANT OF BACILLUS LICHENIFORMIS ENDO-BETA-1,4-GALACTANASE IN COMPLEX WITH GALACTOTRIOSE | 3.2.1.89 |
2GG0 | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GG1 | NMR SOLUTION STRUCTURE OF DOMAIN III OF THE E-PROTEIN OF TICK-BORNE LANGAT FLAVIVIRUS (INCLUDES RDC RESTRAINTS) | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2GG2 | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GG3 | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GG5 | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GG7 | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GG8 | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GG9 | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GGB | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GGC | NOVEL BACTERIAL METHIONINE AMINOPEPTIDASE INHIBITORS | 3.4.11.18 |
2GGK | THE MUTANT A302C OF AGROBACTERIUM RADIOBACTER N-CARBAMOYL-D-AMINO-ACID AMIDOHYDROLASE | 3.5.1.77 |
2GGL | THE MUTANT A222C OF AGROBACTERIUM RADIOBACTER N-CARBAMOYL-D-AMINO ACID AMIDOHYDROLASE | 3.5.1.77 |
2GGV | CRYSTAL STRUCTURE OF THE WEST NILE VIRUS NS2B-NS3 PROTEASE, HIS51ALA MUTANT | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2GH4 | YTER/D143N/DGALA-RHA | 3.2.1 3.2.1.172 |
2GH6 | CRYSTAL STRUCTURE OF A HDAC-LIKE PROTEIN WITH 9,9,9-TRIFLUORO-8-OXO-N-PHENYLNONAN AMIDE BOUND | 3.5.1 |
2GHQ | CTD-SPECIFIC PHOSPHATASE SCP1 IN COMPLEX WITH PEPTIDE C-TERMINAL DOMAIN OF RNA POLYMERASE II | 3.1.3.16 |
2GHT | CTD-SPECIFIC PHOSPHATASE SCP1 IN COMPLEX WITH PEPTIDE FROM C-TERMINAL DOMAIN OF RNA POLYMERASE II | 3.1.3.16 |
2GHU | CRYSTAL STRUCTURE OF FALCIPAIN-2 FROM PLASMODIUM FALCIPARUM | 3.4.22 |
2GI4 | SOLUTION STRUCTURE OF THE LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE FROM CAMPYLOBACTER JEJUNI. | 3.1.3.48 |
2GIE | HINCII BOUND TO COGNATE DNA GTTAAC | 3.1.21.4 |
2GIH | Q138F HINCII BOUND TO COGNATE DNA GTCGAC AND CA2+ | 3.1.21.4 |
2GIQ | HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE NS5B WITH NNI-2 INHIBITOR | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2GIR | HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE NS5B WITH NNI-1 INHIBITOR | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2GJ8 | STRUCTURE OF THE MNME G-DOMAIN IN COMPLEX WITH GDP*ALF4-, MG2+ AND K+ | 3.6 |
2GJ9 | STRUCTURE OF THE MNME G-DOMAIN IN COMPLEX WITH GDP*ALF4-, MG2+ AND RB+ | 3.6 |
2GJA | STRUCTURE OF THE MNME G-DOMAIN IN COMPLEX WITH GDP*ALF4-, MG2+ AND NH4+ | 3.6 |
2GJK | STRUCTURAL AND FUNCTIONAL INSIGHTS INTO THE HUMAN UPF1 HELICASE CORE | 3.6.1 3.6.4 |
2GJP | STRUCTURE OF BACILLUS HALMAPALUS ALPHA-AMYLASE, CRYSTALLIZED WITH THE SUBSTRATE ANALOGUE ACARBOSE AND MALTOSE | 3.2.1.1 3.2.1.98 |
2GJR | STRUCTURE OF BACILLUS HALMAPALUS ALPHA-AMYLASE WITHOUT ANY SUBSTRATE ANALOGUES | 3.2.1.1 3.2.1.98 |
2GJT | CRYSTAL STRUCTURE OF THE HUMAN RECEPTOR PHOSPHATASE PTPRO | 3.1.3.48 |
2GJW | RNA RECOGNITION AND CLEAVAGE BY AN SPLICING ENDONUCLEASE | 3.1.27.9 4.6.1.16 |
2GK1 | X-RAY CRYSTAL STRUCTURE OF NGT-BOUND HEXA | 3.2.1.52 |
2GK6 | STRUCTURAL AND FUNCTIONAL INSIGHTS INTO THE HUMAN UPF1 HELICASE CORE | 3.6.1 3.6.4 |
2GK7 | STRUCTURAL AND FUNCTIONAL INSIGHTS INTO THE HUMAN UPF1 HELICASE CORE | 3.6.1 3.6.4 |
2GKL | CRYSTAL STRUCTURE OF THE ZINC CARBAPENEMASE CPHA IN COMPLEX WITH THE INHIBITOR PYRIDINE-2,4-DICARBOXYLATE | 3.5.2.6 |
2GKO | S41 PSYCHROPHILIC PROTEASE | 3.4.21.62 3.4.21.14 |
2GL9 | CRYSTAL STRUCTURE OF GLYCOSYLASPARAGINASE-SUBSTRATE COMPLEX | 3.5.1.26 |
2GLF | CRYSTAL STRUCTURE OF AMINIPEPTIDASE (M18 FAMILY) FROM THERMOTOGA MARITIMA | 3.4.11 |
2GLQ | X-RAY STRUCTURE OF HUMAN ALKALINE PHOSPHATASE IN COMPLEX WITH STRONTIUM | 3.1.3.1 |
2GMC | STRUCTURE OF C12-LF11 BOUND TO THE DPC MICELLES | 3.4.21 |
2GMK | CRYSTAL STRUCTURE OF ONCONASE DOUBLE MUTANT WITH SPONTANEOUSLY-ASSEMBLED (AMP) 4 STACK | 3.1.27 |
2GMN | CRYSTAL STRUCTURE OF BJP-1, A SUBCLASS B3 METALLO-BETA-LACTAMASE OF BRADYRHIZOBIUM JAPONICUM | 3.5.2.6 |
2GMT | THREE-DIMENSIONAL STRUCTURE OF CHYMOTRYPSIN INACTIVATED WITH (2S) N-ACETYL-L-ALANYL-L-PHENYLALANYL-CHLOROETHYL KETONE: IMPLICATIONS FOR THE MECHANISM OF INACTIVATION OF SERINE PROTEASES BY CHLOROKETONES | 3.4.21.1 |
2GMW | CRYSTAL STRUCTURE OF D,D-HEPTOSE 1.7-BISPHOSPHATE PHOSPHATASE FROM E. COLI. | 3.1.3 3.1.3.82 |
2GNS | DESIGN OF SPECIFIC PEPTIDE INHIBITORS OF PHOSPHOLIPASE A2: CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN A GROUP II PHOSPHOLIPASE A2 AND A DESIGNED PENTAPEPTIDE ALA- LEU- VAL- TYR- LYS AT 2.3 A RESOLUTION | 3.1.1.4 |
2GO3 | CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS LPXC COMPLEXED WITH IMIDAZOLE. | 3.5.1 3.5.1.108 |
2GO4 | CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS LPXC COMPLEXED WITH TU-514 | 3.5.1 3.5.1.108 |
2GOK | CRYSTAL STRUCTURE OF THE IMIDAZOLONEPROPIONASE FROM AGROBACTERIUM TUMEFACIENS AT 1.87 A RESOLUTION | 3.5.2.7 |
2GON | XRAY STRUCTURE OF GAG133-278 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2GP0 | HEPTP CATALYTIC DOMAIN (RESIDUES 44-339), S225D MUTANT | 3.1.3.48 |
2GP9 | CRYSTAL STRUCTURE OF THE SLOW FORM OF THROMBIN IN A SELF-INHIBITED CONFORMATION | 3.4.21.5 |
2GPZ | TRANSTHYRETIN-LIKE PROTEIN FROM SALMONELLA DUBLIN | 3.5.2.17 |
2GQ0 | CRYSTAL STRUCTURE OF THE MIDDLE DOMAIN OF HTPG, THE E. COLI HSP90 | 3.6.4.10 |
2GQ1 | CRYSTAL STRUCTURE OF RECOMBINANT TYPE I FRUCTOSE-1,6-BISPHOSPHATASE FROM ESCHERICHIA COLI COMPLEXED WITH SULFATE IONS | 3.1.3.11 |
2GQC | SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF RHOMBOID INTRAMEMBRANE PROTEASE FROM P. AERUGINOSA | 3.4.21.105 |
2GRC | 1.5 A STRUCTURE OF BROMODOMAIN FROM HUMAN BRG1 PROTEIN, A CENTRAL ATPASE OF SWI/SNF REMODELING COMPLEX | 3.6.1 3.6.4 |
2GRI | NMR STRUCTURE OF THE SARS-COV NON-STRUCTURAL PROTEIN NSP3A | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GSE | CRYSTAL STRUCTURE OF HUMAN DIHYDROPYRIMIDINEASE-LIKE 2 | 3.5.2.2 |
2GSN | STRUCTURE OF XAC NUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE | 3.6.1.9 |
2GSO | STRUCTURE OF XAC NUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE IN COMPLEX WITH VANADATE | 3.6.1.9 |
2GSP | RIBONUCLEASE T1/2',3'-CGPS AND 3'-GMP, 2 DAYS | 3.1.27.3 4.6.1.24 |
2GSU | STRUCTURE OF XAC NUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE IN COMPLEX WITH AMP | 3.6.1.9 |
2GT2 | STRUCTURE OF THE E. COLI GDP-MANNOSE MANNOSYL HYDROLASE | 3.6.1 |
2GT4 | CRYSTAL STRUCTURE OF THE Y103F MUTANT OF THE GDP-MANNOSE MANNOSYL HYDROLASE IN COMPLEX WITH GDP-MANNOSE AND MG+2 | 3.6.1 |
2GT7 | CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PEPTIDASE AT PH 6.0 IN THE SPACE GROUP P21 | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GT8 | CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PEPTIDASE (WITH AN ADDITIONAL ALA AT THE N-TERMINUS OF EACH PROTOMER) IN THE SPACE GROUP P43212 | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GTB | CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PEPTIDASE (WITH AN ADDITIONAL ALA AT THE N-TERMINUS OF EACH PROTOMER) INHIBITED BY AN AZA-PEPTIDE EPOXIDE IN THE SPACE GROUP P43212 | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GTH | CRYSTAL STRUCTURE OF THE WILDTYPE MHV CORONAVIRUS NON-STRUCTURAL PROTEIN NSP15 | 3.6.4.13 |
2GTI | MUTATION OF MHV CORONAVIRUS NON-STRUCTURAL PROTEIN NSP15 (F307L) | 3.6.4.13 |
2GTQ | CRYSTAL STRUCTURE OF AMINOPEPTIDASE N FROM HUMAN PATHOGEN NEISSERIA MENINGITIDIS | 3.4.11.2 |
2GTX | STRUCTURAL BASIS OF CATALYSIS BY MONONUCLEAR METHIONINE AMINOPEPTIDASE | 3.4.11.18 |
2GU0 | CRYSTAL STRUCTURE OF HUMAN ROTAVIRUS NSP2 (GROUP C / BRISTOL STRAIN) | 3.6.4 |
2GU1 | CRYSTAL STRUCTURE OF A ZINC CONTAINING PEPTIDASE FROM VIBRIO CHOLERAE | 3.4 |
2GU2 | CRYSTAL STRUCTURE OF AN ASPARTOACYLASE FROM RATTUS NORVEGICUS | 3.5.1.15 |
2GU4 | E. COLI METHIONINE AMINOPEPTIDASE IN COMPLEX WITH NLEP, 1: 0.5, DI-METALATED | 3.4.11.18 |
2GU5 | E. COLI METHIONINE AMINOPEPTIDASE IN COMPLEX WITH NLEP, 1: 1, DI-METALATED | 3.4.11.18 |
2GU6 | E. COLI METHIONINE AMINOPEPTIDASE IN COMPLEX WITH NLEP, 1: 2, DI-METALATED | 3.4.11.18 |
2GU7 | E. COLI METHIONINE AMINOPEPTIDASE UNLIGANDED, 1:0.5 | 3.4.11.18 |
2GUW | CRYSTAL STRUCTURE OF AMP NUCLEOSIDASE FROM SALMONELLA TYPHIMURIUM LT2 | 3.2.2.4 |
2GUY | ORTHORHOMBIC CRYSTAL STRUCTURE (SPACE GROUP P21212) OF ASPERGILLUS NIGER ALPHA-AMYLASE AT 1.6 A RESOLUTION | 3.2.1.1 |
2GV0 | THE STRUCTURE OF THE ORTHORHOMBIC FORM OF SOFT-SHELLED TURTLE LYSOZYME AT 1.9 ANGSTROMS RESOLUTION | 3.2.1.17 |
2GV1 | NMR SOLUTION STRUCTURE OF THE ACYLPHOSPHATASE FROM ESCHAERICHIA COLI | 3.6.1.7 |
2GV6 | CRYSTAL STRUCTURE OF MATRIPTASE WITH INHIBITOR CJ-730 | 3.4.21 3.4.21.109 |
2GV7 | STRUCTURE OF MATRIPTASE IN COMPLEX WITH INHIBITOR CJ-672 | 3.4.21 3.4.21.109 |
2GV9 | CRYSTAL STRUCTURE OF THE HERPES SIMPLEX VIRUS TYPE 1 DNA POLYMERASE | 2.7.7.7 3.1.26.4 |
2GVF | HCV NS3-4A PROTEASE DOMAIN COMPLEXED WITH A MACROCYCLIC KETOAMIDE INHIBITOR, SCH419021 | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2GVH | CRYSTAL STRUCTURE OF ACYL-COA HYDROLASE (15159470) FROM AGROBACTERIUM TUMEFACIENS AT 2.65 A RESOLUTION | 3.1.2.20 |
2GVN | L-ASPARAGINASE FROM ERWINIA CAROTOVORA IN COMPLEX WITH ASPARTIC ACID | 3.5.1.1 |
2GVU | CRYSTAL STRUCTURE OF DIISOPROPYL FLUOROPHOSPHATASE (DFPASE), MUTANT D229N / N120D | 3.1.8.2 |
2GVV | STRUCTURE OF DIISOPROPYL FLUOROPHOSPHATASE (DFPASE) IN COMPLEX WITH DICYCLOPENTYLPHOSPHOROAMIDATE (DCPPA) | 3.1.8.2 |
2GVW | STRUCTURE OF DIISOPROPYL FLUOROPHOSPHATASE (DFPASE) HOLOENZYME (RT) | 3.1.8.2 |
2GVX | STRUCTURE OF DIISOPROPYL FLUOROPHOSPHATASE (DFPASE), MUTANT D229N / N175D | 3.1.8.2 |
2GVY | MONOCLINIC CRYSTAL FORM OF ASPERGILLUS NIGER ALPHA-AMYLASE IN COMPLEX WITH MALTOSE AT 1.8 A RESOLUTION | 3.2.1.1 |
2GWF | STRUCTURE OF A USP8-NRDP1 COMPLEX | 3.1.2.15 3.4.19.12 |
2GWO | CRYSTAL STRUCTURE OF TMDP | 3.1.3.48 3.1.3.16 |
2GX4 | CRYSTAL STRUCTURE OF SARS CORONAVIRUS 3CL PROTEASE INHIBITOR COMPLEX | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GX6 | RATIONAL STABILIZATION OF E. COLI RIBOSE BINDING PROTEIN | 3.6.3.17 |
2GXB | CRYSTAL STRUCTURE OF THE ZA DOMAIN BOUND TO Z-RNA | 3.5.4 3.5.4.37 |
2GYU | CRYSTAL STRUCTURE OF MUS MUSCULUS ACETYLCHOLINESTERASE IN COMPLEX WITH HI-6 | 3.1.1.7 |
2GYV | CRYSTAL STRUCTURE OF MUS MUSCULUS ACETYLCHOLINESTERASE IN COMPLEX WITH ORTHO-7 | 3.1.1.7 |
2GYW | CRYSTAL STRUCTURE OF MUS MUSCULUS ACETYLCHOLINESTERASE IN COMPLEX WITH OBIDOXIME | 3.1.1.7 |
2GZ5 | HUMAN TYPE 1 METHIONINE AMINOPEPTIDASE IN COMPLEX WITH OVALICIN AT 1.1 ANG | 3.4.11.18 |
2GZ7 | STRUCTURE-BASED DRUG DESIGN AND STRUCTURAL BIOLOGY STUDY OF NOVEL NONPEPTIDE INHIBITORS OF SARS-COV MAIN PROTEASE | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GZ8 | STRUCTURE-BASED DRUG DESIGN AND STRUCTURAL BIOLOGY STUDY OF NOVEL NONPEPTIDE INHIBITORS OF SARS-COV MAIN PROTEASE | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GZ9 | STRUCTURE-BASED DRUG DESIGN AND STRUCTURAL BIOLOGY STUDY OF NOVEL NONPEPTIDE INHIBITORS OF SARS-COV MAIN PROTEASE | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2GZD | CRYSTAL STRUCTURE OF RAB11 IN COMPLEX WITH RAB11-FIP2 | 3.6.5.2 |
2GZH | CRYSTAL STRUCTURE OF RAB11 IN COMPLEX WITH RAB11-FAMILY INTERACTING PROTEIN 2 | 3.6.5.2 |
2GZR | ENTEROBACTIN AND SALMOCHELIN HYDROLASE IROE | 3.1 |
2GZS | ENTEROBACTIN HYDOLASE IROE COMPLEX WITH DFP | 3.1 |
2H02 | STRUCTURAL STUDIES OF PROTEIN TYROSINE PHOSPHATASE BETA CATALYTIC DOMAIN IN COMPLEX WITH INHIBITORS | 3.1.3.48 |
2H03 | STRUCTURAL STUDIES OF PROTEIN TYROSINE PHOSPHATASE BETA CATALYTIC DOMAIN IN COMPLEX WITH INHIBITORS | 3.1.3.48 |
2H04 | STRUCTURAL STUDIES OF PROTEIN TYROSINE PHOSPHATASE BETA CATALYTIC DOMAIN IN COMPLEX WITH INHIBITORS | 3.1.3.48 |
2H0E | CRYSTAL STRUCTURE OF PUCM IN THE ABSENCE OF SUBSTRATE | 3.5.2.17 |
2H0F | CRYSTAL STRUCTURE OF PUCM IN THE PRESENCE OF 8-AZAXANTHINE | 3.5.2.17 |
2H0J | CRYSTAL STRUCTURE OF PUCM IN THE PRESENCE OF 5,6-DIAMINOURACIL | 3.5.2.17 |
2H0P | NMR STRUCTURE OF THE DENGUE-4 VIRUS ENVELOPE PROTEIN DOMAIN III | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2H0Q | CRYSTAL STRUCTURE OF THE PGM DOMAIN OF THE SUPPRESSOR OF T-CELL RECEPTOR (STS-1) | 3.1.3.48 |
2H0R | STRUCTURE OF THE YEAST NICOTINAMIDASE PNC1P | 3.5.1.19 |
2H0T | CRYSTAL STRUCTURE OF THE M69V E166A DOUBLE MUTANT OF SHV-1 B-LACTAMASE COMPLEXED TO CLAVULANIC ACID | 3.5.2.6 |
2H0Y | CRYSTAL STRUCTURE OF THE M69V E166A DOUBLE MUTANT OF SHV-1 B-LACTAMASE COMPLEXED TO SULBACTAM | 3.5.2.6 |
2H10 | CRYSTAL STRUCTURE OF THE M69V E166A DOUBLE MUTANT OF SHV-1 B-LACTAMASE COMPLEXED TO TAZOBACTAM | 3.5.2.6 |
2H1C | CRYSTAL STRUCTURE OF FITACB FROM NEISSERIA GONORRHOEAE | 3.1 |
2H1E | TANDEM CHROMODOMAINS OF BUDDING YEAST CHD1 | 3.6.1 3.6.4 |
2H1I | CRYSTAL STRUCTURE OF THE BACILLUS CEREUS CARBOXYLESTERASE | 3.1.1.1 |
2H1J | 3.1 A X-RAY STRUCTURE OF PUTATIVE OLIGOENDOPEPTIDASE F: CRYSTALS GROWN BY MICROFLUIDIC SEEDING | 3.4.24 |
2H1N | 3.0 A X-RAY STRUCTURE OF PUTATIVE OLIGOENDOPEPTIDASE F: CRYSTALS GROWN BY VAPOR DIFFUSION TECHNIQUE | 3.4.24 |
2H1O | STRUCTURE OF FITAB BOUND TO IR36 DNA FRAGMENT | 3.1 |
2H1U | PORCINE PANCREATIC ELASTASE COMPLEXED WITH METPHELEUGLU AT PH 5.0 | 3.4.21.36 |
2H1X | CRYSTAL STRUCTURE OF 5-HYDROXYISOURATE HYDROLASE (FORMERLY KNOWN AS TRP, TRANSTHYRETIN RELATED PROTEIN) | 3.5.2.17 |
2H2D | THE STRUCTURAL BASIS FOR SIRTUIN SUBSTRATE AFFINITY | 3.5.1 2.3.1.286 |
2H2F | THE STRUCTURAL BASIS FOR SIRTUIN SUBSTRATE AFFINITY | 3.5.1 2.3.1.286 |
2H2G | THE STRUCTURAL BASIS OF SIRTUIN SUBSTRATE AFFINITY | 3.5.1 2.3.1.286 |
2H2H | THE STRUCTURAL BASIS OF SIRTUIN SUBSTRATE SPECIFICITY | 3.5.1 2.3.1.286 |
2H2I | THE STRUCTURAL BASIS OF SIRTUIN SUBSTRATE AFFINITY | 3.5.1 2.3.1.286 |
2H2N | CRYSTAL STRUCTURE OF HUMAN SOLUBLE CALCIUM-ACTIVATED NUCLEOTIDASE (SCAN) WITH CALCIUM ION | 3.6.1.6 |
2H2U | CRYSTAL STRUCTURE OF THE E130Y MUTANT OF HUMAN SOLUBLE CALCIUM-ACTIVATED NUCLEOTIDASE (SCAN) WITH CALCIUM ION | 3.6.1.6 |
2H2Z | CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE WITH AUTHENTIC N AND C-TERMINI | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2H3F | SOLUTION STRUCTURE OF THE HIV-1 MA PROTEIN | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2H3I | SOLUTION STRUCTURE OF THE HIV-1 MYRISTOYLATED MATRIX PROTEIN | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2H3Q | SOLUTION STRUCTURE OF HIV-1 MYRMA BOUND TO DI-C4-PHOSPHATIDYLINOSITOL-(4,5)-BISPHOSPHATE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2H3V | STRUCTURE OF THE HIV-1 MATRIX PROTEIN BOUND TO DI-C8-PHOSPHATIDYLINOSITOL-(4,5)-BISPHOSPHATE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2H3Z | STRUCTURE OF THE HIV-1 MATRIX PROTEIN BOUND TO DI-C4-PHOSPHATIDYLINOSITOL-(4,5)-BISPHOSPHATE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2H40 | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF UNLIGANDED PDE5 | 3.1.4.35 |
2H42 | CRYSTAL STRUCTURE OF PDE5 IN COMPLEX WITH SILDENAFIL | 3.1.4.35 |
2H44 | CRYSTAL STRUCTURE OF PDE5A1 IN COMPLEX WITH ICARISID II | 3.1.4.35 |
2H48 | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (CYS362->ALA, CYS364->ALA, CYS397->ALA) IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2H4C | STRUCTURE OF DABOIATOXIN (HETERODIMERIC PLA2 VENOM) | 3.1.1.4 |
2H4F | SIR2-P53 PEPTIDE-NAD+ | 3.5.1 2.3.1.286 |
2H4G | CRYSTAL STRUCTURE OF PTP1B WITH MONOCYCLIC THIOPHENE INHIBITOR | 3.1.3.48 |
2H4H | SIR2 H116Y MUTANT-P53 PEPTIDE-NAD | 3.5.1 2.3.1.286 |
2H4I | CRYSTAL STRUCTURE OF THE COMPLEX OF PROTEOLYTICALLY PRODUCED C-TERMINAL HALF OF BOVINE LACTOFERRIN WITH LACTOSE AT 2.55 A RESOLUTION | 3.4.21 |
2H4J | SIR2-DEACETYLATED PEPTIDE (FROM ENZYMATIC TURNOVER IN CRYSTAL) | 3.5.1 2.3.1.286 |
2H4K | CRYSTAL STRUCTURE OF PTP1B WITH A MONOCYCLIC THIOPHENE INHIBITOR | 3.1.3.48 |
2H4U | CRYSTAL STRUCTURE OF HUMAN THIOESTERASE SUPERFAMILY MEMBER 2 (CASP TARGET) | 3.1.2.1 3.1.2 3.1.2.2 |
2H4V | CRYSTAL STRUCTURE OF THE HUMAN TYROSINE RECEPTOR PHOSPHATASE GAMMA | 3.1.3.48 |
2H4W | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (GLU390->ASP) IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2H4X | HUMAN BISPHOSPHOGLYCERATE MUTASE COMPLEX WITH 3-PHOSPHOGLYCERATE WITH CRYSTAL GROWTH 90 DAYS | 5.4.2.4 5.4.2.1 3.1.3.13 5.4.2.11 |
2H4Y | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (ARG286->LYS) IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2H4Z | HUMAN BISPHOSPHOGLYCERATE MUTASE COMPLEXED WITH 2,3-BISPHOSPHOGLYCERATE | 5.4.2.4 5.4.2.1 3.1.3.13 5.4.2.11 |
2H51 | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (GLU390->ASP AND ARG286->LYS) IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2H52 | CRYSTAL STRUCTURE OF HUMAN BISPHOSPHOGLYCERATE MUTASE COMPLEX WITH 3-PHOSPHOGLYCERATE (18 DAYS) | 5.4.2.4 5.4.2.1 3.1.3.13 5.4.2.11 |
2H54 | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (THR388->ALA) IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2H56 | CRYSTAL STRUCTURE OF DNA-3-METHYLADENINE GLYCOSIDASE (10174367) FROM BACILLUS HALODURANS AT 2.55 A RESOLUTION | 3.2.2 |
2H59 | SIR2 H116A-DEACETYLATED P53 PEPTIDE-3'-O-ACETYL ADP RIBOSE | 3.5.1 2.3.1.286 |
2H5C | 0.82A RESOLUTION CRYSTAL STRUCTURE OF ALPHA-LYTIC PROTEASE AT PH 5 | 3.4.21.12 |
2H5D | 0.9A RESOLUTION CRYSTAL STRUCTURE OF ALPHA-LYTIC PROTEASE COMPLEXED WITH A TRANSITION STATE ANALOGUE, MEOSUC-ALA-ALA-PRO-VAL BORONIC ACID | 3.4.21.12 |
2H5I | CRYSTAL STRUCTURE OF CASPASE-3 WITH INHIBITOR AC-DEVD-CHO | 3.4.22 3.4.22.56 |
2H5J | CRYSTAL STRUSTURE OF CASPASE-3 WITH INHIBITOR AC-DMQD-CHO | 3.4.22 3.4.22.56 |
2H5S | SA2-13 PENAM SULFONE COMPLEXED TO WT SHV-1 BETA-LACTAMASE | 3.5.2.6 |
2H5X | RUVA FROM MYCOBACTERIUM TUBERCULOSIS | 3.6.1 3.6.4.12 |
2H5Z | CRYSTALLOGRAPHIC STRUCTURE OF DIGESTIVE LYSOZYME 1 FROM MUSCA DOMESTICA BOUND TO CHITOTETRAOSE AT 1.92 A RESOLUTION | 3.2.1.17 |
2H60 | SOLUTION STRUCTURE OF HUMAN BRG1 BROMODOMAIN | 3.6.1 3.6.4 |
2H65 | CRYSTAL STRUSTURE OF CASPASE-3 WITH INHIBITOR AC-VDVAD-CHO | 3.4.22 3.4.22.56 |
2H6A | CRYSTAL STRUCTURE OF THE ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (MONO ZINC FORM) | 3.5.2.6 |
2H6M | AN EPISULFIDE CATION (THIIRANIUM RING) TRAPPED IN THE ACTIVE SITE OF HAV 3C PROTEINASE INACTIVATED BY PEPTIDE-BASED KETONE INHIBITORS | 3.4.22.28 3.6.1.15 2.7.7.48 |
2H6S | SECRETED ASPARTIC PROTEINASE (SAP) 3 FROM CANDIDA ALBICANS | 3.4.23.24 |
2H6T | SECRETED ASPARTIC PROTEINASE (SAP) 3 FROM CANDIDA ALBICANS COMPLEXED WITH PEPSTATIN A | 3.4.23.24 |
2H7J | CRYSTAL STRUCTURE OF CATHEPSIN S IN COMPLEX WITH A NONPEPTIDIC INHIBITOR. | 3.4.22.27 |
2H85 | CRYSTAL STRUCTURE OF NSP 15 FROM SARS | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2H8C | STRUCTURE OF RUSA D70N IN COMPLEX WITH DNA | 3.1.22 3.1.22.4 |
2H8E | STRUCTURE RUSA D70N | 3.1.22 3.1.22.4 |
2H8G | 5'-METHYLTHIOADENOSINE NUCLEOSIDASE FROM ARABIDOPSIS THALIANA | 3.2.2.16 |
2H8N | STRUCTURE OF A GLUTAMINE-RICH DOMAIN FROM HISTONE DEACETYLASE 4 | 3.5.1.98 |
2H9H | AN EPISULFIDE CATION (THIIRANIUM RING) TRAPPED IN THE ACTIVE SITE OF HAV 3C PROTEINASE INACTIVATED BY PEPTIDE-BASED KETONE INHIBITORS | 3.4.22.28 3.6.1.15 2.7.7.48 |
2H9J | STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH NI2-XYLYLBICYCLAM | 3.2.1.17 |
2H9K | STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH NI-CYCLAM | 3.2.1.17 |
2H9T | CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN IN COMPLEX WITH SURAMIN | 3.4.21.5 |
2H9Y | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE COMPLEXED WITH M-(N,N,N-TRIMETHYLAMMONIO)TRIFLUOROACETOPHENONE | 3.1.1.7 |
2HA0 | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE COMPLEXED WITH 4-KETOAMYLTRIMETHYLAMMONIUM | 3.1.1.7 |
2HA2 | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE COMPLEXED WITH SUCCINYLCHOLINE | 3.1.1.7 |
2HA3 | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE COMPLEXED WITH CHOLINE | 3.1.1.7 |
2HA4 | CRYSTAL STRUCTURE OF MUTANT S203A OF MOUSE ACETYLCHOLINESTERASE COMPLEXED WITH ACETYLCHOLINE | 3.1.1.7 |
2HA5 | CRYSTAL STRUCTURE OF MUTANT S203A OF ACETYLCHOLINESTERASE COMPLEXED WITH ACETYLTHIOCHOLINE | 3.1.1.7 |
2HA6 | CRYSTAL STRUCTURE OF MUTANT S203A OF MOUSE ACETYLCHOLINESTERASE COMPLEXED WITH SUCCINYLCHOLINE | 3.1.1.7 |
2HA7 | CRYSTAL STRUCTURE OF MUTANT S203A OF MOUSE ACETYLCHOLINESTERASE COMPLEXED WITH BUTYRYLTHIOCHOLINE | 3.1.1.7 |
2HAD | CRYSTAL STRUCTURE OF HALOALKANE DEHALOGENASE: AN ENZYME TO DETOXIFY HALOGENATED ALKANES | 3.8.1.5 |
2HAH | THE STRUCTURE OF FIV 12S PROTEASE IN COMPLEX WITH TL-3 | 3.4.23.16 2.7.7.49 3.1.13.2 3.1.26.13 |
2HAI | CRYSTAL STRUCTURE OF HCV NS5B RNA POLYMERASE IN COMPLEX WITH NOVEL CLASS OF DIHYDROPYRONE-CONTAINING INHIBITOR. | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2HAL | AN EPISULFIDE CATION (THIIRANIUM RING) TRAPPED IN THE ACTIVE SITE OF HAV 3C PROTEINASE INACTIVATED BY PEPTIDE-BASED KETONE INHIBITORS | 3.4.22.28 3.6.1.15 2.7.7.48 |
2HAW | CRYSTAL STRUCTURE OF FAMILY II INORGANIC PYROPHOSPHATASE IN COMPLEX WITH PNP | 3.6.1.1 |
2HB1 | CRYSTAL STRUCTURE OF PTP1B WITH MONOCYCLIC THIOPHENE INHIBITOR | 3.1.3.48 |
2HB2 | STRUCTURE OF HIV PROTEASE 6X MUTANT IN APO FORM | 3.4.23.16 |
2HB3 | WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH POTENT INHIBITOR GRL06579 | 3.4.23.4 |
2HB4 | STRUCTURE OF HIV PROTEASE NL4-3 IN AN UNLIGANDED STATE | 3.4.23.16 |
2HB5 | CRYSTAL STRUCTURE OF THE MOLONEY MURINE LEUKEMIA VIRUS RNASE H DOMAIN | 3.1.26.4 3.4.23 2.7.7.49 2.7.7.7 2.7.7 3.1 |
2HB6 | STRUCTURE OF CAENORHABDITIS ELEGANS LEUCINE AMINOPEPTIDASE (LAP1) | 3.4.11.1 |
2HB9 | CRYSTAL STRUCTURE OF THE ZINC-BETA-LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA (INHIBITOR 3) | 3.5.2.6 |
2HBJ | STRUCTURE OF THE YEAST NUCLEAR EXOSOME COMPONENT, RRP6P, REVEALS AN INTERPLAY BETWEEN THE ACTIVE SITE AND THE HRDC DOMAIN | 3.1.13 |
2HBK | STRUCTURE OF THE YEAST NUCLEAR EXOSOME COMPONENT, RRP6P, REVEALS AN INTERPLAY BETWEEN THE ACTIVE SITE AND THE HRDC DOMAIN; PROTEIN IN COMPLEX WITH MN | 3.1.13 |
2HBL | STRUCTURE OF THE YEAST NUCLEAR EXOSOME COMPONENT, RRP6P, REVEALS AN INTERPLAY BETWEEN THE ACTIVE SITE AND THE HRDC DOMAIN; PROTEIN IN COMPLEX WITH MN, ZN, AND AMP | 3.1.13 |
2HBM | STRUCTURE OF THE YEAST NUCLEAR EXOSOME COMPONENT, RRP6P, REVEALS AN INTERPLAY BETWEEN THE ACTIVE SITE AND THE HRDC DOMAIN; PROTEIN IN COMPLEX WITH MN, ZN, AND UMP | 3.1.13 |
2HBQ | CRYSTAL STRUCTURE OF WILDTYPE HUMAN CASPASE-1 IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2HBR | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (ARG286->ALA) IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2HBY | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (GLU390->ALA) IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2HBZ | CRYSTAL STRUCTURE OF HUMAN CASPASE-1 (ARG286->ALA, GLU390->ALA) IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK) | 3.4.22.36 |
2HC0 | STRUCTURE OF HIV PROTEASE 6X MUTANT IN COMPLEX WITH AB-2. | 3.4.23.16 |
2HC1 | ENGINEERED CATALYTIC DOMAIN OF PROTEIN TYROSINE PHOSPHATASE HPTPBETA. | 3.1.3.48 |
2HC2 | ENGINEERED PROTEIN TYROSINE PHOSPHATASE BETA CATALYTIC DOMAIN | 3.1.3.48 |
2HC9 | STRUCTURE OF CAENORHABDITIS ELEGANS LEUCINE AMINOPEPTIDASE-ZINC COMPLEX (LAP1) | 3.4.11.1 |
2HCA | CRYSTAL STRUCTURE OF BOVINE LACTOFERRIN C-LOBE LIGANDED WITH GLUCOSE AT 2.8 A RESOLUTION | 3.4.21 |
2HCM | CRYSTAL STRUCTURE OF MOUSE PUTATIVE DUAL SPECIFICITY PHOSPHATASE COMPLEXED WITH ZINC TUNGSTATE, NEW YORK STRUCTURAL GENOMICS CONSORTIUM | 3.1.3.16 3.1.3.48 |
2HCN | CRYSTAL STRUCTURE OF RNA DEPENDENT RNA POLYMERASE DOMAIN FROM WEST NILE VIRUS | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2HCS | CRYSTAL STRUCTURE OF RNA DEPENDANT RNA POLYMERASE DOMAIN OF WEST NILE VIRUS | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2HCT | ACIDIC RESIDUES AT THE ACTIVE SITES OF CD38 AND ADP-RIBOSYL CYCLASE DETERMINE NAAPD SYNTHESIS AND HYDROLYSIS ACTIVITIES | 3.2.2.5 3.2.2.6 2.4.99.20 |
2HD0 | STRUCTURE OF THE CATALYTIC DOMAIN OF HEPATITIS C VIRUS NS2 | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2HD1 | CRYSTAL STRUCTURE OF PDE9 IN COMPLEX WITH IBMX | 3.1.4.35 |
2HD4 | CRYSTAL STRUCTURE OF PROTEINASE K INHIBITED BY A LACTOFERRIN OCTAPEPTIDE GLY-ASP-GLU-GLN-GLY-GLU-ASN-LYS AT 2.15 A RESOLUTION | 3.4.21.64 |
2HD5 | USP2 IN COMPLEX WITH UBIQUITIN | 3.1.2.15 3.4.19.12 |
2HDO | CRYSTAL STRUCTURE OF PUTATIVE PHOSPHOGLYCOLATE PHOSPHATASE (NP_784602.1) FROM LACTOBACILLUS PLANTARUM AT 1.50 A RESOLUTION | 3.1.3.18 3.6.1.1 |
2HDQ | AMPC BETA-LACTAMASE IN COMPLEX WITH 2-CARBOXYTHIOPHENE | 3.5.2.6 |
2HDR | AMPC BETA-LACTAMASE IN COMPLEX WITH 4-AMINO-3-HYDROXYBENZOIC ACID | 3.5.2.6 |
2HDS | AMPC BETA-LACTAMASE IN COMPLEX WITH 4-METHANESULFONYLAMINO BENZOIC ACID | 3.5.2.6 |
2HDU | AMPC BETA-LACTAMASE IN COMPLEX WITH 2-ACETAMIDOTHIOPHENE-3-CARBOXYLIC ACID | 3.5.2.6 |
2HEA | CONTRIBUTION OF WATER MOLECULES IN THE INTERIOR OF A PROTEIN TO THE CONFORMATIONAL STABILITY | 3.2.1.17 |
2HEB | CONTRIBUTION OF WATER MOLECULES IN THE INTERIOR OF A PROTEIN TO THE CONFORMATIONAL STABILITY | 3.2.1.17 |
2HEC | CONTRIBUTION OF WATER MOLECULES IN THE INTERIOR OF A PROTEIN TO THE CONFORMATIONAL STABILITY | 3.2.1.17 |
2HED | CONTRIBUTION OF WATER MOLECULES IN THE INTERIOR OF A PROTEIN TO THE CONFORMATIONAL STABILITY | 3.2.1.17 |
2HEE | CONTRIBUTION OF WATER MOLECULES IN THE INTERIOR OF A PROTEIN TO THE CONFORMATIONAL STABILITY | 3.2.1.17 |
2HEF | CONTRIBUTION OF WATER MOLECULES IN THE INTERIOR OF A PROTEIN TO THE CONFORMATIONAL STABILITY | 3.2.1.17 |
2HEG | PHOSPHO-ASPARTYL INTERMEDIATE ANALOGUE OF APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE | 3.1.3.2 |
2HEZ | BIFIDOBACTERIUM LONGUM BILE SALT HYDROLASE | 3.5.1.24 3.5.1 3.5.1.74 |
2HF0 | BIFIDOBACTERIUM LONGUM BILE SALT HYDROLASE | 3.5.1.24 3.5.1 3.5.1.74 |
2HF2 | DOMAIN SHIFTING CONFIRMS MONOMERIC STRUCTURE OF ESCHERICHIA SUGAR PHOSPHATASE SUPH | 3.1.3.23 |
2HF7 | TRANSITION STATE ANALOGUE OF APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE (ALUMINIUM FLUORIDE COMPLEX) | 3.1.3.2 |
2HFZ | CRYSTAL STRUCTURE OF RNA DEPENDENT RNA POLYMERASE DOMAIN FROM WEST NILE VIRUS | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2HGT | STRUCTURE OF THE HIRUGEN AND HIRULOG 1 COMPLEXES OF ALPHA-THROMBIN | 3.4.21.5 |
2HH5 | CRYSTAL STRUCTURE OF CATHEPSIN S IN COMPLEX WITH A ZINC MEDIATED NON-COVALENT ARYLAMINOETHYL AMIDE | 3.4.22.27 |
2HHA | THE STRUCTURE OF DPP4 IN COMPLEX WITH AN OXADIAZOLE INHIBITOR | 3.4.14.5 |
2HHJ | HUMAN BISPHOSPHOGLYCERATE MUTASE COMPLEXED WITH 2,3-BISPHOSPHOGLYCERATE (15 DAYS) | 5.4.2.4 5.4.2.1 3.1.3.13 5.4.2.11 |
2HHL | CRYSTAL STRUCTURE OF THE HUMAN SMALL CTD PHOSPHATASE 3 ISOFORM 1 | 3.1.3.16 |
2HHM | STRUCTURE OF INOSITOL MONOPHOSPHATASE, THE PUTATIVE TARGET OF LITHIUM THERAPY | 3.1.3.25 3.1.3.94 |
2HHN | CATHEPSIN S IN COMPLEX WITH NON COVALENT ARYLAMINOETHYL AMIDE. | 3.4.22.27 |
2HI0 | CRYSTAL STRUCTURE OF PUTATIVE PHOSPHOGLYCOLATE PHOSPHATASE (YP_619066.1) FROM LACTOBACILLUS DELBRUECKII SUBSP. BULGARICUS ATCC BAA-365 AT 1.51 A RESOLUTION | 3.1.3.18 |
2HIH | CRYSTAL STRUCTURE OF STAPHYLOCOCCUS HYICUS LIPASE | 3.1.1.3 3.1.1.32 |
2HIM | CRYSTAL STRUCTURE AND ALLOSTERIC REGULATION OF THE CYTOPLASMIC ESCHERICHIA COLI L-ASPARAGINASE I | 3.5.1.1 |
2HIS | CELLULOMONAS FIMI XYLANASE/CELLULASE DOUBLE MUTANT E127A/H205N WITH COVALENT CELLOBIOSE | 3.2.1.91 3.2.1.8 |
2HIZ | CRYSTAL STRUCTURE OF HUMAN BETA-SECRETASE (BACE) IN THE PRESENCE OF AN INHIBITOR | 3.4.23.46 |
2HJE | CRYSTAL STRUCTURE OF VIBRIO HARVEYI LUXQ PERIPLASMIC DOMAIN | 2.7.13.3 3.1.3 |
2HJH | CRYSTAL STRUCTURE OF THE SIR2 DEACETYLASE | 3.5.1 2.3.1.286 |
2HJP | CRYSTAL STRUCTURE OF PHOSPHONOPYRUVATE HYDROLASE COMPLEX WITH PHOSPHONOPYRUVATE AND MG++ | 3.11.1.3 |
2HJV | STRUCTURE OF THE SECOND DOMAIN (RESIDUES 207-368) OF THE BACILLUS SUBTILIS YXIN PROTEIN | 3.6.1 3.6.4.13 |
2HKP | SUMO PROTEASE ULP1 WITH THE CATALYTIC CYSTEINE OXIDIZED TO A SULFENIC ACID | 3.4.22 3.4.22.68 |
2HKY | NMR SOLUTION STRUCTURE OF HUMAN RNASE 7 | 3.1.27 |
2HL6 | STRUCTURE OF HOMOLOGOUSLY EXPRESSED FERRULATE ESTERASE OF ASPERGILLUS NIGER IN COMPLEX WITH CAPS | 3.1.1.73 |
2HL8 | SUMO PROTEASE ULP1 WITH THE CATALYTIC CYSTEINE OXIDIZED TO A SULFINIC ACID | 3.4.22 3.4.22.68 |
2HL9 | SUMO PROTEASE ULP1 WITH THE CATALYTIC CYSTEINE OXIDIZED TO A SULFONIC ACID | 3.4.22 3.4.22.68 |
2HLC | HL COLLAGENASE STRUCTURE AT 1.7A RESOLUTION | 3.4.21 3.4.21.49 |
2HLT | SOLUTION STRUCTURE OF BACILLUS SUBTILIS ACYLPHOSPHATASE | 3.6.1.7 |
2HLU | SOLUTION STRUCTURE OF BACILLUS SUBTILIS ACYLPHOSPHATASE | 3.6.1.7 |
2HM1 | CRYSTAL STRUCTURE OF HUMAN BETA-SECRETASE (BACE) IN THE PRESENCE OF AN INHIBITOR (2) | 3.4.23.46 |
2HM7 | CRYSTAL STRUCTURE ANALYSIS OF THE G84S EST2 MUTANT | 3.1.1.1 |
2HMI | HIV-1 REVERSE TRANSCRIPTASE/FRAGMENT OF FAB 28/DNA COMPLEX | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2HMX | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 MATRIX PROTEIN | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2HND | CRYSTAL STRUCTURE OF K101E MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH NEVIRAPINE | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2HNP | CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE 1B | 3.1.3.48 |
2HNQ | CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE 1B | 3.1.3.48 |
2HNT | CRYSTALLOGRAPHIC STRUCTURE OF HUMAN GAMMA-THROMBIN | 3.4.21.5 |
2HNY | CRYSTAL STRUCTURE OF E138K MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH NEVIRAPINE | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2HNZ | CRYSTAL STRUCTURE OF E138K MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH PETT-2 | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2HOB | CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE WITH AUTHENTIC N AND C-TERMINI IN COMPLEX WITH A MICHAEL ACCEPTOR N3 | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2HOH | RIBONUCLEASE T1 (N9A MUTANT) COMPLEXED WITH 2'GMP | 3.1.27.3 4.6.1.24 |
2HOQ | CRYSTAL STRUCTURE OF THE PROBABLE HALOACID DEHALOGENASE (PH1655) FROM PYROCOCCUS HORIKOSHII OT3 | 3 3.1.3 |
2HOW | DIPEPTIDASE (PH0974) FROM PYROCOCCUS HORIKOSHII OT3 | 3.4 |
2HP5 | CRYSTAL STRUCTURE OF THE OXA-10 W154G MUTANT AT PH 7.0 | 3.5.2.6 |
2HP6 | CRYSTAL STRUCTURE OF THE OXA-10 W154A MUTANT AT PH 7.5 | 3.5.2.6 |
2HP9 | CRYSTAL STRUCTURE OF THE OXA-10 W154A MUTANT AT PH 6.0 | 3.5.2.6 |
2HPA | STRUCTURAL ORIGINS OF L(+)-TARTRATE INHIBITION OF HUMAN PROSTATIC ACID PHOSPHATASE | 3.1.3.2 3.1.3.5 |
2HPB | CRYSTAL STRUCTURE OF THE OXA-10 W154A MUTANT AT PH 9.0 | 3.5.2.6 |
2HPE | COMPARISON OF THE STRUCTURES OF HIV-2 PROTEASE COMPLEXES IN THREE CRYSTAL SPACE GROUPS WITH AN HIV-1 PROTEASE COMPLEX STRUCTURE | 3.4.23.47 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2HPF | COMPARISON OF THE STRUCTURES OF HIV-2 PROTEASE COMPLEXES IN THREE CRYSTAL SPACE GROUPS WITH AN HIV-1 PROTEASE COMPLEX STRUCTURE | 3.4.23.47 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2HPJ | CRYSTAL STRUCTURE OF THE PUB DOMAIN OF MOUSE PNGASE | 3.5.1.52 |
2HPL | CRYSTAL STRUCTURE OF THE MOUSE P97/PNGASE COMPLEX | 3.5.1.52 |
2HPO | STRUCTURE OF AMINOPEPTIDASE N FROM E. COLI SUGGESTS A COMPARTMENTALIZED, GATED ACTIVE SITE | 3.4.11.2 |
2HPP | STRUCTURES OF THE NONCOVALENT COMPLEXES OF HUMAN AND BOVINE PROTHROMBIN FRAGMENT 2 WITH HUMAN PPACK-THROMBIN | 3.4.21.5 |
2HPQ | STRUCTURES OF THE NONCOVALENT COMPLEXES OF HUMAN AND BOVINE PROTHROMBIN FRAGMENT 2 WITH HUMAN PPACK-THROMBIN | 3.4.21.5 |
2HPT | CRYSTAL STRUCTURE OF E. COLI PEPN (AMINOPEPTIDASE N)IN COMPLEX WITH BESTATIN | 3.4.11.2 |
2HPZ | CRYSTAL STRUCTURE OF PROTEINASE K COMPLEX WITH A SYNTHETIC PEPTIDE KLKLLVVIRLK AT 1.69 A RESOLUTION | 3.4.21.64 |
2HQE | CRYSTAL STRUCTURE OF HUMAN P100 TUDOR DOMAIN: LARGE FRAGMENT | 3.1.31.1 |
2HQU | HUMAN DUTPASE IN COMPLEX WITH ALPHA,BETA-IMINODUTP AND MAGNESIUM ION | 3.6.1.23 |
2HQX | CRYSTAL STRUCTURE OF HUMAN P100 TUDOR DOMAIN CONSERVED REGION | 3.1.31.1 |
2HR6 | CRYSTAL STRUCTURE OF DUTPASE IN COMPLEX WITH SUBSTRATE ANALOGUE DUDP AND MANGANESE | 3.6.1.23 |
2HRM | CRYSTAL STRUCTURE OF DUTPASE COMPLEXED WITH SUBSTRATE ANALOGUE METHYLENE-DUTP | 3.6.1.23 |
2HRR | CRYSTAL STRUCTURE OF HUMAN LIVER CARBOXYLESTERASE 1 (HCE1) IN COVALENT COMPLEX WITH THE NERVE AGENT TABUN (GA) | 3.1.1.1 3.1.1.13 3.1.1.56 |
2HRV | 2A CYSTEINE PROTEINASE FROM HUMAN RHINOVIRUS 2 | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2HRW | CRYSTAL STRUCTURE OF PHOSPHONOPYRUVATE HYDROLASE | 3.11.1.3 |
2HS1 | ULTRA-HIGH RESOLUTION X-RAY CRYSTAL STRUCTURE OF HIV-1 PROTEASE V32I MUTANT WITH TMC114 (DARUNAVIR) INHIBITOR | 3.4.23.16 |
2HS2 | CRYSTAL STRUCTURE OF M46L MUTANT OF HIV-1 PROTEASE COMPLEXED WITH TMC114 (DARUNAVIR) | 3.4.23.16 |
2HS7 | MULTIPATTERN RIETVELD REFINEMENT WITH PROTEIN POWDER DATA: AN APPROACH TO HIGHER RESOLUTION | 3.2.1.17 |
2HS9 | MULTIPATTERN RIETVELD REFINEMENT WITH PROTEIN POWDER DATA: AN APPROACH TO HIGHER RESOLUTION | 3.2.1.17 |
2HSO | MULTIPATTERN RIETVELD REFINEMENT WITH PROTEIN POWDER DATA: AN APPROACH TO HIGHER RESOLUTION | 3.2.1.17 |
2HSP | SOLUTION STRUCTURE OF THE SH3 DOMAIN OF PHOSPHOLIPASE CGAMMA | 3.1.4.11 |
2HSX | NMR STRUCTURE OF THE NONSTRUCTURAL PROTEIN 1 (NSP1) FROM THE SARS CORONAVIRUS | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2HSZ | CRYSTAL STRUCTURE OF A PREDICTED PHOSPHOGLYCOLATE PHOSPHATASE (HS_0176) FROM HAEMOPHILUS SOMNUS 129PT AT 1.90 A RESOLUTION | 3.1.3.18 |
2HT5 | N8 NEURAMINIDASE | 3.2.1.18 |
2HT7 | N8 NEURAMINIDASE IN OPEN COMPLEX WITH OSELTAMIVIR | 3.2.1.18 |
2HT8 | N8 NEURAMINIDASE IN COMPLEX WITH OSELTAMIVIR | 3.2.1.18 |
2HTQ | N8 NEURAMINIDASE IN COMPLEX WITH ZANAMIVIR | 3.2.1.18 |
2HTR | N8 NEURAMINIDASE IN COMPLEX WITH DANA | 3.2.1.18 |
2HTU | N8 NEURAMINIDASE IN COMPLEX WITH PERAMIVIR | 3.2.1.18 |
2HTV | N4 NEURAMINIDASE | 3.2.1.18 |
2HTW | N4 NEURAMINIDASE IN COMPLEX WITH DANA | 3.2.1.18 |
2HTX | CRYSTAL STRUCTURE ANALYSIS OF HEN EGG WHITE LYSOZYME CROSSLINKED BY POLYMERIZED GLUTARALDEHYDE IN ACIDIC ENVIRONMENT | 3.2.1.17 |
2HU1 | CRYSTAL STRUCTURE ANALYSIS OF HEN EGG WHITE LYSZOYME | 3.2.1.17 |
2HU3 | PARENT STRUCTURE OF HEN EGG WHITE LYSOZYME GROWN IN ACIDIC PH 4.8. REFINEMENT FOR COMPARISON WITH CROSSLINKED MOLECULES OF LYSOZYME | 3.2.1.17 |
2HU5 | BINDING OF INHIBITORS BY ACYLAMINOACYL-PEPTIDASE | 3.4.19.1 |
2HU6 | CRYSTAL STRUCTURE OF HUMAN MMP-12 IN COMPLEX WITH ACETOHYDROXAMIC ACID AND A BICYCLIC INHIBITOR | 3.4.24.65 |
2HU7 | BINDING OF INHIBITORS BY ACYLAMINOACYL PEPTIDASE | 3.4.19.1 |
2HU8 | BINDING OF INHIBITORS BY ACYLAMINOACYL PEPTIDASE | 3.4.19.1 |
2HUB | STRUCTURE OF HEN EGG-WHITE LYSOZYME DETERMINED FROM CRYSTALS GROWN IN PH 7.5 | 3.2.1.17 |
2HUC | STRUCTURAL STUDIES EXAMINING THE SUBSTRATE SPECIFICITY PROFILES OF PC-PLCBC PROTEIN VARIANTS | 3.1.4.3 |
2HUK | CRYSTAL STRUCTURE OF T4 LYSOZYME V131C SYNTHETIC DIMER | 3.2.1.17 |
2HUL | CRYSTAL STRUCTURE OF T4 LYSOZYME S44C SYNTHETIC DIMER | 3.2.1.17 |
2HUM | CRYSTAL STRUCTURE OF T4 LYSOZYME D72C SYNTHETIC DIMER | 3.2.1.17 |
2HVL | CRYSTAL STRUCTURE OF THE HEPTP CATALYTIC DOMAIN C270S MUTANT | 3.1.3.48 |
2HVM | HEVAMINE A AT 1.8 ANGSTROM RESOLUTION | 3.2.1.14 3.2.1.17 |
2HVV | CRYSTAL STRUCTURE OF DCMP DEAMINASE FROM STREPTOCOCCUS MUTANS | 3.5.4.12 |
2HVW | CRYSTAL STRUCTURE OF DCMP DEAMINASE FROM STREPTOCOCCUS MUTANS | 3.5.4.12 |
2HVX | DISCOVERY OF POTENT, ORALLY ACTIVE, NONPEPTIDE INHIBITORS OF HUMAN MAST CELL CHYMASE BY USING STRUCTURE-BASED DRUG DESIGN | 3.4.21.39 |
2HW0 | NMR SOLUTION STRUCTURE OF THE NUCLEASE DOMAIN FROM THE REPLICATOR INITIATOR PROTEIN FROM PORCINE CIRCOVIRUS PCV2 | 3.1.21 2.7.7 3.6.1 |
2HW4 | CRYSTAL STRUCTURE OF HUMAN PHOSPHOHISTIDINE PHOSPHATASE | 3.1.3 3.9.1.3 |
2HWB | A COMPARISON OF THE ANTI-RHINOVIRAL DRUG BINDING POCKET IN HRV14 AND HRV1A | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2HWC | A COMPARISON OF THE ANTI-RHINOVIRAL DRUG BINDING POCKET IN HRV14 AND HRV1A | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2HWD | A COMPARISON OF THE ANTI-RHINOVIRAL DRUG BINDING POCKET IN HRV14 AND HRV1A | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2HWE | A COMPARISON OF THE ANTI-RHINOVIRAL DRUG BINDING POCKET IN HRV14 AND HRV1A | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2HWF | A COMPARISON OF THE ANTI-RHINOVIRAL DRUG BINDING POCKET IN HRV14 AND HRV1A | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2HWH | HCV NS5B ALLOSTERIC INHIBITOR COMPLEX | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2HWI | HCV NS5B ALLOSTERIC INHIBITOR COMPLEX | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2HWK | CRYSTAL STRUCTURE OF VENEZUELAN EQUINE ENCEPHALITIS ALPHAVIRUS NSP2 PROTEASE DOMAIN | 3.4.22 |
2HWL | CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH FIBRINOGEN GAMMA' PEPTIDE | 3.4.21.5 |
2HWT | NMR SOLUTION STRUCTURE OF THE MASTER-REP PROTEIN NUCLEASE DOMAIN (2-95) FROM THE FABA BEAN NECROTIC YELLOWS VIRUS | 3.1.21 2.7.7 3.6.1 |
2HWW | STRUCTURE OF PIN DOMAIN OF HUMAN SMG6 | 3.1 |
2HWX | STRUCTURE OF HUMAN SMG6 E1282C PIN DOMAIN MUTANT. | 3.1 |
2HX5 | CRYSTAL STRUCTURE OF A PUTATIVE THIOESTERASE (PMT_2055) FROM PROCHLOROCOCCUS MARINUS STR. MIT 9313 AT 1.50 A RESOLUTION | 3.1.2.28 |
2HX6 | SOLUTION STRUCTURE ANALYSIS OF THE PHAGE T4 ENDORIBONUCLEASE REGB | 3.1 |
2HXB | DCTP DEAMINASE-DUTPASE FROM METHANOCALDOCOCCUS JANNASCHII | 3.5.4.30 |
2HXD | BIFUNCTIONAL DCTP DEAMINASE-DUTPASE MUTANT ENZYME VARIANT E145A FROM METHANOCALDOCOCCUS JANNASCHII IN COMPLEX WITH ALPHA,BETA-IMIDO DUTP AND MAGNESIUM | 3.5.4.30 |
2HXM | COMPLEX OF UNG2 AND A SMALL MOLECULE SYNTHETIC INHIBITOR | 3.2.2 3.2.2.27 |
2HXP | CRYSTAL STRUCTURE OF THE HUMAN PHOSPHATASE (DUSP9) | 3.1.3.48 3.1.3.16 |
2HXV | CRYSTAL STRUCTURE OF A DIAMINOHYDROXYPHOSPHORIBOSYLAMINOPYRIMIDINE DEAMINASE/ 5-AMINO-6-(5-PHOSPHORIBOSYLAMINO)URACIL REDUCTASE (TM1828) FROM THERMOTOGA MARITIMA AT 1.80 A RESOLUTION | 3.5.4.26 1.1.1.193 |
2HXY | CRYSTAL STRUCTURE OF HUMAN APO-EIF4AIII | 3.6.1 3.6.4.13 |
2HY1 | CRYSTAL STRUCTURE OF RV0805 | 3.1.4.17 3.1.4.53 |
2HY3 | CRYSTAL STRUCTURE OF THE HUMAN TYROSINE RECEPTOR PHOSPHATE GAMMA IN COMPLEX WITH VANADATE | 3.1.3.48 |
2HYK | THE CRYSTAL STRUCTURE OF AN ENDO-BETA-1,3-GLUCANASE FROM ALKALIPHILIC NOCARDIOPSIS SP.STRAIN F96 | 3.2.1.39 |
2HYO | CRYSTAL STRUCTURE OF RV0805 N97A MUTANT | 3.1.4.17 3.1.4.53 |
2HYP | CRYSTAL STRUCTURE OF RV0805 D66A MUTANT | 3.1.4.17 3.1.4.53 |
2HZ6 | THE CRYSTAL STRUCTURE OF HUMAN IRE1-ALPHA LUMINAL DOMAIN | 2.7.11.1 3.1.26 |
2HZP | CRYSTAL STRUCTURE OF HOMO SAPIENS KYNURENINASE | 3.7.1.3 |
2HZY | MOUSE FUMARYLACETOACETATE HYDROLASE COMPLEXES WITH A TRANSITION-STATE MIMIC OF THE COMPLETE SUBSTRATE | 3.7.1.2 |
2I03 | CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE 4 (DPP IV) WITH POTENT ALKYNYL CYANOPYRROLIDINE (ABT-279) | 3.4.14.5 |
2I0U | CRYSTAL STRUCTURES OF PHOSPHOLIPASES A2 FROM VIPERA NIKOLSKII VENOM REVEALING TRITON X-100 BOUND IN HYDROPHOBIC CHANNEL | 3.1.1.4 |
2I0X | HYPOTHETICAL PROTEIN PF1117 FROM PYROCOCCUS FURIOSUS | 3.1 |
2I1A | A RETROVIRAL PROTEASE-LIKE DOMAIN IN THE EUKARYOTIC PROTEIN DDI1 | 3.4.23 |
2I1R | NOVEL THIAZOLONES AS HCV NS5B POLYMERASE INHIBITORS: FURTHER DESIGNS, SYNTHESIS, SAR AND X-RAY COMPLEX STRUCTURE | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2I1V | CRYSTAL STRUCTURE OF PFKFB3 IN COMPLEX WITH ADP AND FRUCTOSE-2,6-BISPHOSPHATE | 2.7.1.105 3.1.3.46 |
2I1Y | CRYSTAL STRUCTURE OF THE PHOSPHATASE DOMAIN OF HUMAN PTP IA-2 | 3.1.3.48 |
2I25 | CRYSTAL STRUCTURE ANALYSIS OF THE NURSE SHARK NEW ANTIGEN RECEPTOR PBLA8 VARIABLE DOMAIN IN COMPLEX WITH LYSOZYME | 3.2.1.17 |
2I26 | CRYSTAL STRUCTURE ANALYSIS OF THE NURSE SHARK NEW ANTIGEN RECEPTOR ANCESTRAL VARIABLE DOMAIN IN COMPLEX WITH LYSOZYME | 3.2.1.17 |
2I33 | THE STRUCTURE OF THE CLASS C ACID PHOSPHATASE FROM BACILLUS ANTHRACIS | 3.1.3.2 |
2I34 | THE CRYSTAL STRUCTURE OF CLASS C ACID PHOSPHATASE FROM BACILLUS ANTHRACIS WITH TUNGSTATE BOUND | 3.1.3.2 |
2I3B | SOLUTION STRUCTURE OF A HUMAN CANCER-RELATED NUCLEOSIDE TRIPHOSPHATASE | 3.6.1.15 |
2I3C | CRYSTAL STRUCTURE OF AN ASPARTOACYLASE FROM HOMO SAPIENS | 3.5.1.15 |
2I3E | SOLUTION STRUCTURE OF CATALYTIC DOMAIN OF GOLDFISH RICH PROTEIN | 3.1.4.37 |
2I3P | K28R MUTANT OF HOMING ENDONUCLEASE I-CREI | 3.1 |
2I3Q | Q44V MUTANT OF HOMING ENDONUCLEASE I-CREI | 3.1 |
2I3R | ENGINEERED CATALYTIC DOMAIN OF PROTEIN TYROSINE PHOSPHATASE HPTPBETA | 3.1.3.48 |
2I3U | STRUCTURAL STUDIES OF PROTEIN TYROSINE PHOSPHATASE BETA CATALYTIC DOMAIN IN COMPLEX WITH INHIBITORS | 3.1.3.48 |
2I42 | CRYSTAL STRUCTURE OF YERSINIA PROTEIN TYROSINE PHOSPHATASE COMPLEXED WITH VANADATE, A TRANSITION STATE ANALOGUE | 3.1.3.48 |
2I47 | CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH INHIBITOR | 3.4.24.86 |
2I4D | CRYSTAL STRUCTURE OF WT HIV-1 PROTEASE WITH GS-8373 | 3.4.23.16 |
2I4E | STRUCTURAL STUDIES OF PROTEIN TYROSINE PHOSPHATASE BETA CATALYTIC DOMAIN IN COMPLEX WITH INHIBITORS | 3.1.3.48 |
2I4G | STRUCTURAL STUDIES OF PROTEIN TYROSINE PHOSPHATASE BETA CATALYTIC DOMAIN IN COMPLEX WITH A SULFAMIC ACID (SOAKING EXPERIMENT) | 3.1.3.48 |
2I4H | STRUCTURAL STUDIES OF PROTEIN TYROSINE PHOSPHATASE BETA CATALYTIC DOMAIN CO-CRYSTALLIZED WITH A SULFAMIC ACID INHIBITOR | 3.1.3.48 |
2I4I | CRYSTAL STRUCTURE OF HUMAN DEAD-BOX RNA HELICASE DDX3X | 3.6.1 3.6.4.13 |
2I4Q | HUMAN RENIN/PF02342674 COMPLEX | 3.4.23.15 |
2I4R | CRYSTAL STRUCTURE OF THE V-TYPE ATP SYNTHASE SUBUNIT F FROM ARCHAEOGLOBUS FULGIDUS. NESG TARGET GR52A. | 3.6.3.14 |
2I4U | HIV-1 PROTEASE WITH TMC-126 | 3.4.23.16 |
2I4V | HIV-1 PROTEASE I84V, L90M WITH TMC126 | 3.4.23.16 |
2I4W | HIV-1 PROTEASE WT WITH GS-8374 | 3.4.23.16 |
2I4X | HIV-1 PROTEASE I84V, L90M WITH GS-8374 | 3.4.23.16 |
2I50 | SOLUTION STRUCTURE OF UBP-M ZNF-UBP DOMAIN | 3.1.2.15 3.4.19.12 |
2I5D | CRYSTAL STRUCTURE OF HUMAN INOSINE TRIPHOSPHATE PYROPHOSPHATASE | 3.6.1.19 3.6.1.9 |
2I5I | CRYSTAL STRUCTURE OF A PUTATIVE CELLOBIOSE-PHOSPHATE CLEAVAGE PROTEIN (EF3048) FROM ENTEROCOCCUS FAECALIS V583 AT 1.70 A RESOLUTION | 3.5.1 |
2I5J | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH DHBNH, AN RNASE H INHIBITOR | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2I5W | STRUCTURE OF HOGG1 CROSSLINKED TO DNA SAMPLING A NORMAL G ADJACENT TO AN OXOG | 3.2.2 4.2.99.18 |
2I5X | ENGINEERING THE PTPBETA CATALYTIC DOMAIN WITH IMPROVED CRYSTALLIZATION PROPERTIES | 3.1.3.48 |
2I65 | STRUCTURAL BASIS FOR THE MECHANISTIC UNDERSTANDING HUMAN CD38 CONTROLLED MULTIPLE CATALYSIS | 3.2.2.5 3.2.2.6 2.4.99.20 |
2I66 | STRUCTURAL BASIS FOR THE MECHANISTIC UNDERSTANDING HUMAN CD38 CONTROLLED MULTIPLE CATALYSIS | 3.2.2.5 3.2.2.6 2.4.99.20 |
2I67 | STRUCTURAL BASIS FOR THE MECHANISTIC UNDERSTANDING HUMAN CD38 CONTROLLED MULTIPLE CATALYSIS | 3.2.2.5 3.2.2.6 2.4.99.20 |
2I6J | CRYSTAL STRUCTURE OF THE COMPLEX OF THE ARCHAEAL SULFOLOBUS PTP-FOLD PHOSPHATASE WITH PHOSPHATE ION | 3.1.3.48 |
2I6M | CRYSTAL STRUCTURE OF THE COMPLEXES OF THE ARCHAEAL SULFOLOBUS PTP-FOLD PHOSPHATASE WITH TUNGSTATE | 3.1.3.48 |
2I6O | CRYSTAL STRUCTURE OF THE COMPLEX OF THE ARCHAEAL SULFOLOBUS PTP-FOLD PHOSPHATASE WITH PHOSPHOPEPTIDES N-G-(P)Y-K-N | 3.1.3.48 |
2I6P | CRYSTAL STRUCTURE OF THE COMPLEX OF THE ARCHAEAL SULFOLOBUS PTP-FOLD PHOSPHATASE WITH PNPP | 3.1.3.48 |
2I6Q | COMPLEMENT COMPONENT C2A | 3.4.21.43 |
2I6S | COMPLEMENT COMPONENT C2A | 3.4.21.43 |
2I6Z | X-RAY DIFFRACTION STUDIES OF ADDUCTS BETWEEN ANTICANCER PLATINUM DRUGS AND HEN EGG WHITE LYSOZYME | 3.2.1.17 |
2I71 | CRYSTAL STRUCTURE OF A CONSERVED PROTEIN OF UNKNOWN FUNCTION FROM SULFOLOBUS SOLFATARICUS P2 | 3.1 |
2I72 | AMPC BETA-LACTAMASE IN COMPLEX WITH 5-DIFORMYLAMINOMETHYL-BENZO[B]THIOPHEN-2-BORONIC ACID | 3.5.2.6 |
2I74 | CRYSTAL STRUCTURE OF MOUSE PEPTIDE N-GLYCANASE C-TERMINAL DOMAIN IN COMPLEX WITH MANNOPENTAOSE | 3.5.1.52 |
2I75 | CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE N4 (PTPN4) | 3.1.3.48 |
2I7A | DOMAIN IV OF HUMAN CALPAIN 13 | 3.4.22 |
2I7D | STRUCTURE OF HUMAN CYTOSOLIC DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH DEOXYURIDINE, ALF4 AND MG2+ | 3.1.3 |
2I7T | STRUCTURE OF HUMAN CPSF-73 | 3.1.27 |
2I7V | STRUCTURE OF HUMAN CPSF-73 | 3.1.27 |
2I8E | STRUCTURE OF SSO1404, A PREDICTED DNA REPAIR-ASSOCIATED PROTEIN FROM SULFOLOBUS SOLFATARICUS P2 | 3.1 |
2I8L | SOLUTION STRUCTURE OF AN ENDOPEPTIDASE HYCI FROM ESCHERICHIA COLI | 3.4 3.4.23.51 |
2I8T | GDP-MANNOSE MANNOSYL HYDROLASE-CALCIUM-GDP-MANNOSE COMPLEX | 3.6.1 |
2I8U | GDP-MANNOSE MANNOSYL HYDROLASE-CALCIUM-GDP PRODUCT COMPLEX | 3.6.1 |
2I9A | CRYSTAL STRUCTURE OF THE FREE AMINOTERMINAL FRAGMENT OF UROKINASE TYPE PLASMINOGEN ACTIVATOR (ATF) | 3.4.21.73 |
2I9B | CRYSTAL STRUCTURE OF ATF-UROKINASE RECEPTOR COMPLEX | 3.4.21.73 |
2I9U | CRYSTAL STRUCTURE OF GUANINE DEAMINASE FROM C. ACETOBUTYLICUM WITH BOUND GUANINE IN THE ACTIVE SITE | 3.5.4.3 |
2IAJ | CRYSTAL STRUCTURE OF K103N/Y181C MUTANT HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH ATP | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2IAO | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE E37Q MUTANT | 3.1.8.2 |
2IAP | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE E21Q MUTANT | 3.1.8.2 |
2IAQ | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE S271A MUTANT | 3.1.8.2 |
2IAR | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE W244H MUTANT | 3.1.8.2 |
2IAS | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE W244F MUTANT | 3.1.8.2 |
2IAT | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE W244L MUTANT | 3.1.8.2 |
2IAU | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE W244Y MUTANT | 3.1.8.2 |
2IAV | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE H287A MUTANT | 3.1.8.2 |
2IAW | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE N175D MUTANT | 3.1.8.2 |
2IAX | CRYSTAL STRUCTURE OF SQUID GANGLION DFPASE D232S MUTANT | 3.1.8.2 |
2IBI | COVALENT UBIQUITIN-USP2 COMPLEX | 3.1.2.15 3.4.19.12 |
2IC3 | CRYSTAL STRUCTURE OF K103N/Y181C MUTANT HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH NONNUCLEOSIDE INHIBITOR HBY 097 | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2IC5 | CRYSTAL STRUCTURE OF HUMAN RAC3 GROWN IN THE PRESENCE OF GPP(NH)P. | 3.6.5.2 |
2IC8 | CRYSTAL STRUCTURE OF GLPG | 3.4.21.105 |
2ICS | CRYSTAL STRUCTURE OF AN ADENINE DEAMINASE | 3.5.4.2 3.1.1 |
2ICU | CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN YEDK FROM ESCHERICHIA COLI | 3.4 |
2ID4 | THE 1.9 A STRUCTURE OF KEX2 IN COMPLEX WITH AN AC-R-E-R-K-CHLOROMETHYL KETONE INHIBITOR. | 3.4.21.61 |
2ID8 | CRYSTAL STRUCTURE OF PROTEINASE K | 3.4.21.64 |
2IDW | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT V82A WITH A POTENT NON-PEPTIDE INHIBITOR (UIC-94017) | 3.4.23.16 |
2IDY | NMR STRUCTURE OF THE SARS-COV NON-STRUCTURAL PROTEIN NSP3A | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2IEH | CRYSTAL STRUCTURE OF HUMAN KINESIN EG5 IN COMPLEX WITH (R)-MON97, A NEW MONASTROL-BASED INHIBITOR THAT BINDS AS (R)-ENANTIOMER | 3.6.4.4 |
2IEN | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE WITH A POTENT NON-PEPTIDE INHIBITOR (UIC-94017) | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2IEO | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT I84V WITH A POTENT NON-PEPTIDE INHIBITOR (UIC-94017) | 3.4.23.16 |
2IER | CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS LPXC COMPLEXED WITH URIDINE 5'-DIPHOSPHATE | 3.5.1 3.5.1.108 |
2IES | CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS LPXC COMPLEXED WITH PYROPHOSPHATE | 3.5.1 3.5.1.108 |
2IEY | CRYSTAL STRUCTURE OF MOUSE RAB27B BOUND TO GDP IN HEXAGONAL SPACE GROUP | 3.6.5.2 |
2IEZ | CRYSTAL STRUCTURE OF MOUSE RAB27B BOUND TO GDP IN MONOCLINIC SPACE GROUP | 3.6.5.2 |
2IF0 | CRYSTAL STRUCTURE OF MOUSE RAB27B BOUND TO GDP IN MONOCLINIC SPACE GROUP | 3.6.5.2 |
2IFD | CRYSTAL STRUCTURE OF A REMOTE BINDING SITE MUTANT, R492L, OF CDC25B PHOSPHATASE CATALYTIC DOMAIN | 3.1.3.48 |
2IFR | CRYSTAL STRUCTURE OF SCYTALIDO-GLUTAMIC PEPTIDASE WITH A PEPTIDE BASED TRANSITION STATE ANALOG | 3.4.23.32 |
2IFV | CRYSTAL STRUCTURE OF AN ACTIVE SITE MUTANT, C473D, OF CDC25B PHOSPHATASE CATALYTIC DOMAIN | 3.1.3.48 |
2IFW | CRYSTAL STRUCTURE OF SCYTALIDO-GLUTAMIC PEPTIDASE WITH A TRANSITION STATE ANALOG INHIBITOR | 3.4.23.32 |
2IGC | STRUCTURE OF SPIN LABELED T4 LYSOZYME MUTANT T115R1A | 3.2.1.17 |
2IGI | CRYSTAL STRUCTURE OF E. COLI OLIGORIBONUCLEASE | 3.1 |
2IGL | CRYSTAL STRUCTURE OF E. COLI YEDX, A TRANSTHYRETIN RELATED PROTEIN | 3.5.2.17 |
2IGX | ACHIRAL, CHEAP AND POTENT INHIBITORS OF PLASMEPSINS II | 3.4.23.39 |
2IGY | ACHIRAL, CHEAP AND POTENT INHIBITORS OF PLASMEPSINS II | 3.4.23.39 |
2IHL | LYSOZYME (E.C.3.2.1.17) (JAPANESE QUAIL) | 3.2.1.17 |
2IHN | CO-CRYSTAL OF BACTERIOPHAGE T4 RNASE H WITH A FORK DNA SUBSTRATE | 3.1.26.4 |
2IHP | YEAST INORGANIC PYROPHOSPHATASE WITH MAGNESIUM AND PHOSPHATE | 3.6.1.1 |
2IHY | STRUCTURE OF THE STAPHYLOCOCCUS AUREUS PUTATIVE ATPASE SUBUNIT OF AN ATP-BINDING CASSETTE (ABC) TRANSPORTER | 3.6.3.34 |
2IIT | HUMAN DIPEPTIDYL PEPTIDASE 4 IN COMPLEX WITH A DIAZEPAN-2-ONE INHIBITOR | 3.4.14.5 |
2IIV | HUMAN DIPEPTIDYL PEPTIDASE 4 IN COMPLEX WITH A DIAZEPAN-2-ONE INHIBITOR | 3.4.14.5 |
2IJD | CRYSTAL STRUCTURE OF THE POLIOVIRUS PRECURSOR PROTEIN 3CD | 3.4.22.28 2.7.7.48 3.4.22.29 3.6.1.15 |
2IJF | CRYSTAL STRUCTURE OF THE POLIOVIRUS RNA-DEPENDENT RNA POLYMERASE FIDELITY MUTANT 3DPOL G64S | 2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28 |
2IJN | ISOTHIAZOLES AS ACTIVE-SITE INHIBITORS OF HCV NS5B POLYMERASE | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2IJO | CRYSTAL STRUCTURE OF THE WEST NILE VIRUS NS2B-NS3 PROTEASE COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2IK0 | YEAST INORGANIC PYROPHOSPHATASE VARIANT E48D WITH MAGNESIUM AND PHOSPHATE | 3.6.1.1 |
2IK1 | YEAST INORGANIC PYROPHOSPHATASE VARIANT Y93F WITH MAGNESIUM AND PHOSPHATE | 3.6.1.1 |
2IK2 | YEAST INORGANIC PYROPHOSPHATASE VARIANT D115E WITH MAGNESIUM AND PHOSPHATE | 3.6.1.1 |
2IK4 | YEAST INORGANIC PYROPHOSPHATASE VARIANT D117E WITH MAGNESIUM AND PHOSPHATE | 3.6.1.1 |
2IK6 | YEAST INORGANIC PYROPHOSPHATASE VARIANT D120E WITH MAGNESIUM AND PHOSPHATE | 3.6.1.1 |
2IK7 | YEAST INORGANIC PYROPHOSPHATASE VARIANT D120N WITH MAGNESIUM AND PHOSPHATE | 3.6.1.1 |
2IK9 | YEAST INORGANIC PYROPHOSPHATASE VARIANT D152E WITH MAGNESIUM AND PHOSPHATE | 3.6.1.1 |
2IKD | SOLUTION STRUCTURE OF THE FIRST CLIP DOMAIN IN PAP2 | 3.4.21 |
2IKE | SOLUTION STRUCTURE OF THE SECOND CLIP DOMAIN IN PAP2 | 3.4.21 |
2IKO | CRYSTAL STRUCTURE OF HUMAN RENIN COMPLEXED WITH INHIBITOR | 3.4.23.15 |
2IKQ | CRYSTAL STRUCTURE OF MOUSE STS-1 PGM DOMAIN IN COMPLEX WITH PHOSPHATE | 3.1.3.48 |
2IKU | CRYSTAL STRUCTURE OF HUMAN RENIN COMPLEXED WITH INHIBITORS | 3.4.23.15 |
2IL2 | CRYSTAL STRUCTURE OF HUMAN RENIN COMPLEXED WITH INHIBITOR | 3.4.23.15 |
2ILN | CRYSTAL STRUCTURE OF THE BOWMAN-BIRK INHIBITOR FROM SNAIL MEDIC SEEDS IN COMPLEX WITH BOVINE TRYPSIN | 3.4.21.4 |
2ILP | CLOSTRIDIUM BOTULINUM SEROTYPE A LIGHT CHAIN INHIBITED BY 4-CHLOROCINNAMIC HYDROXAMATE | 3.4.24.69 |
2ILX | SOLUTION STRUCTURE OF CATALYTIC DOMAIN OF RAT 2',3'-CYCLIC-NUCLEOTIDE 3'-PHOSPHODIESTERASE (CNP) PROTEIN | 3.1.4.37 |
2ILY | CRYSTAL STRUCTURE OF POLIOVIRUS POLYMERASE COMPLEXED WITH ATP AND MG2+ | 2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28 |
2ILZ | CRYSTAL STRUCTURE OF POLIOVIRUS POLYMERASE COMPLEXED WITH GTP AND MN2+ | 2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28 |
2IM0 | CRYSTAL STRUCTURE OF POLIOVIRUS POLYMERASE COMPLEXED WITH CTP AND MG2+ | 2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28 |
2IM1 | CRYSTAL STRUCTURE OF POLIOVIRUS POLYMERASE COMPLEXED WITH CTP AND MN2+ | 2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28 |
2IM2 | CRYSTAL STRUCTURE OF POLIOVIRUS POLYMERASE COMPLEXED WITH UTP AND MG2+ | 2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28 |
2IM3 | CRYSTAL STRUCTURE OF POLIOVIRUS POLYMERASE COMPLEXED WITH UTP AND MN2+ | 2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28 |
2IMA | CLOSTRIDIUM BOTULINUM NEUROTOXIN SEROTYPE A LIGHT CHAIN INHIBITED BY 2,4-DICHLOROCINNAMIC HYDROXAMATE | 3.4.24.69 |
2IMB | CLOSTRIDIUM BOTULINUM NEUROTOXIN SEROTYPE A LIGHT CHAIN INHIBITED BY L-ARGININE HYDROXAMATE | 3.4.24.69 |
2IMC | CLOSTRIDIUM BOTULINUM NEUROTOXIN SEROTYPE A LIGHT CHAIN, RESIDUES 1-424 | 3.4.24.69 |
2IMG | CRYSTAL STRUCTURE OF DUAL SPECIFICITY PROTEIN PHOSPHATASE 23 FROM HOMO SAPIENS IN COMPLEX WITH LIGAND MALATE ION | 3.1.3.48 3.1.3.16 |
2IMO | CRYSTAL STRUCTURE OF ALLANTOATE AMIDOHYDROLASE FROM ESCHERICHIA COLI AT PH 4.6 | 3.5.3 3.5.3.9 |
2IMR | CRYSTAL STRUCTURE OF AMIDOHYDROLASE DR_0824 FROM DEINOCOCCUS RADIODURANS | 3.5.4.40 |
2IMZ | CRYSTAL STRUCTURE OF MTU RECA INTEIN SPLICING DOMAIN | 3.1 |
2IN0 | CRYSTAL STRUCTURE OF MTU RECA INTEIN SPLICING DOMAIN | 3.1 |
2IN2 | NMR STRUCTURE OF THE APO HUMAN RHINOVIRUS 3C PROTEASE (SEROTYPE 14) | 3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48 |
2IN8 | CRYSTAL STRUCTURE OF MTU RECA INTEIN, SPLICING DOMAIN | 3.1 |
2IN9 | CRYSTAL STRUCTURE OF MTU RECA INTEIN, SPLICING DOMAIN | 3.1 |
2IO0 | CRYSTAL STRUCTURE OF HUMAN SENP2 IN COMPLEX WITH PRESUMO-2 | 3.4.22 |
2IO1 | CRYSTAL STRUCTURE OF HUMAN SENP2 IN COMPLEX WITH PRESUMO-3 | 3.4.22 |
2IO2 | CRYSTAL STRUCTURE OF HUMAN SENP2 IN COMPLEX WITH RANGAP1-SUMO-1 | 3.4.22 |
2IO3 | CRYSTAL STRUCTURE OF HUMAN SENP2 IN COMPLEX WITH RANGAP1-SUMO-2 | 3.4.22 |
2IO7 | E. COLI BIFUNCTIONAL GLUTATHIONYLSPERMIDINE SYNTHETASE/AMIDASE INCOMPLEX WITH MG2+ AND AMPPNP | 6.3.1.8 3.5.1.78 |
2IO8 | E. COLI BIFUNCTIONAL GLUTATHIONYLSPERMIDINE SYNTHETASE/AMIDASE INCOMPLEX WITH MG2+ AND ADP | 6.3.1.8 3.5.1.78 |
2IO9 | E. COLI BIFUNCTIONAL GLUTATHIONYLSPERMIDINE SYNTHETASE/AMIDASE INCOMPLEX WITH MG2+ ,GSH AND ADP | 6.3.1.8 3.5.1.78 |
2IOA | E. COLI BIFUNCTIONAL GLUTATHIONYLSPERMIDINE SYNTHETASE/AMIDASE INCOMPLEX WITH MG2+ AND ADP AND PHOSPHINATE INHIBITOR | 6.3.1.8 3.5.1.78 |
2IOB | E. COLI BIFUNCTIONAL GLUTATHIONYLSPERMIDINE SYNTHETASE/AMIDASE APO PROTEIN | 6.3.1.8 3.5.1.78 |
2IOC | THE CRYSTAL STRUCTURE OF TREX1 EXPLAINS THE 3' NUCLEOTIDE SPECIFICITY AND REVEALS A POLYPROLINE II HELIX FOR PROTEIN PARTENRING | 3.1.11.2 |
2IOF | CRYSTAL STRUCTURE OF PHOSPHONOACETALDEHYDE HYDROLASE WITH SODIUM BOROHYDRIDE-REDUCED SUBSTRATE INTERMEDIATE | 3.11.1.1 |
2IOH | CRYSTAL STRUCTURE OF PHOSPHONOACETALDEHYDE HYDROLASE WITH A K53R MUTATION | 3.11.1.1 |
2IOT | CLAVULANIC ACID BOUND TO ELASTASE | 3.4.21.36 |
2IPB | CRYSTAL STRUCTURE OF T159D MUTANT OF S. TYPHIMURIUM PHON PROTEIN | 3.1.3.2 |
2IPH | X-RAY STRUCTURE AT 1.75 A RESOLUTION OF A NOROVIRUS PROTEASE LINKED TO AN ACTIVE SITE DIRECTED PEPTIDE INHIBITOR | 3.4.22 3.6.1.15 3.4.22.66 2.7.7.48 |
2IPP | CRYSTAL STRUCTURE OF THE TETRAGONAL FORM OF HUMAN LIVER CATHEPSIN B | 3.4.22.1 |
2IQ1 | CRYSTAL STRUCTURE OF HUMAN PPM1K | 3.1.3.16 |
2IQ6 | CRYSTAL STRUCTURE OF THE AMINOPEPTIDASE FROM VIBRIO PROTEOLYTICUS IN COMPLEXATION WITH LEUCYL-LEUCYL-LEUCINE. | 3.4.11.10 |
2IQ7 | CRYSTAL STRUCTURE OF THE POLYGALACTURONASE FROM COLLETOTRICHUM LUPINI AND ITS IMPLICATIONS FOR THE INTERACTION WITH POLYGALACTURONASE-INHIBITING PROTEINS | 3.2.1.15 |
2IQG | CRYSTAL STRUCTURE OF HYDROXYETHYL SECONDARY AMINE-BASED PEPTIDOMIMETIC INHIBITOR OF HUMAN BETA-SECRETASE (BACE) | 3.4.23.46 |
2IRV | CRYSTAL STRUCTURE OF GLPG, A RHOMBOID INTRAMEMBRANE SERINE PROTEASE | 3.4.21.105 |
2IRZ | CRYSTAL STRUCTURE OF HUMAN BETA-SECRETASE COMPLEXED WITH INHIBITOR | 3.4.23.46 |
2IS0 | CRYSTAL STRUCTURE OF HUMAN BETA-SECRETASE COMPLEXED WITH INHIBITOR | 3.4.23.46 |
2IS1 | CRYSTAL STRUCTURE OF UVRD-DNA-SO4 COMPLEX | 3.6.1 3.6.4.12 |
2IS2 | CRYSTAL STRUCTURE OF UVRD-DNA BINARY COMPLEX | 3.6.1 3.6.4.12 |
2IS3 | CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNASE T | 3.1.13 |
2IS4 | CRYSTAL STRUCTURE OF UVRD-DNA-ADPNP TERNARY COMPLEX | 3.6.1 3.6.4.12 |
2IS6 | CRYSTAL STRUCTURE OF UVRD-DNA-ADPMGF3 TERNARY COMPLEX | 3.6.1 3.6.4.12 |
2ISD | PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-DELTA1 FROM RAT | 3.1.4.11 |
2ISE | BOTULINUM NEUROTOXIN A LIGHT CHAIN WT CRYSTAL FORM A | 3.4.24.69 |
2ISG | BOTULINUM NEUROTOXIN A LIGHT CHAIN WT CRYSTAL FORM B | 3.4.24.69 |
2ISH | BOTULINUM NEUROTOXIN A LIGHT CHAIN WT CRYSTAL FORM C | 3.4.24.69 |
2ISI | CRYSTAL STRUCTURE OF APE1 FROM HOMO SAPIENS IN A NEW CRYSTAL FORM COMPLEXED WITH A LIGAND | 4.2.99.18 3.1 |
2ITG | CATALYTIC DOMAIN OF HIV-1 INTEGRASE: ORDERED ACTIVE SITE IN THE F185H CONSTRUCT | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2IU0 | CRYSTAL STRUCTURES OF TRANSITION STATE ANALOGUE INHIBITORS OF INOSINE MONOPHOSPHATE CYCLOHYDROLASE | 2.1.2.3 3.5.4.10 |
2IU3 | CRYSTAL STRUCTURES OF TRANSITION STATE ANALOGUE INHIBITORS OF INOSINE MONOPHOSPHATE CYCLOHYDROLASE | 2.1.2.3 3.5.4.10 |
2IUC | STRUCTURE OF ALKALINE PHOSPHATASE FROM THE ANTARCTIC BACTERIUM TAB5 | 3.1.3.1 |
2IUL | HUMAN TACE G13 MUTANT | 3.4.15.1 3.2.1 |
2IUX | HUMAN TACE MUTANT G1234 | 3.2.1 3.4.15.1 |
2IUZ | CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH C2-DICAFFEINE | 3.2.1.14 |
2IVH | CRYSTAL STRUCTURE OF THE NUCLEASE DOMAIN OF COLE7 (H545Q MUTANT) IN COMPLEX WITH AN 18-BP DUPLEX DNA | 3.1 |
2IVK | CRYSTAL STRUCTURE OF THE PERIPLASMIC ENDONUCLEASE VVN COMPLEXED WITH A 16-BP DNA | 3.1 |
2IVN | STRUCTURE OF UP1 PROTEIN | 3.4.24.57 2.3.1.234 |
2IVP | STRUCTURE OF UP1 PROTEIN | 3.4.24.57 2.3.1.234 |
2IVY | CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN SSO1404 FROM SULFOLOBUS SOLFATARICUS P2 | 3.1 |
2IW0 | STRUCTURE OF THE CHITIN DEACETYLASE FROM THE FUNGAL PATHOGEN COLLETOTRICHUM LINDEMUTHIANUM | 3.5.1.41 |
2IW2 | CRYSTAL STRUCTURE OF HUMAN PROLIDASE | 3.4.13.9 |
2IWJ | SOLUTION STRUCTURE OF THE ZN COMPLEX OF HIV-2 NCP(23-49) PEPTIDE, ENCOMPASSING PROTEIN CCHC-LINKER, DISTAL CCHC ZN-BINDING MOTIF AND C- TERMINAL TAIL. | 3.4.23.47 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2IWM | PRECURSOR MUTANT CYS1SER OF PENICILLIN V ACYLASE FROM BACILLUS SPHAERICUS | 3.5.1.11 |
2IX0 | RNASE II | 3.1.13.1 |
2IX1 | RNASE II D209N MUTANT | 3.1.13.1 |
2IX9 | RESPECTIVE ROLE OF PROTEIN FOLDING AND GLYCOSYLATION IN THE THERMAL STABILITY OF RECOMBINANT FERULOYL ESTERASE A | 3.1.1.73 |
2IXA | A-ZYME, N-ACETYLGALACTOSAMINIDASE | 3.2.1.49 |
2IXB | CRYSTAL STRUCTURE OF N-ACETYLGALACTOSAMINIDASE IN COMPLEX WITH GALNAC | 3.2.1.49 |
2IXD | CRYSTAL STRUCTURE OF THE PUTATIVE DEACETYLASE BC1534 FROM BACILLUS CEREUS | 3.5.1 |
2IXS | STRUCTURE OF SDAI RESTRICTION ENDONUCLEASE | 3.1.21.4 |
2IXU | CRYSTAL STRUCTURE OF THE MODULAR CPL-1 ENDOLYSIN COMPLEXED WITH A PEPTIDOGLYCAN ANALOGUE (WILD-TYPE ENDOLYSIN) | 3.2.1.17 |
2IXV | CRYSTAL STRUCTURE OF THE MODULAR CPL-1 ENDOLYSIN COMPLEXED WITH A PEPTIDOGLYCAN ANALOGUE (E94Q MUTANT) | 3.2.1.17 |
2IY0 | SENP1 (MUTANT) SUMO1 RANGAP | 3.4.22 |
2IY1 | SENP1 (MUTANT) FULL LENGTH SUMO1 | 3.4.22 |
2IY9 | CRYSTAL STRUCTURE OF THE A-SUBUNIT OF THE AB5 TOXIN FROM E. COLI | 3.4.21 |
2IYC | SENP1 NATIVE STRUCTURE | 3.4.22 |
2IYD | SENP1 COVALENT COMPLEX WITH SUMO-2 | 3.4.22 |
2IYE | STRUCTURE OF CATALYTIC CPX-ATPASE DOMAIN COPB-B | 3.6.3.10 |
2IYK | CRYSTAL STRUCTURE OF THE UPF2-INTERACTING DOMAIN OF NONSENSE MEDIATED MRNA DECAY FACTOR UPF1 | 3.6.1 3.6.4 |
2IZO | STRUCTURE OF AN ARCHAEAL PCNA1-PCNA2-FEN1 COMPLEX | 3.1 |
2J0E | THREE DIMENSIONAL STRUCTURE AND CATALYTIC MECHANISM OF 6- PHOSPHOGLUCONOLACTONASE FROM TRYPANOSOMA BRUCEI | 3.1.1.31 |
2J0Q | THE CRYSTAL STRUCTURE OF THE EXON JUNCTION COMPLEX AT 3.2 A RESOLUTION | 3.6.4.13 |
2J0S | THE CRYSTAL STRUCTURE OF THE EXON JUNCTION COMPLEX AT 2.2 A RESOLUTION | 3.6.4.13 |
2J0T | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF MMP-1 IN COMPLEX WITH THE INHIBITORY DOMAIN OF TIMP-1 | 3.4.24.7 |
2J0U | THE CRYSTAL STRUCTURE OF EIF4AIII-BARENTSZ COMPLEX AT 3.0 A RESOLUTION | 3.6.4.13 |
2J13 | STRUCTURE OF A FAMILY 4 CARBOHYDRATE ESTERASE FROM BACILLUS ANTHRACIS | 3.5.1 |
2J16 | APO & SULPHATE BOUND FORMS OF SDP-1 | 3.1.3.48 |
2J17 | PTYR BOUND FORM OF SDP-1 | 3.1.3.48 |
2J1A | STRUCTURE OF CBM32 FROM CLOSTRIDIUM PERFRINGENS BETA-N- ACETYLHEXOSAMINIDASE GH84C IN COMPLEX WITH GALACTOSE | 3.2.1.169 |
2J1E | HIGH RESOLUTION CRYSTAL STRUCTURE OF CBM32 FROM A N-ACETYL-BETA- HEXOSAMINIDASE IN COMPLEX WITH LACNAC | 3.2.1.169 |
2J1L | CRYSTAL STRUCTURE OF HUMAN RHO-RELATED GTP-BINDING PROTEIN RHOD | 3.6.5.2 |
2J25 | PARTIALLY DEGLYCOSYLATED GLUCOCERAMIDASE | 3.2.1.45 2.4.1 3.2.1 |
2J2C | CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC 5'-NUCLEOTIDASE II (NT5C2, CN-II) | 3.1.3.5 |
2J2U | CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX | 3.4.21.6 |
2J30 | THE ROLE OF LOOP BUNDLE HYDROGEN BONDS IN THE MATURATION AND ACTIVITY OF (PRO)CASPASE-3 | 3.4.22.56 |
2J31 | THE ROLE OF LOOP BUNDLE HYDROGEN BONDS IN THE MATURATION AND ACTIVITY OF(PRO)CASPASE-3 | 3.4.22.56 |
2J32 | THE ROLE OF LOOP BUNDLE HYDROGEN BONDS IN THE MATURATION AND ACTIVITY OF(PRO)CASPASE-3 | 3.4.22.56 |
2J33 | THE ROLE OF LOOP BUNDLE HYDROGEN BONDS IN THE MATURATION AND ACTIVITY OF (PRO)CASPASE-3 | 3.4.22.56 |
2J34 | CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX | 3.4.21.6 |
2J38 | CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX | 3.4.21.6 |
2J3D | NATIVE MONOCLINIC FORM OF TORPEDO ACETYLCHOLINESTERASE | 3.1.1.7 |
2J3E | DIMERIZATION IS IMPORTANT FOR THE GTPASE ACTIVITY OF CHLOROPLAST TRANSLOCON COMPONENTS ATTOC33 AND PSTOC159 | 3.6.5 |
2J3Q | TORPEDO ACETYLCHOLINESTERASE COMPLEXED WITH FLUOROPHORE THIOFLAVIN T | 3.1.1.7 |
2J43 | ALPHA-GLUCAN RECOGNITION BY FAMILY 41 CARBOHYDRATE-BINDING MODULES FROM STREPTOCOCCAL VIRULENCE FACTORS | 3.2.1.41 |
2J47 | BACTEROIDES THETAIOTAOMICRON GH84 O-GLCNACASE IN COMPLEX WITH A IMIDAZOLE-PUGNAC HYBRID INHIBITOR | 3.2.1.52 3.2.1.169 |
2J4C | STRUCTURE OF HUMAN BUTYRYLCHOLINESTERASE IN COMPLEX WITH 10MM HGCL2 | 3.1.1.8 |
2J4E | THE ITP COMPLEX OF HUMAN INOSINE TRIPHOSPHATASE | 3.6.1.19 3.6.1.9 |
2J4F | TORPEDO ACETYLCHOLINESTERASE - HG HEAVY-ATOM DERIVATIVE | 3.1.1.7 |
2J4G | BACTEROIDES THETAIOTAOMICRON GH84 O-GLCNACASE IN COMPLEX WITH N-BUTYL- THIAZOLINE INHIBITOR | 3.2.1.52 3.2.1.169 |
2J4H | CRYSTAL STRUCTURE OF A H121A ESCHERICHIA COLI DCTP DEAMINASE MUTANT ENZYME | 3.5.4.13 |
2J4I | CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX | 3.4.21.6 |
2J4M | DOUBLE DOCKERIN FROM PIROMYCES EQUI CEL45A | 3.2.1.4 |
2J4N | DOUBLE DOCKERIN FROM PIROMYCES EQUI CEL45A | 3.2.1.4 |
2J4Q | CRYSTAL STRUCTURE OF A E138A ESCHERICHIA COLI DCTP DEAMINASE MUTANT ENZYME IN COMPLEX WITH DTTP | 3.5.4.13 |
2J4T | BIOLOGICAL AND STRUCTURAL FEATURES OF MURINE ANGIOGENIN-4, AN ANGIOGENIC PROTEIN | 3.1.27.5 3.1.27 |
2J5S | STRUCTURAL OF ABDH, A BETA-DIKETONE HYDROLASE FROM THE CYANOBACTERIUM ANABAENA SP. PCC 7120 BOUND TO (S)-3-OXOCYCLOHEXYL ACETIC ACID | 3.7.1.7 |
2J62 | STRUCTURE OF A BACTERIAL O-GLCNACASE IN COMPLEX WITH GLCNACSTATIN | 3.2.1.169 |
2J63 | CRYSTAL STRUCTURE OF AP ENDONUCLEASE LMAP FROM LEISHMANIA MAJOR | 4.2.99.18 3.1 |
2J65 | STRUCTURE OF LPXC FROM AQUIFEX AEOLICUS IN COMPLEX WITH UDP | 3.5.1 3.5.1.108 |
2J67 | THE TIR DOMAIN OF HUMAN TOLL-LIKE RECEPTOR 10 (TLR10) | 3.2.2.6 |
2J68 | BACTERIAL DYNAMIN-LIKE PROTEIN BDLP, GDP BOUND | 3.6.5.5 |
2J6Y | STRUCTURAL AND FUNCTIONAL CHARACTERISATION OF PARTNER SWITCHING REGULATING THE ENVIRONMENTAL STRESS RESPONSE IN BACILLUS SUBTILIS | 3.1.3.3 |
2J6Z | STRUCTURAL AND FUNCTIONAL CHARACTERISATION OF PARTNER-SWITCHING REGULATING THE ENVIRONMENTAL STRESS RESPONSE IN B. SUBTILIS | 3.1.3.3 |
2J70 | STRUCTURAL AND FUNCTIONAL CHARACTERISATION OF PARTNER-SWITCHING REGULATING THE ENVIRONMENTAL STRESS RESPONSE IN B. SUBTILIS | 3.1.3.3 |
2J71 | ALPHA-GLUCAN RECOGNITION BY A FAMILY 41 CARBOHYDRATE-BINDING MODULE FROM THERMOTOGA MARITIMA PULLULANASE PULA | 3.2.1.41 |
2J72 | ALPHA-GLUCAN RECOGNITION BY A FAMILY 41 CARBOHYDRATE-BINDING MODULE FROM THERMOTOGA MARITIMA PULLULANASE PULA | 3.2.1.41 |
2J73 | ALPHA-GLUCAN RCOGNITION BY A FAMILY 41 CARBOHYDRATE-BINDING MODULE FROM THERMOTOGA MARITIMA PULLULANASE PULA | 3.2.1.41 |
2J74 | STRUCTURE OF BETA-1,4-GALACTANASE | 3.2.1.89 |
2J75 | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH NOEUROMYCIN | 3.2.1.21 |
2J77 | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH DEOXYNOJIRIMYCIN | 3.2.1.21 |
2J78 | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH GLUCO- HYDROXIMOLACTAM | 3.2.1.21 |
2J79 | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH GALACTO- HYDROXIMOLACTAM | 3.2.1.21 |
2J7B | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH GLUCO- TETRAZOLE | 3.2.1.21 |
2J7C | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH PHENYLAMINOMETHYL-DERIVED GLUCOIMIDAZOLE | 3.2.1.21 |
2J7D | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH METHOXYCARBONYL-SUBSTITUTED GLUCOIMIDAZOLE | 3.2.1.21 |
2J7E | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH METHYL ACETATE-SUBSTITUTED GLUCOIMIDAZOLE | 3.2.1.21 |
2J7F | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH CARBOXYLATE- SUBSTITUTED GLUCOIMIDAZOLE | 3.2.1.21 |
2J7G | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH METHYL ACETIC ACID-SUBSTITUTED GLUCOIMIDAZOLE | 3.2.1.21 |
2J7H | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH AZAFAGOMINE | 3.2.1.21 |
2J7K | CRYSTAL STRUCTURE OF THE T84A MUTANT EF-G:GDPCP COMPLEX | 3.6.1.48 |
2J7M | CHARACTERIZATION OF A FAMILY 32 CBM | 3.2.1.169 |
2J7U | DENGUE VIRUS NS5 RNA DEPENDENT RNA POLYMERASE DOMAIN | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2J7V | STRUCTURE OF PBP-A | 3.4.16.4 |
2J7W | DENGUE VIRUS NS5 RNA DEPENDENT RNA POLYMERASE DOMAIN COMPLEXED WITH 3' DGTP | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2J83 | ULILYSIN METALLOPROTEASE IN COMPLEX WITH BATIMASTAT. | 3.4.24 |
2J88 | HYALURONIDASE IN COMPLEX WITH A MONOCLONAL IGG FAB FRAGMENT | 3.2.1.35 |
2J8F | CRYSTAL STRUCTURE OF THE MODULAR CPL-1 ENDOLYSIN COMPLEXED WITH A PEPTIDOGLYCAN ANALOGUE (E94Q MUTANT IN COMPLEX WITH A DISACCHARIDE- PENTAPEPTIDE) | 3.2.1.17 |
2J8G | CRYSTAL STRUCTURE OF THE MODULAR CPL-1 ENDOLYSIN COMPLEXED WITH A PEPTIDOGLYCAN ANALOGUE (E94Q MUTANT IN COMPLEX WITH A TETRASACCHARIDE- PENTAPEPTIDE) | 3.2.1.17 |
2J8J | SOLUTION STRUCTURE OF THE A4 DOMAIN OF BLOOD COAGULATION FACTOR XI | 3.4.21.27 |
2J8L | FXI APPLE 4 DOMAIN LOOP-OUT CONFORMATION | 3.4.21.27 |
2J8X | EPSTEIN-BARR VIRUS URACIL-DNA GLYCOSYLASE IN COMPLEX WITH UGI FROM PBS-2 | 3.2.2.3 3.2.2.27 |
2J8Y | STRUCTURE OF PBP-A ACYL-ENZYME COMPLEX WITH PENICILLIN-G | 3.4.16.4 |
2J92 | 3C PROTEASE FROM TYPE A10(61) FOOT-AND-MOUTH DISEASE VIRUS - CRYSTAL PACKING MUTANT (K51Q) | 3.4.22.28 3.4.22.46 3.6.1.15 2.7.7.48 |
2J94 | CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX | 3.4.21.6 |
2J95 | CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX | 3.4.21.6 |
2J97 | HUMAN CORONAVIRUS 229E NON STRUCTURAL PROTEIN 9 (NSP9) | 3.4.19.12 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 2.1.1 |
2J98 | HUMAN CORONAVIRUS 229E NON STRUCTURAL PROTEIN 9 CYS69ALA MUTANT (NSP9) | 3.4.19.12 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 2.1.1 |
2J9A | BLLAP IN COMPLEX WITH MICROGININ FR1 | 3.4.11.1 3.4.11.5 3.4.13.23 |
2J9J | ATOMIC-RESOLUTION CRYSTAL STRUCTURE OF CHEMICALLY-SYNTHESIZED HIV-1 PROTEASE COMPLEXED WITH INHIBITOR JG-365 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2J9K | ATOMIC-RESOLUTION CRYSTAL STRUCTURE OF CHEMICALLY-SYNTHESIZED HIV-1 PROTEASE COMPLEXED WITH INHIBITOR MVT-101 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2J9N | ROBOTICALLY HARVESTED TRYPSIN COMPLEXED WITH BENZAMIDINE CONTAINING POLYPEPTIDE MEDIATED CRYSTAL CONTACTS | 3.4.21.4 |
2J9O | STRUCTURE OF PBP-A, L158E MUTANT | 3.4.16.4 |
2J9P | CRYSTAL STRUCTURE OF THE BACILLUS SUBTILIS PBP4A, AND ITS COMPLEX WITH A PEPTIDOGLYCAN MIMETIC PEPTIDE. | 3.4.16.4 |
2JA9 | STRUCTURE OF THE N-TERMINAL DELETION OF YEAST EXOSOME COMPONENT RRP40 | 3.1.13 |
2JAI | DDAH1 COMPLEXED WITH CITRULLINE | 3.5.3.18 |
2JAJ | DDAH1 COMPLEXED WITH L-257 | 3.5.3.18 |
2JAL | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH CYCLOPHELLITOL | 3.2.1.21 |
2JAO | CRYSTAL STRUCTURE OF D12N VARIANT OF MOUSE CYTOSOLIC 5'(3')- DEOXYRIBONUCLEOTIDASE (CDN) IN COMPLEX WITH DEOXYGUANOSINE 5'- MONOPHOSPHATE | 3.1.3 |
2JAR | CRYSTAL STRUCTURE OF D12N VARIANT OF MOUSE CYTOSOLIC 5'(3')- DEOXYRIBONUCLEOTIDASE (CDN) IN COMPLEX WITH DEOXYURIDINE 5'- MONOPHOSPHATE | 3.1.3 |
2JAU | CRYSTAL STRUCTURE OF D41N VARIANT OF HUMAN MITOCHONDRIAL 5'(3')- DEOXYRIBONUCLEOTIDASE (MDN) IN COMPLEX WITH 3'-AZIDOTHYMIDINE 5'- MONOPHOSPHATE | 3.1.3 |
2JAW | CRYSTAL STRUCTURE OF D41N VARIANT OF HUMAN MITOCHONDRIAL 5'(3')- DEOXYRIBONUCLEOTIDASE (MDN) IN COMPLEX WITH 5-BROMOVINYLDEOXYURIDINE 5'-MONOPHOSPHATE | 3.1.3 |
2JAY | PROTEASOME BETA SUBUNIT PRCB FROM MYCOBACTERIUM TUBERCULOSIS | 3.4.25.1 |
2JAZ | CRYSTAL STRUCTURE OF THE MUTANT N560D OF THE NUCLEASE DOMAIN OF COLE7 IN COMPLEX WITH IM7 | 3.1 |
2JB0 | CRYSTAL STRUCTURE OF THE MUTANT H573A OF THE NUCLEASE DOMAIN OF COLE7 IN COMPLEX WITH IM7 | 3.1 |
2JBF | STRUCTURE OF PBP-A, L158E MUTANT. ACYL-ENZYME COMPLEX WITH PENICILLIN- G. | 3.4.16.4 |
2JBG | CRYSTAL STRUCTURE OF THE MUTANT N560A OF THE NUCLEASE DOMAIN OF COLE7 IN COMPLEX WITH IM7 | 3.1 |
2JBJ | MEMBRANE-BOUND GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH 2-PMPA (2-PHOSPHONOMETHYL-PENTANEDIOIC ACID) | 3.4.17.21 |
2JBK | MEMBRANE-BOUND GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH QUISQUALIC ACID (QUISQUALATE, ALPHA-AMINO-3,5-DIOXO-1,2,4- OXADIAZOLIDINE-2-PROPANOIC ACID) | 3.4.17.21 |
2JBU | CRYSTAL STRUCTURE OF HUMAN INSULIN DEGRADING ENZYME COMPLEXED WITH CO- PURIFIED PEPTIDES. | 3.4.24.56 |
2JBW | CRYSTAL STRUCTURE OF THE 2,6-DIHYDROXY-PSEUDO-OXYNICOTINE HYDROLASE. | 3.7.1 3.7.1.19 |
2JC0 | CRYSTAL STRUCTURE OF HEPATITIS C VIRUS POLYMERASE IN COMPLEX WITH INHIBITOR SB655264 | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2JC1 | CRYSTAL STRUCTURE OF HEPATITIS C VIRUS POLYMERASE IN COMPLEX WITH INHIBITOR SB698223 | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2JC4 | 3'-5' EXONUCLEASE (NEXO) FROM NEISSERIA MENINGITIDIS | 3.1.11.2 |
2JC5 | APURINIC APYRIMIDINIC (AP) ENDONUCLEASE (NAPE) FROM NEISSERIA MENINGITIDIS | 3.1.11.2 |
2JC7 | THE CRYSTAL STRUCTURE OF THE CARBAPENEMASE OXA-24 REVEALS NEW INSIGHTS INTO THE MECHANISM OF CARBAPENEM-HYDROLYSIS | 3.5.2.6 |
2JC9 | CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC 5'-NUCLEOTIDASE II IN COMPLEX WITH ADENOSINE | 3.1.3.5 |
2JCH | STRUCTURAL AND MECHANISTIC BASIS OF PENICILLIN BINDING PROTEIN INHIBITION BY LACTIVICINS | 2.4.1.129 3.4.16.4 |
2JCM | CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC 5'-NUCLEOTIDASE II IN COMPLEX WITH BERYLLIUM TRIFLUORIDE | 3.1.3.5 |
2JDI | GROUND STATE STRUCTURE OF F1-ATPASE FROM BOVINE HEART MITOCHONDRIA (BOVINE F1-ATPASE CRYSTALLISED IN THE ABSENCE OF AZIDE) | 3.6.3.14 |
2JDL | STRUCTURE OF C-TERMINAL REGION OF ACIDIC P2 RIBOSOMAL PROTEIN COMPLEXED WITH TRICHOSANTHIN | 3.2.2.22 |
2JE4 | ATOMIC-RESOLUTION CRYSTAL STRUCTURE OF CHEMICALLY-SYNTHESIZED HIV-1 PROTEASE IN COMPLEX WITH JG-365 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2JE5 | STRUCTURAL AND MECHANISTIC BASIS OF PENICILLIN BINDING PROTEIN INHIBITION BY LACTIVICINS | 2.4.1.129 3.4.16.4 |
2JE6 | STRUCTURE OF A 9-SUBUNIT ARCHAEAL EXOSOME | 3.1.13 |
2JE8 | STRUCTURE OF A BETA-MANNOSIDASE FROM BACTEROIDES THETAIOTAOMICRON | 3.2.1.25 |
2JEA | STRUCTURE OF A 9-SUBUNIT ARCHAEAL EXOSOME BOUND TO RNA | 3.1.13 |
2JEB | STRUCTURE OF A 9-SUBUNIT ARCHAEAL EXOSOME BOUND TO MN IONS | 3.1.13 |
2JEM | NATIVE FAMILY 12 XYLOGLUCANASE FROM BACILLUS LICHENIFORMIS | 3.2.1.4 3.2.1.151 |
2JEN | FAMILY 12 XYLOGLUCANASE FROM BACILLUS LICHENIFORMIS IN COMPLEX WITH LIGAND | 3.2.1.4 3.2.1.151 |
2JEP | NATIVE FAMILY 5 XYLOGLUCANASE FROM PAENIBACILLUS PABULI | 3.2.1.151 3.2.1.4 |
2JEQ | FAMILY 5 XYLOGLUCANASE FROM PAENIBACILLUS PABULI IN COMPLEX WITH LIGAND | 3.2.1.151 3.2.1.4 |
2JET | CRYSTAL STRUCTURE OF A TRYPSIN-LIKE MUTANT (S189D , A226G) CHYMOTRYPSIN. | 3.4.21.1 |
2JEW | CRYSTAL STRUCTURE OF ((2S)-5-AMINO-2-((1-N-PROPYL-1H-IMIDAZOL-4-YL) METHYL)PENTANOIC ACID) UK396,082 A TAFIA INHIBITOR, BOUND TO ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASEB | 3.4.17.2 |
2JEY | MUS MUSCULUS ACETYLCHOLINESTERASE IN COMPLEX WITH HLO-7 | 3.1.1.7 3.1.1.1 |
2JEZ | MUS MUSCULUS ACETYLCHOLINESTERASE IN COMPLEX WITH TABUN AND HLO-7 | 3.1.1.7 3.1.1.1 |
2JF0 | MUS MUSCULUS ACETYLCHOLINESTERASE IN COMPLEX WITH TABUN AND ORTHO-7 | 3.1.1.7 3.1.1.1 |
2JF4 | FAMILY 37 TREHALASE FROM ESCHERICHIA COLI IN COMPLEX WITH VALIDOXYLAMINE | 3.2.1.28 |
2JF6 | STRUCTURE OF INACTIVE MUTANT OF STRICTOSIDINE GLUCOSIDASE IN COMPLEX WITH STRICTOSIDINE | 3.2.1.105 |
2JF7 | STRUCTURE OF STRICTOSIDINE GLUCOSIDASE | 3.2.1.105 |
2JFE | THE CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC BETA-GLUCOSIDASE | 3.2.1.21 |
2JFK | STRUCTURE OF THE MAT DOMAIN OF HUMAN FAS WITH MALONYL-COA | 2.3.1.85 2.3.1.38 2.3.1.39 2.3.1.41 1.1.1.100 4.2.1.59 1.3.1.39 3.1.2.14 |
2JG0 | FAMILY 37 TREHALASE FROM ESCHERICHIA COLI IN COMPLEX WITH 1- THIATREHAZOLIN | 3.2.1.28 |
2JG4 | SUBSTRATE-FREE IDE STRUCTURE IN ITS CLOSED CONFORMATION | 3.4.24.56 |
2JG6 | CRYSTAL STRUCTURE OF A 3-METHYLADENINE DNA GLYCOSYLASE I FROM STAPHYLOCOCCUS AUREUS | 3.2.2.20 |
2JGA | CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC 5'-NUCLEOTIDASE III IN COMPLEX WITH PHOSPHATE AND MAGNESIUM | 3.1.3.5 3.1.3.91 |
2JGE | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY NON-AGED METHAMIDOPHOS | 3.1.1.7 |
2JGF | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY NON-AGED FENAMIPHOS | 3.1.1.7 |
2JGI | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY NON-AGED DIISOPROPYL FLUOROPHOSPHATE (DFP) | 3.1.1.7 |
2JGJ | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY AGED METHAMIDOPHOS | 3.1.1.7 |
2JGK | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY AGED FENAMIPHOS | 3.1.1.7 |
2JGL | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY AGED VX AND SARIN | 3.1.1.7 |
2JGM | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY AGED DIISOPROPYL FLUOROPHOSPHATE (DFP) | 3.1.1.7 |
2JGN | DDX3 HELICASE DOMAIN | 3.6.1 3.6.4.13 |
2JH0 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX | 3.4.21.5 |
2JH2 | X-RAY CRYSTAL STRUCTURE OF A COHESIN-LIKE MODULE FROM CLOSTRIDIUM PERFRINGENS | 3.2.1.169 |
2JH5 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX | 3.4.21.5 |
2JH6 | HUMAN THROMBIN HIRUGEN INHIBITOR COMPLEX | 3.4.21.5 |
2JHJ | 3-METHYLADENINE DNA-GLYCOSYLASE FROM ARCHAEOGLOBUS FULGIDUS | 3.2.2.21 |
2JHN | 3-METHYLADENINE DNA-GLYCOSYLASE FROM ARCHAEOGLOBUS FULGIDUS | 3.2.2.21 |
2JHQ | CRYSTAL STRUCTURE OF URACIL DNA-GLYCOSYLASE FROM VIBRIO CHOLERAE | 3.2.2.3 3.2.2.27 |
2JIC | HIGH RESOLUTION STRUCTURE OF XYLANASE-II FROM ONE MICRON BEAM EXPERIMENT | 3.2.1.8 |
2JID | HUMAN DIPEPTIDYL PEPTIDASE IV IN COMPLEX WITH 1-(3,4-DIMETHOXY-PHENYL) -3-M-TOLYL-PIPERIDINE-4-YLAMINE | 3.4.14.5 |
2JIE | BETA-GLUCOSIDASE B FROM BACILLUS POLYMYXA COMPLEXED WITH 2-F-GLUCOSE | 3.2.1.21 |
2JIH | CRYSTAL STRUCTURE OF HUMAN ADAMTS-1 CATALYTIC DOMAIN AND CYSTEINE- RICH DOMAIN (COMPLEX-FORM) | 3.4.24 |
2JIW | BACTEROIDES THETAIOTAOMICRON GH84 O-GLCNACASE IN COMPLEX WITH 2- ACETYLAMINO-2-DEOXY-1-EPIVALIENAMINE | 3.2.1.52 3.2.1.169 |
2JJB | FAMILY 37 TREHALASE FROM ESCHERICHIA COLI IN COMPLEX WITH CASUARINE-6- O-ALPHA-GLUCOPYRANOSE | 3.2.1.28 |
2JJI | ENDOTHIAPEPSIN IN COMPLEX WITH A GEM-DIOL INHIBITOR. | 3.4.23.22 |
2JJJ | ENDOTHIAPEPSIN IN COMPLEX WITH A GEM-DIOL INHIBITOR. | 3.4.23.22 |
2JJK | FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE -1- PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH A DUAL BINDING AMP SITE INHIBITOR | 3.1.3.11 |
2JJR | V232K, N236D-TRICHOSANTHIN | 3.2.2.22 |
2JKA | NATIVE STRUCTURE OF A FAMILY 97 ALPHA-GLUCOSIDASE FROM BACTEROIDES THETAIOTAOMICRON | 3.2.1.20 3.2.1.3 |
2JKB | CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANB IN COMPLEX WITH 2, 7-ANHYDRO-NEU5AC | 4.2.2.15 3.2.1.18 |
2JKE | STRUCTURE OF A FAMILY 97 ALPHA-GLUCOSIDASE FROM BACTEROIDES THETAIOTAOMICRON IN COMPLEX WITH DEOXYNOJIRIMYCIN | 3.2.1.20 3.2.1.3 |
2JKH | FACTOR XA - CATION INHIBITOR COMPLEX | 3.4.21.6 |
2JKP | STRUCTURE OF A FAMILY 97 ALPHA-GLUCOSIDASE FROM BACTEROIDES THETAIOTAOMICRON IN COMPLEX WITH CASTANOSPERMINE | 3.2.1.20 3.2.1.3 |
2JLQ | DENGUE VIRUS 4 NS3 HELICASE STRUCTURE, APO ENZYME. | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JLR | DENGUE VIRUS 4 NS3 HELICASE IN COMPLEX WITH AMPPNP | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JLS | DENGUE VIRUS 4 NS3 HELICASE IN COMPLEX WITH ADP | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JLU | DENGUE VIRUS 4 NS3 HELICASE IN COMPLEX WITH SSRNA | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JLV | DENGUE VIRUS 4 NS3 HELICASE IN COMPLEX WITH SSRNA AND AMPPNP | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JLW | DENGUE VIRUS 4 NS3 HELICASE IN COMPLEX WITH SSRNA2 | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JLX | DENGUE VIRUS 4 NS3 HELICASE IN COMPLEX WITH SSRNA AND ADP-VANADATE | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JLY | DENGUE VIRUS 4 NS3 HELICASE IN COMPLEX WITH SSRNA AND ADP-PHOSPHATE | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JLZ | DENGUE VIRUS 4 NS3 HELICASE IN COMPLEX WITH SSRNA AND ADP | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JM1 | STRUCTURES AND CHEMICAL SHIFT ASSIGNMENTS FOR THE ADD DOMAIN OF THE ATRX PROTEIN | 3.6.1 3.6.4.12 |
2JMU | NMR STRUCTURE OF THE MOUSE THIAMINE TRIPHOSPHATASE | 3.6.1.28 |
2JMX | OSCP-NT (1-120) IN COMPLEX WITH N-TERMINAL (1-25) ALPHA SUBUNIT FROM F1-ATPASE | 3.6.3.14 |
2JNK | SOLUTION STRUCTURE OF A DOCKERIN-CONTAINING MODULAR PAIR FROM A FAMILY 84 GLYCOSIDE HYDROLASE | 3.2.1.35 |
2JNP | SOLUTION STRUCTURE OF MATRIX METALLOPROTEINASE 3 (MMP-3) IN THE PRESENCE OF N-ISOBUTYL-N-[4-METHOXYPHENYLSULFONYL]GLYCYL HYDROXAMIC ACID (NNGH) | 3.4.24.17 |
2JO0 | THE SOLUTION STRUCTURE OF THE MONOMERIC SPECIES OF THE C TERMINAL DOMAIN OF THE CA PROTEIN OF HIV-1 | 3.4.23.16 |
2JOA | HTRA1 BOUND TO AN OPTIMIZED PEPTIDE: NMR ASSIGNMENT OF PDZ DOMAIN AND LIGAND RESONANCES | 3.4.21 |
2JOG | STRUCTURE OF THE CALCINEURIN-NFAT COMPLEX | 3.1.3.16 |
2JON | SOLUTION STRUCTURE OF THE C-TERMINAL DOMAIN OLE E 9 | 3.2.1.39 |
2JPN | SOLUTION STRUCTURE OF T4 BACTERIOPHAGE HELICASE UVSW.1 | 3.6.1 3.6.4.12 |
2JPR | JOINT REFINEMENT OF THE HIV-1 CA-NTD IN COMPLEX WITH THE ASSEMBLY INHIBITOR CAP-1 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2JQ9 | VPS4A MIT-CHMP1A COMPLEX | 3.6.4.6 |
2JQF | FULL LENGTH LEADER PROTEASE OF FOOT AND MOUTH DISEASE VIRUS C51A MUTANT | 3.4.22.46 3.6.1.15 3.4.22.28 2.7.7.48 |
2JQG | LEADER PROTEASE | 3.4.22.46 3.6.1.15 3.4.22.28 2.7.7.48 |
2JQH | VPS4B MIT | 3.6.4.6 |
2JQK | VPS4B MIT-CHMP2B COMPLEX | 3.6.4.6 |
2JQM | YELLOW FEVER ENVELOPE PROTEIN DOMAIN III NMR STRUCTURE (S288-K398) | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JRC | SOLUTION STRUCTURE OF PEPTIDYL-TRNA HYDROLASE FROM MYCOBACTERIUM TUBERCULOSIS H37RV. | 3.1.1.29 |
2JRI | SOLUTION STRUCTURE OF THE JOSEPHIN DOMAIN OF ATAXIN-3 IN COMPLEX WITH UBIQUITIN MOLECULE. | 3.4.22 3.4.19.12 |
2JSD | SOLUTION STRUCTURE OF MMP20 COMPLEXED WITH NNGH | 3.4.24 |
2JT2 | SOLUTION STRUCTURE OF THE AQUIFEX AEOLICUS LPXC- CHIR-090 COMPLEX | 3.5.1 3.5.1.108 |
2JT5 | SOLUTION STRUCTURE OF MATRIX METALLOPROTEINASE 3 (MMP-3) IN THE PRESENCE OF N-HYDROXY-2-[N-(2-HYDROXYETHYL)BIPHENYL-4-SULFONAMIDE] HYDROXAMIC ACID (MLC88) | 3.4.24.17 |
2JT6 | SOLUTION STRUCTURE OF MATRIX METALLOPROTEINASE 3 (MMP-3) IN THE PRESENCE OF 3-4'-CYANOBYPHENYL-4-YLOXY)-N-HDYDROXYPROPIONAMIDE (MMP-3 INHIBITOR VII) | 3.4.24.17 |
2JTC | 3D STRUCTURE AND BACKBONE DYNAMICS OF SPE B | 3.4.22.10 |
2JU4 | NMR STRUCTURE OF THE GAMMA SUBUNIT OF CGMP PHOSPHODIESTERASE | 3.1.4.17 3.1.4.35 |
2JV6 | YF ED3 PROTEIN NMR STRUCTURE | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2JVB | SOLUTION STRUCTURE OF CATALYTIC DOMAIN OF YDCP2 | 3 3.6.1.62 |
2JXR | STRUCTURE OF YEAST PROTEINASE A | 3.4.23.25 |
2JXY | SOLUTION STRUCTURE OF THE HEMOPEXIN-LIKE DOMAIN OF MMP12 | 3.4.24.65 |
2JYG | SOLUTION STRUCTURE OF THE W184A/M185A MUTANT OF THE CARBOXY-TERMINAL DIMERIZATION DOMAIN OF THE HIV-1 CAPSID PROTEIN | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2JYL | SOLUTION STRUCTURE OF A DOUBLE MUTANT OF THE CARBOXY-TERMINAL DIMERIZATION DOMAIN OF THE HIV-1 CAPSID PROTEIN | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2JYS | SOLUTION STRUCTURE OF SIMIAN FOAMY VIRUS (MAC) PROTEASE | 3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2JYW | SOLUTION STRUCTURE OF C-TERMINAL DOMAIN OF APOBEC3G | 3.5.4 |
2JZD | NMR STRUCTURE OF THE DOMAIN 527-651 OF THE SARS-COV NONSTRUCTURAL PROTEIN NSP3 | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2JZE | NMR STRUCTURE OF THE DOMAIN 527-651 OF THE SARS-COV NONSTRUCTURAL PROTEIN NSP3, SINGLE CONFORMER CLOSEST TO THE MEAN COORDINATES OF AN ENSEMBLE OF TWENTY ENERGY MINIMIZED CONFORMERS | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2JZF | NMR CONFORMER CLOSEST TO THE MEAN COORDINATES OF THE DOMAIN 513-651 OF THE SARS-COV NONSTRUCTURAL PROTEIN NSP3 | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2K11 | SOLUTION STRUCTURE OF HUMAN PANCREATIC RIBONUCLEASE | 3.1.27.5 4.6.1.18 |
2K1G | SOLUTION NMR STRUCTURE OF LIPOPROTEIN SPR FROM ESCHERICHIA COLI K12. NORTHEAST STRUCTURAL GENOMICS TARGET ER541-37-162 | 3.4 3.4.17.13 |
2K1Q | NMR STRUCTURE OF HEPATITIS C VIRUS NS3 SERINE PROTEASE COMPLEXED WITH THE NON-COVALENTLY BOUND PHENETHYLAMIDE INHIBITOR | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2K1R | THE SOLUTION NMR STRUCTURE OF THE COMPLEX BETWEEN MNK1 AND HAH1 MEDIATED BY CU(I) | 3.6.3.4 7.2.2.8 |
2K2G | SOLUTION STRUCTURE OF THE WILD-TYPE CATALYTIC DOMAIN OF HUMAN MATRIX METALLOPROTEINASE 12 (MMP-12) IN COMPLEX WITH A TIGHT-BINDING INHIBITOR | 3.4.24.65 |
2K2J | NMR SOLUTION STRUCTURE OF THE SPLIT PH DOMAIN FROM PHOSPHOLIPASE C GAMMA 2 | 3.1.4.11 |
2K31 | SOLUTION STRUCTURE OF CGMP-BINDING GAF DOMAIN OF PHOSPHODIESTERASE 5 | 3.1.4.35 |
2K3R | PFU RPP21 STRUCTURE AND ASSIGNMENTS | 3.1.26.5 |
2K3W | NMR STRUCTURE OF VPS4A-MIT-CHMP6 | 3.6.4.6 |
2K4E | SOLUTION STRUCTURE OF THE HIV-2 UNMYRISTOYLATED MATRIX PROTEIN | 3.4.23.47 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2K4H | SOLUTION STRUCTURE OF THE HIV-2 MYRISTOYLATED MATRIX PROTEIN | 3.4.23.47 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2K4I | SOLUTION STRUCTURE OF HIV-2 MYRMA BOUND TO DI-C4-PI(4,5)P2 | 3.4.23.47 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2K4P | SOLUTION STRUCTURE OF SHIP2-SAM | 3.1.3.86 |
2K4R | NMR SOLUTION STRUCTURE OF THE NEUROTRYPSIN KRINGLE DOMAIN | 3.4.21 |
2K51 | NMR SOLUTION STRUCTURE OF THE NEUROTRYPSIN KRINGLE DOMAIN | 3.4.21 |
2K6H | NMR STRUCTURE OF AN UNUSUALLY 28 KDA ACTIVE MUTANT OF MAIZE RIBOSOME-INACTIVATING PROTEIN (MOD) | 3.2.2.22 |
2K72 | SOLUTION NMR STRUCTURE OF TOXIN-LIKE POTASSIUM CHANNEL BLOCKING DOMAIN IN MMP23 | 3.4.24 |
2K7J | HUMAN ACYLPHOSPHATASE(ACPH) SURFACE CHARGE-OPTIMIZED | 3.6.1.7 |
2K7K | HUMAN ACYLPHOSPHATASE (ACPH) COMMON TYPE | 3.6.1.7 |
2K7X | SOLUTION STRUCTURE OF C-TERMINAL DOMAIN OF SARS-COV MAIN PROTEASE | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2K7Z | SOLUTION STRUCTURE OF THE CATALYTIC DOMAIN OF PROCASPASE-8 | 3.4.22.61 |
2K87 | NMR STRUCTURE OF A PUTATIVE RNA BINDING PROTEIN (SARS1) FROM SARS CORONAVIRUS | 3.4.19.12 3.4.22 3.4.22.69 |
2K9C | PARAMAGNETIC SHIFTS IN SOLID-STATE NMR OF PROTEINS TO ELICIT STRUCTURAL INFORMATION | 3.4.24.65 |
2KAF | SOLUTION STRUCTURE OF THE SARS-UNIQUE DOMAIN-C FROM THE NONSTRUCTURAL PROTEIN 3 (NSP3) OF THE SEVERE ACUTE RESPIRATORY SYNDROME CORONAVIRUS | 3.4.22 3.4.19.12 3.4.22.69 |
2KAI | REFINED 2.5 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF THE COMPLEX FORMED BY PORCINE KALLIKREIN A AND THE BOVINE PANCREATIC TRYPSIN INHIBITOR. CRYSTALLIZATION, PATTERSON SEARCH, STRUCTURE DETERMINATION, REFINEMENT, STRUCTURE AND COMPARISON WITH ITS COMPONENTS AND WITH THE BOVINE TRYPSIN-PANCREATIC TRYPSIN INHIBITOR COMPLEX | 3.4.21.8 3.4.21.35 |
2KAU | THE CRYSTAL STRUCTURE OF UREASE FROM KLEBSIELLA AEROGENES AT 2.2 ANGSTROMS RESOLUTION | 3.5.1.5 |
2KB0 | CDC42(T35A) | 3.6.5.2 |
2KB5 | SOLUTION NMR STRUCTURE OF EOSINOPHIL CATIONIC PROTEIN/RNASE 3 | 3.1.27 |
2KB6 | SOLUTION STRUCTURE OF ONCONASE C87A/C104A | 3.1.27 |
2KBE | SOLUTION STRUCTURE OF AMINO-TERMINAL DOMAIN OF DBP5P | 3.6.1 3.6.4.13 |
2KBF | SOLUTION STRUCTURE OF CARBOXYL-TERMINAL DOMAIN OF DBP5P | 3.6.1 3.6.4.13 |
2KBO | STRUCTURE, INTERACTION, AND REAL-TIME MONITORING OF THE ENZYMATIC REACTION OF WILD TYPE APOBEC3G | 3.5.4 |
2KC8 | STRUCTURE OF E. COLI TOXIN RELE (R81A/R83A) MUTANT IN COMPLEX WITH ANTITOXIN RELBC (K47-L79) PEPTIDE | 3.1 |
2KC9 | STRUCTURE OF E. COLI TOXIN RELE (R81A/R83A) MUTANT IN THE FREE STATE | 3.1 |
2KDT | PC1/3 DCSG SORTING DOMAIN STRUCTURE IN DPC | 3.4.21.93 |
2KDV | SOLUTION STRUCTURE OF RNA PYROPHOSPHOHYDROLASE RPPH FROM ESCHERICHIA COLI | 3.6.1 |
2KDW | SOLUTION STRUCTURE OF RPPH MUTANT E53A FROM ESCHERICHIA COLI | 3.6.1 |
2KE3 | PC1/3 DCSG SORTING DOMAIN IN CHAPS | 3.4.21.93 |
2KE5 | SOLUTION STRUCTURE AND DYNAMICS OF THE SMALL GTPASE RALB IN ITS ACTIVE CONFORMATION: SIGNIFICANCE FOR EFFECTOR PROTEIN BINDING | 3.6.5.2 |
2KEM | EXTENDED STRUCTURE OF CITIDINE DEAMINASE DOMAIN OF APOBEC3G | 3.5.4 |
2KF3 | BARNASE, LOW PRESSURE REFERENCE NMR STRUCTURE | 3.1.27 |
2KF4 | BARNASE HIGH PRESSURE STRUCTURE | 3.1.27 |
2KF5 | BARNASE BOUND TO D(CGAC), LOW PRESSURE | 3.1.27 |
2KF6 | BARNASE BOUND TO D(CGAC) HIGH PRESSURE | 3.1.27 |
2KHS | SOLUTION STRUCTURE OF SNASE121:SNASE(111-143) COMPLEX | 3.1.31.1 |
2KHX | DROSHA DOUBLE-STRANDED RNA BINDING MOTIF | 3.1.26.3 |
2KHZ | SOLUTION STRUCTURE OF RCL | 3.2.2 |
2KI7 | THE SOLUTION STRUCTURE OF RPP29-RPP21 COMPLEX FROM PYROCOCCUS FURIOSUS | 3.1.26.5 |
2KIE | A PH DOMAIN WITHIN OCRL BRIDGES CLATHRIN MEDIATED MEMBRANE TRAFFICKING TO PHOSPHOINOSITIDE METABOLIS | 3.1.3.36 3.1.3.56 3.1.3.86 |
2KIG | A PH DOMAIN WITHIN OCRL BRIDGES CLATHRIN MEDIATED MEMBRANE TRAFFICKING TO PHOSPHOINOSITIDE METABOLISM | 3.1.3.36 |
2KIJ | SOLUTION STRUCTURE OF THE ACTUATOR DOMAIN OF THE COPPER-TRANSPORTING ATPASE ATP7A | 3.6.3.4 7.2.2.8 |
2KJK | SOLUTION STRUCTURE OF THE SECOND DOMAIN OF THE LISTERIA PROTEIN LIN2157, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET LKR136B | 3.4.21.53 |
2KKN | SOLUTION NMR STRUCTURE OF THEMOTOGA MARITIMA PROTEIN TM1076: NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET VT57 | 3.1.4 |
2KL1 | SOLUTION STRUCTURE OF GTR34C FROM GEOBACILLUS THERMODENITRIFICANS. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET GTR34C | 3.4.21.53 |
2KLH | NMR STRUCTURE OF RCL IN COMPLEX WITH GMP | 3.2.2 |
2KLQ | THE SOLUTION STRUCTURE OF CBD OF HUMAN MCM6 | 3.6.4.12 |
2KLZ | SOLUTION STRUCTURE OF THE TANDEM UIM DOMAIN OF ATAXIN-3 COMPLEXED WITH UBIQUITIN | 3.4.22 3.4.19.12 |
2KMN | SOLUTION STRUCTURE OF PEPTIDE DEFORMYLASE COMPLEXED WITH ACTINONIN | 3.5.1.88 |
2KMU | RECQL4 AMINO-TERMINAL DOMAIN | 3.6.1 3.6.4.12 |
2KMV | SOLUTION STRUCTURE OF THE NUCLEOTIDE BINDING DOMAIN OF THE HUMAN MENKES PROTEIN IN THE ATP-FREE FORM | 3.6.3.4 7.2.2.8 |
2KMX | SOLUTION STRUCTURE OF THE NUCLEOTIDE BINDING DOMAIN OF THE HUMAN MENKES PROTEIN IN THE ATP-BOUND FORM | 3.6.3.4 7.2.2.8 |
2KN7 | STRUCTURE OF THE XPF-SINGLE STRAND DNA COMPLEX | 3.1 |
2KN8 | NMR STRUCTURE OF THE C-TERMINAL DOMAIN OF PUL89 | 3.1 |
2KNF | SOLUTION STRUCTURE AND FUNCTIONAL CHARACTERIZATION OF HUMAN PLASMINOGEN KRINGLE 5 | 3.4.21.7 |
2KNO | NMR SOLUTION STRUCTURE OF SH2 DOMAIN OF THE HUMAN TENSIN LIKE C1 DOMAIN CONTAINING PHOSPHATASE (TENC1) | 3.1.3 3.1.3.48 |
2KNU | SOLUTION STRUCTURE OF THE TRANSMEMBRANE PROXIMAL REGION OF THE HEPATIS C VIRUS E1 GLYCOPROTEIN | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2KOD | A HIGH-RESOLUTION NMR STRUCTURE OF THE DIMERIC C-TERMINAL DOMAIN OF HIV-1 CA | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2KOU | DICER LIKE PROTEIN | 3.1.26 |
2KOY | STRUCTURE OF THE E1064A MUTANT OF THE N-DOMAIN OF WILSON DISEASE ASSOCIATED PROTEIN | 3.6.3.4 7.2.2.8 |
2KP7 | SOLUTION NMR STRUCTURE OF THE MUS81 N-TERMINAL HHH. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET MMT1A | 3.1.22 |
2KPN | SOLUTION NMR STRUCTURE OF A BACTERIAL IG-LIKE (BIG_3) DOMAIN FROM BACILLUS CEREUS. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET BCR147A | 3.4.24.28 |
2KQ3 | SOLUTION STRUCTURE OF SNASE140 | 3.1.31.1 |
2KQ8 | SOLUTION NMR STRUCTURE OF A DOMAIN FROM BT9727_4915 FROM BACILLUS THURINGIENSIS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET BUR95A | 3.5.1.28 |
2KQB | FIRST PBZ DOMAIN OF HUMAN APLF PROTEIN | 4.2.99.18 3.1 |
2KQC | SECOND PBZ DOMAIN OF HUMAN APLF PROTEIN | 4.2.99.18 3.1 |
2KQD | FIRST PBZ DOMAIN OF HUMAN APLF PROTEIN IN COMPLEX WITH RIBOFURANOSYLADENOSINE | 4.2.99.18 3.1 |
2KQE | SECOND PBZ DOMAIN OF HUMAN APLF PROTEIN IN COMPLEX WITH RIBOFURANOSYLADENOSINE | 4.2.99.18 3.1 |
2KQV | SARS CORONAVIRUS-UNIQUE DOMAIN (SUD): THREE-DOMAIN MOLECULAR ARCHITECTURE IN SOLUTION AND RNA BINDING. I: STRUCTURE OF THE SUD-M DOMAIN OF SUD-MC | 3.4.19.12 3.4.22 3.4.22.69 |
2KQW | SARS CORONAVIRUS-UNIQUE DOMAIN (SUD): THREE-DOMAIN MOLECULAR ARCHITECTURE IN SOLUTION AND RNA BINDING. II: STRUCTURE OF THE SUD-C DOMAIN OF SUD-MC | 3.4.19.12 3.4.22 3.4.22.69 |
2KR6 | SOLUTION STRUCTURE OF PRESENILIN-1 CTF SUBUNIT | 3.4.23 |
2KRJ | HIGH-RESOLUTION SOLID-STATE NMR STRUCTURE OF A 17.6 KDA PROTEIN | 3.4.24.65 |
2KSG | SOLUTION STRUCTURE OF DERMCIDIN-1L, A HUMAN ANTIBIOTIC PEPTIDE | 3.4 |
2KSV | THE NMR STRUCTURE OF PROTEIN-GLUTAMINASE FROM CHRYSEOBACTERIUM PROTEOLYTICUM | 3.5.1.44 |
2KU1 | DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | 3.4.25.1 |
2KU2 | DYNAMIC REGULATION OF ARCHAEAL PROTEASOME GATE OPENING AS STUDIED BY TROSY-NMR | 3.4.25.1 |
2KUO | STRUCTURE AND IDENTIFICATION OF ADP-RIBOSE RECOGNITION MOTIFS OF APLF AND ROLE IN THE DNA DAMAGE RESPONSE | 3.1 |
2KV2 | SOLUTION STRUCTURE OF THE HUMAN BLM HRDC DOMAIN | 3.6.4.12 |
2KVR | SOLUTION NMR STRUCTURE OF HUMAN UBIQUITIN SPECIFIC PROTEASE USP7 UBL DOMAIN (RESIDUES 537-664). NESG TARGET HR4395C/ SGC-TORONTO | 3.1.2.15 3.4.19.12 |
2KWA | 1H, 13C AND 15N BACKBONE AND SIDE CHAIN RESONANCE ASSIGNMENTS OF THE N-TERMINAL DOMAIN OF THE HISTIDINE KINASE INHIBITOR KIPI FROM BACILLUS SUBTILIS | 3.5.2.9 |
2KWI | RALB-RLIP76 (RALBP1) COMPLEX | 3.6.5.2 |
2KWT | SOLUTION STRUCTURE OF NS2 [27-59] | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2KWZ | SOLUTION STRUCTURE OF NS2 [60-99] | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2KX3 | THE SOLUTION STRUCTURE OF THE MUTANT OF UBL DOMAIN OF UBLCP1, I5M | 3.1.3.16 |
2KXE | N-TERMINAL DOMAIN OF THE DP1 SUBUNIT OF AN ARCHAEAL D-FAMILY DNA POLYMERASE | 2.7.7.7 3.1.11.1 |
2KYS | NMR STRUCTURE OF THE SARS CORONAVIRUS NONSTRUCTURAL PROTEIN NSP7 IN SOLUTION AT PH 6.5 | 3.4.19.12 3.4.22 3.4.22.69 |
2KYT | SOLUTION STRUCTURE OF THE H-REV107 N-TERMINAL DOMAIN | 3.1.1.4 2.3.1 3.1.1.32 |
2KZQ | S34R STRUCTURE | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2KZR | SOLUTION NMR STRUCTURE OF UBIQUITIN THIOESTERASE OTU1 (EC 3.1.2.-) FROM MUS MUSCULUS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET MMT2A | 3.1.2 3.4.19.12 |
2L0R | CONFORMATIONAL DYNAMICS OF THE ANTHRAX LETHAL FACTOR CATALYTIC CENTER | 3.4.24.83 |
2L0S | SOLUTION STRUCTURE OF HUMAN PLASMINOGEN KRINGLE 3 | 3.4.21.7 |
2L17 | AN ARSENATE REDUCTASE IN THE REDUCED STATE | 1.20.4.1 3.1.3.48 |
2L18 | AN ARSENATE REDUCTASE IN THE PHOSPHATE BINDING STATE | 1.20.4.1 3.1.3.48 |
2L19 | AN ARSENATE REDUCTASE IN THE INTERMEDIATE STATE | 1.20.4.1 3.1.3.48 |
2L2D | SOLUTION NMR STRUCTURE OF HUMAN UBA-LIKE DOMAIN OF OTUD7A_11_83, NESG TARGET HT6304A/OCSP TARGET OTUD7A_11_83/SGC-TORONTO | 3.4.19.12 |
2L37 | 3D SOLUTION STRUCTURE OF ARGININE/GLUTAMATE-RICH POLYPEPTIDE LUFFIN P1 FROM THE SEEDS OF SPONGE GOURD (LUFFA CYLINDRICAL) | 3.2.2.22 |
2L3C | SOLUTION STRUCTURE OF ADAR2 DSRBM1 BOUND TO LSL RNA | 3.5 3.5.4.37 |
2L3F | SOLUTION NMR STRUCTURE OF A PUTATIVE URACIL DNA GLYCOSYLASE FROM METHANOSARCINA ACETIVORANS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET MVR76 | 3.2.2 |
2L3H | NMR STRUCTURE IN A MEMBRANE ENVIRONMENT REVEALS PUTATIVE AMYLOIDOGENIC REGIONS OF THE SEVI PRECURSOR PEPTIDE PAP248-286 | 3.1.3.2 3.1.3.5 |
2L3J | THE SOLUTION STRUCTURE OF THE ADAR2 DSRBM-RNA COMPLEX REVEALS A SEQUENCE-SPECIFIC READ OUT OF THE MINOR GROOVE | 3.5 3.5.4.37 |
2L45 | C-TERMINAL ZINC KNUCKLE OF THE HIVNCP7 WITH DNA | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2L46 | C-TERMINAL ZINC FINGER OF THE HIVNCP7 WITH PLATINATED DNA | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2L47 | SOLUTION STRUCTURE OF THE PLYG CATALYTIC DOMAIN | 3.5.1.28 |
2L4L | STRUCTURAL INSIGHTS INTO THE CTAR DNA RECOGNITION BY THE HIV-1 NUCLEOCAPSID PROTEIN: ROLE OF SUGAR DEOXYRIBOSES IN THE BINDING POLARITY OF NC | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2L4Z | NMR STRUCTURE OF FUSION OF CTIP (641-685) TO LMO4-LIM1 (18-82) | 3.1 |
2L54 | SOLUTION STRUCTURE OF THE ZALPHA DOMAIN MUTANT OF ADAR1 (N43A,Y47A) | 3.5.4 3.5.4.37 |
2L5C | SOLUTION STRUCTURES OF HUMAN PIWI-LIKE 1 PAZ DOMAIN | 3.1.26 |
2L5D | SOLUTION STRUCTURES OF HUMAN PIWI-LIKE 1 PAZ DOMAIN WITH SSRNA (5'-PUGACA) | 3.1.26 |
2L5U | STRUCTURE OF THE FIRST PHD FINGER (PHD1) FROM CHD4 (MI2B) | 3.6.4.12 |
2L6E | NMR STRUCTURE OF THE MONOMERIC MUTANT C-TERMINAL DOMAIN OF HIV-1 CAPSID IN COMPLEX WITH STAPLED PEPTIDE INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2L6K | SOLUTION STRUCTURE OF A NONPHOSPHORYLATED PEPTIDE RECOGNIZING DOMAIN | 3.1.3.48 |
2L6M | STRUCTURE OF C-TERMINAL DSRBD OF THE FISSION YEAST DICER (DCR1) | 3.1.26 3.6.4 |
2L75 | SOLUTION STRUCTURE OF CHD4-PHD2 IN COMPLEX WITH H3K9ME3 | 3.6.4.12 |
2L77 | SOLUTION NMR STRUCTURE OF PAP248-286 IN 50% TFE | 3.1.3.2 3.1.3.5 |
2L78 | DESIGN AND STRUCTURAL ANALYSIS OF ALTERNATIVE HYDROPHOBIC CORE PACKING ARRANGEMENTS IN BACTERIOPHAGE T4 LYSOZYME | 3.2.1.17 |
2L79 | SOLUTION NMR STRUCTURE OF PAP248-286 IN 30% TFE | 3.1.3.2 3.1.3.5 |
2L7Y | SOLUTION STRUCTURE OF A PUTATIVE SURFACE PROTEIN | 3.2.1.96 |
2L80 | SOLUTION STRUCTURE OF THE ZINC FINGER DOMAIN OF USP13 | 3.4.19.12 |
2L8A | STRUCTURE OF A NOVEL CBM3 LACKING THE CALCIUM-BINDING SITE | 3.2.1.4 |
2L8B | TRAI (381-569) | 3.6.4.12 5.6.2.1 |
2L8K | NMR STRUCTURE OF THE ARTERIVIRUS NONSTRUCTURAL PROTEIN 7 ALPHA (NSP7 ALPHA) | 3.4.22 3.4.19.12 3.4.21 2.7.7.48 3.6.4.12 3.6.4.13 |
2L8L | STRUCTURE OF AN ENGINEERED SPLICING INTEIN MUTANT BASED ON MYCOBACTERIUM TUBERCULOSIS RECA | 3.1 |
2L8R | SOLUTION STRUCTURE OF HUMAN PROTEIN C6ORF130 IN COMPLEX WITH ADP-RIBOSE | 3.5.1 3.2.2 |
2L95 | SOLUTION STRUCTURE OF CYTOTOXIC T-LYMPHOCYTE ANTIGENT-2(CTLA PROTEIN), CRAMMER AT PH 6.0 | 3.4 |
2LAA | SOLUTION STRUCUTURE OF THE CBM25-1 OF BETA/ALPHA-AMYLASE FROM PAENIBACILLUS POLYMYXA | 3.2.1.2 3.2.1.1 |
2LAB | SOLUTION STRUCUTURE OF THE CBM25-2 OF BETA/ALPHA-AMYLASE FROM PAENIBACILLUS POLYMYXA | 3.2.1.2 3.2.1.1 |
2LBC | SOLUTION STRUCTURE OF TANDEM UBA OF USP13 | 3.4.19.12 |
2LBM | SOLUTION STRUCTURE OF THE ADD DOMAIN OF ATRX COMPLEXED WITH HISTONE TAIL H3 1-15 K9ME3 | 3.6.4.12 |
2LC9 | SOLUTION STRUCTURE OF A MINOR AND TRANSIENTLY FORMED STATE OF A T4 LYSOZYME MUTANT | 3.2.1.17 |
2LCB | SOLUTION STRUCTURE OF A MINOR AND TRANSIENTLY FORMED STATE OF A T4 LYSOZYME MUTANT | 3.2.1.17 |
2LCF | SOLUTION STRUCTURE OF GPPNHP-BOUND H-RAST35S MUTANT PROTEIN | 3.6.5.2 |
2LCJ | SOLUTION NMR STRUCTURE OF PAB POLII INTEIN | 2.7.7.7 3.1.11.1 |
2LCQ | SOLUTION STRUCTURE OF THE ENDONUCLEASE NOB1 FROM P.HORIKOSHII | 3.1 |
2LD1 | STRUCTURES AND CHEMICAL SHIFT ASSIGNMENTS FOR THE ADD DOMAIN OF THE ATRX PROTEIN | 3.6.4.12 |
2LDI | NMR SOLUTION STRUCTURE OF ZIAAN SUB MUTANT | 3.6.3.5 7.2.2.12 |
2LE8 | THE PROTEIN COMPLEX FOR DNA REPLICATION | 3.6.4.12 |
2LEN | SOLUTION STRUCTURE OF UCHL1 S18Y VARIANT | 3.4.19.12 |
2LEP | SOLUTION STRUCTURE OF N-TERMINAL CYTOSOLIC DOMAIN OF RHOMBOID INTRAMEMBRANE PROTEASE FROM ESCHERICHIA COLI | 3.4.21.105 |
2LF4 | STRUCTURE OF A MONOMERIC MUTANT OF THE HIV-1 CAPSID PROTEIN | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2LFJ | SOLUTION STRUCTURE OF THE MONOMERIC DERIVATIVE OF BS-RNASE | 3.1.27.5 4.6.1.18 |
2LGD | THE HIGH RESOLUTION STRUCTURE OF UBIQUITIN LIKE DOMAIN OF UBLCP1 | 3.1.3.16 |
2LGJ | SOLUTION STRUCTURE OF MSPTH | 3.1.1.29 |
2LGR | SOLUTION STRUCTURE OF HUMAN PROTEIN C6ORF130, A PUTATIVE MACRO DOMAIN | 3.5.1 3.2.2 |
2LHI | SOLUTION STRUCTURE OF CA2+/CNA1 PEPTIDE-BOUND YCAM | 3.1.3.16 |
2LHM | CRYSTAL STRUCTURES OF THE APO-AND HOLOMUTANT HUMAN LYSOZYMES WITH AN INTRODUCED CA2+ BINDING SITE | 3.2.1.17 |
2LIP | PSEUDOMONAS LIPASE OPEN CONFORMATION | 3.1.1.3 |
2LIZ | NMR SOLUTION STRUCTURE OF C-TERMINAL DOMAIN OF SARS-COV MAIN PROTEASE IN 2.5M UREA | 3.4.22 3.4.19.12 3.4.22.69 |
2LJH | NMR STRUCTURE OF DOUBLE-STRANDED RNA-SPECIFIC EDITASE ADAR | 3.5 |
2LJP | BACKBONE 1H, 13C, AND 15N CHEMICAL SHIFT ASSIGNMENTS FOR E.COLI RIBONUCLEASE P PROTEIN | 3.1.26.5 |
2LJV | SOLUTION STRUCTURE OF RHODOSTOMIN G50L MUTANT | 3.4.24 |
2LKT | SOLUTION STRUCTURE OF N-TERMINAL DOMAIN OF HUMAN TIG3 IN 2 M UREA | 3.1.1 2.3.1 3.1.1.32 3.1.1.4 |
2LKV | STAPHYLOCOCCAL NUCLEASE PHS VARIANT | 3.1.31.1 |
2LLZ | GHOS (YJDK) MONOMER | 3.1 |
2LNA | SOLUTION NMR STRUCTURE OF THE MITOCHONDRIAL INNER MEMBRANE DOMAIN (RESIDUES 164-251), FTSH_EXT, FROM THE PARAPLEGIN-LIKE PROTEIN AFG3L2 FROM HOMO SAPIENS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET HR6741A | 3.4.24 |
2LNC | SOLUTION NMR STRUCTURE OF NORWALK VIRUS PROTEASE | 3.4.22.66 3.6.1.15 2.7.7.48 |
2LOZ | THE NOVEL BINDING MODE OF DLC1 AND TENSIN2 PTB DOMAIN | 3.1.3 3.1.3.48 |
2LPR | STRUCTURAL BASIS FOR BROAD SPECIFICITY IN ALPHA-LYTIC PROTEASE MUTANTS | 3.4.21.12 |
2LQB | METAL BINDING REPEAT 2 OF THE WILSON DISEASE PROTEIN (ATP7B) | 3.6.3.4 7.2.2.8 |
2LQJ | SOLUTION STRUCTURE OF THE C-TERMINAL DOMAIN OF THE MGTC PROTEIN FROM MYCOBACTERIUM TUBERCULOSIS | 3.6.3.1 |
2LRO | SOLUTION STRUCTURE, DYNAMICS AND BINDING STUDIES OF CTCBM11 | 3.2.1.4 |
2LRP | SOLUTION STRUCTURE, DYNAMICS AND BINDING STUDIES OF CTCBM11 | 3.2.1.4 |
2LRR | SOLUTION STRUCTURE OF THE R3H DOMAIN FROM HUMAN SMUBP-2 IN COMPLEX WITH 2'-DEOXYGUANOSINE-5'-MONOPHOSPHATE | 3.6.4.12 3.6.4.13 |
2LRS | THE SECOND DSRBD DOMAIN FROM A. THALIANA DICER-LIKE 1 | 3.1.26 |
2LS6 | SOLUTION NMR STRUCTURE OF A NON-CANONICAL GALACTOSE-BINDING CBM32 FROM CLOSTRIDIUM PERFRINGENS | 3.2.1.35 |
2LSN | SOLUTION STRUCTURE OF PFV RNASE H DOMAIN | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1 |
2LT5 | ZYMOGEN-FLG OF THE ONCONASE | 3.1.27 |
2LTJ | CONFORMATIONAL ANALYSIS OF STRH, THE SURFACE-ATTACHED EXO- BETA-D-N-ACETYLGLUCOSAMINIDASE FROM STREPTOCOCCUS PNEUMONIAE | 3.2.1.52 |
2LU1 | PFSUB2 SOLUTION NMR STRUCTURE | 3.4.21.62 |
2LUO | NMR SOLUTION STRUCTURE OF APO-MPTPA | 3.1.3.48 |
2LUQ | SOLUTION STRUCTURE OF DOUBLE-STRANDED RNA BINDING DOMAIN OF S.CEREVISIAE RNASE III (RNT1P) | 3.1.26.3 |
2LUW | SOLUTION STRUCTURE OF VEP C-TER 100 | 3.4.24 |
2LVA | NMR SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF HUMAN USP28, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET HT8470A | 3.4.19.12 |
2LVG | NMR STRUCTURE OF HCV NON-STRUCTURAL PROTEIN AB, NS4B(1-40) | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2LVX | MRH DOMAIN OF THE GLUCOSIDASE II BETA SUBUNIT FROM S. POMBE | 3.2.1.84 |
2LVZ | SOLUTION STRUCTURE OF A EOSINOPHIL CATIONIC PROTEIN-TRISACCHARIDE HEPARIN MIMETIC COMPLEX | 3.1.27 |
2LW1 | THE C-TERMINAL DOMAIN OF THE UUP PROTEIN IS A DNA-BINDING COILED COIL MOTIF | 3.6.1 |
2LWD | SOLUTION STRUCTURE OF SECOND CARD OF HUMAN RIG-I | 3.6.4.13 |
2LWE | SOLUTION STRUCTURE OF MUTANT (T170E) SECOND CARD OF HUMAN RIG-I | 3.6.4.13 |
2LWF | STRUCTURE OF N-TERMINAL DOMAIN OF A PLANT GRX | 3.1 |
2LWI | SOLUTION STRUCTURE OF H-RAST35S MUTANT PROTEIN IN COMPLEX WITH KOBE2601 | 3.6.5.2 |
2LXF | SOLUTION NMR STRUCTURE OF A POTENTIAL ACYLPHOSPHATASE FROM GIARDIA LAMBLIA, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE TARGET GILAA.01396.A | 3.6.1.7 |
2LYA | STRUCTURE OF HIV-1 MYR(-) MATRIX PROTEIN IN COMPLEX WITH 1,2-DIOCTANOYL-SN-PHOSPHATIDYLCHOLINE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2LYB | STRUCTURE OF HIV-1 MYR(-) MATRIX PROTEIN IN COMPLEX WITH 1,2-DIOCTANOYL-SN-PHOSPHATIDYL-L-SERINE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2LYM | CRYSTAL STRUCTURE OF HEN EGG-WHITE LYSOZYME AT A HYDROSTATIC PRESSURE OF 1000 ATMOSPHERES | 3.2.1.17 |
2LYO | CROSS-LINKED CHICKEN LYSOZYME CRYSTAL IN 90% ACETONITRILE-WATER | 3.2.1.17 |
2LYZ | REAL-SPACE REFINEMENT OF THE STRUCTURE OF HEN EGG-WHITE LYSOZYME | 3.2.1.17 |
2LZ2 | THE THREE DIMENSIONAL STRUCTURE OF TURKEY EGG WHITE LYSOZYME AT 2.2 ANGSTROMS RESOLUTION | 3.2.1.17 |
2LZM | STRUCTURE OF BACTERIOPHAGE T4 LYSOZYME REFINED AT 1.7 ANGSTROMS RESOLUTION | 3.2.1.17 |
2LZP | STRUCTURE OF NS2(2-32) GBVB PROTEIN | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2LZQ | STRUCTURE OF NS2(32-57) GBVB PROTEIN | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2LZT | REFINEMENT OF TRICLINIC LYSOZYME. II. THE METHOD OF STEREOCHEMICALLY RESTRAINED LEAST-SQUARES | 3.2.1.17 |
2M00 | SOLUTION STRUCTURE OF STAPHYLOCOCCAL NUCLEASE E43S MUTANT IN THE PRESENCE OF SSDNA AND CD2+ | 3.1.31.1 |
2M0A | SOLUTION STRUCTURE OF MHV NSP3A | 3.4.19.12 3.4.22.69 3.4.22 |
2M0S | SOLUTION STRUCTURE OF THE TRANS-MEMBRANE DOMAIN OF THE NS2A OF DENGUE VIRUS | 3.4.21.91 3.6.1.15 3.6.4.13 |
2M0Z | CIS FORM OF A PHOTOSWITCHABLE PDZ DOMAIN CROSSLINKED WITH AN AZOBENZENE DERIVATIVE | 3.1.3.48 |
2M10 | TRANS FORM OF A PHOTOSWITCHABLE PDZ DOMAIN CROSSLINKED WITH AN AZOBENZENE DERIVATIVE | 3.1.3.48 |
2M17 | UBIQUITIN-LIKE DOMAIN-CONTAINING C-TERMINAL DOMAIN PHOSPHATASE (UBLCP1) | 3.1.3.16 |
2M1C | HADDOCK STRUCTURE OF GTYYBT PAS HOMODIMER | 3.1.4.59 |
2M2F | THE MEMBRAN-PROXIMAL DOMAIN OF ADAM17 | 3.4.24.86 |
2M3D | NMR STRUCTURE OF THE GUCT DOMAIN FROM HUMAN DEAD BOX POLYPEPTIDE 21 | 3.6.4.13 |
2M3Z | NMR SOLUTION STRUCTURE OF HIV-1 NUCLEOCAPSID PROTEIN IN COMPLEX WITH AN INHIBITOR DISPLAYING A 2 INHIBITORS:1 NC STOICHIOMETRY | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2M45 | NMR SOLUTION STRUCTURE OF THE C-TERMINUS OF THE MINICHROMOSOME MAINTENANCE PROTEIN MCM FROM SULFOLOBUS SOLFATARICUS | 3.6.4.12 |
2M4G | SOLUTION STRUCTURE OF THE CORE DOMAIN (11-85) OF THE MURINE NOROVIRUS VPG PROTEIN | 2.7.7.48 3.4.22.66 3.6.1.15 |
2M4H | SOLUTION STRUCTURE OF THE CORE DOMAIN (10-76) OF THE FELINE CALICIVIRUS VPG PROTEIN | 3.6.1.15 2.7.7.48 3.4.22.66 |
2M5C | SOLUTION STRUCTURE OF THE BACILLUS CEREUS METALLO-BETA-LACTAMASE BCII | 3.5.2.6 |
2M5D | SOLUTION STRUCTURE OF THE BACILLUS CEREUS METALLO-BETA-LACTAMASE BCII IN COMPLEX WITH R-THIOMANDELIC ACID | 3.5.2.6 |
2M5L | NS5A308 | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2M5T | SOLUTION STRUCTURE OF THE 2A PROTEINASE FROM A COMMON COLD AGENT, HUMAN RHINOVIRUS RV-C02, STRAIN W12 | 3.4.22.28 3.4.22.29 3.6.1.15 |
2M65 | NMR STRUCTURE OF HUMAN RESTRICTION FACTOR APOBEC3A | 3.5.4 3.5.4.38 |
2M6X | STRUCTURE OF THE P7 CHANNEL OF HEPATITIS C VIRUS, GENOTYPE 5A | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2M73 | SOLUTION STRUCTURE OF THE CALMODULIN-BINDING DOMAIN OF PLANT CALCIUM-ATPASE ACA8 | 3.6.3.8 7.2.2.10 |
2M75 | THE C-TERMINAL REGION OF DISINTEGRIN MODULATE ITS 3D CONFORMATION AND COOPERATE WITH RGD LOOP IN REGULATING RECOGNITIONS OF INTEGRINS | 3.4.24 |
2M7E | SOLUTION STRUCTURE OF THE CALMODULIN-BINDING DOMAIN OF PLANT CALCIUM-ATPASE ACA2 | 3.6.3.8 7.2.2.10 |
2M7F | THE C-TERMINAL REGION OF DISINTEGRIN MODULATE ITS 3D CONFORMATION AND COOPERATE WITH RGD LOOP IN REGULATING INTEGRINS RECOGNITIONS | 3.4.24 |
2M7H | THE C-TERMINAL REGION OF DISINTEGRIN MODULATE ITS 3D CONFORMATION AND COOPERATE WITH RGD LOOP IN REGULATING INTEGRIN ALPHA-IIB BETA-3 RECOGNITION | 3.4.24 |
2M7Y | THE MENGOVIRUS LEADER PROTEIN | 3.6.4.13 3.4.22.28 2.7.7.48 |
2M85 | PHD DOMAIN FROM HUMAN SHPRH | 3.6.4 6.3.2 2.3.2.27 |
2M8L | HIV CAPSID DIMER STRUCTURE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2M8N | HIV-1 CAPSID MONOMER STRUCTURE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2M8P | THE STRUCTURE OF THE W184AM185A MUTANT OF THE HIV-1 CAPSID PROTEIN | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2M9P | NMR STRUCTURE OF AN INHIBITOR BOUND DENGUE NS3 PROTEASE | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2M9Q | NMR STRUCTURE OF AN INHIBITOR BOUND DENGUE NS3 PROTEASE | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2M9U | SOLUTION NMR STRUCTURE OF THE C-TERMINAL DOMAIN (CTD) OF MOLONEY MURINE LEUKEMIA VIRUS INTEGRASE, NORTHEAST STRUCTURAL GENOMICS TARGET OR41A | 3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2MA1 | SOLUTION STRUCTURE OF HRDC1 DOMAIN OF RECQ HELICASE FROM DEINOCOCCUS RADIODURANS | 3.6.4.12 |
2MA3 | NMR SOLUTION STRUCTURE OF THE C-TERMINUS OF THE MINICHROMOSOME MAINTENANCE PROTEIN MCM FROM METHANOTHERMOBACTER THERMAUTOTROPHICUS | 3.6.4.12 |
2MAN | MANNOTRIOSE COMPLEX OF THERMOMONOSPORA FUSCA BETA-MANNANASE | 3.2.1.78 |
2MAS | PURINE NUCLEOSIDE HYDROLASE WITH A TRANSITION STATE INHIBITOR | 3.2.2.1 3.2.2.2 3.2.2.3 |
2MAT | E.COLI METHIONINE AMINOPEPTIDASE AT 1.9 ANGSTROM RESOLUTION | 3.4.11.18 |
2MBC | SOLUTION STRUCTURE OF HUMAN HOLO-PRL-3 IN COMPLEX WITH VANADATE | 3.1.3.48 |
2MC3 | NMR SOLUTION STRUCTURE OF THE WINGED-HELIX DOMAIN FROM MUS81 STRUCTURE-SPECIFIC ENDONUCLEASE | 3.1.22 |
2MCD | BACKBONE 1H, 13C, AND 15N CHEMICAL SHIFT ASSIGNMENTS FOR MURINE NOROVIRUS NS1/2 D94E MUTANT | 2.7.7.48 3.4.22.66 3.6.1.15 |
2MCH | BACKBONE 1H, 13C, AND 15N CHEMICAL SHIFT ASSIGNMENTS FOR MURINE NOROVIRUS NS1/2 CW3 WT | 2.7.7.48 3.4.22.66 3.6.1.15 |
2MCK | BACKBONE 1H, 13C, AND 15N CHEMICAL SHIFT ASSIGNMENTS FOR MURINE NOROVIRUS CR6 NS1/2 PROTEIN | 2.7.7.48 3.4.22.66 3.6.1.15 |
2MCR | SOLUTION STRUCTURE OF SHK-LIKE IMMUNOMODULATORY PEPTIDE FROM BRUGIA MALAYI (FILARIAL WORM) | 3.4.24 |
2MD1 | FRAGMENT BASED APPROACH AND BINDING BEHAVIOR OF LFAMPINB WITH LIPOPOLYSACCHARIDE:BIOPHYSICAL ASPECTS | 3.4.21 |
2MD2 | FRAGMENT BASED APPROACH AND BINDING BEHAVIOR OF LFAMPINB WITH LIPOPOLYSACCHARIDE: BIOPHYSICAL ASPECTS | 3.4.21 |
2MDR | SOLUTION STRUCTURE OF THE THIRD DOUBLE-STRANDED RNA-BINDING DOMAIN (DSRBD3) OF HUMAN ADENOSINE-DEAMINASE ADAR1 | 3.5.4.37 |
2MEA | CHANGES IN CONFORMATIONAL STABILITY OF A SERIES OF MUTANT HUMAN LYSOZYMES AT CONSTANT POSITIONS | 3.2.1.17 |
2MEB | CHANGES IN CONFORMATIONAL STABILITY OF A SERIES OF MUTANT HUMAN LYSOZYMES AT CONSTANT POSITIONS | 3.2.1.17 |
2MEC | CHANGES IN CONFORMATIONAL STABILITY OF A SERIES OF MUTANT HUMAN LYSOZYMES AT CONSTANT POSITIONS | 3.2.1.17 |
2MED | CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME | 3.2.1.17 |
2MEE | CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME | 3.2.1.17 |
2MEF | CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME | 3.2.1.17 |
2MEG | CHANGES IN CONFORMATIONAL STABILITY OF A SERIES OF MUTANT HUMAN LYSOZYMES AT CONSTANT POSITIONS. | 3.2.1.17 |
2MEH | CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME | 3.2.1.17 |
2MEI | CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME | 3.2.1.17 |
2MEV | STRUCTURAL REFINEMENT AND ANALYSIS OF MENGO VIRUS | 3.6.4.13 3.4.22.28 2.7.7.48 |
2MF2 | STRUCTURAL AND BIOPHYSICAL CHARACTERIZATION OF THE MRNA INTERFERASE SAMAZF FROM STAPHYLOCOCCUS AUREUS. | 3.1 |
2MH9 | RESONANCE ASSIGNMENT OF RQC DOMAIN OF HUMAN BLOOM SYNDROME PROTEIN | 3.6.4.12 |
2MIP | CRYSTAL STRUCTURE OF HUMAN IMMUNODEFICIENCY VIRUS (HIV) TYPE 2 PROTEASE IN COMPLEX WITH A REDUCED AMIDE INHIBITOR AND COMPARISON WITH HIV-1 PROTEASE STRUCTURES | 3.4.23.47 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2MJA | SOLUTION STRUCTURE OF DOMAIN-SWAPPED GLPG | 3.4.21.105 |
2MJL | SOLUTION STRUCTURE OF PEPTIDYL-TRNA HYROLASE FROM VIBRIO CHOLERAE | 3.1.1.29 |
2MJP | STRUCTURE-BASED IDENTIFICATION OF THE BIOCHEMICAL FUNCTION OF A HYPOTHETICAL PROTEIN FROM METHANOCOCCUS JANNASCHII:MJ0226 | 3.6.1.66 |
2MK2 | SOLUTION NMR STRUCTURE OF N-TERMINAL DOMAIN (SH2 DOMAIN) OF HUMAN INOSITOL POLYPHOSPHATE PHOSPHATASE-LIKE PROTEIN 1 (INPPL1) (FRAGMENT 20-117), NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET HR9134A | 3.1.3.86 |
2MKB | STRUCTURE OF NS2(113-137) GBVB PROTEIN | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2MKX | SOLUTION STRUCTURE OF LYSM THE PEPTIDOGLYCAN BINDING DOMAIN OF AUTOLYSIN ATLA FROM ENTEROCOCCUS FAECALIS | 3.2.1 |
2MLL | MISTLETOE LECTIN I FROM VISCUM ALBUM | 3.2.2.22 |
2MLR | MEMBRANE BILAYER COMPLEX WITH MATRIX METALLOPROTEINASE-12 AT ITS ALPHA-FACE | 3.4.24.65 |
2MLS | MEMBRANE BILAYER COMPLEX WITH MATRIX METALLOPROTEINASE-12 AT ITS BETA-FACE | 3.4.24.65 |
2MM8 | STRUCTURAL AND BIOCHEMICAL CHARACTERIZATION OF JABURETOX | 3.5.1.5 |
2MMH | UNPHOSPHORYLATED MENGOVIRUS LEADER PROTEIN: NMR STUDIES OF THE PHOSPHORYLATION OF THE MENGOVIRUS LEADER PROTEIN REVEAL STABILIZATION OF INTERMOLECULAR DOMAIN INTERACTIONS | 3.6.4.13 3.4.22.28 2.7.7.48 |
2MMI | MENGOVIRUS LEADER: STRUCTURAL CHARACTERIZATION OF THE MENGOVIRUS LEADER PROTEIN BOUND TO RAN GTPASE BY NUCLEAR MAGNETIC RESONANCE | 3.6.4.13 3.4.22.28 2.7.7.48 |
2MMK | Y41 AND T47 PHOSPHORYLATION OF THE MENGOVIRUS LEADER PROTEIN: NMR STUDIES OF THE PHOSPHORYLATION OF THE MENGOVIRUS LEADER PROTEIN REVEAL STABILIZATION OF INTERMOLECULAR DOMAIN INTERACTIONS | 3.6.4.13 3.4.22.28 2.7.7.48 |
2MML | T47 PHOSPHORYLATION OF THE MENGOVIRUS LEADER PROTEIN: NMR STUDIES OF THE PHOSPHORYLATION OF THE MENGOVIRUS LEADER PROTEIN REVEAL STABILIZATION OF INTERMOLECULAR DOMAIN INTERACTIONS | 3.6.4.13 3.4.22.28 2.7.7.48 |
2MOE | SOLUTION STRUCTURE OF MBD4 METHYL-CYTOSINE BINDING DOMAIN BOUND TO METHYLATED DNA | 3.2.2 |
2MQK | SOLUTION STRUCTURE OF N TERMINAL DOMAIN OF THE MUB AAA+ ATPASE | 3.6.1.3 3.6.1 |
2MQS | TRANSIENT COLLAGEN TRIPLE HELIX BINDING TO A KEY METALLOPROTEINASE IN INVASION AND DEVELOPMENT: SPIN LABELS TO STRUCTURE | 3.4.24.80 |
2MQV | SOLUTION NMR STRUCTURE OF THE U5-PRIMER BINDING SITE (U5-PBS) DOMAIN OF MURINE LEUKEMIA VIRUS RNA GENOME BOUND TO THE RETROVIRAL NUCLEOCAPSID PROTEIN | 3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2MR9 | NMR STRUCTURE OF UBA DOMAIN OF DNA-DAMAGE-INDUCIBLE 1 PROTEIN (DDI1) | 3.4.23 |
2MRP | NMR SOLUTION STRUCTURE OF THE UBIQUITIN LIKE DOMAIN (UBL) OF DNA-DAMAGE-INDUCIBLE 1 PROTEIN (DDI1) | 3.4.23 |
2MS0 | SOLUTION NMR STRUCTURE PF TRNAPRO:MLV-NUCLEOCAPSID (1:2) COMPLEX | 3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2MS1 | SOLUTION NMR STRUCTURE OF TRNAPRO:MLV NUCLEOCAPSID PROTEIN (1:1) COMPLEX | 3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2MSN | NMR STRUCTURE OF A PUTATIVE PHOSPHOGLYCOLATE PHOSPHATASE (NP_346487.1) FROM STREPTOCOCCUS PNEUMONIAE TIGR4 | 3.1.3.18 |
2MTE | SOLUTION STRUCTURE OF DOC48S | 3.2.1.176 |
2MTS | THREE-DIMENSIONAL STRUCTURE AND INTERACTION STUDIES OF HEPATITIS C VIRUS P7 IN 1,2-DIHEXANOYL-SN-GLYCERO-3-PHOSPHOCHOLINE BY SOLUTION NUCLEAR MAGNETIC RESONANCE | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2MUG | PROTECTIVE CELLULAR IMMUNITY AGAINST P. FALCIPARUM MALARIA MEROZOITE IS ASSOCIATED WITH A DIFFERENT P7 AND P8 RESIDUE ORIENTATION IN THE MHC-PEPTIDE-TCR COMPLEX | 3.4.22 |
2MV3 | THE N-DOMAIN OF THE AAA METALLOPROTEINASE YME1 FROM SACCHAROMYCES CEREVISIAE | 3.4.24 |
2MWJ | SOLUTION STRUCTURE OF FAMILY 1 CARBOHYDRATE-BINDING MODULE FROM TRICHODERMA REESEI CEL7A WITH O-MANNOSE RESIDUES AT THR1 AND SER3 | 3.2.1.91 |
2MWK | FAMILY 1 CARBOHYDRATE-BINDING MODULE FROM TRICHODERMA REESEI CEL7A WITH O-MANNOSE RESIDUES AT THR1, SER3, AND SER14 | 3.2.1.91 |
2MXD | SOLUTION STRUCTURE OF VPG OF PORCINE SAPOVIRUS | 3.6.1.15 2.7.7.48 3.4.22.66 |
2MXZ | BACTERIOPHAGE T5 L-ALANOYL-D-GLUTAMATE PEPTIDASE COMLPEX WITH ZN2+ (ENDO T5-ZN2+) | 3.4.24 |
2MY9 | SOLUTION STRUCTURE OF N-TERMINAL DOMAIN OF HUMAN TIG3 | 3.1.1 2.3.1 3.1.1.32 3.1.1.4 |
2MYN | AN ARSENATE REDUCTASE IN REDUCED STATE | 1.20.4.1 3.1.3.48 |
2MYP | AN ARSENATE REDUCTASE IN THE PHOSPHATE BINDING STATE | 1.20.4.1 3.1.3.48 |
2MYT | AN ARSENATE REDUCTASE IN THE INTERMEDIATE STATE | 1.20.4.1 3.1.3.48 |
2MYU | AN ARSENATE REDUCTASE IN OXIDIZED STATE | 1.20.4.1 3.1.3.48 |
2MZE | NMR SOLUTION STRUCTURE OF THE PRO FORM OF HUMAN MATRILYSIN (PROMMP-7) | 3.4.24.23 |
2MZH | NMR SOLUTION STRUCTURE OF THE PRO FORM OF HUMAN MATRILYSIN (PROMMP-7) IN COMPLEX WITH ZWITTERIONIC MEMBRANE | 3.4.24.23 |
2MZI | NMR SOLUTION STRUCTURE OF THE PRO FORM OF HUMAN MATRILYSIN (PROMMP-7) IN COMPLEX WITH ANIONIC MEMBRANE | 3.4.24.23 |
2MZN | NMR STRUCTURE OF THE HLTF HIRAN DOMAIN IN ITS DNA-BOUND CONFORMATION | 2.3.2.27 3.6.4 |
2N16 | SOLUTION STRUCTURE OF G-QUADRUPLEX RECOGNITION DOMAIN OF RHAU | 3.6.4.12 3.6.4.13 |
2N21 | SOLUTION STRUCTURE OF COMPLEX BETWEEN DNA G-QUADRUPLEX AND G-QUADRUPLEX RECOGNITION DOMAIN OF RHAU | 3.6.4.12 3.6.4.13 |
2N42 | EC-NMR STRUCTURE OF HUMAN H-RAST35S MUTANT PROTEIN DETERMINED BY COMBINING EVOLUTIONARY COUPLINGS (EC) AND SPARSE NMR DATA | 3.6.5.2 |
2N46 | EC-NMR STRUCTURE OF HUMAN H-RAST35S MUTANT PROTEIN DETERMINED BY COMBINING EVOLUTIONARY COUPLINGS (EC) AND SPARSE NMR DATA | 3.6.5.2 |
2N5N | STRUCTURE OF AN N-TERMINAL DOMAIN OF CHD4 | 3.6.4.12 |
2N5Z | MYCOBACTERIUM TUBERCULOSIS: A DYNAMIC VIEW OF THE RESUSCITATION PROMOTING FACTOR RPFC CATALYTIC DOMAIN | 3 |
2N6J | SOLUTION STRUCTURE OF ZMP1, A ZINC-DEPENDENT METALLOPROTEASE SECRETED BY CLOSTRIDIUM DIFFICILE | 3.4.24 3.4.24.89 |
2N8R | PRODUCTIVE COMPLEX BETWEEN MMP-12 AND SYNTHETIC TRIPLE-HELICAL COLLAGEN, REVEALED THROUGH PARAMAGNETIC NMR | 3.4.24.65 |
2NA2 | DROSHA QUAD MUTANT DOUBLE-STRANDED RNA BINDING COMPETENT | 3.1.26.3 |
2NAF | SOLUTION STRUCTURE OF PEPTIDYL-TRNA HYDROLASE FROM MYCOBACTERIUM SMEGMATIS | 3.1.1.29 |
2NDK | 20 LOWEST ENERGY ENSEMBLE OF DERMCIDIN (DCD1L) NMR STRUCTURE | 3.4 |
2NGR | TRANSITION STATE COMPLEX FOR GTP HYDROLYSIS BY CDC42: COMPARISONS OF THE HIGH RESOLUTION STRUCTURES FOR CDC42 BOUND TO THE ACTIVE AND CATALYTICALLY COMPROMISED FORMS OF THE CDC42-GAP. | 3.6.5.2 |
2NLK | CRYSTAL STRUCTURE OF D1 AND D2 CATALYTIC DOMAINS OF HUMAN PROTEIN TYROSINE PHOSPHATASE GAMMA (D1+D2 PTPRG) | 3.1.3.48 |
2NLR | STREPTOMYCES LIVIDANS ENDOGLUCANASE (EC: 3.2.1.4) COMPLEX WITH MODIFIED GLUCOSE TRIMER | 3.2.1.4 |
2NM1 | STRUCTURE OF BONT/B IN COMPLEX WITH ITS PROTEIN RECEPTOR | 3.4.24.69 |
2NMM | CRYSTAL STRUCTURE OF HUMAN PHOSPHOHISTIDINE PHOSPHATASE. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET HR1409 | 3.1.3 3.9.1.3 |
2NMV | DAMAGE DETECTION BY THE UVRABC PATHWAY: CRYSTAL STRUCTURE OF UVRB BOUND TO FLUORESCEIN-ADDUCTED DNA | 3.1 |
2NMY | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT V82A WITH A INHIBITOR SAQUINAVIR | 3.4.23.16 |
2NMZ | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT V82A WITH A INHIBITOR SAQUINAVIR | 3.4.23.16 |
2NN3 | STRUCTURE OF PRO-SF-CASPASE-1 | 3.4.22.36 3.4.22 |
2NNK | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT I84V WITH A INHIBITOR SAQUINAVIR | 3.4.23.16 |
2NNP | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT I84V WITH A INHIBITOR SAQUINAVIR | 3.4.23.16 |
2NO4 | CRYSTAL STRUCTURE ANALYSIS OF A DEHALOGENASE | 3.8.1.2 |
2NO5 | CRYSTAL STRUCTURE ANALYSIS OF A DEHALOGENASE WITH INTERMEDIATE COMPLEX | 3.8.1.2 |
2NOB | STRUCTURE OF CATALYTICALLY INACTIVE H270A HUMAN 8-OXOGUANINE GLYCOSYLASE CROSSLINKED TO 8-OXOGUANINE DNA | 3.2.2 4.2.99.18 |
2NOE | STRUCTURE OF CATALYTICALLY INACTIVE G42A HUMAN 8-OXOGUANINE GLYCOSYLASE COMPLEXED TO 8-OXOGUANINE DNA | 3.2.2 4.2.99.18 |
2NOF | STRUCTURE OF Q315F HUMAN 8-OXOGUANINE GLYCOSYLASE PROXIMAL CROSSLINK TO 8-OXOGUANINE DNA | 3.2.2 4.2.99.18 |
2NOH | STRUCTURE OF CATALYTICALLY INACTIVE Q315A HUMAN 8-OXOGUANINE GLYCOSYLASE COMPLEXED TO 8-OXOGUANINE DNA | 3.2.2 4.2.99.18 |
2NOI | STRUCTURE OF G42A HUMAN 8-OXOGUANINE GLYCOSYLASE CROSSLINKED TO UNDAMAGED G-CONTAINING DNA | 3.2.2 4.2.99.18 |
2NOL | STRUCTURE OF CATALYTICALLY INACTIVE HUMAN 8-OXOGUANINE GLYCOSYLASE DISTAL CROSSLINK TO OXOG DNA | 3.2.2 4.2.99.18 |
2NOO | CRYSTAL STRUCTURE OF MUTANT NIKA | 3.6.3.24 |
2NOT | NOTECHIS II-5, NEUROTOXIC PHOSPHOLIPASE A2 FROM NOTECHIS SCUTATUS SCUTATUS | 3.1.1.4 |
2NOZ | STRUCTURE OF Q315F HUMAN 8-OXOGUANINE GLYCOSYLASE DISTAL CROSSLINK TO 8-OXOGUANINE DNA | 3.2.2 4.2.99.18 |
2NP0 | CRYSTAL STRUCTURE OF THE BOTULINUM NEUROTOXIN TYPE B COMPLEXED WITH SYNAPTOTAGAMIN-II ECTODOMAIN | 3.4.24.69 |
2NPH | CRYSTAL STRUCTURE OF HIV1 PROTEASE IN SITU PRODUCT COMPLEX | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2NQ6 | CRYSTAL STRUCTURE OF HUMAN METHIONINE AMINOPEPTIDASE TYPE 1 IN COMPLEX WITH 3-TERT-BUTOXYCARBONYLAMINOPYRIDINE-2-CARBOXYLIC ACID THIAZOLE-2-YLAMIDE | 3.4.11.18 |
2NQ7 | CRYSTAL STRUCTURE OF TYPE 1 HUMAN METHIONINE AMINOPEPTIDASE IN COMPLEX WITH 3-(2,2-DIMETHYLPROPIONYLAMINO)PYRIDINE-2-CARBOXYLIC ACID THIAZOLE-2-YLAMIDE | 3.4.11.18 |
2NQ9 | HIGH RESOLUTION CRYSTAL STRUCTURE OF ESCHERICHIA COLI ENDONUCLEASE IV (ENDO IV) Y72A MUTANT BOUND TO DAMAGED DNA | 3.1.21.2 |
2NQA | CATALYTIC DOMAIN OF HUMAN CALPAIN 8 | 3.4.22.53 |
2NQG | CALPAIN 1 PROTEOLYTIC CORE INACTIVATED BY WR18(S,S), AN EPOXYSUCCINYL-TYPE INHIBITOR. | 3.4.22.52 |
2NQH | HIGH RESOLUTION CRYSTAL STRUCTURE OF ESCHERICHIA COLI ENDONUCLEASE IV (ENDO IV) E261Q MUTANT | 3.1.21.2 |
2NQI | CALPAIN 1 PROTEOLYTIC CORE INACTIVATED BY WR13(R,R), AN EPOXYSUCCINYL-TYPE INHIBITOR. | 3.4.22.52 |
2NQJ | CRYSTAL STRUCTURE OF ESCHERICHIA COLI ENDONUCLEASE IV (ENDO IV) E261Q MUTANT BOUND TO DAMAGED DNA | 3.1.21.2 |
2NQY | CRYSTAL STRUCTURE OF ALKALINE THERMOPHLIC XYLANASE FROM BACILLUS SP. (NCL 86-6-10) WITH COMPLEX XYLOTRIOSE: XYLOTRIOSE CLEAVED TO XYLOBIOSE AND XYLOSE | 3.2.1.8 |
2NR9 | CRYSTAL STRUCTURE OF GLPG, RHOMBOID PEPTIDASE FROM HAEMOPHILUS INFLUENZAE | 3.4.21.105 |
2NRF | CRYSTAL STRUCTURE OF GLPG, A RHOMBOID FAMILY INTRAMEMBRANE PROTEASE | 3.4.21.105 |
2NS6 | CRYSTAL STRUCTURE OF THE MINIMAL RELAXASE DOMAIN OF MOBA FROM PLASMID R1162 | 3.6.1 |
2NSM | CRYSTAL STRUCTURE OF THE HUMAN CARBOXYPEPTIDASE N (KININASE I) CATALYTIC DOMAIN | 3.4.17.3 |
2NSP | CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE D178A MUTANT IN COMPLEX WITH HEXASACCHARIDE I | 3.1.1.11 |
2NST | CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE D178A MUTANT IN COMPLEX WITH HEXASACCHARIDE II | 3.1.1.11 |
2NSX | STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH PHARMACOLOGICAL CHAPERONE PROVIDES INSIGHT INTO GAUCHER DISEASE | 3.2.1.45 2.4.1 3.2.1 |
2NT0 | ACID-BETA-GLUCOSIDASE LOW PH, GLYCEROL BOUND | 3.2.1.45 2.4.1 3.2.1 |
2NT1 | STRUCTURE OF ACID-BETA-GLUCOSIDASE AT NEUTRAL PH | 3.2.1.45 2.4.1 3.2.1 |
2NT2 | CRYSTAL STRUCTURE OF SLINGSHOT PHOSPHATASE 2 | 3.1.3.48 3.1.3.16 |
2NT6 | CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE D178A MUTANT IN COMPLEX WITH HEXASACCHARIDE III | 3.1.1.11 |
2NT7 | CRYSTAL STRUCTURE OF PTP1B-INHIBITOR COMPLEX | 3.1.3.48 |
2NT9 | CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE D178A MUTANT IN COMPLEX WITH HEXASACCHARIDE IV | 3.1.1.11 |
2NTA | CRYSTAL STRUCTURE OF PTP1B-INHIBITOR COMPLEX | 3.1.3.48 |
2NTB | CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE IN COMPLEX WITH HEXASACCHARIDE V | 3.1.1.11 |
2NTG | STRUCTURE OF SPIN-LABELED T4 LYSOZYME MUTANT T115R7 | 3.2.1.17 |
2NTH | STRUCTURE OF SPIN-LABELED T4 LYSOZYME MUTANT L118R1 | 3.2.1.17 |
2NTK | CRYSTAL STRUCTURE OF PURO/IMP FROM METHANOTHERMOBACTER THERMOAUTOTROPHICUS | 3.5.4.10 |
2NTL | CRYSTAL STRUCTURE OF PURO/AICAR FROM METHANOTHERMOBACTER THERMOAUTOTROPHICUS | 3.5.4.10 |
2NTM | CRYSTAL STRUCTURE OF PURO FROM METHANOTHERMOBACTER THERMOAUTOTROPHICUS | 3.5.4.10 |
2NTP | CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE IN COMPLEX WITH HEXASACCHARIDE VI | 3.1.1.11 |
2NTQ | CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE IN COMPLEX WITH HEXASACCHARIDE VII | 3.1.1.11 |
2NTR | CRYSTAL STRUCTURE OF HUMAN BACE-1 BOUND TO INHIBITOR | 3.4.23.46 |
2NU0 | MOLECULAR STRUCTURES OF THE COMPLEXES OF SGPB WITH OMTKY3 AROMATIC P1 VARIANTS TRP18I, HIS18I, PHE18I, AND TYR18I | 3.4.21.81 |
2NU1 | MOLECULAR STRUCTURES OF THE COMPLEXES OF SGPB WITH OMTKY3 AROMATIC P1 VARIANTS TRP18I, HIS18I, PHE18I AND TYR18I | 3.4.21.81 |
2NU2 | ACCOMMODATION OF POSITIVELY-CHARGED RESIDUES IN A HYDROPHOBIC SPECIFICITY POCKET: CRYSTAL STRUCTURES OF SGPB IN COMPLEX WITH OMTKY3 VARIANTS LYS18I AND ARG18I | 3.4.21.81 |
2NU3 | ACCOMMODATION OF POSITIVELY-CHARGED RESIDUES IN A HYDROPHOBIC SPECIFICITY POCKET: CRYSTAL STRUCTURES OF SGPB IN COMPLEX WITH OMTKY3 VARIANTS LYS18I AND ARG18I | 3.4.21.81 |
2NU4 | ACCOMMODATION OF POSITIVELY-CHARGED RESIDUES IN A HYDROPHOBIC SPECIFICITY POCKET: CRYSTAL STRUCTURES OF SGPB IN COMPLEX WITH OMTKY3 VARIANTS LYS18I AND ARG18I | 3.4.21.81 |
2NUC | STAPHLOCOCCAL NUCLEASE, ETHANE THIOL DISULFIDE TO V23C VARIANT | 3.1.31.1 |
2NUE | CRYSTAL STRUCTURE OF RNASE III FROM AQUIFEX AEOLICUS COMPLEXED WITH DS-RNA AT 2.9-ANGSTROM RESOLUTION | 3.1.26.3 |
2NUF | CRYSTAL STRUCTURE OF RNASE III FROM AQUIFEX AEOLICUS COMPLEXED WITH DS-RNA AT 2.5-ANGSTROM RESOLUTION | 3.1.26.3 |
2NUG | CRYSTAL STRUCTURE OF RNASE III FROM AQUIFEX AEOLICUS COMPLEXED WITH DS-RNA AT 1.7-ANGSTROM RESOLUTION | 3.1.26.3 |
2NUI | X-RAY STRUCTURE OF SYNTHETIC [D83A]RNASE A | 3.1.27.5 |
2NUV | CRYSTAL STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH ATENOLOL AT 2.25 A RESOLUTION | 3.4.21 |
2NV0 | STRUCTURE OF THE GLUTAMINASE SUBUNIT PDX2 (YAAE) OF PLP SYNTHASE FROM BACILLUS SUBTILIS | 2.6 4.3.3.6 3.5.1.2 |
2NV5 | CRYSTAL STRUCTURE OF A C-TERMINAL PHOSPHATASE DOMAIN OF RATTUS NORVEGICUS ORTHOLOG OF HUMAN PROTEIN TYROSINE PHOSPHATASE, RECEPTOR TYPE, D (PTPRD) | 3.1.3.48 |
2NVJ | NMR STRUCTURES OF TRANSMEMBRANE SEGMENT FROM SUBUNIT A FROM THE YEAST PROTON V-ATPASE | 3.6.3.14 |
2NW0 | CRYSTAL STRUCTURE OF A LYSIN | 3.2.1.17 |
2NW6 | BURKHOLDERIA CEPACIA LIPASE COMPLEXED WITH S-INHIBITOR | 3.1.1.3 |
2NWD | STRUCTURE OF CHEMICALLY SYNTHESIZED HUMAN LYSOZYME AT 1 ANGSTROM RESOLUTION | 3.2.1.17 |
2NWJ | STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH DISACCHARIDE AT 1.75 A RESOLUTION | 3.4.21 |
2NWN | NEW PHARMACOPHORE FOR SERINE PROTEASE INHIBITION REVEALED BY CRYSTAL STRUCTURE OF HUMAN UROKINASE-TYPE PLASMINOGEN ACTIVATOR COMPLEXED WITH A CYCLIC PEPTIDYL INHIBITOR, UPAIN-1 | 3.4.21.73 |
2NX8 | THE CRYSTAL STRUCTURE OF THE TRNA-SPECIFIC ADENOSINE DEAMINASE FROM STREPTOCOCCUS PYOGENES | 3.5.4 3.5.4.33 |
2NXA | STRUCTURE OF ZN-DEPENDENT METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS R121H, C221D DOUBLE MUTANT | 3.5.2.6 |
2NXD | STRUCTURE OF HIV-1 PROTEASE D25N COMPLEXED WITH RT-RH ANALOGUE PEPTIDE GLY-ALA-ASP-ILE-PHE*TYR-LEU-ASP-GLY-ALA | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2NXF | CRYSTAL STRUCTURE OF A DIMETAL PHOSPHATASE FROM DANIO RERIO LOC 393393 | 3.6.1.13 3.6.1.16 3.6.1.53 |
2NXL | STRUCTURE OF HIV-1 PROTEASE D25N COMPLEXED WITH THE RT-RH ANALOGUE PEPTIDE GLY-ALA-GLU-VAL-PHE*TYR-VAL-ASP-GLY-ALA | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2NXM | STRUCTURE OF HIV-1 PROTEASE D25N COMPLEXED WITH THE RT-RH ANALOGUE PEPTIDE GLY-ALA-GLN-THR-PHE*TYR-VAL-ASP-GLY-ALA | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2NYP | STRUCTURE OF BETA-LACTAMASE II FROM BACILLUS CEREUS. R121H, C221D DOBLE MUTANT WITH TWO ZINC IONS. | 3.5.2.6 |
2NYQ | STRUCTURE OF VIBRIO PROTEOLYTICUS AMINOPEPTIDASE WITH A BOUND TRP FRAGMENT OF DLWCF | 3.4.11.10 |
2NYR | CRYSTAL STRUCTURE OF HUMAN SIRTUIN HOMOLOG 5 IN COMPLEX WITH SURAMIN | 3.5.1 2.3.1 |
2NYT | THE APOBEC2 CRYSTAL STRUCTURE AND FUNCTIONAL IMPLICATIONS FOR AID | 3.5.4 3.5.4.36 |
2NYV | X-RAY CRYSTAL STRUCTURE OF A PHOSPHOGLYCOLATE PHOSPHATASE FROM AQUIFEX AEOLICUS | 3.1.3.18 |
2NYY | CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE A COMPLEXED WITH MONOCLONAL ANTIBODY CR1 | 3.4.24.69 |
2NZ6 | CRYSTAL STRUCTURE OF THE PTPRJ INACTIVATING MUTANT C1239S | 3.1.3.48 |
2NZ8 | N-TERMINAL DHPH CASSETTE OF TRIO IN COMPLEX WITH NUCLEOTIDE-FREE RAC1 | 3.6.5.2 |
2NZ9 | CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE A COMPLEXED WITH MONOCLONAL ANTIBODY AR2 | 3.4.24.69 |
2NZE | STRUCTURE OF BETA-LACTAMASE II FROM BACILLUS CEREUS. R121H, C221S DOUBLE MUTANT. SPACE GROUP P3121. | 3.5.2.6 |
2NZF | STRUCTURE OF BETA-LACTAMASE II FROM BACILLUS CEREUS. R121H, C221S DOUBLE MUTANT. SPACE GROUP C2. | 3.5.2.6 |
2O0H | T4 GP17 ATPASE DOMAIN MUTANT COMPLEXED WITH ATP | 3.6.4 3.1.21 |
2O0J | T4 GP17 ATPASE DOMAIN MUTANT COMPLEXED WITH ADP | 3.6.4 3.1.21 |
2O0K | T4 GP17 ATPASE DOMAIN MUTANT | 3.6.4 3.1.21 |
2O14 | X-RAY CRYSTAL STRUCTURE OF PROTEIN YXIM_BACSU FROM BACILLUS SUBTILIS. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SR595 | 3.1 |
2O1C | STRUCTURE OF THE E. COLI DIHYDRONEOPTERIN TRIPHOSPHATE PYROPHOSPHOHYDROLASE | 3.6.1 3.6.1.67 |
2O1L | STRUCTURE OF A COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH DISACCHARIDE AT 1.97 A RESOLUTION | 3.4.21 |
2O1N | CRYSTAL STRUCTURE OF A COMPLEX OF PHOSPHOLIPASE A2 WITH A PEPTIDE ALA-ILE-ALA-SER AT 2.8 A RESOLUTION | 3.1.1.4 |
2O2H | CRYSTAL STRUCTURE OF HALOALKANE DEHALOGENASE RV2579 FROM MYCOBACTERIUM TUBERCULOSIS COMPLEXED WITH 1,2-DICHLOROETHANE | 3.8.1.5 |
2O2I | CRYSTAL STRUCTURE OF HALOALKANE DEHALOGENASE RV2579 FROM MYCOBACTERIUM TUBERCULOSIS COMPLEXED WITH 1,3-PROPANDIOL | 3.8.1.5 |
2O2X | CRYSTAL STRUCTURE OF A PUTATIVE HAD-LIKE PHOSPHATASE (MLL2559) FROM MESORHIZOBIUM LOTI AT 1.50 A RESOLUTION | 3.1.3.82 |
2O36 | CRYSTAL STRUCTURE OF ENGINEERED THIMET OLIGOPEPTIDASE WITH NEUROLYSIN SPECIFICITY IN NEUROTENSIN CLEAVAGE SITE | 3.4.24.15 |
2O3B | CRYSTAL STRUCTURE COMPLEX OF NUCLEASE A (NUCA) WITH INTRA-CELLULAR INHIBITOR NUIA | 3.1.30 |
2O3C | CRYSTAL STRUCTURE OF ZEBRAFISH APE | 3.1 |
2O3E | CRYSTAL STRUCTURE OF ENGINEERED NEUROLYSIN WITH THIMET OLIGOPEPTIDASE SPECIFICITY FOR NEUROTENSIN CLEAVAGE SITE. | 3.4.24.16 |
2O3H | CRYSTAL STRUCTURE OF THE HUMAN C65A APE | 4.2.99.18 3.1 |
2O3K | YEAST CYTOSINE DEAMINASE D92E TRIPLE MUTANT BOUND TO TRANSITION STATE ANALOGUE HPY | 3.5.4.1 |
2O3Q | STRUCTURAL BASIS FOR FORMATION AND HYDROLYSIS OF CALCIUM MESSENGER CYCLIC ADP-RIBOSE BY HUMAN CD38 | 3.2.2.5 3.2.2.6 2.4.99.20 |
2O3R | STRUCTURAL BASIS FOR FORMATION AND HYDROLYSIS OF CALCIUM MESSENGER CYCLIC ADP-RIBOSE BY HUMAN CD38 | 3.2.2.5 3.2.2.6 2.4.99.20 |
2O3S | STRUCTURAL BASIS FOR FORMATION AND HYDROLYSIS OF CALCIUM MESSENGER CYCLIC ADP-RIBOSE BY HUMAN CD38 | 3.2.2.5 3.2.2.6 2.4.99.20 |
2O3T | STRUCTURAL BASIS FOR FORMATION AND HYDROLYSIS OF CALCIUM MESSENGER CYCLIC ADP-RIBOSE BY HUMAN CD38 | 3.2.2.5 3.2.2.6 2.4.99.20 |
2O3U | STRUCTURAL BASIS FOR FORMATION AND HYDROLYSIS OF CALCIUM MESSENGER CYCLIC ADP-RIBOSE BY HUMAN CD38 | 3.2.2.5 3.2.2.6 2.4.99.20 |
2O3Z | X-RAY CRYSTAL STRUCTURE OF LPXC COMPLEXED WITH 3-HEPTYLOXYBENZOATE | 3.5.1 3.5.1.108 |
2O40 | CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED 203 AMINO ACID 'COVALENT DIMER' HIV-1 PROTEASE MOLECULE | 3.4.23.16 |
2O4E | THE SOLUTION STRUCTURE OF A PROTEIN-PROTEIN INTERACTION MODULE FROM A FAMILY 84 GLYCOSIDE HYDROLASE OF CLOSTRIDIUM PERFRINGENS | 3.2.1.52 3.2.1.169 |
2O4G | STRUCTURE OF TREX1 IN COMPLEX WITH A NUCLEOTIDE | 3.1.11.2 |
2O4H | HUMAN BRAIN ASPARTOACYLASE COMPLEX WITH INTERMEDIATE ANALOG (N-PHOSPHONOMETHYL-L-ASPARTATE) | 3.5.1.15 |
2O4I | STRUCTURE OF TREX1 IN COMPLEX WITH DNA | 3.1.11.2 |
2O4K | CRYSTAL STRUCTURE OF HIV-1 PROTEASE (Q7K) IN COMPLEX WITH ATAZANAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2O4L | CRYSTAL STRUCTURE OF HIV-1 PROTEASE (Q7K, I50V) IN COMPLEX WITH TIPRANAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2O4M | STRUCTURE OF PHOSPHOTRIESTERASE MUTANT I106G/F132G/H257Y | 3.1.8.1 |
2O4N | CRYSTAL STRUCTURE OF HIV-1 PROTEASE (TRM MUTANT) IN COMPLEX WITH TIPRANAVIR | 2.7.7.49 3.1.26.13 3.4.23.16 2.7.7.7 3.1.13.2 2.7.7 3.1 |
2O4Q | STRUCTURE OF PHOSPHOTRIESTERASE MUTANT G60A | 3.1.8.1 |
2O4S | CRYSTAL STRUCTURE OF HIV-1 PROTEASE (Q7K) IN COMPLEX WITH LOPINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2O4W | T4 LYSOZYME CIRCULAR PERMUTANT | 3.2.1.17 |
2O4X | CRYSTAL STRUCTURE OF HUMAN P100 TUDOR DOMAIN | 3.1.31.1 |
2O51 | CRYSTAL STRUCTURE OF BOVINE C-LOBE WITH FRUCTOSE AT 3.0 A RESOLUTION | 3.4.21 |
2O53 | CRYSTAL STRUCTURE OF APO-ASPARTOACYLASE FROM HUMAN BRAIN | 3.5.1.15 |
2O5D | THIAZOLONE-ACYLSULFONAMIDES AS NOVEL HCV NS5B POLYMERASE ALLOSTERIC INHIBITORS: CONVERGENCE OF STRUCTURE-BASED DRUG DESIGN AND X-RAY CRYSTALLOGRAPHIC STUDY | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2O5F | CRYSTAL STRUCTURE OF DR0079 FROM DEINOCOCCUS RADIODURANS AT 1.9 ANGSTROM RESOLUTION | 3.6 3.6.1 |
2O5W | STRUCTURE OF THE E. COLI DIHYDRONEOPTERIN TRIPHOSPHATE PYROPHOSPHOHYDROLASE IN COMPLEX WITH SM+3 AND PYROPHOSPHATE | 3.6.1 3.6.1.67 |
2O6M | H98Q MUTANT OF THE HOMING ENDONUCLEASE I-PPOI COMPLEXED WITH DNA | 3.1 |
2O6X | CRYSTAL STRUCTURE OF PROCATHEPSIN L1 FROM FASCIOLA HEPATICA | 3.4.22.15 3.4.22 |
2O79 | T4 LYSOZYME WITH C-TERMINAL EXTENSION | 3.2.1.17 |
2O7A | T4 LYSOZYME C-TERMINAL FRAGMENT | 3.2.1.17 |
2O7L | THE OPEN-CAP CONFORMATION OF GLPG | 3.4.21.105 |
2O7M | THE C-TERMINAL LOOP OF THE HOMING ENDONUCLEASE I-CREI IS ESSENTIAL FOR DNA BINDING AND CLEAVAGE. IDENTIFICATION OF A NOVEL SITE FOR SPECIFICITY ENGINEERING IN THE I-CREI SCAFFOLD | 3.1 |
2O7R | PLANT CARBOXYLESTERASE AECXE1 FROM ACTINIDIA ERIANTHA WITH ACYL ADDUCT | 3.1.1.1 |
2O7V | CARBOXYLESTERASE AECXE1 FROM ACTINIDIA ERIANTHA COVALENTLY INHIBITED BY PARAOXON | 3.1.1.1 |
2O8A | RAT PP1CGAMMA COMPLEXED WITH MOUSE INHIBITOR-2 | 3.1.3.16 |
2O8G | RAT PP1C GAMMA COMPLEXED WITH MOUSE INHIBITOR-2 | 3.1.3.16 |
2O8H | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF RAT PHOSPHODIESTERASE 10A | 3.1.4.17 3.1.4.35 |
2O8L | STRUCTURE OF V8 PROTEASE FROM STAPHYLOCOCCUS AUREUS | 3.4.21.19 |
2O8M | CRYSTAL STRUCTURE OF THE S139A MUTANT OF HEPATITIS C VIRUS NS3/4A PROTEASE | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2O8O | CRYSTAL STRUCTURE OF CLOSTRIDIUM HISTOLYTICUM COLG COLLAGENASE COLLAGEN-BINDING DOMAIN 3B AT 1.35 ANGSTROM RESOLUTION IN PRESENCE OF CALCIUM | 3.4.24.3 |
2O8T | CRYSTAL STRUCTURE AND BINDING EPITOPES OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR (C122A/N145Q) IN COMPLEX WITH INHIBITORS | 3.4.21.73 |
2O8U | CRYSTAL STRUCTURE AND BINDING EPITOPES OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR (C122A/N145Q/S195A) IN COMPLEX WITH INHIBITORS | 3.4.21.73 |
2O8W | CRYSTAL STRUCTURE AND BINDING EPITOPES OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR (C122A/N145Q/S195A) IN COMPLEX WITH INHIBITORS | 3.4.21.73 |
2O94 | THE 97H/F MUTANT STRUCTURE OF A GLUTAMINE-RICH DOMAIN FROM HISTONE DEACETYLASE 4 | 3.5.1.98 |
2O9J | CRYSTAL STRUCTURE OF CALCIUM ATPASE WITH BOUND MAGNESIUM FLUORIDE AND CYCLOPIAZONIC ACID | 3.6.3.8 7.2.2.10 |
2O9P | BETA-GLUCOSIDASE B FROM PAENIBACILLUS POLYMYXA | 3.2.1.21 |
2O9Q | THE CRYSTAL STRUCTURE OF BOVINE TRYPSIN COMPLEXED WITH A SMALL INHIBITION PEPTIDE ORB2K | 3.4.21.4 |
2O9R | BETA-GLUCOSIDASE B COMPLEXED WITH THIOCELLOBIOSE | 3.2.1.21 |
2O9T | BETA-GLUCOSIDASE B FROM BACILLUS POLYMYXA COMPLEXED WITH GLUCOSE | 3.2.1.21 |
2OA0 | CRYSTAL STRUCTURE OF CALCIUM ATPASE WITH BOUND ADP AND CYCLOPIAZONIC ACID | 3.6.3.8 7.2.2.10 |
2OA8 | CRYSTAL STRUCTURE OF MTREX1 WITH SSDNA | 3.1.11.2 |
2OAG | CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (DPPIV) WITH PYRROLIDINE-CONSTRAINED PHENETHYLAMINE 29G | 3.4.14.5 |
2OAH | CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH INHIBITOR | 3.4.23.46 |
2OAZ | HUMAN METHIONINE AMINOPEPTIDASE-2 COMPLEXED WITH SB-587094 | 3.4.11.18 |
2OB3 | STRUCTURE OF PHOSPHOTRIESTERASE MUTANT H257Y/L303T | 3.1.8.1 |
2OBC | THE CRYSTAL STRUCTURE OF RIBD FROM ESCHERICHIA COLI IN COMPLEX WITH A SUBSTRATE ANALOGUE, RIBOSE 5-PHOSPHATE (BETA FORM), BOUND TO THE ACTIVE SITE OF THE REDUCTASE DOMAIN | 3.5.4.26 1.1.1.193 |
2OBQ | DISCOVERY OF THE HCV NS3/4A PROTEASE INHIBITOR SCH503034. KEY STEPS IN STRUCTURE-BASED OPTIMIZATION | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2OC0 | STRUCTURE OF NS3 COMPLEXED WITH A KETOAMIDE INHIBITOR SCH491762 | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2OC1 | STRUCTURE OF THE HCV NS3/4A PROTEASE INHIBITOR CVS4819 | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2OC2 | STRUCTURE OF TESTIS ACE WITH RXPA380 | 3.4.15.1 3.2.1 |
2OC3 | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN PROTEIN TYROSINE PHOSPHATASE NON-RECEPTOR TYPE 18 | 3.1.3.48 |
2OC7 | STRUCTURE OF HEPATITIS C VIRAL NS3 PROTEASE DOMAIN COMPLEXED WITH NS4A PEPTIDE AND KETOAMIDE SCH571696 | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2OC8 | STRUCTURE OF HEPATITIS C VIRAL NS3 PROTEASE DOMAIN COMPLEXED WITH NS4A PEPTIDE AND KETOAMIDE SCH503034 | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2OCA | THE CRYSTAL STRUCTURE OF T4 UVSW | 3.6.1.8 3.6.4.12 |
2OCD | CRYSTAL STRUCTURE OF L-ASPARAGINASE I FROM VIBRIO CHOLERAE O1 BIOVAR ELTOR STR. N16961 | 3.5.1.1 |
2OCI | CRYSTAL STRUCTURE OF VALACYCLOVIR HYDROLASE COMPLEXED WITH A PRODUCT ANALOGUE | 3.1 |
2OCK | CRYSTAL STRUCTURE OF VALACYCLOVIR HYDROLASE D123N MUTANT | 3.1 |
2OCL | CRYSTAL STRUCTURE OF VALACYCLOVIR HYDROLASE S122A MUTANT | 3.1 |
2OCU | STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH N-(4-HYDROXYPHENYL) ACETAMIDE AT 2.38 A RESOLUTION | 3.4.21 |
2OCV | STRUCTURAL BASIS OF NA+ ACTIVATION MIMICRY IN MURINE THROMBIN | 3.4.21.5 |
2OD2 | CRYSTAL STRUCTURE OF YHST2 I117F MUTANT BOUND TO CARBA-NAD+ AND AN ACETYLATED H4 PEPTIDE | 3.5.1 2.3.1.286 |
2OD3 | HUMAN THROMBIN CHIMERA WITH HUMAN RESIDUES 184A, 186, 186A, 186B, 186C AND 222 REPLACED BY MURINE THROMBIN EQUIVALENTS. | 3.4.21.5 |
2OD7 | CRYSTAL STRUCTURE OF YHST2 BOUND TO THE INTERMEDIATE ANALOGUE ADP-HPD, AND AND ACEYLATED H4 PEPTIDE | 3.5.1 2.3.1.286 |
2OD9 | STRUCTURAL BASIS FOR NICOTINAMIDE INHIBITION AND BASE EXCHANGE IN SIR2 ENZYMES | 3.5.1 2.3.1.286 |
2ODB | THE CRYSTAL STRUCTURE OF HUMAN CDC42 IN COMPLEX WITH THE CRIB DOMAIN OF HUMAN P21-ACTIVATED KINASE 6 (PAK6) | 3.6.5.2 |
2ODJ | CRYSTAL STRUCTURE OF THE OUTER MEMBRANE PROTEIN OPRD FROM PSEUDOMONAS AERUGINOSA | 3.4.21 |
2ODN | MSRECA-DATP COMPLEX | 3.4.99.37 |
2ODP | COMPLEMENT COMPONENT C2A, THE CATALYTIC FRAGMENT OF C3- AND C5-CONVERTASE OF HUMAN COMPLEMENT | 3.4.21.43 |
2ODQ | COMPLEMENT COMPONENT C2A, THE CATALYTIC FRAGMENT OF C3- AND C5-CONVERTASE OF HUMAN COMPLEMENT | 3.4.21.43 |
2ODW | MSRECA-ATP-GAMA-S COMPLEX | 3.4.99.37 |
2ODY | THROMBIN-BOUND BOOPHILIN DISPLAYS A FUNCTIONAL AND ACCESSIBLE REACTIVE-SITE LOOP | 3.4.21.5 |
2OE2 | MSRECA-NATIVE-LOW HUMIDITY 95% | 3.4.99.37 |
2OE4 | HIGH PRESSURE PSUEDO WILD TYPE T4 LYSOZYME | 3.2.1.17 |
2OE7 | HIGH-PRESSURE T4 LYSOZYME | 3.2.1.17 |
2OE9 | HIGH-PRESSURE STRUCTURE OF PSEUDO-WT T4 LYSOZYME | 3.2.1.17 |
2OEA | HIGH-PRESSURE STRUCTURE OF PSEUDO-WT T4 LYSOZYME | 3.2.1.17 |
2OEO | CRYOGENIC CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT TRUNCATED DELTA+PHS I92D | 3.1.31.1 |
2OEP | MSRECA-ADP-COMPLEX | 3.4.99.37 |
2OES | MSRECA-NATIVE-SSB | 3.4.99.37 |
2OF0 | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 5 | 3.4.23.46 |
2OF1 | CRYOGENIC CRYSTAL STRUCTURE OF THE STAPHYLOCOCCAL NUCLEASE VARIANT TRUNCATED DELTA+PHS I92W | 3.1.31.1 |
2OFG | SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF THE ZINC(II) ATPASE ZIAA IN ITS APO FORM | 3.6.3.5 7.2.2.12 |
2OFH | SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF THE ZINC(II) ATPASE ZIAA IN ITS APO FORM | 3.6.3.5 7.2.2.12 |
2OFI | CRYSTAL STRUCTURE OF 3-METHYLADENINE DNA GLYCOSYLASE I (TAG) BOUND TO DNA/3MA | 3.2.2.20 |
2OFK | CRYSTAL STRUCTURE OF 3-METHYLADENINE DNA GLYCOSYLASE I (TAG) | 3.2.2.20 |
2OFO | MSRECA-NATIVE | 3.4.99.37 |
2OG1 | CRYSTAL STRUCTURE OF BPHD, A C-C HYDROLASE FROM BURKHOLDERIA XENOVORANS LB400 | 3.7.1.8 |
2OGJ | CRYSTAL STRUCTURE OF A DIHYDROOROTASE | 3.1.1 |
2OGS | CRYSTAL STRUCTURE OF THE GEOBACILLUS STEAROTHERMOPHILUS CARBOXYLESTERASE EST55 AT PH 6.2 | 3.1.1.1 3.1.1 |
2OGT | CRYSTAL STRUCTURE OF THE GEOBACILLUS STEAROTHERMOPHILUS CARBOXYLESTERASE EST55 AT PH 6.8 | 3.1.1.1 3.1.1 |
2OGZ | CRYSTAL STRUCTURE OF DPP-IV COMPLEXED WITH LILLY ARYL KETONE INHIBITOR | 3.4.14.5 |
2OHE | STRUCTURAL AND MUTATIONAL ANALYSIS OF TRNA-INTRON SPLICING ENDONUCLEASE FROM THERMOPLASMA ACIDOPHILUM DSM 1728 | 3.1.27.9 4.6.1.16 |
2OHK | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH 1-AMINO-ISOQUINOLINE | 3.4.23.46 |
2OHL | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH 2-AMINOQUINOLINE | 3.4.23.46 |
2OHM | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH N~3~-BENZYLPYRIDINE-2,3-DIAMINE | 3.4.23.46 |
2OHN | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH 4-(4-FLUOROBENZYL)PIPERIDINE | 3.4.23.46 |
2OHP | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 3 | 3.4.23.46 |
2OHQ | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 4 | 3.4.23.46 |
2OHR | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 6A | 3.4.23.46 |
2OHS | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 6B | 3.4.23.46 |
2OHT | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 7 | 3.4.23.46 |
2OHU | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 8B | 3.4.23.46 |
2OI0 | CRYSTAL STRUCTURE ANALYSIS 0F THE TNF-A COVERTING ENZYME (TACE) IN COMPLEXED WITH ARYL-SULFONAMIDE | 3.4.24.86 |
2OIE | CRYSTAL STRUCTURE OF RS21-C6 CORE SEGMENT RSCUT | 3.6.1.12 |
2OIG | CRYSTAL STRUCTURE OF RS21-C6 CORE SEGMENT AND DM5CTP COMPLEX | 3.6.1.12 |
2OIN | CRYSTAL STRUCTURE OF HCV NS3-4A R155K MUNTANT | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2OIW | THE STRUCTURE OF A PREDICTED THIOESTERASE FROM BACILLUS STEAROTHERMOPHILUS | 3.1.2 |
2OK5 | HUMAN COMPLEMENT FACTOR B | 3.4.21.47 |
2OK9 | PRTX-I-BPB | 3.1.1.4 |
2OKB | HIGH RESOLUTION CRYSTAL STRUCTURES OF VACCINIA VIRUS DUTPASE | 3.6.1.23 |
2OKD | HIGH RESOLUTION CRYSTAL STRUCTURES OF VACCINIA VIRUS DUTPASE | 3.6.1.23 |
2OKE | HIGH RESOLUTION CRYSTAL STRUCTURES OF VACCINIA VIRUS DUTPASE | 3.6.1.23 |
2OKN | CRYSTAL STRCTURE OF HUMAN PROLIDASE | 3.4.13.9 |
2OKV | C-MYC DNA UNWINDING ELEMENT BINDING PROTEIN | 3.1 3.1.1.96 |
2OKX | CRYSTAL STRUCTURE OF GH78 FAMILY RHAMNOSIDASE OF BACILLUS SP. GL1 AT 1.9 A | 3.2.1.40 |
2OL0 | HIGH RESOLUTION CRYSTAL STRUCTURES OF VACCINIA VIRUS DUTPASE | 3.6.1.23 |
2OL1 | HIGH RESOLUTION CRYSTAL STRUCTURES OF VACCINIA VIRUS DUTPASE | 3.6.1.23 |
2OLE | CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (DPPIV) COMPLEX WITH CYCLIC HYDRAZINE DERIVATIVES | 3.4.14.5 |
2OLG | CRYSTAL STRUCTURE OF THE SERINE PROTEASE DOMAIN OF PROPHENOLOXIDASE ACTIVATING FACTOR-I IN A ZYMOGEN FORM | 3.4.21 |
2OLI | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN A GROUP II PHOSPHOLIPASE A2 AND AN INDOLE DERIVATIVE AT 2.2 A RESOLUTION | 3.1.1.4 |
2OLJ | ABC PROTEIN ARTP IN COMPLEX WITH ADP/MG2+ | 3.6.3.21 |
2OLK | ABC PROTEIN ARTP IN COMPLEX WITH ADP-BETA-S | 3.6.3.21 |
2OLU | STRUCTURAL INSIGHT INTO THE TRANSGLYCOSYLATION STEP OF BACTERIAL CELL WALL BIOSYNTHESIS : APOENZYME | 2.3.2 2.4.1.129 3.4.16.4 |
2OLV | STRUCTURAL INSIGHT INTO THE TRANSGLYCOSYLATION STEP OF BACTERIAL CELL WALL BIOSYNTHESIS : DONOR LIGAND COMPLEX | 2.3.2 2.4.1.129 3.4.16.4 |
2OM6 | HYPOTHETICAL PROTEIN (PROBABLE PHOSPHOSERINE PHOSPH (PH0253) FROM PYROCOCCUS HORIKOSHII OT3 | 3.1.3.3 |
2ONJ | STRUCTURE OF THE MULTIDRUG ABC TRANSPORTER SAV1866 FROM S. AUREUS IN COMPLEX WITH AMP-PNP | 3.6.3 7.6.2 |
2OOD | CRYSTAL STRUCTURE OF GUANINE DEAMINASE FROM BRADYRHIZOBIUM JAPONICUM | 3.5.4.3 |
2OOF | THE CRYSTAL STRUCTURE OF 4-IMIDAZOLONE-5-PROPANOATE AMIDOHYDROLASE FROM ENVIRONMENTAL SAMPLE | 3.5.2.7 |
2OOG | CRYSTAL STRUCTURE OF GLYCEROPHOSPHORYL DIESTER PHOSPHODIESTERASE FROM STAPHYLOCOCCUS AUREUS | 3.1.4.46 |
2OOQ | CRYSTAL STRUCTURE OF THE HUMAN RECEPTOR PHOSPHATASE PTPRT | 3.1.3.48 |
2OOT | A HIGH RESOLUTION STRUCTURE OF LIGAND-FREE HUMAN GLUTAMATE CARBOXYPEPTIDASE II | 3.4.17.21 |
2OP2 | CRYSTAL STRUCTURE OF RNASE DOUBLE-MUTANT V43C R85C WITH EXTRA DISULPHIDE BOND | 3.1.27.5 4.6.1.18 |
2OP3 | THE STRUCTURE OF CATHEPSIN S WITH A NOVEL 2-ARYLPHENOXYACETALDEHYDE INHIBITOR DERIVED BY THE SUBSTRATE ACTIVITY SCREENING (SAS) METHOD | 3.4.22.27 |
2OP6 | PEPTIDE-BINDING DOMAIN OF HEAT SHOCK 70 KDA PROTEIN D PRECURSOR FROM C.ELEGANS | 3.6.4.10 |
2OP9 | SUBSTRATE SPECIFICITY PROFILING AND IDENTIFICATION OF A NEW CLASS OF INHIBITOR FOR THE MAJOR PROTEASE OF THE SARS CORONAVIRUS | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2OPF | CRYSTAL STRUCTURE OF THE DNA REPAIR ENZYME ENDONUCLEASE-VIII (NEI) FROM E. COLI (R252A) IN COMPLEX WITH AP-SITE CONTAINING DNA SUBSTRATE | 3.2.2 4.2.99.18 |
2OPH | HUMAN DIPEPTIDYL PEPTIDASE IV IN COMPLEX WITH AN ALPHA AMINO ACID INHIBITOR | 3.4.14.5 |
2OPP | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW420867X. | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2OPQ | CRYSTAL STRUCTURE OF L100I MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW420867X. | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2OPR | CRYSTAL STRUCTURE OF K101E MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW420867X. | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2OPS | CRYSTAL STRUCTURE OF Y188C MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW420867X. | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2OQ5 | CRYSTAL STRUCTURE OF DESC1, A NEW MEMBER OF THE TYPE II TRANSMEMBRANE SERINE PROTEINASES FAMILY | 3.4.21 |
2OQA | X-RAY SEQUENCE AND CRYSTAL STRUCTURE OF LUFFACULIN 1, A NOVEL TYPE 1 RIBOSOME-INACTIVATING PROTEIN | 3.2.2.22 |
2OQC | CRYSTAL STRUCTURE OF PENICILLIN V ACYLASE FROM BACILLUS SUBTILIS | 3.5.1.11 |
2OQD | CRYSTAL STRUCTURE OF BTHTX-II | 3.1.1.4 |
2OQF | STRUCTURE OF A SYNTHETIC, NON-NATURAL ANALOGUE OF RNASE A: [N71K(ADE), D83A]RNASE A | 3.1.27.5 |
2OQL | STRUCTURE OF PHOSPHOTRIESTERASE MUTANT H254Q/H257F | 3.1.8.1 |
2OQO | CRYSTAL STRUCTURE OF A PEPTIDOGLYCAN GLYCOSYLTRANSFERASE FROM A CLASS A PBP: INSIGHT INTO BACTERIAL CELL WALL SYNTHESIS | 2.4.2 2.4.1.129 3.4.16.4 |
2OQU | HIGH PRESSURE CRYOCOOLING OF CAPILLARY SAMPLE CRYOPROTECTION AND DIFFRACTION PHASING AT LONG WAVELENGTHS | 3.4.21.36 |
2OQV | HUMAN DIPEPTIDYL PEPTIDASE IV (DPP4) WITH PIPERIDINE-CONSTRAINED PHENETHYLAMINE | 3.4.14.5 |
2OQW | THE CRYSTAL STRUCTURE OF SORTASE B FROM B.ANTHRACIS IN COMPLEX WITH AAEK1 | 3.4.22.71 |
2OQZ | THE CRYSTAL STRUCTURE OF SORTASE B FROM B.ANTHRACIS IN COMPLEX WITH AAEK2 | 3.4.22.51 3.4.22.71 |
2OR3 | PRE-OXIDATION COMPLEX OF HUMAN DJ-1 | 3.1.2 3.5.1 3.5.1.124 |
2OR4 | A HIGH RESOLUTION CRYSTAL STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II IN COMPLEX WITH QUISQUALIC ACID | 3.4.17.21 |
2ORY | CRYSTAL STRUCTURE OF M37 LIPASE | 3.1.1.3 |
2OS0 | STRUCTURES OF ACTINONIN BOUND PEPTIDE DEFORMYLASES FROM E. FAECALIS AND S. PYOGENES | 3.5.1.88 |
2OS1 | STRUCTURES OF ACTINONIN BOUND PEPTIDE DEFORMYLASES FROM E. FAECALIS AND S. PYOGENES | 3.5.1.88 |
2OSH | CRYSTAL STRUCTURE OF NATRATOXIN, A SNAKE SPLA2 THAT BLOCKS A-TYPE K+ CHANNEL | 3.1.1.4 |
2OSN | AN ALTERNATE DESCRIPTION OF A CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 FROM BUNGARUS CAERULEUS | 3.1.1.4 |
2OSU | PROBABLE GLUTAMINASE FROM BACILLUS SUBTILIS COMPLEXED WITH 6-DIAZO-5-OXO-L-NORLEUCINE | 3.5.1.2 |
2OSW | ENDO-GLYCOCERAMIDASE II FROM RHODOCOCCUS SP. | 3.2.1.123 |
2OSX | ENDO-GLYCOCERAMIDASE II FROM RHODOCOCCUS SP.: GANGLIOSIDE GM3 COMPLEX | 3.2.1.123 |
2OSY | ENDO-GLYCOCERAMIDASE II FROM RHODOCOCCUS SP.: LACTOSYL-ENZYME INTERMEDIATE | 3.2.1.123 |
2OTD | THE CRYSTAL STRUCTURE OF THE GLYCEROPHOSPHODIESTER PHOSPHODIESTERASE FROM SHIGELLA FLEXNERI 2A | 3.1.4.1 |
2OTF | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND ATENOLOL AT 1.95 A RESOLUTION | 3.1.1.4 |
2OTH | CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF PHOSPHOLIPASE A2 WITH INDOMETHACIN AND NIMESULIDE AT 2.9 A RESOLUTION | 3.1.1.4 |
2OTV | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN BOVINE TRYPSIN AND NICOTINAMIDE AT 1.56 A RESOLUTION | 3.4.21.4 |
2OTY | 1,2-DICHLOROBENZENE IN COMPLEX WITH T4 LYSOZYME L99A | 3.2.1.17 |
2OTZ | N-METHYLANILINE IN COMPLEX WITH T4 LYSOZYME L99A | 3.2.1.17 |
2OU0 | 1-METHYLPYRROLE IN COMPLEX WITH T4 LYSOZYME L99A | 3.2.1.17 |
2OU8 | STRUCTURE OF SPIN-LABELED T4 LYSOZYME MUTANT T115R1 AT ROOM TEMPERATURE | 3.2.1.17 |
2OU9 | STRUCTURE OF SPIN-LABELED T4 LYSOZYME MUTANT T115R1/R119A | 3.2.1.17 |
2OUB | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND ATENOLOL AT 2.75 A RESOLUTION | 3.1.1.4 |
2OUC | CRYSTAL STRUCTURE OF THE MAP KINASE BINDING DOMAIN OF MKP5 | 3.1.3.48 3.1.3.16 |
2OUD | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MKP5 | 3.1.3.48 3.1.3.16 |
2OUK | ABC PROTEIN ARTP IN COMPLEX WITH SULPHATE | 3.6.3.21 |
2OUN | CRYSTAL STRUCTURE OF PDE10A2 IN COMPLEX WITH AMP | 3.1.4.17 3.1.4.35 |
2OUP | CRYSTAL STRUCTURE OF PDE10A | 3.1.4.17 3.1.4.35 |
2OUQ | CRYSTAL STRUCTURE OF PDE10A2 IN COMPLEX WITH GMP | 3.1.4.17 3.1.4.35 |
2OUR | CRYSTAL STRUCTURE OF PDE10A2 MUTANT D674A IN COMPLEX WITH CAMP | 3.1.4.17 3.1.4.35 |
2OUS | CRYSTAL STRUCTURE OF PDE10A2 MUTANT D674A | 3.1.4.17 3.1.4.35 |
2OUU | CRYSTAL STRUCTURE OF PDE10A2 MUTANT D674A IN COMPLEX WITH CGMP | 3.1.4.17 3.1.4.35 |
2OUV | CRYSTAL STRUCTURE OF PDE10A2 MUTANT OF D564N | 3.1.4.17 3.1.4.35 |
2OUY | CRYSTAL STRUCTURE OF PDE10A2 MUTANT D564A IN COMPLEX WITH CAMP. | 3.1.4.17 3.1.4.35 |
2OV2 | THE CRYSTAL STRUCTURE OF THE HUMAN RAC3 IN COMPLEX WITH THE CRIB DOMAIN OF HUMAN P21-ACTIVATED KINASE 4 (PAK4) | 3.6.5.2 |
2OV5 | CRYSTAL STRUCTURE OF THE KPC-2 CARBAPENEMASE | 3.5.2.6 |
2OV6 | THE NMR STRUCTURE OF SUBUNIT F OF THE METHANOGENIC A1AO ATP SYNTHASE AND ITS INTERACTION WITH THE NUCLEOTIDE-BINDING SUBUNIT B | 3.6.3.14 |
2OVV | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF RAT PHOSPHODIESTERASE 10A | 3.1.4.17 3.1.4.35 |
2OVW | ENDOGLUCANASE I COMPLEXED WITH CELLOBIOSE | 3.2.1.4 |
2OVX | MMP-9 ACTIVE SITE MUTANT WITH BARBITURATE INHIBITOR | 3.4.24.35 |
2OVY | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF RAT PHOSPHODIESTERASE 10A | 3.1.4.17 3.1.4.35 |
2OVZ | MMP-9 ACTIVE SITE MUTANT WITH PHOSPHINATE INHIBITOR | 3.4.24.35 |
2OW0 | MMP-9 ACTIVE SITE MUTANT WITH IODINE-LABELED CARBOXYLATE INHIBITOR | 3.4.24.35 |
2OW1 | MMP-9 ACTIVE SITE MUTANT WITH TRIFLUOROMETHYL HYDROXAMATE INHIBITOR | 3.4.24.35 |
2OW2 | MMP-9 ACTIVE SITE MUTANT WITH DIFLUORO BUTANOIC ACID INHIBITOR | 3.4.24.35 |
2OW6 | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH (1R,5S,6S,7R,8S)-1-THIONIABICYCLO[4.3.0]NONAN-5,7,8-TRIOL CHLORIDE | 3.2.1.114 |
2OW7 | GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH (1R,6S,7R,8S)-1-THIONIABICYCLO[4.3.0]NONAN-7,8-DIOL CHLORIDE | 3.2.1.114 |
2OW9 | CRYSTAL STRUCTURE ANALYSIS OF THE MMP13 CATALYTIC DOMAIN IN COMPLEX WITH SPECIFIC INHIBITOR | 3.4.24 |
2OWD | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3 |
2OWE | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2OWM | MOTOR DOMAIN OF NEUROSPORA CRASSA KINESIN-3 (NCKIN3) | 3.6.4.4 |
2OWN | CRYSTAL STRUCTURE OF OLEOYL THIOESTERASE (PUTATIVE) (NP_784467.1) FROM LACTOBACILLUS PLANTARUM AT 2.00 A RESOLUTION | 3.1.2.14 |
2OWQ | CRYSTAL STRUCTURE OF VACCINIA VIRUS URACIL-DNA GLYCOSYLASE | 3.2.2 3.2.2.27 |
2OWZ | R-STATE, CITRATE AND FRU-6-P-BOUND ESCHERICHIA COLI FRUCTOSE-1,6-BISPHOSPHATASE | 3.1.3.11 |
2OX3 | R-STATE, PEP AND FRU-6-P-BOUND, ESCHERICHIA COLI FRUCTOSE-1,6-BISPHOSPHATASE | 3.1.3.11 |
2OXC | HUMAN DEAD-BOX RNA HELICASE DDX20, DEAD DOMAIN IN COMPLEX WITH ADP | 3.6.1 3.6.4.13 |
2OXE | STRUCTURE OF THE HUMAN PANCREATIC LIPASE-RELATED PROTEIN 2 | 3.1.1.3 3.1.1.26 |
2OXM | CRYSTAL STRUCTURE OF A UNG2/MODIFIED DNA COMPLEX THAT REPRESENT A STABILIZED SHORT-LIVED EXTRAHELICAL STATE IN EZYMATIC DNA BASE FLIPPING | 3.2.2.27 |
2OXN | VIBRIO CHOLERAE FAMILY 3 GLYCOSIDE HYDROLASE (NAGZ) IN COMPLEX WITH PUGNAC | 3.2.1.52 |
2OXO | CRYSTALLIZATION AND STRUCTURE DETERMINATION OF THE CORE-BINDING DOMAIN OF BACTERIOPHAGE LAMBDA INTEGRASE | 2.7.7 3.1 |
2OXP | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66D/P117G/H124L/S128A | 3.1.31.1 |
2OXR | PAB0955 CRYSTAL STRUCTURE : A GTPASE IN GDP AND MG BOUND FORM FROM PYROCOCCUS ABYSSI (AFTER GTP HYDROLYSIS) | 3.6.5 |
2OXS | CRYSTAL STRUCTURE OF THE TRYPSIN COMPLEX WITH BENZAMIDINE AT HIGH TEMPERATURE (35 C) | 3.4.21.4 |
2OXT | CRYSTAL STRUCTURE OF MEABAN VIRUS NUCLEOSIDE-2'-O-METHYLTRANSFERASE | 3.4.21.91 3.6.1.15 3.6.4.13 |
2OXU | UNINHIBITED FORM OF HUMAN MMP-12 | 3.4.24.65 |
2OXV | STRUCTURE OF THE A138T PROMISCUOUS MUTANT OF THE ECORI RESTRICTION ENDONUCLEASE BOUND TO ITS COGNATE RECOGNITION SITE. | 3.1.21.4 |
2OXW | HUMAN MMP-12 COMPLEXED WITH THE PEPTIDE IAG | 3.4.24.65 |
2OXZ | HUMAN MMP-12 IN COMPLEX WITH TWO PEPTIDES PQG AND IAG | 3.4.24.65 |
2OY0 | CRYSTAL STRUCTURE OF THE WEST NILE VIRUS METHYLTRANSFERASE | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2OY2 | HUMAN MMP-8 IN COMPLEX WITH PEPTIDE IAG | 3.4.24.34 |
2OY4 | UNINHIBITED HUMAN MMP-8 | 3.4.24.34 |
2OYC | CRYSTAL STRUCTURE OF HUMAN PYRIDOXAL PHOSPHATE PHOSPHATASE | 3.1.3.74 3.1.3.3 |
2OYF | CRYSTAL STRUCTURE OF THE COMPLEX OF PHOSPHOLIPASE A2 WITH INDOLE ACETIC ACID AT 1.2 A RESOLUTION | 3.1.1.4 |
2OYK | ENDO-GLYCOCERAMIDASE II FROM RHODOCOCCUS SP.: CELLOBIOSE-LIKE ISOFAGOMINE COMPLEX | 3.2.1.123 |
2OYL | ENDO-GLYCOCERAMIDASE II FROM RHODOCOCCUS SP.: CELLOBIOSE-LIKE IMIDAZOLE COMPLEX | 3.2.1.123 |
2OYM | ENDO-GLYCOCERAMIDASE II FROM RHODOCOCCUS SP.: FIVE-MEMBERED IMINOCYCLITOL COMPLEX | 3.2.1.123 |
2OYT | CRYSTAL STRUCTURE OF UNG2/DNA(TM) | 3.2.2 3.2.2.27 |
2OZ2 | CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO VINYL SULFONE DERIVED INHIBITOR (K11777) | 3.4.22.51 |
2OZK | STRUCTURE OF AN N-TERMINAL TRUNCATED FORM OF NENDOU (NSP15) FROM SARS-CORONAVIRUS | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2OZM | CRYSTAL STRUCTURE OF RB69 GP43 IN COMPLEX WITH DNA WITH 5-NITP OPPOSITE AN ABASIC SITE ANALOG | 2.7.7.7 3.1.11 |
2OZN | THE COHESIN-DOCKERIN COMPLEX OF NAGJ AND NAGH FROM CLOSTRIDIUM PERFRINGENS | 3.2.1.169 |
2OZR | MMP13 CATALYTIC DOMAIN COMPLEXED WITH 4-{[1-METHYL-2,4-DIOXO-6-(3-PHENYLPROP-1-YN-1-YL)-1,4-DIHYDROQUINAZOLIN-3(2H)-YL]METHYL}BENZOIC ACID | 3.4.24 |
2OZS | CRYSTAL STRUCTURE OF RB69 GP43 IN COMPLEX WITH DNA WITH DATP OPPOSITE DTMP | 2.7.7.7 3.1.11 |
2OZW | SOLUTION STRUCTURE OF HUMAN PHOSPHOHISTIDINE PHOSPHATASE 1 WITH PHOSPHATE LIGAND | 3.1.3 3.9.1.3 |
2OZX | SOLUTION STRUCTURE OF HUMAN PHOSPHOHISTIDINE PHOSPHATASE 1 IN PHOSPHATE FREE FORM | 3.1.3 3.9.1.3 |
2P0R | STRUCTURE OF HUMAN CALPAIN 9 IN COMPLEX WITH LEUPEPTIN | 3.4.22.52 3.4.22 |
2P14 | CRYSTAL STRUCTURE OF SMALL SUBUNIT (R.BSPD6I2) OF THE HETERODIMERIC RESTRICTION ENDONUCLEASE R.BSPD6I | 3.1.21.4 |
2P16 | FACTOR XA IN COMPLEX WITH THE INHIBITOR APIXABAN (BMS-562247) AKA 1-(4-METHOXYPHENYL)-7-OXO-6-(4-(2-OXO-1-PIPERIDINYL)PHENYL)-4,5,6,7-TETRAHYDRO-1H-PYRAZOLO[3, 4-C]PYRIDINE-3-CARBOXAMIDE | 3.4.21.6 |
2P18 | CRYSTAL STRUCTURE OF THE LEISHMANIA INFANTUM GLYOXALASE II | 3.1.2.6 |
2P1D | CRYSTAL STRUCTURE OF DENGUE METHYLTRANSFERASE IN COMPLEX WITH GTP AND S-ADENOSYL-L-HOMOCYSTEINE | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2P1E | CRYSTAL STRUCTURE OF THE LEISHMANIA INFANTUM GLYOXALASE II WITH D-LACTATE AT THE ACTIVE SITE | 3.1.2.6 |
2P1S | CRYSTAL STRUCTURE OF THE C-TERMINAL LOBE OF BOVINE LACTOFERRIN COMPLEXED WITH O-ALPHA-D-GLUCOPYRANOSYL-(1 3)-ALPHA-D-FRUCTOFURANOSYL- (2 1)- ALPHA-D-GLUCOPYRANOSIDE AT 1.93 A RESOLUTION | 3.4.21 |
2P27 | CRYSTAL STRUCTURE OF HUMAN PYRIDOXAL PHOSPHATE PHOSPHATASE WITH MG2+ AT 1.9 A RESOLUTION | 3.1.3.74 3.1.3.3 |
2P2D | CRYSTAL STRUCTURE AND ALLOSTERIC REGULATION OF THE CYTOPLASMIC ESCHERICHIA COLI L-ASPARAGINASE I | 3.5.1.1 |
2P2L | RAC1-GDP-ZINC COMPLEX | 3.6.5.2 |
2P2N | CRYSTAL STRUCTURE AND ALLOSTERIC REGULATION OF THE CYTOPLASMIC ESCHERICHIA COLI L-ASPARAGINASE I | 3.5.1.1 |
2P2Y | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P2Z | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P30 | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P3A | CRYSTAL STRUCTURE OF THE MULTI-DRUG RESISTANT MUTANT SUBTYPE B HIV PROTEASE COMPLEXED WITH TL-3 INHIBITOR | 3.4.23.16 |
2P3B | CRYSTAL STRUCTURE OF THE SUBTYPE B WILD TYPE HIV PROTEASE COMPLEXED WITH TL-3 INHIBITOR | 3.4.23.16 |
2P3C | CRYSTAL STRUCTURE OF THE SUBTYPE F WILD TYPE HIV PROTEASE COMPLEXED WITH TL-3 INHIBITOR | 3.4.23.16 |
2P3D | CRYSTAL STRUCTURE OF THE MULTI-DRUG RESISTANT MUTANT SUBTYPE F HIV PROTEASE COMPLEXED WITH TL-3 INHIBITOR | 3.4.23.16 |
2P3F | CRYSTAL STRUCTURE OF THE FACTOR XA/NAP5 COMPLEX | 3.4.21.6 |
2P3L | CRYSTAL STRUCTURE OF DENGUE METHYLTRANSFERASE IN COMPLEX WITH GPPPA AND S-ADENOSYL-L-HOMOCYSTEINE | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 |
2P3N | THERMOTOGA MARITIMA IMPASE TM1415 | 3.1.3.25 3.1.3.11 |
2P3O | CRYSTAL STRUCTURE OF DENGUE METHYLTRANSFERASE IN COMPLEX WITH 7MEGPPPA AND S-ADENOSYL-L-HOMOCYSTEINE | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 |
2P3Q | CRYSTAL STRUCTURE OF DENGUE METHYLTRANSFERASE IN COMPLEX WITH GPPPG AND S-ADENOSYL-L-HOMOCYSTEINE | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 |
2P3T | CRYSTAL STRUCTURE OF HUMAN FACTOR XA COMPLEXED WITH 3-CHLORO-4-(2-METHYLAMINO-IMIDAZOL-1-YLMETHYL)-THIOPHENE-2-CARBOXYLIC ACID [4-CHLORO-2-(5-CHLORO-PYRIDIN-2-YLCARBAMOYL)-6-METHOXY-PHENYL]-AMIDE | 3.4.21.6 |
2P3U | CRYSTAL STRUCTURE OF HUMAN FACTOR XA COMPLEXED WITH 3-CHLORO-N-(4-CHLORO-2-{[(5-CHLOROPYRIDIN-2-YL)AMINO]CARBONYL}-6-METHOXYPHENYL)-4-[(1-METHYL-1H-IMIDAZOL-2-YL)METHYL]THIOPHENE-2-CARBOXAMIDE {PFIZER 320663} | 3.4.21.6 |
2P3V | THERMOTOGA MARITIMA IMPASE TM1415 | 3.1.3.25 3.1.3.11 |
2P3W | CRYSTAL STRUCTURE OF THE HTRA3 PDZ DOMAIN BOUND TO A PHAGE-DERIVED LIGAND (FGRWV) | 3.4.21 |
2P40 | CRYSTAL STRUCTURE OF DENGUE METHYLTRANSFERASE IN COMPLEX WITH 7MEGPPPG | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 |
2P41 | CRYSTAL STRUCTURE OF DENGUE METHYLTRANSFERASE IN COMPLEX WITH 7MEGPPPG2'OME AND S-ADENOSYL-L-HOMOCYSTEINE | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 |
2P42 | COMPLEX OF A CAMELID SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A AT 1.8A RESOLUTION: SE3-MONO-2 CRYSTAL FORM WITH THREE SE-MET SITES (M34, M51, M83) IN VHH SCAFFOLD | 3.1.27.5 4.6.1.18 |
2P43 | COMPLEX OF A CAMELID SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A AT 1.65A RESOLUTION: SE3-MONO-1 CRYSTAL FORM WITH THREE SE-MET SITES (M34, M51, M83) IN VHH SCAFFOLD | 3.1.27.5 4.6.1.18 |
2P44 | COMPLEX OF A CAMELID SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A AT 1.8A RESOLUTION: SE5A-MONO-1 CRYSTAL FORM WITH FIVE SE-MET SITES (M34, M51, F68M, M83, L86M) IN VHH SCAFFOLD | 3.1.27.5 4.6.1.18 |
2P45 | COMPLEX OF A CAMELID SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A AT 1.1A RESOLUTION: SE5B-ORTHO-1 CRYSTAL FORM WITH FIVE SE-MET SITES (L4M, M34, M51, F68M, M83) IN VHH SCAFFOLD. | 3.1.27.5 4.6.1.18 |
2P46 | COMPLEX OF A CAMELID SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A AT 2.5A RESOLUTION: SE5B-ORTHO-2 CRYSTAL FORM WITH FIVE SE-MET SITES (L4M, M34, M51, F68M, M83) IN VHH SCAFFOLD. | 3.1.27.5 4.6.1.18 |
2P47 | COMPLEX OF A CAMELID SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A AT 2.5A RESOLUTION: SE5B-TRI CRYSTAL FORM WITH FIVE SE-MET SITES (L4M, M34, M51, F68M, M83) IN VHH SCAFFOLD. | 3.1.27.5 4.6.1.18 |
2P48 | COMPLEX OF A CAMELID SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A AT 2.3A RESOLUTION: SE5B-TETRA CRYSTAL FORM WITH FIVE SE-MET SITES (L4M, M34, M51, F68M, M83) IN VHH SCAFFOLD. | 3.1.27.5 4.6.1.18 |
2P49 | COMPLEX OF A CAMELID SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A AT 1.4A RESOLUTION: NATIVE MONO_1 CRYSTAL FORM | 3.1.27.5 4.6.1.18 |
2P4A | X-RAY STRUCTURE OF A CAMELID AFFINITY MATURED SINGLE-DOMAIN VHH ANTIBODY FRAGMENT IN COMPLEX WITH RNASE A | 3.1.27.5 4.6.1.18 |
2P4D | STRUCTURE-ASSISTED DISCOVERY OF VARIOLA MAJOR H1 PHOSPHATASE INHIBITORS | 3.1.3.48 3.1.3.16 3.1.3 |
2P4E | CRYSTAL STRUCTURE OF PCSK9 | 3.4.21 |
2P4J | CRYSTAL STRUCTURE OF BETA-SECRETASE BOND TO AN INHIBITOR WITH ISOPHTHALAMIDE DERIVATIVES AT P2-P3 | 3.4.23.46 |
2P4U | CRYSTAL STRUCTURE OF ACID PHOSPHATASE 1 (ACP1) FROM MUS MUSCULUS | 3.1.3.2 3.1.3.48 |
2P50 | CRYSTAL STRUCTURE OF N-ACETYL-D-GLUCOSAMINE-6-PHOSPHATE DEACETYLASE LIGANDED WITH ZN | 3.5.1.25 |
2P51 | CRYSTAL STRUCTURE OF THE S. POMBE POP2P DEADENYLATION SUBUNIT | 3.1.13.4 |
2P53 | CRYSTAL STRUCTURE OF N-ACETYL-D-GLUCOSAMINE-6-PHOSPHATE DEACETYLASE D273N MUTANT COMPLEXED WITH N-ACETYL PHOSPHONAMIDATE-D-GLUCOSAMINE-6-PHOSPHATE | 3.5.1.25 |
2P5P | CRYSTAL STRUCTURE ANALYSIS OF THE WEST NILE VIRUS ENVELOPE (E) PROTEIN DOMAIN III | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2P5X | CRYSTAL STRUCTURE OF MAF DOMAIN OF HUMAN N-ACETYLSEROTONIN O-METHYLTRANSFERASE-LIKE PROTEIN | 3.6.1.9 2.1.1 |
2P67 | CRYSTAL STRUCTURE OF LAO/AO TRANSPORT SYSTEM KINASE | 2.7 3.6.5 |
2P69 | CRYSTAL STRUCTURE OF HUMAN PYRIDOXAL PHOSPHATE PHOSPHATASE WITH PLP | 3.1.3.74 3.1.3.3 |
2P6B | CRYSTAL STRUCTURE OF HUMAN CALCINEURIN IN COMPLEX WITH PVIVIT PEPTIDE | 3.1.3.16 |
2P6M | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P6N | HUMAN DEAD-BOX RNA HELICASE DDX41, HELICASE DOMAIN | 3.6.1 3.6.4.13 |
2P6O | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P6X | CRYSTAL STRUCTURE OF HUMAN TYROSINE PHOSPHATASE PTPN22 | 3.1.3.48 |
2P6Z | ENZYMATIC AND STRUCTURAL CHARACTERISATION OF AMPHINASE, A NOVEL CYTOTOXIC RIBONUCLEASE FROM RANA PIPIENS OOCYTES | 3.1.27 |
2P74 | CTX-M-9 CLASS A BETA-LACTAMASE APO CRYSTAL STRUCTURE AT 0.88 ANGSTROM RESOLUTION | 3.5.2.6 |
2P75 | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P77 | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P78 | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P79 | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P7S | ENZYMATIC AND STRUCTURAL CHARACTERISATION OF AMPHINASE, A NOVEL CYTOTOXIC RIBONUCLEASE FROM RANA PIPIENS OOCYTES | 3.1.27 |
2P82 | CYSTEINE PROTEASE ATG4A | 3.4.22 |
2P83 | POTENT AND SELECTIVE ISOPHTHALAMIDE S2 HYDROXYETHYLAMINE INHIBITOR OF BACE1 | 3.4.23.46 |
2P86 | THE HIGH RESOLUTION CRYSTAL STRUCTURE OF RHODESAIN, THE MAJOR CATHEPSIN L PROTEASE FROM T. BRUCEI RHODESIENSE, BOUND TO INHIBITOR K11002 | 3.4.22.15 |
2P8E | CRYSTAL STRUCTURE OF THE SERINE/THREONINE PHOSPHATASE DOMAIN OF HUMAN PPM1B | 3.1.3.16 |
2P8H | CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH INHIBITOR | 3.4.23.46 |
2P8N | RICIN A-CHAIN (RECOMBINANT) COMPLEX WITH ADENINE | 3.2.2.22 |
2P8O | CRYSTAL STRUCTURE OF A BENZOHYDROXAMIC ACID/VANADATE COMPLEX BOUND TO CHYMOTRYPSIN A | 3.4.21.1 |
2P8S | HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 IN COMPLEX WITH A CYCLOHEXALAMINE INHIBITOR | 3.4.14.5 |
2P93 | FACTOR XA IN COMPLEX WITH THE INHIBITOR 5-CHLORO-N-(2-(4-(2-OXOPYRIDIN-1(2H)-YL)BENZAMIDO)ETHYL)THIOPHENE-2-CARBOXAMIDE | 3.4.21.6 |
2P94 | FACTOR XA IN COMPLEX WITH THE INHIBITOR 3-CHLORO-N-((1R,2S)-2-(4-(2-OXOPYRIDIN-1(2H)-YL)BENZAMIDO)CYCLOHEXYL)-1H-INDOLE-6-CARBOXAMIDE | 3.4.21.6 |
2P95 | FACTOR XA IN COMPLEX WITH THE INHIBITOR 5-CHLORO-N-((1R,2S)-2-(4-(2-OXOPYRIDIN-1(2H)-YL)BENZAMIDO) CYCLOPENTYL)THIOPHENE-2-CARBOXAMIDE | 3.4.21.6 |
2P98 | E. COLI METHIONINE AMINOPEPTIDASE MONOMETALATED WITH INHIBITOR YE7 | 3.4.11.18 |
2P99 | E. COLI METHIONINE AMINOPEPTIDASE MONOMETALATED WITH INHIBITOR YE6 | 3.4.11.18 |
2P9A | E. COLI METHIONINE AMINOPEPTIDASE DIMETALATED WITH INHIBITOR YE6 | 3.4.11.18 |
2P9V | STRUCTURE OF AMPC BETA-LACTAMASE WITH CROSS-LINKED ACTIVE SITE AFTER EXPOSURE TO SMALL MOLECULE INHIBITOR | 3.5.2.6 |
2P9Y | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2P9Z | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2PA0 | CRYSTAL STRUCTURE OF TTHB049 FROM THERMUS THERMOPHILUS HB8 | 3.1.3.73 |
2PA5 | CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE PTPN9 | 3.1.3.48 |
2PAD | BINDING OF CHLOROMETHYL KETONE SUBSTRATE ANALOGUES TO CRYSTALLINE PAPAIN | 3.4.22.2 |
2PAQ | CRYSTAL STRUCTURE OF THE 5'-DEOXYNUCLEOTIDASE YFBR | 3.1.3.5 3.1.3.89 |
2PAR | CRYSTAL STRUCTURE OF THE 5'-DEOXYNUCLEOTIDASE YFBR MUTANT E72A COMPLEXED WITH CO(2+) AND TMP | 3.1.3.5 3.1.3.89 |
2PAU | CRYSTAL STRUCTURE OF THE 5'-DEOXYNUCLEOTIDASE YFBR MUTANT E72A COMPLEXED WITH CO(2+) AND DAMP | 3.1.3.5 3.1.3.89 |
2PB1 | EXO-B-(1,3)-GLUCANASE FROM CANDIDA ALBICANS IN COMPLEX WITH UNHYDROLYSED AND COVALENTLY LINKED 2,4-DINITROPHENYL-2-DEOXY-2-FLUORO-B-D-GLUCOPYRANOSIDE AT 1.9 A | 3.2.1.58 2.4.1 |
2PB8 | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND PEPTIDE ALA-VAL-TYR-SER AT 2.0 A RESOLUTION | 3.1.1.4 |
2PBG | 6-PHOSPHO-BETA-D-GALACTOSIDASE FORM-B | 3.2.1.85 |
2PBH | CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN B AT 3.3 ANGSTROM RESOLUTION | 3.4.22.1 |
2PBN | CRYSTAL STRUCTURE OF THE HUMAN TYROSINE RECEPTOR PHOSPHATE GAMMA | 3.1.3.48 |
2PBO | E27Q MUTANT OF EXO-B-(1,3)-GLUCANASE FROM CANDIDA ALBICANS AT 1.85 A | 3.2.1.58 2.4.1 |
2PBY | PROBABLE GLUTAMINASE FROM GEOBACILLUS KAUSTOPHILUS HTA426 | 3.5.1.2 |
2PC0 | APO WILD-TYPE HIV PROTEASE IN THE OPEN CONFORMATION | 3.4.23.16 |
2PC2 | LYSOZYME COCRYSTALLIZED WITH TRIS-DIPICOLINATE EU COMPLEX | 3.2.1.17 |
2PC5 | NATIVE CRYSTAL STRUCTURE ANALYSIS ON ARABIDOPSIS DUTPASE | 3.6.1.23 |
2PC8 | E292Q MUTANT OF EXO-B-(1,3)-GLUCANASE FROM CANDIDA ALBICANS IN COMPLEX WITH TWO SEPARATELY BOUND GLUCOPYRANOSIDE UNITS AT 1.8 A | 3.2.1.58 2.4.1 |
2PCJ | CRYSTAL STRUCTURE OF ABC TRANSPORTER (AQ_297) FROM AQUIFEX AEOLICUS VF5 | 3.6.3 7.6.2 |
2PCL | CRYSTAL STRUCTURE OF ABC TRANSPORTER WITH COMPLEX (AQ_297) FROM AQUIFEX AEOLICUS VF5 | 3.6.3 7.6.2 |
2PCR | CRYSTAL STRUCTURE OF MYO-INOSITOL-1(OR 4)-MONOPHOSPHATASE (AQ_1983) FROM AQUIFEX AEOLICUS VF5 | 3.1.3.25 3.1.3.11 |
2PCU | HUMAN CARBOXYPEPTIDASE A4 IN COMPLEX WITH A CLEAVED HEXAPEPTIDE. | 3.4.17 |
2PE4 | STRUCTURE OF HUMAN HYALURONIDASE 1, A HYALURONAN HYDROLYZING ENZYME INVOLVED IN TUMOR GROWTH AND ANGIOGENESIS | 3.2.1.35 |
2PF0 | F258I MUTANT OF EXO-B-(1,3)-GLUCANASE FROM CANDIDA ALBICANS AT 1.9 A | 3.2.1.58 2.4.1 |
2PF1 | STRUCTURE OF BOVINE PROTHROMBIN FRAGMENT 1 REFINED AT 2.25 ANGSTROMS RESOLUTION | 3.4.21.5 |
2PF2 | THE CA+2 ION AND MEMBRANE BINDING STRUCTURE OF THE GLA DOMAIN OF CA-PROTHROMBIN FRAGMENT 1 | 3.4.21.5 |
2PFC | STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS RV0098 | 3.1.2 3.1.2.2 |
2PFJ | CRYSTAL STRUCTURE OF T7 ENDO I RESOLVASE IN COMPLEX WITH A HOLLIDAY JUNCTION | 3.1.21.2 |
2PG3 | CRYSTAL STRUCTURE OF A QUEUOSINE BIOSYNTHESIS PROTEIN QUEC (ECA1155) FROM ERWINIA CAROTOVORA SUBSP. ATROSEPTICA SCRI1043 AT 2.40 A RESOLUTION | 3.5 6.3.4.20 |
2PGB | INHIBITOR-FREE HUMAN THROMBIN MUTANT C191A-C220A | 3.4.21.5 |
2PGF | CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE FROM PLASMODIUM VIVAX IN COMPLEX WITH ADENOSINE | 3.5.4.4 |
2PGJ | CATALYSIS ASSOCIATED CONFORMATIONAL CHANGES REVEALED BY HUMAN CD38 COMPLEXED WITH A NON-HYDROLYZABLE SUBSTRATE ANALOG | 3.2.2.5 3.2.2.6 2.4.99.20 |
2PGL | CATALYSIS ASSOCIATED CONFORMATIONAL CHANGES REVEALED BY HUMAN CD38 COMPLEXED WITH A NON-HYDROLYZABLE SUBSTRATE ANALOG | 3.2.2.5 3.2.2.6 2.4.99.20 |
2PGQ | HUMAN THROMBIN MUTANT C191A-C220A IN COMPLEX WITH THE INHIBITOR PPACK | 3.4.21.5 |
2PGR | CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE FROM PLASMODIUM VIVAX IN COMPLEX WITH PENTOSTATIN | 3.5.4.4 |
2PH6 | CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH INHIBITOR | 3.4.23.46 |
2PH8 | CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH INHIBITOR | 3.4.23.46 |
2PHA | CRYSTAL STRUCTURE OF NATIVE, UNLIGANDED HUMAN ARGINASE AT 1.90 RESOLUTION | 3.5.3.1 |
2PHB | AN ORALLY EFFICACIOUS FACTOR XA INHIBITOR | 3.4.21.6 |
2PHI | A LARGE CONFORMATIONAL CHANGE IS FOUND IN THE CRYSTAL STRUCTURE OF THE PORCINE PANCREATIC PHOSPHOLIPASE A2 POINT MUTANT F63V | 3.1.1.4 |
2PHO | CRYSTAL STRUCTURE OF HUMAN ARGINASE I COMPLEXED WITH THIOSEMICARBAZIDE AT 1.95 RESOLUTION | 3.5.3.1 |
2PI7 | STRUCTURE OF THE CATALYTIC DOMAIN OF THE CHICK RETINAL NEURITE INHIBITOR-RECEPTOR PROTEIN TYROSINE PHOSPHATASE CRYP-2/CPTPRO | 3.1.3.48 |
2PI8 | CRYSTAL STRUCTURE OF E. COLI MLTA WITH BOUND CHITOHEXAOSE | 3.2.1 4.2.2 |
2PIC | E. COLI LYTIC TRANSGLYCOSYLASE MLTA-D308A IN APO-2 FORM | 3.2.1 4.2.2 |
2PIY | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B (S)-2-(3-AMINOMETHYL-PHENYL)-3-{HYDROXY-[(R)-2-METHYL-1-(3-PHENYL-PROPANE-1-SULFONYLAMINO)-PROPYL]-PHOSPHINOYL}-PROPIONIC ACID {ZK 528} COMPLEX | 3.4.17.2 |
2PIZ | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B 2-(3-GUANIDINO-PHENYL)-3-[HYDROXY-(3-PHENYL-PROPYL)-PHOSPHINOYL]-PROPIONIC ACID COMPLEX | 3.4.17.2 |
2PJ0 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B [((R)-1-BENZYLOXYCARBONYLAMINO-2-METHYL-PROPYL)-HYDROXY-PHOSPHINOYLOXY]-(3-GUANIDINO-PHENYL)-ACETIC ACID COMPLEX | 3.4.17.2 |
2PJ1 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B (3-AMINOMETHYL-PHENYL)-[((R)-1-BENZYLOXYCARBONYLAMINO-2-METHYL-PROPYL)-HYDROXY-PHOSPHINOYLOXY]-ACETIC ACID COMPLEX | 3.4.17.2 |
2PJ2 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B 2-(3-AMINOMETHYL-PHENYL)-3-[((R)-1-BENZYLOXYCARBONYLAMINO-2-METHYL-PROPYL)-HYDROXY-PHOSPHINOYL]-PROPIONIC ACID COMPLEX | 3.4.17.2 |
2PJ3 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B (3-GUANIDINO-PHENYL)-{HYDROXY-[(R)-2-METHYL-1-(3-PHENYL-PROPIONYLAMINO)-PROPYL]-PHOSPHINOYLOXY}-ACETIC ACID COMPLEX | 3.4.17.2 |
2PJ4 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B [((R)-BENZYLOXYCARBONYLAMINO-CYCLOHEXYL-METHYL)-HYDROXY-PHOSPHINOYLOXY]-(3-GUANIDINO-PHENYL)-ACETIC ACID COMPLEX | 3.4.17.2 |
2PJ5 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B [((R)-1-BENZYLOXYCARBONYLAMINO-HEXYL)-HYDROXY-PHOSPHINOYLOXY]-(3-GUANIDINO-PHENYL)-ACETIC ACID COMPLEX | 3.4.17.2 |
2PJ6 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B 2-(3-AMINOMETHYL-PHENYL)-3-{HYDROXY-[(R)-2-METHYL-1-(2-PHENYL-ETHANESULFONYLAMINO)-PROPYL]-PHOSPHINOYL}-PROPIONIC ACID COMPLEX | 3.4.17.2 |
2PJ7 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B 2-(3-AMINOMETHYL-PHENYL)-3-[((R)-1-BENZENESULFONYLAMINO-2-METHYL-PROPYL)-HYDROXY-PHOSPHINOYL]-PROPIONIC ACID COMPLEX | 3.4.17.2 |
2PJ8 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B 2-(3-AMINOMETHYL-PHENYL)-3-{[(R)-1-(BIPHENYL-4-SULFONYLAMINO)-2-METHYL-PROPYL]-HYDROXY-PHOSPHINOYL}-PROPIONIC ACID COMPLEX | 3.4.17.2 |
2PJ9 | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B 2-(3-AMINOMETHYL-PHENYL)-3-{[(R)-1-(BENZO[1,2,5]THIADIAZOLE-4-SULFONYLAMINO)-2-METHYL-PROPYL]-HYDROXY-PHOSPHINOYL}-PROPIONIC ACID COMPLEX | 3.4.17.2 |
2PJA | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B 3-{[(R)-1-((S)-2-BENZYLOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-2-METHYL-PROPYL]-HYDROXY-PHOSPHINOYL}-2-(3-GUANIDINO-PHENYL)-PROPIONIC ACID COMPLEX | 3.4.17.2 |
2PJB | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B 2-(3-AMINOMETHYL-PHENYL)-3-{[1-((S)-2-BENZYLOXYCARBONYLAMINO-3-PHENYL-PROPANE-1-SULFONYLAMINO)-2-METHYL-PROPYL]-HYDROXY-PHOSPHINOYL}-PROPIONIC ACID COMPLEX | 3.4.17.2 |
2PJC | CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B ({(R)-1-[(S)-2-BENZYLOXYCARBONYLAMINO-3-(4-HYDROXY-PHENYL)-PROPIONYLAMINO]-2-METHYL-PROPYL}-HYDROXY-PHOSPHINOYLOXY)-(3-GUANIDINO-PHENYL)-ACETIC ACID COMPLEX | 3.4.17.2 |
2PJF | SOLUTION STRUCTURE OF RHODOSTOMIN | 3.4.24 |
2PJG | SOLUTION STRUCTURE OF RHODOSTOMIN D51E MUTANT | 3.4.24 |
2PJI | SOLUTION STRUCTURE OF RHODOSTOMIN P48A MUTANT | 3.4.24 |
2PJJ | E. COLI LYTIC TRANSGLYCOSYLASE MLTA-D308A IN APO-1 FORM | 3.2.1 4.2.2 |
2PJO | RICIN A-CHAIN (RECOMBINANT) COMPLEX WITH N-METHYLUREA | 3.2.2.22 |
2PJR | HELICASE PRODUCT COMPLEX | 3.6.1 3.6.4.12 |
2PJT | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF MMP-13 COMPLEXED WITH WAY-344 | 3.4.24 |
2PK0 | STRUCTURE OF THE S. AGALACTIAE SERINE/THREONINE PHOSPHATASE AT 2.65 RESOLUTION | 3.1.3.16 |
2PK4 | THE REFINED STRUCTURE OF THE EPSILON-AMINOCAPROIC ACID COMPLEX OF HUMAN PLASMINOGEN KRINGLE | 3.4.21.7 |
2PKA | REFINED 2 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF PORCINE PANCREATIC KALLIKREIN A, A SPECIFIC TRYPSIN-LIKE SERINE PROTEINASE. CRYSTALLIZATION, STRUCTURE DETERMINATION, CRYSTALLOGRAPHIC REFINEMENT, STRUCTURE AND ITS COMPARISON WITH BOVINE TRYPSIN | 3.4.21.35 |
2PKC | CRYSTAL STRUCTURE OF CALCIUM-FREE PROTEINASE K AT 1.5 ANGSTROMS RESOLUTION | 3.4.21.64 |
2PKS | THROMBIN IN COMPLEX WITH INHIBITOR | 3.4.21.5 |
2PKY | THE EFFECT OF DEUTERATION ON PROTEIN STRUCTURE A HIGH RESOLUTION COMPARISON OF HYDROGENOUS AND PERDEUTERATED HALOALKANE DEHALOGENASE | 3.8.1.5 |
2PL3 | HUMAN DEAD-BOX RNA HELICASE DDX10, DEAD DOMAIN IN COMPLEX WITH ADP | 3.6.1 3.6.4.13 |
2PLC | PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C FROM LISTERIA MONOCYTOGENES | 3.1.4.10 4.6.1.13 |
2PLD | NUCLEAR MAGNETIC RESONANCE STRUCTURE OF AN SH2 DOMAIN OF PHOSPHOLIPASE C-GAMMA1 COMPLEXED WITH A HIGH AFFINITY BINDING PEPTIDE | 3.1.4.11 |
2PLE | NUCLEAR MAGNETIC RESONANCE STRUCTURE OF AN SH2 DOMAIN OF PHOSPHOLIPASE C-GAMMA1 COMPLEXED WITH A HIGH AFFINITY BINDING PEPTIDE | 3.1.4.11 |
2PLF | THE STRUCTURE OF AIF2GAMMA SUBUNIT FROM THE ARCHAEON SULFOLOBUS SOLFATARICUS IN THE NUCLEOTIDE-FREE FORM. | 3.6.5.3 |
2PLL | CRYSTAL STRUCTURE OF PERDEUTERATED HUMAN ARGINASE I | 3.5.3.1 |
2PLM | CRYSTAL STRUCTURE OF THE PROTEIN TM0936 FROM THERMOTOGA MARITIMA COMPLEXED WITH ZN AND S-INOSYLHOMOCYSTEINE | 3.5.4.28 3.5.4.31 |
2PLQ | CRYSTAL STRUCTURE OF THE AMIDASE FROM GEOBACILLUS PALLIDUS RAPC8 | 3.5.1.4 |
2PLV | STRUCTURAL FACTORS THAT CONTROL CONFORMATIONAL TRANSITIONS AND SEROTYPE SPECIFICITY IN TYPE 3 POLIOVIRUS | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2PLX | TRYPSIN COMPLEXED TO A SYNTHETIC PEPTIDE FROM VERONICA HEDERIFOLIA | 3.4.21.4 |
2PM8 | CRYSTAL STRUCTURE OF RECOMBINANT FULL LENGTH HUMAN BUTYRYLCHOLINESTERASE | 3.1.1.8 |
2PMD | THE STRUCTURES OF AIF2GAMMA SUBUNIT FROM THE ARCHAEON SULFOLOBUS SOLFATARICUS IN THE GDP-BOUND FORM. | 3.6.5.3 |
2PMJ | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND 1, 2 BENZOPYRONE AT 2.4 A RESOLUTION | 3.1.1.4 |
2PMS | CRYSTAL STRUCTURE OF THE COMPLEX OF HUMAN LACTOFERRIN N-LOBE AND LACTOFERRIN-BINDING DOMAIN OF PNEUMOCOCCAL SURFACE PROTEIN A | 3.4.21 |
2PMW | THE CRYSTAL STRUCTURE OF PROPROTEIN CONVERTASE SUBTILISIN KEXIN TYPE 9 (PCSK9) | 3.4.21 |
2PNG | TYPE I RAT FATTY ACID SYNTHASE ACYL CARRIER PROTEIN (ACP) DOMAIN | 2.3.1.85 2.3.1.38 2.3.1.39 2.3.1.41 1.1.1.100 4.2.1.59 1.3.1.39 3.1.2.14 |
2PNM | CRYSTAL STRUCTURE OF VP4 PROTEASE FROM INFECTIOUS PANCREATIC NECROSIS VIRUS (IPNV) IN SPACE GROUP P6122 | 3.4.21 |
2PNQ | CRYSTAL STRUCTURE OF PYRUVATE DEHYDROGENASE PHOSPHATASE 1 (PDP1) | 3.1.3.43 |
2PNS | 1.9 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF A PLANT CYSTEINE PROTEASE ERVATAMIN-C REFINEMENT WITH CDNA DERIVED AMINO ACID SEQUENCE | 3.4.22 |
2PNZ | CRYSTAL STRUCTURE OF THE P. ABYSSI EXOSOME RNASE PH RING COMPLEXED WITH UDP AND GMP | 3.1.13 |
2PO0 | CRYSTAL STRUCTURE OF THE P. ABYSSI EXOSOME RNASE PH RING COMPLEXED WITH ADP IN DOUBLE CONFORMATION | 3.1.13 |
2PO1 | CRYSTAL STRUCTURE OF THE P. ABYSSI EXOSOME RNASE PH RING COMPLEXED WITH A SINGLE STRANDED 10-MER POLY(A) RNA | 3.1.13 |
2PO2 | CRYSTAL STRUCTURE OF THE P. ABYSSI EXOSOME RNASE PH RING COMPLEXED WITH CDP | 3.1.13 |
2POF | CRYSTAL STRUCTURE OF CDP-DIACYLGLYCEROL PYROPHOSPHATASE | 3.6.1.26 |
2POJ | NMR SOLUTION STRUCTURE OF THE INHIBITOR-FREE STATE OF MACROPHAGE METALLOELASTASE (MMP-12) | 3.4.24.65 |
2POO | THERMOSTABLE PHYTASE IN FULLY CALCIUM LOADED STATE | 3.1.3.8 |
2PPL | HUMAN PANCREATIC LIPASE-RELATED PROTEIN 1 | 3.1.1.3 |
2PQ2 | STRUCTURE OF SERINE PROTEINASE K COMPLEX WITH A HIGHLY FLEXIBLE HYDROPHOBIC PEPTIDE AT 1.8A RESOLUTION | 3.4.21.64 |
2PQ5 | CRYSTAL STRUCTURE OF DUAL SPECIFICITY PROTEIN PHOSPHATASE 13 (DUSP13) | 3.1.3.48 3.1.3.16 |
2PQE | SOLUTION STRUCTURE OF PROLINE-FREE MUTANT OF STAPHYLOCOCCAL NUCLEASE | 3.1.31.1 |
2PQG | CRYSTAL STRUCTURE OF INACTIVE RIBOSOME INACTIVATING PROTEIN FROM MAIZE (B-32) | 3.2.2.22 |
2PQI | CRYSTAL STRUCTURE OF ACTIVE RIBOSOME INACTIVATING PROTEIN FROM MAIZE (B-32) | 3.2.2.22 |
2PQJ | CRYSTAL STRUCTURE OF ACTIVE RIBOSOME INACTIVATING PROTEIN FROM MAIZE (B-32), COMPLEX WITH ADENINE | 3.2.2.22 |
2PQX | E. COLI RNASE 1 (IN VIVO FOLDED) | 3.1.27.6 4.6.1.21 |
2PQY | E. COLI RNASE 1 (IN VITRO REFOLDED WITH DSBA ONLY) | 3.1.27.6 4.6.1.21 |
2PQZ | HIV-1 PROTEASE IN COMPLEX WITH A PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2PR3 | FACTOR XA INHIBITOR | 3.4.21.6 |
2PRD | CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM THERMUS THERMOPHILUS | 3.6.1.1 |
2PRE | CRYSTAL STRUCTURE OF PLANT CYSTEINE PROTEASE ERVATAMIN-C COMPLEXED WITH IRREVERSIBLE INHIBITOR E-64 AT 2.7 A RESOLUTION | 3.4.22 |
2PRK | SYNCHROTRON X-RAY DATA COLLECTION AND RESTRAINED LEAST-SQUARES REFINEMENT OF THE CRYSTAL STRUCTURE OF PROTEINASE K AT 1.5 ANGSTROMS RESOLUTION | 3.4.21.14 3.4.21.64 |
2PRO | PRO REGION OF ALPHA-LYTIC PROTEASE | 3.4.21.12 |
2PRQ | X-RAY CRYSTALLOGRAPHIC CHARACTERIZATION OF THE CO(II)-SUBSTITUTED TRIS-BOUND FORM OF THE AMINOPEPTIDASE FROM AEROMONAS PROTEOLYTICA | 3.4.11.10 |
2PSG | REFINED STRUCTURE OF PORCINE PEPSINOGEN AT 1.8 ANGSTROMS RESOLUTION | 3.4.23.1 |
2PSX | CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 5 IN COMPLEX WITH LEUPEPTIN | 3.4.21 |
2PSY | CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 5 IN COMPLEX WITH LEUPEPTIN AND ZINC | 3.4.21 |
2PTC | THE GEOMETRY OF THE REACTIVE SITE AND OF THE PEPTIDE GROUPS IN TRYPSIN, TRYPSINOGEN AND ITS COMPLEXES WITH INHIBITORS | 3.4.21.4 |
2PTD | PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C MUTANT D198E | 3.1.4.10 4.6.1.13 |
2PTH | PEPTIDYL-TRNA HYDROLASE FROM ESCHERICHIA COLI | 3.1.1.29 |
2PTN | ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY | 3.4.21.4 |
2PU2 | AMPC BETA-LACTAMASE WITH BOUND PHTHALAMIDE INHIBITOR | 3.5.2.6 |
2PU3 | STRUCTURAL ADAPTATION OF ENDONUCLEASE I FROM THE COLD-ADAPTED AND HALOPHILIC BACTERIUM VIBRIO SALMONICIDA | 3.1.21.1 |
2PU4 | AMPC BETA-LACAMASE WITH BOUND COVALENT OXADIAZOLE INHIBITOR | 3.5.2.6 |
2PU5 | CRYSTAL STRUCTURE OF A C-C BOND HYDROLASE, BPHD, FROM BURKHOLDERIA XENOVORANS LB400 | 3.7.1 3.7.1.8 |
2PU7 | CRYSTAL STRUCTURE OF S112A/H265A DOUBLE MUTANT OF A C-C HYDROLASE, BPHD, FROM BURKHOLDERIA XENOVORANS LB400 | 3.7.1 3.7.1.8 |
2PUH | CRYSTAL STRUCTURE OF THE S112A MUTANT OF A C-C HYDROLASE, BPHD FROM BURKHOLDERIA XENOVORANS LB400, IN COMPLEX WITH ITS SUBSTRATE HOPDA | 3.7.1 3.7.1.8 |
2PUJ | CRYSTAL STRUCTURE OF THE S112A/H265A DOUBLE MUTANT OF A C-C HYDROLASE, BPHD FROM BURKHOLDERIA XENOVORANS LB400, IN COMPLEX WITH ITS SUBSTRATE HOPDA | 3.7.1 3.7.1.8 |
2PUQ | CRYSTAL STRUCTURE OF ACTIVE SITE INHIBITED COAGULATION FACTOR VIIA IN COMPLEX WITH SOLUBLE TISSUE FACTOR | 3.4.21.21 |
2PUX | CRYSTAL STRUCTURE OF MURINE THROMBIN IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF MURINE PAR3 | 3.4.21.5 |
2PUZ | CRYSTAL STRUCTURE OF IMIDAZOLONEPROPIONASE FROM AGROBACTERIUM TUMEFACIENS WITH BOUND PRODUCT N-FORMIMINO-L-GLUTAMATE | 3.5.2.7 |
2PV9 | CRYSTAL STRUCTURE OF MURINE THROMBIN IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF MURINE PAR4 | 3.4.21.5 |
2PVA | OXIDIZED PENICILLIN V ACYLASE FROM B. SPHAERICUS | 3.5.1.11 |
2PVI | PVUII ENDONUCLEASE COMPLEXED TO AN IODINATED COGNATE DNA | 3.1.21.4 |
2PVS | STRUCTURE OF HUMAN PANCREATIC LIPASE RELATED PROTEIN 2 MUTANT N336Q | 3.1.1.3 3.1.1.26 |
2PVT | CRYSTAL STRUCTURE OF A NEW ISOFORM OF PHOSPHOLIPASE A2 FROM RUSSELLS VIPER AT 2.1 A RESOLUTION | 3.1.1.4 |
2PVV | STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH L-SERINE-O-SULFATE | 3.4.17.21 |
2PVW | A HIGH RESOLUTION STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH 2-(PHOSPHONOMETHYL)PENTANEDIOIC ACID (2-PMPA) | 3.4.17.21 |
2PW3 | STRUCTURE OF THE PDE4D-CAMP COMPLEX | 3.1.4.17 3.1.4.53 |
2PW5 | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT V66Y/P117G/H124L/S128A AT ROOM TEMPERATURE | 3.1.31.1 |
2PW7 | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT V66Y/P117G/H124L/S128A AT 100K | 3.1.31.1 |
2PW8 | CRYSTAL STRUCTURE OF SULFO-HIRUDIN COMPLEXED TO THROMBIN | 3.4.21.5 |
2PWA | CRYSTAL STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH ALANINE BORONIC ACID AT 0.83A RESOLUTION | 3.4.21.64 |
2PWB | CRYSTAL STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH COUMARIN AT 1.9 A RESOLUTION | 3.4.21.64 |
2PWC | HIV-1 PROTEASE IN COMPLEX WITH A AMINO DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2PWM | CRYSTAL STRUCTURE OF HIV-1 CA146 A92E REAL CELL | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2PWR | HIV-1 PROTEASE IN COMPLEX WITH A CARBAMOYL DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2PWS | CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND 2-(4-ISOBUTYL-PHENYL)-PROPIONIC ACID AT 2.2 A RESOLUTION | 3.1.1.4 |
2PWX | CRYSTAL STRUCTURE OF G11A MUTANT OF SARS-COV 3C-LIKE PROTEASE | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2PX1 | CRYSTAL STRUCTURE OF THE COMPLEX OF BOVINE LACTOFERRIN C-LOBE WITH RIBOSE AT 2.5 A RESOLUTION | 3.4.21 |
2PX2 | CRYSTAL STRUCTURE OF THE MURRAY VALLEY ENCEPHALITIS VIRUS NS5 2'-O METHYLTRANSFERASE DOMAIN IN COMPLEX WITH SAH (MONOCLINIC FORM 1) | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2PX4 | CRYSTAL STRUCTURE OF THE MURRAY VALLEY ENCEPHALITIS VIRUS NS5 2'-O METHYLTRANSFERASE DOMAIN IN COMPLEX WITH SAH (MONOCLINIC FORM 2) | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2PX5 | CRYSTAL STRUCTURE OF THE MURRAY VALLEY ENCEPHALITIS VIRUS NS5 2'-O METHYLTRANSFERASE DOMAIN IN COMPLEX WITH SAH (ORTHORHOMBIC CRYSTAL FORM) | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2PX6 | CRYSTAL STRUCTURE OF THE THIOESTERASE DOMAIN OF HUMAN FATTY ACID SYNTHASE INHIBITED BY ORLISTAT | 2.3.1.85 2.3.1.38 2.3.1.39 2.3.1.41 1.1.1.100 4.2.1.59 1.3.1.39 3.1.2.14 |
2PX8 | CRYSTAL STRUCTURE OF THE MURRAY VALLEY ENCEPHALITIS VIRUS NS5 2'-O METHYLTRANSFERASE DOMAIN IN COMPLEX WITH SAH AND 7M-GTP | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2PXA | CRYSTAL STRUCTURE OF THE MURRAY VALLEY ENCEPHALITIS VIRUS NS5 2'-O METHYLTRANSFERASE DOMAIN IN COMPLEX WITH SAH AND GTPG | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2PXC | CRYSTAL STRUCTURE OF THE MURRAY VALLEY ENCEPHALITIS VIRUS NS5 2'-O METHYLTRANSFERASE DOMAIN IN COMPLEX WITH SAM AND GTPA | 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 |
2PY4 | FULL LENGTH STRUCTURE OF THE MYCOBACTERIUM TUBERCULOSIS DUTPASE COMPLEXED WITH MAGNESIUM AND ALPHA,BETA-IMIDO-DUTP. | 3.6.1.23 |
2PY5 | PHI29 DNA POLYMERASE COMPLEXED WITH SINGLE-STRANDED DNA | 2.7.7.7 3.1.11 |
2PYC | CRYSTAL STRUCTURE OF A MONOMERIC PHOSPHOLIPASE A2 FROM RUSSELL'S VIPER AT 1.5A RESOLUTION | 3.1.1.4 |
2PYJ | PHI29 DNA POLYMERASE COMPLEXED WITH PRIMER-TEMPLATE DNA AND INCOMING NUCLEOTIDE SUBSTRATES (TERNARY COMPLEX) | 2.7.7.7 3.1.11 |
2PYK | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT V66Q/P117G/H124L/S128A AT ROOM TEMPERATURE | 3.1.31.1 |
2PYL | PHI29 DNA POLYMERASE COMPLEXED WITH PRIMER-TEMPLATE DNA AND INCOMING NUCLEOTIDE SUBSTRATES (TERNARY COMPLEX) | 2.7.7.7 3.1.11 |
2PYM | HIV-1 PR MUTANT IN COMPLEX WITH NELFINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2PYN | HIV-1 PR MUTANT IN COMPLEX WITH NELFINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2PYU | STRUCTURE OF THE E. COLI INOSINE TRIPHOSPHATE PYROPHOSPHATASE RGDB IN COMPLEX WITH IMP | 3.6.1.19 3.6.1.66 |
2PYZ | CRYSTAL STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH AURAMINE AT 1.8A RESOLUTION | 3.4.21.64 |
2PZD | CRYSTAL STRUCTURE OF THE HTRA2/OMI PDZ DOMAIN BOUND TO A PHAGE-DERIVED LIGAND (WTMFWV) | 3.4.21.108 |
2PZF | MINIMAL HUMAN CFTR FIRST NUCLEOTIDE BINDING DOMAIN AS A HEAD-TO-TAIL DIMER WITH DELTA F508 | 3.6.3.49 5.6.1.6 |
2PZH | YBGC THIOESTERASE (HP0496) FROM HELICOBACTER PYLORI | 3.1.2 |
2PZT | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT V66Q/P117G/H124L/S128A AT 100 K | 3.1.31.1 |
2PZU | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT V66N/P117G/H124L/S128A AT CRYOGENIC TEMPERATURE | 3.1.31.1 |
2PZW | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT V66N/P117G/H124L/S128A AT ROOM TEMPERATURE | 3.1.31.1 |
2Q05 | CRYSTAL STRUCTURE OF TYR/SER PROTEIN PHOSPHATASE FROM VACCINIA VIRUS WR | 3.1.3.48 3.1.3.16 3.1.3 |
2Q09 | CRYSTAL STRUCTURE OF IMIDAZOLONEPROPIONASE FROM ENVIRONMENTAL SAMPLE WITH BOUND INHIBITOR 3-(2,5-DIOXO-IMIDAZOLIDIN-4-YL)-PROPIONIC ACID | 3.5.2.7 |
2Q0H | ABC PROTEIN ARTP IN COMPLEX WITH ADP/MG2+, ATP-GAMMA-S HYDROLYZED | 3.6.3.21 |
2Q0I | STRUCTURE OF PSEUDOMONAS QUINOLONE SIGNAL RESPONSE PROTEIN PQSE | 3.1.2.32 |
2Q0J | STRUCTURE OF PSEUDOMONAS QUINOLONE SIGNAL RESPONSE PROTEIN PQSE | 3.1.2.32 |
2Q0M | TRICARBONYLMANGANESE(I)-LYSOZYME COMPLEX : A STRUCTURALLY CHARACTERIZED ORGANOMETALLIC PROTEIN | 3.2.1.17 |
2Q0S | STRUCTURE OF THE INHIBITOR BOUND FORM OF M. SMEGMATIS ARYL ESTERASE | 3.1.1.2 |
2Q0Z | CRYSTAL STRUCTURE OF Q9P172/SEC63 FROM HOMO SAPIENS. NORTHEAST STRUCTURAL GENOMICS TARGET HR1979. | 3.6.4.13 |
2Q11 | STRUCTURE OF BACE COMPLEXED TO COMPOUND 1 | 3.4.23.46 |
2Q15 | STRUCTURE OF BACE COMPLEXED TO COMPOUND 3A | 3.4.23.46 |
2Q16 | STRUCTURE OF THE E. COLI INOSINE TRIPHOSPHATE PYROPHOSPHATASE RGDB IN COMPLEX WITH ITP | 3.6.1.19 3.6.1.66 |
2Q1J | THE DISCOVERY OF GLYCINE AND RELATED AMINO ACID-BASED FACTOR XA INHIBITORS | 3.4.21.6 |
2Q1P | CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 COMPLEX WITH PROPANOL AT 1.5 A RESOLUTION | 3.1.1.4 |
2Q21 | CRYSTAL STRUCTURES AT 2.2 ANGSTROMS RESOLUTION OF THE CATALYTIC DOMAINS OF NORMAL RAS PROTEIN AND AN ONCOGENIC MUTANT COMPLEXED WITH GSP | 3.6.5.2 |
2Q2B | CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF MOUSE ACYL-COA THIOESTERASE 7 | 3.1.2.2 |
2Q37 | CRYSTAL STRUCTURE OF OHCU DECARBOXYLASE IN THE PRESENCE OF (S)-ALLANTOIN | 4.1.1.97 3.5.2.17 |
2Q3F | X-RAY CRYSTAL STRUCTURE OF PUTATIVE HUMAN RAS-RELATED GTP BINDING D IN COMPLEX WITH GMPPNP | 3.6.5 |
2Q3K | CRYSTAL STRUCTURE OF LYSINE SULFONAMIDE INHIBITOR REVEALS THE DISPLACEMENT OF THE CONSERVED FLAP WATER MOLECULE IN HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2Q3N | AGGLUTININ FROM ABRUS PRECATORIUS (APA-I) | 3.2.2.22 |
2Q3S | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT5G06450 | 3.1.13.1 |
2Q3U | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT5G08170, AGMATINE IMINOHYDROLASE | 3.5.3.12 |
2Q40 | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT2G17340 | 3.1.3 |
2Q42 | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF GLYOXALASE II FROM ARABIDOPSIS THALIANA GENE AT2G31350 | 3.1.2.6 |
2Q43 | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF IAA-AMINOACID HYDROLASE FROM ARABIDOPSIS THALIANA GENE AT5G56660 | 3.5.1 |
2Q47 | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF A PUTATIVE PHOSPHOPROTEIN PHOSPHATASE FROM ARABIDOPSIS THALIANA GENE AT1G05000 | 3.1.3.48 |
2Q4D | ENSEMBLE REFINEMENT OF THE CRYSTAL STRUCTURE OF A LYSINE DECARBOXYLASE-LIKE PROTEIN FROM ARABIDOPSIS THALIANA GENE AT5G11950 | 3.2.2 |
2Q4O | ENSEMBLE REFINEMENT OF THE CRYSTAL STRUCTURE OF A LYSINE DECARBOXYLASE-LIKE PROTEIN FROM ARABIDOPSIS THALIANA GENE AT2G37210 | 3.2.2 |
2Q4P | ENSEMBLE REFINEMENT OF THE CRYSTAL STRUCTURE OF PROTEIN FROM MUS MUSCULUS MM.29898 | 3.6.1.12 |
2Q4T | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF A CYTOSOLIC 5'-NUCLEOTIDASE III FROM MUS MUSCULUS MM.158936 | 3.1.3.5 3.1.3.91 |
2Q4X | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT3G16990 | 3.5.1 3.5.99.2 |
2Q4Z | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF AN ASPARTOACYLASE FROM RATTUS NORVEGICUS | 3.5.1.15 |
2Q51 | ENSEMBLE REFINEMENT OF THE PROTEIN CRYSTAL STRUCTURE OF AN ASPARTOACYLASE FROM HOMO SAPIENS | 3.5.1.15 |
2Q5E | CRYSTAL STRUCTURE OF HUMAN CARBOXY-TERMINAL DOMAIN RNA POLYMERASE II POLYPEPTIDE A SMALL PHOSPHATASE 2 | 3.1.3.16 |
2Q5X | CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF HNUP98 | 3.4.21 |
2Q5Y | CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF HNUP98 | 3.4.21 |
2Q5Z | CRYSTAL STRUCTURE OF IMAZG FROM VIBRIO DAT 722: NTAG-IMAZG (P43212) | 3.6.1.19 |
2Q63 | HIV-1 PR MUTANT IN COMPLEX WITH NELFINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2Q64 | HIV-1 PR MUTANT IN COMPLEX WITH NELFINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2Q6D | CRYSTAL STRUCTURE OF INFECTIOUS BRONCHITIS VIRUS (IBV) MAIN PROTEASE | 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 2.1.1 |
2Q6F | CRYSTAL STRUCTURE OF INFECTIOUS BRONCHITIS VIRUS (IBV) MAIN PROTEASE IN COMPLEX WITH A MICHAEL ACCEPTOR INHIBITOR N3 | 3.4.22 |
2Q6G | CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE H41A MUTANT IN COMPLEX WITH AN N-TERMINAL SUBSTRATE | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2Q6T | CRYSTAL STRUCTURE OF THE THERMUS AQUATICUS DNAB MONOMER | 3.6.1 3.6.4.12 |
2Q73 | CRYSTAL STRUCTURE OF IMAZG FROM VIBRIO DAT 722: CTAG-IMAZG (P41212) | 3.6.1.19 |
2Q74 | MYCOBACTERIUM TUBERCULOSIS SUHB | 3.1.3.25 |
2Q7T | CRYSTAL STRUCTURE OF THE F PLASMID TRAI RELAXASE DOMAIN WITH THE SCISSILE THYMIDINE BASE | 3.6.1 5.6.2.1 3.6.4.12 |
2Q7U | CRYSTAL STRUCTURE OF THE F PLASMID TRAI RELAXASE DOMAIN WITH THE SCISSILE THYMIDINE BASE AND IMIDODIPHOSPHATE | 3.6.1 5.6.2.1 3.6.4.12 |
2Q8J | CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF BOVINE LACTOFERRIN WITH MANNITOL AND MANNOSE AT 2.7 A RESOLUTION | 3.4.21 |
2Q8M | T-LIKE FRUCTOSE-1,6-BISPHOSPHATASE FROM ESCHERICHIA COLI WITH AMP, GLUCOSE 6-PHOSPHATE, AND FRUCTOSE 1,6-BISPHOSPHATE BOUND | 3.1.3.11 |
2Q8W | CRYSTAL STRUCTURE OF PAP-S1ACI, A POKEWEED ANTIVIRAL PROTEIN FROM SEEDS OF PHYTOLACCA ACINOSA | 3.2.2.22 |
2Q92 | E. COLI METHIONINE AMINOPEPTIDASE MN-FORM WITH INHIBITOR B23 | 3.4.11.18 |
2Q93 | E. COLI METHIONINE AMINOPEPTIDASE MN-FORM WITH INHIBITOR B21 | 3.4.11.18 |
2Q94 | E. COLI METHIONINE AMINOPEPTIDASE MN-FORM WITH INHIBITOR A04 | 3.4.11.18 |
2Q95 | E. COLI METHIONINE AMINOPEPTIDASE MN-FORM WITH INHIBITOR A05 | 3.4.11.18 |
2Q96 | E. COLI METHIONINE AMINOPEPTIDASE MN-FORM WITH INHIBITOR A18 | 3.4.11.18 |
2Q9D | STRUCTURE OF SPIN-LABELED T4 LYSOZYME MUTANT A41R1 | 3.2.1.17 |
2Q9E | STRUCTURE OF SPIN-LABELED T4 LYSOZYME MUTANT S44R1 | 3.2.1.17 |
2Q9L | CRYSTAL STRUCTURE OF IMAZG FROM VIBRIO DAT 722: CTAG-IMAZG (P43212) | 3.6.1.19 |
2Q9M | 4-SUBSTITUTED TRINEMS AS BROAD SPECTRUM-LACTAMASE INHIBITORS: STRUCTURE-BASED DESIGN, SYNTHESIS AND BIOLOGICAL ACTIVITY | 3.5.2.6 |
2Q9N | 4-SUBSTITUTED TRINEMS AS BROAD SPECTRUM-LACTAMASE INHIBITORS: STRUCTURE-BASED DESIGN, SYNTHESIS AND BIOLOGICAL ACTIVITY | 3.5.2.6 |
2Q9P | HUMAN DIPHOSPHOINOSITOL POLYPHOSPHATE PHOSPHOHYDROLASE 1, MG-F COMPLEX | 3.6.1.52 3.6.1 |
2QA9 | CRYSTAL STRUCTURE OF THE SECOND TETRAHEDRAL INTERMEDIATES OF SGPB AT PH 4.2 | 3.4.21.81 |
2QAA | CRYSTAL STRUCTURE OF THE SECOND TETRAHEDRAL INTERMEDIATES OF SGPB AT PH 7.3 | 3.4.21.81 |
2QAI | CRYSTAL STRUCTURE OF THE V-TYPE ATP SYNTHASE SUBUNIT F FROM PYROCOCCUS FURIOSUS. NESG TARGET PFR7. | 3.6.3.14 |
2QAK | HIV-1 PR MUTANT IN COMPLEX WITH NELFINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QB6 | SACCHAROMYCES CEREVISIAE CYTOSOLIC EXOPOLYPHOSPHATASE, SULFATE COMPLEX | 3.6.1.11 |
2QB7 | SACCHAROMYCES CEREVISIAE CYTOSOLIC EXOPOLYPHOSPHATASE, PHOSPHATE COMPLEX | 3.6.1.11 |
2QB8 | SACCHAROMYCES CEREVISIAE CYTOSOLIC EXOPOLYPHOSPHATASE, ATP COMPLEX | 3.6.1.11 |
2QBP | CRYSTAL STRUCTURE OF PTP1B-INHIBITOR COMPLEX | 3.1.3.48 |
2QBQ | CRYSTAL STRUCTURE OF PTP1B-INHIBITOR COMPLEX | 3.1.3.48 |
2QBR | CRYSTAL STRUCTURE OF PTP1B-INHIBITOR COMPLEX | 3.1.3.48 |
2QBS | CRYSTAL STRUCTURE OF PTP1B-INHIBITOR COMPLEX | 3.1.3.48 |
2QC2 | CRYSTAL STRUCTURE OF SEVERE ACUTE RESPIRATORY SYNDROME (SARS) 3C-LIKE PROTEASE ASN214ALA MUTANT | 3.4.22 |
2QCA | A NEW CRYSTAL FORM OF BOVINE PANCREATIC RNASE A IN COMPLEX WITH 2'-DEOXYGUANOSINE-5'-MONOPHOSPHATE | 3.1.27.5 4.6.1.18 |
2QCI | HIV-1 PROTEASE MUTANT D30N WITH POTENT ANTIVIRAL INHIBITOR GRL-98065 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QCJ | NATIVE STRUCTURE OF LYP | 3.1.3.48 |
2QCX | CRYSTAL STRUCTURE OF BACILLUS SUBTILIS TENA Y112F MUTANT COMPLEXED WITH FORMYL AMINOMETHYL PYRIMIDINE | 3.5.99.2 |
2QCY | CRYSTAL STRUCTURE OF A MONOMERIC FORM OF SEVERE ACUTE RESPIRATORY SYNDROME (SARS) 3C-LIKE PROTEASE MUTANT | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2QD6 | HIV-1 PROTEASE MUTANT I50V WITH POTENT ANTIVIRAL INHIBITOR GRL-98065 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QD7 | HIV-1 PROTEASE MUTANT V82A WITH POTENT ANTIVIRAL INHIBITOR GRL-98065 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QD8 | HIV-1 PROTEASE MUTANT I84V WITH POTENT ANTIVIRAL INHIBITOR GRL-98065 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QDB | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT E75Q/D21N/T33V/T41I/S59A/P117G/S128A AT 100 K | 3.1.31.1 |
2QDC | CRYSTAL STRUCTURE OF THE HEPTP CATALYTIC DOMAIN D236A MUTANT | 3.1.3.48 |
2QDM | CRYSTAL STRUCTURE OF THE HEPTP CATALYTIC DOMAIN C270S/D236A/Q314A MUTANT | 3.1.3.48 |
2QDP | CRYSTAL STRUCTURE OF THE HEPTP CATALYTIC DOMAIN C270S MUTANT CRYSTALLIZED IN AMMONIUM ACETATE | 3.1.3.48 |
2QDS | CRYSTAL STRUCTURE OF THE ZINC CARBAPENEMASE CPHA IN COMPLEX WITH THE INHIBITOR D-CAPTOPRIL | 3.5.2.6 |
2QDT | STRUCTURAL BASIS FOR THE BROAD-SPECTRUM INHIBITION OF METALLO-{BETA}-LACTAMASES: L1- IS38 COMPLEX | 3.5.2.6 |
2QE2 | STRUCTURE OF HCV NS5B BOUND TO AN ANTHRANILIC ACID INHIBITOR | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2QE5 | STRUCTURE OF HCV NS5B BOUND TO AN ANTHRANILIC ACID INHIBITOR | 2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13 |
2QED | CRYSTAL STRUCTURE OF SALMONELLA THYPHIMURIUM LT2 GLYOXALASE II | 3.1.2.6 |
2QEP | CRYSTAL STRUCTURE OF THE D1 DOMAIN OF PTPRN2 (IA2BETA) | 3.1.3.48 3.1.3 |
2QEQ | CRYSTAL STRUCTURE OF KUNJIN VIRUS NS3 HELICASE | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2QES | CRYSTAL STRUCTURE OF THE RIBOSOME INACTIVATING PROTEIN PDL4 FROM P. DIOICA LEAVES IN COMPLEX WITH ADENINE | 3.2.2.22 |
2QET | STRUCTURE OF THE MUTANT S211A OF THE RIBOSOME INACTIVATING PROTEIN PDL4 FROM P. DIOICA IN COMPLEX WITH ADENINE | 3.2.2.22 |
2QF0 | STRUCTURE OF THE DELTA PDZ TRUNCATION OF THE DEGS PROTEASE | 3.4.21 3.4.21.107 |
2QF3 | STRUCTURE OF THE DELTA PDZ TRUNCATION OF THE DEGS PROTEASE | 3.4.21 3.4.21.107 |
2QFB | CRYSTAL STRUCTURE OF THE REGULATORY DOMAIN OF HUMAN RIG-I WITH BOUND ZN | 3.6.1 3.6.4.13 |
2QFD | CRYSTAL STRUCTURE OF THE REGULATORY DOMAIN OF HUMAN RIG-I WITH BOUND HG | 3.6.1 3.6.4.13 |
2QFE | DISTAL C2-LIKE DOMAIN OF HUMAN CALPAIN-7 | 3.4.22 |
2QFL | STRUCTURE OF SUHB: INOSITOL MONOPHOSPHATASE AND EXTRAGENIC SUPPRESSOR FROM E. COLI | 3.1.3.25 |
2QFP | CRYSTAL STRUCTURE OF RED KIDNEY BEAN PURPLE ACID PHOSPHATASE IN COMPLEX WITH FLUORIDE | 3.1.3.2 |
2QGR | STRUCTURE OF THE R178A MUTANT OF DELTA PDZ DEGS PROTEASE | 3.4.21 3.4.21.107 |
2QHA | FROM STRUCTURE TO FUNCTION: INSIGHTS INTO THE CATALYTIC SUBSTRATE SPECIFICITY AND THERMOSTABILITY DISPLAYED BY BACILLUS SUBTILIS MANNANASE BCMAN | 3.2.1.78 |
2QHC | THE INFLUENCE OF I47A MUTATION ON REDUCED SUSCEPTIBILITY TO THE PROTEASE INHIBITOR LOPINAVIR | 3.4.23.16 |
2QHD | CRYSTAL STRUCTURE OF ECARPHOLIN S (SER49-PLA2) COMPLEXED WITH FATTY ACID | 3.1.1.4 |
2QHE | CRYSTAL STRUCTURE OF SER49-PLA2 (ECARPHOLIN S) FROM ECHIS CARINATUS SOCHUREKI SNAKE VENOM | 3.1.1.4 |
2QHW | CRYSTAL STRUCTURE OF A COMPLEX OF PHOSPHOLIPASE A2 WITH A GRAMINE DERIVATIVE AT 2.2 RESOLUTION | 3.1.1.4 |
2QHY | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-1-AC86 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QHZ | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-1-AC87 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QI0 | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-1-KK80 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QI1 | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-1-KK81 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QI2 | CRYSTAL STRUCTURE OF THE THERMOPLASMA ACIDOPHILUM PELOTA PROTEIN | 3.1 |
2QI3 | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-2-AD94 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QI4 | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-2-AD93 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QI5 | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-2-KC08 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QI6 | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-2-KB98 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QI7 | CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, MIT-2-AD86 IN COMPLEX WITH WILD TYPE HIV-1 PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QIM | CRYSTAL STRUCTURE OF PATHOGENESIS-RELATED PROTEIN LLPR-10.2B FROM YELLOW LUPINE IN COMPLEX WITH CYTOKININ | 3.1.27 |
2QIN | STENOTROPHOMONAS MALTOPHILIA L1 METALLO-BETA-LACTAMASE ASP-120 CYS MUTANT | 3.5.2.6 |
2QIQ | STRUCTURE-BASED DESIGN AND SYNTHESIS AND BIOLOGICAL EVALUATION OF PEPTIDOMIMETIC SARS-3CLPRO INHIBITORS | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2QJC | CRYSTAL STRUCTURE OF A PUTATIVE DIADENOSINE TETRAPHOSPHATASE | 3.6.1.41 |
2QJE | CRYSTAL STRUCTURE OF THE COMPLEX OF BOVINE C-LOBE WITH AMYGDALIN AT 2.3A RESOLUTION | 3.4.21 |
2QJO | CRYSTAL STRUCTURE OF A BIFUNCTIONAL NMN ADENYLYLTRANSFERASE/ADP RIBOSE PYROPHOSPHATASE (NADM) COMPLEXED WITH ADPRP AND NAD FROM SYNECHOCYSTIS SP. | 2.7.7.1 3.6.1 |
2QJR | DIPEPDYL PEPTIDASE IV IN COMPLEX WITH INHIBITOR PZF | 3.4.14.5 |
2QJS | STENOTROPHOMONAS MALTOPHILIA L1 METALLO-BETA-LACTAMASE ASP-120 ASN MUTANT | 3.5.2.6 |
2QJT | CRYSTAL STRUCTURE OF A BIFUNCTIONAL NMN ADENYLYLTRANSFERASE/ADP RIBOSE PYROPHOSPHATASE COMPLEXED WITH AMP AND MN ION FROM FRANCISELLA TULARENSIS | 2.7.7.1 3.6.1 |
2QK5 | STRUCTURE OF BACE1 BOUND TO SCH626485 | 3.4.23.46 |
2QK9 | HUMAN RNASE H CATALYTIC DOMAIN MUTANT D210N IN COMPLEX WITH 18-MER RNA/DNA HYBRID | 3.1.26.4 |
2QKB | HUMAN RNASE H CATALYTIC DOMAIN MUTANT D210N IN COMPLEX WITH 20-MER RNA/DNA HYBRID | 3.1.26.4 |
2QKK | HUMAN RNASE H CATALYTIC DOMAIN MUTANT D210N IN COMPLEX WITH 14-MER RNA/DNA HYBRID | 3.1.26.4 |
2QKM | THE CRYSTAL STRUCTURE OF FISSION YEAST MRNA DECAPPING ENZYME DCP1-DCP2 COMPLEX | 3.6.1.30 |
2QKY | COMPLEX STRUCTURE OF DIPEPTIDYL PEPTIDASE IV AND A OXADIAZOLYL KETONE | 3.4.14.5 |
2QL5 | CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-DMQD-CHO | 3.4.22.60 |
2QL7 | CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-IEPD-CHO | 3.4.22.60 |
2QL9 | CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-DQMD-CHO | 3.4.22.60 |
2QLB | CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-ESMD-CHO | 3.4.22.60 |
2QLF | CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-DNLD-CHO | 3.4.22.60 |
2QLJ | CRYSTAL STRUCTURE OF CASPASE-7 WITH INHIBITOR AC-WEHD-CHO | 3.4.22.60 |
2QLP | BIFUNCTIONAL DCTP DEAMINASE:DUTPASE FROM MYCOBACTERIUM TUBERCULOSIS, APO FORM | 3.5.4.13 3.5.4.30 |
2QLT | CRYSTAL STRUCTURE OF AN ISOFORM OF DL-GLYCEROL-3-PHOSPHATASE, RHR2P, FROM SACCHAROMYCES CEREVISIAE | 3.1.3 3.1.3.21 |
2QLY | CRYSTRAL STRUCTURE OF THE N-TERMINAL SUBUNIT OF HUMAN MALTASE-GLUCOAMYLASE | 3.2.1 3.2.1.20 3.2.1.3 |
2QMD | STRUCTURE OF BACE BOUND TO SCH722924 | 3.4.23.46 |
2QME | CRYSTAL STRUCTURE OF HUMAN RAC3 IN COMPLEX WITH CRIB DOMAIN OF HUMAN P21-ACTIVATED KINASE 1 (PAK1) | 3.6.5.2 |
2QMF | STRUCTURE OF BACE BOUND TO SCH735310 | 3.4.23.46 |
2QMG | STRUCTURE OF BACE BOUND TO SCH745966 | 3.4.23.46 |
2QMJ | CRYSTRAL STRUCTURE OF THE N-TERMINAL SUBUNIT OF HUMAN MALTASE-GLUCOAMYLASE IN COMPLEX WITH ACARBOSE | 3.2.1 3.2.1.20 3.2.1.3 |
2QMK | HUMAN PANCREATIC ALPHA-AMYLASE COMPLEXED WITH NITRITE | 3.2.1.1 |
2QMP | CRYSTAL STRUCTURE OF HIV-1 PROTEASE COMPLEXED WITH PL-100 | 3.4.23.16 |
2QMU | STRUCTURE OF AN ARCHAEAL HETEROTRIMERIC INITIATION FACTOR 2 REVEALS A NUCLEOTIDE STATE BETWEEN THE GTP AND THE GDP STATES | 3.6.5.3 |
2QN0 | STRUCTURE OF BOTULINUM NEUROTOXIN SEROTYPE C1 LIGHT CHAIN PROTEASE | 3.4.24.69 |
2QN6 | STRUCTURE OF AN ARCHAEAL HETEROTRIMERIC INITIATION FACTOR 2 REVEALS A NUCLEOTIDE STATE BETWEEN THE GTP AND THE GDP STATES | 3.6.5.3 |
2QNC | CRYSTAL STRUCTURE OF T4 ENDONUCLEASE VII N62D MUTANT IN COMPLEX WITH A DNA HOLLIDAY JUNCTION | 3.1.22.4 3.1 |
2QNF | CRYSTAL STRUCTURE OF T4 ENDONUCLEASE VII H43N MUTANT IN COMPLEX WITH HETERODUPLEX DNA CONTAINING BASE MISMATCHES | 3.1.22.4 3.1 |
2QNN | HIV-1 PROTEASE IN COMPLEX WITH A MULTIPLE DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QNO | CRYSTAL STRUCTURE OF THE MUTANT E55Q OF THE CELLULASE CEL48F IN COMPLEX WITH A THIO-OLIGOSACCHARIDE | 3.2.1.4 |
2QNP | HIV-1 PROTEASE IN COMPLEX WITH A IODO DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QNQ | HIV-1 PROTEASE IN COMPLEX WITH A CHLORO DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2QOE | HUMAN DIPEPTIDYL PEPTIDASE IV IN COMPLEX WITH A TRIAZOLOPIPERAZINE-BASED BETA AMINO ACID INHIBITOR | 3.4.14.5 |
2QOG | CROTOXIN B, THE BASIC PLA2 FROM CROTALUS DURISSUS TERRIFICUS. | 3.1.1.4 |
2QOM | THE CRYSTAL STRUCTURE OF THE E.COLI ESPP AUTOTRANSPORTER BETA-DOMAIN. | 3.4.21 |
2QP8 | STRUCTURE OF BACE BOUND TO SCH734723 | 3.4.23.46 |
2QPJ | HUMAN NEP COMPLEXED WITH A BIFUNCTIONAL NEP/DPP IV INHIBITOR | 3.4.24.11 |
2QPN | GES-1 BETA-LACTAMASE | 3.5.2.6 |
2QPS | SUGAR TONGS" MUTANT Y380A IN COMPLEX WITH ACARBOSE" | 3.2.1.1 |
2QPU | SUGAR TONGS MUTANT S378P IN COMPLEX WITH ACARBOSE | 3.2.1.1 |
2QQ2 | CRYSTAL STRUCTURE OF C-TERMINAL DOMAIN OF HUMAN ACYL-COA THIOESTERASE 7 | 3.1.2.2 |
2QQF | HST2 BOUND TO ADP-HPD AND ACETYLATED HISTONE H4 | 3.5.1 2.3.1.286 |
2QQG | HST2 BOUND TO ADP-HPD, ACETYLLATED HISTONE H4 AND NICOTINAMIDE | 3.5.1 2.3.1.286 |
2QQU | CRYSTAL STRUCTURE OF A CELL-WALL INVERTASE (D239A) FROM ARABIDOPSIS THALIANA IN COMPLEX WITH SUCROSE | 3.2.1.26 |
2QQV | CRYSTAL STRUCTURE OF A CELL-WALL INVERTASE (E203A) FROM ARABIDOPSIS THALIANA IN COMPLEX WITH SUCROSE | 3.2.1.26 |
2QQW | CRYSTAL STRUCTURE OF A CELL-WALL INVERTASE (D23A) FROM ARABIDOPSIS THALIANA IN COMPLEX WITH SUCROSE | 3.2.1.26 |
2QR5 | AEROPYRUM PERNIX ACYLAMINOACYL PEPTIDASE, H367A MUTANT | 3.4.19.1 |
2QRR | CRYSTAL STRUCTURE OF THE SOLUBLE DOMAIN OF THE ABC TRANSPORTER, ATP-BINDING PROTEIN FROM VIBRIO PARAHAEMOLYTICUS | 3.6.3 7.4.2.11 |
2QRZ | CDC42 BOUND TO GMP-PCP: INDUCED FIT BY EFFECTOR IS REQUIRED | 3.6.5.2 |
2QS9 | CRYSTAL STRUCTURE OF THE HUMAN RETINOBLASTOMA-BINDING PROTEIN 9 (RBBP-9). NESG TARGET HR2978 | 3 |
2QSR | CRYSTAL STRUCTURE OF C-TERMINAL DOMAIN OF TRANSCRIPTION-REPAIR COUPLING FACTOR | 3.6.4 |
2QSU | STRUCTURE OF ARABIDOPSIS THALIANA 5'-METHYLTHIOADENOSINE NUCLEOSIDASE IN APO FORM | 3.2.2.16 |
2QSW | CRYSTAL STRUCTURE OF C-TERMINAL DOMAIN OF ABC TRANSPORTER / ATP-BINDING PROTEIN FROM ENTEROCOCCUS FAECALIS | 3.6.3 7.4.2.11 |
2QT3 | CRYSTAL STRUCTURE OF N-ISOPROPYLAMMELIDE ISOPROPYLAMINOHYDROLASE ATZC FROM PSEUDOMONAS SP. STRAIN ADP COMPLEXED WITH ZN | 3.5.99.4 3.5.4.42 |
2QT7 | CRYSTALLOGRAPHIC STRUCTURE OF THE MATURE ECTODOMAIN OF THE HUMAN RECEPTOR-TYPE PROTEIN-TYROSINE PHOSPHATASE IA-2 AT 1.30 ANGSTROMS | 3.1.3.48 |
2QT9 | HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 IN COMPLEX WITH A 4-ARYL CYCLOHEXYLALANINE INHIBITOR | 3.4.14.5 |
2QTB | HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 IN COMPLEX WITH A 4-ARYL CYCLOHEXYLALANINE INHIBITOR | 3.4.14.5 |
2QTG | CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA 5'-METHYLTHIOADENOSINE NUCLEOSIDASE IN COMPLEX WITH 5'-METHYLTHIOTUBERCIDIN | 3.2.2.16 |
2QTT | CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA 5'-METHYLTHIOADENOSINE NUCLEOSIDASE IN COMPLEX WITH FORMYCIN A | 3.2.2.16 |
2QTW | THE CRYSTAL STRUCTURE OF PCSK9 AT 1.9 ANGSTROMS RESOLUTION REVEALS STRUCTURAL HOMOLOGY TO RESISTIN WITHIN THE C-TERMINAL DOMAIN | 3.4.21 |
2QTY | CRYSTAL STRUCTURE OF MOUSE ADP-RIBOSYLHYDROLASE 3 (MARH3) | 3.2.1.143 3.5.1 3.2.2 |
2QU2 | BACE1 WITH COMPOUND 1 | 3.4.23.46 |
2QU3 | BACE1 WITH COMPOUND 2 | 3.4.23.46 |
2QU9 | CRYSTAL STRUCTURE OF THE COMPLEX OF GROUP II PHOSPHOLIPASE A2 WITH EUGENOL | 3.1.1.4 |
2QUA | CRYSTAL STRUCTURE OF LIPA FROM SERRATIA MARCESCENS | 3.1.1.3 |
2QUE | SATURATION OF SUBSTRATE-BINDING SITE USING TWO NATURAL LIGANDS: CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF PHOSPHOLIPASE A2 WITH ANISIC ACID AND AJMALINE AT 2.25 A RESOLUTION | 3.1.1.4 |
2QUY | TRUNCATED MUTANT ASN175ALA OF PENICILLIN V ACYLASE FROM BACILLUS SPHAERICUS | 3.5.1.11 |
2QUZ | CRYSTAL STRUCTURE OF THE ACTIVATING H-RASK117R MUTANT IN COSTELLO SYNDROME, BOUND TO MG-GDP | 3.6.5.2 |
2QV2 | A ROLE OF THE LOWE SYNDROME PROTEIN OCRL IN EARLY STEPS OF THE ENDOCYTIC PATHWAY | 3.1.3.36 3.1.3.56 3.1.3.86 |
2QV4 | HUMAN PANCREATIC ALPHA-AMYLASE COMPLEXED WITH NITRITE AND ACARBOSE | 3.2.1.1 |
2QV6 | GTP CYCLOHYDROLASE III FROM M. JANNASCHII (MJ0145) COMPLEXED WITH GTP AND METAL IONS | 3.5.4.29 |
2QVB | CRYSTAL STRUCTURE OF HALOALKANE DEHALOGENASE RV2579 FROM MYCOBACTERIUM TUBERCULOSIS | 3.8.1.5 |
2QVD | IDENTIFICATION OF A POTENT ANTI-INFLAMMATORY AGENT FROM THE NATURAL EXTRACT OF PLANT CARDIOSPERMUN HELICACABUM: CRYSTAL STRUCTURE OF THE COMPLEX OF PHOSPHOLIPASE A2 WITH BENZO(G)-1,3-BENZODIOXOLO(5,6-A)QUINOLIZINIUM, 5,6-DIHYDRO-9,10-DIMETHOXY AT 1.93 A RESOLUTION | 3.1.1.4 |
2QVN | CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE FROM PLASMODIUM VIVAX IN COMPLEX WITH GUANOSINE | 3.5.4.4 |
2QVR | E. COLI FRUCTOSE-1,6-BISPHOSPHATASE: CITRATE, FRU-2,6-P2, AND MG2+ BOUND | 3.1.3.11 |
2QVU | PORCINE LIVER FRUCTOSE-1,6-BISPHOSPHATASE COCRYSTALLIZED WITH FRU-2,6-P2 AND MG2+, I(T)-STATE | 3.1.3.11 |
2QVV | PORCINE LIVER FRUCTOSE-1,6-BISPHOSPHATASE COCRYSTALLIZED WITH FRU-2,6-P2 AND ZN2+, I(T)-STATE | 3.1.3.11 |
2QWA | THE X-RAY STRUCTURE OF A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWB | THE X-RAY STRUCTURE OF A COMPLEX OF SIALIC ACID AND A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWC | THE X-RAY STRUCTURE OF A COMPLEX OF NEU5AC2EN AND A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWD | THE X-RAY STRUCTURE OF A COMPLEX OF 4-AMINO-NEU5AC2EN AND A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWE | THE X-RAY STRUCTURE OF A COMPLEX OF 4-GUANIDINO-NEU5AC2EN AND A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWF | THE X-RAY STRUCTURE OF A COMPLEX OF N-ACETYL-4-GUANIDINO-6-METHYL(PROPYL)CARBOXAMIDE-4,5-DIHYDRO-2H-PYRAN-2-CARBOXYLIC ACID AND A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWG | THE X-RAY STRUCTURE OF A COMPLEX OF 5-N-ACETYL-4-AMINO-6-DIETHYLCARBOXAMIDE-4,5-DIHYDRO-2H-PYRAN-2-CARBOXYLIC ACID AND A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWH | THE X-RAY STRUCTURE OF A COMPLEX OF 5-N-ACETYL-5-AMINO-3-(1-ETHYLPROPOXY)-1-CYCLOHEXENE-1-CARBOXYLIC ACID (GS4071) AND A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWI | THE X-RAY STRUCTURE OF A COMPLEX OF N-ACETYL-4-GUANIDINO-6-METHYL(PROPYL)CARBOXAMIDE-4,5-DIHYDRO-2H-PYRAN-2-CARBOXYLIC ACID AND WILDTYPE TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWJ | THE X-RAY STRUCTURE OF A COMPLEX OF 5-N-ACETYL-4-AMINO-6-DIETHYLCARBOXAMIDE-4,5-DIHYDRO-2H-PYRAN-2-CARBOXYLIC ACID AND A DRUG RESISTANT VARIANT R292K OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QWK | THE X-RAY STRUCTURE OF A COMPLEX OF 5-N-ACETYL-5-AMINO-3-(1-ETHYLPROPOXY)-1-CYCLOHEXENE-1-CARBOXYLIC ACID (GS4071) AND WILDTYPE TERN N9 INFLUENZA VIRUS NEURAMINIDASE | 3.2.1.18 |
2QXF | PRODUCT BOUND STRUCTURE OF EXONUCLEASE I AT 1.5 ANGSTROM RESOLUTION | 3.1.11.1 |
2QXG | CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 7 IN COMPLEX WITH ALA-ALA-PHE-CHLOROMETHYLKETONE | 3.4.21.117 |
2QXH | CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 7 IN COMPLEX WITH SUC-ALA-ALA-PRO-PHE-CHLOROMETHYLKETONE | 3.4.21.117 |
2QXI | HIGH RESOLUTION STRUCTURE OF HUMAN KALLIKREIN 7 IN COMPLEX WITH SUC-ALA-ALA-PRO-PHE-CHLOROMETHYLKETONE | 3.4.21.117 |
2QXJ | CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 7 IN COMPLEX WITH SUC-ALA-ALA-PRO-PHE-CHLOROMETHYLKETONE AND COPPER | 3.4.21.117 |
2QXT | CRYSTAL STRUCTURE ANALYSIS OF THE BACILLUS SUBTILIS LIPASE CRYSTALLIZED AT PH 4.5 | 3.1.1.3 |
2QXU | CRYSTAL STRUCTURE ANALYSIS OF THE BACILLUS SUBTILIS LIPASE CRYSTALLIZED AT PH 5.0 | 3.1.1.3 |
2QXX | BIFUNCTIONAL DCTP DEAMINASE: DUTPASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH DTTP | 3.5.4.13 3.5.4.30 |
2QY0 | ACTIVE DIMERIC STRUCTURE OF THE CATALYTIC DOMAIN OF C1R REVEALS ENZYME-PRODUCT LIKE CONTACTS | 3.4.21.41 |
2QY2 | CHARACTERIZATION OF A TRIFUNCTIONAL MIMIVIRUS MRNA CAPPING ENZYME AND CRYSTAL STRUCTURE OF THE RNA TRIPHOSPHATASE DOMAINM. | 3.1.3.33 2.7.7.50 2.1.1.56 |
2QYI | CRYSTAL STRUCTURE OF A BINARY COMPLEX BETWEEN AN ENGINEERED TRYPSIN INHIBITOR AND BOVINE TRYPSIN | 3.4.21.4 |
2QYK | CRYSTAL STRUCTURE OF PDE4A10 IN COMPLEX WITH INHIBITOR NPV | 3.1.4.53 |
2QYL | CRYSTAL STRUCTURE OF PDE4B2B IN COMPLEX WITH INHIBITOR NPV | 3.1.4.53 |
2QYM | CRYSTAL STRUCTURE OF UNLIGANDED PDE4C2 | 3.1.4.53 |
2QYN | CRYSTAL STRUCTURE OF PDE4D2 IN COMPLEX WITH INHIBITOR NPV | 3.1.4.17 3.1.4.53 |
2QYV | CRYSTAL STRUCTURE OF PUTATIVE XAA-HIS DIPEPTIDASE (YP_718209.1) FROM HAEMOPHILUS SOMNUS 129PT AT 2.11 A RESOLUTION | 3.4.13.20 |
2QZ2 | CRYSTAL STRUCTURE OF A GLYCOSIDE HYDROLASE FAMILY 11 XYLANASE FROM ASPERGILLUS NIGER IN COMPLEX WITH XYLOPENTAOSE | 3.2.1.8 |
2QZ3 | CRYSTAL STRUCTURE OF A GLYCOSIDE HYDROLASE FAMILY 11 XYLANASE FROM BACILLUS SUBTILIS IN COMPLEX WITH XYLOTETRAOSE | 3.2.1.8 |
2QZ4 | HUMAN PARAPLEGIN, AAA DOMAIN IN COMPLEX WITH ADP | 3.4.24 |
2QZ6 | FIRST CRYSTAL STRUCTURE OF A PSYCHROPHILE CLASS C BETA-LACTAMASE | 3.5.2.6 |
2QZE | MONOCLINIC MIMIVIRUS CAPPING ENZYME TRIPHOSPHATASE. | 3.1.3.33 2.7.7.50 2.1.1.56 |
2QZK | CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH I21 | 3.4.23.46 |
2QZL | CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH IXS | 3.4.23.46 |
2QZP | CRYSTAL STRUCTURE OF MUTATION OF AN ACYLPTIDE HYDROLASE/ESTERASE FROM AEROPYRUM PERNIX K1 | 3.4.19.1 |
2QZW | SECRETED ASPARTIC PROTEINASE (SAP) 1 FROM CANDIDA ALBICANS | 3.4.23.24 |
2QZX | SECRETED ASPARTIC PROTEINASE (SAP) 5 FROM CANDIDA ALBICANS | 3.4.23.24 |
2R04 | STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2R06 | STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2R07 | STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2R0K | PROTEASE DOMAIN OF HGFA WITH INHIBITOR FAB58 | 3.4.21 |
2R0L | SHORT FORM HGFA WITH INHIBITORY FAB75 | 3.4.21 |
2R11 | CRYSTAL STRUCTURE OF PUTATIVE HYDROLASE (2632844) FROM BACILLUS SUBTILIS AT 1.96 A RESOLUTION | 3.1.1.1 |
2R18 | STRUCTURAL INSIGHTS INTO THE MULTIFUNCTIONAL PROTEIN VP3 OF BIRNAVIRUSES | 3.4.21 |
2R1K | OPDA FROM AGROBACTERIUM RADIOBACTER WITH BOUND DIETHYL PHOSPHATE FROM CRYSTAL SOAKING WITH THE COMPOUND- 1.9 A | 3.1.8.1 |
2R1L | OPDA FROM AGROBACTERIUM RADIOBACTER WITH BOUND DIETHYL THIOPHOSPHATE FROM CRYSTAL SOAKING WITH THE COMPOUND- 1.95 A | 3.1.8.1 |
2R1M | OPDA FROM AGROBACTERIUM RADIOBACTER WITH BOUND PRODUCT DIETHYL PHOSPHATE FROM CRYSTAL SOAKING WITH DIETHYL 4-METHOXYPHENYL PHOSPHATE (450H)- 2.5 A | 3.1.8.1 |
2R1N | OPDA FROM AGROBACTERIUM RADIOBACTER WITH BOUND SLOW SUBSTRATE DIETHYL 4-METHOXYPHENYL PHOSPHATE (20H)- 1.7 A | 3.1.8.1 |
2R1P | OPDA FROM AGROBACTERIUM RADIOBACTER WITH BOUND PRODUCT DIETHYL THIOPHOSPHATE FROM CO-CRYSTALLISATION WITH TETRAETHYL DITHIOPYROPHOSPHATE- 1.8 A | 3.1.8.1 |
2R1T | DOPAMINE QUINONE CONJUGATION TO DJ-1 | 3.1.2 3.5.1 3.5.1.124 |
2R1U | DJ-1 ACTIVATION BY CATECHOL QUINONE MODIFICATION | 3.1.2 3.5.1 3.5.1.124 |
2R1V | NOREPINEPHRINE QUINONE CONJUGATION TO DJ-1 | 3.1.2 3.5.1 3.5.1.124 |
2R29 | NEUTRALIZATION OF DENGUE VIRUS BY A SEROTYPE CROSS-REACTIVE ANTIBODY ELUCIDATED BY CRYOELECTRON MICROSCOPY AND X-RAY CRYSTALLOGRAPHY | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2R2D | STRUCTURE OF A QUORUM-QUENCHING LACTONASE (AIIB) FROM AGROBACTERIUM TUMEFACIENS | 3.1.1.81 |
2R2M | 2-(2-CHLORO-6-FLUOROPHENYL)ACETAMIDES AS POTENT THROMBIN INHIBITORS | 3.4.21.5 |
2R2R | D(ATTAGTTATAACTAAT) COMPLEXED WITH MMLV RT CATALYTIC FRAGMENT | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2R2S | CO(III)BLEOMYCINB2 BOUND TO D(ATTAGTTATAACTAAT) COMPLEXED WITH MMLV RT CATALYTIC FRAGMENT | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2R2T | D(ATTTAGTTAACTAAAT) COMPLEXED WITH MMLV RT CATALYTIC FRAGMENT | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2R2U | CO(III)BLEOMYCINB2 BITHIAZOLE/C-TERMINAL TAIL DOMAIN BOUND TO D(ATTTAGTTAACTAAAT) COMPLEXED WITH MMLV RT CATALYTIC FRAGMENT | 2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1 |
2R2W | UROKINASE PLASMINOGEN ACTIVATOR B-CHAIN-GPPE COMPLEX | 3.4.21.73 |
2R2X | RICIN A-CHAIN (RECOMBINANT) COMPLEX WITH UREA | 3.2.2.22 |
2R38 | I84V HIV-1 PROTEASE MUTANT IN COMPLEX WITH A CARBAMOYL DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2R3D | RICIN A-CHAIN (RECOMBINANT) COMPLEX WITH ACETAMIDE | 3.2.2.22 |
2R3T | I50V HIV-1 PROTEASE MUTANT IN COMPLEX WITH A CARBAMOYL DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2R3U | CRYSTAL STRUCTURE OF THE PDZ DELETION MUTANT OF DEGS | 3.4.21 3.4.21.107 |
2R3W | I84V HIV-1 PROTEASE IN COMPLEX WITH A AMINO DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2R3Y | CRYSTAL STRUCTURE OF THE DEGS PROTEASE IN COMPLEX WITH THE YWF ACTIVATING PEPTIDE | 3.4.21 3.4.21.107 |
2R43 | I50V HIV-1 PROTEASE IN COMPLEX WITH AN AMINO DECORATED PYRROLIDINE-BASED INHIBITOR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2R49 | MUTATIONAL AND STRUCTURAL STUDIES OF E85I REVEAL THE FLEXIBLE LOOPS OF FIBROBACTER SUCCINOGENES 1,3-1,4-BETA-D-GLUCANASEGLUCANASE | 3.2.1.73 |
2R59 | LEUKOTRIENE A4 HYDROLASE COMPLEXED WITH INHIBITOR RB3041 | 3.3.2.6 3.4.11.4 |
2R5O | CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF WZT | 3.6.3.40 |
2R5P | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 SUBTYPE C PROTEASE COMPLEXED WITH INDINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2R5Q | CRYSTAL STRUCTURE ANALYSIS OF HIV-1 SUBTYPE C PROTEASE COMPLEXED WITH NELFINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2R5R | THE CRYSTAL STRUCTURE OF DUF198 FROM NITROSOMONAS EUROPAEA ATCC 19718 | 3.5.4.16 |
2R5U | CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF DNAB HELICASE FROM MYCOBACTERIUM TUBERCULOSIS | 3.6.1 3.6.4.12 3.1 |
2R5W | CRYSTAL STRUCTURE OF A BIFUNCTIONAL NMN ADENYLYLTRANSFERASE/ADP RIBOSE PYROPHOSPHATASE FROM FRANCISELLA TULARENSIS | 2.7.7.1 3.6.1 |
2R62 | CRYSTAL STRUCTURE OF HELICOBACTER PYLORI ATP DEPENDENT PROTEASE, FTSH | 3.4.24 |
2R65 | CRYSTAL STRUCTURE OF HELICOBACTER PYLORI ATP DEPENDENT PROTEASE, FTSH ADP COMPLEX | 3.4.24 |
2R69 | CRYSTAL STRUCTURE OF FAB 1A1D-2 COMPLEXED WITH E-DIII OF DENGUE VIRUS AT 3.8 ANGSTROM RESOLUTION | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2R6A | CRYSTAL FORM BH1 | 3.6.4.12 |
2R6E | CRYSTAL FORM B2 | 3.6.4.12 |
2R6G | THE CRYSTAL STRUCTURE OF THE E. COLI MALTOSE TRANSPORTER | 3.6.3.19 7.5.2.1 |
2R6N | CRYSTAL STRUCTURE OF A PYRROLOPYRIMIDINE INHIBITOR IN COMPLEX WITH HUMAN CATHEPSIN K | 3.4.22.38 |
2R71 | CRYSTAL STRUCTURE OF THE COMPLEX OF BOVINE C-LOBE WITH INOSITOL AT 2.1A RESOLUTION | 3.4.21 |
2R7C | CRYSTALLOGRAPHIC AND BIOCHEMICAL ANALYSIS OF ROTAVIRUS NSP2 WITH NUCLEOTIDES REVEALS AN NDP KINASE LIKE ACTIVITY | 3.6.4 |
2R7J | CRYSTAL STRUCTURE OF ROTAVIRUS NON STRUCTURAL PROTEIN NSP2 WITH H225A MUTATION | 3.6.4 |
2R7P | CRYSTAL STRUCTURE OF H225A NSP2 AND AMPPNP COMPLEX | 3.6.4 |
2R7Y | SELENIUM DERIVATIZED RNA/DNA HYBRID IN COMPLEX WITH RNASE H CATALYTIC DOMAIN MUTANT D132N | 3.1.26.4 |
2R8E | CRYSTAL STRUCTURE OF YRBI FROM ESCHERICHIA COLI IN COMPLEX WITH MG | 3.1.3.45 |
2R8F | CRYSTAL STRUCTURE OF H225A NSP2 AND ATP-GS COMPLEX | 3.6.4 |
2R8N | STRUCTURAL ANALYSIS OF THE UNBOUND FORM OF HIV-1 SUBTYPE C PROTEASE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2R8Q | STRUCTURE OF LMJPDEB1 IN COMPLEX WITH IBMX | 3.1.4.17 3.1.4 |
2R8T | CRYSTAL STRUCTURE OF THE FRUCTOSE 1,6-BISPHOSPHATASE GLPX FROM E.COLI IN THE COMPLEX WITH FRUCTOSE 1,6-BISPHOSPHATE | 3.1.3.11 |
2R8X | CRYSTAL STRUCTURE OF YRBI PHOSPHATASE FROM ESCHERICHIA COLI | 3.1.3.45 |
2R9B | STRUCTURAL ANALYSIS OF PLASMEPSIN 2 FROM PLASMODIUM FALCIPARUM COMPLEXED WITH A PEPTIDE-BASED INHIBITOR | 3.4.23.39 |
2R9C | CALPAIN 1 PROTEOLYTIC CORE INACTIVATED BY ZLAK-3001, AN ALPHA-KETOAMIDE | 3.4.22.52 |
2R9F | CALPAIN 1 PROTEOLYTIC CORE INACTIVATED BY ZLAK-3002, AN ALPHA-KETOAMIDE | 3.4.22.52 |
2R9J | LIGAND RECOGNITION IN C-LOBE: THE CRYSTAL STRUCTURE OF THE COMPLEX OF LACTOFERRIN C-LOBE WITH NICOTINAMIDE AT 2.5 A RESOLUTION | 3.4.21 |
2R9K | CRYSTAL STRUCTURE OF MISTELTOE LECTIN I IN COMPLEX WITH PHLORETAMIDE | 3.2.2.22 |
2R9M | CATHEPSIN S COMPLEXED WITH COMPOUND 15 | 3.4.22.27 |
2R9N | CATHEPSIN S COMPLEXED WITH COMPOUND 26 | 3.4.22.27 |
2R9O | CATHEPSIN S COMPLEXED WITH COMPOUND 8 | 3.4.22.27 |
2R9P | HUMAN MESOTRYPSIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR(BPTI) | 3.4.21.4 |
2R9V | CRYSTAL STRUCTURE OF ATP SYNTHASE SUBUNIT ALPHA (TM1612) FROM THERMOTOGA MARITIMA AT 2.10 A RESOLUTION | 3.6.3.14 7.1.2.2 |
2R9W | AMPC BETA-LACTAMASE WITH BOUND PHTHALAMIDE INHIBITOR | 3.5.2.6 |
2R9X | AMPC BETA-LACTAMASE WITH BOUND PHTHALAMIDE INHIBITOR | 3.5.2.6 |
2RA0 | X-RAY STRUCTURE OF FXA IN COMPLEX WITH 7-FLUOROINDAZOLE | 3.4.21.6 |
2RA3 | HUMAN CATIONIC TRYPSIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR (BPTI) | 3.4.21.4 |
2RAP | THE SMALL G PROTEIN RAP2A IN COMPLEX WITH GTP | 3.6.5.2 |
2RAT | EFFECTS OF TEMPERATURE ON PROTEIN STRUCTURE AND DYNAMICS: X-RAY CRYSTALLOGRAPHIC STUDIES OF THE PROTEIN RIBONUCLEASE-A AT NINE DIFFERENT TEMPERATURES FROM 98 TO 320 K | 3.1.27.5 4.6.1.18 |
2RAY | BETA-CHLOROPHENETOLE IN COMPLEX WITH T4 LYSOZYME L99A | 3.2.1.17 |
2RAZ | 4-(METHYLTHIO)NITROBENZENE IN COMPLEX WITH T4 LYSOZYME L99A | 3.2.1.17 |
2RB0 | 2,6-DIFLUOROBENZYLBROMIDE COMPLEX WITH T4 LYSOZYME L99A | 3.2.1.17 |
2RB1 | 2-ETHOXYPHENOL IN COMPLEX WITH T4 LYSOZYME L99A | 3.2.1.17 |
2RB2 | 3-METHYLBENZYLAZIDE IN COMPLEX WITH T4 LYSOZYME L99A | 3.2.1.17 |
2RB4 | CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF HUMAN DDX25 RNA HELICASE | 3.6.1 3.6.4.13 |
2RBA | STRUCTURE OF HUMAN THYMINE DNA GLYCOSYLASE BOUND TO ABASIC AND UNDAMAGED DNA | 3.2.2 3.2.2.29 |
2RBI | STRUCTURE OF BINASE MUTANT HIS 101 ASN | 3.1.27 |
2RBM | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS I72K AT CRYOGENIC TEMPERATURE | 3.1.31.1 |
2RBN | N-PHENYLGLYCINONITRILE IN COMPLEX WITH T4 LYSOZYME L99A/M102Q | 3.2.1.17 |
2RBO | 2-NITROTHIOPHENE IN COMPLEX WITH T4 LYSOZYME L99A/M102Q | 3.2.1.17 |
2RBP | 2-(N-PROPYLTHIO)ETHANOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q | 3.2.1.17 |
2RBQ | 3-METHYLBENZYLAZIDE IN COMPLEX WITH T4 L99A/M102Q | 3.2.1.17 |
2RBR | 2-PHENOXYETHANOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q | 3.2.1.17 |
2RBS | (R)(+)-3-CHLORO-1-PHENYL-1-PROPANOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q | 3.2.1.17 |
2RCE | DFP MODIFIED DEGS DELTA PDZ | 3.4.21 3.4.21.107 |
2RCN | CRYSTAL STRUCTURE OF THE RIBOSOMAL INTERACTING GTPASE YJEQ FROM THE ENTEROBACTERIAL SPECIES SALMONELLA TYPHIMURIUM. | 3.6.1 |
2RCX | AMPC BETA-LACTAMASE IN COMPLEX WITH (1R)-1-(2-THIOPHEN-2-YL-ACETYLAMINO)-1-(3-(2-CARBOXYVINYL)-PHENYL) METHYLBORONIC ACID | 3.5.2.6 |
2RD3 | CRYSTAL STRUCTURE OF TENA HOMOLOGUE (HP1287) FROM HELICOBACTER PYLORI | 3.5.99.2 |
2RD4 | DESIGN OF SPECIFIC INHIBITORS OF PHOSPHOLIPASE A2: CRYSTAL STRUCTURE OF THE COMPLEX OF PHOSPHOLIPASE A2 WITH PENTAPEPTIDE LEU-VAL-PHE-PHE-ALA AT 2.9 A RESOLUTION | 3.1.1.4 |
2RDF | CRYSTAL STRUCTURE OF STAPHYLOCCOCAL NUCLEASE VIAGAN/E75A VARIANT AT CRYOGENIC TEMPERATURE | 3.1.31.1 |
2REN | STRUCTURE OF RECOMBINANT HUMAN RENIN, A TARGET FOR CARDIOVASCULAR-ACTIVE DRUGS, AT 2.5 ANGSTROMS RESOLUTION | 3.4.23.15 |
2REU | CRYSTAL STRUCTURE OF THE C-TERMINAL OF SAU3AI FRAGMENT | 3.1.21.4 |
2RF2 | HIV REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR 7E (NNRTI) | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2RF6 | CRYSTAL STRUCTURE OF THE VACCINIA VIRUS DUAL-SPECIFICITY PHOSPHATASE VH1 | 3.1.3.48 3.1.3.16 3.1.3 |
2RF8 | CRYSTAL STRUCTURE OF THE MUTANT C2A CONJUGATED BILE ACID HYDROLASE FROM CLOSTRIDIUM PERFRINGENS | 3.5.1.24 3.5.1 |
2RFH | CRYSTAL STRUCTURE ANALYSIS OF CPA-2-BENZYL-3-NITROPROPANOIC ACID COMPLEX | 3.4.17.1 |
2RFL | CRYSTAL STRUCTURE OF THE PUTATIVE PHOSPHOHISTIDINE PHOSPHATASE SIXA FROM AGROBACTERIUM TUMEFACIENS | 5.4.2.1 3.1.3.13 5.4.2.4 |
2RFW | CRYSTAL STRUCTURE OF CELLOBIOHYDROLASE FROM MELANOCARPUS ALBOMYCES | 3.2.1.91 3.2.1 |
2RFY | CRYSTAL STRUCTURE OF CELLOBIOHYDROLASE FROM MELANOCARPUS ALBOMYCES COMPLEXED WITH CELLOBIOSE | 3.2.1.91 3.2.1 |
2RFZ | CRYSTAL STRUCTURE OF CELLOBIOHYDROLASE FROM MELANOCARPUS ALBOMYCES COMPLEXED WITH CELLOTRIOSE | 3.2.1.91 3.2.1 |
2RG0 | CRYSTAL STRUCTURE OF CELLOBIOHYDROLASE FROM MELANOCARPUS ALBOMYCES COMPLEXED WITH CELLOTETRAOSE | 3.2.1.91 3.2.1 |
2RG2 | CRYSTAL STRUCTURE OF VARIANT R18L OF CONJUGATED BILE ACID HYDROLASE FROM CLOSTRIDIUM PERFRINGENS | 3.5.1.24 3.5.1 |
2RG3 | COVALENT COMPLEX STRUCTURE OF ELASTASE | 3.4.21.37 |
2RG9 | CRYSTAL STRUCTURE OF VISCUM ALBUM MISTLETOE LECTIN I IN NATIVE STATE AT 1.95 A RESOLUTION, COMPARISON OF STRUCTURE ACTIVE SITE CONFORMATION IN RICIN AND IN VISCUMIN | 3.2.2.22 |
2RGA | CRYSTAL STRUCTURE OF H-RASQ61I-GPPNHP | 3.6.5.2 |
2RGB | CRYSTAL STRUCTURE OF H-RASQ61K-GPPNHP | 3.6.5.2 |
2RGC | CRYSTAL STRUCTURE OF H-RASQ61V-GPPNHP | 3.6.5.2 |
2RGD | CRYSTAL STRUCTURE OF H-RASQ61L-GPPNHP | 3.6.5.2 |
2RGE | CRYSTAL STRUCTURE OF H-RAS-GPPNHP | 3.6.5.2 |
2RGG | CRYSTAL STRUCTURE OF H-RASQ61I-GPPNHP, TRIGONAL CRYSTAL FORM | 3.6.5.2 |
2RGL | RICE BGLU1 BETA-GLUCOSIDASE, A PLANT EXOGLUCANASE/BETA-GLUCOSIDASE | 3.2.1.21 |
2RGM | RICE BGLU1 BETA-GLUCOSIDASE, A PLANT EXOGLUCANASE/BETA-GLUCOSIDASE | 3.2.1.21 |
2RGU | CRYSTAL STRUCTURE OF COMPLEX OF HUMAN DPP4 AND INHIBITOR | 3.4.14.5 |
2RH1 | HIGH RESOLUTION CRYSTAL STRUCTURE OF HUMAN B2-ADRENERGIC G PROTEIN-COUPLED RECEPTOR. | 3.2.1.17 |
2RH6 | STRUCTURE OF XAC NPP FOR EVALUATION OF REFINEMENT METHODOLOGY | 3.6.1.9 |
2RHB | CRYSTAL STRUCTURE OF NSP15-H234A MUTANT- HEXAMER IN ASYMMETRIC UNIT | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2RHF | D. RADIODURANS RECQ HRDC DOMAIN 3 | 3.6.4.12 |
2RHT | CRYSTAL STRUCTURE OF THE S112A MUTANT OF A C-C HYDROLASE, BPHD FROM BURKHOLDERIA XENOVORANS LB400, IN COMPLEX WITH 3-CL HOPDA | 3.7.1 3.7.1.8 |
2RHW | CRYSTAL STRUCTURE OF THE S112A MUTANT OF A C-C HYDROLASE, BPHD FROM BURKHOLDERIA XENOVORANS LB400, IN COMPLEX WITH 3,10-DI-FLUORO HOPDA | 3.7.1 3.7.1.8 |
2RI0 | CRYSTAL STRUCTURE OF GLUCOSAMINE 6-PHOSPHATE DEAMINASE (NAGB) FROM S. MUTANS | 3.5.99.6 |
2RI1 | CRYSTAL STRUCTURE OF GLUCOSAMINE 6-PHOSPHATE DEAMINASE (NAGB) WITH GLCN6P FROM S. MUTANS | 3.5.99.6 |
2RI6 | CRYSTAL STRUCTURE OF S112A MUTANT OF A C-C HYDROLASE, BPHD FROM BURKHOLDERIA XENOVORANS LB400 | 3.7.1 3.7.1.8 |
2RI8 | PENICILLIUM CITRINUM ALPHA-1,2-MANNOSIDASE COMPLEX WITH GLYCEROL | 3.2.1.113 |
2RI9 | PENICILLIUM CITRINUM ALPHA-1,2-MANNOSIDASE IN COMPLEX WITH A SUBSTRATE ANALOG | 3.2.1.113 |
2RIO | STRUCTURE OF THE DUAL ENZYME IRE1 REVEALS THE BASIS FOR CATALYSIS AND REGULATION OF NON-CONVENTIONAL SPLICING | 2.7.11.1 3.1.26 |
2RIP | STRUCTURE OF DPPIV IN COMPLEX WITH AN INHIBITOR | 3.4.14.5 |
2RJP | CRYSTAL STRUCTURE OF ADAMTS4 WITH INHIBITOR BOUND | 3.4.24.82 |
2RJQ | CRYSTAL STRUCTURE OF ADAMTS5 WITH INHIBITOR BOUND | 3.4.24 |
2RK3 | STRUCTURE OF A104T DJ-1 | 3.1.2 3.5.1 3.5.1.124 |
2RK4 | STRUCTURE OF M26I DJ-1 | 3.1.2 3.5.1 3.5.1.124 |
2RK6 | STRUCTURE OF E163K DJ-1 | 3.1.2 3.5.1 3.5.1.124 |
2RKF | HIV-1 PR RESISTANT MUTANT + LPV | 3.4.23.16 2.7.7.49 3.1.26.13 |
2RKG | HIV-1 PR RESISTANT MUTANT + LPV | 3.4.23.16 2.7.7.49 3.1.26.13 |
2RKI | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH A TRIAZOLE DERIVED NNRTI | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2RKS | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT PHS L38K AT CRYOGENIC TEMPERATURE | 3.1.31.1 |
2RKW | INTERMEDIATE POSITION OF ATP ON ITS TRAIL TO THE BINDING POCKET INSIDE THE SUBUNIT B MUTANT R416W OF THE ENERGY CONVERTER A1AO ATP SYNTHASE | 3.6.3.14 |
2RL3 | CRYSTAL STRUCTURE OF THE OXA-10 W154H MUTANT AT PH 7 | 3.5.2.6 |
2RLA | ALTERING THE BINUCLEAR MANGANESE CLUSTER OF ARGINASE DIMINISHES THERMOSTABILITY AND CATALYTIC FUNCTION | 3.5.3.1 |
2RLC | CRYSTAL STRUCTURE OF THE CONJUGATED BILE ACID HYDROLASE FROM CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH REACTION PRODUCTS GLYCINE AND CHOLATE | 3.5.1.24 3.5.1 |
2RLN | THERMODYNAMIC AND STRUCTURAL CONSEQUENCES OF CHANGING A SULPHUR ATOM TO A METHYLENE GROUP IN THE M13NLE MUTATION IN RIBONUCLEASE S | 3.1.27.5 4.6.1.18 |
2RLT | PHOSPHORYLATED CPI-17 (22-120) | 3.1 |
2RM2 | STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2RMJ | SOLUTION STRUCTURE OF RIG-I C-TERMINAL DOMAIN | 3.6.1 3.6.4.13 |
2RMK | RAC1/PRK1 COMPLEX | 3.6.5.2 |
2RML | SOLUTION STRUCTURE OF THE N-TERMINAL SOLUBLE DOMAINS OF BACILLUS SUBTILIS COPA | 3.6.3 7.2.2.8 |
2RMP | RMP-PEPSTATIN A COMPLEX | 3.4.23.23 |
2RMU | THREE-DIMENSIONAL STRUCTURES OF DRUG-RESISTANT MUTANTS OF HUMAN RHINOVIRUS 14 | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2RMX | SOLUTION STRUCTURE OF THE SHP-1 C-TERMINAL SH2 DOMAIN COMPLEXED WITH A TYROSINE-PHOSPHORYLATED PEPTIDE FROM NKG2A | 3.1.3.48 |
2RN2 | STRUCTURAL DETAILS OF RIBONUCLEASE H FROM ESCHERICHIA COLI AS REFINED TO AN ATOMIC RESOLUTION | 3.1.26.4 |
2RNF | X-RAY CRYSTAL STRUCTURE OF HUMAN RIBONUCLEASE 4 IN COMPLEX WITH D(UP) | 3.1.27 |
2RNK | NMR STRUCTURE OF THE DOMAIN 513-651 OF THE SARS-COV NONSTRUCTURAL PROTEIN NSP3 | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2RNS | REFINEMENT OF THE CRYSTAL STRUCTURE OF RIBONUCLEASE S. COMPARISON WITH AND BETWEEN THE VARIOUS RIBONUCLEASE A STRUCTURES | 3.1.27.5 4.6.1.18 |
2RNT | THREE-DIMENSIONAL STRUCTURE OF RIBONUCLEASE T1 COMPLEXED WITH GUANYLYL-2(PRIME),5(PRIME)-GUANOSINE AT 1.8 ANGSTROMS RESOLUTION | 3.1.27.3 4.6.1.24 |
2ROK | SOLUTION STRUCTURE OF THE CAP-BINDING DOMAIN OF PARN COMPLEXED WITH THE CAP ANALOG | 3.1.13.4 |
2RON | THE EXTERNAL THIOESTERASE OF THE SURFACTIN-SYNTHETASE | 3.1.2 |
2ROP | SOLUTION STRUCTURE OF DOMAINS 3 AND 4 OF HUMAN ATP7B | 3.6.3.4 7.2.2.8 |
2RPA | THE SOLUTION STRUCTURE OF N-TERMINAL DOMAIN OF MICROTUBULE SEVERING ENZYME | 3.6.4.3 5.6.1.1 |
2RPI | THE NMR STRUCTURE OF THE SUBMILLISECOND FOLDING INTERMEDIATE OF THE THERMUS THERMOPHILUS RIBONUCLEASE H | 3.1.26.4 |
2RPZ | SOLUTION STRUCTURE OF THE MONOMERIC FORM OF MOUSE APOBEC2 | 3.5.4 3.5.4.36 |
2RQ6 | SOLUTION STRUCTURE OF THE EPSILON SUBUNIT OF THE F1-ATPASE FROM THERMOSYNECHOCOCCUS ELONGATUS BP-1 | 3.6.3.14 |
2RQA | SOLUTION STRUCTURE OF LGP2 CTD | 3.6.1 3.6.4.13 |
2RQB | SOLUTION STRUCTURE OF MDA5 CTD | 3.6.1 3.6.4.13 |
2RR1 | STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2RRD | STRUCTURE OF HRDC DOMAIN FROM HUMAN BLOOM SYNDROME PROTEIN, BLM | 3.6.4.12 |
2RRK | SOLUTION STRUCTURE OF THE E. COLI ORF135 PROTEIN | 3.6.1 3.6.1.65 |
2RS1 | STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2RS3 | STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2RS5 | STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES | 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48 |
2RS6 | SOLUTION STRUCTURE OF THE N-TERMINAL DSRBD FROM RNA HELICASE A | 3.6.4.13 |
2RS7 | SOLUTION STRUCTURE OF THE SECOND DSRBD FROM RNA HELICASE A | 3.6.4.13 |
2RSC | SOLUTION STRUCTURE OF THE BOMBYX MORI LYSOZYME | 3.2.1.17 |
2RSP | STRUCTURE OF THE ASPARTIC PROTEASE FROM ROUS SARCOMA RETROVIRUS REFINED AT 2 ANGSTROMS RESOLUTION | 3.4.23 |
2RSW | NMR STRUCTURE, LOCALIZATION AND VESICLE FUSION OF CHIKUNGUNYA VIRUS FUSION PEPTIDE | 3.4.21.90 |
2RTX | SOLUTION STRUCTURE OF THE GGQ DOMAIN OF YAEJ PROTEIN FROM ESCHERICHIA COLI | 3.1.1.29 |
2RVE | THE CRYSTAL STRUCTURE OF ECORV ENDONUCLEASE AND OF ITS COMPLEXES WITH COGNATE AND NON-COGNATE DNA SEGMENTS | 3.1.21.4 |
2SAM | STRUCTURE OF THE PROTEASE FROM SIMIAN IMMUNODEFICIENCY VIRUS: COMPLEX WITH AN IRREVERSIBLE NON-PEPTIDE INHIBITOR | 2.7.7.49 3.1.13.2 3.1.26.13 |
2SBT | A COMPARISON OF THE THREE-DIMENSIONAL STRUCTURES OF SUBTILISIN BPN AND SUBTILISIN NOVO | 3.4.21.14 3.4.21.62 |
2SEC | STRUCTURAL COMPARISON OF TWO SERINE PROTEINASE-PROTEIN INHIBITOR COMPLEXES. EGLIN-C-SUBTILISIN CARLSBERG AND CI-2-SUBTILISIN NOVO | 3.4.21.62 |
2SFA | SERINE PROTEINASE FROM STREPTOMYCES FRADIAE ATCC 14544 | 3.4.21 |
2SGA | ELECTRON DENSITY CALCULATIONS AS AN EXTENSION OF PROTEIN STRUCTURE REFINEMENT. STREPTOMYCES GRISEUS PROTEASE AT 1.5 ANGSTROMS RESOLUTION | 3.4.21.80 |
2SGD | ASP 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B AT PH 10.7 | 3.4.21.81 |
2SGE | GLU 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B AT PH 10.7 | 3.4.21.81 |
2SGF | PHE 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B | 3.4.21.81 |
2SGP | PRO 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B AT PH 6.5 | 3.4.21.81 |
2SGQ | GLN 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B AT PH 6.5 | 3.4.21.81 |
2SHP | TYROSINE PHOSPHATASE SHP-2 | 3.1.3.48 |
2SIC | REFINED CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' AND STREPTOMYCES SUBTILISIN INHIBITOR AT 1.8 ANGSTROMS RESOLUTION | 3.4.21.14 3.4.21.62 |
2SIL | THE STRUCTURES OF SALMONELLA TYPHIMURIUM LT2 NEURAMINIDASE AND ITS COMPLEX WITH A TRANSITION STATE ANALOGUE AT 1.6 ANGSTROMS RESOLUTION | 3.2.1.18 |
2SIM | THE STRUCTURES OF SALMONELLA TYPHIMURIUM LT2 NEURAMINIDASE AND ITS COMPLEX WITH A TRANSITION STATE ANALOGUE AT 1.6 ANGSTROMS RESOLUTION | 3.2.1.18 |
2SLI | LEECH INTRAMOLECULAR TRANS-SIALIDASE COMPLEXED WITH 2,7-ANHYDRO-NEU5AC, THE REACTION PRODUCT | 3.2.1.18 4.2.2.15 |
2SNI | STRUCTURAL COMPARISON OF TWO SERINE PROTEINASE-PROTEIN INHIBITOR COMPLEXES. EGLIN-C-SUBTILISIN CARLSBERG AND CI-2-SUBTILISIN NOVO | 3.4.21.14 3.4.21.62 |
2SNM | IN A STAPHYLOCOCCAL NUCLEASE MUTANT THE SIDE-CHAIN OF A LYSINE REPLACING VALINE 66 IS FULLY BURIED IN THE HYDROPHOBIC CORE | 3.1.31.1 |
2SNS | STAPHYLOCOCCAL NUCLEASE. PROPOSED MECHANISM OF ACTION BASED ON STRUCTURE OF ENZYME-THYMIDINE 3(PRIME),5(PRIME)-BIPHOSPHATE-CALCIUM ION COMPLEX AT 1.5-ANGSTROMS RESOLUTION | 3.1.31.1 |
2SNV | THE REFINED STRUCTURE OF SINDBIS VIRUS CORE PROTEIN IN COMPARISON WITH OTHER CHYMOTRYPSIN-LIKE SERINE PROTEINASE STRUCTURES | 3.4.21.90 |
2SNW | SINDBIS VIRUS CAPSID PROTEIN, TYPE3 CRYSTAL FORM | 3.4.21 3.4.21.90 |
2SOB | SN-OB, OB-FOLD SUB-DOMAIN OF STAPHYLOCOCCAL NUCLEASE, NMR, 10 STRUCTURES | 3.1.31.1 |
2SPT | DIFFERENCES IN THE METAL ION STRUCTURE BETWEEN SR-AND CA-PROTHROMBIN FRAGMENT 1 | 3.4.21.5 |
2SRT | CATALYTIC DOMAIN OF HUMAN STROMELYSIN-1 AT PH 5.5 AND 40OC COMPLEXED WITH INHIBITOR | 3.4.24.17 |
2ST1 | THE THREE-DIMENSIONAL STRUCTURE OF BACILLUS AMYLOLIQUEFACIENS SUBTILISIN AT 1.8 ANGSTROMS AND AN ANALYSIS OF THE STRUCTURAL CONSEQUENCES OF PEROXIDE INACTIVATION | 3.4.21.14 3.4.21.62 |
2STA | ANIONIC SALMON TRYPSIN IN COMPLEX WITH SQUASH SEED INHIBITOR (CUCURBITA MAXIMA TRYPSIN INHIBITOR I) | 3.4.21.4 |
2STB | ANIONIC SALMON TRYPSIN IN COMPLEX WITH SQUASH SEED INHIBITOR (CUCURBITA PEPO TRYPSIN INHIBITOR II) | 3.4.21.4 |
2TAA | STRUCTURE AND POSSIBLE CATALYTIC RESIDUES OF TAKA-AMYLASE A | 3.2.1.1 |
2TBS | COLD-ADAPTION OF ENZYMES: STRUCTURAL COMPARISON BETWEEN SALMON AND BOVINE TRYPSINS | 3.4.21.4 |
2TCL | STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN FIBROBLAST COLLAGENASE COMPLEXED WITH AN INHIBITOR | 3.4.24.7 |
2TEC | MOLECULAR DYNAMICS REFINEMENT OF A THERMITASE-EGLIN-C COMPLEX AT 1.98 ANGSTROMS RESOLUTION AND COMPARISON OF TWO CRYSTAL FORMS THAT DIFFER IN CALCIUM CONTENT | 3.4.21.66 |
2TGA | ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY | 3.4.21.4 |
2TGD | LACK OF THE TRANSITION STATE STABILIZATION SITE IS A FACTOR IN THE INACTIVITY OF TRYPSINOGEN, A SERINE PROTEASE ZYMOGEN. STRUCTURE OF DFP INHIBITED BOVINE TRYPSINOGEN AT 2.1 ANGSTROMS RESOLUTION | 3.4.21.4 |
2TGT | ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY | 3.4.21.4 |
2THF | STRUCTURE OF HUMAN ALPHA-THROMBIN Y225F MUTANT BOUND TO D-PHE-PRO-ARG-CHLOROMETHYLKETONE | 3.4.21.5 |
2TIO | LOW PACKING DENSITY FORM OF BOVINE BETA-TRYPSIN IN CYCLOHEXANE | 3.4.21.4 |
2TLD | CRYSTAL STRUCTURE OF AN ENGINEERED SUBTILISIN INHIBITOR COMPLEXED WITH BOVINE TRYPSIN | 3.4.21.4 |
2TLI | THERMOLYSIN (5% ISOPROPANOL SOAKED CRYSTALS) | 3.4.24.27 |
2TLX | THERMOLYSIN (NATIVE) | 3.4.24.27 |
2TMN | CRYSTALLOGRAPHIC STRUCTURAL ANALYSIS OF PHOSPHORAMIDATES AS INHIBITORS AND TRANSITION-STATE ANALOGS OF THERMOLYSIN | 3.4.24.27 |
2TRM | THE THREE-DIMENSIONAL STRUCTURE OF ASN102 MUTANT OF TRYPSIN. ROLE OF ASP102 IN SERINE PROTEASE CATALYSIS | 3.4.21.4 |
2UBP | STRUCTURE OF NATIVE UREASE FROM BACILLUS PASTEURII | 3.5.1.5 |
2ULL | MULTIPLE CONFORMATION STRUCTURE OF ALPHA-LYTIC PROTEASE AT 120 K | 3.4.21.12 |
2UPJ | HIV-1 PROTEASE COMPLEX WITH U100313 ([3-[[3-[CYCLOPROPYL [4-HYDROXY-2OXO-6-[1-(PHENYLMETHYL)PROPYL]-2H-PYRAN-3-YL] METHYL]PHENYL]AMINO]-3-OXO-PROPYL]CARBAMIC ACID TERT-BUTYL ESTER) | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2USH | 5'-NUCLEOTIDASE FROM E. COLI | 3.1.3.5 3.6.1.45 |
2USN | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THIADIAZOLE INHIBITOR PNU-141803 | 3.4.24.17 |
2UUF | THROMBIN-HIRUGEN BINARY COMPLEX AT 1.26A RESOLUTION | 3.4.21.5 |
2UUG | ESCHERICHIA COLI URACIL-DNA GLYCOSYLASE:INHIBITOR COMPLEX WITH H187D MUTANT UDG AND WILD-TYPE UGI | 3.2.2.3 3.2.2.27 |
2UUJ | THROMBIN-HIRUGEN-GW473178 TERNARY COMPLEX AT 1.32A RESOLUTION | 3.4.21.5 |
2UUK | THROMBIN-HIRUGEN-GW420128 TERNARY COMPLEX AT 1.39A RESOLUTION | 3.4.21.5 |
2UUT | THE 2.4 ANGSTROM RESOLUTION STRUCTURE OF THE D346G MUTANT OF THE SAPPORO VIRUS RDRP POLYMERASE | 2.7.7.48 3.6.1.15 3.4.22.66 |
2UUW | 2.75 ANGSTROM STRUCTURE OF THE D347G D348G MUTANT STRUCTURE OF SAPPORO VIRUS RDRP POLYMERASE | 2.7.7.48 3.6.1.15 3.4.22.66 |
2UUY | STRUCTURE OF A TICK TRYPTASE INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN | 3.4.21.4 |
2UWA | CRYSTAL STRUCTURE OF THE NASTURTIUM SEEDLING XYLOGLUCANASE ISOFORM NXG1 | 3.2.1.151 3.2.1.4 2.4.1.207 |
2UWB | CRYSTAL STRUCTURE OF THE NASTURTIUM SEEDLING MUTANT XYLOGLUCANASE ISOFORM NXG1-DELTA-YNIIG | 3.2.1.151 3.2.1.4 2.4.1.207 |
2UWC | CRYSTAL STRUCTURE OF NASTURTIUM XYLOGLUCAN HYDROLASE ISOFORM NXG2 | 3.2.1.151 3.2.1.4 2.4.1.207 |
2UWF | CRYSTAL STRUCTURE OF FAMILY 10 XYLANASE FROM BACILLUS HALODURANS | 3.2.1.8 |
2UWL | SELECTIVE AND DUAL ACTION ORALLY ACTIVE INHIBITORS OF THROMBIN AND FACTOR XA | 3.4.21.6 |
2UWO | SELECTIVE AND DUAL ACTION ORALLY ACTIVE INHIBITORS OF THROMBIN AND FACTOR XA | 3.4.21.6 |
2UWP | FACTOR XA INHIBITOR COMPLEX | 3.4.21.6 |
2UWX | ACTIVE SITE RESTRUCTURING REGULATES LIGAND RECOGNITION IN CLASS A PENICILLIN-BINDING PROTEINS | 2.4.1.129 2.3.2 3.4.16.4 |
2UXS | 2.7A CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE (RV3628) FROM MYCOBACTERIUM TUBERCULOSIS AT PH 7.5 | 3.6.1.1 |
2UXY | ALIPHATIC AMIDASE | 3.5.1.4 |
2UXZ | TWO-CARBON-ELONGATED HIV-1 PROTEASE INHIBITORS WITH A TERTIARY- ALCOHOL-CONTAINING TRANSITION-STATE MIMIC | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2UY0 | TWO-CARBON-ELONGATED HIV-1 PROTEASE INHIBITORS WITH A TERTIARY- ALCOHOL-CONTAINING TRANSITION-STATE MIMIC | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2UY2 | SCCTS1_APO CRYSTAL STRUCTURE | 3.2.1.14 |
2UY3 | SCCTS1_8-CHLOROTHEOPHYLLINE CRYSTAL STRUCTURE | 3.2.1.14 |
2UY4 | SCCTS1_ACETAZOLAMIDE CRYSTAL STRUCTURE | 3.2.1.14 |
2UY5 | SCCTS1_KINETIN CRYSTAL STRUCTURE | 3.2.1.14 |
2UYJ | CRYSTAL STRUCTURE OF E. COLI TDCF WITH BOUND ETHYLENE GLYCOL | 3.5.4 |
2UYK | CRYSTAL STRUCTURE OF E. COLI TDCF WITH BOUND SERINE | 3.5.4 |
2UYN | CRYSTAL STRUCTURE OF E. COLI TDCF WITH BOUND 2-KETOBUTYRATE | 3.5.4 |
2UYP | CRYSTAL STRUCTURE OF E. COLI TDCF WITH BOUND PROPIONATE | 3.5.4 |
2UYR | CRYSTAL STRUCTURE OF BACILLUS CEREUS SPHINGOMYELINASE MUTANT :N57A | 3.1.4.12 |
2UYX | METALLO-BETA-LACTAMASE (1BC2) SINGLE POINT MUTANT D120S | 3.5.2.6 |
2UZ9 | HUMAN GUANINE DEAMINASE (GUAD) IN COMPLEX WITH ZINC AND ITS PRODUCT XANTHINE. | 3.5.4.3 |
2UZG | ZF-UBP DOMAIN OF VDU1 | 3.4.19.12 |
2UZJ | CRYSTAL STRUCTURE OF THE MATURE STREPTOCOCCAL CYSTEINE PROTEASE, MSPEB | 3.4.22.10 |
2UZQ | PROTEIN PHOSPHATASE, NEW CRYSTAL FORM | 3.1.3.48 |
2V00 | X-RAY CRYSTAL STRUCTURE OF ENDOTHIAPEPSIN COMPLEXED WITH COMPOUND 1 | 3.4.23.22 |
2V06 | CRYSTAL STRUCTURE OF THE PPM SER-THR PHOSPHATASE MSPP FROM MYCOBACTERIUM SMEGMATIS AT PH 5.5 | 3.1.3 |
2V0B | SAD STRUCTURE SOLUTION PORCINE PANCREATIC ELASTASE FROM A SELENATE DERIVATIVE | 3.4.21.36 |
2V0E | BRK DOMAIN FROM HUMAN CHD7 | 3.6.1 3.6.4.12 |
2V0F | BRK DOMAIN FROM HUMAN CHD7 | 3.6.1 3.6.4.12 |
2V0R | CRYSTAL STRUCTURE OF A HAIRPIN EXCHANGE VARIANT (LTX) OF THE TARGETING LINE-1 RETROTRANSPOSON ENDONUCLEASE | 2.7.7.49 3.1.21 |
2V0S | CRYSTAL STRUCTURE OF A HAIRPIN EXCHANGE VARIANT (LR1) OF THE TARGETING LINE-1 RETROTRANSPOSON ENDONUCLEASE | 2.7.7.49 3.1.21 |
2V0Z | CRYSTAL STRUCTURE OF RENIN WITH INHIBITOR 10 (ALISKIREN) | 3.4.23.15 |
2V10 | CRYSTAL STRUCTURE OF RENIN WITH INHIBITOR 9 | 3.4.23.15 |
2V11 | CRYSTAL STRUCTURE OF RENIN WITH INHIBITOR 6 | 3.4.23.15 |
2V12 | CRYSTAL STRUCTURE OF RENIN WITH INHIBITOR 8 | 3.4.23.15 |
2V13 | CRYSTAL STRUCTURE OF RENIN WITH INHIBITOR 7 | 3.4.23.15 |
2V16 | CRYSTAL STRUCTURE OF RENIN WITH INHIBITOR 3 | 3.4.23.15 |
2V1O | CRYSTAL STRUCTURE OF N-TERMINAL DOMAIN OF ACYL-COA THIOESTERASE 7 | 3.1.2.2 |
2V1X | CRYSTAL STRUCTURE OF HUMAN RECQ-LIKE DNA HELICASE | 3.6.1 3.6.4.12 |
2V1Z | STRUCTURE OF A TEM-1 BETA-LACTAMASE INSERTANT ALLOSTERICALLY REGULATED BY KANAMYCIN AND ANIONS. | 3.5.2.6 |
2V20 | STRUCTURE OF A TEM-1 BETA-LACTAMASE INSERTANT ALLOSTERICALLY REGULATED BY KANAMYCIN AND ANIONS. COMPLEX WITH SULFATE. | 3.5.2.6 |
2V2F | CRYSTAL STRUCTURE OF PBP1A FROM DRUG-RESISTANT STRAIN 5204 FROM STREPTOCOCCUS PNEUMONIAE | 2.4.1.129 3.4.16.4 |
2V33 | HIGH RESOLUTION CRYSTAL STRUCTURE OF DOMAIN III OF E1 FUSION GLYCOPROTEIN OF SEMLIKI FOREST VIRUS | 3.4.21.90 |
2V35 | PORCINE PANCREATIC ELASTASE IN COMPLEX WITH INHIBITOR JM54 | 3.4.21.36 |
2V36 | CRYSTAL STRUCTURE OF GAMMA-GLUTAMYL TRANSFERASE FROM BACILLUS SUBTILIS | 2.3.2.2 3.4.19.13 |
2V38 | FAMILY 5 ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHAERENS IN COMPLEX WITH CELLOBIO-DERIVED NOEUROMYCIN | 3.2.1.4 |
2V3D | ACID-BETA-GLUCOSIDASE WITH N-BUTYL-DEOXYNOJIRIMYCIN | 3.2.1.45 2.4.1 3.2.1 |
2V3E | ACID-BETA-GLUCOSIDASE WITH N-NONYL-DEOXYNOJIRIMYCIN | 3.2.1.45 2.4.1 3.2.1 |
2V3F | ACID-BETA-GLUCOSIDASE PRODUCED IN CARROT | 3.2.1.45 2.4.1 3.2.1 |
2V3G | STRUCTURE OF A FAMILY 26 LICHENASE IN COMPLEX WITH NOEUROMYCIN | 3.2.1.4 |
2V3H | THROMBIN WITH 3-CYCLE NO F | 3.4.21.5 |
2V3I | HYPOCREA JECORINA CEL7A IN COMPLEX WITH (R)-DIHYDROXY-PHENANTHRENOLOL | 3.2.1.91 |
2V3O | THROMBIN WITH 3-CYCLE WITH F | 3.4.21.5 |
2V3R | HYPOCREA JECORINA CEL7A IN COMPLEX WITH (S)-DIHYDROXY-PHENANTHRENOLOL | 3.2.1.91 |
2V3X | HIS243ALA ESCHERICHIA COLI AMINOPEPTIDASE P IN COMPLEX WITH SUBSTRATE | 3.4.11.9 |
2V3Y | HIS361ALA ESCHERICHIA COLI AMINOPEPTIDASE P IN COMPLEX WITH PRODUCT | 3.4.11.9 |
2V3Z | GLU383ALA ESCHERICHIA COLI AMINOPEPTIDASE P IN COMPLEX WITH SUBSTRATE | 3.4.11.9 |
2V4B | CRYSTAL STRUCTURE OF HUMAN ADAMTS-1 CATALYTIC DOMAIN AND CYSTEINE- RICH DOMAIN (APO-FORM) | 3.4.24 |
2V4N | CRYSTAL STRUCTURE OF SALMONELLA TYPHIMURIUM SURE AT 1.7 ANGSTROM RESOLUTION IN ORTHORHOMBIC FORM | 3.1.3.5 3.1.3.6 3.6.1.11 |
2V4O | CRYSTAL STRUCTURE OF SALMONELLA TYPHIMURIUM SURE AT 2.75 ANGSTROM RESOLUTION IN MONOCLINIC FORM | 3.1.3.5 3.1.3.6 3.1.3.11 3.6.1.11 |
2V4V | CRYSTAL STRUCTURE OF A FAMILY 6 CARBOHYDRATE-BINDING MODULE FROM CLOSTRIDIUM CELLULOLYTICUM IN COMPLEX WITH XYLOSE | 3.2.1.4 |
2V5C | FAMILY 84 GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM PERFRINGENS, 2.1 ANGSTROM STRUCTURE | 3.2.1.52 3.2.1.169 |
2V5D | STRUCTURE OF A FAMILY 84 GLYCOSIDE HYDROLASE AND A FAMILY 32 CARBOHYDRATE-BINDING MODULE IN TANDEM FROM CLOSTRIDIUM PERFRINGENS. | 3.2.1.52 3.2.1.169 |
2V5W | CRYSTAL STRUCTURE OF HDAC8-SUBSTRATE COMPLEX | 3.5.1.98 |
2V5X | CRYSTAL STRUCTURE OF HDAC8-INHIBITOR COMPLEX | 3.5.1.98 |
2V5Y | CRYSTAL STRUCTURE OF THE RECEPTOR PROTEIN TYROSINE PHOSPHATASE MU ECTODOMAIN | 3.1.3.48 |
2V6I | KOKOBERA VIRUS HELICASE | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2V6J | KOKOBERA VIRUS HELICASE: MUTANT MET47THR | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2V6N | CRYSTAL STRUCTURES OF THE SARS-CORONAVIRUS MAIN PROTEINASE INACTIVATED BY BENZOTRIAZOLE COMPOUNDS | 3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2V6X | STRACTURAL INSIGHT INTO THE INTERACTION BETWEEN ESCRT-III AND VPS4 | 3.6.4.6 |
2V6Y | STRUCTURE OF THE MIT DOMAIN FROM A S. SOLFATARICUS VPS4-LIKE ATPASE | 3.6.4.6 |
2V77 | CRYSTAL STRUCTURE OF HUMAN CARBOXYPEPTIDASE A1 | 3.4.17.1 |
2V8B | SAD STRUCTURE SOLUTION OF PROTEINASE K GROWN IN SELENATE SOLUTION | 3.4.21.64 |
2V8D | CRYSTAL STRUCTURE OF MUTANT E159A OF BETA-ALANINE SYNTHASE FROM SACCHAROMYCES KLUYVERI | 3.5.1.6 |
2V8G | CRYSTAL STRUCTURE OF BETA-ALANINE SYNTHASE FROM SACCHAROMYCES KLUYVERI IN COMPLEX WITH THE PRODUCT BETA-ALANINE | 3.5.1.6 |
2V8H | CRYSTAL STRUCTURE OF MUTANT E159A OF BETA-ALANINE SYNTHASE FROM SACCHAROMYCES KLUYVERI IN COMPLEX WITH ITS SUBSTRATE N-CARBAMYL-BETA- ALANINE | 3.5.1.6 |
2V8L | CARBOHYDRATE-BINDING OF THE STARCH BINDING DOMAIN OF RHIZOPUS ORYZAE GLUCOAMYLASE IN COMPLEX WITH BETA-CYCLODEXTRIN AND MALTOHEPTAOSE | 3.2.1.3 |
2V8M | CARBOHYDRATE-BINDING OF THE STARCH BINDING DOMAIN OF RHIZOPUS ORYZAE GLUCOAMYLASE IN COMPLEX WITH BETA-CYCLODEXTRIN AND MALTOHEPTAOSE | 3.2.1.3 |
2V8O | STRUCTURE OF THE MURRAY VALLEY ENCEPHALITIS VIRUS RNA HELICASE TO 1. 9A RESOLUTION | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2V8V | CRYSTAL STRUCTURE OF MUTANT R322A OF BETA-ALANINE SYNTHASE FROM SACCHAROMYCES KLUYVERI | 3.5.1.6 |
2V96 | STRUCTURE OF THE UNPHOTOLYSED COMPLEX OF TCACHE WITH 1-(2- NITROPHENYL)-2,2,2-TRIFLUOROETHYL-ARSENOCHOLINE AT 100K | 3.1.1.7 |
2V9X | E138D VARIANT OF ESCHERICHIA COLI DCTP DEAMINASE IN COMPLEX WITH DUTP | 3.5.4.13 |
2V9Z | STRUCTURE OF THE RHODOCOCCUS HALOALKANE DEHALOGENASE MUTANT WITH ENHANCED ENANTIOSELECTIVITY | 3.8.1.5 |
2VA5 | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 8C | 3.4.23.46 |
2VA6 | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 24 | 3.4.23.46 |
2VA7 | X-RAY CRYSTAL STRUCTURE OF BETA SECRETASE COMPLEXED WITH COMPOUND 27 | 3.4.23.46 |
2VA9 | STRUCTURE OF NATIVE TCACHE AFTER A 9 SECONDS ANNEALING TO ROOM TEMPERATURE DURING THE FIRST 5 SECONDS OF WHICH LASER IRRADIATION AT 266NM TOOK PLACE | 3.1.1.7 |
2VB0 | CRYSTAL STRUCTURE OF COXSACKIEVIRUS B3 PROTEINASE 3C | 3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48 |
2VB1 | HEWL AT 0.65 ANGSTROM RESOLUTION | 3.2.1.17 |
2VBC | CRYSTAL STRUCTURE OF THE NS3 PROTEASE-HELICASE FROM DENGUE VIRUS | 3.4.21.91 3.6.1.15 3.6.4.13 |
2VBE | TAILSPIKE PROTEIN OF BACTERIOPHAGE SF6 | 3.2.1 |
2VBJ | MOLECULAR BASIS OF HUMAN XPC GENE RECOGNITION AND CLEAVAGE BY ENGINEERED HOMING ENDONUCLEASE HETERODIMERS | 3.1 |
2VBK | NATIVE TAILSPIKE PROTEIN OF BACTERIOPHAGE SF6 | 3.2.1 |
2VBL | MOLECULAR BASIS OF HUMAN XPC GENE RECOGNITION AND CLEAVAGE BY ENGINEERED HOMING ENDONUCLEASE HETERODIMERS | 3.1 |
2VBM | TAILSPIKE PROTEIN OF BACTERIOPHAGE SF6 COMPLEXED WITH TETRASACCHARIDE | 3.2.1 |
2VBN | MOLECULAR BASIS OF HUMAN XPC GENE RECOGNITION AND CLEAVAGE BY ENGINEERED HOMING ENDONUCLEASE HETERODIMERS | 3.1 |
2VBO | MOLECULAR BASIS OF HUMAN XPC GENE RECOGNITION AND CLEAVAGE BY ENGINEERED HOMING ENDONUCLEASE HETERODIMERS | 3.1 |
2VC3 | RICIN A-CHAIN (RECOMBINANT) E177D MUTANT WITH A BOUND ACETATE | 3.2.2.22 |
2VC4 | RICIN A-CHAIN (RECOMBINANT) E177D MUTANT | 3.2.2.22 |
2VC5 | STRUCTURAL BASIS FOR NATURAL LACTONASE AND PROMISCUOUS PHOSPHOTRIESTERASE ACTIVITIES | 3.1.8.1 |
2VC9 | FAMILY 89 GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH 2-ACETAMIDO-1,2-DIDEOXYNOJIRMYCIN | 3.2.1.50 |
2VCA | FAMILY 89 GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH BETA-N-ACETYL-D-GLUCOSAMINE | 3.2.1.50 |
2VCB | FAMILY 89 GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH PUGNAC | 3.2.1.50 |
2VCC | FAMILY 89 GLYCOSIDE HYDROLASE FROM CLOSTRIDIUM PERFRINGENS | 3.2.1.50 |
2VCG | CRYSTAL STRUCTURE OF A HDAC-LIKE PROTEIN HDAH FROM BORDETELLA SP. WITH THE BOUND INHIBITOR ST-17 | 3.5.1 |
2VEO | X-RAY STRUCTURE OF CANDIDA ANTARCTICA LIPASE A IN ITS CLOSED STATE. | 3.1.1.3 |
2VES | CRYSTAL STRUCTURE OF LPXC FROM PSEUDOMONAS AERUGINOSA COMPLEXED WITH THE POTENT BB-78485 INHIBITOR | 3.5.1.108 |
2VEU | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B IN COMPLEX WITH AN ISOTHIAZOLIDINONE-CONTAINING INHIBITOR | 3.1.3.48 |
2VEV | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B IN COMPLEX WITH AN ISOTHIAZOLIDINONE-CONTAINING INHIBITOR | 3.1.3.48 |
2VEW | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B IN COMPLEX WITH AN ISOTHIAZOLIDINONE-CONTAINING INHIBITOR | 3.1.3.48 |
2VEX | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B IN COMPLEX WITH AN ISOTHIAZOLIDINONE-CONTAINING INHIBITOR | 3.1.3.48 |
2VEY | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B IN COMPLEX WITH AN ISOTHIAZOLIDINONE-CONTAINING INHIBITOR | 3.1.3.48 |
2VF2 | X-RAY CRYSTAL STRUCTURE OF HSAD FROM MYCOBACTERIUM TUBERCULOSIS | 3.7.1.8 3.7.1.17 |
2VFJ | STRUCTURE OF THE A20 OVARIAN TUMOUR (OTU) DOMAIN | 3.4.19.12 2.3.2 |
2VFM | LOW TEMPERATURE STRUCTURE OF P22 TAILSPIKE PROTEIN FRAGMENT (109-666) | 3.2.1 |
2VFN | LOW TEMPERATURE STRUCTURE OF P22 TAILSPIKE PROTEIN FRAGMENT (109-666), MUTANT V125A | 3.2.1 |
2VFO | LOW TEMPERATURE STRUCTURE OF P22 TAILSPIKE PROTEIN FRAGMENT (109-666), MUTANT V125L | 3.2.1 |
2VFP | LOW TEMPERATURE STRUCTURE OF P22 TAILSPIKE PROTEIN FRAGMENT (109-666), MUTANT V349L | 3.2.1 |
2VFQ | LOW TEMPERATURE STRUCTURE OF P22 TAILSPIKE PROTEIN FRAGMENT (109-666), MUTANT V450A | 3.2.1 |
2VG5 | CRYSTAL STRUCTURES OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXES WITH THIOCARBAMATE NON-NUCLEOSIDE INHIBITORS | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23.16 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2VG6 | CRYSTAL STRUCTURES OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXES WITH THIOCARBAMATE NON-NUCLEOSIDE INHIBITORS | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23.16 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2VG7 | CRYSTAL STRUCTURES OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXES WITH THIOCARBAMATE NON-NUCLEOSIDE INHIBITORS | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23.16 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2VG9 | CRYSTAL STRUCTURE OF LOOP SWAP MUTANT OF NECALLIMASTIX PATRICIARUM XYN11A | 3.2.1.8 |
2VGC | GAMMA-CHYMOTRYPSIN D-PARA-CHLORO-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX | 3.4.21.1 |
2VGD | CRYSTAL STRUCTURE OF ENVIRONMENTAL ISOLATED GH11 IN COMPLEX WITH XYLOBIOSE AND FERULOYL-ARABINO-XYLOTRIOSE | 3.2.1.8 |
2VGJ | CRYSTAL STRUCTURE OF ACTINOMADURA R39 DD-PEPTIDASE COMPLEXED WITH A PEPTIDOGLYCAN-MIMETIC CEPHALOSPORIN | 3.4.16.4 |
2VGK | CRYSTAL STRUCTURE OF ACTINOMADURA R39 DD-PEPTIDASE COMPLEXED WITH A PEPTIDOGLYCAN-MIMETIC CEPHALOSPORIN | 3.4.16.4 |
2VGM | STRUCTURE OF YEAST DOM34 : A PROTEIN RELATED TO TRANSLATION TERMINATION FACTOR ERF1 AND INVOLVED IN NO-GO DECAY. | 3.1 |
2VGN | STRUCTURE OF YEAST DOM34 : A PROTEIN RELATED TO TRANSLATION TERMINATION FACTOR ERF1 AND INVOLVED IN NO-GO DECAY. | 3.1 |
2VH0 | STRUCTURE AND PROPERTY BASED DESIGN OF FACTOR XA INHIBITORS:BIARYL PYRROLIDIN-2-ONES INCORPORATING BASIC HETEROCYCLIC MOTIFS | 3.4.21.6 |
2VH6 | STRUCTURE AND PROPERTY BASED DESIGN OF FACTOR XA INHIBITORS: PYRROLIDIN-2-ONES WITH BIARYL P4 MOTIFS | 3.4.21.6 |
2VH7 | CRYSTAL STRUCTURE OF HUMAN COMMON-TYPE ACYLPHOSPHATASE | 3.6.1.7 |
2VH9 | CRYSTAL STRUCTURE OF NXG1-DELTAYNIIG IN COMPLEX WITH XLLG, A XYLOGLUCAN DERIVED OLIGOSACCHARIDE | 3.2.1.151 3.2.1.4 2.4.1.207 |
2VHF | STRUCTURE OF THE CYLD USP DOMAIN | 3.1.2.15 3.4.19.12 |
2VHH | CRYSTAL STRUCTURE OF A PYRIMIDINE DEGRADING ENZYME FROM DROSOPHILA MELANOGASTER | 3.5.1.6 3.5.1 |
2VHL | THE THREE-DIMENSIONAL STRUCTURE OF THE N-ACETYLGLUCOSAMINE-6- PHOSPHATE DEACETYLASE FROM BACILLUS SUBTILIS | 3.5.1.25 |
2VHS | CATHSILICATEIN, A CHIMERA | 3.4.22.15 |
2VI0 | LICHENASE CTLIC26 IN COMPLEX WITH A THIO-OLIGOSACCHARIDE | 3.2.1.4 |
2VID | SERINE PROTEASE SPLB FROM STAPHYLOCOCCUS AUREUS AT 1.8A RESOLUTION | 3.4.21 |
2VIE | HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-1-BENZYL-2-HYDROXY-3-((1,1,5- TRIMETHYLHEXYL)AMINO)PROPYL)-3-(ETHYLAMINO)-5-(2-OXOPYRROLIDIN-1-YL) BENZAMIDE | 3.4.23.46 |
2VIJ | HUMAN BACE-1 IN COMPLEX WITH 3-(1,1-DIOXIDOTETRAHYDRO-2H-1,2-THIAZIN- 2-YL)-5-(ETHYLAMINO)-N-((1S,2R)-2-HYDROXY-1-(PHENYLMETHYL)-3-(1,2,3,4- TETRAHYDRO-1-NAPHTHALENYLAMINO)PROPYL)BENZAMIDE | 3.4.23.46 |
2VIN | FRAGMENT-BASED DISCOVERY OF MEXILETINE DERIVATIVES AS ORALLY BIOAVAILABLE INHIBITORS OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR | 3.4.21.73 |
2VIO | FRAGMENT-BASED DISCOVERY OF MEXILETINE DERIVATIVES AS ORALLY BIOAVAILABLE INHIBITORS OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR | 3.4.21.73 |
2VIP | FRAGMENT-BASED DISCOVERY OF MEXILETINE DERIVATIVES AS ORALLY BIOAVAILABLE INHIBITORS OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR | 3.4.21.73 |
2VIQ | FRAGMENT-BASED DISCOVERY OF MEXILETINE DERIVATIVES AS ORALLY BIOAVAILABLE INHIBITORS OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR | 3.4.21.73 |
2VIV | FRAGMENT-BASED DISCOVERY OF MEXILETINE DERIVATIVES AS ORALLY BIOAVAILABLE INHIBITORS OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR | 3.4.21.73 |
2VIW | FRAGMENT-BASED DISCOVERY OF MEXILETINE DERIVATIVES AS ORALLY BIOAVAILABLE INHIBITORS OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR | 3.4.21.73 |
2VIY | HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(((1S)-2-(CYCLOHEXYLAMINO)- 1-METHYL-2-OXOETHYL)AMINO)-2-HYDROXY-1-(PHENYLMETHYL)PROPYL)-3-(PENTYLSULFONYL)BENZAMIDE | 3.4.23.46 |
2VIZ | HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(((1S)-2-(CYCLOHEXYLAMINO)- 1-METHYL-2-OXOETHYL)AMINO)-2-HYDROXY-1-(PHENYLMETHYL)PROPYL)-3-(2-OXO- 1-PYRROLIDINYL)-5-(PROPYLOXY)BENZAMIDE | 3.4.23.46 |
2VJ1 | A STRUCTURAL VIEW OF THE INACTIVATION OF THE SARS-CORONAVIRUS MAIN PROTEINASE BY BENZOTRIAZOLE ESTERS | 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2VJ6 | HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(((1S)-2-(CYCLOHEXYLAMINO)- 1-METHYL-2-OXOETHYL)AMINO)-2-HYDROXY-1-(PHENYLMETHYL)PROPYL)-3-(ETHYLAMINO)-5-(2-OXO-1-PYRROLIDINYL)BENZAMIDE | 3.4.23.46 |
2VJ7 | HUMAN BACE-1 IN COMPLEX WITH 3-(ETHYLAMINO)-N-((1S,2R)-2-HYDROXY-1-(PHENYLMETHYL)-3-(((3-(TRIFLUOROMETHYL)PHENYL)METHYL)AMINO)PROPYL)-5-(2-OXO-1-PYRROLIDINYL)BENZAMIDE | 3.4.23.46 |
2VJ8 | COMPLEX OF HUMAN LEUKOTRIENE A4 HYDROLASE WITH A HYDROXAMIC ACID INHIBITOR | 3.3.2.6 3.4.11.4 |
2VJ9 | HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(CYCLOHEXYLAMINO)-2-HYDROXY- 1-(PHENYLMETHYL)PROPYL)-3-(ETHYLAMINO)-5-(2-OXO-1-PYRROLIDINYL) BENZAMIDE | 3.4.23.46 |
2VJA | TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH A NON HYDROLYSABLE SUBSTRATE ANALOGUE, 4-OXO-N,N,N- TRIMETHYLPENTANAMINIUM - ORTHORHOMBIC SPACE GROUP - DATASET A AT 100K | 3.1.1.7 |
2VJB | TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH A NON HYDROLYSABLE SUBSTRATE ANALOGUE, 4-OXO-N,N,N- TRIMETHYLPENTANAMINIUM - ORTHORHOMBIC SPACE GROUP - DATASET D AT 100K | 3.1.1.7 |
2VJC | TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH A NON HYDROLYSABLE SUBSTRATE ANALOGUE, 4-OXO-N,N,N- TRIMETHYLPENTANAMINIUM - ORTHORHOMBIC SPACE GROUP - DATASET A AT 150K | 3.1.1.7 |
2VJD | TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH A NON HYDROLYSABLE SUBSTRATE ANALOGUE, 4-OXO-N,N,N- TRIMETHYLPENTANAMINIUM - ORTHORHOMBIC SPACE GROUP - DATASET C AT 150K | 3.1.1.7 |
2VJX | STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | 3.2.1.25 |
2VK5 | THE STRUCTURE OF CLOSTRIDIUM PERFRINGENS NANI SIALIDASE AND ITS CATALYTIC INTERMEDIATES | 3.2.1.18 |
2VK6 | THE STRUCTURE OF CLOSTRIDIUM PERFRINGENS NANI SIALIDASE AND ITS CATALYTIC INTERMEDIATES | 3.2.1.18 |
2VK7 | THE STRUCTURE OF CLOSTRIDIUM PERFRINGENS NANI SIALIDASE AND ITS CATALYTIC INTERMEDIATES | 3.2.1.18 |
2VK9 | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF ALPHA-TOXIN FROM CLOSTRIDIUM NOVYI | 3.4.22 2.4.1 |
2VKC | SOLUTION STRUCTURE OF THE B3BP SMR DOMAIN | 3 |
2VKD | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF LETHAL TOXIN FROM CLOSTRIDIUM SORDELLII IN COMPLEX WITH UDP-GLC AND MANGANESE ION | 3.4.22 2.4.1 |
2VKH | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF LETHAL TOXIN FROM CLOSTRIDIUM SORDELLII IN COMPLEX WITH UDP-GLC AND CALCIUM ION | 3.4.22 2.4.1 |
2VKM | CRYSTAL STRUCTURE OF GRL-8234 BOUND TO BACE (BETA-SECRETASE) | 3.4.23.46 |
2VKQ | CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC 5'-NUCLEOTIDASE III (CN-III, NT5C3) IN COMPLEX WITH BERYLLIUM TRIFLUORIDE | 3.1.3.5 3.1.3.91 |
2VKY | HEADBINDING DOMAIN OF PHAGE P22 TAILSPIKE C-TERMINALLY FUSED TO ISOLEUCINE ZIPPER PIIGCN4 (CHIMERA I) | 3.2.1 |
2VL1 | CRYSTAL STRUCTURE OF BETA-ALANINE SYNTHASE FROM SACCHAROMYCES KLUYVERI IN COMPLEX WITH A GLY-GLY PEPTIDE | 3.5.1.6 |
2VL4 | STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | 3.2.1.25 |
2VL6 | STRUCTURAL ANALYSIS OF THE SULFOLOBUS SOLFATARICUS MCM PROTEIN N- TERMINAL DOMAIN | 3.6.4.12 |
2VL7 | STRUCTURE OF S. TOKODAII XPD4 | 3.6.4.12 |
2VL8 | CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF LETHAL TOXIN FROM CLOSTRIDIUM SORDELLII IN COMPLEX WITH UDP, CASTANOSPERMINE AND CALCIUM ION | 3.4.22 2.4.1 |
2VLA | CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE BPUJI RECOGNITION DOMAIN IN COMPLEX WITH COGNATE DNA | 3.1.21.4 |
2VLC | CRYSTAL STRUCTURE OF NATURAL CINNAMOMIN (ISOFORM III) | 3.2.2.22 |
2VLD | CRYSTAL STRUCTURE OF A REPAIR ENDONUCLEASE FROM PYROCOCCUS ABYSSI | 3.1 |
2VMF | STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | 3.2.1.25 |
2VMK | CRYSTAL STRUCTURE OF E. COLI RNASE E APOPROTEIN - CATALYTIC DOMAIN | 3.1.4 3.1.26.12 |
2VN4 | GLYCOSIDE HYDROLASE FAMILY 15 GLUCOAMYLASE FROM HYPOCREA JECORINA | 3.2.1.3 |
2VN7 | GLYCOSIDE HYDROLASE FAMILY 15 GLUCOAMYLASE FROM HYPOCREA JECORINA | 3.2.1.3 |
2VND | THE N69Q MUTANT OF VIBRIO CHOLERAE ENDONUCLEASE I | 3.1.21 |
2VNG | FAMILY 51 CARBOHYDRATE BINDING MODULE FROM A FAMILY 98 GLYCOSIDE HYDROLASE PRODUCED BY CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH BLOOD GROUP A-TRISACCHARIDE LIGAND. | 3.2.1 |
2VNL | MUTANT Y108WDEL OF THE HEADBINDING DOMAIN OF PHAGE P22 TAILSPIKE C- TERMINALLY FUSED TO ISOLEUCINE ZIPPER PIIGCN4 (CHIMERA II) | 3.2.1 |
2VNM | HUMAN BACE-1 IN COMPLEX WITH 3-(1,1-DIOXIDOTETRAHYDRO-2H-1,2-THIAZIN- 2-YL)-5-(ETHYLAMINO)-N-((1S,2R)-2-HYDROXY-1-(PHENYLMETHYL)-3-(((3-(TRIFLUOROMETHYL)PHENYL)METHYL)AMINO)PROPYL)BENZAMIDE | 3.4.23.46 |
2VNN | HUMAN BACE-1 IN COMPLEX WITH 7-ETHYL-N-((1S,2R)-2-HYDROXY-1-(PHENYLMETHYL)-3-(((3-(TRIFLUOROMETHYL)PHENYL)METHYL)AMINO)PROPYL)-1- METHYL-3,4-DIHYDRO-1H-(1,2,5)THIADIAZEPINO(3,4,5-HI)INDOLE-9- CARBOXAMIDE 2,2-DIOXIDE | 3.4.23.46 |
2VNO | FAMILY 51 CARBOHYDRATE BINDING MODULE FROM A FAMILY 98 GLYCOSIDE HYDROLASE PRODUCED BY CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH BLOOD GROUP B-TRISACCHARIDE LIGAND. | 3.2.1 |
2VNR | FAMILY 51 CARBOHYDRATE BINDING MODULE FROM A FAMILY 98 GLYCOSIDE HYDROLASE PRODUCED BY CLOSTRIDIUM PERFRINGENS. | 3.2.1 |
2VNT | UROKINASE-TYPE PLASMINOGEN ACTIVATOR INHIBITOR COMPLEX WITH A 1-(7- SULPHOAMIDOISOQUINOLINYL)GUANIDINE | 3.4.21.73 |
2VO5 | STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | 3.2.1.25 |
2VO8 | COHESIN MODULE FROM CLOSTRIDIUM PERFRINGENS ATCC13124 FAMILY 33 GLYCOSIDE HYDROLASE. | 3.2.1 |
2VO9 | CRYSTAL STRUCTURE OF THE ENZYMATICALLY ACTIVE DOMAIN OF THE LISTERIA MONOCYTOGENES BACTERIOPHAGE 500 ENDOLYSIN PLY500 | 3.4.24 |
2VOT | STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | 3.2.1.25 |
2VOY | CRYOEM MODEL OF COPA, THE COPPER TRANSPORTING ATPASE FROM ARCHAEOGLOBUS FULGIDUS | 3.6.3.4 7.2.2.8 |
2VPH | CRYSTAL STRUCTURE OF THE HUMAN PROTEIN TYROSINE PHOSPHATASE, NON- RECEPTOR TYPE 4, PDZ DOMAIN | 3.1.3.48 |
2VPT | CLOSTRIDIUM THERMOCELLUM FAMILY 3 CARBOHYDRATE ESTERASE | 3.1.1.72 |
2VQ4 | CARBOHYDRATE-BINDING OF THE STARCH BINDING DOMAIN OF RHIZOPUS ORYZAE GLUCOAMYLASE IN COMPLEX WITH BETA-CYCLODEXTRIN AND MALTOHEPTAOSE | 3.2.1.3 |
2VQ6 | TORPEDO CALIFORNICA ACETYLCHOLINESTERASE COMPLEXED WITH 2-PAM | 3.1.1.7 |
2VQ9 | RNASE ZF-3E | 3.1.27 |
2VQJ | STRUCTURE OF HDAC4 CATALYTIC DOMAIN BOUND TO A TRIFLUOROMETHYLKETONE INHBITOR | 3.5.1.98 |
2VQM | STRUCTURE OF HDAC4 CATALYTIC DOMAIN BOUND TO A HYDROXAMIC ACID INHBITOR | 3.5.1.98 |
2VQO | STRUCTURE OF HDAC4 CATALYTIC DOMAIN WITH A GAIN-OF-FUNCTION MUATION BOUND TO A TRIFLUOROMETHYLKETONE INHBITOR | 3.5.1.98 |
2VQQ | STRUCTURE OF HDAC4 CATALYTIC DOMAIN (A DOUBLE CYSTEINE-TO-ALANINE MUTANT) BOUND TO A TRIFLUOROMETHYLKETONE INHBITOR | 3.5.1.98 |
2VQR | CRYSTAL STRUCTURE OF A PHOSPHONATE MONOESTER HYDROLASE FROM RHIZOBIUM LEGUMINOSARUM: A NEW MEMBER OF THE ALKALINE PHOSPHATASE SUPERFAMILY | 3.1.4 3.1.3 |
2VQT | STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | 3.2.1.25 |
2VQU | STRUCTURAL AND BIOCHEMICAL EVIDENCE FOR A BOAT-LIKE TRANSITION STATE IN BETA-MANNOSIDASES | 3.2.1.25 |
2VQV | STRUCTURE OF HDAC4 CATALYTIC DOMAIN WITH A GAIN-OF-FUNCTION MUTATION BOUND TO A HYDROXAMIC ACID INHIBITOR | 3.5.1.98 |
2VQW | STRUCTURE OF INHIBITOR-FREE HDAC4 CATALYTIC DOMAIN (WITH GAIN-OF- FUNCTION MUTATION HIS332TYR) | 3.5.1.98 |
2VQX | PRECURSOR OF PROTEALYSIN, METALLOPROTEINASE FROM SERRATIA PROTEAMACULANS. | 3.4.24 |
2VR2 | HUMAN DIHYDROPYRIMIDINASE | 3.5.2.2 |
2VR4 | TRANSITION-STATE MIMICRY IN MANNOSIDE HYDROLYSIS: CHARACTERISATION OF TWENTY SIX INHIBITORS AND INSIGHT INTO BINDING FROM LINEAR FREE ENERGY RELATIONSHIPS AND 3-D STRUCTURE | 3.2.1.25 |
2VR5 | CRYSTAL STRUCTURE OF TREX FROM SULFOLOBUS SOLFATARICUS IN COMPLEX WITH ACARBOSE INTERMEDIATE AND GLUCOSE | 3.2.1 |
2VRI | STRUCTURE OF THE NSP3 X-DOMAIN OF HUMAN CORONAVIRUS NL63 | 3.4.19.12 3.4.22 |
2VRJ | BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH N-OCTYL-5- DEOXY-6-OXA-N-(THIO)CARBAMOYLCALYSTEGINE | 3.2.1.21 |
2VRT | CRYSTAL STRUCTURE OF E. COLI RNASE E POSSESSING M1 RNA FRAGMENTS - CATALYTIC DOMAIN | 3.1.4 3.1.26.12 |
2VRW | CRITICAL STRUCTURAL ROLE FOR THE PH AND C1 DOMAINS OF THE VAV1 EXCHANGE FACTOR | 3.6.5.2 |
2VS2 | NEUTRON DIFFRACTION STRUCTURE OF ENDOTHIAPEPSIN IN COMPLEX WITH A GEM- DIOL INHIBITOR. | 3.4.23.22 |
2VS6 | K173A, R174A, K177A-TRICHOSANTHIN | 3.2.2.22 |
2VS7 | THE CRYSTAL STRUCTURE OF I-DMOI IN COMPLEX WITH DNA AND CA | 3.1 |
2VS8 | THE CRYSTAL STRUCTURE OF I-DMOI IN COMPLEX WITH DNA AND MN | 3.1 |
2VSF | STRUCTURE OF XPD FROM THERMOPLASMA ACIDOPHILUM | 3.6.4.12 |
2VSM | NIPAH VIRUS ATTACHMENT GLYCOPROTEIN IN COMPLEX WITH HUMAN CELL SURFACE RECEPTOR EPHRINB2 | 3.2.1.18 |
2VSO | CRYSTAL STRUCTURE OF A TRANSLATION INITIATION COMPLEX | 3.6.1 3.6.4.13 |
2VSW | THE STRUCTURE OF THE RHODANESE DOMAIN OF THE HUMAN DUAL SPECIFICITY PHOSPHATASE 16 | 3.1.3.16 3.1.3.48 |
2VSX | CRYSTAL STRUCTURE OF A TRANSLATION INITIATION COMPLEX | 3.6.1 3.6.4.13 |
2VT0 | X-RAY STRUCTURE OF A CONJUGATE WITH CONDURITOL-BETA-EPOXIDE OF ACID-BETA-GLUCOSIDASE OVEREXPRESSED IN CULTURED PLANT CELLS | 3.2.1.45 2.4.1 3.2.1 |
2VT6 | NATIVE TORPEDO CALIFORNICA ACETYLCHOLINESTERASE COLLECTED WITH A CUMULATED DOSE OF 9400000 GY | 3.1.1.7 |
2VT7 | NATIVE TORPEDO CALIFORNICA ACETYLCHOLINESTERASE COLLECTED WITH A CUMULATED DOSE OF 800000 GY | 3.1.1.7 |
2VTC | THE STRUCTURE OF A GLYCOSIDE HYDROLASE FAMILY 61 MEMBER, CEL61B FROM THE HYPOCREA JECORINA. | 3.2.1.4 |
2VTF | X-RAY CRYSTAL STRUCTURE OF THE ENDO-BETA-N-ACETYLGLUCOSAMINIDASE FROM ARTHROBACTER PROTOPHORMIAE E173Q MUTANT REVEALS A TIM BARREL CATALYTIC DOMAIN AND TWO ANCILLARY DOMAINS | 3.2.1.96 |
2VU8 | CRYSTAL STRUCTURE OF AN INSECT INHIBITOR WITH A FUNGAL TRYPSIN | 3.4.21.4 |
2VU9 | CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN SEROTYPE A BINDING DOMAIN IN COMPLEX WITH GT1B | 3.4.24.69 |
2VUA | CRYSTAL STRUCTURE OF THE BOTULINUM NEUROTOXIN SEROTYPE A BINDING DOMAIN | 3.4.24.69 |
2VUJ | ENVIRONMENTALLY ISOLATED GH11 XYLANASE | 3.2.1.8 |
2VUL | THERMOSTABLE MUTANT OF ENVIRONMENTALLY ISOLATED GH11 XYLANASE | 3.2.1.8 |
2VUN | THE CRYSTAL STRUCTURE OF ENAMIDASE AT 1.9 A RESOLUTION - A NEW MEMBER OF THE AMIDOHYDROLASE SUPERFAMILY | 3.5.2.18 |
2VUR | CHEMICAL DISSECTION OF THE LINK BETWEEN STREPTOZOTOCIN, O-GLCNAC AND PANCREATIC CELL DEATH | 3.2.1.35 3.2.1.169 |
2VUY | CRYSTAL STRUCTURE OF GLYCOGEN DEBRANCHING EXZYME TREX FROM SULFOLOBUS SOLFATARIUS | 3.2.1 |
2VVC | AMINOPYRROLIDINE FACTOR XA INHIBITOR | 3.4.21.6 |
2VVN | BTGH84 IN COMPLEX WITH NH-BUTYLTHIAZOLINE | 3.2.1.52 3.2.1.169 |
2VVS | BTGH84 STRUCTURE IN COMPLEX WITH PUGNAC | 3.2.1.52 3.2.1.169 |
2VVU | AMINOPYRROLIDINE FACTOR XA INHIBITOR | 3.4.21.6 |
2VVV | AMINOPYRROLIDINE-RELATED TRIAZOLE FACTOR XA INHIBITOR | 3.4.21.6 |
2VVZ | STRUCTURE OF THE CATALYTIC DOMAIN OF STREPTOCOCCUS PNEUMONIAE SIALIDASE NANA | 3.2.1.18 |
2VW0 | CRYSTAL STRUCTURE OF THE NANB SIALIDASE FROM STREPTOCOCCUS PNEUMONIAE | 3.2.1.18 |
2VW1 | CRYSTAL STRUCTURE OF THE NANB SIALIDASE FROM STREPTOCOCCUS PNEUMONIAE | 3.2.1.18 |
2VW2 | CRYSTAL STRUCTURE OF THE NANB SIALIDASE FROM STREPTOCOCCUS PNEUMONIAE | 3.2.1.18 |
2VW8 | CRYSTAL STRUCTURE OF QUINOLONE SIGNAL RESPONSE PROTEIN PQSE FROM PSEUDOMONAS AERUGINOSA | 3.1.2.32 |
2VWB | STRUCTURE OF THE ARCHAEAL KAE1-BUD32 FUSION PROTEIN MJ1130: A MODEL FOR THE EUKARYOTIC EKC-KEOPS SUBCOMPLEX INVOLVED IN TRANSCRIPTION AND TELOMERE HOMEOSTASIS. | 3.4.24.57 2.3.1.234 2.7.11.1 |
2VWL | AMINOPYRROLIDINE FACTOR XA INHIBITOR | 3.4.21.6 |
2VWM | AMINOPYRROLIDINE FACTOR XA INHIBITOR | 3.4.21.6 |
2VWN | AMINOPYRROLIDINE FACTOR XA INHIBITOR | 3.4.21.6 |
2VWO | AMINOPYRROLIDINE FACTOR XA INHIBITOR | 3.4.21.6 |
2VX4 | CELLVIBRIO JAPONICUS MANNANASE CJMAN26C NATIVE FORM | 3.2.1 |
2VX5 | CELLVIBRIO JAPONICUS MANNANASE CJMAN26C MANNOSE-BOUND FORM | 3.2.1 |
2VX6 | CELLVIBRIO JAPONICUS MANNANASE CJMAN26C GAL1MAN4-BOUND FORM | 3.2.1 |
2VX7 | CELLVIBRIO JAPONICUS MANNANASE CJMAN26C MANNOBIOSE-BOUND FORM | 3.2.1 |
2VXR | CRYSTAL STRUCTURE OF THE BOTULINUM NEUROTOXIN SEROTYPE G BINDING DOMAIN | 3.4.24.69 |
2VY0 | THE X-RAY STRUCTURE OF ENDO-BETA-1,3-GLUCANASE FROM PYROCOCCUS FURIOSUS | 3.2.1.39 |
2VYA | CRYSTAL STRUCTURE OF FATTY ACID AMIDE HYDROLASE CONJUGATED WITH THE DRUG-LIKE INHIBITOR PF-750 | 3.5.1.4 3.5.1.99 3.1.1 |
2VYE | CRYSTAL STRUCTURE OF THE DNAC-SSDNA COMPLEX | 3.6.1 3.6.4.12 |
2VYF | CRYSTAL STRUCTURE OF THE DNAC | 3.6.1 3.6.4.12 |
2VYO | CHITIN DEACETYLASE FAMILY MEMBER FROM ENCEPHALITOZOON CUNICULI | 3.5.1.41 |
2VZ8 | CRYSTAL STRUCTURE OF MAMMALIAN FATTY ACID SYNTHASE | 2.3.1.85 1.1.1.100 1.3.1.39 2.3.1.38 2.3.1.39 2.3.1.41 3.1.2.14 4.2.1.59 |
2VZO | CRYSTAL STRUCTURE OF AMYCOLATOPSIS ORIENTALIS EXO-CHITOSANASE CSXA | 3.2.1.165 |
2VZP | ATOMIC RESOLUTION STRUCTURE OF THE C-TERMINAL CBM35 FROM AMYCOLATOPSIS ORIENTALIS EXO-CHITOSANASE CSXA | 3.2.1.165 |
2VZQ | C-TERMINAL CBM35 FROM AMYCOLATOPSIS ORIENTALIS EXO-CHITOSANASE CSXA IN COMPLEX WITH DIGALACTURONIC ACID | 3.2.1.165 |
2VZR | C-TERMINAL CBM35 FROM AMYCOLATOPSIS ORIENTALIS EXO-CHITOSANASE CSXA IN COMPLEX WITH GLUCURONIC ACID | 3.2.1.165 |
2VZS | CHITOSAN PRODUCT COMPLEX OF AMYCOLATOPSIS ORIENTALIS EXO-CHITOSANASE CSXA | 3.2.1.165 |
2VZT | COMPLEX OF AMYCOLATOPSIS ORIENTALIS EXO-CHITOSANASE CSXA E541A WITH PNP-BETA-D-GLUCOSAMINE | 3.2.1.165 |
2VZU | COMPLEX OF AMYCOLATOPSIS ORIENTALIS EXO-CHITOSANASE CSXA D469A WITH PNP-BETA-D-GLUCOSAMINE | 3.2.1.165 |
2W00 | CRYSTAL STRUCTURE OF THE HSDR SUBUNIT OF THE ECOR124I RESTRICTION ENZYME IN COMPLEX WITH ATP | 3.1.21.3 |
2W0D | DOES A FAST NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY- AND X-RAY CRYSTALLOGRAPHY HYBRID APPROACH PROVIDE RELIABLE STRUCTURAL INFORMATION OF LIGAND-PROTEIN COMPLEXES? A CASE STUDY OF METALLOPROTEINASES. | 3.4.24.65 |
2W11 | STRUCTURE OF THE L-2-HALOACID DEHALOGENASE FROM SULFOLOBUS TOKODAII | 3.8.1.2 |
2W12 | HIGH-RESOLUTION CRYSTAL STRUCTURE OF THE P-I SNAKE VENOM METALLOPROTEINASE BAP1 IN COMPLEX WITH A PEPTIDOMIMETIC: INSIGHTS INTO INHIBITOR BINDING | 3.4.24 |
2W13 | HIGH-RESOLUTION CRYSTAL STRUCTURE OF THE P-I SNAKE VENOM METALLOPROTEINASE BAP1 IN COMPLEX WITH A PEPTIDOMIMETIC: INSIGHTS INTO INHIBITOR BINDING | 3.4.24 |
2W14 | HIGH-RESOLUTION CRYSTAL STRUCTURE OF THE P-I SNAKE VENOM METALLOPROTEINASE BAP1 IN COMPLEX WITH A PEPTIDOMIMETIC: INSIGHTS INTO INHIBITOR BINDING | 3.4.24 |
2W15 | HIGH-RESOLUTION CRYSTAL STRUCTURE OF THE P-I SNAKE VENOM METALLOPROTEINASE BAP1 IN COMPLEX WITH A PEPTIDOMIMETIC: INSIGHTS INTO INHIBITOR BINDING | 3.4.24 |
2W1L | THE INTERDEPENDENCE OF WAVELENGTH, REDUNDANCY AND DOSE IN SULFUR SAD EXPERIMENTS: 0.979 A WAVELENGTH 991 IMAGES DATA | 3.2.1.17 |
2W1M | THE INTERDEPENDENCE OF WAVELENGTH, REDUNDANCY AND DOSE IN SULFUR SAD EXPERIMENTS: 2.070 A WAVELENGTH WITH 2THETA 30 DEGREES DATA | 3.2.1.17 |
2W1N | COHESIN AND FIBRONECTIN TYPE-III DOUBLE MODULE CONSTRUCT FROM THE CLOSTRIDIUM PERFRINGENS GLYCOSIDE HYDROLASE GH84C | 3.2.1.52 3.2.1.169 |
2W1Q | UNIQUE LIGAND BINDING SPECIFICITY FOR A FAMILY 32 CARBOHYDRATE- BINDING MODULE FROM THE MU TOXIN PRODUCED BY CLOSTRIDIUM PERFRINGENS | 3.2.1.35 |
2W1S | UNIQUE LIGAND BINDING SPECIFICITY OF A FAMILY 32 CARBOHYDRATE-BINDING MODULE FROM THE MU TOXIN PRODUCED BY CLOSTRIDIUM PERFRINGENS | 3.2.1.35 |
2W1U | A FAMILY 32 CARBOHYDRATE-BINDING MODULE, FROM THE MU TOXIN PRODUCED BY CLOSTRIDIUM PERFRINGENS, IN COMPLEX WITH BETA-D-GLCNAC-BETA(1,3) GALNAC | 3.2.1.35 |
2W1V | CRYSTAL STRUCTURE OF MOUSE NITRILASE-2 AT 1.4A RESOLUTION | 3.5 3.5.1.3 |
2W1X | THE INTERDEPENDENCE OF WAVELENGTH, REDUNDANCY AND DOSE IN SULFUR SAD EXPERIMENTS: 1.284 A WAVELENGTH 360 IMAGES DATA | 3.2.1.17 |
2W1Y | THE INTERDEPENDENCE OF WAVELENGTH, REDUNDANCY AND DOSE IN SULFUR SAD EXPERIMENTS: 1.540 A WAVELENGTH 180 IMAGES DATA | 3.2.1.17 |
2W20 | STRUCTURE OF THE CATALYTIC DOMAIN OF THE NATIVE NANA SIALIDASE FROM STREPTOCOCCUS PNEUMONIAE | 3.2.1.18 |
2W22 | ACTIVATION MECHANISM OF BACTERIAL THERMOALKALOPHILIC LIPASES | 3.1.1.3 |
2W26 | FACTOR XA IN COMPLEX WITH BAY59-7939 | 3.4.21.6 |
2W2D | CRYSTAL STRUCTURE OF A CATALYTICALLY ACTIVE, NON-TOXIC ENDOPEPTIDASE DERIVATIVE OF CLOSTRIDIUM BOTULINUM TOXIN A | 3.4.24.69 |
2W2G | HUMAN SARS CORONAVIRUS UNIQUE DOMAIN | 3.4.22 3.4.19.12 3.4.22.69 |
2W2M | WT PCSK9-DELTAC BOUND TO WT EGF-A OF LDLR | 3.4.21 |
2W2N | WT PCSK9-DELTAC BOUND TO EGF-A H306Y MUTANT OF LDLR | 3.4.21 |
2W2O | PCSK9-DELTAC D374Y MUTANT BOUND TO WT EGF-A OF LDLR | 3.4.21 |
2W2P | PCSK9-DELTAC D374A MUTANT BOUND TO WT EGF-A OF LDLR | 3.4.21 |
2W2Q | PCSK9-DELTAC D374H MUTANT BOUND TO WT EGF-A OF LDLR | 3.4.21 |
2W2W | PLCG2 SPLIT PLECKSTRIN HOMOLOGY (PH) DOMAIN | 3.1.4.11 |
2W35 | STRUCTURES OF ENDONUCLEASE V WITH DNA REVEAL INITIATION OF DEAMINATED ADENINE REPAIR | 3.1.21.7 |
2W36 | STRUCTURES OF ENDONUCLEASE V WITH DNA REVEAL INITIATION OF DEAMINATED ADENINE REPAIR | 3.1.21.7 |
2W39 | GLC(BETA-1-3)GLC DISACCHARIDE IN -1 AND -2 SITES OF LAMINARINASE 16A FROM PHANEROCHAETE CHRYSOSPORIUM | 3.2.1.6 |
2W3I | CRYSTAL STRUCTURE OF FXA IN COMPLEX WITH 4,4-DISUBSTITUTED PYRROLIDINE-1,2-DICARBOXAMIDE INHIBITOR 2 | 3.4.21.6 |
2W3K | CRYSTAL STRUCTURE OF FXA IN COMPLEX WITH 4,4-DISUBSTITUTED PYRROLIDINE-1,2-DICARBOXAMIDE INHIBITOR 1 | 3.4.21.6 |
2W3O | CRYSTAL STRUCTURE OF THE HUMAN PNKP FHA DOMAIN IN COMPLEX WITH AN XRCC1-DERIVED PHOSPHOPEPTIDE | 3.1.3.32 2.7.1.78 |
2W3T | CHLORO COMPLEX OF THE NI-FORM OF E.COLI DEFORMYLASE | 3.5.1.31 3.5.1.88 |
2W3U | FORMATE COMPLEX OF THE NI-FORM OF E.COLI DEFORMYLASE | 3.5.1.31 3.5.1.88 |
2W3Z | STRUCTURE OF A STREPTOCOCCUS MUTANS CE4 ESTERASE | 3.5.1.41 |
2W43 | STRUCTURE OF L-HALOACID DEHALOGENASE FROM S. TOKODAII | 3.1.8.2 3.8.1.2 |
2W45 | EPSTEIN-BARR VIRUS ALKALINE NUCLEASE | 3.1.11 3.1 |
2W46 | CBM35 FROM CELLVIBRIO JAPONICUS ABF62 | 3.2.1.55 |
2W4B | EPSTEIN-BARR VIRUS ALKALINE NUCLEASE D203S MUTANT | 3.1.11 3.1 |
2W4C | HUMAN COMMON-TYPE ACYLPHOSPHATASE VARIANT, A99 | 3.6.1.7 |
2W4D | ACYLPHOSPHATASE VARIANT G91A FROM PYROCOCCUS HORIKOSHII | 3.6.1.7 |
2W4E | STRUCTURE OF AN N-TERMINALLY TRUNCATED NUDIX HYDROLASE DR2204 FROM DEINOCOCCUS RADIODURANS | 3.6.1.13 |
2W4L | HUMAN DCMP DEAMINASE | 3.5.4.12 |
2W4M | THE CRYSTAL STRUCTURE OF HUMAN N-ACETYLNEURAMINIC ACID PHOSPHATASE, NANP | 3.1.3.29 |
2W4P | HUMAN COMMON-TYPE ACYLPHOSPHATASE VARIANT, A99G | 3.6.1.7 |
2W4R | CRYSTAL STRUCTURE OF THE REGULATORY DOMAIN OF HUMAN LGP2 | 3.6.1 3.6.4.13 |
2W4X | BTGH84 IN COMPLEX WITH STZ | 3.2.1.52 3.2.1.169 |
2W52 | 2 BETA-GLUCANS (6-O-GLUCOSYL-LAMINARITRIOSE) IN BOTH DONOR AND ACCEPTOR SITES OF GH16 LAMINARINASE 16A FROM PHANEROCHAETE CHRYSOSPORIUM. | 3.2.1.6 |
2W5F | HIGH RESOLUTION CRYSTALLOGRAPHIC STRUCTURE OF THE CLOSTRIDIUM THERMOCELLUM N-TERMINAL ENDO-1,4-BETA-D-XYLANASE 10B (XYN10B) CBM22-1- GH10 MODULES COMPLEXED WITH XYLOHEXAOSE | 3.2.1.8 |
2W5G | RNASE A-5'-ATP COMPLEX | 3.1.27.5 4.6.1.18 |
2W5I | RNASE A-AP3A COMPLEX | 3.1.27.5 4.6.1.18 |
2W5J | STRUCTURE OF THE C14-ROTOR RING OF THE PROTON TRANSLOCATING CHLOROPLAST ATP SYNTHASE | 3.6.3.14 |
2W5K | RNASE A-NADPH COMPLEX | 3.1.27.5 4.6.1.18 |
2W5L | RNASE A-NADP COMPLEX | 3.1.27.5 4.6.1.18 |
2W5M | RNASE A-PYROPHOSPHATE ION COMPLEX | 3.1.27.5 4.6.1.18 |
2W5N | NATIVE STRUCTURE OF THE GH93 ALPHA-L-ARABINOFURANOSIDASE OF FUSARIUM GRAMINEARUM | 3.2.1.55 |
2W5O | COMPLEX STRUCTURE OF THE GH93 ALPHA-L-ARABINOFURANOSIDASE OF FUSARIUM GRAMINEARUM WITH ARABINOBIOSE | 3.2.1.55 |
2W5V | STRUCTURE OF TAB5 ALKALINE PHOSPHATASE MUTANT HIS 135 ASP WITH MG BOUND IN THE M3 SITE. | 3.1.3.1 |
2W5W | STRUCTURE OF TAB5 ALKALINE PHOSPHATASE MUTANT HIS 135 ASP WITH ZN BOUND IN THE M3 SITE. | 3.1.3.1 |
2W5X | STRUCTURE OF TAB5 ALKALINE PHOSPHATASE MUTANT HIS 135 GLU WITH MG BOUND IN THE M3 SITE. | 3.1.3.1 |
2W66 | BTGH84 IN COMPLEX WITH HQ602 | 3.2.1.52 3.2.1.169 |
2W67 | BTGH84 IN COMPLEX WITH FMA34 | 3.2.1.52 3.2.1.169 |
2W68 | ENHANCING THE RECEPTOR AFFINITY OF THE SIALIC ACID-BINDING DOMAIN OF VIBRIO CHOLERAE SIALIDASE THROUGH MULTIVALENCY | 3.2.1.18 |
2W69 | INFLUENZA POLYMERASE FRAGMENT | 3.1 |
2W6C | ACHE IN COMPLEX WITH A BIS-(-)-NOR-MEPTAZINOL DERIVATIVE | 3.1.1.7 |
2W6D | BACTERIAL DYNAMIN-LIKE PROTEIN LIPID TUBE BOUND | 3.6.5.5 |
2W6F | LOW RESOLUTION STRUCTURES OF BOVINE MITOCHONDRIAL F1-ATPASE DURING CONTROLLED DEHYDRATION: HYDRATION STATE 2. | 3.6.3.14 |
2W7S | SPLA SERINE PROTEASE OF STAPHYLOCOCCUS AUREUS (1.8A) | 3.4.21.19 3.4.21 |
2W7U | SPLA SERINE PROTEASE OF STAPHYLOCOCCUS AUREUS (2.4A) | 3.4.21.19 3.4.21 |
2W87 | XYL-CBM35 IN COMPLEX WITH GLUCURONIC ACID CONTAINING DISACCHARIDE. | 3.2.1 |
2W8S | CRYSTAL STRUCTURE OF A CATALYTICALLY PROMISCUOUS PHOSPHONATE MONOESTER HYDROLASE FROM BURKHOLDERIA CARYOPHYLLI | 3.1.4 3.1 3.1.3 3.1.6 |
2W91 | STRUCTURE OF A STREPTOCOCCUS PNEUMONIAE FAMILY 85 GLYCOSIDE HYDROLASE, ENDO-D. | 3.2.1.96 |
2W92 | STRUCTURE OF A STREPTOCOCCUS PNEUMONIAE FAMILY 85 GLYCOSIDE HYDROLASE, ENDO-D, IN COMPLEX WITH NAG-THIAZOLINE. | 3.2.1.96 |
2W9X | THE ACTIVE SITE OF A CARBOHYDRATE ESTERASE DISPLAYS DIVERGENT CATALYTIC AND NON-CATALYTIC BINDING FUNCTIONS | 3.1.1 3.1.1.72 |
2WA1 | STRUCTURE OF THE METHYLTRANSFERASE DOMAIN FROM MODOC VIRUS, A FLAVIVIRUS WITH NO KNOWN VECTOR (NKV) | 3.4.21.91 3.6.1.15 3.6.4.13 |
2WA2 | STRUCTURE OF THE METHYLTRANSFERASE DOMAIN FROM MODOC VIRUS, A FLAVIVIRUS WITH NO KNOWN VECTOR (NKV) | 3.4.21.91 3.6.1.15 3.6.4.13 |
2WAA | STRUCTURE OF A FAMILY TWO CARBOHYDRATE ESTERASE FROM CELLVIBRIO JAPONICUS | 3.1.1.72 3.1.1 |
2WAB | STRUCTURE OF AN ACTIVE SITE MUTANT OF A FAMILY TWO CARBOHYDRATE ESTERASE FROM CLOSTRIDIUM THERMOCELLUM IN COMPLEX WITH CELLUOHEXASE | 3.2.1.4 3.1.1 3.1.1.72 |
2WAC | EXTENDED TUDOR DOMAIN OF DROSOPHILA MELANOGASTER TUDOR-SN (P100) | 3.1.31.1 |
2WAE | PENICILLIN-BINDING PROTEIN 2B (PBP-2B) FROM STREPTOCOCCUS PNEUMONIAE (STRAIN 5204) | 3.4 |
2WAF | PENICILLIN-BINDING PROTEIN 2B (PBP-2B) FROM STREPTOCOCCUS PNEUMONIAE (STRAIN R6) | 3.4 |
2WAG | THE STRUCTURE OF A FAMILY 25 GLYCOSYL HYDROLASE FROM BACILLUS ANTHRACIS. | 3.2.1.17 |
2WAN | PULLULANASE FROM BACILLUS ACIDOPULLULYTICUS | 3.2.1.41 |
2WAO | STRUCTURE OF A FAMILY TWO CARBOHYDRATE ESTERASE FROM CLOSTRIDIUM THERMOCELLUM IN COMPLEX WITH CELLOHEXAOSE | 3.2.1.4 3.1.1 3.1.1.72 |
2WAP | 3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH THE DRUG-LIKE UREA INHIBITOR PF-3845 | 3.5.1.4 3.5.1.99 3.1.1 |
2WAR | HEN EGG WHITE LYSOZYME E35Q CHITOPENTAOSE COMPLEX | 3.2.1.17 |
2WAX | STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3- FDF PEPTIDE | 3.6.1 3.6.4.13 |
2WAY | STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3- FDF PEPTIDE | 3.6.1 3.6.4.13 |
2WB5 | GLCNACSTATINS ARE NANOMOLAR INHIBITORS OF HUMAN O-GLCNACASE INDUCING CELLULAR HYPER-O-GLCNACYLATION | 3.2.1.35 3.2.1.52 3.2.1.169 |
2WBB | FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE-1- PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH AN AMP SITE INHIBITOR | 3.1.3.11 |
2WBD | FRUCTOSE-1,6-BISPHOSPHATASE(D-FRUCTOSE-1,6-BISPHOSPHATE-1- PHOSPHOHYDROLASE) (E.C.3.1.3.11) COMPLEXED WITH AN AMP SITE INHIBITOR | 3.1.3.11 |
2WBF | CRYSTAL STRUCTURE ANALYSIS OF SERA5E FROM PLASMODIUM FALCIPARUM WITH LOOP 690-700 ORDERED | 3.4.22 |
2WBG | STRUCTURE OF FAMILY 1 BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH 3-IMINO-2-OXA-(+)-CASTANOSPERMINE | 3.2.1.21 |
2WBK | STRUCTURE OF THE MICHAELIS COMPLEX OF BETA-MANNOSIDASE, MAN2A, PROVIDES INSIGHT INTO THE CONFORMATIONAL ITINERARY OF MANNOSIDE HYDROLYSIS | 3.2.1.25 |
2WBN | CRYSTAL STRUCTURE OF THE G2P (LARGE TERMINASE) NUCLEASE DOMAIN FROM THE BACTERIOPHAGE SPP1 | 3.1 3.6.4 |
2WBY | CRYSTAL STRUCTURE OF HUMAN INSULIN-DEGRADING ENZYME IN COMPLEX WITH INSULIN | 3.4.24.56 |
2WC0 | CRYSTAL STRUCTURE OF HUMAN INSULIN DEGRADING ENZYME IN COMPLEX WITH IODINATED INSULIN | 3.4.24.56 |
2WC3 | STRUCTURE OF FAMILY 1 BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH 3-IMINO-2-OXA-(+)-8-EPI-CASTANOSPERMINE | 3.2.1.21 |
2WC4 | STRUCTURE OF FAMILY 1 BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH 3-IMINO-2-THIA-(+)-CASTANOSPERMINE | 3.2.1.21 |
2WC7 | CRYSTAL STRUCTURE OF NOSTOC PUNCTIFORME DEBRANCHING ENZYME(NPDE)(ACARBOSE SOAKED) | 3.2.1.54 |
2WC9 | CRYSTAL STRUCTURE OF THE G2P (LARGE TERMINASE) NUCLEASE DOMAIN FROM THE BACTERIOPHAGE SPP1 WITH BOUND MN | 3.1 3.6.4 |
2WCA | BTGH84 IN COMPLEX WITH N-BUTYL PUGNAC | 3.2.1.52 3.2.1.169 |
2WCG | X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH N-OCTYL(CYCLIC GUANIDINE)-NOJIRIMYCIN IN THE ACTIVE SITE | 3.2.1.45 2.4.1 3.2.1 |
2WCS | CRYSTAL STRUCTURE OF DEBRANCHING ENZYME FROM NOSTOC PUNCTIFORME (NPDE) | 3.2.1.54 |
2WCT | HUMAN SARS CORONAVIRUS UNIQUE DOMAIN (TRICLINIC FORM) | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2WCW | 1.6A RESOLUTION STRUCTURE OF ARCHAEOGLOBUS FULGIDUS HJC, A HOLLIDAY JUNCTION RESOLVASE FROM AN ARCHAEAL HYPERTHERMOPHILE | 3.1.22.4 |
2WCX | CRYSTAL STRUCTURE OF HEPATITIS C VIRUS NS5B POLYMERASE IN COMPLEX WITH THIENOPYRROLE-BASED FINGER-LOOP INHIBITORS | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2WCZ | 1.6A RESOLUTION STRUCTURE OF ARCHAEOGLOBUS FULGIDUS HJC, A HOLLIDAY JUNCTION RESOLVASE FROM AN ARCHAEAL HYPERTHERMOPHILE | 3.1.22.4 |
2WDB | A FAMILY 32 CARBOHYDRATE-BINDING MODULE, FROM THE MU TOXIN PRODUCED BY CLOSTRIDIUM PERFRINGENS, IN COMPLEX WITH BETA-D-GLCNAC-BETA(1,2) MANNOSE | 3.2.1.35 |
2WDP | CRYSTAL STRUCTURE OF LIGAND FREE HUMAN CASPASE-6 | 3.4.22.59 |
2WDT | CRYSTAL STRUCTURE OF PLASMODIUM FALCIPARUM UCHL3 IN COMPLEX WITH THE SUICIDE INHIBITOR UBVME | 3.4.19.12 |
2WE0 | EBV DUTPASE MUTANT CYS4SER | 3.6.1.23 |
2WE1 | EBV DUTPASE MUTANT ASP131ASN WITH BOUND DUMP | 3.6.1.23 |
2WE2 | EBV DUTPASE DOUBLE MUTANT GLY78ASP-ASP131SER WITH DUMP | 3.6.1.23 |
2WE3 | EBV DUTPASE INACTIVE MUTANT DELETED OF MOTIF V | 3.6.1.23 |
2WE6 | CRYSTAL STRUCTURE OF PLASMODIUM FALCIPARUM UBIQUITIN CARBOXYL- TERMINAL HYDROLASE 3 (UCHL3) | 3.4.19.12 |
2WEA | ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL[CYCLO-7[(2R)-((N-VALYL) AMINO)-2-(HYDROXYL-(1S)-1-METHYOXYCARBONYL-2-PHENYLETHOXY) PHOSPHINYLOXY-ETHYL]-1-NAPHTHALENEACETAMIDE], SODIUM SALT | 3.4.23.20 |
2WEB | ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL(2S)-[1-(((N-FORMYL)-L-VALYL)AMINO-2-(2-NAPHTHYL)ETHYL)HYDROXYPHOSPHINYLOXY]-3-PHENYLPROPANOATE, SODIUM SALT | 3.4.23.20 |
2WEC | ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL(2S)-[1-(((N-(1-NAPHTHALENEACETYL))-L-VALYL)AMINOMETHYL)HYDROXY PHOSPHINYLOXY]-3-PHENYLPROPANOATE, SODIUM SALT | 3.4.23.20 |
2WED | ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE MACROCYCLIC INHIBITOR:METHYL[CYCLO-7[(2R)-((N-VALYL)AMINO)-2-(HYDROXYL-(1S)-1-METHYOXYCARBONYL-2-PHENYLETHOXY)PHOSPHINYLOXY-ETHYL]-1-NAPHTHALENEACETAMIDE], SODIUM SALT | 3.4.23.20 |
2WEF | HUMAN 3'(2'), 5'-BISPHOSPHATE NUCLEOTIDASE 1 (BPNT1) IN COMPLEX WITH AMP, PO4 AND MAGNESIUM | 3.1.3.7 |
2WEY | HUMAN PDE-PAPAVERINE COMPLEX OBTAINED BY LIGAND SOAKING OF CROSS- LINKED PROTEIN CRYSTALS | 3.1.4.17 3.1.4.35 |
2WEZ | HUMAN BACE-1 IN COMPLEX WITH 1-ETHYL-N-((1S,2R)-2-HYDROXY-3-(((3-(METHYLOXY)PHENYL)METHYL)AMINO)-1-(PHENYLMETHYL)PROPYL)-4-(2-OXO-1- PYRROLIDINYL)-1H-INDOLE-6-CARBOXAMIDE | 3.4.23.46 |
2WF0 | HUMAN BACE-1 IN COMPLEX WITH 4-ETHYL-N-((1S,2R)-2-HYDROXY-1-(PHENYLMETHYL)-3-(((3-(TRIFLUOROMETHYL)PHENYL)METHYL)AMINO)PROPYL)-8-(2-OXO-1-PYRROLIDINYL)-6-QUINOLINECARBOXAMIDE | 3.4.23.46 |
2WF1 | HUMAN BACE-1 IN COMPLEX WITH 7-ETHYL-N-((1S,2R)-2-HYDROXY-3-(((3-(METHYLOXY)PHENYL(METHYL)AMINO)-1-(PHENYLMETHYL)PROPYL)-1-METHYL-3,4- DIHYDRO-1H-(1,2,5)THIADIAZEPINO(3,4,5-HI)INDOLE-9-CARBOXAMIDE 2,2- DIOXIDE | 3.4.23.46 |
2WF2 | HUMAN BACE-1 IN COMPLEX WITH 8-ETHYL-N-((1S,2R)-2-HYDROXY-3-(((3-(METHYLOXY)PHENYL)METHYL)AMINO)-1-(PHENYLMETHYL)PROPYL)-1-METHYL-3,4,7, 8-TETRAHYDRO-1H,6H-(1,2,5)THIADIAZEPINO(5,4,3-DE)QUINOXALINE-10- CARBOXAMIDE 2,2-DIOXIDE | 3.4.23.46 |
2WF3 | HUMAN BACE-1 IN COMPLEX WITH 6-(ETHYLAMINO)-N-((1S,2R)-2-HYDROXY-3-(((3-(METHYLOXY)PHENYL)METHYL)AMINO)-1-(PHENYLMETHYL)PROPYL)-1-METHYL-1, 3,4,5-TETRAHYDRO-2,1-BENZOTHIAZEPINE-8-CARBOXAMIDE 2,2-DIOXIDE | 3.4.23.46 |
2WF4 | HUMAN BACE-1 IN COMPLEX WITH 6-ETHYL-1-METHYL-N-((1S)-2-OXO-1-(PHENYLMETHYL)-3-(TETRAHYDRO-2H-PYRAN-4-YLAMINO)PROPYL)-1,3,4,6- TETRAHYDRO(1,2)THIAZEPINO(5,4,3-CD)INDOLE-8-CARBOXAMIDE 2,2-DIOXIDE | 3.4.23.46 |
2WFM | CRYSTAL STRUCTURE OF POLYNEURIDINE ALDEHYDE ESTERASE MUTANT (H244A) | 3.1.1.78 |
2WFZ | NON-AGED CONJUGATE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE WITH SOMAN | 3.1.1.7 |
2WG0 | AGED CONJUGATE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE WITH SOMAN (OBTAINED BY IN CRYSTALLO AGING) | 3.1.1.7 |
2WG1 | TERNARY COMPLEX OF THE AGED CONJUGATE OF TORPEDO CALIFORNICA ACEYLCHOLINESTERASE WITH SOMAN AND 2-PAM | 3.1.1.7 |
2WG2 | NON-AGED CONJUGATE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE WITH SOMAN (ALTERNATIVE REFINEMENT) | 3.1.1.7 |
2WG5 | PROTEASOME-ACTIVATING NUCLEOTIDASE (PAN) N-DOMAIN (57-134) FROM ARCHAEOGLOBUS FULGIDUS FUSED TO GCN4 | 3.6.4.8 |
2WG6 | PROTEASOME-ACTIVATING NUCLEOTIDASE (PAN) N-DOMAIN (57-134) FROM ARCHAEOGLOBUS FULGIDUS FUSED TO GCN4, P61A MUTANT | 3.6.4.8 |
2WG7 | STRUCTURE OF ORYZA SATIVA (RICE) PLA2 | 3.1.1.4 |
2WG8 | STRUCTURE OF ORYZA SATIVA (RICE) PLA2, ORTHORHOMBIC CRYSTAL FORM | 3.1.1.4 |
2WG9 | STRUCTURE OF ORYZA SATIVA (RICE) PLA2, COMPLEX WITH OCTANOIC ACID | 3.1.1.4 |
2WGI | CRYSTAL STRUCTURE OF THE ACYL-ENZYME OXA-10 W154A-BENZYLPENICILLIN AT PH 6 | 3.5.2.6 |
2WGP | CRYSTAL STRUCTURE OF HUMAN DUAL SPECIFICITY PHOSPHATASE 14 | 3.1.3.48 3.1.3.16 |
2WGV | CRYSTAL STRUCTURE OF THE OXA-10 V117T MUTANT AT PH 6.5 INHIBITED BY A CHLORIDE ION | 3.5.2.6 |
2WGW | CRYSTAL STRUCTURE OF THE OXA-10 V117T MUTANT AT PH 8.0 | 3.5.2.6 |
2WH7 | THE PARTIAL STRUCTURE OF A GROUP A STREPTPCOCCAL PHAGE-ENCODED TAIL FIBRE HYALURONATE LYASE HYLP2 | 3.2.1.35 |
2WHG | CRYSTAL STRUCTURE OF THE DI-ZINC METALLO-BETA-LACTAMASE VIM-4 FROM PSEUDOMONAS AERUGINOSA | 3.5.2.6 |
2WHH | HIV-1 PROTEASE TETHERED DIMER Q-PRODUCT COMPLEX ALONG WITH NUCLEOPHILIC WATER MOLECULE | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2WHJ | UNDERSTANDING HOW DIVERSE MANNANASES RECOGNISE HETEROGENEOUS SUBSTRATES | 3.2.1.78 |
2WHK | STRUCTURE OF BACILLUS SUBTILIS MANNANASE MAN26 | 3.2.1.78 |
2WHL | UNDERSTANDING HOW DIVERSE MANNANASES RECOGNISE HETEROGENEOUS SUBSTRATES | 3.2.1.78 |
2WHM | CELLVIBRIO JAPONICUS MAN26A E121A AND E320G DOUBLE MUTANT IN COMPLEX WITH MANNOBIOSE | 3.2.1.78 |
2WHO | CRYSTAL STRUCTURE OF HEPATITIS C VIRUS NS5B POLYMERASE FROM 1B GENOTYPE IN COMPLEX WITH A NON-NUCLEOSIDE INHIBITOR | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2WHP | CRYSTAL STRUCTURE OF ACETYLCHOLINESTERASE, PHOSPHONYLATED BY SARIN AND IN COMPLEX WITH HI-6 | 3.1.1.7 |
2WHQ | CRYSTAL STRUCTURE OF ACETYLCHOLINESTERASE, PHOSPHONYLATED BY SARIN (AGED) IN COMPLEX WITH HI-6 | 3.1.1.7 |
2WHR | CRYSTAL STRUCTURE OF ACETYLCHOLINESTERASE IN COMPLEX WITH K027 | 3.1.1.7 |
2WHX | A SECOND CONFORMATION OF THE NS3 PROTEASE-HELICASE FROM DENGUE VIRUS | 3.4.21.91 3.6.1.15 3.6.1 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2WHZ | DIPEPTIDE INHIBITORS OF THERMOLYSIN | 3.4.24.27 |
2WI0 | DIPEPTIDE INHIBITORS OF THERMOLYSIN | 3.4.24.27 |
2WID | NONAGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA1 | 3.1.1.8 |
2WIE | HIGH-RESOLUTION STRUCTURE OF THE ROTOR RING FROM A PROTON DEPENDENT ATP SYNTHASE | 3.6.3.14 |
2WIF | AGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA1 | 3.1.1.8 |
2WIG | NONAGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA4 | 3.1.1.8 |
2WIJ | NONAGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA5 | 3.1.1.8 |
2WIK | NONAGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA6 | 3.1.1.8 |
2WIL | AGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA5 | 3.1.1.8 |
2WIW | CRYSTAL STRUCTURES OF HOLLIDAY JUNCTION RESOLVASES FROM ARCHAEOGLOBUS FULGIDUS BOUND TO DNA SUBSTRATE | 3.1.22.4 |
2WIZ | CRYSTAL STRUCTURES OF HOLLIDAY JUNCTION RESOLVASES FROM ARCHAEOGLOBUS FULGIDUS BOUND TO DNA SUBSTRATE | 3.1.22.4 |
2WJ0 | CRYSTAL STRUCTURES OF HOLLIDAY JUNCTION RESOLVASES FROM ARCHAEOGLOBUS FULGIDUS BOUND TO DNA SUBSTRATE | 3.1.22.4 |
2WJ1 | 3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH 7-PHENYL-1-(4-(PYRIDIN-2-YL)OXAZOL-2-YL)HEPTAN- 1-ONE, AN ALPHA-KETOOXAZOLE | 3.5.1.4 3.5.1.99 3.1.1 |
2WJ2 | 3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH 7-PHENYL-1-(5-(PYRIDIN-2-YL)OXAZOL-2-YL)HEPTAN- 1-ONE, AN ALPHA-KETOOXAZOLE | 3.5.1.4 3.5.1.99 3.1.1 |
2WJA | CRYSTAL STRUCTURE OF THE TYROSINE PHOSPHATASE WZB FROM ESCHERICHIA COLI K30 IN COMPLEX WITH PHOSPHATE. | 3.1.3.48 |
2WJD | CRYSTAL STRUCTURE OF THE TYROSINE PHOSPHATASE CPS4B FROM STEPTOCOCCUS PNEUMONIAE TIGR4. | 3.1.3.48 |
2WJE | CRYSTAL STRUCTURE OF THE TYROSINE PHOSPHATASE CPS4B FROM STEPTOCOCCUS PNEUMONIAE TIGR4. | 3.1.3.48 |
2WJF | CRYSTAL STRUCTURE OF THE TYROSINE PHOSPHATASE CPS4B FROM STEPTOCOCCUS PNEUMONIAE TIGR4 IN COMPLEX WITH PHOSPHATE. | 3.1.3.48 |
2WJO | HUMAN BACE (BETA SECRETASE) IN COMPLEX WITH CYCLOHEXANECARBOXYLIC ACID (2-(2-AM INO-6-PHENOXY-4H-QUINAZOLIN-3-YL)-2 -CYCLOHEXYL-ETHYL)- AMIDE | 3.4.23.46 |
2WJV | CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN HUMAN NONSENSE MEDIATED DECAY FACTORS UPF1 AND UPF2 | 3.6.1 3.6.4 |
2WJY | CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN HUMAN NONSENSE MEDIATED DECAY FACTORS UPF1 AND UPF2 ORTHORHOMBIC FORM | 3.6.1 3.6.4 |
2WK0 | CRYSTAL STRUCTURE OF THE CLASS A BETA-LACTAMASE BS3 INHIBITED BY 6- BETA-IODOPENICILLANATE. | 3.5.2.6 |
2WK2 | CHITINASE A FROM SERRATIA MARCESCENS ATCC990 IN COMPLEX WITH CHITOTRIO-THIAZOLINE DITHIOAMIDE. | 3.2.1.14 |
2WK3 | CRYSTAL STRUCTURE OF HUMAN INSULIN-DEGRADING ENZYME IN COMPLEX WITH AMYLOID-BETA (1-42) | 3.4.24.56 |
2WK4 | DIMERIC STRUCTURE OF D347G D348G MUTANT OF THE SAPPOROVIRUS RNA DEPENDENT RNA POLYMERASE | 3.4.22.66 3.6.1.15 2.7.7.48 |
2WKE | CRYSTAL STRUCTURE OF THE ACTINOMADURA R39 DD-PEPTIDASE INHIBITED BY 6- BETA-IODOPENICILLANATE. | 3.4.16.4 |
2WKG | NOSTOC PUNCTIFORME DEBRANCHING ENZYME (NPDE)(NATIVE FORM) | 3.2.1.54 |
2WKH | CRYSTAL STRUCTURE OF THE ACYL-ENZYME OXA-10 K70C-AMPICILLIN AT PH 7 | 3.5.2.6 |
2WKI | CRYSTAL STRUCTURE OF THE OXA-10 K70C MUTANT AT PH 7.0 | 3.5.2.6 |
2WKL | VELAGLUCERASE ALFA | 3.2.1.45 2.4.1 3.2.1 |
2WKP | STRUCTURE OF A PHOTOACTIVATABLE RAC1 CONTAINING LOV2 WILDTYPE | 3.6.5.2 |
2WKQ | STRUCTURE OF A PHOTOACTIVATABLE RAC1 CONTAINING THE LOV2 C450A MUTANT | 3.6.5.2 |
2WKR | STRUCTURE OF A PHOTOACTIVATABLE RAC1 CONTAINING THE LOV2 C450M MUTANT | 3.6.5.2 |
2WKX | CRYSTAL STRUCTURE OF THE NATIVE E. COLI ZINC AMIDASE AMID | 3.5.1.28 |
2WKZ | HIV-1 PROTEASE INHIBITORS CONTAINING A TERTIARY ALCOHOL IN THE TRANSITION-STATE MIMIC WITH IMPROVED CELL-BASED ANTIVIRAL ACTIVITY | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2WL0 | HIV-1 PROTEASE INHIBITORS CONTAINING A TERTIARY ALCOHOL IN THE TRANSITION-STATE MIMIC WITH IMPROVED CELL-BASED ANTIVIRAL ACTIVITY | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2WLQ | NUCLEOPHILE-DISABLED LAM16A MUTANT HOLDS LAMINARIHEPTAOSE (L7) IN A CYCLICAL CONFORMATION | 3.2.1.6 |
2WLS | CRYSTAL STRUCTURE OF MUS MUSCULUS ACETYLCHOLINESTERASE IN COMPLEX WITH AMTS13 | 3.1.1.7 |
2WLT | THE CRYSTAL STRUCTURE OF HELICOBACTER PYLORI L-ASPARAGINASE AT 1.4 A RESOLUTION | 3.5.1.1 |
2WLY | CHITINASE A FROM SERRATIA MARCESCENS ATCC990 IN COMPLEX WITH CHITOTRIO-THIAZOLINE. | 3.2.1.14 |
2WLZ | CHITINASE A FROM SERRATIA MARCESCENS ATCC990 IN COMPLEX WITH CHITOBIO- THIAZOLINE. | 3.2.1.14 |
2WM0 | CHITINASE A FROM SERRATIA MARCESCENS ATCC990 IN COMPLEX WITH CHITOBIO- THIAZOLINE THIOAMIDE. | 3.2.1.14 |
2WM8 | CRYSTAL STRUCTURE OF HUMAN MAGNESIUM-DEPENDENT PHOSPHATASE 1 OF THE HALOACID DEHALOGENASE SUPERFAMILY (MGC5987) | 3.8.1 3.1.3 3.1.3.48 |
2WMY | CRYSTAL STRUCTURE OF THE TYROSINE PHOSPHATASE WZB FROM ESCHERICHIA COLI K30 IN COMPLEX WITH SULPHATE. | 3.1.3.48 |
2WNE | MUTANT LAMINARINASE 16A CYCLIZES LAMINARIHEPTAOSE | 3.2.1.6 |
2WNH | CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA SP ASR1 PHYTASE | 3.1.3.8 |
2WNI | CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA SP ASR1 PHYTASE | 3.1.3.8 |
2WNR | THE STRUCTURE OF METHANOTHERMOBACTER THERMAUTOTROPHICUS EXOSOME CORE ASSEMBLY | 3.1.13 |
2WNW | THE CRYSTAL STRUCTURE OF SRFJ FROM SALMONELLA TYPHIMURIUM | 3.2.1.75 |
2WO8 | MMP12 COMPLEX WITH A BETA HYDROXY CARBOXYLIC ACID | 3.4.24.65 |
2WO9 | MMP12 COMPLEX WITH A BETA HYDROXY CARBOXYLIC ACID | 3.4.24.65 |
2WOA | MMP12 COMPLEX WITH A BETA HYDROXY CARBOXYLIC ACID | 3.4.24.65 |
2WOC | CRYSTAL STRUCTURE OF THE DINITROGENASE REDUCTASE-ACTIVATING GLYCOHYDROLASE (DRAG) FROM RHODOSPIRILLUM RUBRUM | 3.2.2.24 |
2WOD | CRYSTAL STRUCTURE OF THE DINITROGENASE REDUCTASE-ACTIVATING GLYCOHYDROLASE (DRAG) FROM RHODOSPIRILLUM RUBRUM IN COMPLEX WITH ADP- RIBSOYLLYSINE | 3.2.2.24 |
2WOE | CRYSTAL STRUCTURE OF THE D97N VARIANT OF DINITROGENASE REDUCTASE- ACTIVATING GLYCOHYDROLASE (DRAG) FROM RHODOSPIRILLUM RUBRUM IN COMPLEX WITH ADP-RIBOSE | 3.2.2.24 |
2WOJ | ADP-ALF4 COMPLEX OF S. CEREVISIAE GET3 | 3.6.3.16 3.6 |
2WOM | CRYSTAL STRUCTURE OF UK-453061 BOUND TO HIV-1 REVERSE TRANSCRIPTASE (K103N). | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2WON | CRYSTAL STRUCTURE OF UK-453061 BOUND TO HIV-1 REVERSE TRANSCRIPTASE (WILD-TYPE). | 2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2WOO | NUCLEOTIDE-FREE FORM OF S. POMBE GET3 | 3.6.3.16 3.6 |
2WP7 | CRYSTAL STRUCTURE OF DESUMOYLASE(DUF862) | 3.4.22 3.4 |
2WP8 | YEAST RRP44 NUCLEASE | 3.1.13 |
2WPH | FACTOR IXA SUPERACTIVE TRIPLE MUTANT | 3.4.21.22 |
2WPI | FACTOR IXA SUPERACTIVE DOUBLE MUTANT | 3.4.21.22 |
2WPJ | FACTOR IXA SUPERACTIVE TRIPLE MUTANT, NACL-SOAKED | 3.4.21.22 |
2WPK | FACTOR IXA SUPERACTIVE TRIPLE MUTANT, ETHYLENE GLYCOL-SOAKED | 3.4.21.22 |
2WPL | FACTOR IXA SUPERACTIVE TRIPLE MUTANT, EDTA-SOAKED | 3.4.21.22 |
2WPM | FACTOR IXA SUPERACTIVE MUTANT, EGR-CMK INHIBITED | 3.4.21.22 |
2WPO | HCMV PROTEASE INHIBITOR COMPLEX | 3.4.21 3.4.21.97 |
2WQ5 | NON-ANTIBIOTIC PROPERTIES OF TETRACYCLINES: STRUCTURAL BASIS FOR INHIBITION OF SECRETORY PHOSPHOLIPASE A2. | 3.1.1.4 |
2WQK | CRYSTAL STRUCTURE OF SURE PROTEIN FROM AQUIFEX AEOLICUS | 3.1.3.5 |
2WR0 | STRUCTURES OF INFLUENZA H2 HEMAGGLUTININS | 3.1.1.53 |
2WR1 | STRUCTURE OF INFLUENZA H2 HEMAGGLUTININ WITH HUMAN RECEPTOR | 3.1.1.53 |
2WR2 | STRUCTURE OF INFLUENZA H2 AVIAN HEMAGGLUTININ WITH AVIAN RECEPTOR | 3.1.1.53 |
2WR3 | STRUCTURE OF INFLUENZA H2 DUCK ONTARIO HEMAGGLUTININ WITH AVIAN RECEPTOR | 3.1.1.53 |
2WR4 | STRUCTURE OF INFLUENZA H2 DUCK ONTARIO HEMAGGLUTININ WITH HUMAN RECEPTOR | 3.1.1.53 |
2WR5 | STRUCTURE OF INFLUENZA H2 DUCK ONTARIO HEMAGGLUTININ | 3.1.1.53 |
2WRM | IDENTIFICATION OF NOVEL ALLOSTERIC INHIBITORS OF HEPATITIS C VIRUS NS5B POLYMERASE THUMB DOMAIN (SITE II) BY STRUCTURE-BASED DESIGN | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2WRS | CRYSTAL STRUCTURE OF THE MONO-ZINC METALLO-BETA-LACTAMASE VIM-4 FROM PSEUDOMONAS AERUGINOSA | 3.5.2.6 |
2WSH | STRUCTURE OF BACTERIOPHAGE T4 ENDOII E118A MUTANT | 3.1.21 3.1.21.8 |
2WSK | CRYSTAL STRUCTURE OF GLYCOGEN DEBRANCHING ENZYME GLGX FROM ESCHERICHIA COLI K-12 | 3.2.1.196 |
2WSL | AGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA4 | 3.1.1.8 |
2WSP | THERMOTOGA MARITIMA ALPHA-L-FUCOSYNTHASE, TMD224G, IN COMPLEX WITH ALPHA-L-FUC-(1-2)-BETA-L-FUC-N3 | 3.2.1.51 |
2WT4 | ROOM TEMPERATURE CRYSTAL STRUCTURE OF HELICOBACTER PYLORI L- ASPARAGINASE AT 1.8 A RESOLUTION | 3.5.1.1 |
2WT9 | ACINETOBACTER BAUMANII NICOTINAMIDASE PYRAZINAMIDEASE | 3.5.1.19 3.5.1 |
2WTA | ACINETOBACTER BAUMANII NICOTINAMIDASE PYRAZINAMIDEASE | 3.5.1.19 3.5.1 |
2WU0 | CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA SP ASR1 PHYTASE | 3.1.3.8 |
2WU1 | GLUCOSAMINE-6-PHOSPHATE DEAMINASE COMPLEXED WITH THE ALLOSTERIC ACTIVATOR N-ACETYL-GLUCOAMINE-6-PHOSPHATE BOTH IN THE ACTIVE AND ALLOSTERIC SITES. | 3.5.99.6 |
2WU3 | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE IN COMPLEX WITH FENAMIPHOS AND HI-6 | 3.1.1.7 |
2WU4 | CRYSTAL STRUCTURE OF MOUSE ACETYLCHOLINESTERASE IN COMPLEX WITH FENAMIPHOS AND ORTHO-7 | 3.1.1.7 |
2WUB | CRYSTAL STRUCTURE OF HGFA IN COMPLEX WITH THE ALLOSTERIC NON- INHIBITORY ANTIBODY FAB40.DELTATRP | 3.4.21 |
2WUD | CRYSTAL STRUCTURE OF S114A MUTANT OF HSAD FROM MYCOBACTERIUM TUBERCULOSIS | 3.7.1.8 3.7.1.17 |
2WUE | CRYSTAL STRUCTURE OF S114A MUTANT OF HSAD FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH HOPODA | 3.7.1.8 3.7.1.17 |
2WUF | CRYSTAL STRUCTURE OF S114A MUTANT OF HSAD FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH 4,9DSHA | 3.7.1.8 3.7.1.17 |
2WUG | CRYSTAL STRUCTURE OF S114A MUTANT OF HSAD FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH HOPDA | 3.7.1.8 3.7.1.17 |
2WUV | CRYSTALLOGRAPHIC ANALYSIS OF COUNTER-ION EFFECTS ON SUBTILISIN ENZYMATIC ACTION IN ACETONITRILE | 3.4.21.62 |
2WUW | CRYSTALLOGRAPHIC ANALYSIS OF COUNTER-ION EFFECTS ON SUBTILISIN ENZYMATIC ACTION IN ACETONITRILE (NATIVE DATA) | 3.4.21.62 |
2WV4 | CRYSTAL STRUCTURE OF FOOT-AND-MOUTH DISEASE VIRUS 3C PROTEASE IN COMPLEX WITH A DECAMERIC PEPTIDE CORRESPONDING TO THE VP1-2A CLEAVAGE JUNCTION | 3.4.22.28 3.4.22.46 3.6.1.15 2.7.7.48 |
2WV5 | CRYSTAL STRUCTURE OF FOOT-AND-MOUTH DISEASE VIRUS 3C PROTEASE IN COMPLEX WITH A DECAMERIC PEPTIDE CORRESPONDING TO THE VP1-2A CLEAVAGE JUNCTION WITH A GLN TO GLU SUBSTITUTION AT P1 | 3.4.22.28 3.4.22.46 3.6.1.15 2.7.7.48 |
2WV7 | INTRACELLULAR SUBTILISIN PRECURSOR FROM B. CLAUSII | 3.4.21.62 |
2WV9 | CRYSTAL STRUCTURE OF THE NS3 PROTEASE-HELICASE FROM MURRAY VALLEY ENCEPHALITIS VIRUS | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2WW5 | 3D-STRUCTURE OF THE MODULAR AUTOLYSIN LYTC FROM STREPTOCOCCUS PNEUMONIAE AT 1.6 A RESOLUTION | 3.2.1.17 |
2WWC | 3D-STRUCTURE OF THE MODULAR AUTOLYSIN LYTC FROM STREPTOCOCCUS PNEUMONIAE IN COMPLEX WITH SYNTHETIC PEPTIDOGLYCAN LIGAND | 3.2.1.17 |
2WWD | 3D-STRUCTURE OF THE MODULAR AUTOLYSIN LYTC FROM STREPTOCOCCUS PNEUMONIAE IN COMPLEX WITH PNEUMMOCOCCAL PEPTIDOGLYCAN FRAGMENT | 3.2.1.17 |
2WWT | INTRACELLULAR SUBTILISIN PRECURSOR FROM B. CLAUSII | 3.4.21.62 |
2WWW | CRYSTAL STRUCTURE OF METHYLMALONIC ACIDEMIA TYPE A PROTEIN | 3.6 |
2WWY | STRUCTURE OF HUMAN RECQ-LIKE HELICASE IN COMPLEX WITH A DNA SUBSTRATE | 3.6.1 3.6.4.12 |
2WX3 | ASYMMETRIC TRIMER OF THE HUMAN DCP1A C-TERMINAL DOMAIN | 3 |
2WXD | A MICROMOLAR O-SULFATED THIOHYDROXIMATE INHIBITOR BOUND TO PLANT MYROSINASE | 3.2.3.1 3.2.1.147 |
2WXT | CLOSTRIDIUM PERFRINGENS ALPHA-TOXIN STRAIN NCTC8237 | 3.1.4.3 |
2WXU | CLOSTRIDIUM PERFRINGENS ALPHA-TOXIN STRAIN NCTC8237 MUTANT T74I | 3.1.4.3 |
2WY6 | CLOSTRIDIUM PERFRINGENS ALPHA-TOXIN STRAIN NCTC8237 MUTANT T74I | 3.1.4.3 |
2WYB | THE QUORUM QUENCHING N-ACYL HOMOSERINE LACTONE ACYLASE PVDQ WITH A COVALENTLY BOUND DODECANOIC ACID | 3.5.1.97 |
2WYC | THE QUORUM QUENCHING N-ACYL HOMOSERINE LACTONE ACYLASE PVDQ IN COMPLEX WITH 3-OXO-LAURIC ACID | 3.5.1.97 |
2WYD | THE QUORUM QUENCHING N-ACYL HOMOSERINE LACTONE ACYLASE PVDQ IN COMPLEX WITH DODECANOIC ACID | 3.5.1.97 |
2WYE | THE QUORUM QUENCHING N-ACYL HOMOSERINE LACTONE ACYLASE PVDQ IS AN NTN- HYDROLASE WITH AN UNUSUAL SUBSTRATE-BINDING POCKET | 3.5.1.97 |
2WYG | STRUCTURE AND PROPERTY BASED DESIGN OF FACTOR XA INHIBITORS: PYRROLIDIN-2-ONES WITH MONOARYL P4 MOTIFS | 3.4.21.6 |
2WYH | STRUCTURE OF THE STREPTOCOCCUS PYOGENES FAMILY GH38 ALPHA-MANNOSIDASE | 3.2.1.24 |
2WYI | STRUCTURE OF THE STREPTOCOCCUS PYOGENES FAMILY GH38 ALPHA-MANNOSIDASE COMPLEXED WITH SWAINSONINE | 3.2.1.24 |
2WYJ | STRUCTURE AND PROPERTY BASED DESIGN OF FACTOR XA INHIBITORS: PYRROLIDIN-2-ONES WITH MONOARYL P4 MOTIFS | 3.4.21.6 |
2WYL | APO STRUCTURE OF A METALLO-B-LACTAMASE | 3.1.1 |
2WYM | STRUCTURE OF A METALLO-B-LACTAMASE | 3.1.1 |
2WYN | STRUCTURE OF FAMILY 37 TREHALASE FROM ESCHERICHIA COLI IN COMPLEX WITH A CASUARINE-6-O-A-D-GLUCOSIDE ANALOGUE | 3.2.1.28 |
2WYR | 3-D STRUCTURE OF PHTET1-12S, DODECAMER IN THE ASYMMETRIC UNIT | 3.4.11 |
2WYS | HIGH RESOLUTION CRYSTALLOGRAPHIC STRUCTURE OF THE CLOSTRIDIUM THERMOCELLUM N-TERMINAL ENDO-1,4-BETA-D-XYLANASE 10B (XYN10B) CBM22-1- GH10 MODULES COMPLEXED WITH XYLOHEXAOSE | 3.2.1.8 |
2WYX | NEUTRON STRUCTURE OF A CLASS A BETA-LACTAMASE TOHO-1 E166A R274N R276N TRIPLE MUTANT | 3.5.2.6 |
2WZE | HIGH RESOLUTION CRYSTALLOGRAPHIC STRUCTURE OF THE CLOSTRIDIUM THERMOCELLUM N-TERMINAL ENDO-1,4-BETA-D-XYLANASE 10B (XYN10B) CBM22-1- GH10 MODULES COMPLEXED WITH XYLOHEXAOSE | 3.2.1.8 |
2WZH | BTGH84 D242N IN COMPLEX WITH MEUMB-DERIVED OXAZOLINE | 3.2.1.52 3.2.1.169 |
2WZI | BTGH84 D243N IN COMPLEX WITH 5F-OXAZOLINE | 3.2.1.52 3.2.1.169 |
2WZQ | INSERTION MUTANT E173GP174 OF THE NS3 PROTEASE-HELICASE FROM DENGUE VIRUS | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2WZR | THE STRUCTURE OF FOOT AND MOUTH DISEASE VIRUS SEROTYPE SAT1 | 2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15 |
2WZX | AMP-C BETA-LACTAMASE (PSEUDOMONAS AERUGINOSA)IN COMPLEX WITH COMPOUND M-02 | 3.5.2.6 |
2WZZ | AMP-C BETA-LACTAMASE (PSEUDOMONAS AERUGINOSA)IN COMPLEX WITH COMPOUND M-03 | 3.5.2.6 |
2X01 | CRYSTAL STRUCTURE OF THE OXA-10 S67A MUTANT AT PH 7 | 3.5.2.6 |
2X02 | CRYSTAL STRUCTURE OF THE CLASS D BETA-LACTAMASE OXA-10 AT 1.35 A RESOLUTION | 3.5.2.6 |
2X05 | INHIBITION OF THE EXO-BETA-D-GLUCOSAMINIDASE CSXA BY A GLUCOSAMINE- CONFIGURED CASTANOSPERMINE AND AN AMINO-AUSTRALINE ANALOGUE | 3.2.1.165 |
2X09 | INHIBITION OF THE EXO-BETA-D-GLUCOSAMINIDASE CSXA BY A GLUCOSAMINE- CONFIGURED CASTANOSPERMINE AND AN AMINO-AUSTRALINE ANALOGUE | 3.2.1.165 |
2X0A | MPD-LYSOZYME STRUCTURE AT 55.5 KEV USING A TRIXXEL CSI-ASI BASED DIGITAL IMAGER AND THE NEW ESRF U22 UNDULATOR SOURCE AT ID15 | 3.2.1.17 |
2X0H | BTGH84 MICHAELIS COMPLEX | 3.2.1.52 3.2.1.169 |
2X0Y | SCREENING-BASED DISCOVERY OF DRUG-LIKE O-GLCNACASE INHIBITOR SCAFFOLDS | 3.2.1.52 3.2.1.169 |
2X1V | CRYSTAL STRUCTURE OF THE ACTIVATING H-RAS I163F MUTANT IN COSTELLO SYNDROME, BOUND TO MG-GDP | 3.6.5.2 |
2X2E | DYNAMIN GTPASE DIMER, LONG AXIS FORM | 3.6.5.5 |
2X2F | DYNAMIN 1 GTPASE DIMER, SHORT AXIS FORM | 3.6.5.5 |
2X2Y | CELLULOMONAS FIMI ENDO-BETA-1,4-MANNANASE DOUBLE MUTANT | 3.2.1.78 |
2X36 | STRUCTURE OF THE PROTEOLYTIC DOMAIN OF THE HUMAN MITOCHONDRIAL LON PROTEASE | 3.4.21 3.4.21.53 |
2X3A | ASAP1 INACTIVE MUTANT E294Q, AN EXTRACELLULAR TOXIC ZINC METALLOENDOPEPTIDASE | 3.4.24.39 |
2X3B | ASAP1 INACTIVE MUTANT E294A, AN EXTRACELLULAR TOXIC ZINC METALLOENDOPEPTIDASE | 3.4.24.39 |
2X3C | ASAP1 INACTIVE MUTANT E294Q, AN EXTRACELLULAR TOXIC ZINC METALLOENDOPEPTIDASE | 3.4.24.39 |
2X40 | STRUCTURE OF BETA-GLUCOSIDASE 3B FROM THERMOTOGA NEAPOLITANA IN COMPLEX WITH GLYCEROL | 3.2.1.21 |
2X41 | STRUCTURE OF BETA-GLUCOSIDASE 3B FROM THERMOTOGA NEAPOLITANA IN COMPLEX WITH GLUCOSE | 3.2.1.21 |
2X42 | STRUCTURE OF BETA-GLUCOSIDASE 3B FROM THERMOTOGA NEAPOLITANA IN COMPLEX WITH ALPHA-D-GLUCOSE | 3.2.1.21 |
2X47 | CRYSTAL STRUCTURE OF HUMAN MACROD1 | 3.1.1.106 3.2.2 |
2X4D | CRYSTAL STRUCTURE OF HUMAN PHOSPHOLYSINE PHOSPHOHISTIDINE INORGANIC PYROPHOSPHATE PHOSPHATASE LHPP | 3.6.1.1 3.1.3 |
2X4M | YERSINIA PESTIS PLASMINOGEN ACTIVATOR PLA | 3.4.23.48 |
2X55 | YERSINIA PESTIS PLASMINOGEN ACTIVATOR PLA (NATIVE) | 3.4.23.48 |
2X56 | YERSINIA PESTIS PLASMINOGEN ACTIVATOR PLA (NATIVE) | 3.4.23.48 |
2X6N | HUMAN FOAMY VIRUS INTEGRASE - CATALYTIC CORE. MANGANESE-BOUND STRUCTURE. | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1 |
2X6S | HUMAN FOAMY VIRUS INTEGRASE - CATALYTIC CORE. MAGNESIUM-BOUND STRUCTURE. | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1 |
2X71 | STRUCTURAL BASIS FOR THE INTERACTION OF LACTIVICINS WITH SERINE BETA- LACTAMASES | 3.5.2.6 |
2X74 | HUMAN FOAMY VIRUS INTEGRASE - CATALYTIC CORE. | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1 |
2X78 | HUMAN FOAMY VIRUS INTEGRASE - CATALYTIC CORE. | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1 |
2X7M | CRYSTAL STRUCTURE OF ARCHAEMETZINCIN (AMZA) FROM METHANOPYRUS KANDLERI AT 1.5 A RESOLUTION | 3 3.4 |
2X7V | CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA ENDONUCLEASE IV IN THE PRESENCE OF ZINC | 3.1.21.2 |
2X7W | CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA ENDONUCLEASE IV IN THE PRESENCE OF CADMIUM AND ZINC | 3.1.21.2 |
2X8F | NATIVE STRUCTURE OF ENDO-1,5-ALPHA-L-ARABINANASES FROM BACILLUS SUBTILIS | 3.2.1.99 |
2X8J | INTRACELLULAR SUBTILISIN PRECURSOR FROM B. CLAUSII | 3.4.21.62 |
2X8R | THE STRUCTURE OF A FAMILY GH25 LYSOZYME FROM ASPERGILLUS FUMIGATUS | 3.2.1.17 |
2X8S | CRYSTAL STRUCTURE OF THE ABN2 D171A MUTANT IN COMPLEX WITH ARABINOTRIOSE | 3.2.1.99 |
2X8T | CRYSTAL STRUCTURE OF THE ABN2 H318A MUTANT | 3.2.1.99 |
2X8Y | CRYSTAL STRUCTURE OF ANCE | 3.4.15.1 |
2X8Z | CRYSTAL STRUCTURE OF ANCE-CAPTOPRIL COMPLEX | 3.4.15.1 |
2X90 | CRYSTAL STRUCTURE OF ANCE-ENALAPRILAT COMPLEX | 3.4.15.1 |
2X91 | CRYSTAL STRUCTURE OF ANCE-LISINOPRIL COMPLEX | 3.4.15.1 |
2X92 | CRYSTAL STRUCTURE OF ANCE-RAMIPRILAT COMPLEX | 3.4.15.1 |
2X93 | CRYSTAL STRUCTURE OF ANCE-TRANDOLAPRILAT COMPLEX | 3.4.15.1 |
2X94 | CRYSTAL STRUCTURE OF ANCE-PERINDOPRILAT COMPLEX | 3.4.15.1 |
2X95 | CRYSTAL STRUCTURE OF ANCE-LISINOPRIL-TRYPTOPHAN ANALOGUE, LISW-S COMPLEX | 3.4.15.1 |
2X96 | CRYSTAL STRUCTURE OF ANCE-RXPA380 COMPLEX | 3.4.15.1 |
2X97 | CRYSTAL STRUCTURE OF ANCE-RXP407 COMPLEX | 3.4.15.1 |
2X98 | H.SALINARUM ALKALINE PHOSPHATASE | 3.1.3.1 |
2X9H | CRYSTAL STRUCTURE OF MYOSIN-2 MOTOR DOMAIN IN COMPLEX WITH ADP- METAVANADATE AND PENTACHLOROCARBAZOLE | 3.6.4.1 |
2XAU | CRYSTAL STRUCTURE OF THE PRP43P DEAH-BOX RNA HELICASE IN COMPLEX WITH ADP | 3.6.1 3.6.4.13 |
2XB0 | DNA-BINDING DOMAIN FROM SACCHAROMYCES CEREVISIAE CHROMATIN- REMODELLING PROTEIN CHD1 | 3.6.1 3.6.4 |
2XB2 | CRYSTAL STRUCTURE OF THE CORE MAGO-Y14-EIF4AIII-BARENTSZ-UPF3B ASSEMBLY SHOWS HOW THE EJC IS BRIDGED TO THE NMD MACHINERY | 3.6.1 3.6.4.13 |
2XBD | INTERNAL XYLAN BINDING DOMAIN FROM CELLULOMONAS FIMI XYLANASE D, NMR, MINIMIZED AVERAGE STRUCTURE | 3.2.1.8 3.5.1 |
2XBM | CRYSTAL STRUCTURE OF THE DENGUE VIRUS METHYLTRANSFERASE BOUND TO A 5'- CAPPED OCTAMERIC RNA | 3.4.21.91 3.6.1.15 3.6.4.13 |
2XBR | RAMAN CRYSTALLOGRAPHY OF HEN WHITE EGG LYSOZYME - LOW X-RAY DOSE (0.2 MGY) | 3.2.1.17 |
2XBS | RAMAN CRYSTALLOGRAPHY OF HEN WHITE EGG LYSOZYME - HIGH X-RAY DOSE (16 MGY) | 3.2.1.17 |
2XBV | FACTOR XA IN COMPLEX WITH A PYRROLIDINE-3,4-DICARBOXYLIC ACID INHIBITOR | 3.4.21.6 |
2XBW | FACTOR XA IN COMPLEX WITH A PYRROLIDINE-3,4-DICARBOXYLIC ACID INHIBITOR | 3.4.21.6 |
2XBX | FACTOR XA IN COMPLEX WITH A PYRROLIDINE-3,4-DICARBOXYLIC ACID INHIBITOR | 3.4.21.6 |
2XBY | FACTOR XA IN COMPLEX WITH A PYRROLIDINE-3,4-DICARBOXYLIC ACID INHIBITOR | 3.4.21.6 |
2XC0 | FACTOR XA IN COMPLEX WITH A PYRROLIDINE-3,4-DICARBOXYLIC ACID INHIBITOR | 3.4.21.6 |
2XC4 | FACTOR XA IN COMPLEX WITH A PYRROLIDINE-3,4-DICARBOXYLIC ACID INHIBITOR | 3.4.21.6 |
2XC5 | FACTOR XA IN COMPLEX WITH A PYRROLIDINE-3,4-DICARBOXYLIC ACID INHIBITOR | 3.4.21.6 |
2XCD | STRUCTURE OF YNCF,THE GENOMIC DUTPASE FROM BACILLUS SUBTILIS | 3.6.1.23 |
2XCE | STRUCTURE OF YNCF IN COMPLEX WITH DUPNHPP | 3.6.1.23 |
2XCV | CRYSTAL STRUCTURE OF THE D52N VARIANT OF CYTOSOLIC 5'-NUCLEOTIDASE II IN COMPLEX WITH INOSINE MONOPHOSPHATE AND 2,3-BISPHOSPHOGLYCERATE | 3.1.3.5 |
2XCW | CRYSTAL STRUCTURE OF THE D52N VARIANT OF CYTOSOLIC 5'-NUCLEOTIDASE II IN COMPLEX WITH INOSINE MONOPHOSPHATE AND ATP | 3.1.3.5 |
2XCX | CRYSTAL STRUCTURE OF THE APOFORM OF THE D52N VARIANT OF CYTOSOLIC 5'- NUCLEOTIDASE II | 3.1.3.5 |
2XCY | CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS SIALIDASE | 3.2.1.18 |
2XD0 | A PROCESSED NON-CODING RNA REGULATES A BACTERIAL ANTIVIRAL SYSTEM | 3.1.27.3 3.1 |
2XD1 | ACTIVE SITE RESTRUCTURING REGULATES LIGAND RECOGNITION IN CLASS A PENICILLIN-BINDING PROTEINS | 2.4.1.129 2.3.2 3.4.16.4 |
2XD5 | STRUCTURAL INSIGHTS INTO THE CATALYTIC MECHANISM AND THE ROLE OF STREPTOCOCCUS PNEUMONIAE PBP1B | 2.3.2 2.4.1.129 3.4.16.4 |
2XDB | A PROCESSED NON-CODING RNA REGULATES A BACTERIAL ANTIVIRAL SYSTEM | 3.1.27.3 3.1 |
2XDD | A PROCESSED NON-CODING RNA REGULATES A BACTERIAL ANTIVIRAL SYSTEM | 3.1.27.3 3.1 |
2XDE | CRYSTAL STRUCTURE OF THE COMPLEX OF PF-3450074 WITH AN ENGINEERED HIV CAPSID N TERMINAL DOMAIN | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2XDM | CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD PEPTIDASE AND A PEPTIDOGLYCAN MIMETIC BORONATE INHIBITOR | 3.4.16.4 |
2XDW | INHIBITION OF PROLYL OLIGOPEPTIDASE WITH A SYNTHETIC UNNATURAL DIPEPTIDE | 3.4.21.26 |
2XE4 | STRUCTURE OF OLIGOPEPTIDASE B FROM LEISHMANIA MAJOR | 3.4.21.83 3.4.21.26 |
2XEF | HUMAN GLUTAMATE CARBOXYPEPTIDASE II IN COMPLEX WITH ANTIBODY- RECRUITING MOLECULE ARM-P8 | 3.4.17.21 |
2XEG | HUMAN GLUTAMATE CARBOXYPEPTIDASE II IN COMPLEX WITH ANTIBODY- RECRUITING MOLECULE ARM-P4 | 3.4.17.21 |
2XEI | HUMAN GLUTAMATE CARBOXYPEPTIDASE II IN COMPLEX WITH ANTIBODY- RECRUITING MOLECULE ARM-P2 | 3.4.17.21 |
2XEJ | HUMAN GLUTAMATE CARBOXYPEPTIDASE II IN COMPLEX WITH ARM-M4, UREA- BASED INHIBITOR | 3.4.17.21 |
2XFB | CHIKUNGUNYA E1 E2 ENVELOPE GLYCOPROTEINS FITTED IN SINDBIS VIRUS CRYO- EM MAP | 3.4.21.90 |
2XFF | CRYSTAL STRUCTURE OF BARLEY BETA-AMYLASE COMPLEXED WITH ACARBOSE | 3.2.1.2 |
2XFG | REASSEMBLY AND CO-CRYSTALLIZATION OF A FAMILY 9 PROCESSIVE ENDOGLUCANASE FROM SEPARATELY EXPRESSED GH9 AND CBM3C MODULES | 3.2.1.4 |
2XFI | HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(((1S)-2-(CYCLOHEXYLAMINO)- 1-METHYL-2-OXOETHYL)AMINO)-2-HYDROXY-1-(PHENYLMETHYL)PROPYL)-3-((METHYLSULFONYL)(PHENYL)AMINO)BENZAMIDE | 3.4.23.46 |
2XFJ | HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(((1S)-2-(CYCLOHEXYLAMINO)- 1-METHYL-2-OXOETHYL)AMINO)-2-HYDROXY-1-(PHENYLMETHYL)PROPYL)-3-(ETHYLAMINO)-5-(2-OXO-1-PYRROLIDINYL)BENZAMIDE | 3.4.23.46 |
2XFK | HUMAN BACE-1 IN COMPLEX WITH N-((1S,2R)-3-(((1S)-2-(CYCLOHEXYLAMINO)- 1-METHYL-2-OXOETHYL)AMINO)-2-HYDROXY-1-(PHENYLMETHYL)PROPYL)-3-(ETHYLAMINO)-5-((METHYLSULFONYL)(PHENYL)AMINO)BENZAMIDE | 3.4.23.46 |
2XFM | COMPLEX STRUCTURE OF THE MIWI PAZ DOMAIN BOUND TO METHYLATED SINGLE STRANDED RNA | 3.1.26 |
2XFR | CRYSTAL STRUCTURE OF BARLEY BETA-AMYLASE AT ATOMIC RESOLUTION | 3.2.1.2 |
2XFY | CRYSTAL STRUCTURE OF BARLEY BETA-AMYLASE COMPLEXED WITH ALPHA- CYCLODEXTRIN | 3.2.1.2 |
2XG9 | CRYSTAL STRUCTURE OF BARLEY BETA-AMYLASE COMPLEXED WITH 4-O-ALPHA-D- GLUCOPYRANOSYLMORANOLINE | 3.2.1.2 |
2XGB | CRYSTAL STRUCTURE OF BARLEY BETA-AMYLASE COMPLEXED WITH 2,3- EPOXYPROPYL-ALPHA-D-GLUCOPYRANOSIDE | 3.2.1.2 |
2XGG | STRUCTURE OF TOXOPLASMA GONDII MICRONEMAL PROTEIN 2 A_I DOMAIN | 3.1.1.2 3.4.24.14 |
2XGI | CRYSTAL STRUCTURE OF BARLEY BETA-AMYLASE COMPLEXED WITH 3,4- EPOXYBUTYL ALPHA-D-GLUCOPYRANOSIDE | 3.2.1.2 |
2XGJ | STRUCTURE OF MTR4, A DEXH HELICASE INVOLVED IN NUCLEAR RNA PROCESSING AND SURVEILLANCE | 3.6.4.13 3.6.1 |
2XGR | EXTRACELLULAR ENDONUCLEASE | 3.1.21.1 |
2XH3 | EXTRACELLULAR NUCLEASE | 3.1.21.1 |
2XHI | SEPARATION-OF-FUNCTION MUTANTS UNRAVEL THE DUAL REACTION MODE OF HUMAN 8-OXOGUANINE DNA GLYCOSYLASE | 3.2.2 4.2.99.18 |
2XHL | STRUCTURE OF A FUNCTIONAL DERIVATIVE OF CLOSTRIDIUM BOTULINUM NEUROTOXIN TYPE B | 3.4.24.69 |
2XHM | CRYSTAL STRUCTURE OF ANCE-K26 COMPLEX | 3.4.15.1 |
2XHU | HCV-J4 NS5B POLYMERASE ORTHORHOMBIC CRYSTAL FORM | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XHV | HCV-J4 NS5B POLYMERASE POINT MUTANT ORTHORHOMBIC CRYSTAL FORM | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XHW | HCV-J4 NS5B POLYMERASE TRIGONAL CRYSTAL FORM | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XHY | CRYSTAL STRUCTURE OF E.COLI BGLA | 3.2.1.86 |
2XI2 | HCV-H77 NS5B APO POLYMERASE | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XI3 | HCV-H77 NS5B POLYMERASE COMPLEXED WITH GTP | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XI4 | TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH AFLATOXIN B1 (ORTHORHOMBIC SPACE GROUP) | 3.1.1.7 |
2XI5 | N-TERMINAL ENDONUCLEASE DOMAIN OF LA CROSSE VIRUS L-PROTEIN | 2.7.7.48 3.1 |
2XI7 | N-TERMINAL ENDONUCLEASE DOMAIN OF LA CROSSE VIRUS L-PROTEIN | 2.7.7.48 3.1 |
2XII | CRYSTAL STRUCTURE OF AN ALPHA-L-FUCOSIDASE GH29 FROM BACTEROIDES THETAIOTAOMICRON IN COMPLEX WITH AN EXTENDED 9-FLUORENONE IMINOSUGAR INHIBITOR | 3.2.1.51 |
2XIO | STRUCTURE OF PUTATIVE DEOXYRIBONUCLEASE TATDN1 ISOFORM A | 3.1.21 |
2XIV | STRUCTURE OF RV1477, HYPOTHETICAL INVASION PROTEIN OF MYCOBACTERIUM TUBERCULOSIS | 3.4 |
2XJ7 | BTGH84 IN COMPLEX WITH 6-ACETAMIDO-6-DEOXY-CASTANOSPERMINE | 3.2.1.52 3.2.1.169 |
2XJB | CRYSTAL STRUCTURE OF THE D52N VARIANT OF CYTOSOLIC 5'-NUCLEOTIDASE II IN COMPLEX WITH DEOXYGUANOSINE MONOPHOSPHATE AND DEOXYADENOSINE TRIPHOSPHATE | 3.1.3.5 |
2XJC | CRYSTAL STRUCTURE OF THE D52N VARIANT OF CYTOSOLIC 5'-NUCLEOTIDASE II IN COMPLEX WITH GUANOSINE MONOPHOSPHATE AND DIADENOSINE TETRAPHOSPHATE | 3.1.3.5 |
2XJD | CRYSTAL STRUCTURE OF THE D52N VARIANT OF CYTOSOLIC 5'-NUCLEOTIDASE II IN COMPLEX WITH INORGANIC PHOSPHATE AND DEOXYADENOSINE TRIPHOSPHATE | 3.1.3.5 |
2XJE | CRYSTAL STRUCTURE OF THE D52N VARIANT OF CYTOSOLIC 5'-NUCLEOTIDASE II IN COMPLEX WITH URIDINE 5'-MONOPHOSPHATE AND ADENOSINE TRIPHOSPHATE | 3.1.3.5 |
2XJF | CRYSTAL STRUCTURE OF THE D52N VARIANT OF CYTOSOLIC 5'-NUCLEOTIDASE II WITH A COVALENTLY MODIFIED ASN52 | 3.1.3.5 |
2XJW | LYSOZYME-CO RELEASING MOLECULE ADDUCT | 3.2.1.17 |
2XK1 | CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD-PEPTIDASE AND A BORONATE INHIBITOR | 3.4.16.4 |
2XKV | ATOMIC MODEL OF THE SRP-FTSY EARLY CONFORMATION | 3.6.5.4 |
2XLB | ACETYL XYLAN ESTERASE FROM BACILLUS PUMILUS WITHOUT LIGANDS | 3.1.1.72 3.1.1.6 |
2XLC | ACETYL XYLAN ESTERASE FROM BACILLUS PUMILUS CECT5072 BOUND TO PARAOXON | 3.1.1.72 3.1.1.6 |
2XLI | CRYSTAL STRUCTURE OF THE CSY4-CRRNA COMPLEX, MONOCLINIC FORM | 3.1 |
2XLJ | CRYSTAL STRUCTURE OF THE CSY4-CRRNA COMPLEX, HEXAGONAL FORM | 3.1 |
2XLK | CRYSTAL STRUCTURE OF THE CSY4-CRRNA COMPLEX, ORTHORHOMBIC FORM | 3.1 |
2XLN | CRYSTAL STRUCTURE OF A COMPLEX BETWEEN ACTINOMADURA R39 DD-PEPTIDASE AND A BORONATE INHIBITOR | 3.4.16.4 |
2XM1 | BTGH84 IN COMPLEX WITH N-ACETYL GLUCONOLACTAM | 3.2.1.52 3.2.1.169 |
2XM2 | BTGH84 IN COMPLEX WITH LOGNAC | 3.2.1.52 3.2.1.169 |
2XMB | G117H MUTANT OF HUMAN BUTYRYLCHOLINESTERASE IN COMPLEX WITH SULFATE | 3.1.1.8 |
2XMC | G117H MUTANT OF HUMAN BUTYRYLCHOLINESTERASE IN COMPLEX WITH FLUORIDE ANION | 3.1.1.8 |
2XMD | G117H MUTANT OF HUMAN BUTYRYLCHOLINESTERASE IN COMPLEX WITH ECHOTHIOPHATE | 3.1.1.8 |
2XMG | G117H MUTANT OF HUMAN BUTYRYLCHOLINESTERASE IN COMPLEX WITH VX | 3.1.1.8 |
2XMI | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, COMPLEXED WITH CITRATE | 3.1.4.37 |
2XN0 | STRUCTURE OF ALPHA-GALACTOSIDASE FROM LACTOBACILLUS ACIDOPHILUS NCFM, PTCL4 DERIVATIVE | 3.2.1.22 |
2XN2 | STRUCTURE OF ALPHA-GALACTOSIDASE FROM LACTOBACILLUS ACIDOPHILUS NCFM WITH GALACTOSE | 3.2.1.22 |
2XNI | PROTEIN-LIGAND COMPLEX OF A NOVEL MACROCYCLIC HCV NS3 PROTEASE INHIBITOR DERIVED FROM AMINO CYCLIC BORONATES | 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48 |
2XNS | CRYSTAL STRUCTURE OF HUMAN G ALPHA I1 BOUND TO A DESIGNED HELICAL PEPTIDE DERIVED FROM THE GOLOCO MOTIF OF RGS14 | 3.6.5.1 |
2XOG | FUNCTIONAL AND STRUCTURAL ANALYSES OF N-ACYLSULFONAMIDE-LINKED DINUCLEOSIDE INHIBITORS OF RIBONUCLEASE A | 3.1.27.5 4.6.1.18 |
2XOI | FUNCTIONAL AND STRUCTURAL ANALYSES OF N-ACYLSULFONAMIDE-LINKED DINUCLEOSIDE INHIBITORS OF RIBONUCLEASE A | 3.1.27.5 4.6.1.18 |
2XOM | ATOMIC RESOLUTION STRUCTURE OF TMCBM61 IN COMPLEX WITH BETA-1,4- GALACTOTRIOSE | 3.2.1.89 |
2XON | STRUCTURE OF TMCBM61 IN COMPLEX WITH BETA-1,4-GALACTOTRIOSE AT 1.4 A RESOLUTION | 3.2.1.89 |
2XOV | CRYSTAL STRUCTURE OF E.COLI RHOMBOID PROTEASE GLPG, NATIVE ENZYME | 3.4.21.105 |
2XOW | STRUCTURE OF GLPG IN COMPLEX WITH A MECHANISM-BASED ISOCOUMARIN INHIBITOR | 3.4.21.105 |
2XPH | CRYSTAL STRUCTURE OF HUMAN SENP1 WITH THE BOUND COBALT | 3.4.22 |
2XPK | CELL-PENETRANT, NANOMOLAR O-GLCNACASE INHIBITORS SELECTIVE AGAINST LYSOSOMAL HEXOSAMINIDASES | 3.2.1.52 3.2.1.169 |
2XPY | STRUCTURE OF NATIVE LEUKOTRIENE A4 HYDROLASE FROM SACCHAROMYCES CEREVISIAE | 3.3.2.6 3.4.11 3.3.2.10 |
2XPZ | STRUCTURE OF NATIVE YEAST LTA4 HYDROLASE | 3.3.2.6 3.4.11 3.3.2.10 |
2XQ0 | STRUCTURE OF YEAST LTA4 HYDROLASE IN COMPLEX WITH BESTATIN | 3.3.2.6 3.4.11 3.3.2.10 |
2XQF | X-RAY STRUCTURE OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY RACEMIC VX | 3.1.1.8 |
2XQG | X-RAY STRUCTURE OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY RACEMIC VR | 3.1.1.8 |
2XQI | X-RAY STRUCTURE OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY RACEMIC CVX | 3.1.1.8 |
2XQJ | X-RAY STRUCTURE OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY PURE ENANTIOMER VX-(R) | 3.1.1.8 |
2XQK | X-RAY STRUCTURE OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY PURE ENANTIOMER VX-(S) | 3.1.1.8 |
2XQX | STRUCTURE OF THE FAMILY 32 CARBOHYDRATE-BINDING MODULE FROM STREPTOCOCCUS PNEUMONIAE ENDOD | 3.2.1.96 |
2XQZ | NEUTRON STRUCTURE OF THE PERDEUTERATED TOHO-1 R274N R276N DOUBLE MUTANT BETA-LACTAMASE | 3.5.2.6 |
2XR0 | ROOM TEMPERATURE X-RAY STRUCTURE OF THE PERDEUTERATED TOHO-1 R274N R276N DOUBLE MUTANT BETA-LACTAMASE | 3.5.2.6 |
2XR9 | CRYSTAL STRUCTURE OF AUTOTAXIN (ENPP2) | 3.1.4.39 |
2XRC | HUMAN COMPLEMENT FACTOR I | 3.4.21.45 |
2XRE | DETECTION OF COBALT IN PREVIOUSLY UNASSIGNED HUMAN SENP1 STRUCTURE | 3.4.22 |
2XRG | CRYSTAL STRUCTURE OF AUTOTAXIN (ENPP2) IN COMPLEX WITH THE HA155 BORONIC ACID INHIBITOR | 3.1.4.39 |
2XRI | CRYSTAL STRUCTURE OF HUMAN ERI1 EXORIBONUCLEASE 3 | 3.1 |
2XRM | PROCESSED INTRACELLULAR SUBTILISIN FROM B. CLAUSII | 3.4.21.62 |
2XS3 | STRUCTURE OF KARILYSIN CATALYTIC MMP DOMAIN | 3.4.24 |
2XS4 | STRUCTURE OF KARILYSIN CATALYTIC MMP DOMAIN IN COMPLEX WITH MAGNESIUM | 3.4.24 |
2XSA | OGOGA APOSTRUCTURE | 3.2.1.52 3.2.1.169 |
2XSB | OGOGA PUGNAC COMPLEX | 3.2.1.52 3.2.1.169 |
2XSG | STRUCTURE OF THE GH92 FAMILY GLYCOSYL HYDROLASE CCMAN5 | 3.2.1.24 |
2XSP | STRUCTURE OF CELLOBIOHYDROLASE 1 (CEL7A) FROM HETEROBASIDION ANNOSUM | 3.2.1 |
2XSQ | CRYSTAL STRUCTURE OF HUMAN NUDIX MOTIF 16 (NUDT16) IN COMPLEX WITH IMP AND MAGNESIUM | 3.6.1 3.6.1.62 3.6.1.64 |
2XSS | CRYSTAL STRUCTURE OF GAFB FROM THE HUMAN PHOSPHODIESTERASE 5 | 3.1.4.35 |
2XSW | CRYSTAL STRUCTURE OF HUMAN INPP5E | 3.1.3.36 3.1.3.86 |
2XSZ | THE DODECAMERIC HUMAN RUVBL1:RUVBL2 COMPLEX WITH TRUNCATED DOMAINS II | 3.6.4.12 |
2XT0 | DEHALOGENASE DPPA FROM PLESIOCYSTIS PACIFICA SIR-I | 3.8.1.5 |
2XTH | K2PTBR6 BINDING TO LYSOZYME | 3.2.1.17 |
2XTJ | THE CRYSTAL STRUCTURE OF PCSK9 IN COMPLEX WITH 1D05 FAB | 3.4.21 |
2XTK | CHIA1 FROM ASPERGILLUS FUMIGATUS IN COMPLEX WITH ACETAZOLAMIDE | 3.2.1.14 |
2XTU | STRUCTURE OF E.COLI RHOMBOID PROTEASE GLPG ACTIVE SITE MUTANT, S201T IN TRIGONAL CRYSTAL FORM | 3.4.21.105 |
2XTV | STRUCTURE OF E.COLI RHOMBOID PROTEASE GLPG, ACTIVE SITE MUTANT, S201T, ORTHORHOMBIC CRYSTAL FORM | 3.4.21.105 |
2XTZ | CRYSTAL STRUCTURE OF THE G ALPHA PROTEIN ATGPA1 FROM ARABIDOPSIS THALIANA | 3.6.5.1 |
2XU1 | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2XU2 | CRYSTAL STRUCTURE OF THE HYPOTHETICAL PROTEIN PA4511 FROM PSEUDOMONAS AERUGINOSA | 3.5.2.9 |
2XU3 | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2XU4 | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2XU5 | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2XUA | CRYSTAL STRUCTURE OF THE ENOL-LACTONASE FROM BURKHOLDERIA XENOVORANS LB400 | 3.1.1.24 |
2XUC | NATURAL PRODUCT-GUIDED DISCOVERY OF A FUNGAL CHITINASE INHIBITOR | 3.2.1.14 |
2XUD | CRYSTAL STRUCTURE OF THE Y337A MUTANT OF MOUSE ACETYLCHOLINESTERASE | 3.1.1.7 |
2XUF | CRYSTAL STRUCTURE OF MACHE-Y337A-TZ2PA6 ANTI COMPLEX (1 MTH) | 3.1.1.7 |
2XUG | CRYSTAL STRUCTURE OF MACHE-Y337A-TZ2PA6 ANTI COMPLEX (1 WK) | 3.1.1.7 |
2XUH | CRYSTAL STRUCTURE OF MACHE-Y337A-TZ2PA6 ANTI COMPLEX (10 MTH) | 3.1.1.7 |
2XUI | CRYSTAL STRUCTURE OF MACHE-Y337A-TZ2PA6 SYN COMPLEX (1 WK) | 3.1.1.7 |
2XUJ | CRYSTAL STRUCTURE OF MACHE-Y337A-TZ2PA6 SYN COMPLEX (1 MTH) | 3.1.1.7 |
2XUK | CRYSTAL STRUCTURE OF MACHE-Y337A-TZ2PA6 SYN COMPLEX (10 MTH) | 3.1.1.7 |
2XUO | CRYSTAL STRUCTURE OF MACHE-Y337A MUTANT IN COMPLEX WITH SOAKED TZ2PA6 ANTI INHIBITOR | 3.1.1.7 |
2XUP | CRYSTAL STRUCTURE OF THE MACHE-Y337A MUTANT IN COMPLEX WITH SOAKED TZ2PA6 SYN INHIBITOR | 3.1.1.7 |
2XUQ | CRYSTAL STRUCTURE OF THE MACHE-Y337A MUTANT IN COMPLEX WITH SOAKED TZ2PA6 ANTI-SYN INHIBITORS | 3.1.1.7 |
2XV6 | CRYSTAL STRUCTURE OF THE HIV-1 CAPSID PROTEIN C-TERMINAL DOMAIN (146- 220) IN COMPLEX WITH A CAMELID VHH. | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2XVG | CRYSTAL STRUCTURE OF ALPHA-XYLOSIDASE (GH31) FROM CELLVIBRIO JAPONICUS | 3.2.1 |
2XVK | CRYSTAL STRUCTURE OF ALPHA-XYLOSIDASE (GH31) FROM CELLVIBRIO JAPONICUS IN COMPLEX WITH 5-FLUORO-ALPHA-D-XYLOPYRANOSYL FLUORIDE | 3.2.1 |
2XVL | CRYSTAL STRUCTURE OF ALPHA-XYLOSIDASE (GH31) FROM CELLVIBRIO JAPONICUS IN COMPLEX WITH PENTAERYTHRITOL PROPOXYLATE (5 4 PO OH) | 3.2.1 |
2XVN | A. FUMIGATUS CHITINASE A1 PHENYL-METHYLGUANYLUREA COMPLEX | 3.2.1.14 |
2XVP | CHIA1 FROM ASPERGILLUS FUMIGATUS, APOSTRUCTURE | 3.2.1.14 |
2XW9 | CRYSTAL STRUCTURE OF COMPLEMENT FACTOR D MUTANT S183A | 3.4.21.46 |
2XWA | CRYSTAL STRUCTURE OF COMPLEMENT FACTOR D MUTANT R202A | 3.4.21.46 |
2XWD | X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH 5N,6O-(N'-(N-OCTYL)IMINO)NOJIRIMYCIN IN THE ACTIVE SITE | 3.2.1.45 2.4.1 3.2.1 |
2XWE | X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH 5N,6S-(N'-(N-OCTYL)IMINO)-6-THIONOJIRIMYCIN IN THE ACTIVE SITE | 3.2.1.45 2.4.1 3.2.1 |
2XWH | HCV-J6 NS5B POLYMERASE STRUCTURE AT 1.8 ANGSTROM | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XWY | STRUCTURE OF MK-3281, A POTENT NON-NUCLEOSIDE FINGER-LOOP INHIBITOR, IN COMPLEX WITH THE HEPATITIS C VIRUS NS5B POLYMERASE | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XX6 | STRUCTURE OF THE BACILLUS SUBTILIS PROPHAGE DUTPASE, YOSS | 3.6.1.23 |
2XXA | THE CRYSTAL STRUCTURE OF THE SIGNAL RECOGNITION PARTICLE (SRP) IN COMPLEX WITH ITS RECEPTOR(SR) | 3.6.5.4 |
2XXD | HCV-JFH1 NS5B POLYMERASE STRUCTURE AT 1.9 ANGSTROM | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XXL | CRYSTAL STRUCTURE OF DROSOPHILA GRASS CLIP SERINE PROTEASE OF TOLL PATHWAY | 3.4.21.4 3.4.21 |
2XXM | CRYSTAL STRUCTURE OF THE HIV-1 CAPSID PROTEIN C-TERMINAL DOMAIN IN COMPLEX WITH A CAMELID VHH AND THE CAI PEPTIDE. | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2XXN | STRUCTURE OF THE VIRF4-HAUSP TRAF DOMAIN COMPLEX | 3.4.19.12 |
2XY3 | STRUCTURE OF THE BACILLUS SUBTILIS PROPHAGE DUTPASE WITH DUPNHPP | 3.6.1.23 |
2XY9 | HUMAN ANGIOTENSIN CONVERTING ENZYME IN COMPLEX WITH PHOSPHINIC TRIPEPTIDE | 3.4.15.1 3.2.1 |
2XYA | NON-COVALENT INHIBTORS OF RHINOVIRUS 3C PROTEASE. | 3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48 |
2XYD | HUMAN ANGIOTENISN CONVERTING ENZYME N-DOMAIN IN COMPLEX WITH PHOSPHINIC TRIPEPTIDE | 3.4.15.1 3.2.1 |
2XYE | HIV-1 INHIBITORS WITH A TERTIARY-ALCOHOL-CONTAINING TRANSITION-STATE MIMIC AND VARIOUS P2 AND P1 PRIME SUBSTITUENTS | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2XYF | HIV-1 INHIBITORS WITH A TERTIARY-ALCOHOL-CONTAINING TRANSITION-STATE MIMIC AND VARIOUS P2 AND P1 PRIME SUBSTITUENTS | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2XYG | CASPASE-3:CAS329306 | 3.4.22.56 |
2XYH | CASPASE-3:CAS60254719 | 3.4.22.56 |
2XYL | CELLULOMONAS FIMI XYLANASE/CELLULASE COMPLEXED WITH 2-DEOXY-2-FLUORO-XYLOBIOSE | 3.2.1.91 3.2.1.8 |
2XYM | HCV-JFH1 NS5B T385A MUTANT | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2XYP | CASPASE-3:CAS26049945 | 3.4.22.56 |
2XYQ | CRYSTAL STRUCTURE OF THE NSP16 NSP10 SARS CORONAVIRUS COMPLEX | 2.1.1 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 |
2XYR | CRYSTAL STRUCTURE OF THE NSP16 NSP10 SARS CORONAVIRUS COMPLEX | 2.1.1 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 |
2XYV | CRYSTAL STRUCTURE OF THE NSP16 NSP10 SARS CORONAVIRUS COMPLEX | 2.1.1 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 |
2XZD | CASPASE-3 IN COMPLEX WITH AN INHIBITORY DARPIN-3.4 | 3.4.22.56 |
2XZE | STRUCTURAL BASIS FOR AMSH-ESCRT-III CHMP3 INTERACTION | 3.4.19 |
2XZF | CRYSTAL STRUCTURE OF A COMPLEX BETWEEN THE WILD-TYPE LACTOCOCCUS LACTIS FPG (MUTM) AND AN OXIDIZED PYRIMIDINE CONTAINING DNA AT 293K | 3.2.2.23 4.2.99.18 |
2XZI | THE ASPERGILLUS FUMIGATUS SIALIDASE IS A KDNASE: STRUCTURAL AND MECHANISTIC INSIGHTS | 3.2.1.18 |
2XZJ | THE ASPERGILLUS FUMIGATUS SIALIDASE IS A KDNASE: STRUCTURAL AND MECHANISTIC INSIGHTS | 3.2.1.18 |
2XZK | THE ASPERGILLUS FUMIGATUS SIALIDASE IS A KDNASE: STRUCTURAL AND MECHANISTIC INSIGHTS | 3.2.1.18 |
2XZL | UPF1-RNA COMPLEX | 3.6.4.13 3.6.4 |
2XZO | UPF1 HELICASE - RNA COMPLEX | 3.6.4.13 3.6.4 |
2XZP | UPF1 HELICASE | 3.6.4.13 3.6.4 |
2XZT | CASPASE-3 IN COMPLEX WITH DARPIN-3.4_I78S | 3.4.22.56 |
2XZU | CRYSTAL STRUCTURE OF A COMPLEX BETWEEN THE WILD-TYPE LACTOCOCCUS LACTIS FPG (MUTM) AND AN OXIDIZED PYRIMIDINE CONTAINING DNA AT 310K | 3.2.2.23 4.2.99.18 |
2Y0B | CASPASE-3 IN COMPLEX WITH AN INHIBITORY DARPIN-3.4_S76R | 3.4.22.56 |
2Y0J | TRIAZOLOQUINAZOLINES AS A NOVEL CLASS OF PHOSPHODIESTERASE 10A (PDE10A) INHIBITORS, PART 2, LEAD-OPTIMISATION. | 3.1.4.17 3.1.4.35 |
2Y1H | CRYSTAL STRUCTURE OF THE HUMAN TATD-DOMAIN PROTEIN 3 (TATDN3) | 3.1.21 |
2Y1K | STRUCTURE OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY CBDP (12H SOAK): PHOSPHOSERINE ADDUCT | 3.1.1.8 |
2Y1L | CASPASE-8 IN COMPLEX WITH DARPIN-8.4 | 3.4.22.61 |
2Y1P | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, COMPLEXED WITH CITRATE | 3.1.4.37 |
2Y1T | BACILLUS SUBTILIS PROPHAGE DUTPASE IN COMPLEX WITH DUDP | 3.6.1.23 |
2Y24 | STRUCTURAL BASIS FOR SUBSTRATE RECOGNITION BY ERWINIA CHRYSANTHEMI GH5 GLUCURONOXYLANASE | 3.2.1.8 3.2.1.136 |
2Y28 | CRYSTAL STRUCTURE OF SE-MET AMPD DERIVATIVE | 3.5.1.28 |
2Y2B | CRYSTAL STRUCTURE OF AMPD IN COMPLEX WITH REACTION PRODUCTS | 3.5.1.28 |
2Y2C | CRYSTAL STRUCTURE OF AMPD APOENZYME | 3.5.1.28 |
2Y2D | CRYSTAL STRUCTURE OF AMPD HOLOENZYME | 3.5.1.28 |
2Y2E | CRYSTAL STRUCTURE OF AMPD GROWN AT PH 5.5 | 3.5.1.28 |
2Y2F | CRYSTAL STRUCTURE OF YERSINIA PESTIS YOPH IN COMPLEX WITH AN AMINOOXY- CONTAINING PLATFORM COMPOUND FOR INHIBITOR DESIGN | 3.1.3.48 |
2Y2G | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (A01) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2H | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (ZA2) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2I | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (ZA3) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2J | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (ZA4) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2K | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (ZA5) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2L | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (E06) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2M | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (E08) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2N | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (E07) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2O | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (EO9) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2P | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (Z10) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2Q | PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (Z06) | 2.4.1.129 2.3.2 3.4.16.4 |
2Y2U | NONAGED FORM OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY VX-UPDATE | 3.1.1.7 |
2Y2V | NONAGED FORM OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY SARIN-UPDATE | 3.1.1.7 |
2Y35 | CRYSTAL STRUCTURE OF XRN1-SUBSTRATE COMPLEX | 3.1.13 |
2Y3U | CRYSTAL STRUCTURE OF APO COLLAGENASE G FROM CLOSTRIDIUM HISTOLYTICUM AT 2.55 ANGSTROM RESOLUTION | 3.4.24.3 |
2Y3X | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, COMPLEXED WITH SULFATE | 3.1.4.37 |
2Y4A | UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | 3.4.16.4 |
2Y4S | BARLEY LIMIT DEXTRINASE IN COMPLEX WITH BETA-CYCLODEXTRIN | 3.2.1.41 |
2Y50 | CRYSTAL STRUCTURE OF COLLAGENASE G FROM CLOSTRIDIUM HISTOLYTICUM AT 2. 80 ANGSTROM RESOLUTION | 3.4.24.3 |
2Y55 | UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | 3.4.16.4 |
2Y59 | UNEXPECTED TRICOVALENT BINDING MODE OF BORONIC ACIDS WITHIN THE ACTIVE SITE OF A PENICILLIN BINDING PROTEIN | 3.4.16.4 |
2Y5B | STRUCTURE OF USP21 IN COMPLEX WITH LINEAR DIUBIQUITIN-ALDEHYDE | 3.1.2.15 3.4.19.12 |
2Y5E | BARLEY LIMIT DEXTRINASE IN COMPLEX WITH ALPHA-CYCLODEXTRIN | 3.2.1.41 |
2Y5F | FACTOR XA - CATION INHIBITOR COMPLEX | 3.4.21.6 |
2Y5G | FACTOR XA - CATION INHIBITOR COMPLEX | 3.4.21.6 |
2Y5H | FACTOR XA - CATION INHIBITOR COMPLEX | 3.4.21.6 |
2Y5K | ORALLY ACTIVE AMINOPYRIDINES AS INHIBITORS OF TETRAMERIC FRUCTOSE 1,6- BISPHOSPHATASE | 3.1.3.11 |
2Y5L | ORALLY ACTIVE AMINOPYRIDINES AS INHIBITORS OF TETRAMERIC FRUCTOSE 1,6- BISPHOSPHATASE | 3.1.3.11 |
2Y64 | XYLOPENTAOSE BINDING MUTATED (X-2 L110F) CBM4-2 CARBOHYDRATE BINDING MODULE FROM A THERMOSTABLE RHODOTHERMUS MARINUS XYLANASE | 3.2.1.8 |
2Y6C | THE DISCOVERY OF MMP7 INHIBITORS EXPLOITING A NOVEL SELECTIVITY TRIGGER | 3.4.24.23 |
2Y6D | THE DISCOVERY OF MMP7 INHIBITORS EXPLOITING A NOVEL SELECTIVITY TRIGGER | 3.4.24.23 |
2Y6E | STRUCTURE OF THE D1D2 DOMAIN OF USP4, THE CONSERVED CATALYTIC DOMAIN | 3.1.2.15 3.4.19.12 |
2Y6G | CELLOPENTAOSE BINDING MUTATED (X-2 L110F) CBM4-2 CARBOHYDRATE BINDING MODULE FROM A THERMOSTABLE RHODOTHERMUS MARINUS XYLANASE | 3.2.1.8 |
2Y6H | X-2 L110F CBM4-2 CARBOHYDRATE BINDING MODULE FROM A THERMOSTABLE RHODOTHERMUS MARINUS XYLANASE | 3.2.1.8 |
2Y6I | CRYSTAL STRUCTURE OF COLLAGENASE G FROM CLOSTRIDIUM HISTOLYTICUM IN COMPLEX WITH ISOAMYLPHOSPHONYL-GLY-PRO-ALA AT 3.25 ANGSTROM RESOLUTION | 3.4.24.3 |
2Y6J | X-2 ENGINEERED MUTATED CBM4-2 CARBOHYDRATE BINDING MODULE FROM A THERMOSTABLE RHODOTHERMUS MARINUS XYLANASE | 3.2.1.8 |
2Y6K | XYLOTETRAOSE BOUND TO X-2 ENGINEERED MUTATED CBM4-2 CARBOHYDRATE BINDING MODULE FROM A THERMOSTABLE RHODOTHERMUS MARINUS XYLANASE | 3.2.1.8 |
2Y6L | XYLOPENTAOSE BINDING X-2 ENGINEERED MUTATED CBM4-2 CARBOHYDRATE BINDING MODULE FROM A THERMOSTABLE RHODOTHERMUS MARINUS XYLANASE | 3.2.1.8 |
2Y6T | MOLECULAR RECOGNITION OF CHYMOTRYPSIN BY THE SERINE PROTEASE INHIBITOR ECOTIN FROM YERSINIA PESTIS | 3.4.21.1 |
2Y6U | PEROXISOMAL ALPHA-BETA-HYDROLASE LPX1 (YOR084W) FROM SACCHAROMYCES CEREVISIAE (CRYSTAL FORM II) | 3.1.1 |
2Y6V | PEROXISOMAL ALPHA-BETA-HYDROLASE LPX1 (YOR084W) FROM SACCHAROMYCES CEREVISIAE (CRYSTAL FORM I) | 3.1.1 |
2Y72 | CRYSTAL STRUCTURE OF THE PKD DOMAIN OF COLLAGENASE G FROM CLOSTRIDIUM HISTOLYTICUM AT 1.18 ANGSTROM RESOLUTION. | 3.4.24.3 |
2Y7C | ATOMIC MODEL OF THE OCR-BOUND METHYLASE COMPLEX FROM THE TYPE I RESTRICTION-MODIFICATION ENZYME ECOKI (M2S1). BASED ON FITTING INTO EM MAP 1534. | 3.1.21.3 |
2Y7H | ATOMIC MODEL OF THE DNA-BOUND METHYLASE COMPLEX FROM THE TYPE I RESTRICTION-MODIFICATION ENZYME ECOKI (M2S1). BASED ON FITTING INTO EM MAP 1534. | 3.1.21.3 |
2Y7X | THE DISCOVERY OF POTENT AND LONG-ACTING ORAL FACTOR XA INHIBITORS WITH TETRAHYDROISOQUINOLINE AND BENZAZEPINE P4 MOTIFS | 3.4.21.6 |
2Y7Z | STRUCTURE AND PROPERTY BASED DESIGN OF FACTOR XA INHIBITORS: PYRROLIDIN-2-ONES WITH AMINOINDANE AND PHENYLPYRROLIDINE P4 MOTIFS | 3.4.21.6 |
2Y80 | STRUCTURE AND PROPERTY BASED DESIGN OF FACTOR XA INHIBITORS: PYRROLIDIN-2-ONES WITH AMINOINDANE AND PHENYLPYRROLIDINE P4 MOTIFS | 3.4.21.6 |
2Y81 | STRUCTURE AND PROPERTY BASED DESIGN OF FACTOR XA INHIBITORS: PYRROLIDIN-2-ONES WITH AMINOINDANE AND PHENYLPYRROLIDINE P4 MOTIFS | 3.4.21.6 |
2Y82 | STRUCTURE AND PROPERTY BASED DESIGN OF FACTOR XA INHIBITORS: PYRROLIDIN-2-ONES WITH AMINOINDANE AND PHENYLPYRROLIDINE P4 MOTIFS | 3.4.21.6 |
2Y8C | PLASMODIUM FALCIPARUM DUTPASE IN COMPLEX WITH A TRITYL LIGAND | 3.6.1.23 |
2Y8I | STRUCTURAL BASIS FOR THE ALLOSTERIC INTERFERENCE OF MYOSIN FUNCTION BY MUTANTS G680A AND G680V OF DICTYOSTELIUM MYOSIN-2 | 3.6.4.1 |
2Y8V | STRUCTURE OF CHITINASE, CHIC, FROM ASPERGILLUS FUMIGATUS. | 3.2.1.14 |
2Y8W | STRUCTURE OF CRISPR ENDORIBONUCLEASE CSE3 BOUND TO 20 NT RNA | 3.1 |
2Y8Y | STRUCTURE B OF CRISPR ENDORIBONUCLEASE CSE3 BOUND TO 19 NT RNA | 3.1 |
2Y91 | CRYSTAL STRUCTURE OF CLASS A BETA-LACTAMASE FROM BACILLUS LICHENIFORMIS BS3 WITH CLAVULANIC ACID | 3.5.2.6 |
2Y96 | STRUCTURE OF HUMAN DUAL-SPECIFICITY PHOSPHATASE 27 | 3.1.3.16 3.1.3.48 |
2Y9E | STRUCTURAL BASIS FOR THE ALLOSTERIC INTERFERENCE OF MYOSIN FUNCTION BY MUTANTS G680A AND G680V OF DICTYOSTELIUM MYOSIN-2 | 3.6.4.1 |
2Y9H | STRUCTURE A OF CRISPR ENDORIBONUCLEASE CSE3 BOUND TO 19 NT RNA | 3.1 |
2Y9N | CELLOBIOHYDROLASE I CEL7A FROM TRICHODERMA HARZIANUM AT 2.9 A RESOLUTION | 3.2.1.91 |
2Y9Y | CHROMATIN REMODELING FACTOR ISW1A(DEL_ATPASE) | 3.6.4 |
2Y9Z | CHROMATIN REMODELING FACTOR ISW1A(DEL_ATPASE) IN DNA COMPLEX | 3.6.4 |
2YA4 | CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANA (TIGR4) | 3.2.1.18 |
2YA5 | CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANA (TIGR4) IN COMPLEX WITH SIALIC ACID | 3.2.1.18 |
2YA6 | CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANA (TIGR4) IN COMPLEX WITH DANA | 3.2.1.18 |
2YA8 | CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANA (TIGR4) IN COMPLEX WITH OSELTAMIVIR CARBOXYLATE | 3.2.1.18 |
2YAY | THE CRYSTAL STRUCTURE OF LEISHMANIA MAJOR DUTPASE IN COMPLEX WITH SUBSTRATE ANALOGUE DUPNPP | 3.6.1.23 |
2YAZ | THE CRYSTAL STRUCTURE OF LEISHMANIA MAJOR DUTPASE IN COMPLEX DUMP | 3.6.1.23 |
2YB0 | THE CRYSTAL STRUCTURE OF LEISHMANIA MAJOR DUTPASE IN COMPLEX DEOXYURIDINE | 3.6.1.23 |
2YB1 | STRUCTURE OF AN AMIDOHYDROLASE FROM CHROMOBACTERIUM VIOLACEUM (EFI TARGET EFI-500202) WITH BOUND MN, AMP AND PHOSPHATE. | 3.1.3.97 |
2YB4 | STRUCTURE OF AN AMIDOHYDROLASE FROM CHROMOBACTERIUM VIOLACEUM (EFI TARGET EFI-500202) WITH BOUND SO4, NO METAL | 3.1.3.97 |
2YB9 | CRYSTAL STRUCTURE OF HUMAN NEUTRAL ENDOPEPTIDASE COMPLEXED WITH A HETEROARYLALANINE DIACID. | 3.4.24.11 |
2YBH | NITRATE X-RAY INDUCED REDUCTION ON HEWL CRYSTALS (2.31 MGY). | 3.2.1.17 |
2YBI | NITRATE X-RAY INDUCED REDUCTION ON HEWL CRYSTALS (6.62 MGY) | 3.2.1.17 |
2YBJ | NITRATE X-RAY INDUCED REDUCTION ON HEWL CRYSTALS (12.31 MGY) | 3.2.1.17 |
2YBL | NITRATE X-RAY INDUCED REDUCTION ON HEWL CRYSTALS (17.9 MGY) | 3.2.1.17 |
2YBM | NITRATE X-RAY INDUCED REDUCTION ON HEWL CRYSTALS (23.3 MGY) | 3.2.1.17 |
2YBN | NITRATE X-RAY INDUCED REDUCTION ON HEWL CRYSTALS (28.6 MGY) | 3.2.1.17 |
2YD0 | CRYSTAL STRUCTURE OF THE SOLUBLE DOMAIN OF HUMAN ENDOPLASMIC RETICULUM AMINOPEPTIDASE 1 ERAP1 | 3.4.11 |
2YD1 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-2 MODULE OF DROSOPHILA RECEPTOR PROTEIN TYROSINE PHOSPHATASE DLAR | 3.1.3.48 |
2YD2 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-2 MODULE OF HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE SIGMA | 3.1.3.48 |
2YD3 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-2 MODULE OF HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE SIGMA | 3.1.3.48 |
2YD4 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-2 MODULE OF CHICKEN RECEPTOR PROTEIN TYROSINE PHOSPHATASE SIGMA | 3.1.3.48 |
2YD5 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-2 MODULE OF HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE LAR | 3.1.3.48 |
2YD6 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-2 MODULE OF HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE DELTA | 3.1.3.48 |
2YD7 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-2 MODULE OF HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE DELTA | 3.1.3.48 |
2YD8 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-2 MODULE OF HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE LAR IN COMPLEX WITH SUCROSE OCTASULPHATE | 3.1.3.48 |
2YD9 | CRYSTAL STRUCTURE OF THE N-TERMINAL IG1-3 MODULE OF HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE SIGMA | 3.1.3.48 |
2YDB | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, SOAKED WITH 2',3'-CYCLIC NADP | 3.1.4.37 |
2YDC | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, SOAKED WITH GTP | 3.1.4.37 |
2YDD | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, SOAKED WITH 2',3'-CYCLIC AMP | 3.1.4.37 |
2YDG | ASCORBATE CO-CRYSTALLIZED HEWL. | 3.2.1.17 |
2YDM | STRUCTURAL CHARACTERIZATION OF ANGIOTENSIN-I CONVERTING ENZYME IN COMPLEX WITH A SELENIUM ANALOGUE OF CAPTOPRIL | 3.4.15.1 3.2.1 |
2YDP | STRUCTURE OF THE E242A MUTANT OF THE ALPHA-L-ARABINOFURANOSIDASE ARB93A FROM FUSARIUM GRAMINEARUM IN COMPLEX WITH AN IMINOSUGAR INHIBITOR | 3.2.1.55 |
2YDQ | CPOGA D298N IN COMPLEX WITH HOGA-DERIVED O-GLCNAC PEPTIDE | 3.2.1.52 3.2.1.169 |
2YDR | CPOGA D298N IN COMPLEX WITH P53-DERIVED O-GLCNAC PEPTIDE | 3.2.1.52 3.2.1.169 |
2YDS | CPOGA D298N IN COMPLEX WITH TAB1-DERIVED O-GLCNAC PEPTIDE | 3.2.1.169 |
2YDT | STRUCTURE OF THE ALPHA-L-ARABINOFURANOSIDASE ARB93A FROM FUSARIUM GRAMINEARUM IN COMPLEXE WITH AN IMINOSUGAR INHIBITOR | 3.2.1.55 |
2YDU | CRYSTAL STRUCTURE OF YOPH IN COMPLEX WITH 3-(1,1-DIOXIDO-3- OXOISOTHIAZOLIDIN-5-YL)BENZALDEYDE | 3.1.3.48 |
2YEQ | STRUCTURE OF PHOD | 3.1.3.1 |
2YET | THERMOASCUS GH61 ISOZYME A | 3.2.1.4 |
2YEU | STRUCTURAL AND FUNCTIONAL INSIGHTS OF DR2231 PROTEIN, THE MAZG-LIKE NUCLEOSIDE TRIPHOSPHATE PYROPHOSPHOHYDROLASE FROM DEINOCOCCUS RADIODURANS, COMPLEX WITH GD | 3.6.1.19 |
2YF0 | HUMAN MYOTUBULARIN RELATED PROTEIN 6 (MTMR6) | 3.1.3 3.1.3.95 3.1.3.64 |
2YF3 | CRYSTAL STRUCTURE OF DR2231, THE MAZG-LIKE PROTEIN FROM DEINOCOCCUS RADIODURANS, COMPLEX WITH MANGANESE | 3.6.1.19 |
2YF4 | CRYSTAL STRUCTURE OF DR2231, THE MAZG-LIKE PROTEIN FROM DEINOCOCCUS RADIODURANS, APO STRUCTURE | 3.6.1.19 |
2YF9 | STRUCTURAL AND FUNCTIONAL INSIGHTS OF DR2231 PROTEIN, THE MAZG-LIKE NUCLEOSIDE TRIPHOSPHATE PYROPHOSPHOHYDROLASE FROM DEINOCOCCUS RADIODURANS, NATIVE FORM | 3.6.1.19 |
2YFC | STRUCTURAL AND FUNCTIONAL INSIGHTS OF DR2231 PROTEIN, THE MAZG-LIKE NUCLEOSIDE TRIPHOSPHATE PYROPHOSPHOHYDROLASE FROM DEINOCOCCUS RADIODURANS, COMPLEXED WITH MN AND DUMP | 3.6.1.19 |
2YFD | STRUCTURAL AND FUNCTIONAL INSIGHTS OF DR2231 PROTEIN, THE MAZG-LIKE NUCLEOSIDE TRIPHOSPHATE PYROPHOSPHOHYDROLASE FROM DEINOCOCCUS RADIODURANS, COMPLEXED WITH MG AND DUMP | 3.6.1.19 |
2YFN | GALACTOSIDASE DOMAIN OF ALPHA-GALACTOSIDASE-SUCROSE KINASE, AGASK | 3.2.1.22 2.7 |
2YFO | GALACTOSIDASE DOMAIN OF ALPHA-GALACTOSIDASE-SUCROSE KINASE, AGASK, IN COMPLEX WITH GALACTOSE | 3.2.1.22 2.7 |
2YFY | SERCA IN THE HNE2 STATE COMPLEXED WITH DEBUTANOYL THAPSIGARGIN | 3.6.3.8 7.2.2.10 |
2YG1 | APO STRUCTURE OF CELLOBIOHYDROLASE 1 (CEL7A) FROM HETEROBASIDION ANNOSUM | 3.2.1 |
2YGK | CRYSTAL STRUCTURE OF THE NURA NUCLEASE FROM SULFOLOBUS SOLFATARICUS | 3.1 |
2YH2 | PYROBACULUM CALIDIFONTIS ESTERASE MONOCLINIC FORM | 3.1.1.1 |
2YHW | HIGH-RESOLUTION CRYSTAL STRUCTURES OF N-ACETYLMANNOSAMINE KINASE: INSIGHTS ABOUT SUBSTRATE SPECIFICITY, ACTIVITY AND INHIBITOR MODELLING. | 2.7.1.60 3.2.1.183 |
2YHY | STRUCTURE OF N-ACETYLMANNOSAMINE KINASE IN COMPLEX WITH N- ACETYLMANNOSAMINE AND ADP | 2.7.1.60 3.2.1.183 |
2YI1 | CRYSTAL STRUCTURE OF N-ACETYLMANNOSAMINE KINASE IN COMPLEX WITH N- ACETYL MANNOSAMINE 6-PHOSPHATE AND ADP. | 2.7.1.60 3.2.1.183 |
2YIG | MMP13 IN COMPLEX WITH A NOVEL SELECTIVE NON ZINC BINDING INHIBITOR | 3.4.24 |
2YIH | STRUCTURE OF A PAENIBACILLUS POLYMYXA XYLOGLUCANASE FROM GH FAMILY 44 WITH XYLOGLUCAN | 3.2.1.4 3.2.1.151 |
2YIJ | CRYSTAL STRUCTURE OF PHOSPHOLIPASE A1 | 3.1.1 |
2YIK | CATALYTIC DOMAIN OF CLOSTRIDIUM THERMOCELLUM CELT | 3.2.1.4 3.2.1 |
2YJ2 | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2YJ3 | CONFORMATIONAL CHANGES IN THE CATALYTIC DOMAIN OF THE CPX-ATPASE COPB- B UPON NUCLEOTIDE BINDING | 3.6.3.10 |
2YJ4 | CONFORMATIONAL CHANGES IN THE CATALYTIC DOMAIN OF THE CPX-ATPASE COPB- B UPON NUCLEOTIDE BINDING | 3.6.3.10 |
2YJ5 | CONFORMATIONAL CHANGES IN THE CATALYTIC DOMAIN OF THE CPX-ATPASE COPB- B UPON NUCLEOTIDE BINDING | 3.6.3.10 |
2YJ6 | CONFORMATIONAL CHANGES IN THE CATALYTIC DOMAIN OF THE CPX-ATPASE COPB- B UPON NUCLEOTIDE BINDING | 3.6.3.10 |
2YJ8 | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2YJ9 | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2YJB | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2YJC | CATHEPSIN L WITH A NITRILE INHIBITOR | 3.4.22.15 |
2YJQ | STRUCTURE OF A PAENIBACILLUS POLYMYXA XYLOGLUCANASE FROM GLYCOSIDE HYDROLASE FAMILY 44 | 3.2.1.4 3.2.1.151 |
2YKG | STRUCTURAL INSIGHTS INTO RNA RECOGNITION BY RIG-I | 3.6.4.13 |
2YKK | STRUCTURE OF A PAENIBACILLUS POLYMYXA XYLOGLUCANASE FROM GLYCOSIDE HYDROLASE FAMILY 44 | 3.2.1.4 3.2.1.151 |
2YKM | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH A DIFLUOROMETHYLBENZOXAZOLE (DFMB) PYRIMIDINE THIOETHER DERIVATIVE, A NON-NUCLEOSIDE RT INHIBITOR (NNRTI) | 2.7.7.49 2.7.7.7 3.1.26.13 3.4.23.16 3.1.13.2 2.7.7 3.1 |
2YKN | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH A DIFLUOROMETHYLBENZOXAZOLE (DFMB) PYRIMIDINE THIOETHER DERIVATIVE, A NON-NUCLEOSIDE RT INHIBITOR (NNRTI) | 2.7.7.49 2.7.7.7 3.1.26.13 3.4.23.16 3.1.13.2 2.7.7 3.1 |
2YL6 | INHIBITION OF THE PNEUMOCOCCAL VIRULENCE FACTOR STRH AND MOLECULAR INSIGHTS INTO N-GLYCAN RECOGNITION AND HYDROLYSIS | 3.2.1.52 |
2YL8 | INHIBITION OF THE PNEUMOCOCCAL VIRULENCE FACTOR STRH AND MOLECULAR INSIGHTS INTO N-GLYCAN RECOGNITION AND HYDROLYSIS | 3.2.1.52 |
2YL9 | INHIBITION OF THE PNEUMOCOCCAL VIRULENCE FACTOR STRH AND MOLECULAR INSIGHTS INTO N-GLYCAN RECOGNITION AND HYDROLYSIS | 3.2.1.52 |
2YLA | INHIBITION OF THE PNEUMOCOCCAL VIRULENCE FACTOR STRH AND MOLECULAR INSIGHTS INTO N-GLYCAN RECOGNITION AND HYDROLYSIS | 3.2.1.52 |
2YLK | CARBOHYDRATE-BINDING MODULE CBM3B FROM THE CELLULOSOMAL CELLOBIOHYDROLASE 9A FROM CLOSTRIDIUM THERMOCELLUM | 3.2.1.91 3.2.1 |
2YLL | INHIBITION OF THE PNEUMOCOCCAL VIRULENCE FACTOR STRH AND MOLECULAR INSIGHTS INTO N-GLYCAN RECOGNITION AND HYDROLYSIS | 3.2.1.52 |
2YLM | MECHANISM OF USP7 (HAUSP) ACTIVATION BY ITS C-TERMINAL UBIQUITIN-LIKE DOMAIN (HUBL) AND ALLOSTERIC REGULATION BY GMP-SYNTHETASE. | 3.4.19.12 |
2YMK | CRYSTAL STRUCTURE OF THE HEXAMERIC ANTI-MICROBIAL PEPTIDE CHANNEL DERMCIDIN | 3.4 |
2YNA | CRYSTAL STRUCTURE OF THE MAIN PROTEASE OF CORONAVIRUS HKU4 | 3.4.22.69 3.4.22 3.4.19.12 |
2YNB | CRYSTAL STRUCTURE OF THE MAIN PROTEASE OF CORONAVIRUS HKU4 IN COMPLEX WITH A MICHAEL ACCEPTOR SG85 | 3.4.22.69 3.4.19.12 3.4.22 |
2YNF | HIV-1 REVERSE TRANSCRIPTASE Y188L MUTANT IN COMPLEX WITH INHIBITOR GSK560 | 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 3.4.23.16 2.7.7 3.1 |
2YNG | HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR GSK560 | 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 3.4.23.16 2.7.7 3.1 |
2YNH | HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR GSK500 | 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 3.4.23.16 2.7.7 3.1 |
2YNI | HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR GSK952 | 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 3.4.23.16 2.7.7 3.1 |
2YOC | CRYSTAL STRUCTURE OF PULA FROM KLEBSIELLA OXYTOCA | 3.2.1.41 |
2YOJ | HCV NS5B POLYMERASE COMPLEXED WITH PYRIDONYLINDOLE COMPOUND | 2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 |
2YOK | CELLOBIOHYDROLASE I CEL7A FROM TRICHODERMA HARZIANUM AT 1.7 A RESOLUTION | 3.2.1.91 |
2YOL | WEST NILE VIRUS NS2B-NS3 PROTEASE IN COMPLEX WITH 3,4- DICHLOROPHENYLACETYL-LYS-LYS-GCMA | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2YOZ | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, CRYSTALLIZED WITH 2'-AMPS | 3.1.4.37 |
2YP0 | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, CRYSTALLIZED WITH 2'-AMPS | 3.1.4.37 |
2YPC | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, WITH MUTATION H309S, CRYSTALLIZED WITH 2',3-(SP)-CYCLIC-AMPS | 3.1.4.37 |
2YPE | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, WITH MUTATION H309S, CRYSTALLIZED WITH 2',3'- CYCLIC AMP | 3.1.4.37 |
2YPH | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, WITH MUTATION H230S, CRYSTALLIZED WITH 2',3-(RP)- CYCLIC-AMPS | 3.1.4.37 |
2YPJ | NON-CATALYTIC CARBOHYDRATE BINDING MODULE CBM65B | 3.2.1.4 |
2YPT | CRYSTAL STRUCTURE OF THE HUMAN NUCLEAR MEMBRANE ZINC METALLOPROTEASE ZMPSTE24 MUTANT (E336A) IN COMPLEX WITH A SYNTHETIC CSIM TETRAPEPTIDE FROM THE C-TERMINUS OF PRELAMIN A | 3.4.24.84 |
2YQ9 | CATALYTIC DOMAIN OF MOUSE 2',3'-CYCLIC NUCLEOTIDE 3'- PHOSPHODIESTERASE, WITH MUTATION V321A, CRYSTALLIZED WITH 2'-AMP | 3.1.4.37 |
2YQP | SOLUTION STRUCTURE OF THE ZF-HIT DOMAIN IN DEAD (ASP-GLU-ALA-ASP) BOX POLYPEPTIDE 59 | 3.6.1 3.6.4.13 |
2YRN | SOLUTION STRUCTURE OF THE CH DOMAIN FROM HUMAN NEURON NAVIGATOR 2 | 3.6.1 3.6.4.12 |
2YS0 | SOLUTION STRUCTURE OF THE SOMATOMEDIN B DOMAIN OF HUMAN ECTONUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE FAMILY MEMBER | 3.1.4.1 3.6.1.9 |
2YS1 | SOLUTION STRUCTURE OF THE PH DOMAIN OF DYNAMIN-2 FROM HUMAN | 3.6.5.5 |
2YSX | SOLUTION STRUCTURE OF THE HUMAN SHIP SH2 DOMAIN | 3.1.3.86 3.1.3.56 3.1.3.36 |
2YTW | SOLUTION STRUCTURE OF THE PDZ-DOMAIN OF HUMAN PROTEASE HTRA 1 PRECURSOR | 3.4.21 |
2YU6 | SOLUTION STRUCTURE OF THE YTH DOMAIN IN YTH DOMAIN-CONTAINING PROTEIN 2 | 3.6.4.13 |
2YU7 | SOLUTION STRUCTURE OF THE SHP-1 C-TERMINAL SH2 DOMAIN COMPLEXED WITH A TYROSINE-PHOSPHORYLATED PEPTIDE FROM NKG2A | 3.1.3.48 |
2YV0 | STRUCTURAL AND THERMODYNAMIC ANALYSES OF E. COLI RIBONUCLEASE HI VARIANT WITH QUINTUPLE THERMOSTABILIZING MUTATIONS | 3.1.26.4 |
2YV5 | CRYSTAL STRUCTURE OF YJEQ FROM AQUIFEX AEOLICUS | 3.6.1 |
2YVB | HIGH RESOLUTION X-RAY CRYSTAL STRUCTURE OF TETRAGONAL HEN EGG WHITE LYSOZYME | 3.2.1.17 |
2YVM | CRYSTAL STRUCTURE OF NDX2 IN COMPLEX WITH MG2+ FROM THERMUS THERMOPHILUS HB8 | 3.6.1 |
2YVN | CRYSTAL STRUCTURE OF NDX2 FROM THERMUS THERMOPHILUS HB8 | 3.6.1 |
2YVO | CRYSTAL STRUCTURE OF NDX2 IN COMPLEX WITH MG2+ AND AMP FROM THERMUS THERMOPHILUS HB8 | 3.6.1 |
2YVP | CRYSTAL STRUCTURE OF NDX2 IN COMPLEX WITH MG2+ AND AMPCPR FROM THERMUS THERMOPHILUS HB8 | 3.6.1 |
2YWD | CRYSTAL STRUCTURE OF GLUTAMINE AMIDOTRANSFERASE | 2.6 4.3.3.6 3.5.1.2 |
2YWE | CRYSTAL STRUCTURE OF LEPA FROM AQUIFEX AEOLICUS | 3.6.5 |
2YWF | CRYSTAL STRUCTURE OF GMPPNP-BOUND LEPA FROM AQUIFEX AEOLICUS | 3.6.5 |
2YWG | CRYSTAL STRUCTURE OF GTP-BOUND LEPA FROM AQUIFEX AEOLICUS | 3.6.5 |
2YWH | CRYSTAL STRUCTURE OF GDP-BOUND LEPA FROM AQUIFEX AEOLICUS | 3.6.5 |
2YWJ | CRYSTAL STRUCTURE OF UNCHARACTERIZED CONSERVED PROTEIN FROM METHANOCALDOCOCCUS JANNASCHII | 2.6 4.3.3.6 3.5.1.2 |
2YXO | HISTIDINOL PHOSPHATE PHOSPHATASE COMPLEXED WITH SULFATE | 3.1.3.15 |
2YXP | THE EFFECT OF DEUTERATION ON PROTEIN STRUCTURE A HIGH RESOLUTION COMPARISON OF HYDROGENOUS AND PERDEUTERATED HALOALKANE DEHALOGENASE | 3.8.1.5 |
2YY2 | CRYSTAL STRUCTURE OF THE HUMAN PHOSPHODIESTERASE 9A CATALYTIC DOMAIN COMPLEXED WITH IBMX | 3.1.4.35 |
2YY6 | CRYSTAL STRUCTURE OF THE PHOSPHOGLYCOLATE PHOSPHATASE FROM AQUIFEX AEOLICUS VF5 | 3.1.3.18 |
2YYV | CRYSTAL STRUCTURE OF UNCHARACTERIZED CONSERVED PROTEIN FROM THERMOTOGA MARITIMA | 3.1.3.71 |
2YZ2 | CRYSTAL STRUCTURE OF THE ABC TRANSPORTER IN THE COBALT TRANSPORT SYSTEM | 3.6.3 7 |
2YZ3 | CRYSTALLOGRAPHIC INVESTIGATION OF INHIBITION MODE OF THE VIM-2 METALLO-BETA-LACTAMASE FROM PSEUDOMONAS AERUGINOSA WITH MERCAPTOCARBOXYLATE INHIBITOR | 3.5.2.6 |
2YZ5 | HISTIDINOL PHOSPHATE PHOSPHATASE COMPLEXED WITH PHOSPHATE | 3.1.3.15 |
2YZJ | CRYSTAL STRUCTURE OF DCTP DEAMINASE FROM SULFOLOBUS TOKODAII | 3.6.1.23 |
2YZO | CRYSTAL STRUCTURE OF UNCHARACTERIZED CONSERVED PROTEIN FROM THERMOTOGA MARITIMA | 3.1.3.71 |
2YZS | CRYSTAL STRUCTURE OF UNCHARACTERIZED CONSERVED PROTEIN FROM AQUIFEX AEOLICUS | 3.1 |
2Z00 | CRYSTAL STRUCTURE OF DIHYDROOROTASE FROM THERMUS THERMOPHILUS | 3.5.2.3 |
2Z0B | CRYSTAL STRUCTURE OF CBM20 DOMAIN OF HUMAN PUTATIVE GLYCEROPHOSPHODIESTER PHOSPHODIESTERASE 5 (KIAA1434) | 3.1 3.1.4.2 |
2Z0D | THE CRYSTAL STRUCTURE OF HUMAN ATG4B- LC3(1-120) COMPLEX | 3.4.22 |
2Z0E | THE CRYSTAL STRUCTURE OF HUMAN ATG4B- LC3(1-124) COMPLEX | 3.4.22 |
2Z0J | CRYSTAL STRUCTURE OF UNCHARACTERIZED CONSERVED PROTEIN FROM THERMUS THERMOPHILUS HB8 | 3.1.3.71 |
2Z0M | CRYSTAL STRUCTURE OF HYPOTHETICAL ATP-DEPENDENT RNA HELICASE FROM SULFOLOBUS TOKODAII | 3.6.4.13 |
2Z12 | STRUCTURE OF THE TRANSFORMED MONOCLINIC LYSOZYME BY CONTROLLED DEHYDRATION | 3.2.1.17 |
2Z18 | PHASE TRANSITION OF MONOCLINIC LYSOZYME CRYSTAL SOAKED IN A 10% NACL SOLUTION | 3.2.1.17 |
2Z19 | PHASE TRANSITION OF MONOCLINIC LYSOZYME CRYSTAL SOAKED IN A SATURATED NACL SOLUTION | 3.2.1.17 |
2Z1A | CRYSTAL STRUCTURE OF 5'-NUCLEOTIDASE PRECURSOR FROM THERMUS THERMOPHILUS HB8 | 3.1.3.5 |
2Z1G | CRYSTAL STRUCTURE OF E.COLI RNASE HI SURFACE CHARGED MUTANT(Q4R/T40E/Q72H/Q76K/Q80E/T92K/Q105K) | 3.1.26.4 |
2Z1H | CRYSTAL STRUCTURE OF E.COLI RNASE HI SURFACE CHARGED MUTANT(Q4R/T92K/Q105K/Q113R/Q115K/N143K/T145K) | 3.1.26.4 |
2Z1I | CRYSTAL STRUCTURE OF E.COLI RNASE HI SURFACE CHARGED MUTANT(Q4R/T40E/Q72H/Q76K/Q80E/T92K/Q105K/Q113R/Q115K) | 3.1.26.4 |
2Z1J | CRYSTAL STRUCTURE OF E.COLI RNASE HI SURFACE CHARGED MUTANT(Q4R/T40E/Q72H/Q76K/Q80E/T92K/Q105K/Q113R/Q115K/N143K/T145K) | 3.1.26.4 |
2Z1K | CRYSTAL STRUCTURE OF TTHA1563 FROM THERMUS THERMOPHILUS HB8 | 3.2.1.41 |
2Z1S | BETA-GLUCOSIDASE B FROM PAENIBACILLUS POLYMYXA COMPLEXED WITH CELLOTETRAOSE | 3.2.1.21 |
2Z24 | THR110SER DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2Z25 | THR110VAL DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2Z26 | THR110ALA DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2Z27 | THR109SER DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2Z28 | THR109VAL DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2Z29 | THR109ALA DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2Z2A | THR109GLY DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2Z2B | DELETION 107-116 MUTANT OF DIHYDROOROTASE FROM E. COLI | 3.5.2.3 |
2Z2D | SOLUTION STRUCTURE OF HUMAN MACROPHAGE ELASTASE (MMP-12) CATALYTIC DOMAIN COMPLEXED WITH A GAMMA-KETO BUTANOIC ACID INHIBITOR | 3.4.24.65 |
2Z2E | CRYSTAL STRUCTURE OF CANINE MILK LYSOZYME STABILIZED AGAINST NON-ENZYMATIC DEAMIDATION | 3.2.1.17 |
2Z2F | X-RAY CRYSTAL STRUCTURE OF BOVINE STOMACH LYSOZYME | 3.2.1.17 |
2Z2I | CRYSTAL STRUCTURE OF PEPTIDYL-TRNA HYDROLASE FROM MYCOBACTERIUM TUBERCULOSIS | 3.1.1.29 |
2Z2J | CRYSTAL STRUCTURE OF PEPTIDYL-TRNA HYDROLASE FROM MYCOBACTERIUM TUBERCULOSIS | 3.1.1.29 |
2Z2K | CRYSTAL STRUCTURE OF PEPTIDYL-TRNA HYDROLASE FROM MYCOBACTERIUM TUBERCULOSIS | 3.1.1.29 |
2Z2X | CRYSTAL STRUCTURE OF MATURE FORM OF TK-SUBTILISIN | 3.4.21.62 3.4.21 |
2Z2Y | CRYSTAL STRUCTURE OF AUTOPROCESSED FORM OF TK-SUBTILISIN | 3.4.21.62 3.4.21 |
2Z2Z | CRYSTAL STRUCTURE OF UNAUTOPROCESSED FORM OF TK-SUBTILISIN SOAKED BY 10MM CACL2 | 3.4.21.62 3.4.21 |
2Z30 | CRYSTAL STRUCTURE OF COMPLEX FORM BETWEEN MAT-TK-SUBTILISIN AND TK-PROPEPTIDE | 3.4.21.62 3.4.21 |
2Z37 | CRYSTAL STRUCTURE OF BRASSICA JUNCEA CHITINASE CATALYTIC MODULE (BJCHI3) | 3.2.1.14 |
2Z38 | CRYSTAL STRUCTURE OF CHLORIDE BOUND BRASSICA JUNCEA CHITINASE CATALYTIC MODULE (BJCHI3) | 3.2.1.14 |
2Z39 | CRYSTAL STRUCTURE OF BRASSICA JUNCEA CHITINASE CATALYTIC MODULE GLU234ALA MUTANT (BJCHI3-E234A) | 3.2.1.14 |
2Z3A | CRYSTAL STRUCTURE OF BACILLUS SUBTILIS CODW, A NON-CANONICAL HSLV-LIKE PEPTIDASE WITH AN IMPAIRED CATALYTIC APPARATUS | 3.4.25 3.4.21 |
2Z3B | CRYSTAL STRUCTURE OF BACILLUS SUBTILIS CODW, A NON-CANONICAL HSLV-LIKE PEPTIDASE WITH AN IMPAIRED CATALYTIC APPARATUS | 3.4.25 3.4.21 |
2Z3C | A MECHANISTIC VIEW OF ENZYME INHIBITION AND PEPTIDE HYDROLYSIS IN THE ACTIVE SITE OF THE SARS-COV 3C-LIKE PEPTIDASE | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2Z3D | A MECHANISTIC VIEW OF ENZYME INHIBITION AND PEPTIDE HYDROLYSIS IN THE ACTIVE SITE OF THE SARS-COV 3C-LIKE PEPTIDASE | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2Z3E | A MECHANISTIC VIEW OF ENZYME INHIBITION AND PEPTIDE HYDROLYSIS IN THE ACTIVE SITE OF THE SARS-COV 3C-LIKE PEPTIDASE | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2Z3G | CRYSTAL STRUCTURE OF BLASTICIDIN S DEAMINASE (BSD) | 3.5.4.23 |
2Z3H | CRYSTAL STRUCTURE OF BLASTICIDIN S DEAMINASE (BSD) COMPLEXED WITH DEAMINOHYDROXY BLASTICIDIN S | 3.5.4.23 |
2Z3I | CRYSTAL STRUCTURE OF BLASTICIDIN S DEAMINASE (BSD) MUTANT E56Q COMPLEXED WITH SUBSTRATE | 3.5.4.23 |
2Z3J | CRYSTAL STRUCTURE OF BLASTICIDIN S DEAMINASE (BSD) R90K MUTANT | 3.5.4.23 |
2Z3W | PROLYL TRIPEPTIDYL AMINOPEPTIDASE MUTANT E636A | 3.4.14 3.4.14.12 |
2Z3Z | PROLYL TRIPEPTIDYL AMINOPEPTIDASE MUTANT E636A COMPLEXD WITH AN INHIBITOR | 3.4.14 3.4.14.12 |
2Z4G | HISTIDINOL PHOSPHATE PHOSPHATASE FROM THERMUS THERMOPHILUS HB8 | 3.1.3.15 |
2Z4O | WILD TYPE HIV-1 PROTEASE WITH POTENT ANTIVIRAL INHIBITOR GRL-98065 | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2Z4U | CRYSTAL STRUCTURE OF WILD TYPE PD-L4 FROM PHYTOLACCA DIOICA LEAVES | 3.2.2.22 |
2Z53 | CRYSTAL STRUCTURE OF THE S211A MUTANT OF THE RIBOSOME INACTIVATING PROTEIN PDL4 FROM P. DIOICA LEAVES | 3.2.2.22 |
2Z54 | THE INFLUENCE OF I47A MUTATION ON REDUCED SUSCEPTIBILITY TO THE PROTEASE INHIBITOR LOPINAVIR | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2Z56 | CRYSTAL STRUCTURE OF G56S-PROPEPTIDE:S324A-SUBTILISIN COMPLEX | 3.4.21.62 3.4.21 |
2Z57 | CRYSTAL STRUCTURE OF G56E-PROPEPTIDE:S324A-SUBTILISIN COMPLEX | 3.4.21.62 3.4.21 |
2Z58 | CRYSTAL STRUCTURE OF G56W-PROPEPTIDE:S324A-SUBTILISIN COMPLEX | 3.4.21.62 3.4.21 |
2Z5G | CRYSTAL STRUCTURE OF T1 LIPASE F16L MUTANT | 3.1.1.3 |
2Z62 | CRYSTAL STRUCTURE OF THE TV3 HYBRID OF HUMAN TLR4 AND HAGFISH VLRB.61 | 3.2.2.6 |
2Z63 | CRYSTAL STRUCTURE OF THE TV8 HYBRID OF HUMAN TLR4 AND HAGFISH VLRB.61 | 3.2.2.6 |
2Z64 | CRYSTAL STRUCTURE OF MOUSE TLR4 AND MOUSE MD-2 COMPLEX | 3.2.2.6 |
2Z65 | CRYSTAL STRUCTURE OF THE HUMAN TLR4 TV3 HYBRID-MD-2-ERITORAN COMPLEX | 3.2.2.6 |
2Z66 | CRYSTAL STRUCTURE OF THE VT3 HYBRID OF HUMAN TLR4 AND HAGFISH VLRB.61 | 3.2.2.6 |
2Z6B | CRYSTAL STRUCTURE ANALYSIS OF (GP27-GP5)3 CONJUGATED WITH FE(III) PROTOPORPHYRIN | 3.2.1.17 |
2Z70 | E.COLI RNASE 1 IN COMPLEX WITH D(CGCGATCGCG) | 3.1.27.6 4.6.1.21 |
2Z71 | STRUCTURE OF TRUNCATED MUTANT CYS1GLY OF PENICILLIN V ACYLASE FROM BACILLUS SPHAERICUS CO-CRYSTALLIZED WITH PENICILLIN V | 3.5.1.11 |
2Z72 | NEW STRUCTURE OF COLD-ACTIVE PROTEIN TYROSINE PHOSPHATASE AT 1.1 ANGSTROM | 3.1.3.48 |
2Z79 | HIGH RESOLUTION CRYSTAL STRUCTURE OF A GLYCOSIDE HYDROLASE FAMILY 11 XYLANASE OF BACILLUS SUBTILIS | 3.2.1.8 |
2Z7F | CRYSTAL STRUCTURE OF THE COMPLEX OF HUMAN NEUTROPHIL ELASTASE WITH 1/2SLPI | 3.4.21.37 |
2Z7G | CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE LIGATED WITH EHNA | 3.5.4.4 |
2Z7J | STRUCTURAL INSIGHTS INTO DE MULTIFUNCTIONAL VP3 PROTEIN OF BIRNAVIRUSES:GOLD DERIVATIVE | 3.4.21 |
2Z7X | CRYSTAL STRUCTURE OF THE TLR1-TLR2 HETERODIMER INDUCED BY BINDING OF A TRI-ACYLATED LIPOPEPTIDE | 3.2.2.6 |
2Z80 | CRYSTAL STRUCTURE OF THE TLR1-TLR2 HETERODIMER INDUCED BY BINDING OF A TRI-ACYLATED LIPOPEPTIDE | 3.2.2.6 |
2Z81 | CRYSTAL STRUCTURE OF THE TLR1-TLR2 HETERODIMER INDUCED BY BINDING OF A TRI-ACYLATED LIPOPEPTIDE | 3.2.2.6 |
2Z82 | CRYSTAL STRUCTURE OF THE TLR1-TLR2 HETERODIMER INDUCED BY BINDING OF A TRI-ACYLATED LIPOPEPTIDE | 3.2.2.6 |
2Z83 | CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF JAPANESE ENCEPHALITIS VIRUS NS3 HELICASE/NUCLEOSIDE TRIPHOSPHATASE AT A RESOLUTION 1.8 | 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48 |
2Z84 | INSIGHTS FROM CRYSTAL AND SOLUTION STRUCTURES OF MOUSE UFSP1 | 3.4.22 |
2Z8G | ASPERGILLUS NIGER ATCC9642 ISOPULLULANASE COMPLEXED WITH ISOPANOSE | 3.2.1.57 |
2Z8I | CRYSTAL STRUCTURE OF ESCHERICHIA COLI GAMMA-GLUTAMYLTRANSPEPTIDASE IN COMPLEX WITH AZASERINE | 2.3.2.2 3.4.19.13 |
2Z8J | CRYSTAL STRUCTURE OF ESCHERICHIA COLI GAMMA-GLUTAMYLTRANSPEPTIDASE IN COMPLEX WITH AZASERINE PREPARED IN THE DARK | 2.3.2.2 3.4.19.13 |
2Z8K | CRYSTAL STRUCTURE OF ESCHERICHIA COLI GAMMA-GLUTAMYLTRANSPEPTIDASE IN COMPLEX WITH ACIVICIN | 2.3.2.2 3.4.19.13 |
2Z8X | CRYSTAL STRUCTURE OF EXTRACELLULAR LIPASE FROM PSEUDOMONAS SP. MIS38 | 3.1.1.3 |
2Z8Z | CRYSTAL STRUCTURE OF A PLATINUM-BOUND S445C MUTANT OF PSEUDOMONAS SP. MIS38 LIPASE | 3.1.1.3 |
2Z94 | COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH TDT | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2Z9G | COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH PMA | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2Z9I | CRYSTAL STRUCTURE OF RV0983 FROM MYCOBACTERIUM TUBERCULOSIS- PROTEOLYTICALLY ACTIVE FORM | 3.4.21 3.4.21.107 |
2Z9J | COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH EPDTC | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2Z9K | COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH JMF1600 | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2Z9L | COMPLEX STRUCTURE OF SARS-COV 3C-LIKE PROTEASE WITH JMF1586 | 3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1 |
2ZA4 | CRYSTAL STRUCTURAL ANALYSIS OF BARNASE-BARSTAR COMPLEX | 3.1.27 |
2ZA5 | CRYSTAL STRUCTURE OF HUMAN TRYPTASE WITH POTENT NON-PEPTIDE INHIBITOR | 3.4.21.59 |
2ZAE | CRYSTAL STRUCTURE OF PROTEIN PH1601P IN COMPLEX WITH PROTEIN PH1771P OF ARCHAEAL RIBONUCLEASE P FROM PYROCOCCUS HORIKOSHII OT3 | 3.1.26.5 |
2ZAK | ORTHORHOMBIC CRYSTAL STRUCTURE OF PRECURSOR E. COLI ISOASPARTYL PEPTIDASE/L-ASPARAGINASE (ECAIII) WITH ACTIVE-SITE T179A MUTATION | 3.4.19.5 3.5.1.1 |
2ZAL | CRYSTAL STRUCTURE OF E. COLI ISOASPARTYL AMINOPEPTIDASE/L-ASPARAGINASE IN COMPLEX WITH L-ASPARTATE | 3.4.19.5 3.5.1.1 |
2ZAM | CRYSTAL STRUCTURE OF MOUSE SKD1/VPS4B APO-FORM | 3.6.4.6 |
2ZAN | CRYSTAL STRUCTURE OF MOUSE SKD1/VPS4B ATP-FORM | 3.6.4.6 |
2ZAO | CRYSTAL STRUCTURE OF MOUSE SKD1/VPS4B ADP-FORM | 3.6.4.6 |
2ZAV | ARGINASE I (HOMO SAPIENS): NATIVE AND UNLIGANDED STRUCTURE AT 1.70 A RESOLUTION | 3.5.3.1 |
2ZBD | CRYSTAL STRUCTURE OF THE SR CALCIUM PUMP WITH BOUND ALUMINIUM FLUORIDE, ADP AND CALCIUM | 3.6.3.8 7.2.2.10 |
2ZBE | CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND BEF3 IN THE ABSENCE OF CALCIUM AND TG | 3.6.3.8 7.2.2.10 |
2ZBF | CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND BEF3 AND TG IN THE ABSENCE OF CALCIUM | 3.6.3.8 7.2.2.10 |
2ZBG | CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND ALF4 AND TG IN THE ABSENCE OF CALCIUM | 3.6.3.8 7.2.2.10 |
2ZBH | CRYSTAL STRUCTURE OF THE COMPLEX OF PHOSPHOLIPASE A2 WITH BAVACHALCONE FROM AERVA LANATA AT 2.6 A RESOLUTION | 3.1.1.4 |
2ZBM | CRYSTAL STRUCTURE OF I115M MUTANT COLD-ACTIVE PROTEIN TYROSINE PHOSPHATASE | 3.1.3.48 |
2ZC1 | ORGANOPHOSPHORUS HYDROLASE FROM DEINOCOCCUS RADIODURANS | 3.1.8.1 |
2ZC5 | PENICILLIN-BINDING PROTEIN 1A (PBP 1A) ACYL-ENZYME COMPLEX (BIAPENEM) FROM STREPTOCOCCUS PNEUMONIAE | 2.4.1.129 3.4.16.4 |
2ZC6 | PENICILLIN-BINDING PROTEIN 1A (PBP 1A) ACYL-ENZYME COMPLEX (TEBIPENEM) FROM STREPTOCOCCUS PNEUMONIAE | 2.4.1.129 3.4.16.4 |
2ZC7 | CRYSTAL STRUCTURE OF CLASS C BETA-LACTAMASE ACT-1 | 3.5.2.6 |
2ZC9 | THROMBIN IN COMPLEX WITH INHIBITOR | 3.4.21.5 |
2ZD1 | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH TMC278 (RILPIVIRINE), A NON-NUCLEOSIDE RT INHIBITOR | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23.16 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2ZD8 | SHV-1 CLASS A BETA-LACTAMASE COMPLEXED WITH MEROPENEM | 3.5.2.6 |
2ZDA | EXPLORING THROMBIN S1 POCKET | 3.4.21.5 |
2ZDK | EXPLORING TRYPSIN S3 POCKET | 3.4.21.4 |
2ZDL | EXPLORING TRYPSIN S3 POCKET | 3.4.21.4 |
2ZDM | EXPLORING TRYPSIN S3 POCKET | 3.4.21.4 |
2ZDN | EXPLORING TRYPSIN S3 POCKET | 3.4.21.4 |
2ZDV | EXPLORING THROMBIN S1 POCKET | 3.4.21.5 |
2ZDZ | X-RAY STRUCTURE OF BACE-1 IN COMPLEX WITH COMPOUND 3.B.10 | 3.4.23.46 |
2ZE0 | ALPHA-GLUCOSIDASE GSJ | 3.2.1.20 3.2.1.1 |
2ZE1 | X-RAY STRUCTURE OF BACE-1 IN COMPLEX WITH COMPOUND 6G | 3.4.23.46 |
2ZE2 | CRYSTAL STRUCTURE OF L100I/K103N MUTANT HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH TMC278 (RILPIVIRINE), A NON-NUCLEOSIDE RT INHIBITOR | 2.7.7.49 2.7.7.7 3.1.26.4 3.4.23.16 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2ZE4 | CRYSTAL STRUCTURE OF PHOSPHOLIPASE D FROM STREPTOMYCES ANTIBIOTICUS | 3.1.4.4 |
2ZE9 | CRYSTAL STRUCTURE OF H168A MUTANT OF PHOSPHOLIPASE D FROM STREPTOMYCES ANTIBIOTICUS, AS A COMPLEX WITH PHOSPHATIDYLCHOLINE | 3.1.4.4 |
2ZEC | POTENT, NONPEPTIDE INHIBITORS OF HUMAN MAST CELL TRYPTASE | 3.4.21 3.4.21.59 |
2ZEJ | STRUCTURE OF THE ROC DOMAIN FROM THE PARKINSON'S DISEASE-ASSOCIATED LEUCINE-RICH REPEAT KINASE 2 REVEALS A DIMERIC GTPASE | 2.7.11.1 3.6.5 |
2ZET | CRYSTAL STRUCTURE OF THE SMALL GTPASE RAB27B COMPLEXED WITH THE SLP HOMOLOGY DOMAIN OF SLAC2-A/MELANOPHILIN | 3.6.5.2 |
2ZF0 | EXPLORING THROMBIN S1 POCKET | 3.4.21.5 |
2ZFF | EXPLORING THROMBIN S1-POCKET | 3.4.21.5 |
2ZFP | THROMBIN INIBITION | 3.4.21.5 |
2ZFQ | EXPLORING THROMBIN S3 POCKET | 3.4.21.5 |
2ZFR | EXPLORING THROMBIN S3 POCKET | 3.4.21.5 |
2ZFS | EXPLORING TRYPSIN S3 POCKET | 3.4.21.4 |
2ZFT | EXPLORING TRYPSIN S3 POCKET | 3.4.21.4 |
2ZFY | CRYSTAL STRUCTURE OF HUMAN OTUBAIN 1 | 3.1.2 3.4.19.12 |
2ZG0 | EXPLORING THROMBIN S3 POCKET | 3.4.21.5 |
2ZGA | HIV-1 PROTEASE IN COMPLEX WITH A DIMETHYLALLYL DECORATED PYRROLIDINE BASED INHIBITOR (HEXAGONAL SPACE GROUP) | 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1 |
2ZGB | THROMBIN INHIBITION | 3.4.21.5 |
2ZGC | CRYSTAL STRUCTURE OF ACTIVE HUMAN GRANZYME M | 3.4.21 |
2ZGH | CRYSTAL STRUCTURE OF ACTIVE GRANZYME M BOUND TO ITS PRODUCT | 3.4.21 |
2ZGJ | CRYSTAL STRUCTURE OF D86N-GZMM COMPLEXED WITH ITS OPTIMAL SYNTHESIZED SUBSTRATE | 3.4.21 |
2ZGK | CRYSTAL STRUCTURE OF WILDTYPE AAL | 3.1.21 |
2ZGL | CRYSTAL STRUCTURE OF RECOMBINANT AGROCYBE AEGERITA (RAAL) | 3.1.21 |
2ZGM | CRYSTAL STRUCTURE OF RECOMBINANT AGROCYBE AEGERITA LECTIN,RAAL, COMPLEX WITH LACTOSE | 3.1.21 |
2ZGN | CRYSTAL STRUCTURE OF RECOMBINANT AGROCYBE AEGERITA LECTIN, RAAL, COMPLEX WITH GALACTOSE | 3.1.21 |
2ZGO | CRYSTAL STRUCTURE OF AAL MUTANT H59Q COMPLEX WITH LACTOSE | 3.1.21 |
2ZGP | CRYSTAL STRUCTURE OF AGROCYBE AEGERITA LECTIN AAL MUTANT I25G | 3.1.21 |
2ZGQ | CRYSTAL STRUCTURE OF AAL MUTANT L33A IN P1 SPACEGROUP | 3.1.21 |
2ZGR | CRYSTAL STRUCTURE OF AAL MUTANT L33A IN C2 SPACEGROUP | 3.1.21 |
2ZGS | CRYSTAL STRUCTURE OF AGROCYBE AEGERITA LECTIN AAL MUTANT L47A | 3.1.21 |
2ZGT | CRYSTAL STRUCTURE OF AGROCYBE AEGERITA LECTIN AAL MUTANT F93G | 3.1.21 |
2ZGU | CRYSTAL STRUCTURE AGROCYBE AEGERITA LECTIN AAL MUTANT I144G | 3.1.21 |
2ZGX | THROMBIN INHIBITION | 3.4.21.5 |
2ZHD | EXPLORING TRYPSIN S3 POCKET | 3.4.21.4 |
2ZHE | EXPLORING THROMBIN S3 POCKET | 3.4.21.5 |
2ZHF | EXPLORING THROMBIN S3 POCKET | 3.4.21.5 |
2ZHQ | THROMBIN INHIBITION | 3.4.21.5 |
2ZHR | CRYSTAL STRUCTURE OF BACE1 IN COMPLEX WITH OM99-2 AT PH 5.0 | 3.4.23.46 |
2ZHS | CRYSTAL STRUCTURE OF BACE1 AT PH 4.0 | 3.4.23.46 |
2ZHT | CRYSTAL STRUCTURE OF BACE1 AT PH 4.5 | 3.4.23.46 |
2ZHU | CRYSTAL STRUCTURE OF BACE1 AT PH 5.0 | 3.4.23.46 |
2ZHV | CRYSTAL STRUCTURE OF BACE1 AT PH 7.0 | 3.4.23.46 |