Hits from PDB	Structure Title	EC number
2ZHW	EXPLORING THROMBIN S3 POCKET	3.4.21.5
2ZHX	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH A PROTEINACEOUS INHIBITOR	3.2.2.3 3.2.2.27
2ZI2	THROMBIN INHIBITION	3.4.21.5
2ZIC	CRYSTAL STRUCTURE OF STREPTOCOCCUS MUTANS DEXTRAN GLUCOSIDASE	3.2.1.70
2ZID	CRYSTAL STRUCTURE OF DEXTRAN GLUCOSIDASE E236Q COMPLEX WITH ISOMALTOTRIOSE	3.2.1.70
2ZIJ	CRYSTAL STRUCTURE OF HUMAN LYSOZYME EXPRESSED IN E. COLI.	3.2.1.17
2ZIK	CRYSTAL STRUCTURE OF HUMAN LYSOZYME FROM PICHIA PASTORIS	3.2.1.17
2ZIL	CRYSTAL STRUCTURE OF HUMAN LYSOZYME FROM URINE	3.2.1.17
2ZIQ	THROMBIN INHIBITION	3.4.21.5
2ZIU	CRYSTAL STRUCTURE OF THE MUS81-EME1 COMPLEX	3.1.22
2ZIV	CRYSTAL STRUCTURE OF THE MUS81-EME1 COMPLEX	3.1.22
2ZIW	CRYSTAL STRUCTURE OF THE MUS81-EME1 COMPLEX	3.1.22
2ZIX	CRYSTAL STRUCTURE OF THE MUS81-EME1 COMPLEX	3.1.22
2ZIZ	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE IN TERNARY COMPLEX WITH NAD AND 3-DEAZAADENOSINE	3.3.1.1
2ZJ0	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE IN TERNARY COMPLEX WITH NAD AND 2-FLUOROADENOSINE	3.3.1.1
2ZJ1	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE IN TERNARY COMPLEX WITH NAD AND 3'-KETO-ARISTEROMYCIN	3.3.1.1
2ZJ2	ARCHAEAL DNA HELICASE HJM APO STATE IN FORM 1	3.6.1 3.6.4.12
2ZJ5	ARCHAEAL DNA HELICASE HJM COMPLEXED WITH ADP IN FORM 1	3.6.1 3.6.4.12
2ZJ6	CRYSTAL STRUCTURE OF D337A MUTANT OF PSEUDOMONAS SP. MIS38 LIPASE	3.1.1.3
2ZJ7	CRYSTAL STRUCTURE OF D157A MUTANT OF PSEUDOMONAS SP. MIS38 LIPASE	3.1.1.3
2ZJ8	ARCHAEAL DNA HELICASE HJM APO STATE IN FORM 2	3.6.1 3.6.4.12
2ZJ9	X-RAY CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE (AMPC(D)) FROM AN ESCHERICHIA COLI WITH A TRIPEPTIDE DELETION (GLY286 SER287 ASP288) ON THE H10 HELIX	3.5.2.6
2ZJA	ARCHAEAL DNA HELICASE HJM COMPLEXED WITH AMPPCP IN FORM 2	3.6.1 3.6.4.12
2ZJF	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS EPOXIDE HYDROLASE B COMPLEXED WITH AN INHIBITOR	3.3.2.10
2ZJH	CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH N-(1-BENZYL-PIPERIDIN-4-YL)-4-MERCAPTO-BUTYRAMIDE	3.4.23.46
2ZJI	CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH N-[1-(2,6-DIMETHOXY-BENZYL)-PIPERIDIN-4-YL]-4-MERCAPTO-BUTYRAMIDE	3.4.23.46
2ZJJ	CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH 4-(4-FLUORO-BENZYL)-PIPERAZINE-2-CARBOXYLIC ACID (2-MERCAPTO-ETHYL)-AMIDE	3.4.23.46
2ZJK	CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH 4-(4-FLUORO-BENZYL)-PIPERAZINE-2-CARBOXYLIC ACID(3-MERCAPTO-PROPYL)-AMIDE	3.4.23.46
2ZJL	CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH N-[1-(5-BROMO-2,3-DIMETHOXY-BENZYL)-PIPERIDIN-4-YL]-4-MERCAPTO-BUTYRAMIDE	3.4.23.46
2ZJM	CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH N-[1-(5-CHLORO-2-ISOPROPOXY-3-METHOXY-BENZYL)-PIPERIDIN-4-YL]-2-(4-SULFAMOYL-PHENOXY)-ACETAMIDE	3.4.23.46
2ZJN	CRYSTAL STRUCTURE OF THE HUMAN BACE1 CATALYTIC DOMAIN IN COMPLEX WITH N-[1-(5-CHLORO-2-ISOPROPOXY-3-METHOXY-BENZYL)-PIPERIDIN-4-YL]-2-(2-METHYL-4-SULFAMOYL-PHENOXY)-ACETAMIDE	3.4.23.46
2ZJO	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS NS3 HELICASE WITH A NOVEL INHIBITOR	3.4.21.98 3.4.22 3.6.1.15 3.6.4.13 2.7.7.48
2ZJY	STRUCTURE OF THE K349P MUTANT OF GI ALPHA 1 SUBUNIT BOUND TO ALF4 AND GDP	3.6.5.1
2ZJZ	STRUCTURE OF THE K349P MUTANT OF GI ALPHA 1 SUBUNIT BOUND TO GDP	3.6.5.1
2ZK9	CRYSTAL STRUCTURE OF PROTEIN-GLUTAMINASE	3.5.1
2ZKM	CRYSTAL STRUCTURE OF PHOSPHOLIPASE C BETA 2	3.1.4.11
2ZKS	STRUCTURAL INSIGHTS INTO THE PROTEOLYTIC MACHINERY OF APOPTOSIS-INDUCING GRANZYME M	3.4.21
2ZKU	STRUCTURE OF HEPATITIS C VIRUS NS5B POLYMERASE IN A NEW CRYSTAL FORM	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
2ZL0	CRYSTAL STRUCTURE OF H.PYLORI CLPP	3.4.21.92
2ZL2	CRYSTAL STRUCTURE OF H.PYLORI CLPP IN COMPLEX WITH THE PEPTIDE NVLGFTQ	3.4.21.92
2ZL3	CRYSTAL STRUCTURE OF H.PYLORI CLPP S99A	3.4.21.92
2ZLY	STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE, D370Y MUTANT	3.5.1.46
2ZM0	STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE, G181D/H266N/D370Y MUTANT	3.5.1.46
2ZM2	STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE, A61V/A124V/R187S/F264C/G291R/G338A/D370Y MUTANT (HYB-S4M94)	3.5.1.46
2ZM7	STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE, S112A/G181D MUTANT COMPLEXED WITH 6-AMINOHEXANOATE-DIMER	3.5.1.46
2ZM8	STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE, S112A/D370Y MUTANT COMPLEXED WITH 6-AMINOHEXANOATE-DIMER	3.5.1.46
2ZM9	STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE, A61V/S112A/A124V/R187S/F264C/G291R/G338A/D370Y MUTANT (HYB-S4M94) WITH SUBSTRATE	3.5.1.46
2ZMA	CRYSTAL STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE S112A/G181D/H266N/D370Y MUTANT WITH SUBSTRATE	3.5.1.46
2ZMB	CRYSTAL STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH PARECOXIB AT 2.9 A RESOLUTION	3.4.21
2ZMF	CRYSTAL STRUCTURE OF THE C-TERMINAL GAF DOMAIN OF HUMAN PHOSPHODIESTERASE 10A	3.1.4.17 3.1.4.35
2ZMM	CRYSTAL STRUCTURE OF PTP1B-INHIBITOR COMPLEX	3.1.3.48
2ZN7	CRYSTAL STRUCTURES OF PTP1B-INHIBITOR COMPLEXES	3.1.3.48
2ZNB	METALLO-BETA-LACTAMASE (CADMIUM-BOUND FORM)	3.5.2.6
2ZNK	THROMBIN INHIBITION	3.4.21.5
2ZNL	CRYSTAL STRUCTURE OF PA-PB1 COMPLEX FORM INFLUENZA VIRUS RNA POLYMERASE	3.1
2ZNR	CRYSTAL STRUCTURE OF THE DUB DOMAIN OF HUMAN AMSH-LP	3.1.2.15 3.4.19
2ZNV	CRYSTAL STRUCTURE OF HUMAN AMSH-LP DUB DOMAIN IN COMPLEX WITH LYS63-LINKED UBIQUITIN DIMER	3.1.2.15 3.4.19
2ZO3	BISPHENYLIC THROMBIN INHIBITORS	3.4.21.5
2ZO4	CRYSTAL STRUCTURE OF METALLO-BETA-LACTAMASE FAMILY PROTEIN TTHA1429 FROM THERMUS THERMOPHILUS HB8	3
2ZO9	MALONATE-BOUND STRUCTURE OF THE GLYCEROPHOSPHODIESTERASE FROM ENTEROBACTER AEROGENES (GPDQ) AND CHARACTERIZATION OF THE NATIVE FE2+ METAL ION PREFERENCE	3.1.4.46 3.1.4.53
2ZOA	MALONATE-BOUND STRUCTURE OF THE GLYCEROPHOSPHODIESTERASE FROM ENTEROBACTER AEROGENES (GPDQ) COLLECTED AT 1.280 ANGSTROM	3.1.4.46 3.1.4.53
2ZOF	CRYSTAL STRUCTURE OF MOUSE CARNOSINASE CN2 COMPLEXED WITH MN AND BESTATIN	3.4.13.18
2ZOG	CRYSTAL STRUCTURE OF MOUSE CARNOSINASE CN2 COMPLEXED WITH ZN AND BESTATIN	3.4.13.18
2ZOS	CRYSTAL STRUCTURE OF MANNOSYL-3-PHOSPHOGLYCERATE PHOSPHATASE FROM PYROCOCCUS HORIKOSHII	3.1.3.70
2ZOX	CRYSTAL STRUCTURE OF THE COVALENT INTERMEDIATE OF HUMAN CYTOSOLIC BETA-GLUCOSIDASE	3.2.1.21
2ZP0	HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH BENZYLSULFONAMIDE-D-ILE-GLN-P-AMINOBENZAMIDINE	3.4.21.21
2ZP2	C-TERMINAL DOMAIN OF KIPI FROM BACILLUS SUBTILIS	3.5.2.9
2ZP3	CARBOXYLIC ESTER HYDROLASE, SINGLE MUTANT D49N OF BOVINE PANCREATIC PLA2 ENZYME	3.1.1.4
2ZP4	CARBOXYLIC ESTER HYDROLASE, SINGLE MUTANT H48N OF BOVINE PANCREATIC PLA2 ENZYME	3.1.1.4
2ZP5	CARBOXYLIC ESTER HYDROLASE, SINGLE MUTANT D49K OF BOVINE PANCREATIC PLA2 ENZYME	3.1.1.4
2ZPL	CRYSTAL STRUCTURE ANALYSIS OF PDZ DOMAIN A	3.4.24
2ZPM	CRYSTAL STRUCTURE ANALYSIS OF PDZ DOMAIN B	3.4.24
2ZPO	CRYSTAL STRUCTURE OF GREEN TURTLE EGG WHITE RIBONUCLEASE	3.1.27.5 4.6.1.18
2ZQ0	CRYSTAL STRUCTURE OF SUSB COMPLEXED WITH ACARBOSE	3.2.1.20 3.2.1.3
2ZQ1	EXPLORING TRYPSIN S3 POCKET	3.4.21.4
2ZQ2	EXPLORING TRYPSIN S3 POCKET	3.4.21.4
2ZQ3	THE CRYSTAL STRUCTURE OF THE ORTHORHOMBIC FORM OF HEN EGG WHITE LYSOZYME AT 1.6 ANGSTROMS RESOLUTION	3.2.1.17
2ZQ4	THE CRYSTAL STRUCTURE OF THE ORTHORHOMBIC FORM OF HEN EGG WHITE LYSOZYME AT 2.0 ANGSTROMS RESOLUTION	3.2.1.17
2ZQ7	APO STRUCTURE OF CLASS A BETA-LACTAMASE TOHO-1 E166A/R274N/R276N TRIPLE MUTANT	3.5.2.6
2ZQ8	APO STRUCTURE OF CLASS A BETA-LACTAMASE TOHO-1 R274N/R276N DOUBLE MUTANT	3.5.2.6
2ZQ9	CEPHALOTHIN ACYL-INTERMEDIATE STRUCTURE OF CLASS A BETA-LACTAMASE TOHO-1 E166A/R274N/R276N TRIPLE MUTANT	3.5.2.6
2ZQA	CEFOTAXIME ACYL-INTERMEDIATE STRUCTURE OF CLASS A BETA-LACTA TOHO-1 E166A/R274N/R276N TRIPLE MUTANT	3.5.2.6
2ZQB	CRYSTAL STRUCTURE OF A PSYCHROTROPHIC RNASEHI VARIANT WITH SEXTUPLE THERMOSTABILIZING MUTATIONS	3.1.26.4
2ZQC	AZTREONAM ACYL-INTERMEDIATE STRUCTURE OF CLASS A BETA-LACTAM TOHO-1 E166A/R274N/R276N TRIPLE MUTANT	3.5.2.6
2ZQD	CEFTAZIDIME ACYL-INTERMEDIATE STRUCTURE OF CLASS A BETA-LACT TOHO-1 E166A/R274N/R276N TRIPLE MUTANT	3.5.2.6
2ZQE	CRYSTAL STRUCTURE OF THE SMR DOMAIN OF THERMUS THERMOPHILUS MUTS2	3.1
2ZR0	MSRECA-Q196E MUTANT	3.4.99.37
2ZR1	AGGLUTININ FROM ABRUS PRECATORIUS	3.2.2.22
2ZR7	MSRECA NATIVE FORM II'	3.4.99.37
2ZR9	MSRECA Q196E DATP FORM IV	3.4.99.37
2ZRA	MSRECA Q196E ATPGS	3.4.99.37
2ZRB	MSRECA Q196E FORM II'	3.4.99.37
2ZRC	MSRECA Q196N FORM IV	3.4.99.37
2ZRD	MSRECA Q196N ADP FORM IV	3.4.99.37
2ZRE	MSRECA Q196N ATPGS FORM IV	3.4.99.37
2ZRF	MSRECA Q196N DATP FORM IV	3.4.99.37
2ZRG	MSRECA Q196N DATP FORM II'	3.4.99.37
2ZRH	MSRECA Q196A FORM IV	3.4.99.37
2ZRI	MSRECA Q196A ADP FORM IV	3.4.99.37
2ZRJ	MSRECA Q196A ATPGS FORM IV	3.4.99.37
2ZRK	MSRECA Q196A DATP FORM IV	3.4.99.37
2ZRL	MSRECA Q196A DATP FORM II'	3.4.99.37
2ZRM	MSRECA DATP FORM IV	3.4.99.37
2ZRN	MSRECA FORM IV	3.4.99.37
2ZRO	MSRECA ADP FORM IV	3.4.99.37
2ZRP	MSRECA DATP FORM II'	3.4.99.37
2ZRQ	CRYSTAL STRUCTURE OF S324A-SUBTILISIN	3.4.21.62 3.4.21
2ZSG	CRYSTAL STRUCTURE OF X-PRO AMINOPEPTIDASE FROM THERMOTOGA MARITIMA MSB8	3.4.11.9
2ZSH	STRUCTURAL BASIS OF GIBBERELLIN(GA3)-INDUCED DELLA RECOGNITION BY THE GIBBERELLIN RECEPTOR	3
2ZSI	STRUCTURAL BASIS OF GIBBERELLIN(GA4)-INDUCED DELLA RECOGNITION BY THE GIBBERELLIN RECEPTOR	3
2ZTC	MTRUVA FORM II	3.6.1 3.6.4.12
2ZTD	MTRUVA FORM III	3.6.1 3.6.4.12
2ZTE	MTRUVA FORM IV	3.6.1 3.6.4.12
2ZTI	STRUCTURES OF DIMERIC NONSTANDARD NUCLEOTIDE TRIPHOSPHATE PYROPHOSPHATASE FROM PYROCOCCUS HORIKOSHII OT3: FUNCTIONAL SIGNIFICANCE OF INTERPROTOMER CONFORMATIONAL CHANGES	3.6.1.19 3.6.1.66
2ZTX	COMPLEX STRUCTURE OF CVB3 3C PROTEASE WITH EPDTC	3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48
2ZTY	CRYSTAL STRUCTURE OF 3C PROTEASE FROM CVB3 IN SPACE GROUP C2	3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48
2ZTZ	CRYSTAL STRUCTURE OF 3C PROTEASE FROM CVB3 IN SPACE GROUP P21	3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48
2ZU1	CRYSTAL STRUCTURE OF CVB3 3C PROTEASE MUTANT C147A	3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48
2ZU2	COMPLEX STRUCTURE OF COV 229E 3CL PROTEASE WITH EPDTC	3.4.22 3.4.19.12
2ZU3	COMPLEX STRUCTURE OF CVB3 3C PROTEASE WITH TG-0204998	3.4.22 3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
2ZU4	COMPLEX STRUCTURE OF SARS-COV 3CL PROTEASE WITH TG-0204998	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
2ZU5	COMPLEX STRUCTURE OF SARS-COV 3CL PROTEASE WITH TG-0205486	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
2ZU6	CRYSTAL STRUCTURE OF THE EIF4A-PDCD4 COMPLEX	3.6.1 3.6.4.13
2ZUM	FUNCTIONAL ANALYSIS OF HYPERTHERMOPHILIC ENDOCELLULASE FROM THE ARCHAEON PYROCOCCUS HORIKOSHII	3.2.1.4
2ZUN	FUNCTIONAL ANALYSIS OF HYPERTHERMOPHILIC ENDOCELLULASE FROM THE ARCHAEON PYROCOCCUS HORIKOSHII	3.2.1.4
2ZV3	CRYSTAL STRUCTURE OF PROJECT MJ0051 FROM METHANOCALDOCOCCUS JANNASCHII DSM 2661	3.1.1.29
2ZVD	CRYSTAL STRUCTURE OF PSEUDOMONAS SP. MIS38 LIPASE IN AN OPEN CONFORMATION	3.1.1.3
2ZWB	NEUTRON CRYSTAL STRUCTURE OF WILD TYPE HUMAN LYSOZYME IN D2O	3.2.1.17
2ZWL	HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH HIGHLY SELECTIVE PEPTIDE INHIBITOR	3.4.21.21
2ZWO	CRYSTAL STRUCTURE OF CA2 SITE MUTANT OF PRO-S324A	3.4.21.62 3.4.21
2ZWP	CRYSTAL STRUCTURE OF CA3 SITE MUTANT OF PRO-S324A	3.4.21.62 3.4.21
2ZWS	CRYSTAL STRUCTURE ANALYSIS OF NEUTRAL CERAMIDASE FROM PSEUDOMONAS AERUGINOSA	3.5.1.23
2ZWY	ALPHA-L-FUCOSIDASE	3.2.1.51
2ZWZ	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, CORE1	3.2.1.51
2ZX5	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, F10	3.2.1.51
2ZX6	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, F10-1C	3.2.1.51
2ZX7	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, F10-2C	3.2.1.51
2ZX8	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, F10-2C-O	3.2.1.51
2ZX9	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, B4	3.2.1.51
2ZXA	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, FNJ-ACETYL	3.2.1.51
2ZXB	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, PH-6FNJ	3.2.1.51
2ZXC	CERAMIDASE COMPLEXED WITH C2	3.5.1.23
2ZXD	ALPHA-L-FUCOSIDASE COMPLEXED WITH INHIBITOR, ISO-6FNJ	3.2.1.51
2ZXG	AMINOPEPTIDASE N COMPLEXED WITH THE AMINOPHOSPHINIC INHIBITOR OF PL250, A TRANSITION STATE ANALOGUE	3.4.11.2
2ZXO	CRYSTAL STRUCTURE OF RECJ FROM THERMUS THERMOPHILUS HB8	3.1.11 3.1
2ZXP	CRYSTAL STRUCTURE OF RECJ IN COMPLEX WITH MN2+ FROM THERMUS THERMOPHILUS HB8	3.1.11 3.1
2ZXQ	CRYSTAL STRUCTURE OF ENDO-ALPHA-N-ACETYLGALACTOSAMINIDASE FROM BIFIDOBACTERIUM LONGUM (ENGBF)	3.2.1.97
2ZXR	CRYSTAL STRUCTURE OF RECJ IN COMPLEX WITH MG2+ FROM THERMUS THERMOPHILUS HB8	3.1.11 3.1
2ZYC	CRYSTAL STRUCTURE OF PEPTIDOGLYCAN HYDROLASE FROM SPHINGOMONAS SP. A1	3.2.1
2ZYE	STRUCTURE OF HIV-1 PROTEASE IN COMPLEX WITH POTENT INHIBITOR KNI-272 DETERMINED BY NEUTRON CRYSTALLOGRAPHY	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
2ZYH	MUTANT A. FULGIDUS LIPASE S136A COMPLEXED WITH FATTY ACID FRAGMENT	3.1.1.3
2ZYI	A. FULGIDUS LIPASE WITH FATTY ACID FRAGMENT AND CALCIUM	3.1.1.3
2ZYP	X-RAY STRUCTURE OF HEN EGG-WHITE LYSOZYME WITH POLY(ALLYL AMINE)	3.2.1.17
2ZYR	A. FULGIDUS LIPASE WITH FATTY ACID FRAGMENT AND MAGNESIUM	3.1.1.3
2ZYS	A. FULGIDUS LIPASE WITH FATTY ACID FRAGMENT AND CHLORIDE	3.1.1.3
2ZZD	RECOMBINANT THIOCYANATE HYDROLASE, AIR-OXIDIZED FORM OF HOLO-ENZYME	3.5.5.8
2ZZP	THE CRYSTAL STRUCTURE OF HUMAN ATG4B(C74S)- LC3(1-124) COMPLEX	3.4.22
2ZZU	HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH ETHYLSULFONAMIDE-D-5-(3-CARBOXYBENZYLOXY)-TRP-GLN-P-AMINOBENZAMIDINE	3.4.21.21
3A0F	THE CRYSTAL STRUCTURE OF GEOTRICHUM SP. M128 XYLOGLUCANASE	3.2.1.151
3A1C	CRYSTAL STRUCTURE OF THE P- AND N-DOMAINS OF COPA, A COPPER-TRANSPORTING P-TYPE ATPASE, BOUND WITH AMPPCP-MG	3.6.3 7.2.2.8
3A1D	CRYSTAL STRUCTURE OF THE P- AND N-DOMAINS OF COPA, A COPPER-TRANSPORTING P-TYPE ATPASE, BOUND WITH ADP-MG	3.6.3 7.2.2.8
3A1E	CRYSTAL STRUCTURE OF THE P- AND N-DOMAINS OF HIS462GLN MUTANT COPA, A COPPER-TRANSPORTING P-TYPE ATPASE, BOUND WITH AMPPCP-MG	3.6.3 7.2.2.8
3A1I	CRYSTAL STRUCTURE OF RHODOCOCCUS SP. N-771 AMIDASE COMPLEXED WITH BENZAMIDE	3.5.1.4
3A1J	CRYSTAL STRUCTURE OF THE HUMAN RAD9-HUS1-RAD1 COMPLEX	3.1.11.2
3A1K	CRYSTAL STRUCTURE OF RHODOCOCCUS SP. N771 AMIDASE	3.5.1.4
3A1M	A FUSION PROTEIN OF A BETA HELIX REGION OF GENE PRODUCT 5 AND THE FOLDON REGION OF BACTERIOPHAGE T4	3.2.1.17
3A1R	NEUTRON CRYSTAL STRUCTURE ANALYSIS OF BOVINE PANCREATIC RIBONUCLEASE A	3.1.27.5 4.6.1.18
3A21	CRYSTAL STRUCTURE OF STREPTOMYCES AVERMITILIS BETA-L-ARABINOPYRANOSIDASE	3.2.1.22
3A22	CRYSTAL STRUCTURE OF BETA-L-ARABINOPYRANOSIDASE COMPLEXED WITH L-ARABINOSE	3.2.1.22
3A23	CRYSTAL STRUCTURE OF BETA-L-ARABINOPYRANOSIDASE COMPLEXED WITH D-GALACTOSE	3.2.1.22
3A24	CRYSTAL STRUCTURE OF BT1871 RETAINING GLYCOSIDASE	3.2.1.22
3A29	CRYSTAL STRUCTURE OF HUMAN LIVER FBPASE IN COMPLEX WITH TRICYCLIC INHIBITOR	3.1.3.11
3A2L	CRYSTAL STRUCTURE OF DBJA (MUTANT DBJA DELTA)	3.8.1.5
3A2M	CRYSTAL STRUCTURE OF DBJA (WILD TYPE TYPE I)	3.8.1.5
3A2N	CRYSTAL STRUCTURE OF DBJA (WILD TYPE TYPE II P21)	3.8.1.5
3A2O	CRYSTAL STRUCTURE OF HIV-1 PROTEASE COMPLEXED WITH KNI-1689	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
3A2P	STRUCTURE OF 6-AMINOHEXANOATE CYCLIC DIMER HYDROLASE	3.5.2.12
3A2Q	STRUCTURE OF 6-AMINOHEXANOATE CYCLIC DIMER HYDROLASE COMPLEXED WITH SUBSTRATE	3.5.2.12
3A2Y	E. COLI GSP AMIDASE C59A COMPLEXED WITH GSP	6.3.1.8 3.5.1.78
3A2Z	E. COLI GSP AMIDASE CYS59 SULFENIC ACID	6.3.1.8 3.5.1.78
3A30	E. COLI GSP AMIDASE C59 ACETATE MODIFICATION	6.3.1.8 3.5.1.78
3A34	EFFECT OF ARIGININE ON LYSOZYME	3.2.1.17
3A36	STRUCTURAL INSIGHT INTO THE MEMBRANE INSERTION OF TAIL-ANCHORED PROTEINS BY GET3	3.6.3.16 3.6
3A37	STRUCTURAL INSIGHT INTO THE MEMBRANE INSERTION OF TAIL-ANCHORED PROTEINS BY GET3	3.6.3.16 3.6
3A3D	CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM HAEMOPHILUS INFLUENZAE	3.4.16.4 3.4.21
3A3E	CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM HAEMOPHILUS INFLUENZAE, COMPLEXED WITH NOVEL BETA-LACTAM (CMV)	3.4.16.4
3A3F	CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM HAEMOPHILUS INFLUENZAE,COMPLEXED WITH NOVEL BETA-LACTAM (FMZ)	3.4.16.4
3A3H	CELLOTRIOSE COMPLEX OF THE ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHERANS AT 1.6 A RESOLUTION	3.2.1.4
3A3I	CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 (DACB) FROM HAEMOPHILUS INFLUENZAE, COMPLEXED WITH AMPICILLIN (AIX)	3.4.16.4
3A3J	CRYSTAL STRUCTURES OF PENICILLIN BINDING PROTEIN 5 FROM HAEMOPHILUS INFLUENZAE	3.4.16.4
3A3N	CRYSTAL STRUCTURE OF COMPLEX BETWEEN SA-SUBTILISIN AND TK-PROPEPTIDE WITH DELETION OF THE TWO C-TERMINAL RESIDUES	3.4.21
3A3O	CRYSTAL STRUCTURE OF COMPLEX BETWEEN SA-SUBTILISIN AND TK-PROPEPTIDE WITH DELETION OF THE FIVE C-TERMINAL RESIDUES	3.4.21
3A3P	CRYSTAL STRUCTURE OF COMPLEX BETWEEN E201A/SA-SUBTILISIN AND TK-PROPEPTIDE	3.4.21
3A3Q	STRUCTURE OF N59D HEN EGG-WHITE LYSOZYME IN COMPLEX WITH (GLCNAC)3	3.2.1.17
3A3R	STRUCTURE OF N59D HEN EGG-WHITE LYSOZYME	3.2.1.17
3A3V	CRYSTAL STRUCTURE OF REDUCING-END-XYLOSE RELEASING EXO-OLIGOXYLANASE Y198F MUTANT	3.2.1.156
3A3W	STRUCTURE OF OPDA MUTANT (G60A/A80V/S92A/R118Q/K185R/Q206P/D208G/I260T/G273S) WITH DIETHYL 4-METHOXYPHENYL PHOSPHATE BOUND IN THE ACTIVE SITE	3.1.8.1
3A3X	STRUCTURE OF OPDA MUTANT (G60A/A80V/R118Q/K185R/Q206P/D208G/I260T/G273S)	3.1.8.1
3A42	CRYSTAL STRUCTURE OF MVNEI1	3.2.2.23 4.2.99.18
3A45	CRYSTAL STRUCTURE OF MVNEI1_2	3.2.2.23 4.2.99.18
3A46	CRYSTAL STRUCTURE OF MVNEI1/THF COMPLEX	3.2.2.23 4.2.99.18
3A47	CRYSTAL STRUCTURE OF ISOMALTASE FROM SACCHAROMYCES CEREVISIAE	3.2.1.10
3A4A	CRYSTAL STRUCTURE OF ISOMALTASE FROM SACCHAROMYCES CEREVISIAE	3.2.1.10
3A4J	ARPTE (K185R/D208G/N265D/T274N)	3.1.8.1
3A4K	CRYSTAL STRUCTURAL ANALYSIS OF HINDIII RESTRICTION ENDONUCLEASE IN COMPLEX WITH COGNATE DNA AND DIVALENT CATIONS AT 2.17 ANGSTROM RESOLUTION	3.1.21.4
3A4W	CRYSTAL STRUCTURES OF CATALYTIC SITE MUTANTS OF ACTIVE DOMAIN 2 OF THERMOSTABLE CHITINASE FROM PYROCOCCUS FURIOSUS COMPLEXED WITH CHITO-OLIGOSACCHARIDES	3.2.1.14
3A4X	CRYSTAL STRUCTURES OF CATALYTIC SITE MUTANTS OF ACTIVE DOMAIN 2 OF THERMOSTABLE CHITINASE FROM PYROCOCCUS FURIOSUS COMPLEXED WITH CHITO-OLIGOSACCHARIDES	3.2.1.14
3A4Y	CRYSTAL STRUCTURE OF H61A MUTANT TTHA0252 FROM THERMUS THERMOPHILUS HB8	3.1
3A54	CRYSTAL STRUCTURE OF THE A47Q1 MUTANT OF PRO-PROTEIN-GLUTAMINASE	3.5.1
3A55	CRYSTAL STRUCTURE OF THE A47Q2 MUTANT OF PRO- PROTEIN-GLUTAMINASE	3.5.1
3A56	CRYSTAL STRUCTURE OF PRO- PROTEIN-GLUTAMINASE	3.5.1
3A5E	CRYSTAL STRUCTURE OF 5K RNASE SA	3.1.27.3 4.6.1.24
3A5J	CRYSTAL STRUCTURE OF PROTEIN-TYROSINE PHOSPHATASE 1B	3.1.3.48
3A5K	CRYSTAL STRUCTURE OF PROTEIN-TYROSINE PHOSPHATASE 1B	3.1.3.48
3A5V	CRYSTAL STRUCTURE OF ALPHA-GALACTOSIDASE I FROM MORTIERELLA VINACEA	3.2.1.22
3A64	CRYSTAL STRUCTURE OF CCCEL6C, A GLYCOSIDE HYDROLASE FAMILY 6 ENZYME, FROM COPRINOPSIS CINEREA	3.2.1.91 3.2.1
3A65	CRYSTAL STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE S112A/G181D/H266N MUTANT WITH SUBSTRATE	3.5.1.46
3A66	CRYSTAL STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE S112A/G181D/H266N/D370Y MUTANT WITH SUBSTRATE	3.5.1.46
3A6D	CREATININASE COMPLEXED WITH 1-METHYLGUANIDINE	3.5.2.10
3A6E	W174F MUTANT CREATININASE, TYPE I	3.5.2.10
3A6H	W154A MUTANT CREATININASE	3.5.2.10
3A6J	E122Q MUTANT CREATININASE COMPLEXED WITH CREATINE	3.5.2.10
3A6O	CRYSTAL STRUCTURE OF THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE 2/ACARBOSE COMPLEX	3.2.1.135
3A6S	CRYSTAL STRUCTURE OF THE MUTT PROTEIN	3.6.1 3.6.1.55
3A6T	CRYSTAL STRUCTURE OF MUTT-8-OXO-DGMP COMPLEX	3.6.1 3.6.1.55
3A6U	CRYSTAL STRUCTURE OF MUTT-8-OXO-DGMP-MN(II) COMPLEX	3.6.1 3.6.1.55
3A6V	CRYSTAL STRUCTURE OF THE MUTT PROTEIN IN MN(II) BOUND HOLO FORM	3.6.1 3.6.1.55
3A6Z	CRYSTAL STRUCTURE OF PSEUDOMONAS SP. MIS38 LIPASE (PML) IN THE OPEN CONFORMATION FOLLOWING DIALYSIS AGAINST CA-FREE BUFFER	3.1.1.3
3A70	CRYSTAL STRUCTURE OF PSEUDOMONAS SP. MIS38 LIPASE IN COMPLEX WITH DIETHYL PHOSPHATE	3.1.1.3
3A71	HIGH RESOLUTION STRUCTURE OF PENICILLIUM CHRYSOGENUM ALPHA-L-ARABINANASE	3.2.1.55
3A72	HIGH RESOLUTION STRUCTURE OF PENICILLIUM CHRYSOGENUM ALPHA-L-ARABINANASE COMPLEXED WITH ARABINOBIOSE	3.2.1.55
3A75	CRYSTAL STRUCTURE OF GLUTAMATE COMPLEX OF HALOTOLERANT γ-GLUTAMYLTRANSPEPTIDASE FROM BACILLUS SUBTILIS	2.3.2.2 3.4.19.13
3A79	CRYSTAL STRUCTURE OF TLR2-TLR6-PAM2CSK4 COMPLEX	3.2.2.6
3A7B	CRYSTAL STRUCTURE OF TLR2-STREPTOCOCCUS PNEUMONIAE LIPOTEICHOIC ACID COMPLEX	3.2.2.6
3A7C	CRYSTAL STRUCTURE OF TLR2-PE-DTPA COMPLEX	3.2.2.6
3A7N	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE FROM MYCOBACTERIUM TUBERCULOSIS	3.2.2.3 3.2.2.27
3A7Q	STRUCTURAL BASIS FOR SPECIFIC RECOGNITION OF REELIN BY ITS RECEPTORS	3.4.21
3A7S	CATALYTIC DOMAIN OF UCH37	3.4.19.12
3A7T	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH 4-FORMYLBENZIMIDAMIDE	3.4.21.4
3A7V	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH 3-FORMYLBENZIMIDAMIDE	3.4.21.4
3A7W	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((TETRAHYDRO-2H-PYRAN-2-YLOXYIMINO)METHYL)BENZIMIDAMIDE (SOAKING 4HOURS)	3.4.21.4
3A7X	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)ACETIC ACID (SOAKING 45SECONDS)	3.4.21.4
3A7Y	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((1-METHYLPIPERIDIN-3-YLOXYIMINO)METHYL)BENZIMIDAMIDE (SOAKING 2HOURS)	3.4.21.4
3A7Z	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((1-METHYLPIPERIDIN-4-YLOXYIMINO)METHYL)BENZIMIDAMIDE (SOAKING 3HOURS)	3.4.21.4
3A80	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)-2-METHYLPROPANOIC ACID (SOAKING 40SECONDS)	3.4.21.4
3A81	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((2-NICOTINOYLHYDRAZONO)METHYL)BENZIMIDAMIDE (SOAKING 8 HOURS)	3.4.21.4
3A82	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH PRE-SYNTHESIZED (E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)ACETIC ACID	3.4.21.4
3A83	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH PRE-SYNTHESIZED (E)-4-((2-NICOTINOYLHYDRAZONO)METHYL)BENZIMIDAMIDE	3.4.21.4
3A84	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH(E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)ACETIC ACID (SOAKING 5 SECONDS)	3.4.21.4
3A85	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)ACETIC ACID (SOAKING 15 SECONDS)	3.4.21.4
3A86	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)ACETIC ACID (SOAKING 30 SECONDS)	3.4.21.4
3A87	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((2-NICOTINOYLHYDRAZONO)METHYL)BENZIMIDAMIDE (SOAKING 5 MINUTES)	3.4.21.4
3A88	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((2-NICOTINOYLHYDRAZONO)METHYL)BENZIMIDAMIDE (SOAKING 30 MINUTES)	3.4.21.4
3A89	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((2-NICOTINOYLHYDRAZONO)METHYL)BENZIMIDAMIDE (SOAKING 4 HOURS)	3.4.21.4
3A8A	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH 4-FORMYLBENZIMIDAMIDE AND ANILINE	3.4.21.4
3A8B	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-4-((4-BROMOPHENYLIMINO)METHYL)BENZIMIDAMIDE	3.4.21.4
3A8C	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)ACETIC ACID (SOAKING WITH MIXTURE OF [(E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)ACETIC ACID] AND [(E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)-2-METHYLPROPANOIC ACID])	3.4.21.4
3A8D	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (E)-2-(4-CARBAMIMIDOYLBENZYLIDENEAMINOOXY)ACETIC ACID (UNDER ANILINE-FREE CONDITION)	3.4.21.4
3A8Z	CRYSTAL STRUCTURE OF HEN EGG WHITE LYSOZYME	3.2.1.17
3A90	CRYSTAL STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH 1MM RHCL3	3.2.1.17
3A91	CRYSTAL STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH 5MM RHCL3	3.2.1.17
3A92	CRYSTAL STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH 10MM RHCL3	3.2.1.17
3A93	CRYSTAL STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH 30MM RHCL3	3.2.1.17
3A94	CRYSTAL STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH 100MM RHCL3	3.2.1.17
3A95	CRYSTAL STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH 100MM RHCL3 AT PH3.8	3.2.1.17
3A96	CRYSTAL STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH 100MM RHCL3 AT PH2.2	3.2.1.17
3A9B	CCCEL6C, A GLYCOSIDE HYDROLASE FAMILY 6 ENZYME, COMPLEXED WITH CELLOBIOSE	3.2.1.91 3.2.1
3AA2	A52I E. COLI RNASE HI	3.1.26.4
3AA3	A52L E. COLI RNASE HI	3.1.26.4
3AA4	A52V E.COLI RNASE HI	3.1.26.4
3AA5	A52F E.COLI RNASE HI	3.1.26.4
3AAF	STRUCTURE OF WRN RQC DOMAIN BOUND TO DOUBLE-STRANDED DNA	3.6.1 3.6.4.12 3.1
3AAL	CRYSTAL STRUCTURE OF ENDONUCLEASE IV FROM GEOBACILLUS KAUSTOPHILUS	3.1.21.2
3AAM	CRYSTAL STRUCTURE OF ENDONUCLEASE IV FROM THERMUS THERMOPHILUS HB8	3.1.21.2
3AAS	BOVINE BETA-TRYPSIN BOUND TO META-GUANIDINO SCHIFF BASE COPPER (II) CHELATE	3.4.21.4
3AAU	BOVINE BETA-TRYPSIN BOUND TO META-DIGUANIDINO SCHIFF BASE COPPER (II) CHELATE	3.4.21.4
3AAV	BOVINE BETA-TRYPSIN BOUND TO META-DIAMIDINO SCHIFF BASE COPPER (II) CHELATE	3.4.21.4
3AB6	CRYSTAL STRUCTURE OF NAG3 BOUND LYSOZYME FROM MERETRIX LUSORIA	3.2.1.17
3ABX	CCCEL6C, A GLYCOSIDE HYDROLASE FAMILY 6 ENZYME, COMPLEXED WITH P-NITROPHENYL BETA-D-CELLOTRIOSIDE	3.2.1.91 3.2.1
3AC9	CRYSTAL STRUCTURE OF HUMAN NUDT5 COMPLEXED WITH 8-OXO-DGDP AND MANGANESE	3.6.1.13 3.6.1.58 2.7.7.96
3ACA	CRYSTAL STRUCTURE OF HUMAN NUDT5 COMPLEXED WITH 8-OXO-DADP AND MANGANESE	3.6.1.13 3.6.1.58 2.7.7.96
3ACF	CRYSTAL STRUCTURE OF CARBOHYDRATE-BINDING MODULE FAMILY 28 FROM CLOSTRIDIUM JOSUI CEL5A IN A LIGAND-FREE FORM	3.2.1.4
3ACG	CRYSTAL STRUCTURE OF CARBOHYDRATE-BINDING MODULE FAMILY 28 FROM CLOSTRIDIUM JOSUI CEL5A IN COMPLEX WITH CELLOBIOSE	3.2.1.4
3ACH	CRYSTAL STRUCTURE OF CARBOHYDRATE-BINDING MODULE FAMILY 28 FROM CLOSTRIDIUM JOSUI CEL5A IN COMPLEX WITH CELLOTETRAOSE	3.2.1.4
3ACI	CRYSTAL STRUCTURE OF CARBOHYDRATE-BINDING MODULE FAMILY 28 FROM CLOSTRIDIUM JOSUI CEL5A IN COMPLEX WITH CELLOPENTAOSE	3.2.1.4
3AEH	INTEGRAL MEMBRANE DOMAIN OF AUTOTRANSPORTER HBP	3.4.21
3AFB	CRYSTAL STRUCTURES OF CATALYTIC SITE MUTANTS OF ACTIVE DOMAIN 2 OF CHITINASE FROM PYROCOCCUS FURIOSUS	3.2.1.14
3AFG	CRYSTAL STRUCTURE OF PRON-TK-SP FROM THERMOCOCCUS KODAKARAENSIS	3.4.21.62
3AFI	CRYSTAL STRUCTURE OF DBJA (HIS-DBJA)	3.8.1.5
3AFK	CRYSTAL STRUCTURE OF AGROCYBE AEGERITA LECTIN AAL COMPLEXED WITH THOMSEN-FRIEDENREICH ANTIGEN	3.1.21
3AGD	CRYSTAL STRUCTURE OF MGLU IN ITS NATIVE FORM IN THE PRESENCE OF 4.3M NACL	3.5.1.2
3AGE	CRYSTAL STRUCTURE OF MGLU IN ITS L-GLUTAMATE BINDING FORM IN THE PRESENCE OF 4.3M NACL	3.5.1.2
3AGF	CRYSTAL STRUCTURE OF BACILLUS GLUTAMINASE IN THE PRESENCE OF 4.3M NACL	3.5.1.2
3AGG	X-RAY ANALYSIS OF LYSOZYME IN THE ABSENCE OF ARG	3.2.1.17
3AGH	X-RAY ANALYSIS OF LYSOZYME IN THE PRESENCE OF 200 MM ARG	3.2.1.17
3AGI	HIGH RESOLUTION X-RAY ANALYSIS OF ARG-LYSOZYME COMPLEX IN THE PRESENCE OF 500 MM ARG	3.2.1.17
3AGN	CRYSTAL STRUCTURE OF USTILAGO SPHAEROGENA RIBONUCLEASE U2 COMPLEXED WITH ADENOSINE 3'-MONOPHOSPHATE	3.1.27.4 4.6.1.20
3AGO	CRYSTAL STRUCTURE OF USTILAGO SPHAEROGENA RIBONUCLEASE U2 COMPLEXED WITH ADENOSINE 3'-MONOPHOSPHATE	3.1.27.4 4.6.1.20
3AGR	CRYSTAL STRUCTURE OF NUCLEOSIDE TRIPHOSPHATE HYDROLASES FROM NEOSPORA CANINUM	3.6.1.15
3AHS	CRYSTAL STRUCTURE OF USTILAGO SPHAEROGENA RIBONUCLEASE U2B	3.1.27.4 4.6.1.20
3AHT	CRYSTAL STRUCTURE OF RICE BGLU1 E176Q MUTANT IN COMPLEX WITH LAMINARIBIOSE	3.2.1.21
3AHV	SEMI-ACTIVE E176Q MUTANT OF RICE BGLU1 COVALENT COMPLEX WITH 2-DEOXY-2-FLUOROGLUCOSIDE	3.2.1.21
3AHW	CRYSTAL STRUCTURE OF USTILAGO SPHAEROGENA RIBONUCLEASE U2 COMPLEXED WITH ADENOSINE 2'-MONOPHOSPHATE	3.1.27.4 4.6.1.20
3AHZ	CRYSTAL STRUCTURE OF BETA-GLUCOSIDASE FROM TERMITE NEOTERMES KOSHUNENSIS IN COMPLEX WITH TRIS	3.2.1.21
3AI0	CRYSTAL STRUCTURE OF BETA-GLUCOSIDASE FROM TERMITE NEOTERMES KOSHUNENSIS IN COMPLEX WITH PARA-NITROPHENYL-BETA-D-GLUCOPYRANOSIDE	3.2.1.21
3AI8	CATHEPSIN B IN COMPLEX WITH THE NITROXOLINE	3.4.22.1
3AID	A NEW CLASS OF HIV-1 PROTEASE INHIBITOR: THE CRYSTALLOGRAPHIC STRUCTURE, INHIBITION AND CHEMICAL SYNTHESIS OF AN AMINIMIDE PEPTIDE ISOSTERE	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
3AIG	ADAMALYSIN II WITH PEPTIDOMIMETIC INHIBITOR POL656	3.4.24.46
3AIK	CRYSTAL STRUCTURE OF A HSL-LIKE CARBOXYLESTERASE FROM SULFOLOBUS TOKODAII	3.1.1.1
3AIL	CRYSTAL STRUCTURE OF A HSL-LIKE CARBOXYLESTERASE FROM SULFOLOBUS TOKODAII COMPLEXED WITH PARAOXON	3.1.1.1
3AIM	R267E MUTANT OF A HSL-LIKE CARBOXYLESTERASE FROM SULFOLOBUS TOKODAII	3.1.1.1
3AIN	R267G MUTANT OF A HSL-LIKE CARBOXYLESTERASE FROM SULFOLOBUS TOKODAII	3.1.1.1
3AIO	R267K MUTANT OF A HSL-LIKE CARBOXYLESTERASE FROM SULFOLOBUS TOKODAII	3.1.1.1
3AIQ	CRYSTAL STRUCTURE OF BETA-GLUCOSIDASE IN WHEAT COMPLEXED WITH AN AGLYCONE DIMBOA	3.2.1.21 3.2.1.182
3AIR	CRYSTAL STRUCTURE OF BETA-GLUCOSIDASE IN WHEAT COMPLEXED WITH 2-DEOXY-2-FLUOROGLUCOSIDE AND DINITROPHENOL	3.2.1.21 3.2.1.182
3AIS	CRYSTAL STRUCTURE OF A MUTANT BETA-GLUCOSIDASE IN WHEAT COMPLEXED WITH DIMBOA-GLC	3.2.1.21 3.2.1.182
3AIU	CRYSTAL STRUCTURE OF BETA-GLUCOSIDASE IN RYE	3.2.1.21 3.2.1.182
3AIV	CRYSTAL STRUCTURE OF BETA-GLUCOSIDASE IN RYE COMPLEXED WITH AN AGLYCONE DIMBOA	3.2.1.21 3.2.1.182
3AIW	CRYSTAL STRUCTURE OF BETA-GLUCOSIDASE IN RYE COMPLEXED WITH 2-DEOXY-2-FLUOROGLUCOSIDE AND DINITROPHENOL	3.2.1.21 3.2.1.182
3AJ3	CRYSTAL STRUCTURE OF SELENOMETHIONINE SUBSTITUTED 4-PYRIDOXOLACTONASE FROM MESORHIZOBIUM LOTI	3.1.1.27
3AJ7	CRYSTAL STRUCTURE OF ISOMALTASE FROM SACCHAROMYCES CEREVISIAE	3.2.1.10
3AJ8	X-RAY ANALYSIS OF CRYSTAL OF PROTEINASE K OBTAINED FROM H2O SOLUTION USING PEG 8000	3.4.21.64
3AJ9	X-RAY ANALYSIS OF CRYSTAL OF PROTEINASE K OBTAINED FROM D2O SOLUTION USING PEG 8000	3.4.21.64
3AJA	CRYSTAL STRUCTURE OF MSMEG_6394	3.1.1
3AJN	STRUCTURAL BASIS OF GLYCINE AMIDE ON SUPPRESSION OF PROTEIN AGGREGATION BY HIGH RESOLUTION X-RAY ANALYSIS	3.2.1.17
3AKF	CRYSTAL STRUCTURE OF EXO-1,5-ALPHA-L-ARABINOFURANOSIDASE	3.2.1.55
3AKG	CRYSTAL STRUCTURE OF EXO-1,5-ALPHA-L-ARABINOFURANOSIDASE COMPLEXED WITH ALPHA-1,5-L-ARABINOFURANOBIOSE	3.2.1.55
3AKH	CRYSTAL STRUCTURE OF EXO-1,5-ALPHA-L-ARABINOFURANOSIDASE COMPLEXED WITH ALPHA-1,5-L-ARABINOFURANOTRIOSE	3.2.1.55
3AKI	CRYSTAL STRUCTURE OF EXO-1,5-ALPHA-L-ARABINOFURANOSIDASE COMPLEXED WITH ALPHA-L-ARABINOFURANOSYL AZIDO	3.2.1.55
3AKP	CRYSTAL STRUCTURE OF XYLANASE FROM TRICHODERMA LONGIBRACHIATUM	3.2.1.8
3AKQ	CRYSTAL STRUCTURE OF XYLANASE FROM TRICHODERMA LONGIBRACHIATUM	3.2.1.8
3AKR	CRYSTAL STRUCTURE OF XYLANASE FROM TRICHODERMA LONGIBRACHIATUM	3.2.1.8
3AKS	CRYSTAL STRUCTURE OF XYLANASE FROM TRICHODERMA LONGIBRACHIATUM	3.2.1.8
3AKT	CRYSTAL STRUCTURE OF XYLANASE FROM TRICHODERMA LONGIBRACHIATUM	3.2.1.8
3ALF	CRYSTAL STRUCTURE OF CLASS V CHITINASE FROM NICOTIANA TOBACCUM	3.2.1.14
3ALG	CRYSTAL STRUCTURE OF CLASS V CHITINASE (E115Q MUTANT) FROM NICOTIANA TOBACCUM IN COMPLEX WITH NAG4	3.2.1.14
3ALY	CRYSTAL STRUCTURE OF RNASE HI FROM SULFOLOBUS TOKODAII WITH C-TERMINAL DELETION	3.1.26.4
3AMC	CRYSTAL STRUCTURES OF THERMOTOGA MARITIMA CEL5A, APO FORM AND DIMER/AU	3.2.1.4
3AMD	CRYSTAL STRUCTURES OF THERMOTOGA MARITIMA CEL5A, APO FORM AND TETRAMER/AU	3.2.1.4
3AMG	CRYSTAL STRUCTURES OF THERMOTOGA MARITIMA CEL5A IN COMPLEX WITH CELLOBIOSE SUBSTRATE, MUTANT FORM	3.2.1.4
3AMH	CRYSTAL STRUCTURE OF CELLULASE 12A FROM THERMOTOGA MARITIMA	3.2.1.4
3AMI	THE CRYSTAL STRUCTURE OF THE M16B METALLOPEPTIDASE SUBUNIT FROM SPHINGOMONAS SP. A1	3.4.24
3AMJ	THE CRYSTAL STRUCTURE OF THE HETERODIMER OF M16B PEPTIDASE FROM SPHINGOMONAS SP. A1	3.4.24
3AMM	CELLOTETRAOSE COMPLEX OF CELLULASE 12A FROM THERMOTOGA MARITIMA	3.2.1.4
3AMN	E134C-CELLOBIOSE COMPLEX OF CELLULASE 12A FROM THERMOTOGA MARITIMA	3.2.1.4
3AMP	E134C-CELLOTETRAOSE COMPLEX OF CELLULASE 12A FROM THERMOTOGA MARITIMA	3.2.1.4
3AMQ	E134C-CELLOBIOSE CO-CRYSTAL OF CELLULASE 12A FROM THERMOTOGA MARITIMA	3.2.1.4
3AMR	CRYSTAL STRUCTURES OF BACILLUS SUBTILIS ALKALINE PHYTASE IN COMPLEX WITH CA2+, CO2+, NI2+, MG2+ AND MYO-INOSITOL HEXASULFATE	3.1.3.8
3AMS	CRYSTAL STRUCTURES OF BACILLUS SUBTILIS ALKALINE PHYTASE IN COMPLEX WITH CA2+, CD2+, CO2+, NI2+, MG2+ AND MYO-INOSITOL HEXASULFATE	3.1.3.8
3ANI	CRYSTAL STRUCTURE OF UNSATURATED GLUCURONYL HYDROLASE MUTANT D175N FROM STREPTCOCCUS AGALACTIAE	3.2.1 3.2.1.180
3ANJ	CRYSTAL STRUCTURE OF UNSATURATED GLUCURONYL HYDROLASE FROM STREPTCOCCUS AGALACTIAE	3.2.1 3.2.1.180
3ANK	CRYSTAL STRUCTURE OF UNSATURATED GLUCURONYL HYDROLASE MUTANT D175N FROM STREPTCOCCUS AGALACTIAE COMPLEXED WITH DGLCA-GALNAC6S	3.2.1 3.2.1.180
3ANS	HUMAN SOLUBLE EPOXIDE HYDROLASE IN COMPLEX WITH A SYNTHETIC INHIBITOR	3.3.2.10 3.1.3.76
3ANT	HUMAN SOLUBLE EPOXIDE HYDROLASE IN COMPLEX WITH A SYNTHETIC INHIBITOR	3.3.2.10 3.1.3.76
3AO1	FRAGMENT-BASED APPROACH TO THE DESIGN OF LIGANDS TARGETING A NOVEL SITE IN HIV-1 INTEGRASE	2.7.7.49 3.1.13.2 3.1.26.13
3AO2	FRAGMENT-BASED APPROACH TO THE DESIGN OF LIGANDS TARGETING A NOVEL SITE ON HIV-1 INTEGRASE	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
3AO3	FRAGMENT-BASED APPROACH TO THE DESIGN OF LIGANDS TARGETING A NOVEL SITE ON HIV-1 INTEGRASE	2.7.7.49 3.1.13.2 3.1.26.13
3AO4	FRAGMENT-BASED APPROACH TO THE DESIGN OF LIGANDS TARGETING A NOVEL SITE ON HIV-1 INTEGRASE	2.7.7.49 3.1.13.2 3.1.26.13
3AO5	FRAGMENT-BASED APPROACH TO THE DESIGN OF LIGANDS TARGETING A NOVEL SITE ON HIV-1 INTEGRASE	2.7.7.49 3.1.13.2 3.1.26.13
3AO9	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF SEQUENCE-SPECIFIC RIBONUCLEASE	3.1
3AOF	CRYSTAL STRUCTURES OF THERMOTOGA MARITIMA CEL5A IN COMPLEX WITH MANNOTRIOSE SUBSTRATE	3.2.1.4
3AON	CRYSTAL STRUCTURE OF THE CENTRAL AXIS (NTPD-NTPG) IN THE CATALYTIC PORTION OF ENTEROCOCCUS HIRAE V-TYPE SODIUM ATPASE	3.6.3.14
3APM	CRYSTAL STRUCTURE OF THE HUMAN SNP PAD4 PROTEIN	3.5.3.15
3APN	CRYSTAL STRUCTURE OF THE HUMAN WILD-TYPE PAD4 PROTEIN	3.5.3.15
3APP	STRUCTURE AND REFINEMENT OF PENICILLOPEPSIN AT 1.8 ANGSTROMS RESOLUTION	3.4.23.20
3APR	BINDING OF A REDUCED PEPTIDE INHIBITOR TO THE ASPARTIC PROTEINASE FROM RHIZOPUS CHINENSIS. IMPLICATIONS FOR A MECHANISM OF ACTION	3.4.23.6 3.4.23.21
3AQU	CRYSTAL STRUCTURE OF A CLASS V CHITINASE FROM ARABIDOPSIS THALIANA	3.2.1.14
3AR2	CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND AMPPCP AND CA2+	3.6.3.8 7.2.2.10
3AR3	CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND ADP AND TG	3.6.3.8 7.2.2.10
3AR4	CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND ATP AND TG IN THE ABSENCE OF CA2+	3.6.3.8 7.2.2.10
3AR5	CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND TNP-AMP AND TG	3.6.3.8 7.2.2.10
3AR6	CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND TNP-ADP AND TG IN THE ABSENCE OF CALCIUM	3.6.3.8 7.2.2.10
3AR7	CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND TNP-ATP AND TG IN THE ABSENCE OF CA2+	3.6.3.8 7.2.2.10
3AR8	CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND ALF4, TNP-AMP AND TG	3.6.3.8 7.2.2.10
3AR9	CALCIUM PUMP CRYSTAL STRUCTURE WITH BOUND BEF3, TNP-AMP AND TG IN THE ABSENCE OF CALCIUM	3.6.3.8 7.2.2.10
3ARA	DISCOVERY OF NOVEL URACIL DERIVATIVES AS POTENT HUMAN DUTPASE INHIBITORS	3.6.1.23
3ARN	HUMAN DUTPASE IN COMPLEX WITH NOVEL URACIL DERIVATIVE	3.6.1.23
3ARO	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - APO STRUCTURE	3.2.1.14
3ARP	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH DEQUALINIUM	3.2.1.14
3ARQ	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH IDARUBICIN	3.2.1.14
3ARR	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH PENTOXIFYLLINE	3.2.1.14
3ARS	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - APO STRUCTURE OF MUTANT W275G	3.2.1.14
3ART	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - W275G MUTANT COMPLEX STRUCTURE WITH DEQUALINIUM	3.2.1.14
3ARU	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - W275G MUTANT COMPLEX STRUCTURE WITH PENTOXIFYLLINE	3.2.1.14
3ARV	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH SANGUINARINE	3.2.1.14
3ARW	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH CHELERYTHRINE	3.2.1.14
3ARX	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH PROPENTOFYLLINE	3.2.1.14
3ARY	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH 2-(IMIDAZOLIN-2-YL)-5-ISOTHIOCYANATOBENZOFURAN	3.2.1.14
3ARZ	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - COMPLEX STRUCTURE WITH 2-(IMIDAZOLIN-2-YL)-5-ISOTHIOCYANATOBENZOFURAN	3.2.1.14
3AS0	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - W275G MUTANT COMPLEX STRUCTURE WITH SANGUINARINE	3.2.1.14
3AS1	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - W275G MUTANT COMPLEX STRUCTURE WITH CHELERYTHRINE	3.2.1.14
3AS2	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - W275G MUTANT COMPLEX STRUCTURE WITH PROPENTOFYLLINE	3.2.1.14
3AS3	CRYSTAL STRUCTURE ANALYSIS OF CHITINASE A FROM VIBRIO HARVEYI WITH NOVEL INHIBITORS - W275G MUTANT COMPLEX STRUCTURE WITH 2-(IMIDAZOLIN-2-YL)-5-ISOTHIOCYANATOBENZOFURAN	3.2.1.14
3ASM	CRYSTAL STRUCTURE OF Q54A MUTANT PROTEIN OF BST-RNASE HIII	3.1.26.4
3ATG	ENDO-1,3-BETA-GLUCANASE FROM CELLULOSIMICROBIUM CELLULANS	3.2.1.39
3ATI	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (3-METHOXYPHENYL)METHANAMINE	3.4.21.4
3ATK	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH CYCLOHEPTANAMINE	3.4.21.4
3ATL	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH BENZAMIDINE	3.4.21.4
3ATM	CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH 2-(1H-INDOL-3-YL)ETHANAMINE	3.4.21.4
3ATN	GLYCINE ETHYL ESTER SHIELDING ON THE AROMATIC SURFACES OF LYSOZYME: IMPLICATION FOR SUPPRESSION OF PROTEIN AGGREGATION	3.2.1.17
3ATO	GLYCINE ETHYL ESTER SHIELDING ON THE AROMATIC SURFACES OF LYSOZYME: IMPLICATION FOR SUPPRESSION OF PROTEIN AGGREGATION	3.2.1.17
3ATW	STRUCTURE-BASED DESIGN, SYNTHESIS, EVALUATION OF PEPTIDE-MIMETIC SARS 3CL PROTEASE INHIBITORS	3.4.22.69 3.4.19.12 3.4.22
3AUK	CRYSTAL STRUCTURE OF A LIPASE FROM GEOBACILLUS SP. SBS-4S	3.1.1.3
3AUZ	CRYSTAL STRUCTURE OF MRE11 WITH MANGANESE	3.1
3AV0	CRYSTAL STRUCTURE OF MRE11-RAD50 BOUND TO ATP S	3.1
3AV9	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVA	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVB	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVC	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVF	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVG	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVH	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVI	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVJ	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVK	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVL	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVM	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVN	CRYSTAL STRUCTURES OF NOVEL ALLOSTERIC PEPTIDE INHIBITORS OF HIV INTEGRASE IN THE LEDGF BINDING SITE	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
3AVZ	STRUCTURE OF SARS 3CL PROTEASE WITH PEPTIDIC ALDEHYDE INHIBITOR CONTAINING CYCLOHEXYL SIDE CHAIN	3.4.22.69 3.4.19.12 3.4.22
3AW0	STRUCTURE OF SARS 3CL PROTEASE WITH PEPTIDIC ALDEHYDE INHIBITOR	3.4.22.69 3.4.19.12 3.4.22
3AW1	STRUCTURE OF SARS 3CL PROTEASE AUTO-PROTEOLYSIS RESISTANT MUTANT IN THE ABSENT OF INHIBITOR	3.4.22.69 3.4.19.12 3.4.22
3AW6	CRYSTAL STRUCTURE OF TETRAGONAL HEN EGG WHITE LYSOZYME AT 84.2% RELATIVE HUMIDITY	3.2.1.17
3AW7	CRYSTAL STRUCTURE OF TETRAGONAL HEN EGG WHITE LYSOZYME AT 71.9% RELATIVE HUMIDITY	3.2.1.17
3AWE	CRYSTAL STRUCTURE OF PTEN-LIKE DOMAIN OF CI-VSP (248-576)	3.1.3
3AWG	CRYSTAL STRUCTURE OF PTEN-LIKE DOMAIN OF CI-VSP G356A MUTANT (248-576)	3.1.3
3AXD	THE TRUNCATED FIBROBACTER SUCCINOGENES 1,3-1,4-BETA-D-GLUCANASE V18Y/W203Y IN APO-FORM	3.2.1.73
3AXE	THE TRUNCATED FIBROBACTER SUCCINOGENES 1,3-1,4-BETA-D-GLUCANASE V18Y/W203Y IN COMPLEX WITH CELLOTETRAOSE (CELLOBIOSE DENSITY WAS OBSERVED)	3.2.1.73
3AXH	CRYSTAL STRUCTURE OF ISOMALTASE IN COMPLEX WITH ISOMALTOSE	3.2.1.10
3AXI	CRYSTAL STRUCTURE OF ISOMALTASE IN COMPLEX WITH MALTOSE	3.2.1.10
3AXX	FUNCTIONAL ANALYSIS OF HYPERTHERMOPHILIC ENDOCELLULASE FROM THE ARCHAEON PYROCOCCUS HORIKOSHII	3.2.1.4
3AYK	CATALYTIC FRAGMENT OF HUMAN FIBROBLAST COLLAGENASE COMPLEXED WITH CGS-27023A, NMR, MINIMIZED AVERAGE STRUCTURE	3.4.24.7
3AYQ	CRYSTAL STRUCTURE OF INHIBITOR BOUND LYSOZYME FROM MERETRIX LUSORIA	3.2.1.17
3AYR	GH5 ENDOGLUCANASE EGLA FROM A RUMINAL FUNGUS	3.2.1.4
3AYS	GH5 ENDOGLUCANASE FROM A RUMINAL FUNGUS IN COMPLEX WITH CELLOTRIOSE	3.2.1.4
3AYU	CRYSTAL STRUCTURE OF MMP-2 ACTIVE SITE MUTANT IN COMPLEX WITH APP-DRIVED DECAPEPTIDE INHIBITOR	3.4.24.24
3AZ4	CRYSTAL STRUCTURE OF CO/O-HEWL	3.2.1.17
3AZ5	CRYSTAL STRUCTURE OF PT/O-HEWL	3.2.1.17
3AZ6	CRYSTAL STRUCTURE OF CO/T-HEWL	3.2.1.17
3AZ7	CRYSTAL STRUCTURE OF PT/T-HEWL	3.2.1.17
3AZR	DIVERSE SUBSTRATES RECOGNITION MECHANISM REVEALED BY THERMOTOGA MARITIMA CEL5A STRUCTURES IN COMPLEX WITH CELLOBIOSE	3.2.1.4
3AZS	DIVERSE SUBSTRATES RECOGNITION MECHANISM REVEALED BY THERMOTOGA MARITIMA CEL5A STRUCTURES IN COMPLEX WITH MANNOTRIOSE	3.2.1.4
3AZT	DIVERSE SUBSTRATES RECOGNITION MECHANISM REVEALED BY THERMOTOGA MARITIMA CEL5A STRUCTURES IN COMPLEX WITH CELLOTETRAOSE	3.2.1.4
3AZX	CRYSTAL STRUCTURE OF THE LAMINARINASE CATALYTIC DOMAIN FROM THERMOTOGA MARITIMA MSB8	3.2.1.39
3AZY	CRYSTAL STRUCTURE OF THE LAMINARINASE CATALYTIC DOMAIN FROM THERMOTOGA MARITIMA MSB8	3.2.1.39
3AZZ	CRYSTAL STRUCTURE OF THE LAMINARINASE CATALYTIC DOMAIN FROM THERMOTOGA MARITIMA MSB8 IN COMPLEX WITH GLUCONOLACTONE	3.2.1.39
3B00	CRYSTAL STRUCTURE OF THE LAMINARINASE CATALYTIC DOMAIN FROM THERMOTOGA MARITIMA MSB8 IN COMPLEX WITH CETYLTRIMETHYLAMMONIUM BROMIDE	3.2.1.39
3B01	CRYSTAL STRUCTURE OF THE LAMINARINASE CATALYTIC DOMAIN FROM THERMOTOGA MARITIMA MSB8	3.2.1.39
3B12	CRYSTAL STRUCTURE OF THE FLUOROACETATE DEHALOGENASE D104 MUTANT FROM BURKHOLDERIA SP. FA1 IN COMPLEX WITH FLUOROACETATE	3.8.1.3
3B18	RV0098 OF MYCOBACTERIUM TUBERCULOSIS WITH ORDERED LOOP BETWEEN BETA-4 AND BETA-5	3.1.2 3.1.2.2
3B1T	CRYSTAL STRUCTURE OF HUMAN PEPTIDYLARGININE DEIMINASE 4 IN COMPLEX WITH O-CL-AMIDINE	3.5.3.15
3B1U	CRYSTAL STRUCTURE OF HUMAN PEPTIDYLARGININE DEIMINASE 4 IN COMPLEX WITH O-F-AMIDINE	3.5.3.15
3B23	CRYSTAL STRUCTURE OF THROMBIN-VARIEGIN COMPLEX: INSIGHTS OF A NOVEL MECHANISM OF INHIBITION AND DESIGN OF TUNABLE THROMBIN INHIBITORS	3.4.21.5
3B2E	CRYSTAL STRUCTURE OF S. CEREVISIAE GET3 IN THE OPEN CONFORMATION IN COMPLEX WITH GET1 CYTOSOLIC DOMAIN	3.6.3.16 3.6
3B2P	CRYSTAL STRUCTURE OF E. COLI AMINOPEPTIDASE N IN COMPLEX WITH ARGININE	3.4.11.2
3B2Q	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
3B2R	CRYSTAL STRUCTURE OF PDE5A1 CATALYTIC DOMAIN IN COMPLEX WITH VARDENAFIL	3.1.4.35
3B2X	CRYSTAL STRUCTURE OF E. COLI AMINOPEPTIDASE N IN COMPLEX WITH LYSINE	3.4.11.2
3B34	CRYSTAL STRUCTURE OF E. COLI AMINOPEPTIDASE N IN COMPLEX WITH PHENYLALANINE	3.4.11.2
3B35	CRYSTAL STRUCTURE OF THE M180A MUTANT OF THE AMINOPEPTIDASE FROM VIBRIO PROTEOLYTICUS	3.4.11.10
3B36	STRUCTURE OF M26L DJ-1	3.1.2 3.5.1 3.5.1.124
3B37	CRYSTAL STRUCTURE OF E. COLI AMINOPEPTIDASE N IN COMPLEX WITH TYROSINE	3.4.11.2
3B38	STRUCTURE OF A104V DJ-1	3.1.2 3.5.1 3.5.1.124
3B3A	STRUCTURE OF E163K/R145E DJ-1	3.1.2 3.5.1 3.5.1.124
3B3B	CRYSTAL STRUCTURE OF E. COLI AMINOPEPTIDASE N IN COMPLEX WITH TRYPTOPHAN	3.4.11.2
3B3C	CRYSTAL STRUCTURE OF THE M180A MUTANT OF THE AMINOPEPTIDASE FROM VIBRIO PROTEOLYTICUS IN COMPLEX WITH LEUCINE PHOSPHONIC ACID	3.4.11.10
3B3S	CRYSTAL STRUCTURE OF THE M180A MUTANT OF THE AMINOPEPTIDASE FROM VIBRIO PROTEOLYTICUS IN COMPLEX WITH LEUCINE	3.4.11.10
3B3T	CRYSTAL STRUCTURE OF THE D118N MUTANT OF THE AMINOPEPTIDASE FROM VIBRIO PROTEOLYTICUS	3.4.11.10
3B3V	CRYSTAL STRUCTURE OF THE S228A MUTANT OF THE AMINOPEPTIDASE FROM VIBRIO PROTEOLYTICUS	3.4.11.10
3B3W	CRYSTAL STRUCTURE OF THE S228A MUTANT OF THE AMINOPEPTIDASE FROM VIBRIO PROTEOLYTICUS IN COMPLEX WITH LEUCINE	3.4.11.10
3B3X	CRYSTAL STRUCTURE OF CLASS A BETA-LACTAMASE OF BACILLUS LICHENIFORMIS BS3 WITH AMINOCITRATE	3.5.2.6
3B44	CRYSTAL STRUCTURE OF GLPG W136A MUTANT	3.4.21.105
3B45	CRYSTAL STRUCTURE OF GLPG AT 1.9A RESOLUTION	3.4.21.105
3B4R	SITE-2 PROTEASE FROM METHANOCALDOCOCCUS JANNASCHII	3.4.24
3B5L	CRYSTAL STRUCTURE OF A NOVEL ENGINEERED RETROALDOLASE: RA-61	3.2.1.8
3B5Q	CRYSTAL STRUCTURE OF A PUTATIVE SULFATASE (NP_810509.1) FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 AT 2.40 A RESOLUTION	3.1.6
3B5X	CRYSTAL STRUCTURE OF MSBA FROM VIBRIO CHOLERAE	3.6.3 7.5.2.6
3B60	CRYSTAL STRUCTURE OF MSBA FROM SALMONELLA TYPHIMURIUM WITH AMPPNP, HIGHER RESOLUTION FORM	3.6.3 7.5.2.6
3B69	T CRUZI TRANS-SIALIDASE COMPLEX WITH BENZOYLATED NANA DERIVATIVE	3.2.1.18
3B6E	CRYSTAL STRUCTURE OF HUMAN DECH-BOX RNA HELICASE MDA5 (MELANOMA DIFFERENTIATION-ASSOCIATED PROTEIN 5), DECH-DOMAIN	3.6.1 3.6.4.13
3B6L	CRYSTAL STRUCTURE OF LYSOZYME FOLDED IN SDS AND 2-METHYL-2,4-PENTANEDIOL	3.2.1.17
3B6O	STRUCTURE OF TREX1 IN COMPLEX WITH A NUCLEOTIDE AND AN INHIBITOR ION (LITHIUM)	3.1.11.2
3B6P	STRUCTURE OF TREX1 IN COMPLEX WITH A NUCLEOTIDE AND INHIBITOR IONS (SODIUM AND ZINC)	3.1.11.2
3B72	CRYSTAL STRUCTURE OF LYSOZYME FOLDED IN SDS AND 2-METHYL-2,4-PENTANEDIOL	3.2.1.17
3B7C	CRYSTAL STRUCTURE OF A NTF-2 LIKE PROTEIN OF UNKNOWN FUNCTION (SO_0125) FROM SHEWANELLA ONEIDENSIS MR-1 AT 1.70 A RESOLUTION	3.5.1.1
3B7E	NEURAMINIDASE OF A/BREVIG MISSION/1/1918 H1N1 STRAIN IN COMPLEX WITH ZANAMIVIR	3.2.1.18
3B7G	HUMAN DEAD-BOX RNA HELICASE DDX20, CONSERVED DOMAIN I (DEAD) IN COMPLEX WITH AMPPNP (ADENOSINE-(BETA,GAMMA)-IMIDOTRIPHOSPHATE)	3.6.1 3.6.4.13
3B7I	CRYSTAL STRUCTURE OF THE S228A MUTANT OF THE AMINOPEPTIDASE FROM VIBRIO PROTEOLYTICUS IN COMPLEX WITH LEUCINE PHOSPHONIC ACID	3.4.11.10
3B7K	HUMAN ACYL-COENZYME A THIOESTERASE 12	3.1.2.1
3B7M	CRYSTAL STRUCTURE OF A MESO-ACTIVE THERMO-STABLE CELLULASE (MT CEL12A) DERIVED BY MAKING NON-CONTIGUOUS MUTATIONS IN THE ACTIVE SURFACE OF THE CEL12A CELLULASE OF RHODOTHERMUS MARINUS	3.2.1.4
3B7O	CRYSTAL STRUCTURE OF THE HUMAN TYROSINE PHOSPHATASE SHP2 (PTPN11) WITH AN ACCESSIBLE ACTIVE SITE	3.1.3.48
3B7R	LEUKOTRIENE A4 HYDROLASE COMPLEXED WITH INHIBITOR RB3040	3.3.2.6 3.4.11.4
3B7S	[E296Q]LTA4H IN COMPLEX WITH RSR SUBSTRATE	3.3.2.6 3.4.11.4
3B7T	[E296Q]LTA4H IN COMPLEX WITH ARG-ALA-ARG SUBSTRATE	3.3.2.6 3.4.11.4
3B7U	LEUKOTRIENE A4 HYDROLASE COMPLEXED WITH KELATORPHAN	3.3.2.6 3.4.11.4
3B7V	HIV-1 PROTEASE COMPLEXED WITH GEM-DIOL-AMINE TETRAHEDRAL INTERMEDIATE NLLTQI	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
3B80	HIV-1 PROTEASE MUTANT I54V COMPLEXED WITH GEM-DIOL-AMINE INTERMEDIATE NLLTQI	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
3B8B	CRYSTAL STRUCTURE OF CYSQ FROM BACTEROIDES THETAIOTAOMICRON, A BACTERIAL MEMBER OF THE INOSITOL MONOPHOSPHATASE FAMILY	3.1.3.7
3B8F	CRYSTAL STRUCTURE OF THE CYTIDINE DEAMINASE FROM BACILLUS ANTHRACIS	3.5.4.4
3B8J	Q191A MUTANT OF DEGS-DELTAPDZ	3.4.21 3.4.21.107
3B8S	CRYSTAL STRUCTURE OF WILD-TYPE CHITINASE A FROM VIBRIO HARVEYI	3.2.1.14
3B8Z	HIGH RESOLUTION CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF ADAMTS-5 (AGGRECANASE-2)	3.4.24
3B92	NOVEL THIO-BASED TACE INHIBITORS PART 2: RATIONAL DESIGN, SYNTHESIS AND SAR OF THIOL-CONTANING ARYL SUFONES	3.4.24.86
3B9A	CRYSTAL STRUCTURE OF VIBRIO HARVEYI CHITINASE A COMPLEXED WITH HEXASACCHARIDE	3.2.1.14
3B9D	CRYSTAL STRUCTURE OF VIBRIO HARVEYI CHITINASE A COMPLEXED WITH PENTASACCHARIDE	3.2.1.14
3B9E	CRYSTAL STRUCTURE OF INACTIVE MUTANT E315M CHITINASE A FROM VIBRIO HARVEYI	3.2.1.14
3B9F	1.6 A STRUCTURE OF THE PCI-THROMBIN-HEPARIN COMPLEX	3.4.21.5
3B9G	CRYSTAL STRUCTURE OF LOOP DELETION MUTANT OF TRYPANOSOMA VIVAX NUCLEOSIDE HYDROLASE (3GTVNH) IN COMPLEX WITH IMMH	3.2.2.1
3B9R	SERCA CA2+-ATPASE E2 ALUMINIUM FLUORIDE COMPLEX WITHOUT THAPSIGARGIN	3.6.3.8 7.2.2.10
3B9X	CRYSTAL STRUCTURE OF THE E. COLI PYRIMIDINE NUCLEOSIDE HYDROLASE YEIK IN COMPLEX WITH INOSINE	3.2.2.8
3BA0	CRYSTAL STRUCTURE OF FULL-LENGTH HUMAN MMP-12	3.4.24.65
3BA6	STRUCTURE OF THE CA2E1P PHOSPHOENZYME INTERMEDIATE OF THE SERCA CA2+-ATPASE	3.6.3.8 7.2.2.10
3BAI	HUMAN PANCREATIC ALPHA AMYLASE WITH BOUND NITRATE	3.2.1.1
3BAJ	HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH NITRATE AND ACARBOSE	3.2.1.1
3BAK	N298S MUTANT OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH NITRATE	3.2.1.1
3BAM	RESTRICTION ENDONUCLEASE BAMHI COMPLEX WITH DNA AND MANGANESE IONS (POST-REACTIVE COMPLEX)	3.1.21.4
3BAW	HUMAN PANCREATIC ALPHA-AMYLASE COMPLEXED WITH AZIDE	3.2.1.1
3BAX	N298S VARIANT OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH AZIDE	3.2.1.1
3BAY	N298S VARIANT OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH NITRATE AND ACARBOSE	3.2.1.1
3BB1	CRYSTAL STRUCTURE OF TOC34 FROM PISUM SATIVUM IN COMPLEX WITH MG2+ AND GMPPNP	3.6.5
3BB3	CRYSTAL STRUCTURE OF TOC33 FROM ARABIDOPSIS THALIANA IN COMPLEX WITH GDP AND MG2+	3.6.5
3BB4	CRYSTAL STRUCTURE OF TOC33 FROM ARABIDOPSIS THALIANA IN COMPLEX WITH MG2+ AND GMPPNP	3.6.5
3BC1	CRYSTAL STRUCTURE OF THE COMPLEX RAB27A-SLP2A	3.6.5.2
3BC2	METALLO BETA-LACTAMASE II FROM BACILLUS CEREUS 569/H/9 AT PH 6.0, MONOCLINIC CRYSTAL FORM	3.5.2.6
3BC3	EXPLORING INHIBITOR BINDING AT THE S SUBSITES OF CATHEPSIN L	3.4.22.15
3BC4	I84V HIV-1 PROTEASE IN COMPLEX WITH A PYRROLIDINE DIESTER	3.4.23.16
3BC9	ALPHA-AMYLASE B IN COMPLEX WITH ACARBOSE	3.2.1.1 3.2.1.98
3BCD	ALPHA-AMYLASE B IN COMPLEX WITH MALTOTETRAOSE AND ALPHA-CYCLODEXTRIN	3.2.1.1 3.2.1.98
3BCF	ALPHA-AMYLASE B FROM HALOTHERMOTHRIX ORENII	3.2.1.1 3.2.1.98
3BCM	CRYSTAL STRUCTURE OF THE UNSWAPPED FORM OF P19A/L28Q/N67D BS-RNASE	3.1.27.5 4.6.1.18
3BCN	CRYSTAL STRUCTURE OF A PAPAIN-LIKE CYSTEINE PROTEASE ERVATAMIN-A COMPLEXED WITH IRREVERSIBLE INHIBITOR E-64	3.4.22
3BCO	CRYSTAL STRUCTURE OF THE SWAPPED FORM OF P19A/L28Q/N67D BS-RNASE	3.1.27.5 4.6.1.18
3BCP	CRYSTAL STRUCTURE OF THE SWAPPED NON COVALENT FORM OF P19A/L28Q/N67D BS-RNASE	3.1.27.5 4.6.1.18
3BDC	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS AT CRYOGENIC TEMPERATURE	3.1.31.1
3BDF	CRYSTAL STRUCTURE OF METAL-FREE E. COLI ALKALINE PHOSPHATASE (T155V)	3.1.3.1
3BDG	CRYSTAL STRUCTURE OF WILD-TYPE/T155V MIXED DIMER OF E. COLI ALKALINE PHOSPHATASE	3.1.3.1
3BDH	CRYSTAL STRUCTURE OF ZINC-DEFICIENT WILD-TYPE E. COLI ALKALINE PHOSPHATASE	3.1.3.1
3BDL	CRYSTAL STRUCTURE OF A TRUNCATED HUMAN TUDOR-SN	3.1.31.1
3BEB	CRYSTAL STRUCTURE OF E. COLI PENICILLIN-BINDING PROTEIN 5 IN COMPLEX WITH A PEPTIDE-MIMETIC PENICILLIN	3.4.16.4 3.5.2.6
3BEC	CRYSTAL STRUCTURE OF E. COLI PENICILLIN-BINDING PROTEIN 5 IN COMPLEX WITH A PEPTIDE-MIMETIC CEPHALOSPORIN	3.4.16.4 3.5.2.6
3BEF	CRYSTAL STRUCTURE OF THROMBIN BOUND TO THE EXTRACELLULAR FRAGMENT OF PAR1	3.4.21.5
3BEI	CRYSTAL STRUCTURE OF THE SLOW FORM OF THROMBIN IN A SELF_INHIBITED CONFORMATION	3.4.21.5
3BEQ	NEURAMINIDASE OF A/BREVIG MISSION/1/1918 H1N1 STRAIN	3.2.1.18
3BER	HUMAN DEAD-BOX RNA-HELICASE DDX47, CONSERVED DOMAIN I IN COMPLEX WITH AMP	3.6.1 3.6.4.13
3BEU	NA+-DEPENDENT ALLOSTERY MEDIATES COAGULATION FACTOR PROTEASE ACTIVE SITE SELECTIVITY	3.4.21.4
3BEZ	CRYSTAL STRUCTURE OF ESCHERICHIA COLI SIGNAL PEPTIDE PEPTIDASE (SPPA), SEMET CRYSTALS	3.4.21
3BF0	CRYSTAL STRUCTURE OF ESCHERICHIA COLI SIGNAL PEPTIDE PEPTIDASE (SPPA), NATIVE CRYSTALS	3.4.21
3BF6	THROMBIN:SURAMIN COMPLEX	3.4.21.5
3BF7	1.1 RESOLUTION STRUCTURE OF YBFF, A NEW ESTERASE FROM ESCHERICHIA COLI: A UNIQUE SUBSTRATE-BINDING CREVICE GENERATED BY DOMAIN ARRANGEMENT	3.1
3BF8	1.1 RESOLUTION STRUCTURE OF YBFF, A NEW ESTERASE FROM ESCHERICHIA COLI: A UNIQUE SUBSTRATE-BINDING CREVICE GENERATED BY DOMAIN ARRANGEMENT	3.1
3BFC	CLASS A BETA-LACTAMASE SED-G238C COMPLEXED WITH IMIPENEM	3.5.2.6
3BFD	CRYSTAL STRUCTURE OF THE CLASS A BETA-LACTAMASE SED-G238C MUTANT FROM CITROBACTER SEDLAKII	3.5.2.6
3BFE	CRYSTAL STRUCTURE OF THE CLASS A BETA-LACTAMASE SED-1 FROM CITROBACTER SEDLAKII	3.5.2.6
3BFF	CLASS A BETA-LACTAMASE SED-G238C COMPLEXED WITH FAROPENEM	3.5.2.6
3BFG	CLASS A BETA-LACTAMASE SED-G238C COMPLEXED WITH MEROPENEM	3.5.2.6
3BFK	CRYSTAL STRUCTURE OF PLASMODIUM FALCIPARUM RAB11A IN COMPLEX WITH GDP	3.6.5.2
3BFO	CRYSTAL STRUCTURE OF IG-LIKE C2-TYPE 2 DOMAIN OF THE HUMAN MUCOSA-ASSOCIATED LYMPHOID TISSUE LYMPHOMA TRANSLOCATION PROTEIN 1	3.4.22
3BG4	THE CRYSTAL STRUCTURE OF GUAMERIN IN COMPLEX WITH CHYMOTRYPSIN AND THE DEVELOPMENT OF AN ELASTASE-SPECIFIC INHIBITOR	3.4.21.1
3BG8	CRYSTAL STRUCTURE OF FACTOR XIA IN COMPLEX WITH CLAVATADINE A	3.4.21.27
3BGA	CRYSTAL STRUCTURE OF BETA-GALACTOSIDASE FROM BACTEROIDES THETAIOTAOMICRON VPI-5482	3.2.1.23
3BGB	HIV-1 PROTEASE IN COMPLEX WITH A ISOBUTYL DECORATED OLIGOAMINE	3.4.23.16
3BGC	HIV-1 PROTEASE IN COMPLEX WITH A BENZYL DECORATED OLIGOAMINE	3.4.23.16
3BGO	AZIDE COMPLEX OF ENGINEERED SUBTILISIN SUBT_BACAM	3.4.21.62
3BGR	CRYSTAL STRUCTURE OF K103N/Y181C 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
3BGY	TRICLINIC STRUCTURE OF MIMIVIRUS CAPPING ENZYME TRIPHOSPHATASE AT 1.65 A	3.1.3.33 2.7.7.50 2.1.1.56
3BH0	ATPASE DOMAIN OF G40P	3.6.4.12
3BH4	HIGH RESOLUTION CRYSTAL STRUCTURE OF BACILLUS AMYLOLIQUEFACIENS ALPHA-AMYLASE	3.2.1.1
3BHD	CRYSTAL STRUCTURE OF HUMAN THIAMINE TRIPHOSPHATASE (THTPA)	3.6.1.28
3BHE	HIV-1 PROTEASE IN COMPLEX WITH A THREE ARMED PYRROLIDINE DERIVATIVE	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
3BHX	X-RAY STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH A TRANSITION STATE ANALOG OF ASP-GLU	3.4.17.21
3BI0	X-RAY STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH A TRANSITION STATE ANALOG OF GLU-GLU	3.4.17.21
3BI1	X-RAY STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH A TRANSITION STATE ANALOG OF METHOTREXATE-GLU	3.4.17.21
3BIF	6-PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE EMPTY 6-PF-2K ACTIVE SITE	2.7.1.105 3.1.3.46
3BIG	CRYSTAL STRUCTURE OF THE FRUCTOSE-1,6-BISPHOSPHATASE GLPX FROM E.COLI IN COMPLEX WITH INORGANIC PHOSPHATE	3.1.3.11
3BIH	CRYSTAL STRUCTURE OF FRUCTOSE-1,6-BISPHOSPHATASE FROM E.COLI GLPX	3.1.3.11
3BIR	DISECTING HISTIDINE INTERACTIONS IN RIBONUCLEASE T1 BY ASN AND GLN SUBSTITUTIONS	3.1.27.3 4.6.1.24
3BIU	HUMAN THROMBIN-IN COMPLEX WITH UB-THR10	3.4.21.5
3BIV	HUMAN THROMBIN-IN COMPLEX WITH UB-THR11	3.4.21.5
3BJC	CRYSTAL STRUCTURE OF THE PDE5A CATALYTIC DOMAIN IN COMPLEX WITH A NOVEL INHIBITOR	3.1.4.35
3BJK	CRYSTAL STRUCTURE OF HI0827, A HEXAMERIC BROAD SPECIFICITY ACYL-COENZYME A THIOESTERASE: THE ASP44ALA MUTANT ENZYME	3.1.2
3BJM	CRYSTAL STRUCTURE OF HUMAN DPP-IV IN COMPLEX WITH (1S,3S, 5S)-2-[(2S)-2-AMINO-2-(3-HYDROXYTRICYCLO[3.3.1.13,7]DEC-1- YL)ACETYL]-2-AZABICYCLO[3.1.0]HEXANE-3-CARBONITRILE (CAS), (1S,3S,5S)-2-((2S)-2-AMINO-2-(3-HYDROXYADAMANTAN-1- YL)ACETYL)-2-AZABICYCLO[3.1.0]HEXANE-3-CARBONITRILE (IUPAC), OR BMS-477118	3.4.14.5
3BJW	CRYSTAL STRUCTURE OF ECARPHOLIN S COMPLEXED WITH SURAMIN	3.1.1.4
3BJX	STRUCTURE OF A GROUP I HALOACID DEHALOGENASE FROM PSEUDOMONAS PUTIDA STRAIN PP3	3.8.1.2
3BK1	CRYSTAL STRUCTURE ANALYSIS OF RNASE J	3 3.1
3BK2	CRYSTAL STRUCTURE ANALYSIS OF THE RNASE J/UMP COMPLEX	3 3.1
3BKK	TESIS ACE CO-CRYSTAL STRUCTURE WITH KETONE ACE INHIBITOR KAF	3.4.15.1 3.2.1
3BKL	TESTIS ACE CO-CRYSTAL STRUCTURE WITH KETONE ACE INHIBITOR KAW	3.4.15.1 3.2.1
3BL5	CRYSTAL STRUCTURE OF QUEC FROM BACILLUS SUBTILIS: AN ENZYME INVOLVED IN PREQ1 BIOSYNTHESIS	3.5 6.3.4.20
3BL6	CRYSTAL STRUCTURE OF STAPHYLOCOCCUS AUREUS 5'-METHYLTHIOADENOSINE/S-ADENOSYLHOMOCYSTEINE NUCLEOSIDASE IN COMPLEX WITH FORMYCIN A	3.2.2.9 3.2.2.16
3BL7	SYNTHETIC GENE ENCODED DCPS BOUND TO INHIBITOR DG156844	3 3.6.1.59
3BL9	SYNTHETIC GENE ENCODED DCPS BOUND TO INHIBITOR DG157493	3 3.6.1.59
3BLA	SYNTHETIC GENE ENCODED DCPS BOUND TO INHIBITOR DG153249	3 3.6.1.59
3BLB	CRYSTAL STRUCTURE OF GOLGI MANNOSIDASE II IN COMPLEX WITH SWAINSONINE AT 1.3 ANGSTROM RESOLUTION	3.2.1.114
3BLK	ROLE OF AROMATIC RESIDUES IN STARCH BINDING	3.2.1.1
3BLM	REFINED CRYSTAL STRUCTURE OF BETA-LACTAMASE FROM STAPHYLOCOCCUS AUREUS PC1 AT 2.0	3.5.2.6
3BLP	ROLE OF AROMATIC RESIDUES IN HUMAN SALIVARY ALPHA-AMYLASE	3.2.1.1
3BLS	AMPC BETA-LACTAMASE FROM ESCHERICHIA COLI	3.5.2.6
3BLT	CRYSTAL STRUCTURES OF YOPH COMPLEXED WITH PVSN AND PVS, INHIBITORS OF YOPH WHICH CO-VALENT BIND TO CYS OF ACTIVE SITE	3.1.3.48
3BLU	CRYSTAL STRUCTURE YOPH COMPLEXED WITH INHIBITOR PVS	3.1.3.48
3BM4	CRYSTAL STRUCTURE OF HUMAN ADP-RIBOSE PYROPHOSPHATASE NUDT5 IN COMPLEX WITH MAGNESIUM AND AMPCPR	3.6.1.13 3.6.1 3.6.1.58 2.7.7.96
3BM6	AMPC BETA-LACTAMASE IN COMPLEX WITH A P.CARBOXYPHENYLBORONIC ACID	3.5.2.6
3BM8	CRYSTAL STRUCTURE OF YOPH MUTANT D356A COMPLEXED WITH IRREVERSIBLE INHIBITOR PVSN	3.1.3.48
3BMX	BETA-N-HEXOSAMINIDASE (YBBD) FROM BACILLUS SUBTILIS	3.2.1.52
3BN9	CRYSTAL STRUCTURE OF MT-SP1 IN COMPLEX WITH FAB INHIBITOR E2	3.4.21.109
3BO5	CRYSTAL STRUCTURE OF METHYLTRANSFERASE DOMAIN OF HUMAN HISTONE-LYSINE N-METHYLTRANSFERASE SETMAR	2.1.1.43 2.1.1.357 3.1
3BOK	STRUCTURE OF THE C. BOTULINUM NEUROTOXIN SEROTYPE A APO-ENZYME	3.4.24.69
3BON	STRUCTURE OF THE C. BOTULINUM NEUROTOXIN SEROTYPE A WITH ZN2+ COFACTOR BOUND	3.4.24.69
3BOO	STRUCTURE OF THE C. BOTULINUM NEUROTOXIN SEROTYPE A WITH AN INHIBITORY PEPTIDE BOUND	3.4.24.69
3BOR	CRYSTAL STRUCTURE OF THE DEADC DOMAIN OF HUMAN TRANSLATION INITIATION FACTOR 4A-2	3.6.1 3.6.4.13
3BOW	STRUCTURE OF M-CALPAIN IN COMPLEX WITH CALPASTATIN	3.4.22.53
3BP2	ROLE OF THE N-TERMINUS IN THE INTERACTION OF PANCREATIC PHOSPHOLIPASE A2 WITH AGGREGATED SUBSTRATES. PROPERTIES AND CRYSTAL STRUCTURE OF TRANSAMINATED PHOSPHOLIPASE A2	3.1.1.4
3BPB	CRYSTAL STRUCTURE OF THE DIMETHYLARGININE DIMETHYLAMINOHYDROLASE H162G ADDUCT WITH S-METHYL-L-THIOCITRULLINE	3.5.3.18
3BPF	CRYSTAL STRUCTURE OF FALCIPAIN-2 WITH ITS INHIBITOR, E64	3.4.22
3BPM	CRYSTAL STRUCTURE OF FALCIPAIN-3 WITH ITS INHIBITOR, LEUPEPTIN	3.4.22
3BPP	1510-N MEMBRANE PROTEASE K138A MUTANT SPECIFIC FOR A STOMATIN HOMOLOG FROM PYROCOCCUS HORIKOSHII	3.4.21
3BPS	PCSK9:EGF-A COMPLEX	3.4.21
3BPT	CRYSTAL STRUCTURE OF HUMAN BETA-HYDROXYISOBUTYRYL-COA HYDROLASE IN COMPLEX WITH QUERCETIN	3.1.2.4
3BQ8	CRYSTAL STRUCTURE OF THE E.COLI PHOQ SENSOR DOMAIN	2.7.13.3 3.1.3
3BQ9	CRYSTAL STRUCTURE OF PREDICTED NUCLEOTIDE-BINDING PROTEIN FROM IDIOMARINA BALTICA OS145	3.2.2.4
3BQA	CRYSTAL STRUCTURE OF AN E.COLI PHOQ SENSOR DOMAIN MUTANT	2.7.13.3 3.1.3
3BR8	CRYSTAL STRUCTURE OF ACYLPHOSPHATASE FROM BACILLUS SUBTILIS	3.6.1.7
3BR9	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL PYRIDAZINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3BRA	BACE-1 COMPLEXED WITH COMPOUND 1	3.4.23.46
3BRH	PROTEIN TYROSINE PHOSPHATASE PTPN-22 (LYP) BOUND TO THE MONO-PHOSPHORYLATED LCK ACTIVE SITE PEPTIDE	3.1.3.48
3BRM	CRYSTAL STRUCTURE OF THE COVALENT COMPLEX BETWEEN THE BACILLUS SUBTILIS GLUTAMINASE YBGJ AND 5-OXO-L-NORLEUCINE FORMED BY REACTION OF THE PROTEIN WITH 6-DIAZO-5-OXO-L-NORLEUCINE	3.5.1.2
3BSA	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL PYRIDAZINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3BSC	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL PYRIDAZINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3BSF	CRYSTAL STRUCTURE OF THE MTA/SAH NUCLEOSIDASE	3.2.2.9
3BSG	BARLEY ALPHA-AMYLASE ISOZYME 1 (AMY1) H395A MUTANT	3.2.1.1
3BSH	BARLEY ALPHA-AMYLASE ISOZYME 1 (AMY1) DOUBLE MUTANT Y105A/Y380A IN COMPLEX WITH INHIBITOR ACARBOSE	3.2.1.1
3BSN	NORWALK VIRUS POLYMERASE BOUND TO 5-NITROCYTIDINE TRIPHOSPHATE AND PRIMER-TEMPLATE RNA	2.7.7.48 3.4.22.66 3.6.1.15
3BSO	NORWALK VIRUS POLYMERASE BOUND TO CYTIDINE 5'-TRIPHOSPHATE AND PRIMER-TEMPLATE RNA	2.7.7.48 3.4.22.66 3.6.1.15
3BSQ	CRYSTAL STRUCTURE OF HUMAN KALLIKREIN 7 PRODUCED AS A SECRETION PROTEIN IN E.COLI	3.4.21.117
3BSU	HYBRID-BINDING DOMAIN OF HUMAN RNASE H1 IN COMPLEX WITH 12-MER RNA/DNA	3.1.26.4
3BT1	STRUCTURE OF UROKINASE RECEPTOR, UROKINASE AND VITRONECTIN COMPLEX	3.4.21.73
3BT2	STRUCTURE OF UROKINASE RECEPTOR, UROKINASE AND VITRONECTIN COMPLEX	3.4.21.73
3BTA	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN SEROTYPE A	3.4.24.69
3BTD	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN THE BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI.	3.4.21.4
3BTE	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI.	3.4.21.4
3BTF	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI.	3.4.21.4
3BTG	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI	3.4.21.4
3BTH	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI	3.4.21.4
3BTK	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI	3.4.21.4
3BTM	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI	3.4.21.4
3BTQ	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI	3.4.21.4
3BTT	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI	3.4.21.4
3BTW	THE CRYSTAL STRUCTURES OF THE COMPLEXES BETWEEN BOVINE BETA-TRYPSIN AND TEN P1 VARIANTS OF BPTI	3.4.21.4
3BU4	RIBONUCLEASE T1 COMPLEX WITH 2'GMP	3.1.27.3 4.6.1.24
3BUB	GOLGI ALPHA-MANNOSIDASE II WITH AN EMPTY ACTIVE SITE	3.2.1.114
3BUD	GOLGI MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT WITH AN EMPTY ACTIVE SITE	3.2.1.114
3BUF	BACE-1 COMPLEXED WITH COMPOUND 2	3.4.23.46
3BUG	BACE-1 COMPLEXED WITH COMPOUND 3	3.4.23.46
3BUH	BACE-1 COMPLEXED WITH COMPOUND 4	3.4.23.46
3BUI	GOLGI MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT COMPLEX WITH TRIS	3.2.1.114
3BUP	GOLGI ALPHA-MANNOSIDASE II D341N ACID-BASE CATALYST MUTANT WITH BOUND MANNOSE	3.2.1.114
3BUQ	GOLGI ALPHA-MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT WITH BOUND MANNOSE.	3.2.1.114
3BV9	STRUCTURE OF THROMBIN BOUND TO THE INHIBITOR FM19	3.4.21.5
3BVA	CYSTAL STRUCTURE OF HIV-1 ACTIVE SITE MUTANT D25N AND P2-NC ANALOG 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
3BVB	CYSTAL STRUCTURE OF HIV-1 ACTIVE SITE MUTANT D25N AND INHIBITOR DARUNAVIR	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
3BVT	GOLGI MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT COMPLEX WITH METHYL (ALPHA-D-MANNOPYRANOSYL)-(1->3)-S-ALPHA-D-MANNOPYRANOSIDE	3.2.1.114
3BVU	GOLGI MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT COMPLEX WITH METHYL(ALPHA-D-MANNOPYRANOSYL)-(1->3)-S-[(ALPHA-D-MANNOPYRANOSYL)-(1->6)]-ALPHA-D-MANNOPYRANOSIDE	3.2.1.114
3BVV	GOLGI MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT COMPLEX WITH METHYL ALPHA-D-MANNOPYRANOSYL-(1->3)-[6-THIO-ALPHA-D-MANNOPYRANOSYL-(1->6)]-BETA-D-MANNOPYRANOSIDE	3.2.1.114
3BVW	GOLGI MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT COMPLEX WITH METHYL (2-DEOXY-2-ACETAMIDO-BETA-D-GLUCOPYRANOSYL)-(1->2)-ALPHA-D-MANNOPYRANOSYL- (1->3)-[ALPHA-D-MANNOPYRANOSYL-(1->6)-6-THIO-ALPHA-D-MANNOPYRANOSYL- (1->6)]-BETA-D-MANNOPYRANOSIDE	3.2.1.114
3BVX	GOLGI MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT COMPLEX WITH METHYL (2-DEOXY-2-ACETAMIDO-BETA-D-GLUCOPYRANOSYL)-(1->2)-(ALPHA-D-MANNOPYRANOSYL)- (1->3)-[(ALPHA-D-MANNOPYRANOSYL)-(1->6)-(ALPHA-D-MANNOPYRANOSYL)-(1->6)]-BETA-D-MANNOPYRANOSIDE	3.2.1.114
3BWE	CRYSTAL STRUCTURE OF AGGREGATED FORM OF DJ1	3.1.2 3.5.1 3.5.1.124
3BWH	ATOMIC RESOLUTION STRUCTURE OF CUCURMOSIN, A NOVEL TYPE 1 RIP FROM THE SARCOCARP OF CUCURBITA MOSCHATA	3.2.2.22
3BWI	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH AN ACETATE ION BOUND AT THE ACTIVE SITE	3.4.24.69
3BWK	CRYSTAL STRUCTURE OF FALCIPAIN-3 WITH ITS INHIBITOR, K11017	3.4.22
3BWV	CRYSTAL STRUCTURE OF DEOXYRIBONUCLEOTIDASE-LIKE PROTEIN (NP_764060.1) FROM STAPHYLOCOCCUS EPIDERMIDIS ATCC 12228 AT 1.55 A RESOLUTION	3.1.3
3BX1	COMPLEX BETWEEN THE BARLEY ALPHA-AMYLASE/SUBTILISIN INHIBITOR AND THE SUBTILISIN SAVINASE	3.4.21.62
3BXM	STRUCTURE OF AN INACTIVE MUTANT OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II [GCPII(E424A)] IN COMPLEX WITH N-ACETYL-ASP-GLU (NAAG)	3.4.17.21
3BXR	CRYSTAL STRUCTURES OF HIGHLY CONSTRAINED SUBSTRATE AND HYDROLYSIS PRODUCTS BOUND TO HIV-1 PROTEASE. IMPLICATIONS FOR CATALYTIC MECHANISM	3.4.23.16
3BXS	CRYSTAL STRUCTURES OF HIGHLY CONSTRAINED SUBSTRATE AND HYDROLYSIS PRODUCTS BOUND TO HIV-1 PROTEASE. IMPLICATIONS FOR CATALYTIC MECHANISM	3.4.23.16
3BY4	STRUCTURE OF OVARIAN TUMOR (OTU) DOMAIN IN COMPLEX WITH UBIQUITIN	3.4.19.12
3BYC	JOINT NEUTRON AND X-RAY STRUCTURE OF DIISOPROPYL FLUOROPHOSPHATASE. DEUTERIUM OCCUPANCIES ARE 1-Q, WHERE Q IS OCCUPANCY OF H	3.1.8.2
3BYD	CRYSTAL STRUCTURE OF BETA-LACTAMASE OXY-1-1 FROM KLEBSIELLA OXYTOCA	3.5.2.6
3C0R	STRUCTURE OF OVARIAN TUMOR (OTU) DOMAIN IN COMPLEX WITH UBIQUITIN	3.4.19.12
3C0W	I-SCEI IN COMPLEX WITH A BOTTOM NICKED DNA SUBSTRATE	3.1
3C0X	I-SCEI IN COMPLEX WITH A TOP NICKED DNA SUBSTRATE	3.1
3C0Y	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN HISTONE DEACETYLASE HDAC7	3.5.1.98
3C0Z	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN HISTONE DEACETYLASE HDAC7 IN COMPLEX WITH SAHA	3.5.1.98
3C10	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN HISTONE DEACETYLASE HDAC7 IN COMPLEX WITH TRICHOSTATIN A (TSA)	3.5.1.98
3C17	HEXAGONAL CRYSTAL STRUCTURE OF PRECURSOR E. COLI ISOASPARTYL PEPTIDASE/L-ASPARAGINASE (ECAIII) WITH ACTIVE-SITE T179A MUTATION	3.4.19.5 3.5.1.1
3C1E	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L125K AT CRYOGENIC TEMPERATURE	3.1.31.1
3C1F	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS V104K AT CRYOGENIC TEMPERATURE	3.1.31.1
3C1K	CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH INHIBITOR 15	3.4.21.5
3C1U	D192N MUTANT OF RHAMNOGALACTURONAN ACETYLESTERASE	3.1.1 3.1.1.86
3C27	CYANOFLUOROPHENYLACETAMIDES AS ORALLY EFFICACIOUS THROMBIN INHIBITORS	3.4.21.5
3C2T	EVOLUTION OF CHLORELLA VIRUS DUTPASE	3.6.1.23
3C30	CRYSTAL STRUCTURE OF THE VIBRIO CHOLERAE LUXQ PERIPLASMIC DOMAIN (SEMET)	2.7.13.3 3.1.3
3C38	CRYSTAL STRUCTURE OF THE PERIPLASMIC DOMAIN OF VIBRIO CHOLERAE LUXQ	2.7.13.3 3.1.3
3C3I	EVOLUTION OF CHLORELLA VIRUS DUTPASE	3.6.1.23
3C3J	CRYSTAL STRUCTURE OF TAGATOSE-6-PHOSPHATE KETOSE/ALDOSE ISOMERASE FROM ESCHERICHIA COLI	3.5.99
3C41	ABC PROTEIN ARTP IN COMPLEX WITH AMP-PNP/MG2+	3.6.3.21
3C43	HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 IN COMPLEX WITH A FLOUROOLEFIN INHIBITOR	3.4.14.5
3C45	HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 IN COMPLEX WITH A FLUOROOLEFIN INHIBITOR	3.4.14.5
3C4B	STRUCTURE OF RNASEIIIB AND DSRNA BINDING DOMAINS OF MOUSE DICER	3.1.26 3.1.26.3
3C4J	ABC PROTEIN ARTP IN COMPLEX WITH ATP-GAMMA-S	3.6.3.21
3C4O	CRYSTAL STRUCTURE OF THE SHV-1 BETA-LACTAMASE/BETA-LACTAMASE INHIBITOR PROTEIN (BLIP) E73M/S130K/S146M COMPLEX	3.5.2.6
3C4P	CRYSTAL STRUCTURE OF THE SHV-1 BETA-LACTAMASE/BETA-LACTAMASE INHIBITOR PROTEIN (BLIP) E73M COMPLEX	3.5.2.6
3C4T	STRUCTURE OF RNASEIIIB AND DSRNA BINDING DOMAINS OF MOUSE DICER	3.1.26 3.1.26.3
3C58	CRYSTAL STRUCTURE OF A COMPLEX BETWEEN THE WILD-TYPE LACTOCOCCUS LACTIS FPG (MUTM) AND A N7-BENZYL-FAPY-DG CONTAINING DNA	4.2.99.18 3.2.2.23
3C5A	CRYSTAL STRUCTURE OF THE C-TERMINAL DELETED MUTANT OF THE CLASS A CARBAPENEMASE KPC-2 AT 1.23 ANGSTROM	3.5.2.6
3C5C	CRYSTAL STRUCTURE OF HUMAN RAS-LIKE, FAMILY 12 PROTEIN IN COMPLEX WITH GDP	3.6.5.2
3C5K	CRYSTAL STRUCTURE OF HUMAN HDAC6 ZINC FINGER DOMAIN	3.5.1.98 3.5.1
3C5V	PP2A-SPECIFIC METHYLESTERASE APO FORM (PME)	3.1.1.89
3C6B	REACTION PRODUCT OF PARAOXON AND S-FORMYLGLUTATHIONE HYDROLASE W197I MUTANT	3.1.2.12
3C6E	CRYSTAL STRUCTURE OF THE PRECURSOR MEMBRANE PROTEIN- ENVELOPE PROTEIN HETERODIMER FROM THE DENGUE 2 VIRUS AT NEUTRAL PH	3.4.21.91 3.6.1.15 3.6.4.13
3C6T	CRYSTAL STRUCTURE OF HIV REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR 14	2.7.7.49 2.7.7.7 3.4.23.16 3.1.26.13 3.1.13.2 2.7.7 3.1
3C6U	CRYSTAL STRUCTURE OF HIV REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR 22	2.7.7.49 2.7.7.7 3.4.23.16 3.1.26.13 3.1.13.2 2.7.7 3.1
3C7E	CRYSTAL STRUCTURE OF A GLYCOSIDE HYDROLASE FAMILY 43 ARABINOXYLAN ARABINOFURANOHYDROLASE FROM BACILLUS SUBTILIS.	3.2.1.55
3C7F	CRYSTAL STRUCTURE OF A GLYCOSIDE HYDROLASE FAMILY 43 ARABINOXYLAN ARABINOFURANOHYDROLASE FROM BACILLUS SUBTILIS IN COMPLEX WITH XYLOTRIOSE.	3.2.1.55
3C7G	CRYSTAL STRUCTURE OF A GLYCOSIDE HYDROLASE FAMILY 43 ARABINOXYLAN ARABINOFURANOHYDROLASE FROM BACILLUS SUBTILIS IN COMPLEX WITH XYLOTETRAOSE.	3.2.1.55
3C7H	CRYSTAL STRUCTURE OF GLYCOSIDE HYDROLASE FAMILY 43 ARABINOXYLAN ARABINOFURANOHYDROLASE FROM BACILLUS SUBTILIS IN COMPLEX WITH AXOS-4-0.5.	3.2.1.55
3C7O	CRYSTAL STRUCTURE OF A GLYCOSIDE HYDROLASE FAMILY 43 ARABINOXYLAN ARABINOFURANOHYDROLASE FROM BACILLUS SUBTILIS IN COMPLEX WITH CELLOTETRAOSE.	3.2.1.55
3C7T	CRYSTAL STRUCTURE OF THE ECDYSONE PHOSPHATE PHOSPHATASE, EPPASE, FROM BOMBIX MORI IN COMPLEX WITH TUNGSTATE	3.1.3 3.1.3.48
3C7U	STRUCTURAL INSIGHT INTO THE KINETICS AND CP OF INTERACTIONS BETWEEN TEM-1-LACTAMASE AND BLIP	3.5.2.6
3C7V	STRUCTURAL INSIGHT INTO THE KINETICS AND DELTA-CP OF INTERACTIONS BETWEEN TEM-1 BETA-LACTAMASE AND BLIP	3.5.2.6
3C7W	CONTRIBUTIONS OF ALL 20 AMINO ACIDS AT SITE 96 TO THE STABILITY AND STRUCTURE OF T4 LYSOZYME	3.2.1.17
3C7X	HEMOPEXIN-LIKE DOMAIN OF MATRIX METALLOPROTEINASE 14	3.4.24.80
3C7Y	MUTANT R96A OF T4 LYSOZYME IN WILDTYPE BACKGROUND AT 298K	3.2.1.17
3C7Z	T4 LYSOZYME MUTANT D89A/R96H AT ROOM TEMPERATURE	3.2.1.17
3C80	T4 LYSOZYME MUTANT R96Y AT ROOM TEMPERATURE	3.2.1.17
3C81	MUTANT K85A OF T4 LYSOZYME IN WILDTYPE BACKGROUND AT ROOM TEMPERATURE	3.2.1.17
3C82	BACTERIOPHAGE LYSOZYME T4 LYSOZYME MUTANT K85A/R96H	3.2.1.17
3C83	BACTERIOPHAGE T4 LYSOZYME MUTANT D89A IN WILDTYPE BACKGROUND AT ROOM TEMPERATURE	3.2.1.17
3C86	OPDA FROM AGROBACTERIUM RADIOBACTER WITH BOUND PRODUCT DIETHYL THIOPHOSPHATE FROM CRYSTAL SOAKING WITH TETRAETHYL DITHIOPYROPHOSPHATE- 1.8 A	3.1.8.1
3C88	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH INHIBITORY PEPTIDE RRGC	3.4.24.69
3C89	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH INHIBITORY PEPTIDE RRGM	3.4.24.69
3C8A	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH INHIBITORY PEPTIDE RRGL	3.4.24.69
3C8B	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH INHIBITORY PEPTIDE RRGI	3.4.24.69
3C8Q	CONTRIBUTION OF ALL 20 AMINO ACIDS AT SITE 96 TO THE STABILITY AND STRUCTURE OF T4 LYSOZYME	3.2.1.17
3C8R	CONTRIBUTIONS OF ALL 20 AMINO ACIDS AT SITE 96 TO STABILITY AND STRUCTURE OF T4 LYSOZYME	3.2.1.17
3C8S	CONTRIBUTIONS OF ALL 20 AMINO ACIDS AT SITE 96 TO THE STABILITY AND STRUCTURE OF T4 LYSOZYME	3.2.1.17
3C90	THE 1.25 A RESOLUTION STRUCTURE OF PHOSPHORIBOSYL-ATP PYROPHOSPHOHYDROLASE FROM MYCOBACTERIUM TUBERCULOSIS, CRYSTAL FORM II	3.6.1.31
3C94	EXOI/SSB-CT COMPLEX	3.1.11.1
3C95	EXONUCLEASE I (APO)	3.1.11.1
3C9E	CRYSTAL STRUCTURE OF THE CATHEPSIN K : CHONDROITIN SULFATE COMPLEX.	3.4.22.38
3C9Q	CRYSTAL STRUCTURE OF THE UNCHARACTERIZED HUMAN PROTEIN C8ORF32 WITH BOUND PEPTIDE	3.5.1.122
3C9X	CRYSTAL STRUCTURE OF TRICHODERMA REESEI ASPARTIC PROTEINASE	3.4.23.18
3C9Z	SAMBUCUS NIGRA AGGLUTININ II (SNA-II), TETRAGONAL CRYSTAL FORM	3.2.2.22
3CA0	SAMBUCUS NIGRA AGGLUTININ II (SNA-II), HEXAGONAL CRYSTAL FORM	3.2.2.22
3CA1	SAMBUCUS NIGRA AGGLUTININ II (SNA-II)- TETRAGONAL CRYSTAL FORM- COMPLEXED TO GALACTOSE	3.2.2.22
3CA3	CRYSTAL STRUCTURE OF SAMBUCUS NIGRA AGGLUTININ II (SNA-II)-TETRAGONAL CRYSTAL FORM- COMPLEXED TO N-ACETYLGALACTOSAMINE	3.2.2.22
3CA4	SAMBUCUS NIGRA AGGLUTININ II, TETRAGONAL CRYSTAL FORM- COMPLEXED TO LACTOSE	3.2.2.22
3CA5	CRYSTAL STRUCTURE OF SAMBUCUS NIGRA AGGLUTININ II (SNA-II)-TETRAGONAL CRYSTAL FORM- COMPLEXED TO ALPHA1 METHYLGALACTOSE	3.2.2.22
3CA6	SAMBUCUS NIGRA AGGLUTININ II (SNA-II)- TETRAGONAL CRYSTAL FORM- COMPLEXED TO TN ANTIGEN	3.2.2.22
3CA9	EVOLUTION OF CHLORELLA VIRUS DUTPASE	3.6.1.23
3CAE	STRUCTURE OF NNQQNY AS AN INSERT IN T7 ENDONUCLEASE I	3.1.21.2
3CAH	SAMBUCUS NIGRA AGGUTININ II. TETRAGONAL CRYSTAL FORM- COMPLEXED TO FUCOSE	3.2.2.22
3CAK	X-RAY STRUCTURE OF WT PTE WITH ETHYL PHOSPHATE	3.1.8.1
3CB2	CRYSTAL STRUCTURE OF HUMAN GAMMA-TUBULIN BOUND TO GDP	3.6.5.6
3CB7	THE CRYSTALLOGRAPHIC STRUCTURE OF THE DIGESTIVE LYSOZYME 2 FROM MUSCA DOMESTICA AT 1.9 ANG.	3.2.1.17
3CBH	THREE-DIMENSIONAL STRUCTURE OF CELLOBIOHYDROLASE FROM TRICHODERMA REESEI	3.2.1.91
3CBI	CRYSTAL STRUCTURE OF THE TERNARY COMPLEX OF PHOSPHOLIPASE A2 WITH AJMALINE AND ANISIC ACID AT 3.1 A RESOLUTION	3.1.1.4
3CBJ	CHAGASIN-CATHEPSIN B COMPLEX	3.4.22.1
3CBK	CHAGASIN-CATHEPSIN B	3.4.22.1
3CBT	CRYSTAL STRUCTURE OF SC4828, A UNIQUE PHOSPHATASE FROM STREPTOMYCES COELICOLOR	3.1.3.5
3CBW	CRYSTAL STRUCTURE OF THE YDHT PROTEIN FROM BACILLUS SUBTILIS	3.2.1.78
3CC1	CRYSTAL STRUCTURE OF A PUTATIVE ALPHA-N-ACETYLGALACTOSAMINIDASE (BH1870) FROM BACILLUS HALODURANS C-125 AT 2.00 A RESOLUTION	3.2.1.49 3.2.1.22
3CCB	CRYSTAL STRUCTURE OF HUMAN DPP4 IN COMPLEX WITH A BENZIMIDAZOLE DERIVATIVE	3.4.14.5
3CCC	CRYSTAL STRUCTURE OF HUMAN DPP4 IN COMPLEX WITH A BENZIMIDAZOLE DERIVATIVE	3.4.14.5
3CDO	BACTERIOPHAGE T4 LYSOZYME MUTANT R96V IN WILDTYPE BACKGROUND AT LOW TEMPERATURE	3.2.1.17
3CDQ	CONTRIBUTIONS OF ALL 20 AMINO ACIDS AT SITE 96 TO THE STABILITY AND STRUCTURE OF T4 LYSOZYME	3.2.1.17
3CDR	R96Q MUTANT OF WILDTYPE PHAGE T4 LYSOZYME AT 298 K	3.2.1.17
3CDT	CONTRIBUTIONS OF ALL 20 AMINO ACIDS AT SITE 96 TO THE STABILITY AND STRUCTURE OF T4 LYSOZYME	3.2.1.17
3CDU	CRYSTAL STRUCTURE OF COXSACKIEVIRUS B3 RNA-DEPENDENT RNA POLYMERASE (3DPOL) IN COMPLEX WITH A PYROPHOSPHATE	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
3CDV	CONTRIBUTIONS OF ALL 20 AMINO ACIDS AT SITE 96 TO THE STABILITY AND STRUCTURE OF T4 LYSOZYME	3.2.1.17
3CDW	CRYSTAL STRUCTURE OF COXSACKIEVIRUS B3 RNA-DEPENDENT RNA POLYMERASE (3DPOL) IN COMPLEX WITH PROTEIN PRIMER VPG AND A PYROPHOSPHATE	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
3CE6	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE IN TERNARY COMPLEX WITH NAD AND ADENOSINE	3.3.1.1
3CED	CRYSTAL STRUCTURE OF THE C-TERMINAL NIL DOMAIN OF AN ABC TRANSPORTER PROTEIN HOMOLOGUE FROM STAPHYLOCOCCUS AUREUS	3.6.3 7.4.2.11
3CEL	ACTIVE-SITE MUTANT E212Q DETERMINED AT PH 6.0 WITH CELLOBIOSE BOUND IN THE ACTIVE SITE	3.2.1.91
3CEN	FACTOR XA IN COMPLEX WITH THE INHIBITOR N-(2-(((5-CHLORO-2-PYRIDINYL) AMINO)SULFONYL)PHENYL)-4-(2-OXO-1(2H)-PYRIDINYL)BENZAMIDE	3.4.21.6
3CEV	ARGINASE FROM BACILLUS CALDEVELOX, COMPLEXED WITH L-ARGININE	3.5.3.1
3CF1	STRUCTURE OF P97/VCP IN COMPLEX WITH ADP/ADP.ALFX	3.6.4.6
3CF3	STRUCTURE OF P97/VCP IN COMPLEX WITH ADP	3.6.4.6
3CFL	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN C-LOBE OF BOVINE LACTOFERRIN AND 5-CHLORO-6'-METHYL-3-[4-(METHYLSULFONYL)PHENYL]-2,3'-BIPYRIDINE AT 2.25 A RESOLUTION	3.4.21
3CG5	CRYSTAL STRUCTURE OF THE COVALENT ADDUCT FORMED BETWEEN TB B-LACTAMASE AND CLAVULANATE	3.5.2.6
3CG7	CRYSTAL STRUCTURE OF CELL-DEATH RELATED NUCLEASE 4 (CRN-4)	3.1
3CGY	CRYSTAL STRUCTURE OF SALMONELLA SENSOR KINASE PHOQ CATALYTIC DOMAIN IN COMPLEX WITH RADICICOL	2.7.13.3 3.1.3
3CGZ	CRYSTAL STRUCTURE OF SALMONELLA SENSOR KINASE PHOQ CATALYTIC DOMAIN	2.7.13.3 3.1.3
3CH0	CRYSTAL STRUCTURE OF GLYCEROPHOSPHORYL DIESTER PHOSPHODIESTERASE (YP_677622.1) FROM CYTOPHAGA HUTCHINSONII ATCC 33406 AT 1.50 A RESOLUTION	3.1.4.46
3CH2	CRYSTAL STRUCTURE ANALYSIS OF SERA5E FROM PLASMODIUM FALCIPARUM	3.4.22
3CH3	CRYSTAL STRUCTURE ANALYSIS OF SERA5E FROM PLASMODIUM FALCIPARUM	3.4.22
3CH7	CRYSTAL STRUCTURE OF 6-PHOSPHOGLUCONOLACTONASE FROM LEISHMANIA BRAZILIENSIS	3.1.1.17 3.1.1.31
3CH9	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH DIMETHYLGUANYLUREA	3.2.1.14
3CHC	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH MONOPEPTIDE	3.2.1.14
3CHD	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH DIPEPTIDE	3.2.1.14
3CHE	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH TRIPEPTIDE	3.2.1.14
3CHF	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH TETRAPEPTIDE	3.2.1.14
3CHO	CRYSTAL STRUCTURE OF LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH 2-AMINO-N-[4-(PHENYLMETHOXY)PHENYL]-ACETAMIDE	3.3.2.6 3.4.11.4
3CHP	CRYSTAL STRUCTURE OF LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH (3S)-3-AMINO-4-OXO-4-[(4-PHENYLMETHOXYPHENYL)AMINO]BUTANOIC ACID	3.3.2.6 3.4.11.4
3CHQ	CRYSTAL STRUCTURE OF LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH N5-[4-(PHENYLMETHOXY)PHENYL]-L-GLUTAMINE	3.3.2.6 3.4.11.4
3CHR	CRYSTAL STRUCTURE OF LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH 4-AMINO-N-[4-(PHENYLMETHOXY)PHENYL]-BUTANAMIDE	3.3.2.6 3.4.11.4
3CHS	CRYSTAL STRUCTURE OF LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH (2S)-2-AMINO-5-[[4-[(2S)-2-HYDROXY-2-PHENYL-ETHOXY]PHENYL]AMINO]-5-OXO-PENTANOIC ACID	3.3.2.6 3.4.11.4
3CI8	CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF LACTOFERRIN WITH VITAMIN B3 (NIACIN) AT 2.4 A RESOLUTION	3.4.21
3CIA	CRYSTAL STRUCTURE OF COLD-AMINOPEPTIDASE FROM COLWELLIA PSYCHRERYTHRAEA	3.4.11 3.4.11.2
3CIB	STRUCTURE OF BACE BOUND TO SCH727596	3.4.23.46
3CIC	STRUCTURE OF BACE BOUND TO SCH709583	3.4.23.46
3CID	STRUCTURE OF BACE BOUND TO SCH726222	3.4.23.46
3CIV	CRYSTAL STRUCTURE OF THE ENDO-BETA-1,4-MANNANASE FROM ALICYCLOBACILLUS ACIDOCALDARIUS	3.2.1.78
3CIZ	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE NS5B IN COMPLEX WITH SMALL MOLECULE FRAGMENTS	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CJ0	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE NS5B IN COMPLEX WITH SMALL MOLECULE FRAGMENTS	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CJ1	STRUCTURE OF RATTUS NORVEGICUS NTPDASE2	3.6.1.5 3.6.1
3CJ2	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE NS5B IN COMPLEX WITH OPTIMIZED SMALL MOLECULE FRAGMENTS	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CJ3	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE NS5B IN COMPLEX WITH OPTIMIZED SMALL MOLECULE FRAGMENTS	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CJ4	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE NS5B IN COMPLEX WITH OPTIMIZED SMALL MOLECULE FRAGMENTS	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CJ5	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE NS5B IN COMPLEX WITH OPTIMIZED SMALL MOLECULE FRAGMENTS	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CJ7	STRUCTURE OF RATTUS NORVEGICUS NTPDASE2 IN COMPLEX WITH AMP	3.6.1.5 3.6.1
3CJ9	STRUCTURE OF RATTUS NORVEGICUS NTPDASE2 IN COMPLEX WITH CALCIUM, AMP AND PHOSPHATE	3.6.1.5 3.6.1
3CJA	STRUCTURE OF RATTUS NORVEGICUS NTPDASE2 IN COMPLEX WITH CALCIUM AND AMPPNP	3.6.1.5 3.6.1
3CK2	CRYSTAL STRUCTURE OF CONSERVED UNCHARACTERIZED PROTEIN (PREDICTED PHOSPHOESTERASE COG0622) FROM STREPTOCOCCUS PNEUMONIAE TIGR4	3.1.4
3CKI	CRYSTAL STRUCTURE OF THE TACE-N-TIMP-3 COMPLEX	3.4.24.86
3CKP	CRYSTAL STRUCTURE OF BACE-1 IN COMPLEX WITH INHIBITOR	3.4.23.46
3CKR	CRYSTAL STRUCTURE OF BACE-1 IN COMPLEX WITH INHIBITOR	3.4.23.46
3CKT	HIV-1 PROTEASE IN COMPLEX WITH A DIMETHYLALLYL DECORATED PYRROLIDINE BASED INHIBITOR (ORTHOROMBIC 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
3CKZ	N1 NEURAMINIDASE H274Y + ZANAMIVIR	3.2.1.18
3CL0	N1 NEURAMINIDASE H274Y + OSELTAMIVIR	3.2.1.18
3CL4	CRYSTAL STRUCTURE OF BOVINE CORONAVIRUS HEMAGGLUTININ-ESTERASE	3.1.1.53
3CL5	STRUCTURE OF CORONAVIRUS HEMAGGLUTININ-ESTERASE IN COMPLEX WITH 4,9-O-DIACETYL SIALIC ACID	3.1.1.53
3CL6	CRYSTAL STRUCTURE OF PUUE ALLANTOINASE	3.5.2.5
3CL7	CRYSTAL STRUCTURE OF PUUE ALLANTOINASE IN COMPLEX WITH HYDANTOIN	3.5.2.5
3CL8	CRYSTAL STRUCTURE OF PUUE ALLANTOINASE COMPLEXED WITH ACA	3.5.2.5
3CLV	CRYSTAL STRUCTURE OF RAB5A FROM PLASMODIUM FALCIPARUM, PFB0500C	3.6.5.2
3CM3	HIGH RESOLUTION CRYSTAL STRUCTURE OF THE VACCINIA VIRUS DUAL-SPECIFICITY PHOSPHATASE VH1	3.1.3.48 3.1.3
3CM5	CRYSTAL STRUCTURE OF CELL-DEATH RELATED NUCLEASE 4 (CRN-4) BOUND WITH MN	3.1
3CM6	CRYSTAL STRUCTURE OF CELL-DEATH RELATED NUCLEASE 4 (CRN-4) BOUND WITH ER	3.1
3CM8	A RNA POLYMERASE SUBUNIT STRUCTURE FROM VIRUS	3.1
3CMD	CRYSTAL STRUCTURE OF PEPTIDE DEFORMYLASE FROM VRE-E.FAECIUM	3.5.1.88
3CMJ	CRYSTAL STRUCTURE OF ENGINEERED BETA-GLUCOSIDASE FROM SOIL METAGENOME	3.2.1.21
3CMR	E. COLI ALKALINE PHOSPHATASE MUTANT R166S IN COMPLEX WITH PHOSPHATE	3.1.3.1
3CMS	ENGINEERING ENZYME SUB-SITE SPECIFICITY: PREPARATION, KINETIC CHARACTERIZATION AND X-RAY ANALYSIS AT 2.0-ANGSTROMS RESOLUTION OF VAL111PHE SITE-MUTATED CALF CHYMOSIN	3.4.23.4
3CMZ	TEM-1 CLASS-A BETA-LACTAMASE L201P MUTANT APO STRUCTURE	3.5.2.6
3CN7	CRYSTAL STRUCTURE ANALYSIS OF THE CARBOXYLESTERASE PA3859 FROM PSEUDOMONAS AERUGINOSA PAO1- MONOCLINIC CRYSTAL FORM	3.1.1.1
3CN9	CRYSTAL STRUCTURE ANALYSIS OF THE CARBOXYLESTERASE PA3859 FROM PSEUDOMONAS AERUGINOSA PAO1- ORTHORHOMBIC CRYSTAL FORM	3.1.1.1
3CNQ	PROSUBTILISIN SUBSTRATE COMPLEX OF SUBTILISIN SUBT_BACAM	3.4.21.62
3CO0	SUBSTRATE COMPLEX OF FLUORIDE-SENSITIVE ENGINEERED SUBTILISIN SUBT_BACAM	3.4.21.62
3CO9	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL PYRIDAZINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CON	CRYSTAL STRUCTURE OF THE HUMAN NRAS GTPASE BOUND WITH GDP	3.6.5.2
3COU	CRYSTAL STRUCTURE OF HUMAN NUDIX MOTIF 16 (NUDT16)	3.6.1 3.6.1.62 3.6.1.64
3CP7	CRYSTAL STRUCTURE OF A THERMOSTABLE SERINE PROTEASE AL20 FROM EXTREMOPHILIC MICROOGANISM	3.4.21.1
3CPA	X-RAY CRYSTALLOGRAPHIC INVESTIGATION OF SUBSTRATE BINDING TO CARBOXYPEPTIDASE A AT SUBZERO TEMPERATURE	3.4.17.1
3CPE	CRYSTAL STRUCTURE OF T4 GP17	3.6.4 3.1.21
3CPM	PLANT PEPTIDE DEFORMYLASE PDF1B CRYSTAL STRUCTURE	3.5.1.88
3CPU	SUBSITE MAPPING OF THE ACTIVE SITE OF HUMAN PANCREATIC ALPHA-AMYLASE USING SUBSTRATES, THE PHARMACOLOGICAL INHIBITOR ACARBOSE, AND AN ACTIVE SITE VARIANT	3.2.1.1
3CQ8	TERNARY COMPLEX OF THE L415F MUTANT RB69 EXO(-)POLYMERASE	2.7.7.7 3.1.11
3CQB	CRYSTAL STRUCTURE OF HEAT SHOCK PROTEIN HTPX DOMAIN FROM VIBRIO PARAHAEMOLYTICUS RIMD 2210633	3.4.24
3CQL	CRYSTAL STRUCTURE OF GH FAMILY 19 CHITINASE FROM CARICA PAPAYA	3.2.1.14
3CR9	CRYSTAL STRUCTURE OF THE COMPLEX OF LACTOFERRIN WITH 6-(HYDROXYMETHYL)OXANE-2,3,4,5-TETROL AT 3.49 A RESOLUTION	3.4.21
3CRA	CRYSTAL STRUCTURE OF ESCHERICHIA COLI MAZG, THE REGULATOR OF NUTRITIONAL STRESS RESPONSE	3.6.1.8
3CRB	CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF LACTOFERRIN WITH 2-CHROMENONE AT 2.6 A RESOLUTION	3.4.21
3CRC	CRYSTAL STRUCTURE OF ESCHERICHIA COLI MAZG, THE REGULATOR OF NUTRITIONAL STRESS RESPONSE	3.6.1.8
3CRV	XPD_HELICASE	3 3.6.4.12
3CRW	XPD_APO	3 3.6.4.12
3CS0	CRYSTAL STRUCTURE OF DEGP24	3.4.21.107
3CS2	CRYSTAL STRUCTURE OF PTE G60A MUTANT	3.1.8.1
3CS7	FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-(4-METHOXYPHENYL)-6-(4-(1-(PYRROLIDIN-1-YLMETHYL)CYCLOPROPYL)PHENYL)-3-(TRIFLUOROMETHYL)-5,6-DIHYDRO-1H-PYRAZOLO[3,4-C]PYRIDIN-7(4H)-ONE	3.4.21.6
3CSK	STRUCTURE OF DPP III FROM SACCHAROMYCES CEREVISIAE	3.4.14.4
3CSO	HCV POLYMERASE IN COMPLEX WITH A 1,5 BENZODIAZEPINE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CSS	CRYSTAL STRUCTURE OF 6-PHOSPHOGLUCONOLACTONASE FROM LEISHMANIA GUYANENSIS	3.1.1.17 3.1.1.31
3CTK	CRYSTAL STRUCTURE OF THE TYPE 1 RIP BOUGANIN	3.2.2.22
3CTR	CRYSTAL STRUCTURE OF THE RRM-DOMAIN OF THE POLY(A)-SPECIFIC RIBONUCLEASE PARN BOUND TO M7GTP	3.1.13.4
3CTT	CRYSTAL COMPLEX OF N-TERMINAL HUMAN MALTASE-GLUCOAMYLASE WITH CASUARINE	3.2.1.20 3.2.1.3
3CTZ	STRUCTURE OF HUMAN CYTOSOLIC X-PROLYL AMINOPEPTIDASE	3.4.11.9
3CU9	HIGH RESOLUTION CRYSTAL STRUCTURE OF 1,5-ALPHA-L-ARABINANASE FROM GEOBACILLUS STEAROTHERMOPHILUS	3.2.1.99
3CUF	CELLULOMONAS FIMI XYLANASE/CELLULASE CEX (CF XYN10A) IN COMPLEX WITH CELLOBIOSE-LIKE ISOFAGOMINE	3.2.1.91 3.2.1.8
3CUG	CELLULOMONAS FIMI XYLANASE/CELLULASE CEX (CF XYN10A) IN COMPLEX WITH CELLOTETRAOSE-LIKE ISOFAGOMINE	3.2.1.91 3.2.1.8
3CUH	CELLULOMONAS FIMI XYLANASE/CELLULASE CEX (CF XYN10A) IN COMPLEX WITH CELLOTRIOSE-LIKE ISOFAGOMINE	3.2.1.91 3.2.1.8
3CUI	CELLULOMONAS FIMI XYLANASE/CELLULASE CEX (CF XYN10A) IN COMPLEX WITH SULFUR SUBSTITUTED BETA-1,4 XYLOTETRAOSE	3.2.1.91 3.2.1.8
3CUJ	CELLULOMONAS FIMI XYLANASE/CELLULASE CEX (CF XYN10A) IN COMPLEX WITH SULFUR SUBSTITUTED BETA-1,4 XYLOPENTAOSE.	3.2.1.91 3.2.1.8
3CV5	GOLGI MANNOSIDASE II D204A CATALYTIC NUCLEOPHILE MUTANT COMPLEX WITH 3ALPHA,6ALPHA-MANNOPENTAOSE	3.2.1.114
3CVK	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL PYRIDAZINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3CVS	CRYSTAL STRUCTURE OF AN ALKA HOST/GUEST COMPLEX 8OXOGUANINE:ADENINE BASE PAIR	3.2.2.21
3CVT	CRYSTAL STRUCTURE OF AN ALKA HOST/GUEST COMPLEX 8OXOGUANINE:CYTOSINE BASE PAIR	3.2.2.21
3CW7	CRYSTAL STRUCTURE OF AN ALKA HOST/GUEST COMPLEX 8OXOGUANINE:CYTOSINE BASE PAIR	3.2.2.21
3CWA	CRYSTAL STRUCTURE OF AN ALKA HOST/GUEST COMPLEX 8OXOGUANINE:CYTOSINE BASE PAIR	3.2.2.21
3CWE	PTP1B IN COMPLEX WITH A PHOSPHONIC ACID INHIBITOR	3.1.3.48
3CWS	CRYSTAL STRUCTURE OF AN ALKA HOST/GUEST COMPLEX 2'-FLUORO-2'-DEOXYINOSINE:THYMINE BASE PAIR	3.2.2.21
3CWT	CRYSTAL STRUCTURE OF AN ALKA HOST/GUEST COMPLEX 2'-FLUORO-2'-DEOXYINOSINE:ADENINE BASE PAIR	3.2.2.21
3CWU	CRYSTAL STRUCTURE OF AN ALKA HOST/GUEST COMPLEX 2'-FLUORO-2'-DEOXY-1,N6-ETHENOADENINE:THYMINE BASE PAIR	3.2.2.21
3CWW	CRYSTAL STRUCTURE OF IDE-BRADYKININ COMPLEX	3.4.24.56
3CXM	LEISHMANIA NAIFFI URACIL-DNA GLYCOSYLASE IN COMPLEX WITH 5-BROMOURACIL	3.2.2 3.2.2.27
3CXU	STRUCTURE OF A Y149F MUTANT OF EPOXIDE HYDROLASE FROM SOLANUM TUBEROSUM	3.3.2.10
3CY6	CRYSTAL STRUCTURE OF E18Q DJ-1	3.1.2 3.5.1 3.5.1.124
3CYE	CYRSTAL STRUCTURE OF THE NATIVE 1918 H1N1 NEURAMINIDASE FROM A CRYSTAL WITH LATTICE-TRANSLOCATION DEFECTS	3.2.1.18
3CYF	CRYSTAL STRUCTURE OF E18N DJ-1	3.1.2 3.5.1 3.5.1.124
3CYW	EFFECT OF FLAP MUTATIONS ON STRUCTURE OF HIV-1 PROTEASE AND INHIBITION BY SAQUINAVIR AND DARUNAVIR	3.4.23.16
3CYX	CRYSTAL STRUCTURE OF HIV-1 MUTANT I50V AND INHIBITOR SAQUINAVIRA	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
3CZ4	NATIVE APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE FROM E. COLI	3.1.3.2
3CZ8	CRYSTAL STRUCTURE OF PUTATIVE SPORULATION-SPECIFIC GLYCOSYLASE YDHD FROM BACILLUS SUBTILIS	3.2
3CZ9	CRYSTAL STRUCTURE OF E18L DJ-1	3.1.2 3.5.1 3.5.1.124
3CZA	CRYSTAL STRUCTURE OF E18D DJ-1	3.1.2 3.5.1 3.5.1.124
3CZD	CRYSTAL STRUCTURE OF HUMAN GLUTAMINASE IN COMPLEX WITH L-GLUTAMATE	3.5.1.2
3CZE	CRYSTAL STRUCTURE ANALYSIS OF SUCROSE HYDROLASE (SUH)- TRIS COMPLEX	3.2.1.48
3CZG	CRYSTAL STRUCTURE ANALYSIS OF SUCROSE HYDROLASE (SUH)-GLUCOSE COMPLEX	3.2.1.48
3CZK	CRYSTAL STRUCTURE ANALYSIS OF SUCROSE HYDROLASE(SUH) E322Q-SUCROSE COMPLEX	3.2.1.48
3CZL	CRYSTAL STRUCTURE ANALYSIS OF SUCROSE HYDROLASE(SUH) E322Q-GLUCOSE COMPLEX	3.2.1.48
3CZN	GOLGI ALPHA-MANNOSIDASE II (D204A NUCLEOPHILE MUTANT) IN COMPLEX WITH GNMAN5GN	3.2.1.114
3CZS	GOLGI ALPHA-MANNOSIDASE II (D204A NUCLEOPHILE MUTANT)	3.2.1.114
3CZX	THE CRYSTAL STRUCTURE OF THE PUTATIVE N-ACETYLMURAMOYL-L-ALANINE AMIDASE FROM NEISSERIA MENINGITIDIS	3.5.1.28
3D03	1.9A STRUCTURE OF GLYCEROPHOSHPHODIESTERASE (GPDQ) FROM ENTEROBACTER AEROGENES	3.1.4.46 3.1.4.53
3D0F	STRUCTURE OF THE BIG_1156.2 DOMAIN OF PUTATIVE PENICILLIN-BINDING PROTEIN MRCA FROM NITROSOMONAS EUROPAEA ATCC 19718	2.4.2 2.4.1.129 3.4.16.4
3D0G	CRYSTAL STRUCTURE OF SPIKE PROTEIN RECEPTOR-BINDING DOMAIN FROM THE 2002-2003 SARS CORONAVIRUS HUMAN STRAIN COMPLEXED WITH HUMAN-CIVET CHIMERIC RECEPTOR ACE2	3.4.17.23 3.4.17
3D0H	CRYSTAL STRUCTURE OF SPIKE PROTEIN RECEPTOR-BINDING DOMAIN FROM THE 2002-2003 SARS CORONAVIRUS CIVET STRAIN COMPLEXED WITH HUMAN-CIVET CHIMERIC RECEPTOR ACE2	3.4.17.23 3.4.17
3D0I	CRYSTAL STRUCTURE OF SPIKE PROTEIN RECEPTOR-BINDING DOMAIN FROM THE 2005-2006 SARS CORONAVIRUS CIVET STRAIN COMPLEXED WITH HUMAN-CIVET CHIMERIC RECEPTOR ACE2	3.4.17.23 3.4.17
3D0P	INSIGHTS INTO RNA/DNA HYBRID RECOGNITION AND PROCESSING BY RNASE H FROM THE CRYSTAL STRUCTURE OF A NON-SPECIFIC ENZYME-DSDNA COMPLEX	3.1.26.4
3D11	CRYSTAL STRUCTURES OF THE NIPAH G ATTACHMENT GLYCOPROTEIN	3.2.1.18
3D1R	STRUCTURE OF E. COLI GLPX WITH ITS SUBSTRATE FRUCTOSE 1,6-BISPHOSPHATE	3.1.3.11
3D1X	CRYSTAL STRUCTURE OF HIV-1 MUTANT I54M AND INHIBITOR SAQUINAVIR	3.4.23.16
3D1Y	CRYSTAL STRUCTURE OF HIV-1 MUTANT I54V AND INHIBITOR SAQUINA	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
3D1Z	CRYSTAL STRUCTURE OF HIV-1 MUTANT I54M AND INHIBITOR DARUNAVIR	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
3D20	CRYSTAL STRUCTURE OF HIV-1 MUTANT I54V AND INHIBITOR DARUNAVIA	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
3D23	MAIN PROTEASE OF HCOV-HKU1	3.4.22 3.4.19.12 3.4.22.69
3D27	E. COLI METHIONINE AMINOPEPTIDASE WITH FE INHIBITOR W29	3.4.11.18
3D28	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL BENZISOTHIAZOLE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3D2A	STRUCTURE OF 1-17A4, A THERMOSTABLE MUTANT OF BACILLUS SUBTILIS LIPASE OBTAINED THROUGH DIRECTED EVOLUTION	3.1.1.3
3D2B	STRUCTURE OF 2D9, A THERMOSTABLE MUTANT OF BACILLUS SUBTILIS LIPASE OBTAINED THROUGH DIRECTED EVOLUTION	3.1.1.3
3D2O	CRYSTAL STRUCTURE OF MANGANESE-METALLATED GTP CYCLOHYDROLASE TYPE IB	3.5.4.16
3D2Y	COMPLEX OF THE N-ACETYLMURAMYL-L-ALANINE AMIDASE AMID FROM E.COLI WITH THE SUBSTRATE ANHYDRO-N-ACETYLMURAMIC ACID-L-ALA-D-GAMMA-GLU-L-LYS	3.5.1.28
3D2Z	COMPLEX OF THE N-ACETYLMURAMYL-L-ALANINE AMIDASE AMID FROM E.COLI WITH THE PRODUCT L-ALA-D-GAMMA-GLU-L-LYS	3.5.1.28
3D3D	BACTERIOPHAGE LAMBDA LYSOZYME COMPLEXED WITH A CHITOHEXASACCHARIDE	3.2.1.17 4.2.2
3D3H	CRYSTAL STRUCTURE OF A COMPLEX OF THE PEPTIDOGLYCAN GLYCOSYLTRANSFERASE DOMAIN FROM AQUIFEX AEOLICUS AND NERYL MOENOMYCIN A	2.4.2 2.4.1.129 3.4.16.4
3D3I	CRYSTAL STRUCTURAL OF ESCHERICHIA COLI K12 YGJK, A GLUCOSIDASE BELONGING TO GLYCOSIDE HYDROLASE FAMILY 63	3.2.1
3D3L	THE 2.6 A CRYSTAL STRUCTURE OF THE LIPOXYGENASE DOMAIN OF HUMAN ARACHIDONATE 12-LIPOXYGENASE, 12S-TYPE (CASP TARGET)	1.13.11.31 1.13.11 1.13.11.33 3.3.2
3D3P	CRYSTAL STRUCTURE OF PDE4B CATALYTIC DOMAIN IN COMPLEX WITH A PYRAZOLOPYRIDINE INHIBITOR	3.1.4.17 3.1.4.53
3D3T	CRYSTAL STRUCTURE OF HIV-1 CRF01_AE IN COMPLEX WITH THE SUBSTRATE P1-P6	3.4.23.16
3D3Z	CRYSTAL STRUCTURE OF ACTIBIND A T2 RNASE	3.1.27.1 4.6.1.19
3D42	CRYSTAL STRUCTURE OF HEPTP IN COMPLEX WITH A MONOPHOSPHORYLATED ERK2 PEPTIDE	3.1.3.48
3D44	CRYSTAL STRUCTURE OF HEPTP IN COMPLEX WITH A DUALLY PHOSPHORYLATED ERK2 PEPTIDE MIMETIC	3.1.3.48
3D45	CRYSTAL STRUCTURE OF MOUSE PARN IN COMPLEX WITH M7GPPPG	3.1.13.4
3D49	THROMBIN INHIBITION	3.4.21.5
3D4B	CRYSTAL STRUCTURE OF SIR2TM IN COMPLEX WITH ACETYL P53 PEPTIDE AND DADME-NAD+	3.5.1 2.3.1.286
3D4D	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS Y91E AT CRYOGENIC TEMPERATURE	3.1.31.1
3D4F	SHV-1 BETA-LACTAMASE COMPLEX WITH LN1-255	3.5.2.6
3D4L	HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 IN COMPLEX WITH A NOVEL INHIBITOR	3.4.14.5
3D4S	CHOLESTEROL BOUND FORM OF HUMAN BETA2 ADRENERGIC RECEPTOR.	3.2.1.17
3D4U	BOVINE THROMBIN-ACTIVATABLE FIBRINOLYSIS INHIBITOR (TAFIA) IN COMPLEX WITH TICK-DERIVED CARBOXYPEPTIDASE INHIBITOR.	3.4.17.20
3D4V	CRYSTAL STRUCTURE OF AN ALKA HOST/GUEST COMPLEX N7METHYLGUANINE:CYTOSINE BASE PAIR	3.2.2.21
3D4W	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS A109R AT CRYOGENIC TEMPERATURE	3.1.31.1
3D4Y	GOLGI MANNOSIDASE II COMPLEX WITH MANNOIMIDAZOLE	3.2.1.114
3D4Z	GOLGI MANNOSIDASE II COMPLEX WITH GLUCO-IMIDAZOLE	3.2.1.114
3D50	GOLGI MANNOSIDASE II COMPLEX WITH N-OCTYL-6-EPI-VALIENAMINE	3.2.1.114
3D51	GOLGI MANNOSIDASE II COMPLEX WITH GLUCO-HYDROXYIMINOLACTAM	3.2.1.114
3D52	GOLGI MANNOSIDASE II COMPLEX WITH AN N-ARYL CARBAMATE DERIVATIVE OF GLUCO-HYDROXYIMINOLACTAM	3.2.1.114
3D53	2.2 A CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM RICKETTSIA PROWAZEKII	3.6.1.1
3D59	CRYSTAL STRUCTURE OF HUMAN PLASMA PLATELET ACTIVATING FACTOR ACETYLHYDROLASE	3.1.1.47
3D5E	CRYSTAL STRUCTURE OF HUMAN PLASMA PLATELET ACTIVATING FACTOR ACETYLHYDROLASE COVALENTLY INHIBITED BY PARAOXON	3.1.1.47
3D5M	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL PYRIDAZINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3D5Y	HIGH RESOLUTION CRYSTAL STRUCTURE OF 1,5-ALPHA-ARABINANASE CATALYTIC MUTANT (ABNBE201A)	3.2.1.99
3D5Z	CRYSTAL STRUCTURE ANALYSIS OF 1,5-ALPHA-ARABINANASE CATALYTIC MUTANT (ABNBE201A) COMPLEXED TO ARABINOTRIOSE	3.2.1.99
3D60	CRYSTAL STRUCTURE ANALYSIS OF 1,5-ALPHA-ARABINANASE CATALYTIC MUTANT (D27A)	3.2.1.99
3D61	CRYSTAL STRUCTURE ANALYSIS OF 1,5-ALPHA-ARABINANASE CATALYTIC MUTANT (ABNBD147A) COMPLEXED TO ARABINOBIOSE	3.2.1.99
3D62	DEVELOPMENT OF BROAD-SPECTRUM HALOMETHYL KETONE INHIBITORS AGAINST CORONAVIRUS MAIN PROTEASE 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
3D63	CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM BURKHOLDERIA PSEUDOMALLEI	3.6.1.1
3D64	CRYSTAL STRUCTURE OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE FROM BURKHOLDERIA PSEUDOMALLEI	3.3.1.1
3D65	CRYSTAL STRUCTURE OF TEXTILININ-1, A KUNITZ-TYPE SERINE PROTEASE INHIBITOR FROM THE AUSTRALIAN COMMON BROWN SNAKE VENOM, IN COMPLEX WITH TRYPSIN	3.4.21.4
3D66	CRYSTAL STRUCTURE OF THROMBIN-ACTIVATABLE FIBRINOLYSIS INHIBITOR (TAFI)	3.4.17.20
3D67	CRYSTAL STRUCTURE OF THROMBIN-ACTIVATABLE FIBRINOLYSIS INHIBITOR (TAFI) IN COMPLEX WITH 2-GUANIDINO-ETHYL-MERCAPTOSUCCINIC ACID (GEMSA)	3.4.17.20
3D68	CRYSTAL STRUCTURE OF A T325I/T329I/H333Y/H335Q MUTANT OF THROMBIN-ACTIVATABLE FIBRINOLYSIS INHIBITOR (TAFI-IIYQ)	3.4.17.20
3D6C	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT PHS L38E AT CRYOGENIC TEMPERATURE	3.1.31.1
3D6E	CRYSTAL STRUCTURE OF THE ENGINEERED 1,3-1,4-BETA-GLUCANASE PROTEIN FROM BACILLUS LICHENIFORMIS	3.2.1.73
3D6F	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 WITH A NATURALLY-OCCURRING ARG240->GLN SUBSTITUTION IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK)	3.4.22.36
3D6H	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 WITH A NATURALLY-OCCURRING ASN263->SER SUBSTITUTION IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK)	3.4.22.36
3D6M	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 WITH A NATURALLY-OCCURRING LYS319->ARG SUBSTITUTION IN COMPLEX WITH 3-[2-(2-BENZYLOXYCARBONYLAMINO-3-METHYL-BUTYRYLAMINO)-PROPIONYLAMINO]-4-OXO-PENTANOIC ACID (Z-VAD-FMK)	3.4.22.36
3D6N	CRYSTAL STRUCTURE OF AQUIFEX DIHYDROOROTASE ACTIVATED BY ASPARTATE TRANSCARBAMOYLASE	3.5.2.3
3D6O	THE RNASE A- 5'-DEOXY-5'-N-(ETHYL ISONIPECOTATYL)URIDINE COMPLEX	3.1.27.5 4.6.1.18
3D6P	RNASE A- 5'-DEOXY-5'-N-MORPHOLINOURIDINE COMPLEX	3.1.27.5 4.6.1.18
3D6Q	THE RNASE A- 5'-DEOXY-5'-N-PIPERIDINOURIDINE COMPLEX	3.1.27.5 4.6.1.18
3D6S	CRYSTAL STRUCTURE OF MITE ALLERGEN DER F 1	3.4.22.65
3D6T	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
3D7B	THE RIBONUCLEASE A- 5'-DEOXY-5'-N-PYRROLIDINOURIDINE COMPLEX	3.1.27.5 4.6.1.18
3D7D	A HIGH RESOLUTION CRYSTAL STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN A COMPLEX WITH DCFBD, A UREA-BASED INHIBITOR	3.4.17.21
3D7F	A HIGH RESOLUTION CRYSTAL STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN A COMPLEX WITH DCIT, A UREA-BASED INHIBITOR	3.4.17.21
3D7G	A HIGH RESOLUTION CRYSTAL STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN A COMPLEX WITH DCMC, A UREA-BASED INHIBITOR	3.4.17.21
3D7H	A HIGH RESOLUTION CRYSTAL STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN A COMPLEX WITH DCIBZL, A UREA-BASED INHIBITOR	3.4.17.21
3D7R	CRYSTAL STRUCTURE OF A PUTATIVE ESTERASE FROM STAPHYLOCOCCUS AUREUS	3.1
3D7W	MISTLETOE LECTIN I IN COMPLEX WITH ZEATIN	3.2.2.22
3D81	SIR2-S-ALKYLAMIDATE COMPLEX CRYSTAL STRUCTURE	3.5.1 2.3.1.286
3D8B	CRYSTAL STRUCTURE OF HUMAN FIDGETIN-LIKE PROTEIN 1 IN COMPLEX WITH ADP	3.6.4
3D8G	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS I72R AT CRYOGENIC TEMPERATURE	3.1.31.1
3D8Y	RNASE A- 5'-DEOXY-5'-N-PIPERIDINOTHYMIDINE COMPLEX	3.1.27.5 4.6.1.18
3D8Z	RNASE A- 5'-DEOXY-5'-N-PYRROLIDINOTHYMIDINE COMPLEX	3.1.27.5 4.6.1.18
3D91	HUMAN RENIN IN COMPLEX WITH REMIKIREN	3.4.23.15
3D9A	HIGH RESOLUTION CRYSTAL STRUCTURE STRUCTURE OF HYHEL10 FAB COMPLEXED TO HEN EGG LYSOZYME	3.2.1.17
3D9C	CRYSTAL STRUCTURE PTP1B COMPLEX WITH ARYL SELENINIC ACID	3.1.3.48
3D9Q	PROTEINASE K BY LB NANOTEMPLATE METHOD BEFORE HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DA7	A CONFORMATIONALLY STRAINED, CIRCULAR PERMUTANT OF BARNASE	3.1.27
3DA9	CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH INHIBITOR	3.4.21.5
3DAI	CRYSTAL STRUCTURE OF THE BROMODOMAIN OF THE HUMAN ATAD2	3.6.1
3DBA	CRYSTAL STRUCTURE OF THE CGMP-BOUND GAF A DOMAIN FROM THE PHOTORECEPTOR PHOSPHODIESTERASE 6C	3.1.4.35
3DBK	PSEUDOMONAS AERUGINOSA ELASTASE WITH PHOSPHORAMIDON	3.4.24.26
3DC0	CRYSTAL STRUCTURE OF NATIVE ALPHA-AMYLASE FROM BACILLUS SP. KR-8104	3.2.1.1
3DC8	CRYSTAL STRUCTURE OF DIHYDROPYRIMIDINASE FROM SINORHIZOBIUM MELILOTI	3.5.2.2
3DCK	X-RAY STRUCTURE OF D25N CHEMICAL ANALOGUE OF HIV-1 PROTEASE COMPLEXED WITH KETOMETHYLENE ISOSTERE INHIBITOR	3.4.23.16
3DCN	GLOMERELLA CINGULATA APO CUTINASE	3.1.1.74
3DCP	CRYSTAL STRUCTURE OF THE PUTATIVE HISTIDINOL PHOSPHATASE HISK FROM LISTERIA MONOCYTOGENES. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET LMR141.	3.1.3.15
3DCR	X-RAY STRUCTURE OF HIV-1 PROTEASE AND HYDRATED FORM OF KETOMETHYLENE ISOSTERE INHIBITOR	3.4.23.16
3DCY	CRYSTAL STRUCTURE A TP53-INDUCED GLYCOLYSIS AND APOPTOSIS REGULATOR PROTEIN FROM HOMO SAPIENS.	3.1.3.46
3DD5	GLOMERELLA CINGULATA E600-CUTINASE COMPLEX	3.1.1.74
3DDA	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH A SNAP-25 PEPTIDE	3.4.24.69
3DDB	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH A SUBSTRATE ANALOG PEPTIDE	3.4.24.69
3DDC	CRYSTAL STRUCTURE OF NORE1A IN COMPLEX WITH RAS	3.6.5.2
3DDF	GOLGI MANNOSIDASE II COMPLEX WITH (3R,4R,5R)-3,4-DIHYDROXY-5-({[(1R)-2-HYDROXY-1 PHENYLETHYL]AMINO}METHYL) PYRROLIDIN-2-ONE	3.2.1.114
3DDG	GOLGI MANNOSIDASE II COMPLEX WITH (3R,4R,5R)-3,4-DIHYDROXY-5-({[(1R)-2-HYDROXY-1 PHENYLETHYL]AMINO}METHYL) METHYLPYRROLIDIN-2-ONE	3.2.1.114
3DDK	COXSACKIEVIRUS B3 3DPOL RNA DEPENDENT RNA POLYMERASE	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3DDU	PROLYL OLIGOPEPTIDASE WITH GSK552	3.4.21.26
3DDZ	PROTEINASE K BY LB NANOTEMPLATE METHOD AFTER THE FIRST STEP OF HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DE0	PROTEINASE K BY LB NANOTEMPLATE METHOD AFTER THE SECOND STEP OF HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DE1	PROTEINASE K BY LB NANOTEMPLATE METHOD AFTER THE THIRD STEP OF HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DE2	PROTEINASE K BY LB NANOTEMPLATE METHOD AFTER THE FOURTH STEP OF HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DE3	PROTEINASE K BY CLASSICAL HANGING DROP METHOD BEFORE HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DE4	PROTEINASE K BY CLASSICAL HANGING DROP METHOD AFTER THE FIRST STEP OF HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DE5	ROTEINASE K BY CLASSICAL HANGING DROP METHOD AFTER THE SECOND STEP OF HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DE6	PROTEINASE K BY CLASSICAL HANGING DROP METHOD AFTER THE THIRD STEP OF HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DE7	PROTEINASE K BY CLASSICAL HANGING DROP METHOD AFTER THE FOURTH STEP OF HIGH X-RAY DOSE ON ESRF ID23-1 BEAMLINE	3.4.21.64
3DEA	GLOMERELLA CINGULATA PETFP-CUTINASE COMPLEX	3.1.1.74
3DEB	CRYSTAL STRUCTURE OF APO FORM (ZINC REMOVED) OF THE BOTULINUM NEUROTOXIN TYPE C LIGHT CHAIN	3.4.24.69
3DEC	CRYSTAL STRUCTURE OF A GLYCOSYL HYDROLASES FAMILY 2 PROTEIN FROM BACTEROIDES THETAIOTAOMICRON	3.2.1.23
3DEF	CRYSTAL STRUCTURE OF TOC33 FROM ARABIDOPSIS THALIANA, DIMERIZATION DEFICIENT MUTANT R130A	3.6.5.2 3.6.5
3DEH	CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3,4-TRIONE DERIVATIVE INHIBITORS	3.4.22.56
3DEI	CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3,4-TRIONE DERIVATIVE INHIBITORS	3.4.22.56
3DEJ	CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3,4-TRIONE DERIVATIVE INHIBITORS	3.4.22.56
3DEK	CRYSTAL STRUCTURES OF CASPASE-3 WITH BOUND ISOQUINOLINE-1,3,4-TRIONE DERIVATIVE INHIBITORS	3.4.22.56
3DEM	CUB1-EGF-CUB2 DOMAIN OF HUMAN MASP-1/3	3.4.21
3DF0	CALCIUM-DEPENDENT COMPLEX BETWEEN M-CALPAIN AND CALPASTATIN	3.4.22.53
3DF9	CRYSTAL STRUCTURE OF E. COLI MTA/SAH NUCLEOSIDASE IN COMPLEX WITH BNT-DADMEIMMA	3.2.2.9
3DFJ	CRYSTAL STRUCTURE OF HUMAN PROSTASIN	3.4.21
3DFL	CRYSTAL STRUCTURE OF HUMAN PROSTASIN COMPLEXED TO 4-GUANIDINOBENZOIC ACID	3.4.21
3DGT	THE 1.5 A CRYSTAL STRUCTURE OF ENDO-1,3-BETA-GLUCANASE FROM STREPTOMYCES SIOYAENSIS	3.2.1.39
3DGV	CRYSTAL STRUCTURE OF THROMBIN ACTIVATABLE FIBRINOLYSIS INHIBITOR (TAFI)	3.4.17.20
3DH1	CRYSTAL STRUCTURE OF HUMAN TRNA-SPECIFIC ADENOSINE-34 DEAMINASE SUBUNIT ADAT2	3.5.4 3.5.4.33
3DH5	CRYSTAL STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE A (WILD-TYPE)	3.1.27.5 4.6.1.18
3DH6	CRYSTAL STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE A VARIANT (V47A)	3.1.27.5 4.6.1.18
3DH8	STRUCTURE OF PSEUDOMONAS QUINOLONE SIGNAL RESPONSE PROTEIN PQSE	3.1.2.32
3DHA	AN ULTRAL HIGH RESOLUTION STRUCTURE OF N-ACYL HOMOSERINE LACTONE HYDROLASE WITH THE PRODUCT N-HEXANOYL-L-HOMOSERINE BOUND AT AN ALTERNATIVE SITE	3.1.1 3.1.1.81
3DHB	1.4 ANGSTROM STRUCTURE OF N-ACYL HOMOSERINE LACTONE HYDROLASE WITH THE PRODUCT N-HEXANOYL-L-HOMOSERINE BOUND AT THE CATALYTIC METAL CENTER	3.1.1 3.1.1.81
3DHC	1.3 ANGSTROM STRUCTURE OF N-ACYL HOMOSERINE LACTONE HYDROLASE WITH THE PRODUCT N-HEXANOYL-L-HOMOCYSTEINE BOUND TO THE CATALYTIC METAL CENTER	3.1.1 3.1.1.81
3DHK	BISPHENYLIC THROMBIN INHIBITORS	3.4.21.5
3DHP	PROBING THE ROLE OF AROMATIC RESIDUES AT THE SECONDARY SACCHARIDE BINDING SITES OF HUMAN SALIVARY ALPHA-AMYLASE IN SUBSTRATE HYDROLYSIS AND BACTERIAL BINDING	3.2.1.1
3DHQ	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS A90R AT CRYOGENIC TEMPERATURE	3.1.31.1
3DHU	CRYSTAL STRUCTURE OF AN ALPHA-AMYLASE FROM LACTOBACILLUS PLANTARUM	3.2.1.1
3DHX	CRYSTAL STRUCTURE OF ISOLATED C2 DOMAIN OF THE METHIONINE UPTAKE TRANSPORTER	3.6.3 7.4.2.11
3DHY	CRYSTAL STRUCTURES OF MYCOBACTERIUM TUBERCULOSIS S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE IN TERNARY COMPLEX WITH SUBSTRATE AND INHIBITORS	3.3.1.1
3DI6	HIV-1 RT WITH PYRIDAZINONE NON-NUCLEOSIDE 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
3DI7	CRYSTAL STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE A VARIANT (V54A)	3.1.27.5 4.6.1.18
3DI8	CRYSTAL STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE A VARIANT (V57A)	3.1.27.5 4.6.1.18
3DI9	CRYSTAL STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE A VARIANT (I81A)	3.1.27.5 4.6.1.18
3DIB	CRYSTAL STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE A VARIANT (I106A)	3.1.27.5 4.6.1.18
3DIC	CRYSTAL STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE A VARIANT (V108A)	3.1.27.5 4.6.1.18
3DJ8	SYNTHESIS OF (2S)-2-AMINO-7,8-EPOXYOCTANOIC ACID AND STRUCTURE OF ITS METAL-BRIDGING COMPLEX WITH HUMAN ARGINASE I	3.5.3.1
3DJK	WILD TYPE HIV-1 PROTEASE WITH POTENT ANTIVIRAL INHIBITOR GRL-0255A	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
3DJO	BOVINE SEMINAL RIBONUCLEASE URIDINE 2' PHOSPHATE COMPLEX	3.1.27.5 4.6.1.18
3DJP	BOVINE SEMINAL RIBONUCLEASE- URIDINE 3' PHOSPHATE COMPLEX	3.1.27.5 4.6.1.18
3DJQ	BOVINE SEMINAL RIBONUCLEASE- URIDINE 5' DIPHOSPHATE COMPLEX	3.1.27.5 4.6.1.18
3DJV	BOVINE SEMINAL RIBONUCLEASE- CYTIDINE 3' PHOSPHATE COMPLEX	3.1.27.5 4.6.1.18
3DJX	BOVINE SEMINAL RIBONUCLEASE- CYTIDINE 5' PHOSPHATE COMPLEX	3.1.27.5 4.6.1.18
3DJY	NONAGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN	3.1.1.8
3DK1	WILD TYPE HIV-1 PROTEASE WITH POTENT ANTIVIRAL INHIBITOR GRL-0105A	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
3DKB	CRYSTAL STRUCTURE OF A20, 2.5 ANGSTROM	3 2.3.2 3.4.19.12
3DKE	POLAR AND NON-POLAR CAVITIES IN PHAGE T4 LYSOZYME	3.2.1.17
3DKK	AGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN	3.1.1.8
3DKP	HUMAN DEAD-BOX RNA-HELICASE DDX52, CONSERVED DOMAIN I IN COMPLEX WITH ADP	3.6.1 3.6.4.13
3DKT	CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA ENCAPSULIN	3.4
3DKU	CRYSTAL STRUCTURE OF NUDIX HYDROLASE ORF153, YMFB, FROM ESCHERICHIA COLI K-1	3.6.1
3DL4	NON-AGED FORM OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY TABUN- UPDATE	3.1.1.7
3DL7	AGED FORM OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY TABUN- UPDATE	3.1.1.7
3DLE	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GF128590.	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
3DLG	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW564511.	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
3DLJ	CRYSTAL STRUCTURE OF HUMAN CARNOSINE DIPEPTIDASE 1	3.4.13.20
3DLK	CRYSTAL STRUCTURE OF AN ENGINEERED FORM OF THE HIV-1 REVERSE TRANSCRIPTASE, RT69A	2.7.7.49 2.7.7.7 3.4.23.16 3.1.26.13 3.1.13.2 2.7.7 3.1
3DLR	CRYSTAL STRUCTURE OF THE CATALYTIC CORE DOMAIN FROM PFV INTEGRASE	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3DM2	CRYSTAL STRUCTURE OF HIV-1 K103N MUTANT REVERSE TRANSCRIPTASE IN COMPLEX WITH GW564511.	2.7.7.49 2.7.7.7 3.1.26.4 3.1.13.2 3.1.26.13
3DM6	BETA-SECRETASE 1 COMPLEXED WITH STATINE-BASED INHIBITOR	3.4.23.46
3DMJ	CRYSTAL STRUCTURE OF HIV-1 V106A AND Y181C MUTANT REVERSE TRANSCRIPTASE IN COMPLEX WITH GW564511.	2.7.7.49 2.7.7.7 3.1.26.4 3.1.13.2 3.1.26.13
3DMN	THE CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF A POSSILBE DNA HELICASE FROM LACTOBACILLUS PLANTARUN WCFS1	3.6.4.12
3DMO	1.6 A CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE FROM BURKHOLDERIA PSEUDOMALLEI	3.5.4.5
3DMU	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT PHS T62K AT CRYOGENIC TEMPERATURE	3.1.31.1
3DMV	FREE OF LIGAND BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DMX	BENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DMZ	HEXAFLUOROBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DN0	PENTAFLUOROBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DN1	CHLOROPENTAFLUOROBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DN2	BROMOPENTAFLUOROBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DN3	IODOPENTAFLUOROBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DN4	IODOBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DN6	1,3,5-TRIFLUORO-2,4,6-TRICHLOROBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT	3.2.1.17
3DN8	IODOPENTAFLUOROBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT (SELENO VERSION)	3.2.1.17
3DNA	IODOBENZENE BINDING IN THE HYDROPHOBIC CAVITY OF T4 LYSOZYME L99A MUTANT (SELENO VERSION)	3.2.1.17
3DNG	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MMP-8 AND A NON-ZINC CHELATING INHIBITOR	3.4.24.34
3DNI	CRYSTALLOGRAPHIC REFINEMENT AND STRUCTURE OF DNASE I AT 2 ANGSTROMS RESOLUTION	3.1.21.1
3DNM	CRYSTAL STRUCTURE HORMONE-SENSITIVE LIPASE FROM A METAGENOME LIBRARY	3.1.1
3DNZ	THERMOLYSIN BY LB NANOTEMPLATE METHOD BEFORE HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.4.24.27
3DO0	THERMOLYSIN BY CLASSICAL HANGING DROP METHOD AFTER HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.4.24.27
3DO1	THERMOLYSIN BY CLASSICAL HANGING DROP METHOD BEFORE HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.4.24.27
3DO2	THERMOLYSIN BY LB NANOTEMPLATE METHOD AFTER HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.4.24.27
3DOH	CRYSTAL STRUCTURE OF A THERMOSTABLE ESTERASE	3.1.1.1
3DOI	CRYSTAL STRUCTURE OF A THERMOSTABLE ESTERASE COMPLEX WITH PARAOXON	3.1.1.1
3DOK	CRYSTAL STRUCTURE OF K103N MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW678248.	2.7.7.49 2.7.7.7 3.1.26.4 3.1.13.2 3.1.26.13
3DOL	CRYSTAL STRUCTURE OF L100I MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW695634.	2.7.7.49 2.7.7.7 3.1.26.4 3.1.13.2 3.1.26.13
3DOX	X-RAY STRUCTURE OF HIV-1 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
3DP9	CRYSTAL STRUCTURE OF VIBRIO CHOLERAE 5'-METHYLTHIOADENOSINE/S-ADENOSYL HOMOCYSTEINE NUCLEOSIDASE (MTAN) COMPLEXED WITH BUTYLTHIO-DADME-IMMUCILLIN A	3.2.2.9
3DPC	STRUCTURE OF E.COLI ALKALINE PHOSPHATASE MUTANT IN COMPLEX WITH A PHOSPHORYLATED PEPTIDE	3.1.3.1
3DPE	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MMP-8 AND A NON-ZINC CHELATING INHIBITOR	3.4.24.34
3DPF	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MMP-8 AND A NON-ZINC CHELATING INHIBITOR	3.4.24.34
3DPG	SGRAI WITH NONCOGNATE DNA BOUND	3.1.21.4
3DPH	HIV-1 CAPSID C-TERMINAL DOMAIN MUTANT (L211S)	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
3DPR	HUMAN RHINOVIRUS 2 BOUND TO A CONCATAMER OF THE VLDL RECEPTOR MODULE V3	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3DR2	STRUCTURAL AND FUNCTIONAL ANALYSES OF XC5397 FROM XANTHOMONAS CAMPESTRIS: A GLUCONOLACTONASE IMPORTANT IN GLUCOSE SECONDARY METABOLIC PATHWAYS	3.1.1.17
3DRP	HIV REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR R8E	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
3DRR	HIV REVERSE TRANSCRIPTASE Y181C MUTANT IN COMPLEX WITH INHIBITOR R8E	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
3DRS	HIV REVERSE TRANSCRIPTASE K103N MUTANT IN COMPLEX WITH INHIBITOR R8D	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
3DS0	HIV-1 CAPSID C-TERMINAL DOMAIN MUTANT (N183A) IN COMPLEX WITH AN INHIBITOR OF PARTICLE ASSEMBLY (CAI)	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
3DS1	HIV-1 CAPSID C-TERMINAL DOMAIN MUTANT (E187A) IN COMPLEX WITH AN INHIBITOR OF PARTICLE ASSEMBLY (CAI)	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
3DS2	HIV-1 CAPSID C-TERMINAL DOMAIN MUTANT (Y169A)	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
3DS3	HIV-1 CAPSID C-TERMINAL DOMAIN MUTANT (Y169A) IN COMPLEX WITH AN INHIBITOR OF PARTICLE ASSEMBLY (CAI)	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
3DS4	HIV-1 CAPSID C-TERMINAL DOMAIN MUTANT (L211S) IN COMPLEX WITH AN INHIBITOR OF PARTICLE ASSEMBLY (CAI)	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
3DS5	HIV-1 CAPSID C-TERMINAL DOMAIN MUTANT (N183A)	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
3DS9	A POTENT PEPTIDOMIMETIC INHIBITOR OF BOTULINUM NEUROTOXIN SEROTYPE A HAS A VERY DIFFERENT CONFORMATION THAN SNAP-25 SUBSTRATE	3.4.24.69
3DSC	CRYSTAL STRUCTURE OF P. FURIOSUS MRE11 DNA SYNAPTIC COMPLEX	3.1
3DSD	CRYSTAL STRUCTURE OF P. FURIOSUS MRE11-H85S BOUND TO A BRANCHED DNA AND MANGANESE	3.1
3DSE	A POTENT PEPTIDOMIMETIC INHIBITOR OF BOTULINUM NEUROTOXIN SEROTYPE A HAS A VERY DIFFERENT CONFORMATION THAN SNAP-25 SUBSTRATE	3.4.24.69
3DSL	THE THREE-DIMENSIONAL STRUCTURE OF BOTHROPASIN, THE MAIN HEMORRHAGIC FACTOR FROM BOTHROPS JARARACA VENOM.	3.4.24.49
3DSR	ADP IN TRANSITION BINDING SITE IN THE SUBUNIT B OF THE ENERGY CONVERTER A1AO ATP SYNTHASE	3.6.3.14
3DT0	UNDERSTANDING THROMBIN INHIBITION	3.4.21.5
3DT6	CRYSTAL STRUCTURE OF BOVIN BRAIN PLATELET ACTIVATING FACTOR ACETYLHYDROLASE COVALENTLY INHIBITED BY PARAOXON	3.1.1.47
3DT8	CRYSTAL STRUCTURE OF BOVIN BRAIN PLATELET ACTIVATING FACTOR ACETYLHYDROLASE COVALENTLY INHIBITED BY SARIN	3.1.1.47
3DT9	CRYSTAL STRUCTURE OF BOVIN BRAIN PLATELET ACTIVATING FACTOR ACETYLHYDROLASE COVALENTLY INHIBITED BY SOMAN	3.1.1.47
3DTE	CRYSTAL STRUCTURE OF THE IRRE PROTEIN, A CENTRAL REGULATOR OF DNA DAMAGE REPAIR IN DEINOCOCCACEAE	3.4.24
3DTI	CRYSTAL STRUCTURE OF THE IRRE PROTEIN, A CENTRAL REGULATOR OF DNA DAMAGE REPAIR IN DEINOCOCCACEAE	3.4.24
3DTJ	HIV-1 CAPSID C-TERMINAL DOMAIN MUTANT (E187A)	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
3DTK	CRYSTAL STRUCTURE OF THE IRRE PROTEIN, A CENTRAL REGULATOR OF DNA DAMAGE REPAIR IN DEINOCOCCACEAE	3.4.24
3DTM	INCREASED FOLDING STABILITY OF TEM-1 BETA-LACTAMASE BY IN-VITRO SELECTION	3.5.2.6
3DUX	UNDERSTANDING THROMBIN INHIBITION	3.4.21.5
3DUY	CRYSTAL STRUCTURE OF HUMAN BETA-SECRETASE IN COMPLEX WITH NVP-AFJ144	3.4.23.46
3DV1	CRYSTAL STRUCTURE OF HUMAN BETA-SECRETASE IN COMPLEX WITH NVP-ARV999	3.4.23.46
3DV5	CRYSTAL STRUCTURE OF HUMAN BETA-SECRETASE IN COMPLEX WITH NVP-BAV544	3.4.23.46
3DVO	SGRAI WITH COGNATE DNA AND CALCIUM BOUND	3.1.21.4
3DVQ	PROTEINASE K BY LB NANOTEMPLATE METHOD BEFORE HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.4.21.64
3DVR	PROTEINASE K BY LB NANOTEMPLATE METHOD AFTER THE FIRST STEP OF HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.4.21.64
3DVS	PROTEINASE K BY LB NANOTMPLATE METHOD AFTER THE SECOND STEP OF HIGH DOSE ON ESRF ID14-2 BEAMLINE	3.4.21.64
3DW0	CRYSTAL STRUCTURE OF THE CLASS A CARBAPENEMASE KPC-2 AT 1.6 ANGSTROM RESOLUTION	3.5.2.6
3DW1	PROTEINASE K BY LB NANOTEMPLATE METHOD AFTER THE THIRD STEP HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.4.21.64
3DW3	PROTEINASE K BY CLASSICAL HANGING DROP METHOD BEFORE HIGH X RAY DOSE ON ESRF ID 14-2 BEAMLINE	3.4.21.64
3DW9	SGRAI WITH COGNATE DNA AND MANGANESE BOUND	3.1.21.4
3DWB	STRUCTURE OF HUMAN ECE-1 COMPLEXED WITH PHOSPHORAMIDON	3.4.24.71
3DWC	TRYPANOSOMA CRUZI METALLOCARBOXYPEPTIDASE 1	3.4.17.19
3DWE	PROTEINASE K BY CLASSICAL HANGING DROP METHOD AFTER HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.4.21.64
3DWK	IDENTIFICATION OF DYNAMIC STRUCTURAL MOTIFS INVOLVED IN PEPTIDOGLYCAN GLYCOSYLTRANSFER	2.4.1.129 3.4.16.4
3DWZ	MEROPENEM COVALENT ADDUCT WITH TB BETA-LACTAMASE	3.5.2.6
3DX0	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH MANNOSTATIN A AT PH 5.75	3.2.1.114
3DX1	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH MANNOSTATIN ANALOG (1S,2S,3R,4R)-4-AMINOCYCLOPENTANE-1,2,3-TRIOL	3.2.1.114
3DX2	GOLGI MANNOSIDASE II COMPLEX WITH MANNOSTATIN B	3.2.1.114
3DX3	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH MANNOSTATIN ANALOG (1R,2R,3S,4R,5R)-5-AMINOCYCLOPENTANE-1,2,3,4-TETRAOL	3.2.1.114
3DX4	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH MANNOSTATIN ANALOG (1R,2R,3R,4S,5R)-4-AMINO-5-METHOXYCYCLOPENTANE-1,2,3-TRIOL	3.2.1.114
3DXG	RIBONUCLEASE A- URIDINE 5' PHOSPHATE COMPLEX	3.1.27.5 4.6.1.18
3DXH	RIBONUCLEASE A URIDINE 5' DIPHOSPHATE COMPLEX	3.1.27.5 4.6.1.18
3DXS	CRYSTAL STRUCTURE OF A COPPER BINDING DOMAIN FROM HMA7, A P-TYPE ATPASE	3.6.3.4 7.2.2.8
3DY8	HUMAN PHOSPHODIESTERASE 9 IN COMPLEX WITH PRODUCT 5'-GMP (E+P COMPLEX)	3.1.4.35
3DYA	HIV-1 RT WITH NON-NUCLEOSIDE INHIBITOR ANNULATED PYRAZOLE 1	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
3DYB	PROTEINASE K- DIGALACTURONIC ACID COMPLEX	3.4.21.64
3DYC	STRUCTURE OF E322Y ALKALINE PHOSPHATASE IN COMPLEX WITH INORGANIC PHOSPHATE	3.1.3.1
3DYL	HUMAN PHOSPHDIESTERASE 9 SUBSTRATE COMPLEX (ES COMPLEX)	3.1.4.35
3DYM	E. COLI (LACZ) BETA-GALACTOSIDASE (H418E)	3.2.1.23
3DYN	HUMAN PHOSPHODIESTRASE 9 IN COMPLEX WITH CGMP (ZN INHIBITED)	3.1.4.35
3DYQ	HUMAN PHOSPHODIESTRASE 9 (INHIBITED BY OMITTING DIVALENT CATION) IN COMPLEX WITH CGMP	3.1.4.35
3DYS	HUMAN PHOSPHODIESTRASE-5'GMP COMPLEX (EP), PRODUCED BY SOAKING WITH 20MM CGMP+20 MM MNCL2+20 MM MGCL2 FOR 2 HOURS, AND FLASH-COOLED TO LIQUID NITROGEN TEMPERATURE WHEN SUBSTRATE WAS STILL ABUDANT.	3.1.4.35
3DZE	CRYSTAL STRUCTURE OF BOVINE COUPLING FACTOR B BOUND WITH CADMIUM	3.6.3.14
3DZF	CRYSTAL STRUCTURE OF HUMAN CD38 EXTRACELLULAR DOMAIN COMPLEXED WITH A COVALENT INTERMEDIATE, ARA-F-RIBOSE-5'-PHOSPHATE	3.2.2.5 3.2.2.6 2.4.99.20
3DZG	CRYSTAL STRUCTURE OF HUMAN CD38 EXTRACELLULAR DOMAIN, ARA-F-RIBOSE-5'-PHOSPHATE/NICOTINAMIDE COMPLEX	3.2.2.5 3.2.2.6 2.4.99.20
3DZH	CRYSTAL STRUCTURE OF HUMAN CD38 EXTRACELLULAR DOMAIN, GTP COMPLEX	3.2.2.5 3.2.2.6 2.4.99.20
3DZI	CRYSTAL STRUCTURE OF HUMAN CD38 EXTRACELLULAR DOMAIN, RIBOSE-5'-PHOSPHATE INTERMEDIATE/GTP COMPLEX	3.2.2.5 3.2.2.6 2.4.99.20
3DZJ	CRYSTAL STRUCTURE OF HUMAN CD38 EXTRACELLULAR DOMAIN E226Q MUTANT, NMN COMPLEX	3.2.2.5 3.2.2.6 2.4.99.20
3DZK	CRYSTAL STRUCTURE OF HUMAN CD38 EXTRACELLULAR DOMAIN, NMN COMPLEX	3.2.2.5 3.2.2.6 2.4.99.20
3E01	HIV-RT WITH NON-NUCLEOSIDE INHIBITOR ANNULATED PYRAZOLE 2	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
3E0L	COMPUTATIONALLY DESIGNED AMMELIDE DEAMINASE	3.5.4.3
3E0N	THE X-RAY STRUCTURE OF HUMAN PROSTASIN IN COMPLEX WITH DFFR-CHLOROMETHYL KETONE INHIBITOR	3.4.21
3E0P	THE X-RAY STRUCTURE OF HUMAN PROSTASIN IN COMPLEX WITH A COVALENT BENZOXAZOLE INHIBITOR	3.4.21
3E15	6-PHOSPHOGLUCONOLACTONASE FROM PLASMODIUM VIVAX	3.1.1.31
3E16	X-RAY STRUCTURE OF HUMAN PROSTASIN IN COMPLEX WITH BENZOXAZOLE WARHEAD PEPTIDOMIMIC, LYSINE IN P3	3.4.21
3E1S	STRUCTURE OF AN N-TERMINAL TRUNCATION OF DEINOCOCCUS RADIODURANS RECD2	3.6.4.12
3E1U	THE CRYSTAL STRUCTURE OF THE ANTI-VIRAL APOBEC3G CATALYTIC DOMAIN	3.5.4
3E1X	THE CRYSTAL STRUCTURE OF APO PROSTASIN AT 1.7 ANGSTROMS RESOLUTION	3.4.21
3E2D	THE 1.4 A CRYSTAL STRUCTURE OF THE LARGE AND COLD-ACTIVE VIBRIO SP. ALKALINE PHOSPHATASE	3.1.3.1
3E2J	CRYSTAL STRUCTURE OF BOVINE COUPLING FACTOR B	3.6.3.14
3E2K	CRYSTAL STRUCTURE OF THE KPC-2 BETA-LACTAMASE/BETA-LACTAMASE INHIBITOR PROTEIN (BLIP)	3.5.2.6
3E2L	CRYSTAL STRUCTURE OF THE KPC-2 BETA-LACTAMASE/BETA-LACTAMASE INHIBITOR PROTEIN (BLIP)	3.5.2.6
3E3D	STRUCTURE OF HEN EGG WHITE LYSOZYME WITH THE MAGIC TRIANGLE I3C	3.2.1.17
3E3H	CRYSTAL STRUCTURE OF THE OP HYDROLASE MUTANT FROM BREVUNDIMONAS DIMINUTA	3.1.8.1
3E3T	STRUCTURE OF PORCINE PANCREATIC ELASTASE WITH THE MAGIC TRIANGLE I3C	3.4.21.36
3E3U	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PEPTIDE DEFORMYLASE IN COMPLEX WITH INHIBITOR	3.5.1.88
3E3Z	CRYSTAL STRUCTURE OF BOVINE COUPLING FACTOR B BOUND WITH PHENYLARSINE OXIDE	3.6.3.14
3E4A	HUMAN IDE-INHIBITOR COMPLEX AT 2.6 ANGSTROM RESOLUTION	3.4.24.56
3E4C	PROCASPASE-1 ZYMOGEN DOMAIN CRYSTAL STRUCTURE	3.4.22.36
3E4D	STRUCTURAL AND KINETIC STUDY OF AN S-FORMYLGLUTATHIONE HYDROLASE FROM AGROBACTERIUM TUMEFACIENS	3.1.2.12
3E4G	CRYSTAL STRUCTURE OF BOVINE COUPLING FACTOR B, G28E MUTANT	3.6.3.14
3E4Z	CRYSTAL STRUCTURE OF HUMAN INSULIN DEGRADING ENZYME IN COMPLEX WITH INSULIN-LIKE GROWTH FACTOR II	3.4.24.56
3E51	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL PYRIDAZINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3E54	ARCHAEAL INTRON-ENCODED HOMING ENDONUCLEASE I-VDI141I COMPLEXED WITH DNA	3.1
3E5S	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L103K AT CRYOGENIC TEMPERATURE	3.1.31.1
3E6K	X-RAY STRUCTURE OF HUMAN ARGINASE I: THE MUTANT D183A IN COMPLEX WITH ABH	3.5.3.1
3E6P	CRYSTAL STRUCTURE OF HUMAN MEIZOTHROMBIN DESF1	3.4.21.5
3E6V	X-RAY STRUCTURE OF HUMAN ARGINASE I-D183N MUTANT: THE COMPLEX WITH ABH	3.5.3.1
3E74	CRYSTAL STRUCTURE OF E. COLI ALLANTOINASE WITH IRON IONS AT THE METAL CENTER	3.5.2.5
3E7A	CRYSTAL STRUCTURE OF PROTEIN PHOSPHATASE-1 BOUND TO THE NATURAL TOXIN NODULARIN-R	3.1.3.16
3E7B	CRYSTAL STRUCTURE OF PROTEIN PHOSPHATASE-1 BOUND TO THE NATURAL TOXIN INHIBITOR TAUTOMYCIN	3.1.3.16
3E7F	CRYSTAL STRUCTURE OF 6-PHOSPHOGLUCONOLACTONASE FROM TRYPANOSOMA BRUCEI COMPLEXED WITH 6-PHOSPHOGLUCONIC ACID	3.1.1.17 3.1.1.31
3E81	STRUCTURE-FUNCTION ANALYSIS OF 2-KETO-3-DEOXY-D-GLYCERO-D-GALACTO-NONONATE-9-PHOSPHATE (KDN) PHOSPHATASE DEFINES A NEW CLAD WITHIN THE TYPE C0 HAD SUBFAMILY	3.1.3.103
3E84	STRUCTURE-FUNCTION ANALYSIS OF 2-KETO-3-DEOXY-D-GLYCERO-D-GALACTO-NONONATE-9-PHOSPHATE (KDN) PHOSPHATASE DEFINES A NEW CLAD WITHIN THE TYPE C0 HAD SUBFAMILY	3.1.3.103
3E85	CRYSTAL STRUCTURE OF PATHOGENESIS-RELATED PROTEIN LLPR-10.2B FROM YELLOW LUPINE IN COMPLEX WITH DIPHENYLUREA	3.1.27
3E8L	THE CRYSTAL STRUCTURE OF THE DOUBLE-HEADED ARROWHEAD PROTEASE INHIBITOR A IN COMPLEX WITH TWO TRYPSINS	3.4.21.4
3E8M	STRUCTURE-FUNCTION ANALYSIS OF 2-KETO-3-DEOXY-D-GLYCERO-D-GALACTO-NONONATE-9-PHOSPHATE (KDN) PHOSPHATASE DEFINES A NEW CLAD WITHIN THE TYPE C0 HAD SUBFAMILY	3.1.3.103
3E8Q	X-RAY STRUCTURE OF RAT ARGINASE I-T135A: THE UNLIGANDED COMPLEX	3.5.3.1
3E8R	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH HYDROXAMATE INHIBITOR	3.4.24.86
3E8Z	X-RAY STRUCTURE OF RAT ARGINASE I-N130A MUTANT: THE UNLIGANDED COMPLEX	3.5.3.1
3E90	WEST NILE VI RUS NS2B-NS3PROTEASE IN COMPLEXED WITH INHIBITOR NAPH-KKR-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
3E91	CRYSTAL STRUCTURE OF SARS-COV MPRO MUTANT IN P21 AT PH6.9	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
3E9B	X-RAY STRUCTURE OF RAT ARGINASE I-T135A MUTANT: THE COMPLEX WITH BEC	3.5.3.1
3E9C	STRUCTURE OF A TRYPTIC CORE FRAGMENT OF TIGAR FROM DANIO RERIO	3.1.3.46
3E9D	STRUCTURE OF FULL-LENGTH TIGAR FROM DANIO RERIO	3.1.3.46
3E9E	STRUCTURE OF FULL-LENGTH H11A MUTANT FORM OF TIGAR FROM DANIO RERIO	3.1.3.46
3E9K	CRYSTAL STRUCTURE OF HOMO SAPIENS KYNURENINASE-3-HYDROXYHIPPURIC ACID INHIBITOR COMPLEX	3.7.1.3
3E9S	A NEW CLASS OF PAPAIN-LIKE PROTEASE/DEUBIQUITINASE INHIBITORS BLOCKS SARS VIRUS REPLICATION	3.4.22 3.4.19.12 3.4.22.69
3E9X	CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF LACTOFERRIN WITH NIMESULIDE AT 2.7 A RESOLUTION	3.4.21
3EA7	CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE TRIPLE MUTANT STI/A IN 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
3EA8	CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE TRIPLE MUTANT STI/A IN SPACE GROUP C2	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
3EA9	CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE QUADRUPLE MUTANT STIF/A WITH ONE MOLECULE IN ONE ASYMMETRIC UNIT	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
3EAJ	CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE QUADRUPLE MUTANT STIF/A WITH TWO MOLECULES IN ONE ASYMMETRIC UNIT	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
3EAX	CRYSTAL STRUCTURE PTP1B COMPLEX WITH SMALL MOLECULE COMPOUND LZP-6	3.1.3.48
3EAY	CRYSTAL STRUCTURE OF THE HUMAN SENP7 CATALYTIC DOMAIN	3.4.22
3EB1	CRYSTAL STRUCTURE PTP1B COMPLEX WITH SMALL MOLECULE INHIBITOR LZP-25	3.1.3.48
3EB8	VIRA	3.4.22
3EB9	CRYSTAL STRUCTURE OF 6-PHOSPHOGLUCONOLACTONASE FROM TRYPANOSOMA BRUCEI COMPLEXED WITH CITRATE	3.1.1.17 3.1.1.31
3EBC	STRUCTURE OF N141A HINCII WITH COGNATE DNA	3.1.21.4
3EBG	STRUCTURE OF THE M1 ALANYLAMINOPEPTIDASE FROM MALARIA	3.4.11
3EBH	STRUCTURE OF THE M1 ALANYLAMINOPEPTIDASE FROM MALARIA COMPLEXED WITH BESTATIN	3.4.11
3EBI	STRUCTURE OF THE M1 ALANYLAMINOPEPTIDASE FROM MALARIA COMPLEXED WITH THE PHOSPHINATE DIPEPTIDE ANALOG	3.4.11
3EBJ	CRYSTAL STRUCTURE OF AN AVIAN INFLUENZA VIRUS PROTEIN	3.1
3EBL	CRYSTAL STRUCTURE OF RICE GID1 COMPLEXED WITH GA4	3
3EBN	A SPECIAL DIMERIZATION OF SARS-COV MAIN PROTEASE C-TERMINAL DOMAIN DUE TO DOMAIN-SWAPPING	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
3EBQ	CRYSTAL STRUCTURE OF HUMAN PPPDE1	3.4.22 3.4
3EBZ	HIGH RESOLUTION HIV-2 PROTEASE STRUCTURE IN COMPLEX WITH CLINICAL DRUG DARUNAVIR	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
3EC0	HIGH RESOLUTION HIV-2 PROTEASE STRUCTURE IN COMPLEX WITH ANTIVIRAL INHIBITOR GRL-06579A	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
3ECA	CRYSTAL STRUCTURE OF ESCHERICHIA COLI L-ASPARAGINASE, AN ENZYME USED IN CANCER THERAPY (ELSPAR)	3.5.1.1
3ECG	HIGH RESOLUTION HIV-2 PROTEASE STRUCTURE IN COMPLEX WITH ANTIVIRAL INHIBITOR GRL-98065	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
3ECM	CRYSTAL STRUCTURE OF THE UNLIGANDED PDE8A CATALYTIC DOMAIN	3.1.4.17 3.1.4.53
3ECN	CRYSTAL STRUCTURE OF PDE8A CATALYTIC DOMAIN IN COMPLEX WITH IBMX	3.1.4.17 3.1.4.53
3ECP	CRYSTAL STRUCTURE OF TN5 TRANSPOSASE COMPLEXED WITH 5' PHOSPHORYLATED TRANSPOSON END DNA	3.1
3ECY	CRYSTAL STRUCTURAL ANALYSIS OF DROSOPHILA MELANOGASTER DUTPASE	3.6.1.23
3ED1	CRYSTAL STRUCTURE OF RICE GID1 COMPLEXED WITH GA3	3
3ED5	THE CRYSTAL STRUCTURE OF YFNB FROM BACILLUS SUBTILIS SUBSP. SUBTILIS STR. 168	3
3EDD	STRUCTURAL BASE FOR CYCLODEXTRIN HYDROLYSIS	3.2.1.54
3EDE	STRUCTURAL BASE FOR CYCLODEXTRIN HYDROLYSIS	3.2.1.54
3EDF	STRUCTURAL BASE FOR CYCLODEXTRIN HYDROLYSIS	3.2.1.54
3EDG	CRYSTAL STRUCTURE OF BONE MORPHOGENETIC PROTEIN 1 PROTEASE DOMAIN	3.4.24.19
3EDH	CRYSTAL STRUCTURE OF BONE MORPHOGENETIC PROTEIN 1 PROTEASE DOMAIN IN COMPLEX WITH PARTIALLY BOUND DMSO	3.4.24.19
3EDI	CRYSTAL STRUCTURE OF TOLLOID-LIKE PROTEASE 1 (TLL-1) PROTEASE DOMAIN	3.4.24
3EDJ	STRUCTURAL BASE FOR CYCLODEXTRIN HYDROLYSIS	3.2.1.54
3EDK	STRUCTURAL BASE FOR CYCLODEXTRIN HYDROLYSIS	3.2.1.54
3EDQ	CRYSTAL STRUCTURE OF CASPASE-3 WITH INHIBITOR AC-LDESD-CHO	3.4.22.56
3EDR	THE CRYSTAL STRUCTURE OF CASPASE-7 IN COMPLEX WITH ACETYL-LDESD-CHO	3.4.22.60
3EDX	CRYSTAL STRUCTURE OF THE W215A/E217A MUTANT OF MURINE THROMBIN	3.4.21.5
3EDY	CRYSTAL STRUCTURE OF THE PRECURSOR FORM OF HUMAN TRIPEPTIDYL-PEPTIDASE 1	3.4.14.9
3EDZ	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH HYDROXAMATE INHIBITOR	3.4.24.86
3EE0	CRYSTAL STRUCTURE OF THE W215A/E217A MUTANT OF HUMAN THROMBIN (SPACE GROUP P2(1)2(1)2(1))	3.4.21.5
3EE1	NOVEL FOLD OF VIRA, A TYPE III SECRETION SYSTEM EFFECTOR PROTEIN FROM SHIGELLA FLEXNERI	3.4.22
3EE6	CRYSTAL STRUCTURE ANALYSIS OF TRIPEPTIDYL PEPTIDASE -I	3.4.14.9
3EE7	CRYSTAL STRUCTURE OF SARS-COV NSP9 G104E	3.4.22 3.4.19.12 3.4.22.69
3EEB	STRUCTURE OF THE V. CHOLERAE RTX CYSTEINE PROTEASE DOMAIN	3.4.22 6.3.2
3EEF	CRYSTAL STRUCTURE OF N-CARBAMOYLSARCOSINE AMIDASE FROM THERMOPLASMA ACIDOPHILUM	3.5.1.59
3EEI	CRYSTAL STRUCTURE OF 5'-METHYLTHIOADENOSINE/S-ADENOSYLHOMOCYSTEINE NUCLEOSIDASE FROM NEISSERIA MENINGITIDIS IN COMPLEX WITH METHYLTHIO-IMMUCILLIN-A	3.2.2.16 3.2.2.9
3EES	STRUCTURE OF THE RNA PYROPHOSPHOHYDROLASE BDRPPH	3.6.1
3EEU	STRUCTURE OF THE RNA PYROPHOSPHOHYDROLASE BDRPPH IN COMPLEX WITH HOLMIUM	3.6.1
3EF0	THE STRUCTURE OF FCP1, AN ESSENTIAL RNA POLYMERASE II CTD PHOSPHATASE	3.1.3.16
3EF1	THE STRUCTURE OF FCP1, AN ESSENTIAL RNA POLYMERASE II CTD PHOSPHATASE	3.1.3.16
3EF3	CUT-1A; NCN-PT-PINCER-CUTINASE HYBRID	3.1.1.74
3EF5	STRUCTURE OF THE RNA PYROPHOSPHOHYDROLASE BDRPPH IN COMPLEX WITH DGTP	3.6.1
3EG5	CRYSTAL STRUCTURE OF MDIA1-TSH GBD-FH3 IN COMPLEX WITH CDC42-GMPPNP	3.6.5.2
3EGG	CRYSTAL STRUCTURE OF A COMPLEX BETWEEN PROTEIN PHOSPHATASE 1 ALPHA (PP1) AND THE PP1 BINDING AND PDZ DOMAINS OF SPINOPHILIN	3.1.3.16
3EGH	CRYSTAL STRUCTURE OF A COMPLEX BETWEEN PROTEIN PHOSPHATASE 1 ALPHA (PP1), THE PP1 BINDING AND PDZ DOMAINS OF SPINOPHILIN AND THE SMALL NATURAL MOLECULAR TOXIN NODULARIN-R	3.1.3.16
3EGJ	N-ACETYLGLUCOSAMINE-6-PHOSPHATE DEACETYLASE FROM VIBRIO CHOLERAE.	3.5.1.25
3EGK	KNOBLE INHIBITOR	3.4.21.5
3EH8	CRYSTAL STRUCTURE OF Y2 I-ANII VARIANT (F13Y/S111Y)/DNA COMPLEX WITH CALCIUM	3.1
3EHW	HUMAN DUTPASE IN COMPLEX WITH ALPHA,BETA-IMIDO-DUTP AND MG2+: VISUALIZATION OF THE FULL-LENGTH C-TERMINI IN ALL MONOMERS AND SUGGESTION FOR AN ADDITIONAL METAL ION BINDING SITE	3.6.1.23
3EHX	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR (R)-2-(BIPHENYL-4-YLSULFONAMIDO)-4-METHYLPENTANOIC ACID	3.4.24.65
3EHY	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR (R)-2-(4-METHOXYPHENYLSULFONAMIDO)PROPANOIC ACID	3.4.24.65
3EIF	1.9 ANGSTROM CRYSTAL STRUCTURE OF THE ACTIVE FORM OF THE C5A PEPTIDASE FROM STREPTOCOCCUS PYOGENES (SCPA)	3.4.21.110
3EIM	METAL EXCHANGE IN THERMOLYSIN	3.4.24.27
3EIO	CRYSTAL STRUCTURE ANALYSIS OF DPPIV INHIBITOR	3.4.14.5
3EIQ	CRYSTAL STRUCTURE OF PDCD4-EIF4A	3.6.1 3.6.4.13
3EIU	A SECOND TRANSIENT POSITION OF ATP ON ITS TRAIL TO THE NUCLEOTIDE-BINDING SITE OF SUBUNIT B OF THE MOTOR PROTEIN A1AO ATP SYNTHASE	3.6.3.14
3EIY	CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM BURKHOLDERIA PSEUDOMALLEI WITH BOUND PYROPHOSPHATE	3.6.1.1
3EIZ	CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM BURKHOLDERIA PSEUDOMALLEI, H32 CRYSTAL FORM	3.6.1.1
3EJ0	CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM BURKHOLDERIA PSEUDOMALLEI WITH BOUND N-(PYRIDIN-3-YLMETHYL) ANILINE, H32 CRYSTAL FORM	3.6.1.1
3EJ2	CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM BURKHOLDERIA PSEUDOMALLEI WITH BOUND 5-AMINO-1-(4-CHLOROPHENYL)-1H-PYRAZOLE-4-CARBONITRILE, H32 CRYSTAL FORM	3.6.1.1
3EJ5	COMPLEX OF RICIN A CHAIN AND PYRIMIDINE-BASED INHIBITOR	3.2.2.22
3EJF	CRYSTAL STRUCTURE OF IBV X-DOMAIN AT PH 8.5	3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 2.1.1
3EJG	CRYSTAL STRUCTURE OF HCOV-229E X-DOMAIN	3.4.22 3.4.19.12 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 2.1.1
3EJI	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L36K AT CRYOGENIC TEMPERATURE	3.1.31.1
3EJP	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH 5-SUBSTITUTED SWAINSONINE ANALOG: (5R)-5-[2'-OXO-2'-(PHENYL)ETHYL]-SWAINSONINE	3.2.1.114
3EJQ	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH 5-SUBSTITUED SWAINSONINE ANALOG: (5R)-5-[2'-OXO-2'-(4-METHYLPHENYL)ETHYL]-SWAINSONINE	3.2.1.114
3EJR	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH 5-SUBSTITUED SWAINSONINE ANALOG: (5R)-5-[2'-OXO-2'-(4-TERT-BUTYLPHENYL)ETHYL]-SWAINSONINE	3.2.1.114
3EJS	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH 5-SUBSTITUTED SWAINSONINE ANALOG: (5S)-5-[2'-(4-TERT-BUTYLPHENYL)ETHYL]-SWAINSONINE	3.2.1.114
3EJT	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH 5-SUBSTITUTED SWAINSONINE ANALOG:(5R)-5-[2'-(4-TERT-BUTYLPHENYL)ETHYL]-SWAINSONINE	3.2.1.114
3EJU	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH 5-SUBSTITUTED SWAINSONINE ANALOG:(5S)-5-[2'-OXO-2'-(4-TERT-BUTYLPHENYL)ETHYL]-SWAINSONINE	3.2.1.114
3EKE	CRYSTAL STRUCTURE OF IBV X-DOMAIN AT PH 5.6	3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 2.1.1
3EKP	CRYSTAL STRUCTURE OF THE INHIBITOR AMPRENAVIR (APV) IN COMPLEX WITH A MULTI-DRUG RESISTANT HIV-1 PROTEASE VARIANT (L10I/G48V/I54V/V64I/V82A)REFER: FLAP+ IN CITATION	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
3EKQ	CRYSTAL STRUCTURE OF INHIBITOR SAQUINAVIR (SQV) IN COMPLEX WITH MULTI-DRUG RESISTANT HIV-1 PROTEASE (L63P/V82T/I84V) (REFERRED TO AS ACT IN PAPER)	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
3EKT	CRYSTAL STRUCTURE OF THE INHIBITOR DARUNAVIR (DRV) IN COMPLEX WITH A MULTI-DRUG RESISTANT HIV-1 PROTEASE VARIANT (L10F/G48V/I54V/V64I/V82A) (REFER: FLAP+ IN CITATION.)	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
3EKV	CRYSTAL STRUCTURE OF THE WILD TYPE HIV-1 PROTEASE WITH THE INHIBITOR, AMPRENAVIR	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
3EKW	CRYSTAL STRUCTURE OF THE INHIBITOR ATAZANAVIR (ATV) IN COMPLEX WITH A MULTI-DRUG RESISTANCE HIV-1 PROTEASE VARIANT (L10I/G48V/I54V/V64I/V82A) REFER: FLAP+ IN CITATION.	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
3EKX	CRYSTAL STRUCTURE OF THE WILD-TYPE HIV-1 PROTEASE WITH THE INHIBITOR, 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
3EKY	CRYSTAL STRUCTURE OF WILD-TYPE HIV PROTEASE IN COMPLEX WITH THE INHIBITOR, 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
3EL0	CRYSTAL STRUCTURE OF THE INHIBITOR NELFINAVIR (NFV) IN COMPLEX WITH A MULTI-DRUG RESISTANT HIV-1 PROTEASE VARIANT (L10I/G48V/I54V/V64I/V82A) (REFER: FLAP+ IN CITATION)	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
3EL1	CRYSTAL STRUCTURE OF WILD-TYPE HIV PROTEASE IN COMPLEX WITH THE INHIBITOR, 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
3EL4	CRYSTAL STRUCTURE OF INHIBITOR SAQUINAVIR (SQV) COMPLEXED WITH THE MULTIDRUG HIV-1 PROTEASE VARIANT L63P/V82T/I84V	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
3EL5	CRYSTAL STRUCTURE OF NELFINAVIR (NFV) COMPLEXED WITH A MULTIDRUG VARIANT (ACT) (V82T/I84V) OF HIV-1 PROTEASE	3.1.26.4 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
3EL9	CRYSTAL STRUCTURE OF ATAZANAVIR (ATV) IN COMPLEX WITH A MULTIDRUG HIV-1 PROTEASE (V82T/I84V)	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
3ELA	CRYSTAL STRUCTURE OF ACTIVE SITE INHIBITED COAGULATION FACTOR VIIA MUTANT IN COMPLEX WITH SOLUBLE TISSUE FACTOR	3.4.21.21
3ELM	CRYSTAL STRUCTURE OF MMP-13 COMPLEXED WITH INHIBITOR 24F	3.4.24
3ELO	CRYSTAL STRUCTURE OF HUMAN PANCREATIC PROPHOSPHOLIPASE A2	3.1.1.4
3EM3	CRYSTAL STRUCTURE OF AMPRENAVIR (APV) IN COMPLEX WITH A DRUG RESISTANT HIV-1 PROTEASE VARIANT (I50L/A71V).	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
3EM4	CRYSTAL STRUCTURE OF ATAZANAVIR (ATV) IN COMPLEX WITH I50L/A71V DRUG-RESISTANT 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
3EM6	CRYSTAL STRUCTURE OF I50L/A71V MUTANT OF HIV-1 PROTEASE IN COMPLEX WITH INHIBITOR DARUNAVIR	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
3EMC	CRYSTAL STRUCTURE OF XYNB, AN INTRACELLULAR XYLANASE FROM PAENIBACILLUS BARCINONENSIS	3.2.1.8
3EMJ	2.2 A CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM RICKETTSIA PROWAZEKII (P21 FORM)	3.6.1.1
3EML	THE 2.6 A CRYSTAL STRUCTURE OF A HUMAN A2A ADENOSINE RECEPTOR BOUND TO ZM241385.	3.2.1.17
3EMQ	CRYSTAL STRUCTURE OF XILANASE XYNB FROM PAENIBACILLUS BARCELONENSIS COMPLEXED WITH AN INHIBITOR	3.2.1.8
3EMS	EFFECT OF ARIGININE ON LYSOZYME	3.2.1.17
3EMU	CRYSTAL STRUCTURE OF A LEUCINE RICH REPEAT AND PHOSPHATASE DOMAIN CONTAINING PROTEIN FROM ENTAMOEBA HISTOLYTICA	3.1.3
3EMZ	CRYSTAL STRUCTURE OF XYLANASE XYNB FROM PAENIBACILLUS BARCINONENSIS COMPLEXED WITH A CONDURAMINE DERIVATIVE	3.2.1.8
3EN0	THE STRUCTURE OF CYANOPHYCINASE	3.4.15.6
3EN9	STRUCTURE OF THE METHANOCOCCUS JANNASCHII KAE1-BUD32 FUSION PROTEIN	3.4.24.57 2.3.1.234 2.7.11.1
3ENG	STRUCTURE OF ENDOGLUCANASE V CELLOBIOSE COMPLEX	3.2.1.4
3ENH	CRYSTAL STRUCTURE OF CGI121/BUD32/KAE1 COMPLEX	3.4.24.57 2.3.1.234 2.7.11.1
3ENO	CRYSTAL STRUCTURE OF PYROCOCCUS FURIOSUS PCC1 IN COMPLEX WITH THERMOPLASMA ACIDOPHILUM KAE1	3.4.24.57 2.3.1.234 2.7.11.1
3ENS	CRYSTAL STRUCTURE OF HUMAN FXA IN COMPLEX WITH METHYL (2Z)-3-[(3-CHLORO-1H-INDOL-7-YL)AMINO]-2-CYANO-3-{[(3S)-2-OXO-1-(2-OXO-2-PYRROLIDIN-1-YLETHYL)AZEPAN-3-YL]AMINO}ACRYLATE	3.4.21.6
3EO3	CRYSTAL STRUCTURE OF THE N-ACETYLMANNOSAMINE KINASE DOMAIN OF HUMAN GNE PROTEIN	5.1.3.14 2.7.1.60 3.2.1.183
3EO5	CRYSTAL STRUCTURE OF THE RESUSCITATION PROMOTING FACTOR RPFB	3
3EOQ	THE CRYSTAL STRUCTURE OF PUTATIVE ZINC PROTEASE BETA-SUBUNIT FROM THERMUS THERMOPHILUS HB8	3.4.24.56
3EPC	CRYOEM STRUCTURE OF POLIOVIRUS RECEPTOR BOUND TO POLIOVIRUS TYPE 1	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3EPF	CRYOEM STRUCTURE OF POLIOVIRUS RECEPTOR BOUND TO POLIOVIRUS TYPE 2	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3EPR	CRYSTAL STRUCTURE OF PUTATIVE HAD SUPERFAMILY HYDROLASE FROM STREPTOCOCCUS AGALACTIAE.	3.1.3
3EPS	THE CRYSTAL STRUCTURE OF ISOCITRATE DEHYDROGENASE KINASE/PHOSPHATASE FROM E. COLI	2.7.11.5 3.1.3
3EPW	CRYSTAL STRUCTURE OF TRYPANOSOMA VIVAX NUCLEOSIDE HYDROLASE IN COMPLEX WITH THE INHIBITOR (2R,3R,4S)-1-[(4-HYDROXY-5H-PYRROLO[3,2-D]PYRIMIDIN-7-YL)METHYL]-2-(HYDROXYMETHYL)PYRROLIDIN-3,4-DIOL	3.2.2.1
3EPX	CRYSTAL STRUCTURE OF TRYPANOSOMA VIVAX NUCLEOSIDE HYDROLASE IN COMPLEX WITH THE INHIBITOR (2R,3R,4S)-2-(HYDROXYMETHYL)-1-(QUINOLIN-8-YLMETHYL)PYRROLIDIN-3,4-DIOL	3.2.2.1
3EQ0	THROMBIN INHIBITOR	3.4.21.5
3EQ7	PROLYL OLIGOPEPTIDASE COMPLEXED WITH R-PRO-(DECARBOXY-PRO)-TYPE INHIBITORS	3.4.21.26
3EQ8	PROLYL OLIGOPEPTIDASE COMPLEXED WITH R-PRO-(DECARBOXY-PRO)-TYPE INHIBITORS	3.4.21.26
3EQ9	PROLYL OLIGOPEPTIDASE COMPLEXED WITH R-PRO-(DECARBOXY-PRO)-TYPE INHIBITORS	3.4.21.26
3EQA	CATALYTIC DOMAIN OF GLUCOAMYLASE FROM ASPERGILLUS NIGER COMPLEXED WITH TRIS AND GLYCEROL	3.2.1.3
3EQN	CRYSTAL STRUCTURE OF BETA-1,3-GLUCANASE FROM PHANEROCHAETE CHRYSOSPORIUM (LAM55A)	3.2.1.58
3EQO	CRYSTAL STRUCTURE OF BETA-1,3-GLUCANASE FROM PHANEROCHAETE CHRYSOSPORIUM (LAM55A) GLUCONOLACTONE COMPLEX	3.2.1.58
3EQT	CRYSTAL STRUCTURE OF HUMAN LGP2 C-TERMINAL DOMAIN IN COMPLEX WITH DSRNA	3.6.1 3.6.4.13
3EQU	CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN 2 FROM NEISSERIA GONORRHOEAE	3.4.16.4
3EQV	CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN 2 FROM NEISSERIA GONORRHOEAE CONTAINING FOUR MUTATIONS ASSOCIATED WITH PENICILLIN RESISTANCE	3.4.16.4
3ER3	THE ACTIVE SITE OF ASPARTIC PROTEINASES	3.4.23.6 3.4.23.22
3ER5	THE ACTIVE SITE OF ASPARTIC PROTEINASES	3.4.23.6 3.4.23.22
3ERB	THE CRYSTAL STRUCTURE OF C2B, A FRAGMENT OF COMPLEMENT COMPONENT C2 PRODUCED DURING C3-CONVERTASE FORMATION	3.4.21.43
3ERJ	CRYSTAL STRUCTURE OF THE PEPTIDYL-TRNA HYDROLASE AF2095 FROM ARCHAEGLOBUS FULGIDIS. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET GR4	3.1.1.29
3ERO	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS I72E AT CRYOGENIC TEMPERATURE	3.1.31.1
3ERQ	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT L25K AT CRYOGENIC TEMPERATURE	3.1.31.1
3ESA	CUT-1B; NCN-PT-PINCER-CUTINASE HYBRID	3.1.1.74
3ESB	CUT-1C; NCN-PT-PINCER-CUTINASE HYBRID	3.1.1.74
3ESC	CUT-2A; NCN-PT-PINCER-CUTINASE HYBRID	3.1.1.74
3ESD	CUT-2B; NCN-PT-PINCER-CUTINASE HYBRID	3.1.1.74
3ESQ	CRYSTAL STRUCTURE OF CALCIUM-BOUND D,D-HEPTOSE 1.7-BISPHOSPHATE PHOSPHATASE FROM E. COLI	3.1.3 3.1.3.82
3ESR	CRYSTAL STRUCTURE OF D,D-HEPTOSE1.7-BISPHOSPHATE PHOSPHATASE FROM E. COLI IN COMPLEX WITH CALCIUM AND PHOSPHATE	3.1.3 3.1.3.82
3EST	STRUCTURE OF NATIVE PORCINE PANCREATIC ELASTASE AT 1.65 ANGSTROMS RESOLUTION	3.4.21.36
3ESW	COMPLEX OF YEAST PNGASE WITH GLCNAC2-IAC.	3.5.1.52
3ET4	STRUCTURE OF RECOMBINANT HAEMOPHILUS INFLUENZAE E(P4) ACID PHOSPHATASE	3.1.3.2
3ET5	STRUCTURE OF RECOMBINANT HAEMOPHILUS INFLUENZAE E(P4) ACID PHOSPHATASE COMPLEXED WITH TUNGSTATE	3.1.3.2
3ETI	STRUCTURE OF A CUBIC CRYSTAL FORM OF X (ADRP) DOMAIN FROM FCOV	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
3EU0	CRYSTAL STRUCTURE OF THE S-NITROSYLATED CYS215 OF PTP1B	3.1.3.48
3EUG	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
3EUX	CRYSTAL STRUCTURE OF CROSSLINKED RIBONUCLEASE A	3.1.27.5 4.6.1.18
3EUY	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 50% DIOXANE	3.1.27.5 4.6.1.18
3EUZ	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 50% DIMETHYLFORMAMIDE	3.1.27.5 4.6.1.18
3EV0	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 70% DIMETHYL SULFOXIDE	3.1.27.5 4.6.1.18
3EV1	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 70% HEXANEDIOL	3.1.27.5 4.6.1.18
3EV2	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 70% ISOPROPANOL	3.1.27.5 4.6.1.18
3EV3	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 70% T-BUTANOL	3.1.27.5 4.6.1.18
3EV4	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 50% TRIFLUOROETHANOL	3.1.27.5 4.6.1.18
3EV5	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 1M TRIMETHYLAMINE N-OXIDE	3.1.27.5 4.6.1.18
3EV6	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN 50% R,S,R-BISFURANOL	3.1.27.5 4.6.1.18
3EVA	CRYSTAL STRUCTURE OF YELLOW FEVER VIRUS METHYLTRANSFERASE COMPLEXED WITH S-ADENOSYL-L-HOMOCYSTEINE	2.1.1.56 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.57
3EVB	CRYSTAL STRUCTURE OF YELLOW FEVER VIRUS METHYLTRANSFERASE COMPLEXED WITH S-ADENOSYL-L-HOMOCYSTEINE	2.1.1.56 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.57
3EVC	CRYSTAL STRUCTURE OF GTP COMPLEX OF YELLOW FEVER VIRUS METHYLTRANSFERASE AND S-ADENOSYL-L-HOMOCYSTEINE	2.1.1.56 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.57
3EVD	CRYSTAL STRUCTURE OF GTP COMPLEX OF YELLOW FEVER VIRUS METHYLTRANSFERASE AND S-ADENOSYL-L-HOMOCYSTEINE	2.1.1.56 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.57
3EVE	CRYSTAL STRUCTURE OF GPPPA COMPLEX OF YELLOW FEVER VIRUS METHYLTRANSFERASE AND S-ADENOSYL-L-HOMOCYSTEINE	2.1.1.56 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.57
3EVF	CRYSTAL STRUCTURE OF ME7-GPPPA COMPLEX OF YELLOW FEVER VIRUS METHYLTRANSFERASE AND S-ADENOSYL-L-HOMOCYSTEINE	2.1.1.56 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.57
3EVG	CRYSTAL STRUCTURE OF DENGUE-2 VIRUS METHYLTRANSFERASE COMPLEXED WITH S-ADENOSYL-L-HOMOCYSTEINE	2.1.1.56 2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.57
3EVQ	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L25E AT CRYOGENIC TEMPERATURE	3.1.31.1
3EVY	CRYSTAL STRUCTURE OF A FRAGMENT OF A PUTATIVE TYPE I RESTRICTION ENZYME R PROTEIN FROM BACTEROIDES FRAGILIS	3.1.21.3
3EW5	STRUCTURE OF THE TETRAGONAL CRYSTAL FORM OF X (ADRP) DOMAIN FROM FCOV	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
3EW8	CRYSTAL STRUCTURE ANALYSIS OF HUMAN HDAC8 D101L VARIANT	3.5.1.98
3EWC	CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE FROM PLASMODIAL VIVAX IN COMPLEX WITH MT-COFORMYCIN	3.5.4.4
3EWD	CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE MUTANT (DELTA ASP172) FROM PLASMODIUM VIVAX IN COMPLEX WITH MT-COFORMYCIN	3.5.4.4
3EWF	CRYSTAL STRUCTURE ANALYSIS OF HUMAN HDAC8 H143A VARIANT COMPLEXED WITH SUBSTRATE.	3.5.1.98
3EWJ	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH CARBOXYLATE INHIBITOR	3.4.24.86
3EWO	IBV NSP3 ADRP DOMAIN	3.4.22
3EWP	COMPLEX OF SUBSTRATE ADP-RIBOSE WITH IBV NSP3 ADRP DOMAIN	3.4.22
3EWQ	HCOV-229E NSP3 ADRP DOMAIN	3.4.22 3.4.19.12
3EWR	COMPLEX OF SUBSTRATE ADP-RIBOSE WITH HCOV-229E NSP3 ADRP DOMAIN	3.4.22 3.4.19.12
3EWS	HUMAN DEAD-BOX RNA-HELICASE DDX19 IN COMPLEX WITH ADP	3.6.1 3.6.4.13
3EX8	COMPLEX STRUCTURE OF BACILLUS SUBTILIS RIBG REDUCTION MECHANISM IN RIBOFLAVIN BIOSYNTHESIS	3.5.4.26 1.1.1.193
3EXC	STRUCTURE OF THE RNA'SE SSO8090 FROM SULFOLOBUS SOLFATARICUS	3.1.26 3.1
3EXD	SULFUR-SAD PHASED HEWL CRYSTAL	3.2.1.17
3EXM	CRYSTAL STRUCTURE OF THE PHOSPHATASE SC4828 WITH THE NON-HYDROLYZABLE NUCLEOTIDE GPCP	3.6.1.6
3EXO	CRYSTAL STRUCTURE OF BACE1 BOUND TO INHIBITOR	3.4.23.46
3EXU	A GLYCOSIDE HYDROLASE FAMILY 11 XYLANASE WITH AN EXTENDED THUMB REGION	3.2.1.8
3EY1	A CONFORMATIONAL TRANSITION IN THE STRUCTURE OF A 2'-THIOMETHYL-MODIFIED DNA VISUALIZED AT HIGH RESOLUTION	3.1.26.4
3EYD	STRUCTURE OF HCV NS3-4A PROTEASE WITH AN INHIBITOR DERIVED FROM A BORONIC ACID	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3EZ8	CRYSTAL STRUCTURE OF ENDOGLUCANASE CEL9A FROM THE THERMOACIDOPHILIC ALICYCLOBACILLUS ACIDOCALDARIUS	3.2.1.4
3EZG	CRYSTAL STRUCTURE OF E18Q DJ-1 WITH OXIDIZED C106	3.1.2 3.5.1 3.5.1.124
3EZP	CRYSTAL STRUCTURE ANALYSIS OF HUMAN HDAC8 D101N VARIANT	3.5.1.98
3EZT	CRYSTAL STRUCTURE ANALYSIS OF HUMAN HDAC8 D101E VARIANT	3.5.1.98
3EZZ	CRYSTAL STRUCTURE OF HUMAN MKP-2	3.1.3.48 3.1.3.16
3F06	CRYSTAL STRUCTURE ANALYSIS OF HUMAN HDAC8 D101A VARIANT.	3.5.1.98
3F07	CRYSTAL STRUCTURE ANALYSIS OF HUMAN HDAC8 COMPLEXED WITH APHA IN A NEW MONOCLINIC CRYSTAL FORM	3.5.1.98
3F0R	CRYSTAL STRUCTURE ANALYSIS OF HUMAN HDAC8 COMPLEXED WITH TRICHOSTATIN A IN A NEW MONOCLINIC CRYSTAL FORM	3.5.1.98
3F0Z	CRYSTAL STRUCTURE OF CLOSTRIDIUM ACETOBUTYLICUM 8-OXOGUANINE GLYCOSYLASE/LYASE IN ITS APO-FORM	3.2.2 4.2.99.18
3F10	CRYSTAL STRUCTURE OF CLOSTRIDIUM ACETOBUTYLICUM 8-OXOGUANINE DNA GLYCOSYLASE IN COMPLEX WITH 8-OXOGUANOSINE	3.2.2 4.2.99.18
3F15	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR (S)-N-(2,3-DIHYDROXYPROPYL)-4-METHOXY-N-(2-NITROSO-2-OXOETHYL)BENZENESULFONAMIDE	3.4.24.65
3F16	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR (R)-N-(3-HYDROXY-1-NITROSO-1-OXOPROPAN-2-YL)-4-METHOXYBENZENESULFONAMIDE	3.4.24.65
3F17	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR N-(2-NITROSO-2-OXOETHYL)BIPHENYL-4-SULFONAMIDE	3.4.24.65
3F18	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR 4-FLUORO-N-(2-HYDROXYETHYL)-N-(2-NITROSO-2-OXOETHYL)BENZENESULFONAMIDE	3.4.24.65
3F19	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR 4-FLUORO-N-(2-NITROSO-2-OXOETHYL)BENZENESULFONAMIDE	3.4.24.65
3F1A	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR N-(2-NITROSO-2-OXOETHYL)BENZENESULFONAMIDE	3.4.24.65
3F21	CRYSTAL STRUCTURE OF ZALPHA IN COMPLEX WITH D(CACGTG)	3.5.4 3.5.4.37
3F22	CRYSTAL STRUCTURE OF ZALPHA IN COMPLEX WITH D(CGTACG)	3.5.4 3.5.4.37
3F23	CRYSTAL STRUCTURE OF ZALPHA IN COMPLEX WITH D(CGGCCG)	3.5.4 3.5.4.37
3F28	THERMOLYSIN INHIBITION	3.4.24.27
3F2K	STRUCTURE OF THE TRANSPOSASE DOMAIN OF HUMAN HISTONE-LYSINE N-METHYLTRANSFERASE SETMAR	2.1.1.43 2.1.1.357 3.1
3F2P	THERMOLYSIN INHIBITION	3.4.24.27
3F3K	THE STRUCTURE OF UNCHARACTERIZED PROTEIN YKR043C FROM SACCHAROMYCES CEREVISIAE.	3.1.3.37
3F41	STRUCTURE OF THE TANDEMLY REPEATED PROTEIN TYROSINE PHOSPHATASE LIKE PHYTASE FROM MITSUOKELLA MULTACIDA	3.1.3.8
3F49	ANION-TRIGGERED ENGINEERED SUBTILISIN SUBT_BACAM	3.4.21.62
3F4A	STRUCTURE OF YGR203W, A YEAST PROTEIN TYROSINE PHOSPHATASE OF THE RHODANESE FAMILY	3.1.3.16 3.1.3
3F4F	CRYSTAL STRUCTURE OF DUT1P, A DUTPASE FROM SACCHAROMYCES CEREVISIAE	3.6.1.23
3F4V	SEMI-ACTIVE E176Q MUTANT OF RICE BGLU1, A PLANT EXOGLUCANASE/BETA-GLUCOSIDASE	3.2.1.21
3F5D	CRYSTAL STRUCTURE OF A PROTEIN OF UNKNOWN FUNCTION FROM BACILLUS SUBTILIS	3.2
3F5J	SEMI-ACTIVE E176Q MUTANT OF RICE BGLU1, A PLANT EXOGLUCANASE/BETA-GLUCOSIDASE	3.2.1.21
3F5K	SEMI-ACTIVE E176Q MUTANT OF RICE BGLU1, A PLANT EXOGLUCANASE/BETA-GLUCOSIDASE	3.2.1.21
3F5L	SEMI-ACTIVE E176Q MUTANT OF RICE BGLU1, A PLANT EXOGLUCANASE/BETA-GLUCOSIDASE	3.2.1.21
3F5O	CRYSTAL STRUCTURE OF HTHEM2(UNDECAN-2-ONE-COA) COMPLEX	3.1.2 3.1.2.2
3F5V	C2 CRYSTAL FORM OF MITE ALLERGEN DER P 1	3.4.22.65
3F67	CRYSTAL STRUCTURE OF PUTATIVE DIENELACTONE HYDROLASE FROM KLEBSIELLA PNEUMONIAE SUBSP. PNEUMONIAE MGH 78578	3.1.1
3F68	THROMBIN INHIBITION	3.4.21.5
3F6U	CRYSTAL STRUCTURE OF HUMAN ACTIVATED PROTEIN C (APC) COMPLEXED WITH PPACK	3.4.21.69
3F6Y	CONFORMATIONAL CLOSURE OF THE CATALYTIC SITE OF HUMAN CD38 INDUCED BY CALCIUM	3.2.2.5 3.2.2.6 2.4.99.20
3F6Z	CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA MLIC IN COMPLEX WITH HEN EGG WHITE LYSOZYME	3.2.1.17
3F71	CRYSTAL STRUCTURE OF E18D DJ-1 WITH OXIDIZED C106	3.1.2 3.5.1 3.5.1.124
3F75	ACTIVATED TOXOPLASMA GONDII CATHEPSIN L (TGCPL) IN COMPLEX WITH ITS PROPEPTIDE	3.4.22.15
3F7M	CRYSTAL STRUCTURE OF APO CUTICLE-DEGRADING PROTEASE (VER112) FROM VERTICILLIUM PSALLIOTAE	3.4.21
3F7O	CRYSTAL STRUCTURE OF CUTICLE-DEGRADING PROTEASE FROM PAECILOMYCES LILACINUS (PL646)	3.4.21
3F80	(S)-2-AMINO-6-NITROHEXANOIC ACID BINDS TO HUMAN ARGINASE I THROUGH MULTIPLE NITRO-METAL COORDINATION INTERACTIONS IN THE BINUCLEAR MANGANESE CLUSTER. RESOLUTION 1.60 A.	3.5.3.1
3F81	INTERACTION OF VHR WITH SA3	3.1.3.48 3.1.3.16
3F8G	THE X-RAY STRUCTURE OF A DIMERIC VARIANT OF HUMAN PANCREATIC RIBONUCLEASE WITH HIGH CYTOTOXIC AND ANTITUMOR ACTIVITIES	3.1.27.5 4.6.1.18
3F8S	CRYSTAL STRUCTURE OF DIPEPTIDYL PEPTIDASE IV IN COMPLEX WITH INHIBITOR	3.4.14.5
3F8V	EVAULAUTION AT ATOMIC RESOLUTION OF THE ROLE OF STRAIN IN DESTABILIZING THE TEMPERATURE SENSITIVE T4 LYSOZYME MUTANT ARG96-->HIS	3.2.1.17
3F96	CRYSTAL STRUCTURE OF HUMAN PLASMA PLATELET ACTIVATING FACTOR ACETYLHYDROLASE COVALENTLY INHIBITED BY SARIN	3.1.1.47
3F97	CRYSTAL STRUCTURE OF HUMAN PLASMA PLATELET ACTIVATING FACTOR ACETYLHYDROLASE COVALENTLY INHIBITED BY SOMAN	3.1.1.47
3F98	CRYSTAL STRUCTURE OF HUMAN PLASMA PLATELET ACTIVATING FACTOR ACETYLHYDROLASE COVALENTLY INHIBITED BY TABUN	3.1.1.47
3F99	W354F YERSINIA ENTEROCOLITICA PTPASE APO FORM	3.1.3.48
3F9A	W354F YERSINIA ENTEROCOLITICA PTPASE COMPLEXED WITH TUNGSTATE	3.1.3.48
3F9B	W354F YERSINIA ENTEROCOLITICA PTPASE COMPLEXED WITH DIVANADATE	3.1.3.48
3F9C	CRYSTAL STRUCTURE OF HUMAN PLASMA PLATELET ACTIVATING FACTOR ACETYLHYDROLASE COVALENTLY INHIBITED BY DIISOPROPYLFLUOROPHOSPHATE	3.1.1.47
3F9E	CRYSTAL STRUCTURE OF THE S139A MUTANT OF SARS-CORONOVIRUS 3C-LIKE PROTEASE	3.4.22 3.4.19.12 3.4.22.69
3F9F	CRYSTAL STRUCTURE OF THE F140A MUTANT OF SARS-CORONOVIRUS 3C-LIKE PROTEASE AT PH 6.0	3.4.22 3.4.19.12 3.4.22.69
3F9G	CRYSTAL STRUCTURE OF THE F140A MUTANT OF SARS-CORONOVIRUS 3C-LIKE PROTEASE AT PH 6.5	3.4.22 3.4.19.12 3.4.22.69
3F9H	CRYSTAL STRUCTURE OF THE F140A MUTANT OF SARS-CORONOVIRUS 3C-LIKE PROTEASE AT PH 7.6	3.4.22 3.4.19.12 3.4.22.69
3F9L	EVAULAUTION AT ATOMIC RESOLUTION OF THE ROLE OF STRAIN IN DESTABILIZING THE TEMPERATURE SENSITIVE T4 LYSOZYME MUTANT ARG96-->HIS	3.2.1.17
3F9O	CRYSTAL STRUCTURE OF THE DI-ZINC CARBAPENEMASE CPHA FROM AEROMONAS HYDROPHILA	3.5.2.6
3F9Q	RE-REFINEMENT OF UNCOMPLEXED PLASMEPSIN II FROM PLASMODIUM FALCIPARUM.	3.4.23.39
3F9V	CRYSTAL STRUCTURE OF A NEAR FULL-LENGTH ARCHAEAL MCM: FUNCTIONAL INSIGHTS FOR AN AAA+ HEXAMERIC HELICASE	3 3.6.4.12
3FA0	EVAULAUTION AT ATOMIC RESOLUTION OF THE ROLE OF STRAIN IN DESTABILIZING THE TEMPERATURE SENSITIVE T4 LYSOZYME MUTANT ARG96-->HIS	3.2.1.17
3FAD	EVAULAUTION AT ATOMIC RESOLUTION OF THE ROLE OF STRAIN IN DESTABILIZING THE TEMPERATURE SENSITIVE T4 LYSOZYME MUTANT ARG96-->HIS	3.2.1.17
3FAI	THE DI ZINC CARBAPENEMASE CPHA N220G MUTANT	3.5.2.6
3FAK	STRUCTURAL AND FUNCTIONAL ANALYSIS OF A HORMONE-SENSITIVE LIPASE LIKE ESTE5 FROM A METAGENOME LIBRARY	3.1.1
3FAN	CRYSTAL STRUCTURE OF CHYMOTRYPSIN-LIKE PROTEASE/PROTEINASE (3CLSP/NSP4) OF PORCINE REPRODUCTIVE AND RESPIRATORY SYNDROME VIRUS (PRRSV)	3.4.21.114
3FAO	CRYSTAL STRUCTURE OF S118A MUTANT 3CLSP OF PRRSV	3.4.21.114
3FAU	CRYSTAL STRUCTURE OF HUMAN SMALL-MUTS RELATED DOMAIN	3
3FB0	METAL EXCHANGE IN THERMOLYSIN	3.4.24.27
3FBD	CRYSTAL STRUCTURE OF THE NUCLEASE DOMAIN OF COLE7(D493Q MUTANT) IN COMPLEX WITH AN 18-BP DUPLEX DNA	3.1
3FBM	D431N MUTANT VP2 PROTEIN OF INFECTIOUS BURSAL DISEASE VIRUS; DERIVED T=1 PARTICLES	3.4.21
3FBO	METAL EXCHANGE IN THERMOLYSIN	3.4.24.27
3FBP	STRUCTURE REFINEMENT OF FRUCTOSE-1,6-BISPHOSPHATASE AND ITS FRUCTOSE 2,6-BISPHOSPHATE COMPLEX AT 2.8 ANGSTROMS RESOLUTION	3.1.3.11
3FBW	STRUCTURE OF RHODOCOCCUS RHODOCHROUS HALOALKANE DEHALOGENASE DHAA MUTANT C176Y	3.8.1.5
3FBX	CRYSTAL STRUCTURE OF THE LYSOSOMAL 66.3 KDA PROTEIN FROM MOUSE SOLVED BY S-SAD	3.1.1
3FCF	COMPLEX OF UNG2 AND A FRAGMENT-BASED DESIGNED INHIBITOR	3.2.2 3.2.2.27
3FCI	COMPLEX OF UNG2 AND A FRAGMENT-BASED DESIGNED INHIBITOR	3.2.2 3.2.2.27
3FCK	COMPLEX OF UNG2 AND A FRAGMENT-BASED DESIGN INHIBITOR	3.2.2 3.2.2.27
3FCL	COMPLEX OF UNG2 AND A FRAGMENT-BASED DESIGNED INHIBITOR	3.2.2 3.2.2.27
3FCQ	THERMOLYSIN INHIBITION	3.4.24.27
3FCX	CRYSTAL STRUCTURE OF HUMAN ESTERASE D	3.1.2.12 3.1.1.56
3FCY	CRYSTAL STRUCTURE OF ACETYL XYLAN ESTERASE 1 FROM THERMOANAEROBACTERIUM SP. JW/SL YS485	3.1.1.72 3.1.1.41
3FCZ	ADAPTIVE PROTEIN EVOLUTION GRANTS ORGANISMAL FITNESS BY IMPROVING CATALYSIS AND FLEXIBILITY	3.5.2.6
3FD2	CRYSTAL STRUCTURE OF MMSOI/DNA COMPLEX WITH CALCIUM	3.1
3FD7	CRYSTAL STRUCTURE OF ONCONASE C87A/C104A-ONC	3.1.27
3FDB	CRYSTAL STRUCTURE OF A PUTATIVE PLP-DEPENDENT BETA-CYSTATHIONASE (AECD, DIP1736) FROM CORYNEBACTERIUM DIPHTHERIAE AT 1.99 A RESOLUTION	3
3FDF	CRYSTAL STRUCTURE OF THE SERINE PHOSPHATASE OF RNA POLYMERASE II CTD (SSU72 SUPERFAMILY) FROM DROSOPHILA MELANOGASTER. ORTHORHOMBIC CRYSTAL FORM. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET FR253.	3.1.3.16
3FDG	THE CRYSTAL STRUCTURE OF THE DIPEPTIDASE AC, METALLO PEPTIDASE. MEROPS FAMILY M19	3.4.13.19
3FE0	X-RAY CRYSTAL STRUCTURE OF WILD TYPE HUMAN LYSOZYME IN D2O	3.2.1.17
3FE2	HUMAN DEAD-BOX RNA HELICASE DDX5 (P68), CONSERVED DOMAIN I IN COMPLEX WITH ADP	3.6.1 3.6.4.13
3FEC	CRYSTAL STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE III (GCPIII/NAALADASE II), PSEUDO-UNLIGANDED	3.4.17.21
3FED	THE HIGH RESOLUTION STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE III (GCPIII/NAALADASE II) IN COMPLEX WITH A TRANSITION STATE ANALOG OF GLU-GLU	3.4.17.21
3FEE	THE HIGH RESOLUTION STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE III (GCPIII/NAALADASE II) IN COMPLEX WITH QUISQUALIC ACID	3.4.17.21
3FEF	CRYSTAL STRUCTURE OF PUTATIVE GLUCOSIDASE LPLD FROM BACILLUS SUBTILIS	3.2.1.67
3FF3	THE HIGH RESOLUTION STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE III (GCPIII/NAALADASE II) IN COMPLEX WITH L-GLUTAMATE	3.4.17.21
3FFG	FACTOR XA IN COMPLEX WITH THE INHIBITOR (R)-6-(2'-((3- HYDROXYPYRROLIDIN-1-YL)METHYL)BIPHENYL-4-YL)-1-(3-(5-OXO-4,5-DIHYDRO-1H-1,2,4-TRIAZOL-3-YL)PHENYL)-3-(TRIFLUOROMETHYL)-5,6-DIHYDRO-1H-PYRAZOLO[3,4-C]PYRIDIN- 7(4H)-ONE	3.4.21.6
3FFI	HIV-1 RT WITH PYRIDONE NON-NUCLEOSIDE 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
3FFU	STRUCTURE OF THE RNA PYROPHOSPHOHYDROLASE BDRPPH IN COMPLEX WITH GTP AND MAGNESIUM	3.6.1
3FG5	CRYSTAL STRUCTURE DETERMINATION OF A TERNARY COMPLEX OF PHOSPHOLIPASE A2 WITH A PENTAPEPTIDE FLSYK AND AJMALINE AT 2.5 A RESOLUTION	3.1.1.4
3FGD	DRUGSCORE FP: THERMOYLSIN IN COMPLEX WITH FRAGMENT.	3.4.24.27
3FGO	CRYSTAL STRUCTURE OF THE E2 MAGNESIUM FLUORIDE COMPLEX OF THE (SR) CA2+-ATPASE WITH BOUND CPA AND AMPPCP	3.6.3.8 7.2.2.10
3FGR	TWO CHAIN FORM OF THE 66.3 KDA PROTEIN AT 1.8 ANGSTROEM	3.1.1
3FGT	TWO CHAIN FORM OF THE 66.3 KDA PROTEIN FROM MOUSE LACKING THE LINKER PEPTIDE	3.1.1
3FGW	ONE CHAIN FORM OF THE 66.3 KDA PROTEIN	3.1.1
3FH2	THE CRYSTAL STRUCTURE OF THE PROBABLE ATP-DEPENDENT PROTEASE (HEAT SHOCK PROTEIN) FROM CORYNEBACTERIUM GLUTAMICUM	3
3FH4	CRYSTAL STRUCTURE OF RECOMBINANT VIBRIO PROTEOLYTICUS AMINOPEPTIDASE	3.4.11.10
3FH5	LEUKOTRIENE A4 HYDROLASE COMPLEXED WITH INHIBITOR (2R)-2-[(4-BENZYLPHENOXY)METHYL]PYRROLIDINE.	3.3.2.6 3.4.11.4
3FH6	CRYSTAL STRUCTURE OF THE RESTING STATE MALTOSE TRANSPORTER FROM E. COLI	3.6.3.19 7.5.2.1
3FH7	LEUKOTRIENE A4 HYDROLASE COMPLEXED WITH INHIBITOR 4-[(2S)-2-{[4-(4-CHLOROPHENOXY)PHENOXY]METHYL}PYRROLIDIN-1-YL]BUTANOATE.	3.3.2.6 3.4.11.4
3FH8	LEUKOTRIENE A4 HYDROLASE COMPLEXED WITH INHIBITOR 1-[2-(4-BENZYLPHENOXY)ETHYL]PYRROLIDINE.	3.3.2.6 3.4.11.4
3FHA	STRUCTURE OF ENDO-BETA-N-ACETYLGLUCOSAMINIDASE A	3.2.1.96
3FHD	CRYSTAL STRUCTURE OF THE SHUTOFF AND EXONUCLEASE PROTEIN FROM KAPOSIS SARCOMA ASSOCIATED HERPESVIRUS	3.1
3FHE	LEUKOTRIENE A4 HYDROLASE COMPLEXED WITH INHIBITOR N-[3-(4-BENZYLPHENOXY)PROPYL]-N-METHYL-BETA-ALANINE.	3.3.2.6 3.4.11.4
3FHF	CRYSTAL STRUCTURE OF METHANOCALDOCOCCUS JANNASCHII 8-OXOGUANINE DNA GLYCOSYLASE (MJOGG)	3.2.2 4.2.99.18
3FHG	CRYSTAL STRUCTURE OF SULFOLOBUS SOLFATARICUS 8-OXOGUANINE DNA GLYCOSYLASE (SSOGG)	3.2.2 4.2.99.18
3FHO	STRUCTURE OF S. POMBE DBP5	3.6.1 3.6.4.13
3FHQ	STRUCTURE OF ENDO-BETA-N-ACETYLGLUCOSAMINIDASE A	3.2.1.96
3FHT	CRYSTAL STRUCTURE OF HUMAN DBP5 IN COMPLEX WITH AMPPNP AND RNA	3.6.1 3.6.4.13
3FI5	CRYSTAL STRUCTURE OF T4 LYSOZYME MUTANT R96W	3.2.1.17
3FI7	CRYSTAL STRUCTURE OF THE AUTOLYSIN AUTO (LMO1076) FROM LISTERIA MONOCYTOGENES, CATALYTIC DOMAIN	3.2.1.96
3FIE	CRYSTAL STRUCTURE OF CLOSTRIDIUM BOTULINUM NEUROTOXIN SEROTYPE F CATALYTIC DOMAIN WITH AN INHIBITOR (INH1)	3.4.24.69
3FII	CRYSTAL STRUCTURE OF CLOSTRIDIUM BOTULINUM NEUROTOXIN SEROTYPE F CATALYTIC DOMAIN WITH AN INHIBITOR (INH2)	3.4.24.69
3FIT	FHIT (FRAGILE HISTIDINE TRIAD PROTEIN) IN COMPLEX WITH ADENOSINE/SULFATE AMP ANALOG	3.6.1.29
3FIV	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
3FJU	ASCARIS SUUM CARBOXYPEPTIDASE INHIBITOR IN COMPLEX WITH HUMAN CARBOXYPEPTIDASE A1	3.4.17.1
3FKT	CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH SPIROPIPERDINE IMINOHYDANTOIN INHIBITOR	3.4.23.46
3FKV	AMPC K67R MUTANT COMPLEXED WITH BENZO(B)THIOPHENE-2-BORONIC ACID (BZB)	3.5.2.6
3FKW	AMPC K67R MUTANT APO STRUCTURE	3.5.2.6
3FKZ	X-RAY STRUCTURE OF THE NON COVALENT SWAPPED FORM OF THE S16G/T17N/A19P/A20S/K31C/S32C MUTANT OF BOVINE PANCREATIC RIBONUCLEASE	3.1.27.5 4.6.1.18
3FL0	X-RAY STRUCTURE OF THE NON COVALENT SWAPPED FORM OF THE Q28L/K31C/S32C MUTANT OF BOVINE PANCREATIC RIBONUCLEASE IN COMPLEX WITH 2'-DEOXYCYTIDINE-2'-DEOXYGUANOSINE-3',5'-MONOPHOSPHATE	3.1.27.5 4.6.1.18
3FL1	X-RAY STRUCTURE OF THE NON COVALENT SWAPPED FORM OF THE A19P/Q28L/K31C/S32C MUTANT OF BOVINE PANCREATIC RIBONUCLEASE IN COMPLEX WITH 2'-DEOXYCYTIDINE-2'-DEOXYGUANOSINE-3',5'-MONOPHOSPHATE	3.1.27.5 4.6.1.18
3FL3	X-RAY STRUCTURE OF THE LIGAND FREE NON COVALENT SWAPPED FORM OF THE A19P/Q28L/K31C/S32C MUTANT OF BOVINE PANCREATIC RIBONUCLEASE	3.1.27.5 4.6.1.18
3FLA	RIFR - TYPE II THIOESTERASE FROM RIFAMYCIN NRPS/PKS BIOSYNTHETIC PATHWAY - FORM 1	3.1.2
3FLB	RIFR - TYPE II THIOESTERASE FROM RIFAMYCIN NRPS/PKS BIOSYNTHETIC PATHWAY - FORM 2	3.1.2
3FLD	CRYSTAL STRUCTURE OF THE TRAI C-TERMINAL DOMAIN	3.6.1 5.6.2.1 3.6.4.12
3FLF	THERMOLYSIN INHIBITION	3.4.24.27
3FM3	CRYSTAL STRUCTURE OF AN ENCEPHALITOZOON CUNICULI METHIONINE AMINOPEPTIDASE TYPE 2	3.4.11.18
3FMQ	CRYSTAL STRUCTURE OF AN ENCEPHALITOZOON CUNICULI METHIONINE AMINOPEPTIDASE TYPE 2 WITH ANGIOGENESIS INHIBITOR FUMAGILLIN BOUND	3.4.11.18
3FMR	CRYSTAL STRUCTURE OF AN ENCEPHALITOZOON CUNICULI METHIONINE AMINOPEPTIDASE TYPE 2 WITH ANGIOGENESIS INHIBITOR TNP470 BOUND	3.4.11.18
3FMV	CRYSTAL STRUCTURE OF THE SERINE PHOSPHATASE OF RNA POLYMERASE II CTD (SSU72 SUPERFAMILY) FROM DROSOPHILA MELANOGASTER. MONOCLINIC CRYSTAL FORM. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET FR253.	3.1.3.16
3FNS	CRYSTAL STRUCTURE OF HISTO-ASPARTIC PROTEASE (HAP) FROM PLASMODIUM FALCIPARUM	3.4.23
3FNT	CRYSTAL STRUCTURE OF PEPSTATIN A BOUND HISTO-ASPARTIC PROTEASE (HAP) FROM PLASMODIUM FALCIPARUM	3.4.23
3FO5	HUMAN START DOMAIN OF ACYL-COENZYME A THIOESTERASE 11 (ACOT11)	3.1.2 3.1.2.2
3FO7	SIMULTANEOUS INHIBITION OF ANTI-COAGULATION AND INFLAMMATION: CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 COMPLEXED WITH INDOMETHACIN AT 1.4 A RESOLUTION REVEALS THE PRESENCE OF THE NEW COMMON LIGAND BINDING SITE	3.1.1.4
3FOR	THERMOLYSIN COMPLEXED WITH BNPA (2-BENZYL-3-NITRO PROPANOIC ACID AMIDE)	3.4.24.27
3FP6	ANIONIC TRYPSIN IN COMPLEX WITH BOVINE PANCREATIC TRYPSIN INHIBITOR (BPTI) DETERMINED TO THE 1.49 A RESOLUTION LIMIT	3.4.21.4
3FP7	ANIONIC TRYPSIN VARIANT S195A IN COMPLEX WITH BOVINE PANCREATIC TRYPSIN INHIBITOR (BPTI) CLEAVED AT THE SCISSILE BOND (LYS15-ALA16) DETERMINED TO THE 1.46 A RESOLUTION LIMIT	3.4.21.4
3FP8	ANIONIC TRYPSIN VARIANT S195A IN COMPLEX WITH BOVINE PANCREATIC TRYPSIN INHIBITOR (BPTI) DETERMINED TO THE 1.46 A RESOLUTION LIMIT	3.4.21.4
3FPB	THE STRUCTURE OF SARCOPLASMIC RETICULUM CA2+-ATPASE BOUND TO CYCLOPIAZONIC ACID WITH ATP	3.6.3.8 7.2.2.10
3FPS	THE STRUCTURE OF SARCOPLASMIC RETICULUM CA2+-ATPASE BOUND TO CYCLOPIAZONIC AND ADP	3.6.3.8 7.2.2.10
3FQ3	CRYSTAL STRUCTURE OF INORGANIC PHOSPHATASE FROM BRUCELLA MELITENSIS	3.6.1.1
3FQD	CRYSTAL STRUCTURE OF THE S. POMBE RAT1-RAI1 COMPLEX	3.1.13
3FQG	CRYSTAL STRUCTURE OF THE S. POMBE RAI1	3.6.1
3FQI	CRYSTAL STRUCTURE OF THE MOUSE DOM3Z	3.6.1 3.1.13
3FQJ	CRYSTAL STRUCTURE OF THE MOUSE DOM3Z IN COMPLEX WITH GDP	3.6.1 3.1.13
3FQK	HEPATITIS C VIRUS POLYMERASE NS5B (BK 1-570) WITH HCV-796 INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3FQL	HEPATITIS C VIRUS POLYMERASE NS5B (CON1 1-570) WITH HCV-796 INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3FQM	CRYSTAL STRUCTURE OF A NOVEL DIMERIC FORM OF HCV NS5A DOMAIN I PROTEIN	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3FQQ	CRYSTAL STRUCTURE OF A NOVEL DIMERIC FORM OF HCV NS5A DOMAIN I PROTEIN	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3FRG	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B2B IN COMPLEX WITH A QUINOLINE INHIBITOR	3.1.4.17 3.1.4.53
3FRY	CRYSTAL STRUCTURE OF THE COPA C-TERMINAL METAL BINDING DOMAIN	3.6.3 7.2.2.8
3FRZ	CRYSTAL STRUCTURE OF HCV NS5B RNA POLYMERASE IN COMPLEX WITH PF868554	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3FS5	CRYSTAL STRUCTURE OF SACCHAROMYCES CEREVISIAE YGR203W, A HOMOLOG OF SINGLE-DOMAIN RHODANESE AND CDC25 PHOSPHATASE CATALYTIC DOMAIN	3.1.3
3FSI	CRYSTAL STRUCTURE OF A TRYPANOCIDAL 4,4'-BIS(IMIDAZOLINYLAMINO)DIPHENYLAMINE BOUND TO DNA	2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1
3FSM	CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED 203 AMINO ACID 'COVALENT DIMER' [L-ALA51,D-ALA51'] HIV-1 PROTEASE MOLECULE	3.4.23.16
3FSN	CRYSTAL STRUCTURE OF RPE65 AT 2.14 ANGSTROM RESOLUTION	5.2.1.7 3.1.1.64 5.3.3.22
3FTJ	CRYSTAL STRUCTURE OF THE PERIPLASMIC REGION OF MACB FROM ACTINOBACILLUS ACTINOMYCETEMCOMITANS	3.6.3 7.6.2
3FTS	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH RESVERATROL	3.3.2.6 3.4.11.4
3FTU	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH DIHYDRORESVERATROL	3.3.2.6 3.4.11.4
3FTV	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT N-(PYRIDIN-3-YLMETHYL)ANILINE	3.3.2.6 3.4.11.4
3FTW	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENTS N-(PYRIDIN-3-YLMETHYL)ANILINE AND ACETATE	3.3.2.6 3.4.11.4
3FTX	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH DIHYDRORESVERATROL AND BESTATIN	3.3.2.6 3.4.11.4
3FTY	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT 3-(BENZYLOXY)PYRIDIN-2-AMINE	3.3.2.6 3.4.11.4
3FTZ	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT 2-(PYRIDIN-3-YLMETHOXY)ANILINE	3.3.2.6 3.4.11.4
3FU0	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT 4-(4-FLUOROBENZOYL)PYRIDINE	3.3.2.6 3.4.11.4
3FU3	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT 4-(2-AMINO-1,3-THIAZOL-4-YL)PHENOL	3.3.2.6 3.4.11.4
3FU5	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH (5-THIOPHEN-2-YLTHIOPHEN-2-YL)METHYLAMINE	3.3.2.6 3.4.11.4
3FU6	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT (4-THIOPHEN-2-YLPHENYL)METHANAMINE	3.3.2.6 3.4.11.4
3FUD	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH N-METHYL-1-(2-THIOPHEN-2-YLPHENYL)METHANAMINE	3.3.2.6 3.4.11.4
3FUE	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT 5-CHLOROINDOLE AND BESTATIN	3.3.2.6 3.4.11.4
3FUF	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT 5-FLUOROINDOLE AND BESTATIN	3.3.2.6 3.4.11.4
3FUH	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH FRAGMENT 5-HYDROXYINDOLE AND BESTATIN	3.3.2.6 3.4.11.4
3FUI	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH N-BENZYL-4-[(2R)-PYRROLIDIN-2-YLMETHOXY]ANILINE	3.3.2.6 3.4.11.4
3FUJ	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH 5-[2-(1H-PYRROL-1-YL)ETHOXY]-1H-INDOLE	3.3.2.6 3.4.11.4
3FUK	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH 1-[2-(1H-INDOL-5-YLOXY)ETHYL]PIPERIDINE-4-CARBOXYLIC ACID	3.3.2.6 3.4.11.4
3FUL	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH PYRIDIN-4-YL[4-(2-PYRROLIDIN-1-YLETHOXY)PHENYL]METHANONE	3.3.2.6 3.4.11.4
3FUM	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH (R)-PYRIDIN-4-YL[4-(2-PYRROLIDIN-1-YLETHOXY)PHENYL]METHANOL	3.3.2.6 3.4.11.4
3FUN	LEUKOTRIENE A4 HYDROLASE IN COMPLEX WITH {4-[(2R)-PYRROLIDIN-2-YLMETHOXY]PHENYL}(4-THIOPHEN-3-YLPHENYL)METHANONE	3.3.2.6 3.4.11.4
3FUO	THE CRYSTAL STRUCTURE OF RECEPTOR BINDING DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A	3.4.24.69
3FUQ	GLYCOSYLATED SV2 AND GANGLIOSIDES AS DUAL RECEPTORS FOR BOTULINUM NEUROTOXIN SEROTYPE F	3.4.24.69
3FV3	SECRETED ASPARTIC PROTEASE 1 FROM CANDIDA PARAPSILOSIS IN COMPLEX WITH PEPSTATIN A	3.4.23.24
3FV4	THERMOLYSIN INHIBITION	3.4.24.27
3FV7	OXA-24 BETA-LACTAMASE COMPLEX WITH SA4-44 INHIBITOR	3.5.2.6
3FVF	THE CRYSTAL STRUCTURE OF PROSTASIN COMPLEXED WITH CAMOSTAT AT 1.6 ANGSTROMS RESOLUTION	3.4.21
3FVI	CRYSTAL STRUCTURE OF COMPLEX OF PHOSPHOLIPASE A2 WITH OCTYL SULFATES	3.1.1.4
3FVJ	CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 1B CRYSTALLIZED IN THE PRESENCE OF OCTYL SULFATE	3.1.1.4
3FVL	CRYSTALLOGIC STUDIES ON THE COMPLEX OF CARBOXYPEPTIDASE A WITH INHIBITORS USING ALPHA-HYDROXY KETONE AS ZINC-BINDING GROUP	3.4.17.1
3FVP	THERMOLYSIN INHIBITION	3.4.24.27
3FVQ	CRYSTAL STRUCTURE OF THE NUCLEOTIDE BINDING DOMAIN FBPC COMPLEXED WITH ATP	3.6.3.30 7.2.2.7
3FVR	CRYSTAL STRUCTURE OF ACETYL XYLAN ESTERASE FROM BACILLUS PUMILUS, MONOCLINIC CRYSTAL FORM I	3.1.1.6
3FVY	CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE III	3.4.14.4
3FW6	CRYSTAL STRUCTURE OF CELM2, A BIFUNCTIONAL GLUCANASE-XYLANASE PROTEIN FROM A METAGENOME LIBRARY	3.2.1.4
3FWH	STRUCTURE OF HALOALKANE DEHALOGENASE MUTANT DHA15 (I135F/C176Y) FROM RHODOCOCCUS RHODOCHROUS	3.8.1.5
3FWL	CRYSTAL STRUCTURE OF THE FULL-LENGTH TRANSGLYCOSYLASE PBP1B FROM ESCHERICHIA COLI	2.4.1.129 3.4 3.4.16.4
3FWX	THE CRYSTAL STRUCTURE OF THE PEPTIDE DEFORMYLASE FROM VIBRIO CHOLERAE O1 BIOVAR EL TOR STR. N16961	3.5.1.88
3FX5	STRUCTURE OF HIV-1 PROTEASE IN COMPLEX WITH POTENT INHIBITOR KNI-272 DETERMINED BY HIGH RESOLUTION X-RAY CRYSTALLOGRAPHY	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
3FX6	X-RAY CRYSTALLOGRAPHIC STUDIES ON THE COMPLEX OF CARBOXYPEPTIDASE A WITH THE INHIBITOR USING ALPHA-NITRO KETONE AS THE ZINC-BINDING GROUP	3.4.17.1
3FXI	CRYSTAL STRUCTURE OF THE HUMAN TLR4-HUMAN MD-2-E.COLI LPS RA COMPLEX	3.2.2.6
3FXJ	CRYSTAL STRUCTURE OF HUMAN PROTEIN PHOSPHATASE 1A (PPM1A) BOUND WITH PHOSPHATE AT 3 MM OF MN2+	3.1.3.16
3FXK	CRYSTAL STRUCTURE OF HUMAN PROTEIN PHOSPHATASE 1A (PPM1A) BOUND WITH PHOSPHATE AT 10 MM OF MN2+	3.1.3.16
3FXL	CRYSTAL STRUCTURE OF HUMAN PROTEIN PHOSPHATASE 1A (PPM1A) BOUND WITH CITRATE AT 1 MM OF MN2+	3.1.3.16
3FXM	CRYSTAL STRUCTURE OF HUMAN PROTEIN PHOSPHATASE 1A (PPM1A) BOUND WITH CITRATE AT 10 MM OF MN2+	3.1.3.16
3FXO	CRYSTAL STRUCTURE OF HUMAN PROTEIN PHOSPHATASE 1A (PPM1A) BOUND WITH PHOSPHATE AT 1 MM OF MN2+	3.1.3.16
3FXP	THERMOLYSIN INHIBITION	3.4.24.27
3FXS	METAL EXCHANGE IN THERMOLYSIN	3.4.24.27
3FXT	CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF HUMAN NUDT6	3.6.1
3FXY	ACIDIC MAMMALIAN CHINASE, CATALYTIC DOMAIN	3.2.1.14
3FY1	THE ACIDIC MAMMALIAN CHITINASE CATALYTIC DOMAIN IN COMPLEX WITH METHYLALLOSAMIDIN	3.2.1.14
3FYZ	OXA-24 BETA-LACTAMASE COMPLEX WITH SA4-17 INHIBITOR	3.5.2.6
3FZ0	INOSINE-GUANOSINE NUCLEOSIDE HYDROLASE (IG-NH)	3.2.2.1
3FZC	OXA-24 BETA-LACTAMASE COMPLEX WITH SA3-53 INHIBITOR	3.5.2.6
3FZD	MUTATION OF ASN28 DISRUPTS THE ENZYMATIC ACTIVITY AND DIMERIZATION OF SARS 3CLPRO	3.4.22 3.4.19.12 3.4.22.69
3FZI	1.9 ANGSTROM STRUCTURE OF THE THERMOPHILIC EXONUCLEASE III HOMOLOGUE MTH0212	3.1.11.2 4.2.99.18
3FZQ	CRYSTAL STRUCTURE OF PUTATIVE HALOACID DEHALOGENASE-LIKE HYDROLASE (YP_001086940.1) FROM CLOSTRIDIUM DIFFICILE 630 AT 2.10 A RESOLUTION	3.1.3
3FZY	CRYSTAL STRUCTURE OF PRE-CLEAVAGE FORM OF CYSTEINE PROTEASE DOMAIN FROM VIBRIO CHOLERAE RTXA TOXIN	3.4.22 6.3.2
3FZZ	STRUCTURE OF GRC	3.4.21
3G00	MTH0212 IN COMPLEX WITH A 9BP BLUNT END DSDNA AT 1.7 ANGSTROM	3.1.11.2 4.2.99.18
3G01	STRUCTURE OF GRC MUTANT E192R/E193G	3.4.21
3G02	STRUCTURE OF ENANTIOSELECTIVE MUTANT OF EPOXIDE HYDROLASE FROM ASPERGILLUS NIGER GENERATED BY DIRECTED EVOLUTION	3.3.2.9 3.3.2.3
3G0A	MTH0212 WITH TWO BOUND MANGANESE IONS	3.1.11.2 4.2.99.18
3G0B	CRYSTAL STRUCTURE OF DIPEPTIDYL PEPTIDASE IV IN COMPLEX WITH TAK-322	3.4.14.5
3G0H	HUMAN DEAD-BOX RNA HELICASE DDX19, IN COMPLEX WITH AN ATP-ANALOGUE AND RNA	3.6.1 3.6.4.13
3G0I	COMPLEX OF ASPERGILLUS NIGER EPOXIDE HYDROLASE WITH VALPROMIDE (2-PROPYLPENTANAMIDE)	3.3.2.9 3.3.2.3
3G0Q	CRYSTAL STRUCTURE OF MUTY BOUND TO ITS INHIBITOR DNA	3.2.2 3.2.2.31
3G0R	COMPLEX OF MTH0212 AND AN 8BP DSDNA WITH DISTORTED ENDS	3.1.11.2 4.2.99.18
3G0V	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN FROM THE ROUS SARCOMA VIRUS CAPSID PROTEIN: MUTANT D179A	3.4.23
3G0Z	STRUCTURE OF S. POMBE POP2P - ZN2+ AND MN2+ BOUND FORM	3.1.13.4
3G10	STRUCTURE OF S. POMBE POP2P - MG2+ AND MN2+ BOUND FORM	3.1.13.4
3G1G	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN FROM THE ROUS SARCOMA VIRUS CAPSID PROTEIN: HIGH PH	3.4.23
3G1I	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE ROUS SARCOMA VIRUS CAPSID PROTEIN: INTERMEDIATE PH	3.4.23
3G1K	MTH0212 (WT) CRYSTALLIZED IN A MONOCLINIC SPACE GROUP	3.1.11.2 4.2.99.18
3G1P	CRYSTALS STRUCTURE OF PHNP FROM E.COLI K-12	3.1.4.55
3G1U	CRYSTAL STRUCTURE OF LEISHMANIA MAJOR S-ADENOSYLHOMOCYSTEINE HYDROLASE	3.3.1.1
3G21	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE ROUS SARCOMA VIRUS CAPSID PROTEIN: LOW PH	3.4.23
3G26	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE ROUS SARCOMA VIRUS CAPSID PROTEIN: MUTANT A184C	3.4.23
3G27	STRUCTURE OF A PUTATIVE BACTERIOPHAGE PROTEIN FROM ESCHERICHIA COLI STR. K-12 SUBSTR. MG1655	3.1
3G28	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE ROUS SARCOMA VIRUS CAPSID PROTEIN: MUTANT D179N, LOW PH	3.4.23
3G29	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE ROUS SARCOMA VIRUS CAPSID PROTEIN: D179N MUTANT, NEUTRAL PH	3.4.23
3G2C	MTH0212 IN COMPLEX WITH A SHORT SSDNA (CGTA)	3.1.11.2 4.2.99.18
3G2D	COMPLEX OF MTH0212 AND A 4 BP DSDNA WITH 3'-OVERHANG	3.1.11.2 4.2.99.18
3G2Y	CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 1 (GF4)	3.5.2.6
3G2Z	CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 2 (GZ2)	3.5.2.6
3G30	CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 3 (G30)	3.5.2.6
3G31	CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 4 (GF1)	3.5.2.6
3G32	CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 6 (3G3)	3.5.2.6
3G34	CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 11 (1CE)	3.5.2.6
3G35	CTX-M-9 CLASS A BETA-LACTAMASE COMPLEXED WITH COMPOUND 12 (F13)	3.5.2.6
3G38	THE CATALYTICALLY INACTIVE MUTANT MTH0212 (D151N) IN COMPLEX WITH AN 8 BP DSDNA	3.1.11.2 4.2.99.18
3G3C	MTH0212 (WT) IN COMPLEX WITH A 6BP DSDNA CONTAINING A SINGLE ONE NUCLEOTIDE LONG 3'-OVERHANG	3.1.11.2 4.2.99.18
3G3N	PDE7A CATALYTIC DOMAIN IN COMPLEX WITH 3-(2,6-DIFLUOROPHENYL)-2-(METHYLTHIO)QUINAZOLIN-4(3H)-ONE	3.1.4.17 3.1.4.53
3G3V	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME (V131R1) AT 291 K	3.2.1.17
3G3W	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME (T151R1) AT 291 K	3.2.1.17
3G3X	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME (T151R1) AT 100 K	3.2.1.17
3G3Y	MTH0212 IN COMPLEX WITH SSDNA IN SPACE GROUP P32	3.1.11.2 4.2.99.18
3G42	CRYSTAL STRUCTURE OF TACE WITH TRYPTOPHAN SULFONAMIDE DERIVATIVE INHIBITOR	3.4.24.86
3G45	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 4B WITH REGULATORY DOMAIN AND D155988	3.1.4.17 3.1.4.53
3G4E	CRYSTAL STRUCTURE OF HUMAN SENESCENCE MARKER PROTEIN-30(SMP30)(CALCIUM BOUND)	3.1.1.17
3G4H	CRYSTAL STRUCTURE OF HUMAN SENESCENCE MARKER PROTEIN-30 (ZINC BOUND)	3.1.1.17
3G4I	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 4D WITH D155871	3.1.4.17 3.1.4.53
3G4K	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 4D WITH ROLIPRAM	3.1.4.17 3.1.4.53
3G4L	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 4D WITH ROFLUMILAST	3.1.4.17 3.1.4.53
3G4P	OXA-24 BETA-LACTAMASE AT PH 7.5	3.5.2.6
3G4T	MTH0212 (WT) IN COMPLEX WITH A 7BP DSDNA	3.1.11.2 4.2.99.18
3G58	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 4D WITH D155988/PMNPQ	3.1.4.17 3.1.4.53
3G5I	CRYSTAL STRUCTURE OF THE E.COLI RIHA PYRIMIDINE NUCLEOSIDASE BOUND TO A IMINORIBITOL-BASED INHIBITOR	3.2.2.8 3.2
3G5K	STRUCTURE AND ACTIVITY OF HUMAN MITOCHONDRIAL PEPTIDE DEFORMYLASE, A NOVEL CANCER TARGET	3.5.1.88
3G5P	STRUCTURE AND ACTIVITY OF HUMAN MITOCHONDRIAL PEPTIDE DEFORMYLASE, A NOVEL CANCER TARGET	3.5.1.88
3G65	CRYSTAL STRUCTURE OF THE HUMAN RAD9-RAD1-HUS1 DNA DAMAGE CHECKPOINT COMPLEX	3.1.11.2
3G6L	THE CRYSTAL STRUCTURE OF A CHITINASE CRCHI1 FROM THE NEMATOPHAGOUS FUNGUS CLONOSTACHYS ROSEA	3.2.1.14
3G6M	CRYSTAL STRUCTURE OF A CHITINASE CRCHI1 FROM THE NEMATOPHAGOUS FUNGUS CLONOSTACHYS ROSEA IN COMPLEX WITH A POTENT INHIBITOR CAFFEINE	3.2.1.14
3G6N	CRYSTAL STRUCTURE OF AN EFPDF COMPLEX WITH MET-ALA-SER	3.5.1.88
3G6Z	DESIGN AND PREPARATION OF POTENT, NON-PEPTIDIC, BIOAVAILABLE RENIN INHIBITORS	3.4.23.15
3G70	DESIGN AND PREPARATION OF POTENT, NON-PEPTIDIC, BIOAVAILABLE RENIN INHIBITORS	3.4.23.15
3G72	DESIGN AND PREPARATION OF POTENT, NON-PEPTIDIC, BIOAVAILABLE RENIN INHIBITORS	3.4.23.15
3G77	BACTERIAL CYTOSINE DEAMINASE V152A/F316C/D317G MUTANT	3.5.4.1 3.5.4
3G7N	CRYSTAL STRUCTURE OF A TRIACYLGLYCEROL LIPASE FROM PENICILLIUM EXPANSUM AT 1.3	3.1.1.3
3G7T	CRYSTAL STRUCTURE OF DENGUE VIRUS TYPE 1 ENVELOPE PROTEIN IN THE POSTFUSION CONFORMATION	3.4.21.91 3.6.1.15 3.6.4.13
3G86	HEPATITIS C VIRUS POLYMERASE NS5B (BK 1-570) WITH THIAZINE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3G8F	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN A GROUP II PHOSPHOLIPASE A2 AND DESIGNED PEPTIDE INHIBITOR CARBOBENZOXY-DEHYDRO-VAL-ALA-ARG-SER AT 1.2 A RESOLUTION	3.1.1.4
3G8G	CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 AMMODYTOXIN A FROM VIPERA AMMODYTES AMMODYTES	3.1.1.4
3G8H	CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 AMMODYTOXIN C FROM VIPERA AMMODYTES AMMODYTES	3.1.1.4
3G8Q	A CYTIDINE DEAMINASE EDITS C-TO-U IN TRANSFER RNAS IN ARCHAEA	3.5.4.35
3G8V	THE RATIONALLY DESIGNED CATALYTICALLY INACTIVE MUTANT MTH0212(D151N)	3.1.11.2 4.2.99.18
3G91	1.2 ANGSTROM STRUCTURE OF THE EXONUCLEASE III HOMOLOGUE MTH0212	3.1.11.2 4.2.99.18
3G9D	CRYSTAL STRUCTURE GLYCOHYDROLASE	3.2.2.24
3G9T	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY P-NITROPHENYL BUTYRATE FOR 5SEC	3.1.1
3G9U	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY P-NITROPHENYL BUTYRATE FOR 5MIN	3.1.1
3G9X	STRUCTURE OF HALOALKANE DEHALOGENASE DHAA14 MUTANT I135F FROM RHODOCOCCUS RHODOCHROUS	3.8.1.5
3G9Z	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY P-NITROPHENYL CAPRYLATE	3.1.1
3GA2	CRYSTAL STRUCTURE OF THE ENDONUCLEASE_V (BSU36170) FROM BACILLUS SUBTILIS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SR624	3.1.21.7
3GA3	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF HUMAN MDA5	3.6.1 3.6.4.13
3GA6	MTH0212 IN COMPLEX WITH TWO DNA HELICES	3.1.11.2 4.2.99.18
3GA7	1.55 ANGSTROM CRYSTAL STRUCTURE OF AN ACETYL ESTERASE FROM SALMONELLA TYPHIMURIUM	3.1.1
3GB0	CRYSTAL STRUCTURE OF AMINOPEPTIDASE PEPT (NP_980509.1) FROM BACILLUS CEREUS ATCC 10987 AT 2.04 A RESOLUTION	3.4.11
3GBO	CRYSTAL STRUCTURE OF BMOOMPALPHA-I, A NON-HEMORRHAGIC METALLOPROTEINASE ISOLATED FROM BOTHROPS MOOJENI SNAKE VENOM	3.4.24
3GBS	CRYSTAL STRUCTURE OF ASPERGILLUS ORYZAE CUTINASE	3.1.1.74
3GC6	STRUCTURAL INSIGHTS INTO THE CATALYTIC MECHANISM OF CD38: EVIDENCE FOR A CONFORMATIONALLY FLEXIBLE COVALENT ENZYME-SUBSTRATE COMPLEX.	3.2.2.5 2.4.99.20 3.2.2.6
3GCB	GAL6 (YEAST BLEOMYCIN HYDROLASE) MUTANT C73A/DELTAK454	3.4.22 3.4.22.40
3GCD	STRUCTURE OF THE V. CHOLERAE RTX CYSTEINE PROTEASE DOMAIN IN COMPLEX WITH AN AZA-LEUCINE PEPTIDE INHIBITOR	3.4.22 6.3.2
3GCG	CRYSTAL STRUCTURE OF MAP AND CDC42 COMPLEX	3.6.5.2
3GCH	CHEMISTRY OF CAGED ENZYMES. BINDING OF PHOTOREVERSIBLE CINNAMATES TO CHYMOTRYPSIN	3.4.21.1
3GCI	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN A NEW ISOFORM OF PHOSPHOLIPASE A2 WITH C-TERMINAL AMYLOID BETA HEPTAPEPTIDE AT 2 A RESOLUTION	3.1.1.4
3GCN	CRYSTAL STRUCTURE OF DEGS H198P/D320A MUTANT MODIFIED BY DFP IN COMPLEX WITH OMP PEPTIDE (YQF)	3.4.21 3.4.21.107
3GCO	CRYSTAL STRUCTURE OF DEGS H198P/D320A MUTANT MODIFIED BY DFP IN COMPLEX WITH DNRDGNVYQF OMP PEPTIDE	3.4.21 3.4.21.107
3GCW	PCSK9:EGFA(H306Y)	3.4.21
3GCX	PCSK9:EGFA (PH 7.4)	3.4.21
3GCZ	YOKOSE VIRUS METHYLTRANSFERASE IN COMPLEX WITH ADOMET	2.1.1.57 3.4.21.91 3.6.1.15 3.6.4.13
3GD0	CRYSTAL STRUCTURE OF LAMINARIPENTAOSE-PRODUCING BETA-1,3-GLUCANASE	3.2.1.39
3GD9	CRYSTAL STRUCTURE OF LAMINARIPENTAOSE-PRODUCING BETA-1,3-GLUCANASE IN COMPLEX WITH LAMINARITETRAOSE	3.2.1.39
3GDB	CRYSTAL STRUCTURE OF SPR0440 GLYCOSIDE HYDROLASE DOMAIN, ENDO-D FROM STREPTOCOCCUS PNEUMONIAE R6	3.2.1.96
3GDS	CRYSTAL STRUCTURE OF DEGS H198P/D320A MUTANT MODIFIED BY DFP IN COMPLEX WITH DNRDGNVYYF PEPTIDE	3.4.21 3.4.21.107
3GDU	CRYSTAL STRUCTURE OF DEGS H198P/D320A MUTANT MODIFIED BY DFP AND IN COMPLEX WITH YRF PEPTIDE	3.4.21 3.4.21.107
3GDV	CRYSTAL STRUCTURE OF DEGS H198P/D320A MUTANT MODIFIED BY DFP AND IN COMPLEX WITH YQF PEPTIDE	3.4.21 3.4.21.107
3GEE	CRYSTAL STRUCTURE OF MNME FROM CHLOROBIUM TEPIDUM IN COMPLEX WITH GDP AND FOLINIC ACID	3.6
3GEH	CRYSTAL STRUCTURE OF MNME FROM NOSTOC IN COMPLEX WITH GDP, FOLINIC ACID AND ZN	3.6
3GEI	CRYSTAL STRUCTURE OF MNME FROM CHLOROBIUM TEPIDUM IN COMPLEX WITH GCP	3.6
3GEL	O-METHYLPHOSPHORYLATED TORPEDO ACETYLCHOLINESTERASE OBTAINED BY REACTION WITH METHYL PARAOXON (AGED)	3.1.1.7
3GF0	BIFUNCTIONAL DCTP DEAMINASE-DUTPASE MUTANT ENZYME VARIANT E145Q FROM METHANOCALDOCOCCUS JANNASCHII IN COMPLEX WITH PYROPHOSPHATE AND MAGNESIUM	3.5.4.30
3GFO	STRUCTURE OF CBIO1 FROM CLOSTRIDIUM PERFRINGENS: PART OF THE ABC TRANSPORTER COMPLEX CBIONQ.	3.6.3
3GFP	STRUCTURE OF THE C-TERMINAL DOMAIN OF THE DEAD-BOX PROTEIN DBP5	3.6.1 3.6.4.13
3GFT	HUMAN K-RAS (Q61H) IN COMPLEX WITH A GTP ANALOGUE	3.6.5.2
3GG6	CRYSTAL STRUCTURE OF THE NUDIX DOMAIN OF HUMAN NUDT18	3.6.1 3.6.1.58
3GGA	HIV PROTEASE INHIBITORS WITH PSEUDO-SYMMETRIC CORES	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
3GGR	CRYSTAL STRUCTURE OF THE HUMAN RAD9-HUS1-RAD1 COMPLEX	3.1.11.2
3GGU	HIV PR DRUG RESISTANT PATIENT'S VARIANT IN COMPLEX WITH DARUNAVIR	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
3GGV	HIV PROTEASE, PSEUDO-SYMMETRIC INHIBITORS	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
3GGX	HIV PROTEASE, PSEUDO-SYMMETRIC INHIBITORS	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
3GH1	CRYSTAL STRUCTURE OF PREDICTED NUCLEOTIDE-BINDING PROTEIN FROM VIBRIO CHOLERAE	3.2.2.4
3GH3	STRUCTURAL INSIGHTS INTO THE CATALYTIC MECHANISM OF CD38: EVIDENCE FOR A CONFORMATIONALLY FLEXIBLE COVALENT ENZYME-SUBSTRATE COMPLEX.	3.2.2.5 2.4.99.20 3.2.2.6
3GH4	CRYSTAL STRUCTURE OF BETA-HEXOSAMINIDASE FROM PAENIBACILLUS SP. TS12	3.2.1.52
3GH5	CRYSTAL STRUCTURE OF BETA-HEXOSAMINIDASE FROM PAENIBACILLUS SP. TS12 IN COMPLEX WITH GLCNAC	3.2.1.52
3GH7	CRYSTAL STRUCTURE OF BETA-HEXOSAMINIDASE FROM PAENIBACILLUS SP. TS12 IN COMPLEX WITH GALNAC	3.2.1.52
3GHH	STRUCTURAL INSIGHTS INTO THE CATALYTIC MECHANISM OF CD38: EVIDENCE FOR A CONFORMATIONALLY FLEXIBLE COVALENT ENZYME-SUBSTRATE COMPLEX.	3.2.2.5 2.4.99.20 3.2.2.6
3GHM	CRYSTAL STRUCTURE OF THE EXOSITE-CONTAINING FRAGMENT OF HUMAN ADAMTS13 (FORM-1)	3.4.24 3.4.24.87
3GHN	CRYSTAL STRUCTURE OF THE EXOSITE-CONTAINING FRAGMENT OF HUMAN ADAMTS13 (FORM-2)	3.4.24 3.4.24.87
3GI0	CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED 203 AMINO ACID 'COVALENT DIMER' [L-ALA51,D-ALA51'] HIV-1 PROTEASE MOLECULE COMPLEXED WITH JG-365 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
3GI4	CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, KB60 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
3GI5	CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, KB62 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
3GI6	CRYSTAL STRUCTURE OF PROTEASE INHIBITOR, AD78 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
3GIC	STRUCTURE OF THROMBIN MUTANT DELTA(146-149E) IN THE FREE FORM	3.4.21.5
3GIP	CRYSTAL STRUCTURE OF N-ACYL-D-GLUTAMATE DEACYLASE FROM BORDETELLA BRONCHISEPTICA COMPLEXED WITH ZINC, ACETATE AND FORMATE IONS.	3.5.1.82
3GIQ	CRYSTAL STRUCTURE OF N-ACYL-D-GLUTAMATE DEACYLASE FROM BORDETELLA BRONCHISEPTICA COMPLEXED WITH ZINC AND PHOSPHONATE INHIBITOR, A MIMIC OF THE REACTION TETRAHEDRAL INTERMEDIATE.	3.5.1.82
3GIS	CRYSTAL STRUCTURE OF NA-FREE THROMBIN IN COMPLEX WITH THROMBOMODULIN	3.4.21.5
3GIU	1.25 ANGSTROM CRYSTAL STRUCTURE OF PYRROLIDONE-CARBOXYLATE PEPTIDASE (PCP) FROM STAPHYLOCOCCUS AUREUS	3.4.19.3
3GJQ	CASPASE-3 BINDS DIVERSE P4 RESIDUES IN PEPTIDES	3.4.22.56
3GJR	CASPASE-3 BINDS DIVERSE P4 RESIDUES IN PEPTIDES	3.4.22.56
3GJS	CASPASE-3 BINDS DIVERSE P4 RESIDUES IN PEPTIDES	3.4.22.56
3GJT	CASPASE-3 BINDS DIVERSE P4 RESIDUES IN PEPTIDES	3.4.22.56
3GKL	FOLLOWING EVOLUTIONARY PATHS TO HIGH AFFINITY AND SELECTIVITY PROTEIN-PROTEIN INTERACTIONS USING COLICIN7 AND IMMUNITY PROTEINS	3.1
3GL1	CRYSTAL STRUCTURE OF ATPASE DOMAIN OF SSB1 CHAPERONE, A MEMBER OF THE HSP70 FAMILY, FROM SACCHAROMYCES CEREVISIAE	3.6.4.10
3GLJ	A POLYMORPH OF CARBOXYPEPTIDASE B ZYMOGEN STRUCTURE	3.4.17.2
3GLQ	CRYSTAL STRUCTURE OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE FROM BURKHOLDERIA PSEUDOMALLEI IN COMPLEX WITH 9-BETA-D-ARABINO-FURANSYL-ADENINE	3.3.1.1
3GLR	CRYSTAL STRUCTURE OF HUMAN SIRT3 WITH ACETYL-LYSINE ACECS2 PEPTIDE	3.5.1 2.3.1.286
3GLS	CRYSTAL STRUCTURE OF HUMAN SIRT3	3.5.1 2.3.1.286
3GLT	CRYSTAL STRUCTURE OF HUMAN SIRT3 WITH ADPR BOUND TO THE ACECS2 PEPTIDE CONTAINING A THIOACETYL LYSINE	3.5.1 2.3.1.286
3GLU	CRYSTAL STRUCTURE OF HUMAN SIRT3 WITH ACECS2 PEPTIDE	3.5.1 2.3.1.286
3GLY	REFINED CRYSTAL STRUCTURES OF GLUCOAMYLASE FROM ASPERGILLUS AWAMORI VAR. X100	3.2.1.3
3GM8	CRYSTAL STRUCTURE OF A BETA-GLYCOSIDASE FROM BACTEROIDES VULGATUS	3.2.1
3GMW	CRYSTAL STRUCTURE OF BETA-LACTAMSE INHIBITORY PROTEIN-I (BLIP-I) IN COMPLEX WITH TEM-1 BETA-LACTAMASE	3.5.2.6
3GMZ	CRYSTAL OF HUMAN ARGINASE IN COMPLEX WITH L-ORNITHINE. RESOLUTION 1.43 A.	3.5.3.1
3GN0	CRYSTAL STRUCTURE OF HUMAN ARGINASE I IN COMPLEX WITH DIFLUOROMETHYLORNITHINE (DFMO)	3.5.3.1
3GNA	CRYSTAL STRUCTURE OF THE RAG1 NONAMER-BINDING DOMAIN WITH DNA	3.1 2.3.2.27
3GNB	CRYSTAL STRUCTURE OF THE RAG1 NONAMER-BINDING DOMAIN WITH DNA	3.1 2.3.2.27
3GNO	CRYSTAL STRUCTURE OF A RICE OS3BGLU6 BETA-GLUCOSIDASE	3.2.1.21
3GNP	CRYSTAL STRUCTURE OF A RICE OS3BGLU6 BETA-GLUCOSIDASE WITH OCTYL-BETA-D-THIO-GLUCOSIDE	3.2.1.21
3GNR	CRYSTAL STRUCTURE OF A RICE OS3BGLU6 BETA-GLUCOSIDASE WITH COVALENTLY BOUND 2-DEOXY-2-FLUOROGLUCOSIDE TO THE CATALYTIC NUCLEOPHILE E396	3.2.1.21
3GNV	HCV NS5B POLYMERASE IN COMPLEX WITH 1,5 BENZODIAZEPINE INHIBITOR 1B	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3GNW	HCV NS5B POLYMERASE IN COMPLEX WITH 1,5 BENZODIAZEPINE INHIBITOR 4C	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3GO8	MUTM ENCOUNTERING AN INTRAHELICAL 8-OXOGUANINE (OXOG) LESION IN EC3-LOOP DELETION COMPLEX	3.2.2.23 4.2.99.18
3GOC	CRYSTAL STRUCTURE OF THE ENDONUCLEASE V (SAV1684) FROM STREPTOMYCES AVERMITILIS. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SVR196	3.1.21.7
3GOD	STRUCTURAL BASIS FOR DNASE ACTIVITY OF A CONSERVED PROTEIN IMPLICATED IN CRISPR-MEDIATED ANTIVIRAL DEFENSE	3.1
3GOL	HCV NS5B POLYMERASE IN COMPLEX WITH 1,5 BENZODIAZEPINE INHIBITOR (R)-11D	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3GOV	CRYSTAL STRUCTURE OF THE CATALYTIC REGION OF HUMAN MASP-1	3.4.21
3GP1	MUTM ENCOUNTERING AN INTRAHELICAL 8-OXOGUANINE (OXOG) LESION IN EC3-V222P COMPLEX	4.2.99.18 3.2.2.23
3GP8	CRYSTAL STRUCTURE OF THE BINARY COMPLEX OF RECD2 WITH DNA	3.6.4.12
3GPG	CRYSTAL STRUCTURE OF MACRO DOMAIN OF CHIKUNGUNYA VIRUS	2.1.1 2.7.7 3.1.3.33 3.4.22 3.6.1.15 3.6.4.13 3.1.3.84 2.7.7.19 2.7.7.48
3GPL	CRYSTAL STRUCTURE OF THE TERNARY COMPLEX OF RECD2 WITH DNA AND ADPNP	3.6.4.12
3GPO	CRYSTAL STRUCTURE OF MACRO DOMAIN OF CHIKUNGUNYA VIRUS IN COMPLEX WITH ADP-RIBOSE	2.1.1 2.7.7 3.1.3.33 3.4.22 3.6.1.15 3.6.4.13 3.1.3.84 2.7.7.19 2.7.7.48
3GPP	MUTM ENCOUNTERING AN INTRAHELICAL 8-OXOGUANINE (OXOG) LESION IN EC3-T224P COMPLEX	4.2.99.18 3.2.2.23
3GPQ	CRYSTAL STRUCTURE OF MACRO DOMAIN OF CHIKUNGUNYA VIRUS IN COMPLEX WITH RNA	2.1.1 2.7.7 3.1.3.33 3.4.22 3.6.1.15 3.6.4.13 3.1.3.84 2.7.7.19 2.7.7.48
3GPU	MUTM ENCOUNTERING AN INTRAHELICAL 8-OXOGUANINE (OXOG) LESION IN EC4-LOOP DELETION COMPLEX	4.2.99.18 3.2.2.23
3GPX	SEQUENCE-MATCHED MUTM INTERROGATION COMPLEX 4 (IC4)	4.2.99.18 3.2.2.23
3GPY	SEQUENCE-MATCHED MUTM LESION RECOGNITION COMPLEX 3 (LRC3)	4.2.99.18 3.2.2.23
3GQ3	MUTM ENCOUNTERING AN INTRAHELICAL 8-OXOGUANINE (OXOG) LESION IN EC5-LOOP DELETION COMPLEX	4.2.99.18 3.2.2.23
3GQ4	SEQUENCE-MATCHED MUTM LESION RECOGNITION COMPLEX 5 (LRC5)	4.2.99.18 3.2.2.23
3GQ5	SEQUENCE-MATCHED MUTM INTERROGATION COMPLEX 5 (IC5)	4.2.99.18 3.2.2.23
3GQB	CRYSTAL STRUCTURE OF THE A3B3 COMPLEX FROM V-ATPASE	3.6.3.14 7.1.2.2
3GQE	CRYSTAL STRUCTURE OF MACRO DOMAIN OF VENEZUELAN EQUINE ENCEPHALITIS VIRUS	2.1.1 2.7.7 3.1.3.33 3.4.22 3.6.1.15 3.6.4.13 3.1.3.84 2.7.7.19 2.7.7.48
3GQO	CRYSTAL STRUCTURE OF MACRO DOMAIN OF VENEZUELAN EQUINE ENCEPHALITIS VIRUS IN COMPLEX WITH ADP-RIBOSE	2.1.1 2.7.7 3.1.3.33 3.4.22 3.6.1.15 3.6.4.13 3.1.3.84 2.7.7.19 2.7.7.48
3GQZ	AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT-BASED INHIBITOR	3.5.2.6
3GR2	AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT-BASED INHIBITOR	3.5.2.6
3GRH	CRYSTAL STRUCTURE OF ESCHERICHIA COLI YBHC	3.1.2
3GRI	THE CRYSTAL STRUCTURE OF A DIHYDROOROTASE FROM STAPHYLOCOCCUS AUREUS	3.5.2.3
3GRJ	AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT-BASED INHIBITOR	3.5.2.6
3GRN	CRYSTAL STRUCTURE OF MUTT PROTEIN FROM METHANOSARCINA MAZEI GO1	3.6.1
3GRO	HUMAN PALMITOYL-PROTEIN THIOESTERASE 1	3.1.2.22
3GS6	VIBRIO CHOLEREA FAMILY 3 GLYCOSIDE HYDROLASE (NAGZ)IN COMPLEX WITH N-BUTYRYL-PUGNAC	3.2.1.52
3GSG	AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT-BASED INHIBITOR	3.5.2.6
3GSM	VIBRIO CHOLERAE FAMILY 3 GLYCOSIDE HYDROLASE (NAGZ) BOUND TO N-VALERYL-PUGNAC	3.2.1.52
3GSP	RIBONUCLEASE T1 COMPLEXED WITH 2',3'-CGPS + 3'-GMP, 4 DAYS	3.1.27.3 4.6.1.24
3GSZ	STRUCTURE OF THE GENOTYPE 2B HCV POLYMERASE	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3GT3	STRUCTURE OF PROTEINASE K WITH THE MAD TRIANGLE B3C	3.4.21.64
3GT4	STRUCTURE OF PROTEINASE K WITH THE MAGIC TRIANGLE I3C	3.4.21.64
3GTC	AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT-BASED INHIBITOR	3.5.2.6
3GTN	CRYSTAL STRUCTURE OF XYNC FROM BACILLUS SUBTILIS 168	3.2.1.136
3GUI	T4 LYSOZYME M102E/L99A MUTANT WITH BURIED CHARGE IN APOLAR CAVITY--APO STRUCTURE	3.2.1.17
3GUJ	T4 LYSOZYME M102E/L99A MUTANT WITH BURIED CHARGE IN APOLAR CAVITY--BENZENE BINDING	3.2.1.17
3GUK	T4 LYSOZYME M102E/L99A MUTANT WITH BURIED CHARGE IN APOLAR CAVITY--TOLUENE BINDING	3.2.1.17
3GUL	T4 LYSOZYME M102E/L99A MUTANT WITH BURIED CHARGE IN APOLAR CAVITY--ETHYLBENZENE BINDING	3.2.1.17
3GUM	T4 LYSOZYME M102E/L99A MUTANT WITH BURIED CHARGE IN APOLAR CAVITY--P-XYLENE BINDING	3.2.1.17
3GUN	T4 LYSOZYME M102E/L99A MUTANT WITH BURIED CHARGE IN APOLAR CAVITY--ANILINE BINDING	3.2.1.17
3GUO	T4 LYSOZYME M102E/L99A MUTANT WITH BURIED CHARGE IN APOLAR CAVITY--PHENOL BINDING	3.2.1.17
3GUP	T4 LYSOZYME M102E/L99A MUTANT WITH BURIED CHARGE IN APOLAR CAVITY--PYRIDINE BINDING	3.2.1.17
3GUU	X-RAY STRUCTURE OF CANDIDA ANTARCTICA LIPASE A	3.1.1.3
3GV4	CRYSTAL STRUCTURE OF HUMAN HDAC6 ZINC FINGER DOMAIN AND UBIQUITIN C-TERMINAL PEPTIDE RLRGG	3.5.1.98 3.5.1
3GV9	AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT-BASED INHIBITOR	3.5.2.6
3GVB	AMPC BETA-LACTAMASE IN COMPLEX WITH FRAGMENT-BASED INHIBITOR	3.5.2.6
3GVE	CRYSTAL STRUCTURE OF CALCINEURIN-LIKE PHOSPHOESTERASE YFKN FROM BACILLUS SUBTILIS	3.1.3.6 3.1.4.16 3.1.3.5
3GVF	1.7 ANGSTROM CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM BURKHOLDERIA PSEUDOMALLEI BOUND WITH PHOSPHATE	3.6.1.1
3GVJ	CRYSTAL STRUCTURE OF AN ENDO-NEURAMINIDASENF MUTANT	3.2.1.129
3GVK	CRYSTAL STRUCTURE OF ENDO-NEURAMINIDASE NF MUTANT	3.2.1.129
3GVL	CRYSTAL STRUCTURE OF ENDO-NEURAMINIDASENF	3.2.1.129
3GVP	HUMAN SAHH-LIKE DOMAIN OF HUMAN ADENOSYLHOMOCYSTEINASE 3	3.3.1.1
3GW5	CRYSTAL STRUCTURE OF HUMAN RENIN COMPLEXED WITH A NOVEL INHIBITOR	3.4.23.15
3GW6	INTRAMOLECULAR CHAPERONE	3.2.1.129
3GWB	CRYSTAL STRUCTURE OF PEPTIDASE M16 INACTIVE DOMAIN FROM PSEUDOMONAS FLUORESCENS. NORTHEAST STRUCTURAL GENOMICS TARGET PLR293L	3.4.24
3GWI	CRYSTAL STRUCTURE OF MG-ATPASE NUCLEOTIDE BINDING DOMAIN	3.6.3.2 7.2.2.14
3GWT	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B2B IN COMPLEX WITH A QUINOLINE INHIBITOR	3.1.4.17 3.1.4.53
3GXD	CRYSTAL STRUCTURE OF APO ACID-BETA-GLUCOSIDASE PH 4.5	3.2.1.45 2.4.1 3.2.1
3GXF	CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH ISOFAGOMINE AT NEUTRAL PH	3.2.1.45 2.4.1 3.2.1
3GXI	CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE AT PH 5.5	3.2.1.45 2.4.1 3.2.1
3GXK	THE CRYSTAL STRUCTURE OF G-TYPE LYSOZYME FROM ATLANTIC COD (GADUS MORHUA L.) IN COMPLEX WITH NAG OLIGOMERS SHEDS NEW LIGHT ON SUBSTRATE BINDING AND THE CATALYTIC MECHANISM. NATIVE STRUCTURE TO 1.9	3.2.1.17
3GXM	CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE AT PH 4.5, PHOSPHATE CRYSTALLIZATION CONDITION	3.2.1.45 2.4.1 3.2.1
3GXN	CRYSTAL STRUCTURE OF APO ALPHA-GALACTOSIDASE A AT PH 4.5	3.2.1.22 3.2.1.47
3GXP	CRYSTAL STRUCTURE OF ACID-ALPHA-GALACTOSIDASE A COMPLEXED WITH GALACTOSE AT PH 4.5	3.2.1.22 3.2.1.47
3GXR	THE CRYSTAL STRUCTURE OF G-TYPE LYSOZYME FROM ATLANTIC COD (GADUS MORHUA L.) IN COMPLEX WITH NAG OLIGOMERS SHEDS NEW LIGHT ON SUBSTRATE BINDING AND THE CATALYTIC MECHANISM. STRUCTURE WITH NAG TO 1.7	3.2.1.17
3GXT	CRYSTAL STRUCTURE OF ALPHA-GALACTOSIDASE A AT PH 4.5 COMPLEXED WITH 1-DEOXYGALACTONIJIRIMYCIN	3.2.1.22 3.2.1.47
3GXV	THREE-DIMENSIONAL STRUCTURE OF N-TERMINAL DOMAIN OF DNAB HELICASE FROM HELICOBACTER PYLORI AND ITS INTERACTIONS WITH PRIMASE	3.6.1 3.6.4.12
3GY2	A COMPARATIVE STUDY ON THE INHIBITION OF BOVINE BETA-TRYPSIN BY BIS-BENZAMIDINES DIMINAZENE AND PENTAMIDINE BY X-RAY CRYSTALLOGRAPHY AND ITC	3.4.21.4
3GY3	A COMPARATIVE STUDY ON THE INHIBITION OF BOVINE BETA-TRYPSIN BY BIS-BENZAMIDINES DIMINAZENE AND PENTAMIDINE BY X-RAY CRYSTALLOGRAPHY AND ITC	3.4.21.4
3GY4	A COMPARATIVE STUDY ON THE INHIBITION OF BOVINE BETA-TRYPSIN BY BIS-BENZAMIDINES DIMINAZENE AND PENTAMIDINE BY X-RAY CRYSTALLOGRAPHY AND ITC	3.4.21.4
3GY5	A COMPARATIVE STUDY ON THE INHIBITION OF BOVINE BETA-TRYPSIN BY BIS-BENZAMIDINES DIMINAZENE AND PENTAMIDINE BY X-RAY CRYSTALLOGRAPHY AND ITC	3.4.21.4
3GY6	A COMPARATIVE STUDY ON THE INHIBITION OF BOVINE BETA-TRYPSIN BY THE BIS-BENZAMIDINES DIMINAZENE AND PENTAMIDINE	3.4.21.4
3GY7	A COMPARATIVE STUDY ON THE INHIBITION OF BOVINE BETA-TRYPSIN BY BIS-BENZAMIDINES DIMINAZENE AND PENTAMIDINE BY X-RAY CRYSTALLOGRAPHY AND ITC	3.4.21.4
3GY8	A COMPARATIVE STUDY ON THE INHIBITION OF BOVINE BETA-TRYPSIN BY BIS-BENZAMIDINES DIMINAZENE AND PENTAMIDINE BY X-RAY CRYSTALLOGRAPHY AND ITC	3.4.21.4
3GYG	CRYSTAL STRUCTURE OF YHJK (HALOACID DEHALOGENASE-LIKE HYDROLASE PROTEIN) FROM BACILLUS SUBTILIS	3.1.3.92
3GYL	STRUCTURE OF PROSTASIN AT 1.3 ANGSTROMS RESOLUTION IN COMPLEX WITH A CALCIUM ION.	3.4.21
3GYM	STRUCTURE OF PROSTASIN IN COMPLEX WITH APROTININ	3.4.21
3GYN	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL MONOCYCLIC DIHYDROPYRIDINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3GZF	STRUCTURE OF THE C-TERMINAL DOMAIN OF NSP4 FROM FELINE CORONAVIRUS	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
3GZJ	CRYSTAL STRUCTURE OF POLYNEURIDINE ALDEHYDE ESTERASE COMPLEXED WITH 16-EPI-VELLOSIMINE	3.1.1.78
3GZK	STRUCTURE OF A. ACIDOCALDARIUS CELLULASE CELA	3.2.1.4
3H08	CRYSTAL STRUCTURE OF THE RIBONUCLEASE H1 FROM CHLOROBIUM TEPIDUM	3.1.26.4
3H09	THE STRUCTURE OF HAEMOPHILUS INFLUENZAE IGA1 PROTEASE	3.4.21.72
3H0B	DISCOVERY OF AMINOHETEROCYCLES AS A NOVEL BETA-SECRETASE INHIBITOR CLASS	3.4.23.46
3H0C	CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (CD26) IN COMPLEX WITH A REVERSED AMIDE INHIBITOR	3.4.14.5
3H0E	3,4-DIHYDROPYRIMIDO(1,2-A)INDOL-10(2H)-ONES AS POTENT NON-PEPTIDIC INHIBITORS OF CASPASE-3	3.4.22.56
3H0O	THE IMPORTANCE OF CH-PI STACKING INTERACTIONS BETWEEN CARBOHYDRATE AND AROMATIC RESIDUES IN TRUNCATED FIBROBACTER SUCCINOGENES 1,3-1,4-BETA-D-GLUCANASE	3.2.1.73
3H0X	CRYSTAL STRUCTURE OF PEPTIDE-BINDING DOMAIN OF KAR2 PROTEIN FROM SACCHAROMYCES CEREVISIAE	3.6.4.10
3H16	CRYSTAL STRUCTURE OF A BACTERIA TIR DOMAIN, PDTIR FROM PARACOCCUS DENITRIFICANS	3.2.2.6
3H17	CRYSTAL STRUCTURE OF ESTE5-PMSF (I)	3.1.1
3H18	CRYSTAL STRUCTURE OF ESTE5-PMSF (II)	3.1.1
3H19	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY METHYL ALCOHOL	3.1.1
3H1A	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY ETHYL ALCOHOL	3.1.1
3H1B	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY ISOPROPYL ALCOHOL	3.1.1
3H1P	MATURE CASPASE-7 I213A WITH DEVD-CHO INHIBITOR BOUND TO ACTIVE SITE	3.4.22.60
3H1X	SIMULTANEOUS INHIBITION OF ANTI-COAGULATION AND INFLAMMATION: CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 COMPLEXED WITH INDOMETHACIN AT 1.4 A RESOLUTION REVEALS THE PRESENCE OF THE NEW COMMON LIGAND BINDING SITE	3.1.1.4
3H2G	CRYSTAL STRUCTURE OF A RICE CELL WALL DEGRADING ESTERASE LIPA FROM XANTHOMONAS ORYZAE	3.1.1
3H2H	CRYSTAL STRUCTURE OF G231F MUTANT OF THE RICE CELL WALL DEGRADING ESTERASE LIPA FROM XANTHOMONAS ORYZAE	3.1.1
3H2I	CRYSTAL STRUCTURE OF N228W MUTANT OF THE RICE CELL WALL DEGRADING ESTERASE LIPA FROM XANTHOMONAS ORYZAE	3.1.1
3H2J	CRYSTAL STRUCTURE OF THE RICE CELL WALL DEGRADING ESTERASE LIPA FROM XANTHOMONAS ORYZAE	3.1.1
3H2K	CRYSTAL STRUCTURE OF A LIGAND-BOUND FORM OF THE RICE CELL WALL DEGRADING ESTERASE LIPA FROM XANTHOMONAS ORYZAE	3.1.1
3H2L	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE IN COMPLEX WITH A NOVEL BICYCLIC DIHYDRO-PYRIDINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3H2W	STRUCTURE OF A. ACIDOCALDARIUS CELLULASE CELA IN COMPLEX WITH CELLOBIOSE	3.2.1.4
3H2X	CRYSTAL STRUCTURE OF THE HUMAN LYMPHOID TYROSINE PHOSPHATASE CATALYTIC DOMAIN	3.1.3.48
3H3K	STRUCTURE OF A. ACIDOCALDARIUS CELLULASE CELA IN COMPLEX WITH CELLOTETRAOSE	3.2.1.4
3H41	CRYSTAL STRUCTURE OF A NLPC/P60 FAMILY PROTEIN (BCE_2878) FROM BACILLUS CEREUS ATCC 10987 AT 1.79 A RESOLUTION	3.4.14.13
3H42	CRYSTAL STRUCTURE OF PCSK9 IN COMPLEX WITH FAB FROM LDLR COMPETITIVE ANTIBODY	3.4.21
3H44	CRYSTAL STRUCTURE OF INSULIN DEGRADING ENZYME IN COMPLEX WITH MACROPHAGE INFLAMMATORY PROTEIN 1 ALPHA	3.4.24.56
3H47	X-RAY STRUCTURE OF HEXAMERIC 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
3H4R	CRYSTAL STRUCTURE OF E. COLI RECE EXONUCLEASE	3.1.11
3H4W	STRUCTURE OF A CA+2 DEPENDENT PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C (PI-PLC) ENZYME FROM STREPTOMYCES ANTIBIOTICUS	3.1.4.11
3H4X	STRUCTURE OF A CA+2 DEPENDENT PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C (PI-PLC) ENZYME FROM STREPTOMYCES ANTIBIOTICUS	3.1.4.11
3H53	CRYSTAL STRUCTURE OF HUMAN ALPHA-N-ACETYLGALACTOSAMINIDASE	3.2.1.49
3H54	CRYSTAL STRUCTURE OF HUMAN ALPHA-N-ACETYLGALACTOSAMINIDASE,COMPLEX WITH GALNAC	3.2.1.49
3H55	CRYSTAL STRUCTURE OF HUMAN ALPHA-N-ACETYLGALACTOSAMINIDASE, COMPLEX WITH GALACTOSE	3.2.1.49
3H59	HEPATITIS C VIRUS POLYMERASE NS5B WITH THIAZINE INHIBITOR 2	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3H5B	CRYSTAL STRUCTURE OF WILD TYPE HIV-1 PROTEASE WITH NOVEL P1'-LIGAND GRL-02031	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
3H5K	CRYSTAL STRUCTURE OF THE RIBOSOME INACTIVATING PROTEIN PDL1	3.2.2.22
3H5S	HEPATITIS C VIRUS POLYMERASE NS5B WITH SACCHARIN INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3H5U	HEPATITIS C VIRUS POLYMERASE NS5B WITH SACCHARIN INHIBITOR 1	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3H5X	CRYSTAL STRUCTURE OF 2'-AMINO-2'-DEOXY-CYTIDINE-5'-TRIPHOSPHATE BOUND TO NOROVIRUS GII RNA POLYMERASE	2.7.7.48 3.4.22.66 3.6.1.15
3H5Y	NOROVIRUS POLYMERASE+PRIMER/TEMPLATE+CTP COMPLEX AT 6 MM MNCL2	2.7.7.48 3.4.22.66 3.6.1.15
3H60	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C)WITH TWO MN2+ ATOMS	3.1.3.16
3H61	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C) WITH TWO MN2+ ATOMS ORIGINALLY SOAKED WITH NORCANTHARIDIN (WHICH IS PRESENT IN THE STRUCTURE IN THE HYDROLYZED FORM)	3.1.3.16
3H62	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C) WITH TWO MN2+ ATOMS COMPLEXED WITH CANTHARIDIC ACID	3.1.3.16
3H63	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C) WITH TWO MN2+ ATOMS ORIGINALLY SOAKED WITH CANTHARIDIN (WHICH IS PRESENT IN THE STRUCTURE IN THE HYDROLYZED FORM)	3.1.3.16
3H64	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C) WITH TWO MN2+ ATOMS COMPLEXED WITH ENDOTHALL	3.1.3.16
3H66	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C) WITH TWO ZN2+ ATOMS	3.1.3.16
3H67	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C)WITH TWO ZN2+ ATOMS COMPLEXED WITH CANTHARIDIC ACID	3.1.3.16
3H68	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C)WITH TWO ZN2+ ATOMS ORIGINALLY SOAKED WITH CANTHARIDIN (WHICH IS PRESENT IN THE STRUCTURE IN THE HYDROLYZED FORM)	3.1.3.16
3H69	CATALYTIC DOMAIN OF HUMAN SERINE/THREONINE PHOSPHATASE 5 (PP5C) WITH TWO ZN2+ ATOMS COMPLEXED WITH ENDOTHALL	3.1.3.16
3H6D	STRUCTURE OF THE MYCOBACTERIUM TUBERCULOSIS DUTPASE D28N MUTANT	3.6.1.23
3H6M	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS V104E AT CRYOGENIC TEMPERATURE	3.1.31.1
3H6S	STRUCTURE OF CLITOCYPIN - CATHEPSIN V COMPLEX	3.4.22.43
3H6X	CRYSTAL STRUCTURE OF DUTPASE FROM STREPTOCOCCUS MUTANS	3.6.1.23
3H71	CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE D39 NEURAMINIDASE A PRECURSOR (NANA)	3.2.1.18
3H72	CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE D39 NEURAMINIDASE A PRECURSOR (NANA) IN COMPLEX WITH NANA	3.2.1.18
3H73	CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE D39 NEURAMINIDASE A PRECURSOR (NANA) IN COMPLEX WITH DANA	3.2.1.18
3H7C	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA AGMATINE DEIMINASE FROM CELL FREE EXPRESSION	3.5.3.12
3H7D	THE CRYSTAL STRUCTURE OF THE CATHEPSIN K VARIANT M5 IN COMPLEX WITH CHONDROITIN-4-SULFATE	3.4.22.38
3H7I	STRUCTURE OF THE METAL-FREE D132N T4 RNASE H	3.1.26.4
3H7K	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA AGMATINE DEIMINASE COMPLEXED WITH A COVALENTLY BOUND REACTION INTERMEDIATE	3.5.3.12
3H84	CRYSTAL STRUCTURE OF GET3	3.6.3.16 3.6
3H87	RV0301 RV0300 TOXIN ANTITOXIN COMPLEX FROM MYCOBACTERIUM TUBERCULOSIS	3.1
3H89	A COMBINED CRYSTALLOGRAPHIC AND MOLECULAR DYNAMICS STUDY OF CATHEPSIN-L RETRO-BINDING INHIBITORS(COMPOUND 4)	3.4.22.15
3H8B	A COMBINED CRYSTALLOGRAPHIC AND MOLECULAR DYNAMICS STUDY OF CATHEPSIN-L RETRO-BINDING INHIBITORS(COMPOUND 9)	3.4.22.15
3H8C	A COMBINED CRYSTALLOGRAPHIC AND MOLECULAR DYNAMICS STUDY OF CATHEPSIN-L RETRO-BINDING INHIBITORS (COMPOUND 14)	3.4.22.15
3H8E	LOW PH NATIVE STRUCTURE OF LEUCINE AMINOPEPTIDASE FROM PSEUDOMONAS PUTIDA	3.4.11.1 3.4.11.10
3H8J	NATIVE T4 RNASE H IN THE ABSENCE OF DIVALENT METAL IONS	3.1.26.4
3H8S	STRUCTURE OF D19N T4 RNASE H IN THE PRESENCE OF DIVALENT MAGNESIUM	3.1.26.4
3H8W	STRUCTURE OF D132N T4 RNASE H IN THE PRESENCE OF DIVALENT MAGNESIUM	3.1.26.4
3H95	CRYSTAL STRUCTURE OF THE NUDIX DOMAIN OF NUDT6	3.6.1
3H98	CRYSTAL STRUCTURE OF HCV NS5B 1B WITH (1,1-DIOXO-2H-[1,2,4]BENZOTHIADIAZIN-3-YL) AZOLO[1,5-A]PYRIMIDINE DERIVATIVE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3H9U	S-ADENOSYL HOMOCYSTEINE HYDROLASE (SAHH) FROM TRYPANOSOMA BRUCEI	3.3.1.1
3HAB	THE STRUCTURE OF DPP4 IN COMPLEX WITH PIPERIDINE FUSED BENZIMIDAZOLE 25	3.4.14.5
3HAC	THE STRUCTURE OF DPP-4 IN COMPLEX WITH PIPERIDINE FUSED IMIDAZOPYRIDINE 34	3.4.14.5
3HAT	ACTIVE SITE MIMETIC INHIBITION OF THROMBIN	3.4.21.5
3HAU	CRYSTAL STRUCTURE OF CHEMICALLY SYNTHESIZED HIV-1 PROTEASE WITH REDUCED ISOSTERE MVT-101 INHIBITOR	3.4.23.16
3HAW	CRYSTAL STRUCTURE OF [L-ALA51/51']HIV-1 PROTEASE WITH REDUCED ISOSTERE MVT-101 INHIBITOR	3.4.23.16
3HB0	STRUCTURE OF EDEYA2 COMPLEXED WITH BEF3	3.1.3.48
3HB2	PRTC METHIONINE MUTANTS: M226I	3.4.24 3.4.24.40
3HBD	CLASS IV CHITINASE STRUCTURE FROM PICEA ABIES AT 1.8A	3.2.1.14
3HBE	CLASS IV CHITINASE STRUCTURE FROM PICEA ABIES AT 1.55A	3.2.1.14
3HBH	CLASS IV CHITINASE STRUCTURE FROM PICEA ABIES AT 2.25A	3.2.1.14
3HBM	CRYSTAL STRUCTURE OF PSEG FROM CAMPYLOBACTER JEJUNI	3.6.1.57
3HBN	CRYSTAL STRUCTURE PSEG-UDP COMPLEX FROM CAMPYLOBACTER JEJUNI	3.6.1.57
3HBO	CRYSTAL STRUCTURE OF CHEMICALLY SYNTHESIZED [D-ALA51/51']HIV-1 PROTEASE	3.4.23.16
3HBR	CRYSTAL STRUCTURE OF OXA-48 BETA-LACTAMASE	3.5.2.6
3HBU	PRTC METHIONINE MUTANTS: M226H DESY	3.4.24 3.4.24.40
3HBV	PRTC METHIONINE MUTANTS: M226A IN-HOUSE	3.4.24 3.4.24.40
3HC7	CRYSTAL STRUCTURE OF LYSIN B FROM MYCOBACTERIOPHAGE D29	3.1
3HC8	INVESTIGATION OF AMINOPYRIDIOPYRAZINONES AS PDE5 INHIBITORS: EVALUATION OF MODIFICATIONS TO THE CENTRAL RING SYSTEM.	3.1.4.35 3.1.4.53
3HD0	CRYSTAL STRUCTURE OF TM1865, AN ENDONUCLEASE V FROM THERMOTOGA MARITIMA	3.1.21.7
3HD3	HIGH RESOLUTION CRYSTAL STRUCTURE OF CRUZAIN BOUND TO THE VINYL SULFONE INHIBITOR SMDC-256047	3.4.22.51
3HDA	PRTC METHIONINE MUTANTS: M226A_DESY	3.4.24 3.4.24.40
3HDB	CRYSTAL STRUCTURE OF AAHIV, A METALLOPROTEINASE FROM VENOM OF AGKISTRODON ACUTUS	3.4.24
3HDE	CRYSTAL STRUCTURE OF FULL-LENGTH ENDOLYSIN R21 FROM PHAGE 21	3.2.1.17
3HDF	CRYSTAL STRUCTURE OF TRUNCATED ENDOLYSIN R21 FROM PHAGE 21	3.2.1.17
3HDK	CRYSTAL STRUCTURE OF CHEMICALLY SYNTHESIZED [AIB51/51']HIV-1 PROTEASE	3.4.23.16
3HDZ	IDENTIFICATION, SYNTHESIS, AND SAR OF AMINO SUBSTITUTED PYRIDO[3,2B]PRYAZIONES AS POTENT AND SELECTIVE PDE5 INHIBITORS	3.1.4.35 3.1.4.53
3HEA	THE L29P/L124I MUTATION OF PSEUDOMONAS FLUORESCENS ESTERASE	3.1.1.2 1
3HEJ	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS T62R AT CRYOGENIC TEMPERATURE	3.1.31.1
3HFQ	CRYSTAL STRUCTURE OF THE LP_2219 PROTEIN FROM LACTOBACILLUS PLANTARUM. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET LPR118.	3.1.1.31
3HFW	CRYSTAL STRUCTURE OF HUMAN ADP-RIBOSYLHYDROLASE 1 (HARH1)	3.2.2.19
3HG2	HUMAN ALPHA-GALACTOSIDASE CATALYTIC MECHANISM 1. EMPTY ACTIVE SITE	3.2.1.22 3.2.1.47
3HG3	HUMAN ALPHA-GALACTOSIDASE CATALYTIC MECHANISM 2. SUBSTRATE BOUND	3.2.1.22 3.2.1.47
3HG4	HUMAN ALPHA-GALACTOSIDASE CATALYTIC MECHANISM 3. COVALENT INTERMEDIATE	3.2.1.22 3.2.1.47
3HG5	HUMAN ALPHA-GALACTOSIDASE CATALYTIC MECHANISM 4. PRODUCT BOUND	3.2.1.22 3.2.1.47
3HG6	CRYSTAL STRUCTURE OF THE RECOMBINANT ONCONASE FROM RANA PIPIENS	3.1.27
3HGN	STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH A POTENT PEPTIDYL INHIBITOR FR130180 DETERMINED BY NEUTRON CRYSTALLOGRAPHY	3.4.21.36
3HGP	STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH A POTENT PEPTIDYL INHIBITOR FR130180 DETERMINED BY HIGH RESOLUTION CRYSTALLOGRAPHY	3.4.21.36
3HGZ	CRYSTAL STRUCTURE OF HUMAN INSULIN-DEGRADING ENZYME IN COMPLEX WITH AMYLIN	3.4.24.56
3HH3	NEW AZABORINE COMPOUNDS BIND TO THE T4 LYSOZYME L99A CAVITY - 1,2-DIHYDRO-1,2-AZABORINE	3.2.1.17
3HH4	NEW AZABORINE COMPOUNDS BIND TO THE T4 LYSOZYME L99A CAVITY - BENZENE AS CONTROL	3.2.1.17
3HH5	NEW AZABORINE COMPOUNDS BIND TO THE T4 LYSOZYME L99A CAVITY - 1-ETHYL-2-HYDRO-1,2-AZABORINE	3.2.1.17
3HH6	NEW AZABORINE COMPOUNDS BIND TO THE T4 LYSOZYME L99A CAVITY -ETHYLBENZENE AS CONTROL	3.2.1.17
3HHA	CRYSTAL STRUCTURE OF CATHEPSIN L IN COMPLEX WITH AZ12878478	3.4.22.15
3HHI	CRYSTAL STRUCTURE OF CATHEPSIN B FROM T. BRUCEI IN COMPLEX WITH CA074	3.4.22
3HHK	HCV NS5B POLYMERASE COMPLEX WITH A SUBSTITUTED BENZOTHIADIZINE	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
3HI0	CRYSTAL STRUCTURE OF PUTATIVE EXOPOLYPHOSPHATASE (17739545) FROM AGROBACTERIUM TUMEFACIENS STR. C58 (DUPONT) AT 2.30 A RESOLUTION	3.6.1.11
3HI4	SWITCHING CATALYSIS FROM HYDROLYSIS TO PERHYDROLYSIS IN P. FLUORESCENS ESTERASE	3.1.1.2 1
3HIB	CRYSTAL STRUCTURE OF THE SECOND SEC63 DOMAIN OF YEAST BRR2	3.6.1 3.6.4.13
3HIO	CRYSTAL STRUCTURE OF RICIN A-CHAIN IN COMPLEX WITH THE CYCLIC TETRANUCLEOTIDE INHIBITOR, A TRANSITION STATE ANALOGUE	3.2.2.22
3HIQ	CRYSTAL STRUCTURE OF SAPORIN-L1 MUTANT (Y73A) FROM SAPONARIA OFFICINALIS	3.2.2.22
3HIS	CRYSTAL STRUCTURE OF SAPORIN-L1 FROM SAPONARIA OFFICINALIS	3.2.2.22
3HIT	CRYSTAL STRUCTURE OF SAPORIN-L1 IN COMPLEX WITH THE DINUCLEOTIDE INHIBITOR, A TRANSITION STATE ANALOGUE	3.2.2.22
3HIV	CRYSTAL STRUCTURE OF SAPORIN-L1 IN COMPLEX WITH THE TRINUCLEOTIDE INHIBITOR, A TRANSITION STATE ANALOGUE	3.2.2.22
3HIW	CRYSTAL STRUCTURE OF SAPORIN-L1 IN COMPLEX WITH THE CYCLIC TETRANUCLEOTIDE INHIBITOR, A TRANSITION STATE ANALOGUE	3.2.2.22
3HJH	A RIGID N-TERMINAL CLAMP RESTRAINS THE MOTOR DOMAINS OF THE BACTERIAL TRANSCRIPTION-REPAIR COUPLING FACTOR	3.6.1 3.6.4
3HJR	CRYSTAL STRUCTURE OF SERINE PROTEASE OF AEROMONAS SOBRIA	3.4.21
3HJU	CRYSTAL STRUCTURE OF HUMAN MONOGLYCERIDE LIPASE	3.1.1.23
3HK3	CRYSTAL STRUCTURE OF MURINE THROMBIN MUTANT W215A/E217A (ONE MOLECULE IN THE ASYMMETRIC UNIT)	3.4.21.5
3HK6	CRYSTAL STRUCTURE OF MURINE THROMBIN MUTANT W215A/E217A (TWO MOLECULES IN THE ASYMMETRIC UNIT)	3.4.21.5
3HKI	CRYSTAL STRUCTURE OF MURINE THROMBIN MUTANT W215A/E217A IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR1	3.4.21.5
3HKJ	CRYSTAL STRUCTURE OF HUMAN THROMBIN MUTANT W215A/E217A IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR1	3.4.21.5
3HKM	CRYSTAL STRUCTURE OF RICE(ORYZA SATIVA) RRP46	3.1.13
3HKW	HCV NS5B GENOTYPE 1A IN COMPLEX WITH 1,5 BENZODIAZEPINE INHIBITOR 6	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3HKX	CRYSTAL STRUCTURE ANALYSIS OF AN AMIDASE FROM NESTERENKONIA SP.	3.5.1.4
3HKY	HCV NS5B POLYMERASE GENOTYPE 1B IN COMPLEX WITH 1,5 BENZODIAZEPINE 6	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3HL8	CRYSTAL STRUCTURE OF EXONUCLEASE I IN COMPLEX WITH INHIBITOR BCBP	3.1.11.1
3HLH	DIISOPROPYL FLUOROPHOSPHATASE (DFPASE), ACTIVE SITE MUTANTS	3.1.8.2
3HLI	DIISOPROPYL FLUOROPHOSPHATASE (DFPASE), ACTIVE SITE MUTANTS	3.1.8.2
3HLK	CRYSTAL STRUCTURE OF HUMAN MITOCHONDRIAL ACYL-COA THIOESTERASE (ACOT2)	3.1.2.2
3HLO	CRYSTAL STRUCTURE OF CHEMICALLY SYNTHESIZED 'COVALENT DIMER' [GLY51/D-ALA51']HIV-1 PROTEASE	3.4.23.16
3HLW	CTX-M-9 S70G IN COMPLEX WITH CEFOTAXIME	3.5.2.6
3HM7	CRYSTAL STRUCTURE OF ALLANTOINASE FROM BACILLUS HALODURANS C-125	3.5.2.5
3HMB	MUTANT ENDOLYSIN FROM BACILLUS SUBTILIS	3.5.1.28
3HMV	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B2B IN COMPLEX WITH A TETRAHYDROBENZOTHIOPHENE INHIBITOR	3.1.4.17 3.1.4.53
3HMY	CRYSTAL STRUCTURE OF HCR/T COMPLEXED WITH GT2	3.4.24.68
3HN1	CRYSTAL STRUCTURE OF HCR/T COMPLEXED WITH GT2 AND LACTOSE	3.4.24.68
3HN3	HUMAN BETA-GLUCURONIDASE AT 1.7 A RESOLUTION	3.2.1.31
3HN6	CRYSTAL STRUCTURE OF GLUCOSAMINE-6-PHOSPHATE DEAMINASE FROM BORRELIA BURGDORFERI	3.5.99.6
3HO6	STRUCTURE-FUNCTION ANALYSIS OF INOSITOL HEXAKISPHOSPHATE-INDUCED AUTOPROCESSING IN CLOSTRIDIUM DIFFICILE TOXIN A	3.4.22 2.4.1
3HOA	CRYSTAL STRUCTURE OF THE THERMUS THERMOPHILUS M32 CARBOXYPEPTIDASE	3.4.17.19
3HOH	RIBONUCLEASE T1 (THR93GLN MUTANT) COMPLEXED WITH 2'GMP	3.1.27.3 4.6.1.24
3HOS	CRYSTAL STRUCTURE OF THE MARINER MOS1 PAIRED END COMPLEX WITH MG	2.7.7 3.1
3HOT	CRYSTAL STRUCTURE OF THE MOS1 MARINER PAIRED END COMPLEX WITH MN	2.7.7 3.1
3HP9	CRYSTAL STRUCTURE OF SSB/EXONUCLEASE I IN COMPLEX WITH INHIBITOR CFAM	3.1.11.1
3HPG	VISNA VIRUS INTEGRASE (RESIDUES 1-219) IN COMPLEX WITH LEDGF IBD: EXAMPLES OF OPEN INTEGRASE DIMER-DIMER INTERFACES	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 3.1.13.2 3.6.1.23 2.7.7 3.1
3HPH	CLOSED TETRAMER OF VISNA VIRUS INTEGRASE (RESIDUES 1-219) IN COMPLEX WITH LEDGF IBD	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 3.1.13.2 3.6.1.23 2.7.7 3.1
3HPT	CRYSTAL STRUCTURE OF HUMAN FXA IN COMPLEX WITH (S)-2-CYANO-1-(2-METHYLBENZOFURAN-5-YL)-3-(2-OXO-1-(2-OXO-2-(PYRROLIDIN-1-YL)ETHYL)AZEPAN-3-YL)GUANIDINE	3.4.21.6
3HQC	CRYSTAL STRUCTURE OF PHOSPHOTYROSINE-BINDING DOMAIN FROM THE HUMAN TENSIN-LIKE C1 DOMAIN-CONTAINING PHOSPHATASE (TENC1)	3.1.3 3.1.3.48
3HQF	CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE ECORII N-TERMINAL EFFECTOR-BINDING DOMAIN IN COMPLEX WITH COGNATE DNA	3.1.21.4
3HQG	CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE ECORII CATALYTIC C-TERMINAL DOMAIN IN COMPLEX WITH COGNATE DNA	3.1.21.4
3HQW	DISCOVERY OF NOVEL INHIBITORS OF PDE10A	3.1.4.17 3.1.4.35
3HQY	DISCOVERY OF NOVEL INHIBITORS OF PDE10A	3.1.4.17 3.1.4.35
3HQZ	DISCOVERY OF NOVEL INHIBITORS OF PDE10A	3.1.4.17 3.1.4.35
3HR1	DISCOVERY OF NOVEL INHIBITORS OF PDE10A	3.1.4.17 3.1.4.35
3HR9	THE TRUNCATED FIBROBACTER SUCCINOGENES 1,3-1,4-BETA-D-GLUCANASE F40I MUTANT	3.2.1.73
3HRE	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-9 S70G	3.5.2.6
3HSC	THREE-DIMENSIONAL STRUCTURE OF THE ATPASE FRAGMENT OF A 70K HEAT-SHOCK COGNATE PROTEIN	3.6.1.3
3HSW	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH 2-METHOXYCYCLOHEXA-2-5-DIENE-1,4-DIONE	3.1.1.4
3HT6	2-METHYLPHENOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HT7	2-ETHYLPHENOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HT8	5-CHLORO-2-METHYLPHENOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HT9	2-METHOXYPHENOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HTB	2-PROPYLPHENOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HTC	THE STRUCTURE OF A COMPLEX OF RECOMBINANT HIRUDIN AND HUMAN ALPHA-THROMBIN	3.4.21.5
3HTD	(Z)-THIOPHENE-2-CARBOXALDOXIME IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HTF	4-CHLORO-1H-PYRAZOLE IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HTG	2-ETHOXY-3,4-DIHYDRO-2H-PYRAN IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HU2	STRUCTURE OF P97 N-D1 R86A MUTANT IN COMPLEX WITH ATPGS	3.6.4.6
3HU3	STRUCTURE OF P97 N-D1 R155H MUTANT IN COMPLEX WITH ATPGS	3.6.4.6
3HU8	2-ETHOXYPHENOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HU9	NITROSOBENZENE IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HUA	4,5,6,7-TETRAHYDROINDOLE IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HUK	BENZYLACETATE IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HUM	CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 FROM STAPHYLOCOCCUS AUREUS COL IN COMPLEX WITH CEFOTAXIME	3.4.16.4
3HUN	CRYSTAL STRUCTURE OF PENICILLIN BINDING PROTEIN 4 FROM STAPHYLOCOCCUS AUREUS COL IN COMPLEX WITH AMPICILLIN	3.4.16.4
3HUO	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-9 S70G IN COMPLEX WITH BENZYLPENICILLIN	3.5.2.6
3HUQ	THIENO[3,2-B]THIOPHENE IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
3HV8	CRYSTAL STRUCTURE OF FIMX EAL DOMAIN FROM PSEUDOMONAS AERUGINOSA BOUND TO C-DI-GMP	3.1.4.52
3HV9	CRYSTAL STRUCTURE OF FIMX EAL DOMAIN FROM PSEUDOMONAS AERUGINOSA	3.1.4.52
3HVF	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-9 S70G IN COMPLEX WITH HYDROLYZED BENZYLPENICILLIN	3.5.2.6
3HVO	STRUCTURE OF THE GENOTYPE 2B HCV POLYMERASE BOUND TO A NNI	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3HVP	CONSERVED FOLDING IN RETROVIRAL PROTEASES. CRYSTAL STRUCTURE OF A SYNTHETIC 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
3HVQ	CRYSTAL STRUCTURE OF A COMPLEX BETWEEN PROTEIN PHOSPHATASE 1 ALPHA (PP1) AND THE PP1 BINDING AND PDZ DOMAINS OF NEURABIN	3.1.3.16
3HVT	STRUCTURAL BASIS OF ASYMMETRY IN THE HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 REVERSE TRANSCRIPTASE HETERODIMER	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
3HW3	THE CRYSTAL STRUCTURE OF AVIAN INFLUENZA VIRUS PA_N IN COMPLEX WITH UMP	3.1
3HW4	CRYSTAL STRUCTURE OF AVIAN INFLUENZA A VIRUS IN COMPLEX WITH TMP	3.1
3HW5	CRYSTAL STRUCTURE OF AVIAN INFLUENZA VIRUS PA_N IN COMPLEX WITH AMP	3.1
3HW6	CRYSTAL STRUCTURE OF AVIAN INFLUENZA VIRUS PA_N IN COMPLEX WITH MN	3.1
3HWL	CRYSTAL STRUCTURE OF T4 LYSOZYME WITH THE UNNATURAL AMINO ACID P-ACETYL-L-PHENYLALANINE INCORPORATED AT POSITION 131	3.2.1.17
3HWN	CATHEPSIN L WITH AZ13010160	3.4.22.15
3HWP	CRYSTAL STRUCTURE AND COMPUTATIONAL ANALYSES PROVIDE INSIGHTS INTO THE CATALYTIC MECHANISM OF 2, 4-DIACETYLPHLOROGLUCINOL HYDROLASE PHLG FROM PSEUDOMONAS FLUORESCENS	3.7.1.24
3HY7	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF ADAMTS-5 IN COMPLEX WITH MARIMASTAT	3.4.24
3HY9	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF ADAMTS-5 IN COMPLEX WITH AN AMINO-2-INDANOL COMPOUND	3.4.24
3HYC	CRYSTAL STRUCTURE OF E. COLI PHOSPHATASE YRBI, WITH MG, TETRAGONAL FORM	3.1.3.45
3HYF	CRYSTAL STRUCTURE OF HIV-1 RNASE H P15 WITH ENGINEERED E. COLI LOOP AND ACTIVE SITE INHIBITOR	3.1.26.4
3HYG	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF ADAMTS-5 IN COMPLEX WITH AN AMINO-2-INDANOL COMPOUND	3.4.24
3HZA	CRYSTAL STRUCTURE OF DUTPASE H145W MUTANT	3.6.1.23
3HZC	CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED 203 AMINO ACID 'COVALENT DIMER' [GLY51;AIB51']HIV-1 PROTEASE MOLECULE COMPLEXED WITH MVT-101 REDUCED ISOSTERE INHIBITOR	3.4.23.16
3HZX	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT D+PHS/V66K AT PH 9 DETERMINED AT 100 K	3.1.31.1
3I06	CRYSTAL STRUCTURE OF CRUZAIN COVALENTLY BOUND TO A PURINE NITRILE	3.4.22.51
3I0R	CRYSTAL STRUCTURE OF HIV REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR 3	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
3I0S	CRYSTAL STRUCTURE OF HIV REVERSE TRANSCRIPTASE IN COMPLEX WITH INHIBITOR 7	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
3I0V	BACILLUS CEREUS METALLO-BETA-LACTAMASE: APO FORM	3.5.2.6
3I0W	CRYSTAL STRUCTURE OF CLOSTRIDIUM ACETOBUTYLICUM 8-OXOGUANINE GLYCOSYLASE/LYASE IN COMPLEX WITH DSDNA CONTAINING CYTOSINE OPPOSITE TO 8-OXOG	3.2.2 4.2.99.18
3I0X	CRYSTAL STRUCTURE OF CLOSTRIDIUM ACETOBUTYLICUM 8-OXOGUANINE GLYCOSYLASE/LYASE IN COMPLEX WITH DSDNA CONTAINING ADENINE OPPOSITE TO 8-OXOG	3.2.2 4.2.99.18
3I11	COBALT-SUBSTITUTED METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS	3.5.2.6
3I13	BACILLUS CEREUS ZN-DEPENDENT METALLO-BETA-LACTAMASE AT PH 5.8	3.5.2.6
3I14	COBALT-SUBSTITUTED METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS: RESIDUE CYS168 PARTIALLY OXIDIZED	3.5.2.6
3I15	COBALT-SUBSTITUTED METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS: RESIDUE CYS168 FULLY OXIDIZED	3.5.2.6
3I18	CRYSTAL STRUCTURE OF THE PDZ DOMAIN OF THE SDRC-LIKE PROTEIN (LMO2051) FROM LISTERIA MONOCYTOGENES, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET LMR166B	3.4.21.53
3I1C	CRYSTAL STRUCTURE OF A NOVEL ENGINEERED DIELS-ALDERASE: DA_20_00_A74I	3.1.8.2
3I1E	CRYSTAL STRUCTURE OF THE PDZ DOMAIN OF THE SDRC-LIKE PROTEIN (LIN2157) FROM LISTERIA INNOCUA, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET LKR136C	3.4.21.53
3I1F	GAMMA-SUBUNIT OF THE TRANSLATION INITIATION FACTOR 2 FROM S. SOLFATARICUS IN COMPLEX WITH GPP(CH2)P	3.6.5.3
3I1K	STRUCTURE OF PORCINE TOROVIRUS HEMAGGLUTININ-ESTERASE	3.1.1.53
3I1L	STRUCTURE OF PORCINE TOROVIRUS HEMAGGLUTININ-ESTERASE IN COMPLEX WITH ITS RECEPTOR	3.1.1.53
3I1U	CARBOXYPEPTIDASE A INHIBITED BY A THIIRANE MECHANISM-BASED INACTIVATOR	3.4.17.1
3I1Y	CRYSTAL STRUCTURE OF SOLUBLE EPOXIDE HYDROLASE	3.3.2.10 3.1.3.76
3I25	POTENT BETA-SECRETASE 1 HYDROXYETHYLENE INHIBITOR	3.4.23.46
3I26	STRUCTURE OF BOVINE TOROVIRUS HEMAGGLUTININ-ESTERASE	3.1.1.53
3I27	STRUCTURE OF BOVINE TOROVIRUS HEMAGGLUTININ-ESTERASE IN COMPLEX WITH RECEPTOR	3.1.1.53
3I28	CRYSTAL STRUCTURE OF SOLUBLE EPOXIDE HYDROLASE	3.3.2.10 3.1.3.76
3I29	CRYSTAL STRUCTURE OF A BINARY COMPLEX BETWEEN AN MUTANT TRYPSIN INHIBITOR WITH BOVINE TRYPSIN	3.4.21.4
3I2E	CRYSTAL STRUCTURE OF HUMAN DIMETHYLARGININE DYMETHYLAMINOHYDROLASE-1 (DDAH-1)	3.5.3.18
3I2F	COCAINE ESTERASE WITH MUTATIONS T172R / G173Q, BOUND TO DTT ADDUCT	3.1.1 3.1.1.84
3I2G	COCAINE ESTERASE WITH MUTATION G173Q, BOUND TO DTT ADDUCT	3.1.1 3.1.1.84
3I2H	COCAINE ESTERASE WITH MUTATION L169K, BOUND TO DTT ADDUCT	3.1.1 3.1.1.84
3I2I	COCAINE ESTERASE WITH MUTATION T172R, BOUND TO DTT ADDUCT	3.1.1 3.1.1.84
3I2J	COCAINE ESTERASE, WILD TYPE, WITHOUT A LIGAND	3.1.1 3.1.1.84
3I2K	COCAINE ESTERASE, WILD TYPE, BOUND TO A DTT ADDUCT	3.1.1 3.1.1.84
3I2L	CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED [ALLO-ILE50/50']HIV-1 PROTEASE MOLECULE COMPLEXED WITH MVT-101 REDUCED ISOSTERE INHIBITOR	3.4.23.16
3I2Y	PROTEINASE K BY CLASSICAL HANGING DROP METHOD BEFORE HIGH X-RAY DOSE ON ID14-2 BEAMLINE AT ESRF	3.4.21.64
3I30	PROTEINASE K BY CLASSICAL HANGING DROP METHOD AFTER HIGH X-RAY DOSE ON ID14-2 BEAMLINE AT ESRF	3.4.21.64
3I34	PROTEINASE K BY LB NANOTEMPLATE METHOD AFTER HIGH X-RAY DOSE ON ID14-2 BEAMLINE AT ESRF	3.4.21.64
3I36	CRYSTAL STRUCTURE OF RAT PROTEIN TYROSINE PHOSPHATASE ETA CATALYTIC DOMAIN	3.1.3.48
3I37	PROTEINASE K BY LB NANOTEMPLATE METHOD BEFORE HIGH X-RAY DOSE ON ID14-2 BEAMLINE AT ESRF	3.4.21.64
3I3S	CRYSTAL STRUCTURE OF H-RAS WITH THR50 REPLACED BY ISOLEUCINE	3.6.5.2
3I3T	CRYSTAL STRUCTURE OF COVALENT UBIQUITIN-USP21 COMPLEX	3.1.2.15 3.4.19.12
3I4A	CRYSTAL STRUCTURE OF DIMETHYLARGININE DIMETHYLAMINOHYDROLASE-1 (DDAH-1) IN COMPLEX WITH N5-(1-IMINOPROPYL)-L-ORNITHINE	3.5.3.18
3I4H	CRYSTAL STRUCTURE OF CAS6 IN PYROCOCCUS FURIOSUS	3.1
3I4I	CRYSTAL STRUCTURE OF A PROKARYOTIC BETA-1,3-1,4-GLUCANASE (LICHENASE) DERIVED FROM A MOUSE HINDGUT METAGENOME	3.2.1.73
3I4L	STRUCTURAL CHARACTERIZATION FOR THE NUCLEOTIDE BINDING ABILITY OF SUBUNIT A WITH AMP-PNP OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3I4Q	STRUCTURE OF A PUTATIVE INORGANIC PYROPHOSPHATASE FROM THE OIL-DEGRADING BACTERIUM OLEISPIRA ANTARCTICA	3.6.1.1
3I4U	CRYSTAL STRUCTURE ANALYSIS OF A HELICASE ASSOCIATED DOMAIN	3.6.1 3.6.4.13
3I50	CRYSTAL STRUCTURE OF THE WEST NILE VIRUS ENVELOPE GLYCOPROTEIN IN COMPLEX WITH THE E53 ANTIBODY FAB	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
3I5K	CRYSTAL STRUCTURE OF THE NS5B POLYMERASE FROM HEPATITIS C VIRUS (HCV) STRAIN JFH1	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3I5V	CRYSTAL STRUCTURE OF BETA TOXIN 275-280 FROM STAPHYLOCOCCUS AUREUS	3.1.4.3
3I5X	STRUCTURE OF MSS116P BOUND TO SSRNA AND AMP-PNP	3.6.1 3.6.4.13
3I5Y	STRUCTURE OF MSS116P BOUND TO SSRNA CONTAINING A SINGLE 5-BRU AND AMP-PNP	3.6.1 3.6.4.13
3I61	STRUCTURE OF MSS116P BOUND TO SSRNA AND ADP-BERYLLIUM FLUORIDE	3.6.1 3.6.4.13
3I62	STRUCTURE OF MSS116P BOUND TO SSRNA AND ADP-ALUMINUM FLUORIDE	3.6.1 3.6.4.13
3I67	RIBONUCLEASE A BY LB NANOTEMPLATE METHOD AFTER HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.1.27.5 4.6.1.18
3I6B	CRYSTAL STRUCTURE OF YRBI LACKING THE LAST 8 RESIDUES, IN COMPLEX WITH KDO AND INORGANIC PHOSPHATE	3.1.3.45
3I6F	RIBONUCLEASE A BY CLASSICAL HANGING DROP METHOD BEFORE HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.1.27.5 4.6.1.18
3I6H	RIBONUCLEASE A BY LB NANOTEMPLATE METHOD BEFORE HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.1.27.5 4.6.1.18
3I6J	RIBONUCLEASE A BY CLASSICAL HANGING DROP METHOD AFTER HIGH X-RAY DOSE ON ESRF ID14-2 BEAMLINE	3.1.27.5 4.6.1.18
3I6M	3D STRUCTURE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE COMPLEXED WITH N-PIPERIDINOPROPYL-GALANTHAMINE	3.1.1.7
3I6O	CRYSTAL STRUCTURE OF WILD TYPE HIV-1 PROTEASE WITH MACROCYCLIC INHIBITOR GRL-0216A	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
3I6S	CRYSTAL STRUCTURE OF THE PLANT SUBTILISIN-LIKE PROTEASE SBT3	3.4.21
3I6Y	STRUCTURE OF AN ESTERASE FROM THE OIL-DEGRADING BACTERIUM OLEISPIRA ANTARCTICA	3.1.1.2 3.1.2.12
3I6Z	3D STRUCTURE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE COMPLEXED WITH N-SACCHARINOHEXYL-GALANTHAMINE	3.1.1.7
3I72	STRUCTURAL CHARACTERIZATION FOR THE NUCLEOTIDE BINDING ABILITY OF SUBUNIT A WITH SO4 OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3I73	STRUCTURAL CHARACTERIZATION FOR THE NUCLEOTIDE BINDING ABILITY OF SUBUNIT A WITH ADP OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3I74	CRYSTAL STRUCTURE OF THE PLANT SUBTILISIN-LIKE PROTEASE SBT3 IN COMPLEX WITH A CHLOROMETHYLKETONE INHIBITOR	3.4.21
3I76	THE CRYSTAL STRUCTURE OF THE ORTHORHOMBIC FORM OF THE PUTATIVE HAD-HYDROLASE YFNB FROM BACILLUS SUBTILIS BOUND TO MAGNESIUM REVEALS INTERDOMAIN MOVEMENT	3
3I77	35/99/170-LOOPS OF FXA IN SGT	3.4.21.4
3I78	35/99/170/186/220-LOOPS OF FXA IN SGT	3.4.21.4
3I7E	CO-CRYSTAL STRUCTURE OF HIV-1 PROTEASE BOUND TO A MUTANT RESISTANT INHIBITOR UIC-98038	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
3I7G	MMP-13 IN COMPLEX WITH A NON ZINC-CHELATING INHIBITOR	3.4.24
3I7I	MMP-13 IN COMPLEX WITH A NON ZINC-CHELATING INHIBITOR	3.4.24
3I7W	HIGH PRESSURE STRUCTURE OF WILD-TYPE RNASE A (0.67 GPA)	3.1.27.5 4.6.1.18
3I7X	HIGH PRESSURE STRUCTURE OF I106A RNASE A VARIANT (0.35 GPA)	3.1.27.5 4.6.1.18
3I7Y	HIGH PRESSURE STRUCTURE OF I106A VARIANT OF RNASE A (0.48 GPA)	3.1.27.5 4.6.1.18
3I7Z	PROTEIN TYROSINE PHOSPHATASE 1B - TRANSITION STATE ANALOG FOR THE FIRST CATALYTIC STEP	3.1.3.48
3I80	PROTEIN TYROSINE PHOSPHATASE 1B - TRANSITION STATE ANALOG FOR THE SECOND CATALYTIC STEP	3.1.3.48
3I86	CRYSTAL STRUCTURE OF THE P60 DOMAIN FROM M. AVIUM SUBSPECIES PARATUBERCULOSIS ANTIGEN MAP1204	3.4.19.11
3I8D	THE PAIRING GEOMETRY OF THE HYDROPHOBIC THYMINE ANALOG 2,4-DIFLUOROTOLUENE IN DUPLEX DNA AS ANALYZED BY X-RAY CRYSTALLOGRAPHY	3.1.26.4
3I8V	CRYSTAL STRUCTURE OF HUMAN PDE4A WITH 4-(3-BUTOXY-4-METHOXYPHENYL)METHYL-2-IMIDAZOLIDONE	3.1.4.17 3.1.4.53
3I8W	CRYSTAL STRUCTURE OF A METALLACARBORANE INHIBITOR BOUND TO HIV 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
3I93	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS DUTPASE STOP138T MUTANT	3.6.1.23
3I98	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF INORGANIC PYROPHOSPHATASE AT 298K FROM ARCHAEON THERMOCOCCUS THIOREDUCENS	3.6.1.1
3I9J	CRYSTAL STRUCTURE OF ADP RIBOSYL CYCLASE COMPLEXED WITH A SUBSTRATE ANALOG AND A PRODUCT NICOTINAMIDE	3.2.2.5 3.2.2.6 2.4.99.20
3I9K	CRYSTAL STRUCTURE OF ADP RIBOSYL CYCLASE COMPLEXED WITH SUBSTRATE NAD	3.2.2.5 3.2.2.6 2.4.99.20
3I9L	CRYSTAL STRUCTURE OF ADP RIBOSYL CYCLASE COMPLEXED WITH N1-CIDPR	3.2.2.5 3.2.2.6 2.4.99.20
3I9M	CRYSTAL STRUCTURE OF HUMAN CD38 COMPLEXED WITH AN ANALOG ARA-2'F-ADPR	3.2.2.5 3.2.2.6 2.4.99.20
3I9N	CRYSTAL STRUCTURE OF HUMAN CD38 COMPLEXED WITH AN ANALOG RIBO-2'F-ADP RIBOSE	3.2.2.5 3.2.2.6 2.4.99.20
3I9O	CRYSTAL STRUCTURE OF ADP RIBOSYL CYCLASE COMPLEXED WITH RIBO-2'F-ADP RIBOSE	3.2.2.5 3.2.2.6 2.4.99.20
3IA2	PSEUDOMONAS FLUORESCENS ESTERASE COMPLEXED TO THE R-ENANTIOMER OF A SULFONATE TRANSITION STATE ANALOG	3.1.1.2 1
3IA9	CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED [D25N]HIV-1 PROTEASE MOLECULE COMPLEXED WITH MVT-101 REDUCED ISOSTERE INHIBITOR	3.4.23.16
3IAB	CRYSTAL STRUCTURE OF RNASE P /RNASE MRP PROTEINS POP6, POP7 IN A COMPLEX WITH THE P3 DOMAIN OF RNASE MRP RNA	3.1.26.5
3IAD	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 4D WITH BOUND ALLOSTERIC MODULATOR	3.1.4.17 3.1.4.53
3IAK	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 4D (PDE4D) WITH PAPAVERINE.	3.1.4.17 3.1.4.53
3IAN	CRYSTAL STRUCTURE OF A CHITINASE FROM LACTOCOCCUS LACTIS SUBSP. LACTIS	3.2.1.14
3IAR	THE CRYSTAL STRUCTURE OF HUMAN ADENOSINE DEAMINASE	3.5.4.4
3IAW	CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED 203 AMINO ACID 'COVALENT DIMER' [GLY51;AIB51']HIV-1 PROTEASE MOLECULE COMPLEXED WITH MVT-101 REDUCED ISOSTERE INHIBITOR AT 1.6 A RESOLUTION	3.4.23.16
3IAY	TERNARY COMPLEX OF DNA POLYMERASE DELTA	2.7.7.7 3.1.11
3IAZ	STRUCTURAL BASIS OF THE PREVENTION OF NSAID-INDUCED DAMAGE OF THE GASTROINTESTINAL TRACT BY C-TERMINAL HALF (C-LOBE) OF BOVINE COLOSTRUM PROTEIN LACTOFERRIN: BINDING AND STRUCTURAL STUDIES OF THE C-LOBE COMPLEX WITH ASPIRIN	3.4.21
3IB0	STRUCTURAL BASIS OF THE PREVENTION OF NSAID-INDUCED DAMAGE OF THE GASTROINTESTINAL TRACT BY C-TERMINAL HALF (C-LOBE) OF BOVINE COLOSTRUM PROTEIN LACTOFERRIN: BINDING AND STRUCTURAL STUDIES OF C-LOBE COMPLEX WITH DICLOFENAC	3.4.21
3IB1	STRUCTURAL BASIS OF THE PREVENTION OF NSAID-INDUCED DAMAGE OF THE GASTROINTESTINAL TRACT BY C-TERMINAL HALF (C-LOBE) OF BOVINE COLOSTRUM PROTEIN LACTOFERRIN: BINDING AND STRUCTURAL STUDIES OF C-LOBE COMPLEX WITH INDOMETHACIN	3.4.21
3IB2	STRUCTURE OF THE COMPLEX OF C-TERMINAL HALF (C-LOBE) OF BOVINE LACTOFERRIN WITH ALPHA-METHYL-4-(2-METHYLPROPYL) BENZENE ACETIC ACID	3.4.21
3IB7	CRYSTAL STRUCTURE OF FULL LENGTH RV0805	3.1.4.17 3.1.4.53
3IB8	CRYSTAL STRUCTURE OF FULL LENGTH RV0805 IN COMPLEX WITH 5'-AMP	3.1.4.17 3.1.4.53
3IBC	CRYSTAL STRUCTURE OF CASPASE-7 INCOMPLEX WITH ACETYL-YVAD-CHO	3.4.22.60
3IBF	CRYSTAL STRUCTURE OF UNLIGANDED CASPASE-7	3.4.22.60
3IBG	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS GET3 WITH BOUND ADP	3.6.3.16 3.6
3IBJ	X-RAY STRUCTURE OF PDE2A	3.1.4.17
3IBX	CRYSTAL STRUCTURE OF F47Y VARIANT OF TENA (HP1287) FROM HELICOBACTER PYLORI	3.5.99.2
3IC1	CRYSTAL STRUCTURE OF ZINC-BOUND SUCCINYL-DIAMINOPIMELATE DESUCCINYLASE FROM HAEMOPHILUS INFLUENZAE	3.5.1.18
3ICE	RHO TRANSCRIPTION TERMINATION FACTOR BOUND TO RNA AND ADP-BEF3	3.6.1 3.6.4
3ICF	STRUCTURE OF PROTEIN SERINE/THREONINE PHOSPHATASE FROM SACCHAROMYCES CEREVISIAE WITH SIMILARITY TO HUMAN PHOSPHATASE PP5	3.1.3.16
3ICO	CRYSTAL STRUCTURE OF 6-PHOSPHOGLUCONOLACTONASE FROM MYCOBACTERIUM TUBERCULOSIS	3.1.1.31
3ICV	STRUCTURAL CONSEQUENCES OF A CIRCULAR PERMUTATION ON LIPASE B FROM CANDIDA ANTARTICA	3.1.1.3
3ICW	STRUCTURE OF A CIRCULAR PERMUTATION ON LIPASE B FROM CANDIDA ANTARTICA WITH BOUND SUICIDE INHIBITOR	3.1.1.3
3ID1	CRYSTAL STRUCTURE OF RSEP PDZ1 DOMAIN	3.4.24
3ID2	CRYSTAL STRUCTURE OF RSEP PDZ2 DOMAIN	3.4.24
3ID3	CRYSTAL STRUCTURE OF RSEP PDZ2 I304A DOMAIN	3.4.24
3ID4	CRYSTAL STRUCTURE OF RSEP PDZ2 DOMAIN FUSED GKASPV PEPTIDE	3.4.24
3IDA	THERMOSTABLE COCAINE ESTERASE WITH MUTATIONS L169K AND G173Q, BOUND TO DTT ADDUCT	3.1.1 3.1.1.84
3IDE	STRUCTURE OF IPNV SUBVIRAL PARTICLE	3.4.21
3IDO	CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE FROM ENTAMOEBA HISTOLYTICA WITH A PHOSPHOTYROSINE CRUDE MIMIC HEPES MOLECULE IN THE ACTIVE SITE	3.1.3.2
3IDQ	CRYSTAL STRUCTURE OF S. CEREVISIAE GET3 AT 3.7 ANGSTROM RESOLUTION	3.6.3.16 3.6
3IDZ	CRYSTAL STRUCTURE OF S378Q MUTANT TTHA0252 FROM THERMUS THERMOPHILUS HB8	3.1
3IE0	CRYSTAL STRUCTURE OF S378Y MUTANT TTHA0252 FROM THERMUS THERMOPHILUS HB8	3.1
3IE1	CRYSTAL STRUCTURE OF H380A MUTANT TTHA0252 FROM THERMUS THERMOPHILUS HB8 COMPLEXED WITH RNA	3.1
3IE2	CRYSTAL STRUCTURE OF H400V MUTANT TTHA0252 FROM THERMUS THERMOPHILUS HB8	3.1
3IEJ	PYRAZOLE-BASED CATHEPSIN S INHIBITORS WITH ARYLALKYNES AS P1 BINDING ELEMENTS	3.4.22.27
3IEK	CRYSTAL STRUCTURE OF NATIVE TTHA0252 FROM THERMUS THERMOPHILUS HB8	3.1
3IEL	CRYSTAL STRUCTURE OF TTHA0252 FROM THERMUS THERMOPHILUS HB8 COMPLEXED WITH UMP	3.1
3IEM	CRYSTAL STRUCTURE OF TTHA0252 FROM THERMUS THERMOPHILUS HB8 COMPLEXED WITH RNA ANALOG	3.1
3IEY	CRYSTAL STRUCTURE OF THE FUNCTIONAL NANOARCHAEUM EQUITANS TRNA SPLICING ENDONUCLEASE	3.1.27.9 4.6.1.16
3IF5	CRYSTAL STRUCTURE ANALYSIS OF MGLU	3.5.1.2
3IF6	CRYSTAL STRUCTURE OF OXA-46 BETA-LACTAMASE FROM P. AERUGINOSA	3.5.2.6
3IFE	1.55 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF PEPTIDASE T (PEPT-1) FROM BACILLUS ANTHRACIS STR. 'AMES ANCESTOR'.	3.4.11.4
3IFJ	CRYSTAL STRUCTURE OF MTU RECA INTEIN, SPLICING DOMAIN	3.1
3IFW	CRYSTAL STRUCTURE OF THE S18Y VARIANT OF UBIQUITIN CARBOXY TERMINAL HYDROLASE L1 BOUND TO UBIQUITIN VINYLMETHYLESTER.	3.4.19.12 6
3IG1	HIV-1 REVERSE TRANSCRIPTASE WITH THE INHIBITOR BETA-THUJAPLICINOL BOUND AT THE RNASE H ACTIVE SITE	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
3IG6	LOW MOLECULAR WEIGTH HUMAN UROKINASE TYPE PLASMINOGEN ACTIVATOR 2-[6-(3'-AMINOMETHYL-BIPHENYL-3-YLOXY)-4-(3-DIMETHYLAMINO-PYRROLIDIN-1-YL)-3,5-DIFLUORO-PYRIDIN-2-YLOXY]-4-DIMETHYLAMINO-BENZOIC ACID COMPLEX	3.4.21.73
3IGB	BACE-1 WITH COMPOUND 3	3.4.23.46
3IGD	CRYSTAL STRUCTURE OF MTU RECA INTEIN, SPLICING DOMAIN	3.1
3IGU	CRYSTAL STRUCTURE OF HUMAN ALPHA-N-ACETYLGALACTOSAMINIDASE, COVALENT INTERMEDIATE	3.2.1.49
3IGV	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE WITH A NOVEL MONOCYCLIC DIHYDRO-PYRIDINONE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3IH7	CRYSTAL STRUCTURE OF CATALYTICALLY ACTIVE HUMAN 8-OXOGUANINE GLYCOSYLASE DISTALLY CROSSLINKED TO GUANINE-CONTAINING DNA	3.2.2 4.2.99.18
3IH8	CRYSTAL STRUCTURE ANALYSIS OF MGLU IN ITS NATIVE FORM	3.5.1.2
3IH9	CRYSTAL STRUCTURE ANALYSIS OF MGLU IN ITS TRIS FORM	3.5.1.2
3IHA	CRYSTAL STRUCTURE ANALYSIS OF MGLU IN ITS GLUTAMATE FORM	3.5.1.2
3IHB	CRYSTAL STRUCTURE ANALYSIS OF MGLU IN ITS TRIS AND GLUTAMATE FORM	3.5.1.2
3IHO	THE C-TERMINAL GLYCOSYLASE DOMAIN OF HUMAN MBD4	3.2.2
3IHP	COVALENT UBIQUITIN-USP5 COMPLEX	3.1.2.15 3.4.19.12
3IHR	CRYSTAL STRUCTURE OF UCH37	3.4.19.12
3II1	STRUCTURAL CHARACTERIZATION OF DIFUNCTIONAL GLUCANASE-XYLANSE CELM2	3.2.1.4
3IIQ	CRYSTALLOGRAPHIC ANALYSIS OF BACTERIAL SIGNAL PEPTIDASE IN TERNARY COMPLEX WITH ARYLOMYCIN A2 AND A BETA-SULTAM INHIBITOR	3.4.21.89
3IIT	FACTOR XA IN COMPLEX WITH A CIS-1,2-DIAMINOCYCLOHEXANE DERIVATIVE	3.4.21.6
3IJ3	1.8 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF CYTOSOL AMINOPEPTIDASE FROM COXIELLA BURNETII	3.4.11.1
3IJ5	1.95 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF 3-DEOXY-D-MANNO-OCTULOSONATE 8-PHOSPHATE PHOSPHATASE FROM YERSINIA PESTIS	3.1.3.45
3IJ7	DIRECTED 'IN SITU' ELONGATION AS A STRATEGY TO CHARACTERIZE THE COVALENT GLYCOSYL-ENZYME CATALYTIC INTERMEDIATE OF HUMAN PANCREATIC A-AMYLASE	3.2.1.1
3IJ8	DIRECTED 'IN SITU' ELONGATION AS A STRATEGY TO CHARACTERIZE THE COVALENT GLYCOSYL-ENZYME CATALYTIC INTERMEDIATE OF HUMAN PANCREATIC A-AMYLASE	3.2.1.1
3IJ9	DIRECTED 'IN SITU' ELONGATION AS A STRATEGY TO CHARACTERIZE THE COVALENT GLYCOSYL-ENZYME CATALYTIC INTERMEDIATE OF HUMAN PANCREATIC A-AMYLASE	3.2.1.1
3IJF	CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE FROM MYCOBACTERIUM TUBERCULOSIS	3.5.4.5
3IJU	CHICKEN EGG WHITE LYSOZYME BY HIGHLY ORDERED APA (ANODIC POROUS ALUMINA) NANOTEMPLATE CRYSTALLIZATION METHOD	3.2.1.17
3IJV	CHICKEN EGG WHITE LYSOZYME BY CLASSICAL HANGING DROP VAPOUR DIFFUSION METHOD	3.2.1.17
3IKJ	STRUCTURAL CHARACTERIZATION FOR THE NUCLEOTIDE BINDING ABILITY OF SUBUNIT A MUTANT S238A OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3ILF	CRYSTAL STRUCTURE OF PORPHYRANASE A (PORA) IN COMPLEX WITH NEO-PORPHYROTETRAOSE	3.2.1.178
3ILY	APO CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE FROM ENTAMOEBA HISTOLYTICA FEATURING A DISORDERED ACTIVE SITE	3.1.3.2
3IM1	STRUCTURE OF THE C-TERMINAL SEC63 UNIT OF YEAST BRR2, P212121 FORM	3.6.1 3.6.4.13
3IM2	STRUCTURE OF THE C-TERMINAL SEC63 UNIT OF YEAST BRR2, P41212 FORM	3.6.1 3.6.4.13
3IMA	COMPLEX STRUCTURE OF TAROCYSTATIN AND PAPAIN	3.4.22.2
3IN3	BACE1 WITH COMPOUND 30	3.4.23.46
3IN4	BACE1 WITH COMPOUND 38	3.4.23.46
3IND	BACE1 WITH THE AMINOHYDANTOIN COMPOUND 29	3.4.23.46
3INE	BACE1 WITH THE AMINOHYDANTOIN COMPOUND S-34	3.4.23.46
3INF	BACE1 WITH THE AMINOHYDANTOIN COMPOUND 37	3.4.23.46
3INH	BACE1 WITH THE AMINOHYDANTOIN COMPOUND R-58	3.4.23.46
3INW	HSP90 N-TERMINAL DOMAIN WITH POCHOXIME A	3.6.4.10
3INX	HSP90 N-TERMINAL DOMAIN WITH POCHOXIME B	3.6.4.10
3IO3	GET3 WITH ADP FROM D. HANSENII IN CLOSED FORM	3.6
3IOF	CRYSTAL STRUCTURE OF CPHA N220G MUTANT WITH INHIBITOR 10A	3.5.2.6
3IOG	CRYSTAL STRUCTURE OF CPHA N220G MUTANT WITH INHIBITOR 18	3.5.2.6
3IQA	CRYSTAL STRUCTURE OF BLAC COVALENTLY BOUND WITH DORIPENEM	3.5.2.6
3IQS	CRYSTAL STRUCTURE OF THE ANTI-VIRAL APOBEC3G CATALYTIC DOMAIN	3.5.4
3IQW	AMPPNP COMPLEX OF C. THERM. GET3	3.6
3IQX	ADP COMPLEX OF C.THERM. GET3 IN CLOSED FORM	3.6
3IR2	CRYSTAL STRUCTURE OF THE APOBEC3G CATALYTIC DOMAIN	3.5.4
3IRC	CRYSTAL STRUCTURE ANALYSIS OF DENGUE-1 ENVELOPE PROTEIN DOMAIN III	3.4.21.91 3.6.1.15 3.6.4.13
3IRQ	CRYSTAL STRUCTURE OF A Z-Z JUNCTION	3.5.4 3.5.4.37
3IRR	CRYSTAL STRUCTURE OF A Z-Z JUNCTION (WITH HEPES INTERCALATING)	3.5.4 3.5.4.37
3IRT	CRYSTAL STRUCTURE OF THE I93M MUTANT OF UBIQUITIN CARBOXY-TERMINAL HYDROLASE L1	3.4.19.12 6
3IRU	CRYSTAL STRUCTURE OF PHOSHONOACETALDEHYDE HYDROLASE LIKE PROTEIN FROM OLEISPIRA ANTARCTICA	3.11.1.1
3IRX	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH THE NON-NUCLEOSIDE RT INHIBITOR (E)-S-METHYL 5-(1-(3,7-DIMETHYL-2-OXO-2,3-DIHYDROBENZO[D]OXAZOL-5-YL)-5-(5-METHYL-1,3,4-OXADIAZOL-2-YL)PENT-1-ENYL)-2-METHOXY-3-METHYLBENZOTHIOATE.	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
3IS9	CRYSTAL STRUCTURE OF THE HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH THE ALKENYLDIARYLMETHANE (ADAM) NON-NUCLEOSIDE RT INHIBITOR DIMETHYL 3,3'-(6-METHOXY-6-OXOHEX-1-ENE-1,1-DIYL)BIS(5-CYANO-6-METHOXYBENZOATE).	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
3ISG	STRUCTURE OF THE CLASS D BETA-LACTAMASE OXA-1 IN COMPLEX WITH DORIPENEM	3.5.2.6
3ISM	CRYSTAL STRUCTURE OF THE ENDOG/ENDOGI COMPLEX: MECHANISM OF ENDOG INHIBITION	3.1.30
3ISN	CRYSTAL STRUCTURE OF HIV-1 RT BOUND TO A 6-VINYLPYRIMIDINE 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
3ISZ	CRYSTAL STRUCTURE OF MONO-ZINC FORM OF SUCCINYL-DIAMINOPIMELATE DESUCCINYLASE FROM HAEMOPHILUS INFLUENZAE	3.5.1.18
3IT0	CRYSTAL STRUCTURE FRANCISELLA TULARENSIS HISTIDINE ACID PHOSPHATASE COMPLEXED WITH PHOSPHATE	3.1.3.2
3IT1	CRYSTAL STRUCTURE FRANCISELLA TULARENSIS HISTIDINE ACID PHOSPHATASE COMPLEXED WITH L(+)-TARTRATE	3.1.3.2
3IT2	CRYSTAL STRUCTURE OF LIGAND-FREE FRANCISELLA TULARENSIS HISTIDINE ACID PHOSPHATASE	3.1.3.2
3IT3	CRYSTAL STRUCTURE FRANCISELLA TULARENSIS HISTIDINE ACID PHOSPHATASE D261A MUTANT COMPLEXED WITH SUBSTRATE 3'-AMP	3.1.3.2
3IT5	CRYSTAL STRUCTURE OF THE LASA VIRULENCE FACTOR FROM PSEUDOMONAS AERUGINOSA	3.4.24
3IT7	CRYSTAL STRUCTURE OF THE LASA VIRULENCE FACTOR FROM PSEUDOMONAS AERUGINOSA	3.4.24
3ITH	CRYSTAL STRUCTURE OF THE HIV-1 REVERSE TRANSCRIPTASE BOUND TO A 6-VINYLPYRIMIDINE 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
3ITI	STRUCTURE OF BOVINE TRYPSIN WITH THE MAD TRIANGLE B3C	3.4.21.4
3ITM	CATALYTIC DOMAIN OF HPDE2A	3.1.4.17
3ITN	CRYSTAL STRUCTURE OF PSEUDO-ACTIVATED PROCASPASE-3	3.4.22.56
3ITP	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS F34K AT CRYOGENIC TEMPERATURE	3.1.31.1
3ITU	HPDE2A CATALYTIC DOMAIN COMPLEXED WITH IBMX	3.1.4.17
3IU7	M. TUBERCULOSIS METHIONINE AMINOPEPTIDASE WITH MN INHIBITOR A02	3.4.11.18
3IU8	M. TUBERCULOSIS METHIONINE AMINOPEPTIDASE WITH NI INHIBITOR T03	3.4.11.18
3IU9	M. TUBERCULOSIS METHIONINE AMINOPEPTIDASE WITH NI INHIBITOR T07	3.4.11.18
3IUC	CRYSTAL STRUCTURE OF THE HUMAN 70KDA HEAT SHOCK PROTEIN 5 (BIP/GRP78) ATPASE DOMAIN IN COMPLEX WITH ADP	3.6.4.10
3IUO	THE CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE ATP-DEPENDENT DNA HELICASE RECQ FROM PORPHYROMONAS GINGIVALIS TO 1.6A	3.6.4.12
3IUT	THE CRYSTAL STRUCTURE OF CRUZAIN IN COMPLEX WITH A TETRAFLUOROPHENOXYMETHYL KETONE INHIBITOR	3.4.22.51
3IUY	CRYSTAL STRUCTURE OF DDX53 DEAD-BOX DOMAIN	3.6.1 3.6.4.13
3IV2	CRYSTAL STRUCTURE OF MATURE APO-CATHEPSIN L C25A MUTANT	3.4.22.15
3IV8	N-ACETYLGLUCOSAMINE-6-PHOSPHATE DEACETYLASE FROM VIBRIO CHOLERAE COMPLEXED WITH FRUCTOSE 6-PHOSPHATE	3.5.1.25
3IVH	DESIGN AND SYNTHESIS OF POTENT BACE-1 INHIBITORS WITH CELLULAR ACTIVITY: STRUCTURE-ACTIVITY RELATIONSHIP OF P1 SUBSTITUENTS	3.4.23.46
3IVI	DESIGN AND SYNTHESIS OF POTENT BACE-1 INHIBITORS WITH CELLULAR ACTIVITY: STRUCTURE-ACTIVITY RELATIONSHIP OF P1 SUBSTITUENTS	3.4.23.46
3IVZ	CRYSTAL STRUCTURE OF HYPERTHERMOPHILIC NITRILASE	3.5.1.6 3.5.5.1
3IW3	CRYSTAL STRUCTURE OF HYPERTHERMOPHILIC NITRILASE	3.5.1.6 3.5.5.1
3IWI	X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC OMEGA LOOP INSERTION (H210AAA) MUTANT BETA-LACTAMASE AT 1.64 ANGSTROM RESOLUTION	3.5.2.6
3IWM	THE OCTAMERIC 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
3IWO	X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC Y221G MUTANT BETA-LACTAMASE AT 1.90 ANGSTROM RESOLUTION	3.5.2.6
3IWQ	X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC E219K MUTANT BETA-LACTAMASE AT 1.84 ANGSTROM RESOLUTION	3.5.2.6
3IWR	CRYSTAL STRUCTURE OF CLASS I CHITINASE FROM ORYZA SATIVA L. JAPONICA	3.2.1.14
3IWV	CRYSTAL STRUCTURE OF Y116T MUTANT OF 5-HYDROXYISOURATE HYDROLASE (TRP)	3.5.2.17
3IWW	CRYSTAL STRUCTURE OF HUMAN GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN A COMPLEX WITH DBIBZL, A UREA-BASED INHIBITOR	3.4.17.21
3IX7	CRYSTAL STRUCTURE OF A DOMAIN OF FUNCTIONALLY UNKNOWN PROTEIN FROM THERMUS THERMOPHILUS HB8	3.1
3IXB	X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC E219K MUTANT BETA-LACTAMASE COMPLEXED WITH BENZO(B)THIOPHENE-2-BORONIC ACID (BZB) AT 1.63 ANGSTROM RESOLUTION	3.5.2.6
3IXD	X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC V298E MUTANT BETA-LACTAMASE AT 2.64 ANGSTROM RESOLUTION	3.5.2.6
3IXG	X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC T70I MUTANT BETA-LACTAMASE WITH AND WITHOUT BENZO(B)THIOPHENE-2-BORONIC ACID BOUND AT 2.14 ANGSTROM RESOLUTION	3.5.2.6
3IXH	X-RAY CRYSTAL STRUCTURE OF THE EXTENDED-SPECTRUM AMPC Y221G MUTANT BETA-LACTAMASE IN COMPLEX WITH CEFOTAXIME AT 2.3 ANGSTROM RESOLUTION	3.5.2.6
3IXJ	CRYSTAL STRUCTURE OF BETA-SECRETASE 1 IN COMPLEX WITH SELECTIVE BETA-SECRETASE 1 INHIBITOR	3.4.23.46
3IXK	POTENT BETA-SECRETASE 1 INHIBITOR	3.4.23.46
3IXO	CRYSTAL STRUCTURE OF UNCOMPLEXED HIV_1 PROTEASE SUBTYPE A	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
3IXZ	PIG GASTRIC H+/K+-ATPASE COMPLEXED WITH ALUMINIUM FLUORIDE	3.6.3.10 7.2.2.19
3IYA	ASSOCIATION OF THE PR PEPTIDES WITH DENGUE VIRUS BLOCKS MEMBRANE FUSION AT ACIDIC PH	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
3IYB	POLIOVIRUS EARLY RNA-RELEASE INTERMEDIATE	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3IYC	POLIOVIRUS LATE RNA-RELEASE INTERMEDIATE	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3IYW	WEST NILE VIRUS IN COMPLEX WITH FAB FRAGMENTS OF MAB CR4354 (FITTED COORDINATES OF ENVELOPE PROTEINS AND FAB FRAGMENTS OF ONE ICOSAHEDRAL ASU)	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
3IZQ	STRUCTURE OF THE DOM34-HBS1-GDPNP COMPLEX BOUND TO A TRANSLATING RIBOSOME	3.1
3J05	THREE-DIMENSIONAL STRUCTURE OF DENGUE VIRUS SEROTYPE 1 COMPLEXED WITH HMAB 14C10 FAB	3.4.21.91 3.6.1.15 3.6.4.13
3J08	HIGH RESOLUTION HELICAL RECONSTRUCTION OF THE BACTERIAL P-TYPE ATPASE COPPER TRANSPORTER COPA	3.6.3 7.2.2.8
3J09	HIGH RESOLUTION HELICAL RECONSTRUCTION OF THE BACTERIAL P-TYPE ATPASE COPPER TRANSPORTER COPA	3.6.3 7.2.2.8
3J0B	CRYO-EM RECONSTRUCTION OF WEST NILE 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
3J0F	SINDBIS VIRION	3.4.21.90
3J15	MODEL OF RIBOSOME-BOUND ARCHAEAL PELOTA AND ABCE1	3.1
3J1P	ATOMIC MODEL OF RABBIT HEMORRHAGIC DISEASE VIRUS	3.4.22.66
3J22	THE ENTEROVIRUS 71 A-PARTICLE	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3J23	THE ENTEROVIRUS 71 EMPTY CAPSID	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3J2J	EMPTY COXSACKIEVIRUS A9 CAPSID	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3J42	OBSTRUCTION OF DENGUE VIRUS MATURATION BY FAB FRAGMENTS OF THE 2H2 ANTIBODY	3.4.21.91 3.6.1.15 3.6.4.13
3J48	CRYO-EM STRUCTURE OF POLIOVIRUS 135S PARTICLES	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3J4G	STRUCTURE OF LYSOZYME SOLVED BY MICROED TO 2.9 A	3.2.1.17
3J5V	PHUZ201 FILAMENT	3.6.5
3J6K	2.5A STRUCTURE OF LYSOZYME SOLVED BY MICROED	3.2.1.17
3J7T	CALCIUM ATPASE STRUCTURE WITH TWO BOUND CALCIUM IONS DETERMINED BY ELECTRON CRYSTALLOGRAPHY OF THIN 3D CRYSTALS	3.6.3.8 7.2.2.10
3J8F	CRYO-EM RECONSTRUCTION OF POLIOVIRUS-RECEPTOR COMPLEX	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3J95	STRUCTURE OF ADP-BOUND N-ETHYLMALEIMIDE SENSITIVE FACTOR DETERMINED BY SINGLE PARTICLE CRYOELECTRON MICROSCOPY	3.6.4.6
3J9B	ELECTRON CRYO-MICROSCOPY OF AN RNA POLYMERASE	3.1
3J9F	POLIOVIRUS COMPLEXED WITH SOLUBLE, DEGLYCOSYLATED POLIOVIRUS RECEPTOR (PVR) AT 4 DEGREES C	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3JAU	THE CRYOEM MAP OF EV71 MATURE VIRON IN COMPLEX WITH THE FAB FRAGMENT OF ANTIBODY D5	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3JBC	COMPLEX OF POLIOVIRUS WITH VHH PVSP29F	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3JBD	COMPLEX OF POLIOVIRUS WITH VHH PVSP6A	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3JBE	COMPLEX OF POLIOVIRUS WITH VHH PVSS8A	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3JBF	COMPLEX OF POLIOVIRUS WITH VHH PVSP19B	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3JBG	COMPLEX OF POLIOVIRUS WITH VHH PVSS21E	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3JBQ	DOMAIN ORGANIZATION AND CONFORMATIONAL PLASTICITY OF THE G PROTEIN EFFECTOR, PDE6	3.1.4.35
3JBW	CRYO-ELECTRON MICROSCOPY STRUCTURE OF RAG PAIRED COMPLEX (WITH NBD, NO SYMMETRY)	3.1 6.3.2 2.3.2.27
3JBX	CRYO-ELECTRON MICROSCOPY STRUCTURE OF RAG SIGNAL END COMPLEX (C2 SYMMETRY)	3.1 6.3.2 2.3.2.27
3JBY	CRYO-ELECTRON MICROSCOPY STRUCTURE OF RAG PAIRED COMPLEX (C2 SYMMETRY)	3.1 6.3.2 2.3.2.27
3JCA	CORE MODEL OF THE MOUSE MAMMARY TUMOR VIRUS INTASOME	3.6.1.23 3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
3JD7	THE NOVEL ASYMMETRIC ENTRY INTERMEDIATE OF A PICORNAVIRUS CAPTURED WITH NANODISCS	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3JQ5	PHOSPHOLIPASE A2 PREVENTS THE AGGREGATION OF AMYLOID BETA PEPTIDES: CRYSTAL STRUCTURE OF THE COMPLEX OF PHOSPHOLIPASE A2 WITH OCTAPEPTIDE FRAGMENT OF AMYLOID BETA PEPTIDE, ASP-ALA-GLU-PHE-ARG-HIS-ASP-SER AT 2 A RESOLUTION	3.1.1.4
3JQL	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND A HEXAPEPTIDE FRAGMENT OF AMYLOID BETA PEPTIDE, LYS-LEU-VAL-PHE-PHE-ALA AT 1.2 A RESOLUTION	3.1.1.4
3JQW	CRYSTAL STRUCTURE OF CLOSTRIDIUM HISTOLYTICUM COLH COLLAGENASE COLLAGEN-BINDING DOMAIN 3 AT 2 ANGSTROM RESOLUTION IN PRESENCE OF CALCIUM	3.4.24.3
3JQX	CRYSTAL STRUCTURE OF CLOSTRIDIUM HISTOLYTICUM COLH COLLAGENASE COLLAGEN BINDING DOMAIN 3 AT 2.2 ANGSTROM RESOLUTION IN THE PRESENCE OF CALCIUM AND CADMIUM	3.4.24.3
3JR3	SIR2 BOUND TO ACETYLATED PEPTIDE	3.5.1 2.3.1.286
3JR4	MUTM INTERROGATING AN EXTRAHELICAL G	4.2.99.18 3.2.2.23
3JR5	MUTM LESION RECOGNITION CONTROL COMPLEX WITH N174C CROSSLINKING SITE	4.2.99.18 3.2.2.23
3JR6	SEQUENTIAL REORGANIZATION OF BETA-SHEET TOPOLOGY BY INSERTION OF A SINGLE STRAND	3.2.1.17
3JR8	CRYSTAL STRUCTURE OF BTHTX-II (ASP49-PLA2 FROM BOTHROPS JARARACUSSU SNAKE VENOM) WITH CALCIUM IONS	3.1.1.4
3JRN	CRYSTAL STRUCTURE OF TIR DOMAIN FROM ARABIDOPSIS THALIANA	3.2.2.6
3JRO	NUP84-NUP145C-SEC13 EDGE ELEMENT OF THE NPC LATTICE	3.4.21
3JRP	SEC13 WITH NUP145C (AA109-179) INSERTION BLADE	3.4.21
3JRQ	CRYSTAL STRUCTURE OF (+)-ABA-BOUND PYL1 IN COMPLEX WITH ABI1	3.1.3.16
3JRU	CRYSTAL STRUCTURE OF LEUCYL AMINOPEPTIDASE (PEPA) FROM XOO0834,XANTHOMONAS ORYZAE PV. ORYZAE KACC10331	3.4.11.1 3.4.11.10
3JS5	CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE FROM ENTAMOEBA HISTOLYTICA WITH HEPES IN THE ACTIVE SITE. HIGH RESOLUTION, ALTERNATIVE CRYSTAL FORM WITH 1 MOLECULE IN ASYMMETRIC UNIT	3.1.3.2
3JSB	CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF THE LYMPHOCYTIC CHORIOMENINGITIS VIRUS L PROTEIN	2.7.7.48 3.1
3JSI	HUMAN PHOSPHODIESTERASE 9 IN COMPLEX WITH INHIBITOR	3.1.4.35
3JSM	K65R MUTANT HIV-1 REVERSE TRANSCRIPTASE CROSS-LINKED TO DS-DNA AND COMPLEXED WITH TENOFOVIR-DIPHOSPHATE AS THE INCOMING NUCLEOTIDE SUBSTRATE	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
3JSO	CLASSIC PROTEIN WITH A NEW TWIST: CRYSTAL STRUCTURE OF A LEXA REPRESSOR DNA COMPLEX	3.4.21.88
3JSP	CLASSIC PROTEIN WITH A NEW TWIST: CRYSTAL STRUCTURE OF A LEXA REPRESSOR DNA COMPLEX	3.4.21.88
3JSW	HUMAN PDE9 IN COMPLEX WITH SELECTIVE INHIBITOR	3.1.4.35
3JTI	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 WITH BETA-AMYLOID FRAGMENT, LYS-GLY-ALA-ILE-ILE-GLY-LEU-MET AT 1.8 A RESOLUTION	3.1.1.4
3JU1	CRYSTAL STRUCTURE OF ENOYL-COA HYDRATASE/ISOMERASE FAMILY PROTEIN	3.1.2.4
3JU4	CRYSTAL STRUCTURE ANALYSIS OF ENDOSIALIDASENF AT 0.98 A RESOLUTION	3.2.1.129
3JUG	CRYSTAL STRUCTURE OF ENDO-BETA-1,4-MANNANASE FROM THE ALKALIPHILIC BACILLUS SP. N16-5	3.2.1.78
3JUR	THE CRYSTAL STRUCTURE OF A HYPERTHERMOACTIVE EXOPOLYGALACTURONASE FROM THERMOTOGA MARITIMA	3.2.1.15
3JUU	CRYSTAL STRUCTURE OF PORPHYRANASE B (PORB) FROM ZOBELLIA GALACTANIVORANS	3.2.1.178
3JVI	PRODUCT STATE MIMIC CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE FROM ENTAMOEBA HISTOLYTICA	3.1.3.2
3JVW	HIV-1 PROTEASE MUTANT G86A WITH SYMMETRIC INHIBITOR DMP323	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
3JVY	HIV-1 PROTEASE MUTANT G86A WITH DARUNAVIR	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
3JW1	CRYSTAL STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE COMPLEXED WITH URIDINE-5'-MONOPHOSPHATE AT 1.60 A RESOLUTION	3.1.27.5 4.6.1.18
3JW2	HIV-1 PROTEASE MUTANT G86S WITH DARUNAVIR	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
3JW8	CRYSTAL STRUCTURE OF HUMAN MONO-GLYCERIDE LIPASE	3.1.1.23
3JWE	CRYSTAL STRUCTURE OF HUMAN MONO-GLYCERIDE LIPASE IN COMPLEX WITH SAR629	3.1.1.23
3JWQ	CRYSTAL STRUCTURE OF CHIMERIC PDE5/PDE6 CATALYTIC DOMAIN COMPLEXED WITH SILDENAFIL	3.1.4.35
3JWR	CRYSTAL STRUCTURE OF CHIMERIC PDE5/PDE6 CATALYTIC DOMAIN COMPLEXED WITH 3-ISOBUTYL-1-METHYLXANTHINE (IBMX) AND PDE6 GAMMA-SUBUNIT INHIBITORY PEPTIDE 70-87.	3.1.4.35
3JXF	CA-LIKE DOMAIN OF HUMAN PTPRZ	3.1.3.48
3JXG	CA-LIKE DOMAIN OF MOUSE PTPRG	3.1.3.48
3JXH	CA-LIKE DOMAIN OF HUMAN PTPRG	3.1.3.48
3JYF	THE CRYSTAL STRUCTURE OF A 2,3-CYCLIC NUCLEOTIDE 2-PHOSPHODIESTERASE/3-NUCLEOTIDASE BIFUNCTIONAL PERIPLASMIC PRECURSOR PROTEIN FROM KLEBSIELLA PNEUMONIAE SUBSP. PNEUMONIAE MGH 78578	3.1.3.6 3.1.4.16
3JYH	HUMAN DIPEPTIDYL PEPTIDASE DPP7	3.4.14.2
3JYI	STRUCTURAL AND BIOCHEMICAL EVIDENCE THAT A TEM-1 {BETA}-LACTAMASE ASN170GLY ACTIVE SITE MUTANT ACTS VIA SUBSTRATE-ASSISTED CATALYSIS	3.5.2.6
3JYT	K65R MUTANT HIV-1 REVERSE TRANSCRIPTASE CROSS-LINKED TO DS-DNA AND COMPLEXED WITH DATP AS THE INCOMING NUCLEOTIDE SUBSTRATE	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
3JYU	CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAINS OF THE UBIQUITIN SPECIFIC PEPTIDASE 4 (USP4)	3.1.2.15 3.4.19.12
3JZ1	CRYSTAL STRUCTURE OF HUMAN THROMBIN MUTANT N143P IN E:NA+ FORM	3.4.21.5
3JZ2	CRYSTAL STRUCTURE OF HUMAN THROMBIN MUTANT N143P IN E* FORM	3.4.21.5
3JZE	1.8 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF DIHYDROOROTASE (PYRC) FROM SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHIMURIUM STR. LT2	3.5.2.3
3K0V	REMOVAL OF SUGARS AND SUGARS-LIKE MOLECULES FROM THE SOLUTION BY C-LOBE OF LACTOFERRIN: CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE WITH BETA-D-GLUCOPYRANOSYL-(1->4)-BETA-D-GALACTOPYRANOSYL-(1->4)-ALPHA-D-GLUCOPYRANOSE AT 1.9 A RESOLUTION	3.4.21
3K0W	CRYSTAL STRUCTURE OF THE TANDEM IG-LIKE C2-TYPE 2 DOMAINS OF THE HUMAN MUCOSA-ASSOCIATED LYMPHOID TISSUE LYMPHOMA TRANSLOCATION PROTEIN 1	3.4.22
3K1W	NEW CLASSES OF POTENT AND BIOAVAILABLE HUMAN RENIN INHIBITORS	3.4.23.15
3K24	CRYSTAL STRUCTURE OF MATURE APO-CATHEPSIN L C25A MUTANT IN COMPLEX WITH GLN-LEU-ALA PEPTIDE	3.4.22.15
3K2I	HUMAN ACYL-COENZYME A THIOESTERASE 4	3.1.2.2 3.1.2.3
3K2P	HIV-1 REVERSE TRANSCRIPTASE ISOLATED RNASEH DOMAIN WITH THE INHIBITOR BETA-THUJAPLICINOL BOUND AT THE ACTIVE SITE	3.1.26.4 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
3K2R	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME MUTANT K65V1/R76V1	3.2.1.17
3K2U	CRYSTAL STRUCTURE OF HGFA IN COMPLEX WITH THE ALLOSTERIC INHIBITORY ANTIBODY FAB40	3.4.21
3K2Z	CRYSTAL STRUCTURE OF A LEXA PROTEIN FROM THERMOTOGA MARITIMA	3.4.21.88
3K35	CRYSTAL STRUCTURE OF HUMAN SIRT6	3.5.1 2.3.1.286
3K36	CRYSTAL STRUCTURE OF B/PERTH NEURAMINIDASE	3.2.1.18
3K37	CRYSTAL STRUCTURE OF B/PERTH NEURAMINIDASE IN COMPLEX WITH PERAMIVIR	3.2.1.18
3K3C	THE N-TERMINAL PAS DOMAIN CRYSTAL STRUCTURE OF RV1364C FROM MYCOBACTERIUM TUBERCULOSIS AT 1.62	3.1.3.16 2.7.11.1
3K3D	THE N-TERMINAL PAS DOMAIN CRYSTAL STRUCTURE OF RV1364C FROM MYCOBACTERIUM TUBERCULOSIS AT 2.3 ANGSTROM	3.1.3.16 2.7.11.1
3K3E	CRYSTAL STRUCTURE OF THE PDE9A CATALYTIC DOMAIN IN COMPLEX WITH (R)-BAY73-6691	3.1.4.35
3K3H	CRYSTAL STRUCTURE OF THE PDE9A CATALYTIC DOMAIN IN COMPLEX WITH (S)-BAY73-6691	3.1.4.35
3K3T	E185A MUTANT OF PEPTIDOGLYCAN HYDROLASE FROM SPHINGOMONAS SP. A1	3.2.1
3K3W	THERMOSTABLE PENICILLIN G ACYLASE FROM ALCALIGENES FAECALIS IN ORTHORHOMBIC FORM	3.5.1.11
3K46	CRYSTAL STRUCTURE OF FULL-LENGTH E. COLI BETA-GLUCURONIDASE	3.2.1.31
3K4A	CRYSTAL STRUCTURE OF SELENOMETHIONINE SUBSTITUTED E. COLI BETA-GLUCURONIDASE	3.2.1.31
3K4D	CRYSTAL STRUCTURE OF E. COLI BETA-GLUCURONIDASE WITH THE GLUCARO-D-LACTAM INHIBITOR BOUND	3.2.1.31
3K4P	ASPERGILLUS NIGER PHYTASE	3.1.3.8
3K4Q	ASPERGILLUS NIGER PHYTASE IN COMPLEX WITH MYO-INOSITOL HEXAKIS SULFATE	3.1.3.8
3K4S	THE STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN PDE4D WITH 4-(3-BUTOXY-4-METHOXYPHENYL)METHYL-2-IMIDAZOLIDONE	3.1.4.17 3.1.4.53
3K4V	NEW CRYSTAL FORM OF HIV-1 PROTEASE/SAQUINAVIR STRUCTURE REVEALS CARBAMYLATION OF N-TERMINAL PROLINE	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
3K5C	HUMAN BACE-1 COMPLEX WITH NB-216	3.4.23.46
3K5D	CRYSTAL STRUCTURE OF BACE-1 IN COMPLEX WITH AHM178	3.4.23.46
3K5E	THE STRUCTURE OF HUMAN KINESIN-LIKE MOTOR PROTEIN KIF11/KSP/EG5 IN COMPLEX WITH ADP AND ENASTROL.	3.6.4.4
3K5F	HUMAN BACE-1 COMPLEX WITH AYH011	3.4.23.46
3K5G	HUMAN BACE-1 COMPLEX WITH BJC060	3.4.23.46
3K65	CRYSTAL STRUCTURE OF PRETHOMBIN-2/FRAGMENT-2 COMPLEX	3.4.21.5
3K6K	CRYSTAL STRUCTURE AT 2.2 ANGSTROM OF HSL-HOMOLOG ESTE7 FROM A METAGENOME LIBRARY	3.1.1
3K6L	THE STRUCTURE OF E.COLI PEPTIDE DEFORMYLASE (PDF) IN COMPLEX WITH PEPTIDOMIMETIC LIGAND BB2827	3.5.1.88
3K6Y	CRYSTAL STRUCTURE OF RV3671C PROTEASE FROM M. TUBERCULOSIS, ACTIVE FORM	3.4.21
3K6Z	CRYSTAL STRUCTURE OF RV3671C PROTEASE, INACTIVE FORM	3.4.21
3K7E	CRYSTAL STRUCTURE OF HUMAN LIGAND-FREE MATURE CASPASE-6	3.4.22.59
3K7F	CRYSTAL STRUCTURE ANALYSIS OF A PHENHEXYL/OXAZOLE/CARBOXYPYRIDINE ALPHA-KETOHETEROCYCLE INHIBITOR BOUND TO A HUMANIZED VARIANT OF FATTY ACID AMIDE HYDROLASE'	3.5.1 3.5.1.99 3.1.1
3K7L	STRUCTURES OF TWO ELAPID SNAKE VENOM METALLOPROTEASES WITH DISTINCT ACTIVITIES HIGHLIGHT THE DISULFIDE PATTERNS IN THE D DOMAIN OF ADAMALYSIN FAMILY PROTEINS	3.4.24
3K7N	STRUCTURES OF TWO ELAPID SNAKE VENOM METALLOPROTEASES WITH DISTINCT ACTIVITIES HIGHLIGHT THE DISULFIDE PATTERNS IN THE D DOMAIN OF ADAMALYSIN FAMILY PROTEINS	3.4.24
3K83	CRYSTAL STRUCTURE ANALYSIS OF A BIPHENYL/OXAZOLE/CARBOXYPYRIDINE ALPHA-KETOHETEROCYCLE INHIBITOR BOUND TO A HUMANIZED VARIANT OF FATTY ACID AMIDE HYDROLASE	3.5.1 3.5.1.99 3.1.1
3K84	CRYSTAL STRUCTURE ANALYSIS OF A OLEYL/OXADIAZOLE/PYRIDINE INHIBITOR BOUND TO A HUMANIZED VARIANT OF FATTY ACID AMIDE HYDROLASE	3.5.1 3.5.1.99 3.1.1
3K8K	CRYSTAL STRUCTURE OF SUSG	3.2.1.1
3K8L	CRYSTAL STRUCTURE OF SUSG-D498N MUTANT WITH MALTOHEPTAOSE	3.2.1.1
3K8M	CRYSTAL STRUCTURE OF SUSG WITH ACARBOSE	3.2.1.1
3K8Y	ALLOSTERIC MODULATION OF H-RAS GTPASE	3.6.5.2
3K9B	CRYSTAL STRUCTURE OF HUMAN LIVER CARBOXYLESTERASE 1 (HCE1) IN COVALENT COMPLEX WITH THE NERVE AGENT CYCLOSARIN (GF)	3.1.1.1 3.1.1.13 3.1.1.56
3K9J	TRANSPOSASE DOMAIN OF METNASE	2.1.1.43 2.1.1.357 3.1
3K9K	TRANSPOSASE DOMAIN OF METNASE	2.1.1.43 2.1.1.357 3.1
3K9L	ALLOSTERIC MODULATION OF H-RAS GTPASE	3.6.5.2
3K9M	CATHEPSIN B IN COMPLEX WITH STEFIN A	3.4.22.1
3K9N	ALLOSTERIC MODULATION OF H-RAS GTPASE	3.6.5.2
3K9X	X-RAY CRYSTAL STRUCTURE OF HUMAN FXA IN COMPLEX WITH (S)-N-((2-METHYLBENZOFURAN-5-YLAMINO)(2-OXO-1-(2-OXO-2- (PYRROLIDIN-1-YL)ETHYL)AZEPAN-3- YLAMINO)METHYLENE)NICOTINAMIDE	3.4.21.6
3KA2	CRYSTAL STRUCTURE OF CHEMICALLY SYNTHESIZED 203 AMINO ACID 'COVALENT DIMER' [L-ALA;GLY51']HIV-1 PROTEASE MOLECULE COMPLEXED WITH MVT-101 REDUCED ISOSTERE INHIBITOR AT 1.4 A RESOLUTION	3.4.23.16
3KAM	HEN EGG WHITE LYSOZYME DERIVATIZED WITH RHENIUM(I) DIAQUATRICARBONYL CATION	3.2.1.17
3KBB	CRYSTAL STRUCTURE OF PUTATIVE BETA-PHOSPHOGLUCOMUTASE FROM THERMOTOGA MARITIMA	3.1.3
3KBP	KIDNEY BEAN PURPLE ACID PHOSPHATASE	3.1.3.2
3KBZ	CRYSTAL STRUCTURE OF HUMAN LIVER FBPASE IN COMPLEX WITH TRICYCLIC INHIBITOR 6	3.1.3.11
3KC0	CRYSTAL STRUCTURE OF HUMAN LIVER FBPASE IN COMPLEX WITH TRICYCLIC INHIBITOR 10B	3.1.3.11
3KC1	CRYSTAL STRUCTURE OF HUMAN LIVER FBPASE IN COMPLEX WITH TRICYCLIC INHIBITOR 19A	3.1.3.11
3KCH	BARANASE CROSSLINKED BY GLUTARALDEHYDE	3.1.27
3KD1	CLOSED BINARY COMPLEX OF AN RB69 GP43 FINGERS DOMAIN MUTANT COMPLEXED WITH AN ACYCLIC GMP TERMINATED PRIMER TEMPLATE PAIR.	2.7.7.7 3.1.11
3KD3	CRYSTAL STRUCTURE OF A PHOSPHOSERINE PHOSPHOHYDROLASE-LIKE PROTEIN FROM FRANCISELLA TULARENSIS SUBSP. TULARENSIS SCHU S4	3.1.3.3
3KD5	CLOSED TERNARY COMPLEX OF AN RB69 GP43 FINGERS DOMAIN MUTANT COMPLEXED WITH AN ACYCLIC GMP TERMINATED PRIMER TEMPLATE PAIR AND PHOSPHONOFORMIC ACID.	2.7.7.7 3.1.11
3KDB	CRYSTAL STRUCTURE OF HIV-1 PROTEASE (Q7K, L33I, L63I) IN COMPLEX WITH KNI-10006	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
3KDC	CRYSTAL STRUCTURE OF HIV-1 PROTEASE (Q7K, L33I, L63I) IN COMPLEX WITH KNI-10074	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
3KDD	CRYSTAL STRUCTURE OF HIV-1 PROTEASE (Q7K, L33I, L63I) IN COMPLEX WITH KNI-10265	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
3KDS	APO-FTSH CRYSTAL STRUCTURE	3.4.24
3KE0	CRYSTAL STRUCTURE OF N370S GLUCOCEREBROSIDASE AT ACIDIC PH.	3.2.1.45 2.4.1 3.2.1
3KE6	THE CRYSTAL STRUCTURE OF THE RSBU AND RSBW DOMAINS OF RV1364C FROM MYCOBACTERIUM TUBERCULOSIS	3.1.3.16 2.7.11.1
3KEC	CRYSTAL STRUCTURE OF HUMAN MMP-13 COMPLEXED WITH A PHENYL-2H-TETRAZOLE COMPOUND	3.4.24
3KED	CRYSTAL STRUCTURE OF AMINOPEPTIDASE N IN COMPLEX WITH 2,4-DIAMINOBUTYRIC ACID	3.4.11.2
3KEE	HCV NS3/NS4A COMPLEXED WITH NON-COVALENT MACROCYCLIC COMPOUND TMC435	3.4.21.98 2.7.7.48 3.6.1.15 3.6.4.13
3KEH	CRYSTAL STRUCTURE OF N370S GLUCOCEREBROSIDASE MUTANT AT PH 7.4	3.2.1.45 2.4.1 3.2.1
3KEJ	CRYSTAL STRUCTURE OF HUMAN MMP-13 COMPLEXED WITH A (PYRIDIN-4-YL)-2H-TETRAZOLE COMPOUND	3.4.24
3KEK	CRYSTAL STRUCTURE OF HUMAN MMP-13 COMPLEXED WITH A (PYRIDIN-4-YL)-2H-TETRAZOLE COMPOUND	3.4.24
3KEP	CRYSTAL STRUCTURE OF THE AUTOPROTEOLYTIC DOMAIN FROM THE NUCLEAR PORE COMPLEX COMPONENT NUP145 FROM SACCHAROMYCES CEREVISIAE	3.4.21
3KES	CRYSTAL STRUCTURE OF THE AUTOPROTEOLYTIC DOMAIN FROM THE NUCLEAR PORE COMPLEX COMPONENT NUP145 FROM SACCHAROMYCES CEREVISIAE IN THE HEXAGONAL, P61 SPACE GROUP	3.4.21
3KF0	HIV PROTEASE WITH FRAGMENT 4D9 BOUND	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
3KF2	THE HCV NS3/NS4A PROTEASE APO STRUCTURE	3.4.21.98 2.7.7.48 3.6.1.15 3.6.4.13
3KF3	STRUCTURE OF FRUCTOFURANOSIDASE FROM SCHWANNIOMYCES OCCIDENTALIS COMPLEXED WITH FRUCTOSE	3.2.1.26
3KF5	STRUCTURE OF INVERTASE FROM SCHWANNIOMYCES OCCIDENTALIS	3.2.1.26
3KFN	HIV PROTEASE (PR) WITH INHIBITOR TL-3 AND FRAGMENT HIT 4D9 BY SOAKING	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
3KFP	HIV PROTEASE (PR) WITH INHIBITOR TL-3 BOUND, AND DMSOS IN EXO SITE	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
3KFQ	UNREDUCED CATHEPSIN V IN COMPLEX WITH STEFIN A	3.4.22.43
3KFR	HIV PROTEASE (PR) DIMER WITH INHIBITOR TL-3 BOUND AND FRAGMENT 1F1 IN THE OUTSIDE/TOP OF FLAP	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
3KFS	HIV PROTEASE (PR) DIMER WITH INHIBITOR TL-3 BOUND AND FRAGMENT 2F4 IN THE OUTSIDE/TOP OF FLAP	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
3KG4	CRYSTAL STRUCTURE OF AN UNCHARACTERIZED PROTEIN FROM MANNHEIMIA SUCCINICIPRODUCENS	3.1
3KGG	X-RAY STRUCTURE OF PERDEUTERATED DIISOPROPYL FLUOROPHOSPHATASE (DFPASE): PERDEUTERATION OF PROTEINS FOR NEUTRON DIFFRACTION	3.1.8.2
3KGP	CRYSTAL STRUCTURES OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR IN COMPLEX WITH 4-(AMINOMETHYL) BENZOIC ACID AND 4-(AMINOMETHYL-PHENYL)-METHANOL	3.4.21.73
3KGQ	CARBOXYPEPTIDASE A LIGANDED TO AN ORGANIC SMALL-MOLECULE: CONFORMATIONAL CHANGES	3.4.17.1
3KHV	CRYSTAL STRUCTURES OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR IN COMPLEX WITH 4-(AMINOMETHYL) BENZOIC ACID AND 4-(AMINOMETHYL-PHENYL)-METHANOL	3.4.21.73
3KHX	CRYSTAL STRUCTURE OF STAPHYLOCOCCUS AUREUS METALLOPEPTIDASE (SAPEP/DAPE) IN THE APO-FORM	3.4.13
3KHZ	CRYSTAL STRUCTURE OF R350A MUTANT OF STAPHYLOCOCCUS AUREUS METALLOPEPTIDASE (SAPEP/DAPE) IN THE APO-FORM	3.4.13
3KI8	CRYSTAL STRUCTURE OF HYPERTHERMOPHILIC NITRILASE	3.5.1.6 3.5.5.1
3KI9	CRYSTAL STRUCTURE OF STAPHYLOCOCCUS AUREUS METALLOPEPTIDASE (SAPEP/DAPE) IN THE MN2+ BOUND FORM	3.4.13
3KID	THE CRYSTAL STRUCTURES OF 2-AMINOBENZOTHIAZOLE-BASED INHIBITORS IN COMPLEXES WITH UROKINASE-TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
3KIO	MOUSE RNASE H2 COMPLEX	3.1.26.4
3KIV	RECOMBINANT KRINGLE IV-10/M66 VARIANT OF HUMAN APOLIPOPROTEIN(A)	3.4.21
3KJ7	CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF BOVINE LACTOFERRIN WITH DEXTRIN AT 1.9 A RESOLUTION	3.4.21
3KJF	CASPASE 3 BOUND TO A COVALENT INHIBITOR	3.4.22.56
3KJN	CASPASE 8 BOUND TO A COVALENT INHIBITOR	3.4.22.61
3KJQ	CASPASE 8 WITH COVALENT INHIBITOR	3.4.22.61
3KJV	HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH DNA	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
3KJZ	CRYSTAL STRUCTURE OF NATIVE PEPTIDYL-TRNA HYDROLASE FROM MYCOBACTERIUM SMEGMATIS	3.1.1.29
3KK0	CRYSTAL STRUCTURE OF PARTIALLY FOLDED INTERMEDIATE STATE OF PEPTIDYL-TRNA HYDROLASE FROM MYCOBACTERIUM SMEGMATIS	3.1.1.29
3KK1	HIV-1 REVERSE TRANSCRIPTASE-DNA COMPLEX WITH NUCEOTIDE INHIBITOR GS-9148-DIPHOSPHATE BOUND IN NUCLEOTIDE SITE	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
3KK2	HIV-1 REVERSE TRANSCRIPTASE-DNA COMPLEX WITH DATP BOUND IN THE NUCLEOTIDE BINDING SITE	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
3KK3	HIV-1 REVERSE TRANSCRIPTASE-DNA COMPLEX WITH GS-9148 TERMINATED PRIMER	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
3KKL	CRYSTAL STRUCTURE OF FUNCTIONALLY UNKNOWN HSP33 FROM SACCHAROMYCES CEREVISIAE	3.2 4.2.1.130
3KKM	CRYSTAL STRUCTURE OF H-RAS T35S IN COMPLEX WITH GPPNHP	3.6.5.2
3KKN	CRYSTAL STRUCTURE OF H-RAS T35S IN COMPLEX WITH GPPNHP	3.6.5.2
3KKO	CRYSTAL STRUCTURE OF M-RAS P40D/D41E/L51R IN COMPLEX WITH GPPNHP	3.6.5.2
3KKP	CRYSTAL STRUCTURE OF M-RAS P40D IN COMPLEX WITH GPPNHP	3.6.5.2
3KKQ	CRYSTAL STRUCTURE OF M-RAS P40D IN COMPLEX WITH GDP	3.6.5.2
3KKR	CRYSTAL STRUCTURE OF CATALYTIC CORE DOMAIN OF BIV INTEGRASE IN CRYSTAL FORM I	3.4.23 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
3KKS	CRYSTAL STRUCTURE OF CATALYTIC CORE DOMAIN OF BIV INTEGRASE IN CRYSTAL FORM II	3.4.23 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
3KKT	CRYSTAL STRUCTURE OF HUMAN PDE4B WITH 5-[3-[(1S,2S,4R)-BICYCLO[2.2.1]HEPT-2-YLOXY]-4-METHOXYP HENYL]TETRAHYDRO-2(1H)-PYRIMIDINONE REVEALS ORDERING OF THE C-TERMINAL HELIX RESIDUES 502-509.	3.1.4.17 3.1.4.53
3KKU	CRUZAIN IN COMPLEX WITH A NON-COVALENT LIGAND	3.4.22.51
3KL0	CRYSTAL STRUCTURE OF THE GLUCURONOXYLAN XYLANOHYDROLASE XYNC FROM BACILLUS SUBTILIS	3.2.1.136
3KL3	CRYSTAL STRUCTURE OF LIGAND BOUND XYNC	3.2.1.136
3KL4	RECOGNITION OF A SIGNAL PEPTIDE BY THE SIGNAL RECOGNITION PARTICLE	3.6.5.4
3KL5	STRUCTURE ANALYSIS OF A XYLANASE FROM GLYCOSYL HYDROLASE FAMILY THIRTY: CARBOHYDRATE LIGAND COMPLEXES REVEAL THIS FAMILY OF ENZYMES UNIQUE MECHANISM OF SUBSTRATE SPECIFICITY AND RECOGNITION	3.2.1.136
3KL6	DISCOVERY OF TETRAHYDROPYRIMIDIN-2(1H)-ONE DERIVATIVE TAK-442: A POTENT, SELECTIVE AND ORALLY ACTIVE FACTOR XA INHIBITOR	3.4.21.6
3KLC	CRYSTAL STRUCTURE OF HYPERTHERMOPHILIC NITRILASE	3.5.1.6 3.5.5.1
3KLG	CRYSTAL STRUCTURE OF AZT-RESISTANT HIV-1 REVERSE TRANSCRIPTASE CROSSLINKED TO PRE-TRANSLOCATION AZTMP-TERMINATED DNA (COMPLEX N)	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
3KLI	CRYSTAL STRUCTURE OF UNLIGANDED AZT-RESISTANT HIV-1 REVERSE TRANSCRIPTASE	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
3KLV	M296I G62S MUTANT OF FOOT-AND-MOUTH DISEASE VIRUS RNA-POLYMERASE IN COMPLEX WITH A TEMPLATE- PRIMER RNA	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
3KM3	CRYSTAL STRUCTURE OF EOXYCYTIDINE TRIPHOSPHATE DEAMINASE FROM ANAPLASMA PHAGOCYTOPHILUM AT 2.1A RESOLUTION	3.5.4.13
3KM4	OPTIMIZATION OF ORALLY BIOAVAILABLE ALKYL AMINE RENIN INHIBITORS	3.4.23.15
3KM8	CRYSTAL STRUCTUORE OF ADENOSINE DEAMINASE FROM MUS MUSCULUS COMPLEXED WITH 9-DEAZAINOSINE	3.5.4.4
3KMC	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH TARTRATE-BASED INHIBITOR	3.4.24.86
3KME	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH PHENYL-PYRROLIDINYL-TARTRATE INHIBITOR	3.4.24.86
3KMQ	G62S MUTANT OF FOOT-AND-MOUTH DISEASE VIRUS RNA-POLYMERASE IN COMPLEX WITH A TEMPLATE- PRIMER RNA, TETRAGONAL STRUCTURE	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
3KMS	G62S MUTANT OF FOOT-AND-MOUTH DISEASE VIRUS RNA-POLYMERASE IN COMPLEX WITH A TEMPLATE- PRIMER RNA TRIGONAL STRUCTURE	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
3KMX	STRUCTURE OF BACE BOUND TO SCH346572	3.4.23.46
3KMY	STRUCTURE OF BACE BOUND TO SCH12472	3.4.23.46
3KN0	STRUCTURE OF BACE BOUND TO SCH708236	3.4.23.46
3KN2	HCV NS3 PROTEASE DOMAIN WITH KETOAMIDE INHIBITOR	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3KNA	M296I MUTANT OF FOOT-AND-MOUTH DISEASE VIRUS RNA-POLYMERASE IN COMPLEX WITH A TEMPLATE- PRIMER RNA	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
3KNF	CRYSTAL STRUCTURE OF D-TYR-TRNA(TYR) DEACYLASE FROM PLASMODIUM FALCIPARUM	3.1 3.1.1.96
3KNP	CRYSTAL STRUCTURE OF DTD FROM PLASMODIUM FALCIPARUM	3.1 3.1.1.96
3KNR	BACILLUS CEREUS METALLO-BETA-LACTAMASE CYS221ASP MUTANT, 1 MM ZN(II)	3.5.2.6
3KNS	BACILLUS CEREUS METALLO-BETA-LACTAMASE CYS221ASP MUTANT, 20 MM ZN(II)	3.5.2.6
3KNT	CRYSTAL STRUCTURE OF METHANOCALDOCOCCUS JANNASCHII 8-OXOGUANINE GLYCOSYLASE/LYASE IN COMPLEX WITH 15MER DNA CONTAINING 8-OXOGUANINE	3.2.2 4.2.99.18
3KNX	HCV NS3 PROTEASE DOMAIN WITH P1-P3 MACROCYCLIC KETOAMIDE INHIBITOR	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
3KO3	D-TYROSYL-TRNA(TYR) DEACYLASE FROM PLASMODIUM FALCIPARUM INCOMPLEX WITH ADP, OBTAINED THROUGH SOAKING NATIVE ENZYME CRYSTAL WITH THE ATP	3.1 3.1.1.96
3KO4	CRYSTAL STRUCTURE OF D-TYR-TRNA(TYR) DEACYLASE FROM PLASMODIUM FALCIPARUM IN COMPLEX WITH ADP	3.1 3.1.1.96
3KO5	D-TYR-TRNA(TYR) DEACYLASE FROM PLASMODIUM FALCIPARUM IN COMPLEX WITH ADP	3.1 3.1.1.96
3KO7	DTD FROM PLASMODIUM FALCIPARUM IN COMPLEX WITH D-LYSINE	3.1 3.1.1.96
3KO9	DTD FROM PLASMODIUM FALCIPARUM IN COMPLEX WITH D-ARGININE	3.1 3.1.1.96
3KOA	M296I MUTANT OF FOOT-AND-MOUTH DISEASE VIRUS RNA-POLYMERASE IN COMPLEX WITH A TEMPLATE- PRIMER RNA AND GTP	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
3KOB	DTD FROM PLASMODIUM FALCIPARUM IN COMPLEX WITH D-GLUTAMIC ACID	3.1 3.1.1.96
3KOC	DTD FROM PLASMODIUM FALCIPARUM IN COMPLEX WITH D-HISTIDINE	3.1 3.1.1.96
3KOD	DTD FROM PLASMODIUM FALCIPARUM IN COMPLEX WITH D-SERINE	3.1 3.1.1.96
3KOO	CRYSTAL STRUCTURE OF SOLUBLE EPOXIDE HYDROLASE	3.3.2.10 3.1.3.76
3KOU	STRUCTURAL INSIGHTS INTO THE CATALYTIC MECHANISM OF CD38: EVIDENCE FOR A CONFORMATIONALLY FLEXIBLE COVALENT ENZYME-SUBSTRATE COMPLEX.	3.2.2.5 2.4.99.20 3.2.2.6
3KQB	FACTOR XA IN COMPLEX WITH THE INHIBITOR N-(3-FLUORO-2'- (METHYLSULFONYL)BIPHENYL-4-YL)-1-(3-(5-OXO-4,5-DIHYDRO-1H- 1,2,4-TRIAZOL-3-YL)PHENYL)-3-(TRIFLUOROMETHYL)-1H- PYRAZOLE-5-CARBOXAMIDE	3.4.21.6
3KQC	FACTOR XA IN COMPLEX WITH THE INHIBITOR 6-(2'- (METHYLSULFONYL)BIPHENYL-4-YL)-1-(3-(5-OXO-4,5-DIHYDRO-1H- 1,2,4-TRIAZOL-3-YL)PHENYL)-3-(TRIFLUOROMETHYL)-5,6- DIHYDRO-1H-PYRAZOLO[3,4-C]PYRIDIN-7(4H)-ONE	3.4.21.6
3KQD	FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-(3-(5-OXO-4,5- DIHYDRO-1H-1,2,4-TRIAZOL-3-YL)PHENYL)-6-(2'-(PYRROLIDIN-1- YLMETHYL)BIPHENYL-4-YL)-3-(TRIFLUOROMETHYL)-5,6-DIHYDRO- 1H-PYRAZOLO[3,4-C]PYRIDIN-7(4H)-ONE	3.4.21.6
3KQE	FACTOR XA IN COMPLEX WITH THE INHIBITOR 3-METHYL-1-(3-(5- OXO-4,5-DIHYDRO-1H-1,2,4-TRIAZOL-3-YL)PHENYL)-6-(2'- (PYRROLIDIN-1-YLMETHYL)BIPHENYL-4-YL)-5,6-DIHYDRO-1H- PYRAZOLO[3,4-C]PYRIDIN-7(4H)-ONE	3.4.21.6
3KQH	THREE CONFORMATIONAL SNAPSHOTS OF THE HEPATITIS C VIRUS NS3 HELICASE REVEAL A RATCHET TRANSLOCATION MECHANISM	3.4.21.98 3.6.1.15 3.6.1 3.4.22 3.6.4.13 2.7.7.48
3KQK	THREE CONFORMATIONAL SNAPSHOTS OF THE HEPATITIS C VIRUS NS3 HELICASE REVEAL A RATCHET TRANSLOCATION MECHANISM	3.4.21.98 3.6.1.15 3.6.1 3.4.22 3.6.4.13 2.7.7.48
3KQL	THREE CONFORMATIONAL SNAPSHOTS OF THE HEPATITIS C VIRUS NS3 HELICASE REVEAL A RATCHET TRANSLOCATION MECHANISM	3.4.21.98 3.6.1.15 3.6.1 3.4.22 3.6.4.13 2.7.7.48
3KQN	THREE CONFORMATIONAL SNAPSHOTS OF THE HEPATITIS C VIRUS NS3 HELICASE REVEAL A RATCHET TRANSLOCATION MECHANISM	3.4.21.98 3.6.1.15 3.6.1 3.4.22 3.6.4.13 2.7.7.48
3KRN	CRYSTAL STRUCTURE OF C. ELEGANS CELL-DEATH-RELATED NUCLEASE 5(CRN-5)	3.1.13
3KRY	CRYSTAL STRUCTURE OF MMP-13 IN COMPLEX WITH SC-78080	3.4.24
3KSE	UNREDUCED CATHEPSIN L IN COMPLEX WITH STEFIN A	3.4.22.15
3KSK	CRYSTAL STRUCTURE OF SINGLE CHAIN PVUII	3.1.21.4
3KT2	CRYSTAL STRUCTURE OF N88D MUTANT 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
3KT5	CRYSTAL STRUCTURE OF N88S MUTANT 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
3KT9	APRATAXIN FHA DOMAIN	3 3.6.1.71 3.6.1.72
3KTG	STRUCTURE OF CLPP FROM BACILLUS SUBTILIS IN MONOCLINIC CRYSTAL FORM	3.4.21.92
3KTH	STRUCTURE OF CLPP FROM BACILLUS SUBTILIS IN ORTHOROMBIC CRYSTAL FORM	3.4.21.92
3KTI	STRUCTURE OF CLPP IN COMPLEX WITH ADEP1	3.4.21.92
3KTJ	STRUCTURE OF CLPP IN COMPLEX WITH ADEP2 IN MONOCLINIC CRYSTAL FORM	3.4.21.92
3KTU	STRUCTURE OF HUMAN 8-OXOGUANINE GLYCOSYLASE 1 BOUND TO FLUORNINATED OXOG-CONTAINING DNA	3.2.2 4.2.99.18
3KTZ	STRUCTURE OF GAP31	3.2.2.22
3KU0	STRUCTURE OF GAP31 WITH ADENINE AT ITS BINDING POCKET	3.2.2.22
3KUC	COMPLEX OF RAP1A(E30D/K31E)GDP WITH RAFRBD(A85K/N71R)	3.6.5.2
3KUD	COMPLEX OF RAS-GDP WITH RAFRBD(A85K)	3.6.5.2
3KUV	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA THIOESTERASE FLK - T42S MUTANT IN COMPLEX WITH ACETATE.	3 3.1.2.29
3KUW	STRUCTURAL BASIS OF THE ACTIVITY ANS SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA THIOESTERASE FLK - T42S MUTANT IN COMPLEX WITH FLUORO-ACETATE	3 3.1.2.29
3KV2	HIGH RESOLUTION STRUCTURE OF HUMAN ARGINASE I IN COMPLEX WITH THE STRONG INHIBITOR N(OMEGA)-HYDROXY-NOR-L-ARGININE (NOR-NOHA)	3.5.3.1
3KV7	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA THIOESTERASE FLK - WILD TYPE FLK IN COMPLEX WITH ACETATE	3 3.1.2.29
3KV8	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA THIOESTERASE FLK - WILD TYPE FLK IN COMPLEX WITH FLUORO-ACETATE	3 3.1.2.29
3KVC	CRYSTAL STRUCTURE OF BOVINE RPE65 AT 1.9 ANGSTROM RESOLUTION	3.1.1.64 5.2.1.7 5.3.3.22
3KVF	CRYSTAL STRUCTURE OF THE I93M MUTANT OF UBIQUITIN CARBOXY TERMINAL HYDROLASE L1 BOUND TO UBIQUITIN VINYLMETHYLESTER	3.4.19.12 6
3KVI	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA THIOESTERASE FLK - T42A MUTANT IN COMPLEX WITH FLUORO-ACETATE	3 3.1.2.29
3KVN	CRYSTAL STRUCTURE OF THE FULL-LENGTH AUTOTRANSPORTER ESTA FROM PSEUDOMONAS AERUGINOSA	3.1.1.1
3KVU	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA FLK - T42S MUTANT IN COMPLEX WITH ACETYL-COA	3 3.1.2.29
3KVZ	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA THIESTERASE FLK - WILD TYPE FLK IN COMPLEX WITH FACCPAN	3 3.1.2.29
3KW1	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA FLK - WILD TYPE FLK IN COMPLEX WITH FACOPAN	3 3.1.2.29
3KW5	CRYSTAL STRUCTURE OF UBIQUITIN CARBOXY TERMINAL HYDROLASE L1 BOUND TO UBIQUITIN VINYLMETHYLESTER	3.4.19.12 6
3KW9	X-RAY STRUCTURE OF CATHEPSIN K COVALENTLY BOUND TO A TRIAZINE LIGAND	3.4.22.38
3KWB	STRUCTURE OF CATK COVALENTLY BOUND TO A DIOXO-TRIAZINE INHIBITOR	3.4.22.38
3KWF	HUMAN DPP-IV WITH CARMEGLIPTIN (S)-1-((2S,3S,11BS)-2-AMINO-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-A]ISOQUINOLIN-3-YL)-4-FLUOROMETHYL-PYRROLIDIN-2-ONE	3.4.14.5
3KWJ	STRUCTURE OF HUMAN DPP-IV WITH (2S,3S,11BS)-3-(3-FLUOROMETHYL-PHENYL)-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-A]ISOQUINOLIN-2-YLAMINE	3.4.14.5
3KWX	CHEMICALLY MODIFIED TAKA ALPHA-AMYLASE	3.2.1.1
3KWZ	CATHEPSIN K IN COMPLEX WITH A NON-SELECTIVE 2-CYANO-PYRIMIDINE INHIBITOR	3.4.22.38
3KX0	CRYSTAL STRUCTURE OF THE PAS DOMAIN OF RV1364C	3.1.3.16 2.7.11.1
3KX1	CATHEPSIN K IN COMPLEX WITH A SELECTIVE 2-CYANO-PYRIMIDINE INHIBITOR	3.4.22.38
3KX2	CRYSTAL STRUCTURE OF PRP43P IN COMPLEX WITH ADP	3.6.1 3.6.4.13
3KX7	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA FLK - APO WILD TYPE FLK	3 3.1.2.29
3KX8	STRUCTURAL BASIS OF THE ACTIVITY AND SUBSTRATE SPECIFICITY OF THE FLUOROACETYL-COA THIOESTERASE FLK	3.1.2.29
3KYH	SACCHAROMYCES CEREVISIAE CET1-CEG1 CAPPING APPARATUS	3.1.3.33
3KYR	BACE-1 IN COMPLEX WITH A NORSTATINE TYPE INHIBITOR	3.4.23.46
3L07	METHYLENETETRAHYDROFOLATE DEHYDROGENASE/METHENYLTETRAHYDROFOLATE CYCLOHYDROLASE, PUTATIVE BIFUNCTIONAL PROTEIN FOLD FROM FRANCISELLA TULARENSIS.	1.5.1.5 3.5.4.9
3L0B	CRYSTAL STRUCTURE OF SCP1 PHOSPHATASE D206A MUTANT PHOSPHORYL-INTERMEDIATE	3.1.3.16
3L0C	CRYSTAL STRUCTURE OF SCP1 PHOSPHATASE D206A MUTANT WITH TRAPPED INORGANIC PHOSPHATE	3.1.3.16
3L0O	STRUCTURE OF RNA-FREE RHO TRANSCRIPTION TERMINATION FACTOR FROM THERMOTOGA MARITIMA	3.6.1 3.6.4
3L0T	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH HYDANTOIN INHIBITOR	3.4.24.86
3L0V	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH THE FIRST HYDANTOIN INHIBITOR OCCUPYING THE S1' POCKET	3.4.24.86
3L0Y	CRYSTAL STRUCTURE OF SCP1 PHOSPHATASE D98A MUTANT	3.1.3.16
3L1H	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY FECL3	3.1.1
3L1I	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY CUSO4	3.1.1
3L1J	CRYSTAL STRUCTURE OF ESTE5, WAS SOAKED BY ZNSO4	3.1.1
3L1K	SAD STRUCTURE SOLUTION OF PROTEINASE K GROWN IN POTASSIUM TELLURATE SOLUTION	3.4.21.64
3L1U	CRYSTAL STRUCTURE OF CALCIUM-BOUND GMHB FROM E. COLI.	3.1.3 3.1.3.82
3L1V	CRYSTAL STRUCTURE OF GMHB FROM E. COLI IN COMPLEX WITH CALCIUM AND PHOSPHATE.	3.1.3 3.1.3.82
3L24	CRYSTAL STRUCTURE OF THE NERVE AGENT DEGRADING ORGANOPHOSPHATE ANHYDROLASE/PROLIDASE IN COMPLEX WITH INHIBITORS	3.4.13.9 3.1.8.2 3.1.8.1
3L2B	CRYSTAL STRUCTURE OF THE CBS AND DRTGG DOMAINS OF THE REGULATORY REGION OF CLOSTRIDIUM PERFRINGENS PYROPHOSPHATASE COMPLEXED WITH ACTIVATOR, DIADENOSINE TETRAPHOSPHATE	3.6.1.1
3L2L	X-RAY CRYSTALLOGRAPHIC ANALYSIS OF PIG PANCREATIC ALPHA-AMYLASE WITH LIMIT DEXTRIN AND OLIGOSACCHARIDE	3.2.1.1
3L2M	X-RAY CRYSTALLOGRAPHIC ANALYSIS OF PIG PANCREATIC ALPHA-AMYLASE WITH ALPHA-CYCLODEXTRIN	3.2.1.1
3L2Q	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN APO FORM	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3L2R	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3L2U	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND GS9137 (ELVITEGRAVIR)	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3L2V	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MANGANESE AND MK0518 (RALTEGRAVIR)	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3L2W	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MANGANESE AND GS9137 (ELVITEGRAVIR)	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3L2X	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME MUTANT 115-119RX	3.2.1.17
3L30	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 COMPLEXED WITH DIHYDROXYBERBERINE	3.1.1.4
3L31	CRYSTAL STRUCTURE OF THE CBS AND DRTGG DOMAINS OF THE REGULATORY REGION OF CLOSTRIDIUM PERFRINGENS PYROPHOSPHATASE COMPLEXED WITH THE INHIBITOR, AMP	3.6.1.1
3L33	HUMAN MESOTRYPSIN COMPLEXED WITH AMYLOID PRECURSOR PROTEIN INHIBITOR(APPI)	3.4.21.4
3L38	BACE1 IN COMPLEX WITH THE AMINOPYRIDINE COMPOUND 44	3.4.23.46
3L3A	BACE-1 WITH THE AMINOPYRIDINE COMPOUND 32	3.4.23.46
3L3N	TESTIS ACE CO-CRYSTAL STRUCTURE WITH NOVEL INHIBITOR LISW	3.4.15.1 3.2.1
3L3T	HUMAN MESOTRYPSIN COMPLEXED WITH AMYLOID PRECURSOR PROTEIN INHIBITOR VARIANT (APPIR15K)	3.4.21.4
3L3U	CRYSTAL STRUCTURE OF THE HIV-1 INTEGRASE CORE DOMAIN TO 1.4A	2.7.7.49 3.1.13.2 3.1.26.13
3L3V	STRUCTURE OF HIV-1 INTEGRASE CORE DOMAIN IN COMPLEX WITH SUCROSE	2.7.7.49 3.1.13.2 3.1.26.13
3L43	CRYSTAL STRUCTURE OF THE DYNAMIN 3 GTPASE DOMAIN BOUND WITH GDP	3.6.5.5
3L4E	1.5A CRYSTAL STRUCTURE OF A PUTATIVE PEPTIDASE E PROTEIN FROM LISTERIA MONOCYTOGENES EGD-E	3.4.21
3L4T	CRYSTAL COMPLEX OF N-TERMINAL HUMAN MALTASE-GLUCOAMYLASE WITH BJ2661	3.2.1.20 3.2.1.3
3L4U	CRYSTAL COMPLEX OF N-TERMINAL HUMAN MALTASE-GLUCOAMYLASE WITH DE-O-SULFONATED KOTALANOL	3.2.1.20 3.2.1.3
3L4V	CRYSTAL COMPLEX OF N-TERMINAL HUMAN MALTASE-GLUCOAMYLASE WITH KOTALANOL	3.2.1.20 3.2.1.3
3L4W	CRYSTAL COMPLEX OF N-TERMINAL HUMAN MALTASE-GLUCOAMYLASE WITH MIGLITOL	3.2.1.20 3.2.1.3
3L4X	CRYSTAL COMPLEX OF N-TERMINAL HUMAN MALTASE-GLUCOAMYLASE WITH NR4-8	3.2.1.20 3.2.1.3
3L4Y	CRYSTAL COMPLEX OF N-TERMINAL HUMAN MALTASE-GLUCOAMYLASE WITH NR4-8II	3.2.1.20 3.2.1.3
3L4Z	CRYSTAL COMPLEX OF N-TERMINAL HUMAN MALTASE-GLUCOAMYLASE WITH SALACINOL	3.2.1.20 3.2.1.3
3L57	CRYSTAL STRUCTURE OF THE PLASMID PCU1 TRAI RELAXASE DOMAIN	3.6.1
3L58	STRUCTURE OF BACE BOUND TO SCH589432	3.4.23.46
3L59	STRUCTURE OF BACE BOUND TO SCH710413	3.4.23.46
3L5B	STRUCTURE OF BACE BOUND TO SCH713601	3.4.23.46
3L5C	STRUCTURE OF BACE BOUND TO SCH723871	3.4.23.46
3L5D	STRUCTURE OF BACE BOUND TO SCH723873	3.4.23.46
3L5E	STRUCTURE OF BACE BOUND TO SCH736062	3.4.23.46
3L5F	STRUCTURE OF BACE BOUND TO SCH736201	3.4.23.46
3L5K	THE CRYSTAL STRUCTURE OF HUMAN HALOACID DEHALOGENASE-LIKE HYDROLASE DOMAIN CONTAINING 1A (HDHD1A)	3.1.3.96
3L64	T4 LYSOZYME S44E/WT*	3.2.1.17
3L6N	CRYSTAL STRUCTURE OF METALLO-BETA-LACTAMASE IND-7	3.5.2.6
3L6P	CRYSTAL STRUCTURE OF DENGUE VIRUS 1 NS2B/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
3L6T	CRYSTAL STRUCTURE OF AN N-TERMINAL MUTANT OF THE PLASMID PCU1 TRAI RELAXASE DOMAIN	3.6.1
3L7G	CRYSTAL STRUCTURE OF ORGANOPHOSPHATE ANHYDROLASE/PROLIDASE	3.4.13.9 3.1.8.2 3.1.8.1
3L7Z	CRYSTAL STRUCTURE OF THE S. SOLFATARICUS ARCHAEAL EXOSOME	3.1.13
3L85	CRYSTAL STRUCTURE OF HUMAN NUDT5 COMPLEXED WITH 8-OXO-DGMP	3.6.1.13 3.6.1.58 2.7.7.96
3L87	THE CRYSTAL STRUCTURE OF SMU.143C FROM STREPTOCOCCUS MUTANS UA159	3.5.1.88
3L8B	CRYSTAL STRUCTURE OF A REPLICATIVE DNA POLYMERASE BOUND TO THE OXIDIZED GUANINE LESION GUANIDINOHYDANTOIN	2.7.7.7 3.1.11
3L8E	CRYSTAL STRUCTURE OF APO FORM OF D,D-HEPTOSE 1.7-BISPHOSPHATE PHOSPHATASE FROM E. COLI	3.1.3 3.1.3.82
3L8F	CRYSTAL STRUCTURE OF D,D-HEPTOSE 1.7-BISPHOSPHATE PHOSPHATASE FROM E. COLI COMPLEXED WITH MAGNESIUM AND PHOSPHATE	3.1.3 3.1.3.82
3L8G	CRYSTAL STRUCTURE OF D,D-HEPTOSE 1.7-BISPHOSPHATE PHOSPHATASE FROM E. COLI COMPLEXED WITH D-GLYCERO-D-MANNO-HEPTOSE 1 ,7-BISPHOSPHATE	3.1.3 3.1.3.82
3L8H	CRYSTAL STRUCTURE OF D,D-HEPTOSE 1.7-BISPHOSPHATE PHOSPHATASE FROM B. BRONCHISEPTICA COMPLEXED WITH MAGNESIUM AND PHOSPHATE	3.1.3.82
3L8Y	COMPLEX OF RAS WITH CYCLEN	3.6.5.2
3L8Z	H-RAS WILDTYPE NEW CRYSTAL FORM	3.6.5.2
3L91	STRUCTURE OF PSEUDOMONAS AERUGIONSA PVDQ BOUND TO OCTANOATE	3.5.1.97
3L94	STRUCTURE OF PVDQ COVALENTLY ACYLATED WITH MYRISTATE	3.5.1.97
3LA4	CRYSTAL STRUCTURE OF THE FIRST PLANT UREASE FROM JACK BEAN (CANAVALIA ENSIFORMIS)	3.5.1.5
3LAC	CRYSTAL STRUCTURE OF BACILLUS ANTHRACIS PYRROLIDONE-CARBOXYLATE PEPTIDASE, PCP	3.4.19.3
3LAK	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH N1-HETEROCYCLE PYRIMIDINEDIONE NON-NUCLEOSIDE 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
3LAL	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH N1-ETHYL PYRIMIDINEDIONE NON-NUCLEOSIDE 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
3LAM	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH N1-PROPYL PYRIMIDINEDIONE NON-NUCLEOSIDE 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
3LAN	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH N1-BUTYL PYRIMIDINEDIONE NON-NUCLEOSIDE 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
3LAQ	STRUCTURE-BASED ENGINEERING OF SPECIES SELECTIVITY IN THE UPA-UPAR INTERACTION	3.4.21.73
3LAT	CRYSTAL STRUCTURE OF STAPHYLOCOCCUS PEPTIDOGLYCAN HYDROLASE AMIE	3.5.1.28 3.2.1.96
3LB9	CRYSTAL STRUCTURE OF THE B. CIRCULANS CPA123 CIRCULAR PERMUTANT	3.2.1.8
3LBH	RAS SOAKED IN CALCIUM ACETATE	3.6.5.2
3LBI	RAS SOAKED IN MAGNESIUM ACETATE AND BACK SOAKED IN CALCIUM ACETATE	3.6.5.2
3LBN	RAS SOAKED IN MAGNESIUM ACETATE	3.6.5.2
3LC3	BENZOTHIOPHENE INHIBITORS OF FACTOR IXA	3.4.21.22
3LC5	SELECTIVE BENZOTHIOPHINE INHIBITORS OF FACTOR IXA	3.4.21.22
3LC6	THE ALTERNATIVE CONFORMATION STRUCTURE OF ISOCITRATE DEHYDROGENASE KINASE/PHOSPHATASE FROM E. COLI	2.7.11.5 3.1.3
3LC9	RICIN A-CHAIN VARIANT 1-33/44-198 WITH ENGINEERED DISULFIDE BOND	3.2.2.22
3LCB	THE CRYSTAL STRUCTURE OF ISOCITRATE DEHYDROGENASE KINASE/PHOSPHATASE IN COMPLEX WITH ITS SUBSTRATE, ISOCITRATE DEHYDROGENASE, FROM ESCHERICHIA COLI.	2.7.11.5 3.1.3
3LCE	CRYSTAL STRUCTURE OF OXA-10 BETA-LACTAMASE COVALENTLY BOUND TO CYCLOBUTANONE BETA-LACTAM MIMIC	3.5.2.6
3LCR	THIOESTERASE FROM TAUTOMYCETIN BIOSYNTHHETIC PATHWAY	3.1.2 1.1.1.100 1.3.1.39 2.3.1.38 2.3.1.39 2.3.1.41 4.2.1.59
3LD1	CRYSTAL STRUCTURE OF IBV NSP2A	3.4.22
3LD3	CRYSTAL STRUCTURE OF INORGANIC PHOSPHATASE FROM ANAPLASMA PHAGOCYTOPHILUM AT 1.75A RESOLUTION	3.6.1.1
3LDL	CRYSTAL STRUCTURE OF HUMAN GRP78 (70KDA HEAT SHOCK PROTEIN 5 / BIP) ATPASE DOMAIN IN COMPLEX WITH ATP	3.6.4.10
3LDN	CRYSTAL STRUCTURE OF HUMAN GRP78 (70KDA HEAT SHOCK PROTEIN 5 / BIP) ATPASE DOMAIN IN APO FORM	3.6.4.10
3LDO	CRYSTAL STRUCTURE OF HUMAN GRP78 (70KDA HEAT SHOCK PROTEIN 5 / BIP) ATPASE DOMAIN IN COMPLEX WITH AMPPNP	3.6.4.10
3LDP	CRYSTAL STRUCTURE OF HUMAN GRP78 (70KDA HEAT SHOCK PROTEIN 5 / BIP) ATPASE DOMAIN IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.6.4.10
3LDS	CRYSTAL STRUCTURE OF RB69 GP43 WITH DNA AND DATP OPPOSITE 8-OXOG	2.7.7.7 3.1.11
3LDX	DISCOVERY AND CLINICAL EVALUATION OF RWJ-671818, A THROMBIN INHIBITOR WITH AN OXYGUANIDINE P1 MOTIF	3.4.21.5
3LE7	CRYSTAL STRUCTURE OF PD-L1 FROM P. DIOICA IN COMPLEX WITH ADENINE	3.2.2.22
3LE9	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF TACE WITH INDAZOLINONE-PHENYL-HYDANTOIN INHIBITOR	3.4.24.86
3LEA	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF TACE WITH ISOINDOLINONE-BIPHENYL-HYDANTOIN INHIBITOR	3.4.24.86
3LEZ	CRYSTAL STRUCTURE OF A HALOTOLERANT BACTERIAL BETA-LACTAMASE	3.5.2.6
3LFU	CRYSTAL STRUCTURE OF E. COLI UVRD	3.6.1 3.6.4.12
3LFV	CRYSTAL STRUCTURE OF UNLIGANDED PDE5A GAF DOMAIN	3.1.4.35
3LFY	CTD OF TAROCYSTATIN IN COMPLEX WITH PAPAIN	3.4.22.2
3LG2	A YKR043C/ FRUCTOSE-1,6-BISPHOSPHATE PRODUCT COMPLEX FOLLOWING LIGAND SOAKING	3.1.3.11 3.1.3.37
3LGD	CRYSTAL STRUCTURE OF HUMAN ADENOSINE DEAMINASE GROWTH FACTOR, ADENOSINE DEAMINASE TYPE 2 (ADA2)	3.5.4.4
3LGG	CRYSTAL STRUCTURE OF HUMAN ADENOSINE DEAMINASE GROWTH FACTOR, ADENOSINE DEAMINASE TYPE 2 (ADA2) COMPLEXED WITH TRANSITION STATE ANALOGUE, COFORMYCIN	3.5.4.4
3LGI	STRUCTURE OF THE PROTEASE DOMAIN OF DEGS (DEGS-DELTAPDZ) AT 1.65 A	3.4.21 3.4.21.107
3LGP	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH BENZIMIDAZOLYL-THIENYL-TARTRATE BASED INHIBITOR	3.4.24.86
3LGR	XYLANASE II FROM TRICHODERMA REESEI COCRYSTALLIZED WITH TRIS-DIPICOLINATE EUROPIUM	3.2.1.8
3LGS	A. THALIANA MTA NUCLEOSIDASE IN COMPLEX WITH S-ADENOSYLHOMOCYSTEINE	3.2.2.16
3LGT	Y162A/H198P DOUBLE MUTANT OF DEGS-DELTAPDZ PROTEASE	3.4.21 3.4.21.107
3LGU	Y162A MUTANT OF THE DEGS-DELTAPDZ PROTEASE	3.4.21 3.4.21.107
3LGV	H198P MUTANT OF THE DEGS-DELTAPDZ PROTEASE	3.4.21 3.4.21.107
3LGW	H198P/T167V DOUBLE MUTANT OF DEGS-DELTAPDZ PROTEASE	3.4.21 3.4.21.107
3LGY	R178A MUTANT OF THE DEGS-DELTAPDZ PROTEASE	3.4.21 3.4.21.107
3LH1	Q191A MUTANT OF THE DEGS-DELTAPDZ	3.4.21 3.4.21.107
3LH3	DFP MODIFIED DEGS DELTA PDZ	3.4.21 3.4.21.107
3LHG	BACE1 IN COMPLEX WITH THE AMINOHYDANTOIN COMPOUND 4G	3.4.23.46
3LHI	CRYSTAL STRUCTURE OF PUTATIVE 6-PHOSPHOGLUCONOLACTONASE(YP_207848.1) FROM NEISSERIA GONORRHOEAE FA 1090 AT 1.33 A RESOLUTION	3.1.1.31
3LHL	CRYSTAL STRUCTURE OF A PUTATIVE AGMATINASE FROM CLOSTRIDIUM DIFFICILE	3.5.3.11
3LHM	CRYSTAL STRUCTURES OF THE APO-AND HOLOMUTANT HUMAN LYSOZYMES WITH AN INTRODUCED CA2+ BINDING SITE	3.2.1.17
3LI3	DIISOPROPYL FLUOROPHOSPHATASE (DFPASE), D121E MUTANT	3.1.8.2
3LI4	DIISOPROPYL FLUOROPHOSPHATASE (DFPASE), N120D,N175D,D229N MUTANT	3.1.8.2
3LI5	DIISOPROPYL FLUOROPHOSPHATASE (DFPASE), E21Q,N120D,N175D,D229N MUTANT	3.1.8.2
3LII	RECOMBINANT HUMAN ACETYLCHOLINESTERASE	3.1.1.7
3LIK	HUMAN MMP12 IN COMPLEX WITH NON-ZINC CHELATING INHIBITOR	3.4.24.65
3LIL	HUMAN MMP12 IN COMPLEX WITH NON-ZINC CHELATING INHIBITOR	3.4.24.65
3LIP	OPEN CONFORMATION OF PSEUDOMONAS CEPACIA LIPASE	3.1.1.3
3LIR	HUMAN MMP12 IN COMPLEX WITH NON-ZINC CHELATING INHIBITOR	3.4.24.65
3LIW	FACTOR XA IN COMPLEX WITH (R)-2-(1-ADAMANTYLCARBAMOYLAMINO)-3-(3-CARBAMIDOYL-PHENYL)-N-PHENETHYL-PROPIONIC ACID AMIDE	3.4.21.6
3LIZ	CRYSTAL STRUCTURE OF BLA G 2 COMPLEXED WITH FAB 4C3	3.4.23
3LJ0	IRE1 COMPLEXED WITH ADP AND QUERCETIN	2.7.11.1 3.1.26
3LJ1	IRE1 COMPLEXED WITH CDK1/2 INHIBITOR III	2.7.11.1 3.1.26
3LJ2	IRE1 COMPLEXED WITH JAK INHIBITOR I	2.7.11.1 3.1.26
3LJ6	3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH THE DRUG-LIKE UREA INHIBITOR PF-3845 AT 2.42A RESOLUTION	3.5.1 3.5.1.99 3.1.1
3LJ7	3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH CARBAMATE INHIBITOR URB597	3.5.1 3.5.1.99 3.1.1
3LJ8	CRYSTAL STRUCTURE OF MKP-4	3.1.3.48 3.1.3.16
3LJC	CRYSTAL STRUCTURE OF LON N-TERMINAL DOMAIN.	3.4.21.53
3LJG	HUMAN MMP12 IN COMPLEX WITH NON-ZINC CHELATING INHIBITOR	3.4.24.65
3LJJ	BOVINE TRYPSIN IN COMPLEX WITH UB-THR 10	3.4.21.4
3LJO	BOVINE TRYPSIN IN COMPLEX WITH UB-THR 11	3.4.21.4
3LJQ	CRYSTAL STRUCTURE OF THE GLYCOSYLASPARAGINASE T152C APO-PRECURSOR	3.5.1.26
3LJT	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF ADAMTS-5 IN COMPLEX WITH AN AMINO-2-INDANOL COMPOUND	3.4.24
3LJZ	CRYSTAL STRUCTURE OF HUMAN MMP-13 COMPLEXED WITH AN AMINO-2-INDANOL COMPOUND	3.4.24
3LK6	BETA-N-HEXOSAMINIDASE N318D MUTANT (YBBD_N318D) FROM BACILLUS SUBTILIS	3.2.1.52
3LK8	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR PARAMETHOXY-SULFONYL-GLYCINE HYDROXAMATE	3.4.24.65
3LKA	CATALYTIC DOMAIN OF HUMAN MMP-12 COMPLEXED WITH HYDROXAMIC ACID AND PARAMETHOXY-SULFONYL AMIDE	3.4.24.65
3LKH	INHIBITORS OF HEPATITIS C VIRUS POLYMERASE: SYNTHESIS AND CHARACTERIZATION OF NOVEL 6-FLUORO-N-[2-HYDROXY-1(S)-BENZAMIDES	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3LKW	CRYSTAL STRUCTURE OF DENGUE VIRUS 1 NS2B/NS3 PROTEASE ACTIVE SITE 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
3LKZ	STRUCTURAL AND FUNCTIONAL ANALYSES OF A CONSERVED HYDROPHOBIC POCKET OF FLAVIVIRUS 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
3LL4	STRUCTURE OF THE H13A MUTANT OF YKR043C IN COMPLEX WITH FRUCTOSE-1,6-BISPHOSPHATE	3.1.3.11 3.1.3.37
3LL8	CRYSTAL STRUCTURE OF CALCINEURIN IN COMPLEX WITH AKAP79 PEPTIDE	3.1.3.16
3LLM	CRYSTAL STRUCTURE ANALYSIS OF A RNA HELICASE	3.6.1 3.6.4.13
3LLU	CRYSTAL STRUCTURE OF THE NUCLEOTIDE-BINDING DOMAIN OF RAS-RELATED GTP-BINDING PROTEIN C	3.6.5
3LMN	OLIGOMERIC STRUCTURE OF THE DUSP DOMAIN OF HUMAN USP15	3.1.2.15 3.4.19.12
3LMS	STRUCTURE OF HUMAN ACTIVATED THROMBIN-ACTIVATABLE FIBRINOLYSIS INHIBITOR, TAFIA, IN COMPLEX WITH TICK-DERIVED FUNNELIN INHIBITOR, TCI.	3.4.17.20
3LMT	CRYSTAL STRUCTURE OF DTD FROM PLASMODIUM FALCIPARUM	3.1 3.1.1.96
3LMU	CRYSTAL STRUCTURE OF DTD FROM PLASMODIUM FALCIPARUM	3.1 3.1.1.96
3LMV	D-TYR-TRNA(TYR) DEACYLASE FROM PLASMODIUM FALCIPARUM IN COMPLEX WITH HEPES	3.1 3.1.1.96
3LMW	CRYSTAL STRUCTURE OF IOTA-CARRAGEENASE FAMILY GH82 FROM A. FORTIS IN ABSENCE OF CHLORIDE IONS	3.2.1.157
3LMY	THE CRYSTAL STRUCTURE OF BETA-HEXOSAMINIDASE B IN COMPLEX WITH PYRIMETHAMINE	3.2.1.52
3LN2	CRYSTAL STRUCTURE OF A CHARGE ENGINEERED HUMAN LYSOZYME VARIANT	3.2.1.17
3LNK	STRUCTURE OF BACE BOUND TO SCH743813	3.4.23.46
3LNP	CRYSTAL STRUCTURE OF AMIDOHYDROLASE FAMILY PROTEIN OLEI01672_1_465 FROM OLEISPIRA ANTARCTICA	3.5.4.28 3.5.4.31
3LNX	SECOND PDZ DOMAIN FROM HUMAN PTP1E	3.1.3.48
3LNY	SECOND PDZ DOMAIN FROM HUMAN PTP1E IN COMPLEX WITH RA-GEF2 PEPTIDE	3.1.3.48
3LO0	CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM EHRLICHIA CHAFFEENSIS	3.6.1.1
3LO5	CRYSTAL STRUCTURE OF THE DOMINANT NEGATIVE S17N MUTANT OF RAS	3.6.5.2
3LO7	CRYSTAL STRUCTURE OF PBPA FROM MYCOBACTERIUM TUBERCULOSIS	3.4.16.4
3LOB	CRYSTAL STRUCTURE OF FLOCK HOUSE VIRUS CALCIUM MUTANT	3.4.23.44
3LOJ	STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS DUTPASE H145A MUTANT	3.6.1.23
3LON	HCV NS3-4A PROTEASE DOMAIN WITH KETOAMIDE INHIBITOR NARLAPREVIR	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
3LOU	CRYSTAL STRUCTURE OF FORMYLTETRAHYDROFOLATE DEFORMYLASE (YP_105254.1) FROM BURKHOLDERIA MALLEI ATCC 23344 AT 1.90 A RESOLUTION	3.5.1.10
3LOX	HCV NS3-4A PROTEASE DOMAIN WITH A KETOAMIDE INHIBITOR DERIVATIVE OF BOCEPREVIR BOUND	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
3LP0	HIV-1 REVERSE TRANSCRIPTASE WITH 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
3LP1	HIV-1 REVERSE TRANSCRIPTASE WITH 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
3LP2	HIV-1 REVERSE TRANSCRIPTASE WITH 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
3LP3	P15 HIV RNASEH DOMAIN WITH INHIBITOR MK3	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
3LP4	CRYSTAL STRUCTURE OF HUMAN ARGINASE I IN COMPLEX WITH L-LYSINE, 1.90A RESOLUTION.	3.5.3.1
3LP7	CRYSTAL STRUCTURE OF HUMAN ARGINASE I IN COMPLEX WITH INHIBITOR N(OMEGA)-HYDROXY-L-ARGININE (NOHA), 2.04A RESOLUTION	3.5.3.1
3LPA	CRYSTAL STRUCTURE OF A SUBTILISIN-LIKE PROTEASE	3.4.21
3LPC	CRYSTAL STRUCTURE OF A SUBTILISIN-LIKE PROTEASE	3.4.21
3LPD	CRYSTAL STRUCTURE OF A SUBTILISIN-LIKE PROTEASE	3.4.21
3LPF	STRUCTURE OF E. COLI BETA-GLUCURONIDASE BOUND WITH A NOVEL, POTENT INHIBITOR 1-((6,7-DIMETHYL-2-OXO-1,2-DIHYDROQUINOLIN-3-YL)METHYL)-1-(2-HYDROXYETHYL)-3-(3-METHOXYPHENYL)THIOUREA	3.2.1.31
3LPG	STRUCTURE OF E. COLI BETA-GLUCURONIDASE BOUND WITH A NOVEL, POTENT INHIBITOR 3-(2-FLUOROPHENYL)-1-(2-HYDROXYETHYL)-1-((6-METHYL-2-OXO-1,2-DIHYDROQUINOLIN-3-YL)METHYL)UREA	3.2.1.31
3LPI	STRUCTURE OF BACE BOUND TO SCH745132	3.4.23.46
3LPJ	STRUCTURE OF BACE BOUND TO SCH743641	3.4.23.46
3LPK	STRUCTURE OF BACE BOUND TO SCH747123	3.4.23.46
3LPP	CRYSTAL COMPLEX OF N-TERMINAL SUCRASE-ISOMALTASE WITH KOTALANOL	3.2.1.10 3.2.1.48
3LPR	STRUCTURAL BASIS FOR BROAD SPECIFICITY IN ALPHA-LYTIC PROTEASE MUTANTS	3.4.21.12
3LPT	HIV INTEGRASE	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
3LPU	HIV INTEGRASE	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
3LQ0	ZYMOGEN STRUCTURE OF CRAYFISH ASTACIN METALLOPEPTIDASE	3.4.24.21
3LQB	CRYSTAL STRUCTURE OF THE HATCHING ENZYME ZHE1 FROM THE ZEBRAFISH DANIO RERIO	3.4.24
3LQW	CRYSTAL STRUCTURE OF DEOXYURIDINE 5-TRIPHOSPHATE NUCLEOTIDOHYDROLASE FROM ENTAMOEBA HISTOLYTICA	3.6.1.23
3LRK	STRUCTURE OF ALFA-GALACTOSIDASE (MEL1) FROM SACCHAROMYCES CEREVISIAE	3.2.1.22
3LRL	STRUCTURE OF ALFA-GALACTOSIDASE (MEL1) FROM SACCHAROMYCES CEREVISIAE WITH MELIBIOSE	3.2.1.22
3LRM	STRUCTURE OF ALFA-GALACTOSIDASE FROM SACCHAROMYCES CEREVISIAE WITH RAFFINOSE	3.2.1.22
3LRN	CRYSTAL STRUCTURE OF HUMAN RIG-I CTD BOUND TO A 14 BP GC 5' PPP DSRNA	3.6.1 3.6.4.13
3LRR	CRYSTAL STRUCTURE OF HUMAN RIG-I CTD BOUND TO A 12 BP AU RICH 5' PPP DSRNA	3.6.1 3.6.4.13
3LRY	CRYSTAL STRUCTURE OF SYNTHETIC HIV-1 CAPSID C-TERMINAL DOMAIN (CCA)	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
3LS2	CRYSTAL STRUCTURE OF AN S-FORMYLGLUTATHIONE HYDROLASE FROM PSEUDOALTEROMONAS HALOPLANKTIS TAC125	3.1.1 3.1.2.12
3LS7	CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH XENON	3.4.24.27
3LT3	CRYSTAL STRUCTURE OF RV3671C FROM M. TUBERCULOSIS H37RV, SER343ALA MUTANT, INACTIVE FORM	3.4.21
3LU9	CRYSTAL STRUCTURE OF HUMAN THROMBIN MUTANT S195A IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR1	3.4.21.5
3LUC	CRYSTAL STRUCTURE OF MID DOMAIN FROM HAGO2	3.1.26
3LUD	CRYSTAL STRUCTURE OF MID DOMAIN FROM HAGO2 IN COMPLEX WITH AMP	3.1.26
3LUG	CRYSTAL STRUCTURE OF MID DOMAIN FROM HAGO2 IN COMPLEX WITH CMP	3.1.26
3LUH	CRYSTAL STRUCTURE OF MID DOMAIN FROM HAGO2 IN COMPLEX WITH GMP	3.1.26
3LUJ	CRYSTAL STRUCTURE OF MID DOMAIN FROM HAGO2 IN COMPLEX WITH UMP	3.1.26
3LUK	CRYSTAL STRUCTURE OF MID DOMAIN FROM HAGO2	3.1.26
3LUM	STRUCTURE OF ULILYSIN MUTANT M290L	3.4.24
3LUN	STRUCTURE OF ULILYSIN MUTANT M290C	3.4.24
3LUZ	CRYSTAL STRUCTURE OF EXTRAGENIC SUPPRESSOR PROTEIN SUHB FROM BARTONELLA HENSELAE, VIA COMBINED IODIDE SAD MOLECULAR REPLACEMENT	3.1.3.25
3LV0	CRYSTAL STRUCTURE OF EXTRAGENIC SUPPRESSOR PROTEIN SUHB FROM BARTONELLA HENSELAE, NATIVE	3.1.3.25
3LW8	SHIGELLA IPGB2 IN COMPLEX WITH HUMAN RHOA, GDP AND MG2+ (COMPLEX A)	3.6.5.2
3LWD	CRYSTAL STRUCTURE OF PUTATIVE 6-PHOSPHOGLUCONOLACTONASE (YP_574786.1) FROM CHROMOHALOBACTER SALEXIGENS DSM 3043 AT 1.88 A RESOLUTION	3.1.1.31
3LWN	SHIGELLA IPGB2 IN COMPLEX WITH HUMAN RHOA, GDP AND MG2+ (COMPLEX B)	3.6.5.2
3LWT	CRYSTAL STRUCTURE OF THE YEAST SAC1: IMPLICATIONS FOR ITS PHOSPHOINOSITIDE PHOSPHATASE FUNCTION	3.1.3 3.1.3.64
3LX0	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS D21N AT CRYOGENIC TEMPERATURE	3.1.31.1
3LX9	INTERCONVERSION OF HUMAN LYSOSOMAL ENZYME SPECIFICITIES	3.2.1.22 3.2.1.47
3LXA	INTERCONVERSION OF HUMAN LYSOSOMAL ENZYME SPECIFICITIES	3.2.1.22 3.2.1.47
3LXB	INTERCONVERSION OF HUMAN LYSOSOMAL ENZYME SPECIFICITIES	3.2.1.22 3.2.1.47
3LXC	INTERCONVERSION OF HUMAN LYSOSOMAL ENZYME SPECIFICITIES	3.2.1.22 3.2.1.47
3LXG	CRYSTAL STRUCTURE OF RAT PHOSPHODIESTERASE 10A IN COMPLEX WITH LIGAND WEB-3	3.1.4.17 3.1.4.35
3LXO	THE CRYSTAL STRUCTURE OF RIBONUCLEASE A IN COMPLEX WITH THYMIDINE-3'-MONOPHOSPHATE	3.1.27.5 4.6.1.18
3LXR	SHIGELLA IPGB2 IN COMPLEX WITH HUMAN RHOA AND GDP (COMPLEX C)	3.6.5.2
3LXS	CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO VINYL SULFONE DERIVED INHIBITOR (WRR483)	3.4.22.51
3LXU	CRYSTAL STRUCTURE OF TRIPEPTIDYL PEPTIDASE 2 (TPP II)	3.4.14.10
3LY0	CRYSTAL STRUCTURE OF METALLO PEPTIDASE FROM RHODOBACTER SPHAEROIDES LIGANDED WITH PHOSPHINATE MIMIC OF DIPEPTIDE L-ALA-D-ALA	3.4.13.19
3LY3	CRYSTAL STRUCTURE OF FLUOROPHORE-LABELED CLASS A BETA-LACTAMASE PENP	3.5.2.6
3LY4	CRYSTAL STRUCTURE OF FLUOROPHORE-LABELED CLASS A -LACTAMASE PENP-E166CB IN COMPLEX WITH PENICILLIN G	3.5.2.6
3LY5	DDX18 DEAD-DOMAIN	3.6.1 3.6.4.13
3LYE	CRYSTAL STRUCTURE OF OXALOACETATE ACETYLHYDROLASE	3.7.1.1
3LYM	CRYSTAL STRUCTURE OF HEN EGG-WHITE LYSOZYME AT A HYDROSTATIC PRESSURE OF 1000 ATMOSPHERES	3.2.1.17
3LYO	CROSS-LINKED CHICKEN LYSOZYME CRYSTAL IN 95% ACETONITRILE-WATER	3.2.1.17
3LYT	COMPARISON OF RADIATION-INDUCED DECAY AND STRUCTURE REFINEMENT FROM X-RAY DATA COLLECTED FROM LYSOZYME CRYSTALS AT LOW AND AMBIENT TEMPERATURES	3.2.1.17
3LYZ	REAL-SPACE REFINEMENT OF THE STRUCTURE OF HEN EGG-WHITE LYSOZYME	3.2.1.17
3LZ2	STRUCTURE DETERMINATION OF TURKEY EGG WHITE LYSOZYME USING LAUE DIFFRACTION	3.2.1.17
3LZ7	CRYSTAL STRUCTURE OF THIOESTERASE HI1161 EC3.1.2.- FROM HAEMOPHILUS INFLUENZAE. ORTHOROMBIC CRYSTAL FORM. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET IR63	3.1.2
3LZI	RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DATP OPPOSITE 7,8-DIHYDRO-8-OXOGUANINE	2.7.7.7 3.1.11
3LZJ	RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE 7,8-DIHYDRO-8-OXOGUANINE	2.7.7.7 3.1.11
3LZM	STRUCTURAL STUDIES OF MUTANTS OF T4 LYSOZYME THAT ALTER HYDROPHOBIC STABILIZATION	3.2.1.17
3LZS	CRYSTAL STRUCTURE OF HIV-1 CRF01_AE PROTEASE IN COMPLEX WITH DARUNAVIR	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
3LZT	REFINEMENT OF TRICLINIC LYSOZYME AT ATOMIC RESOLUTION	3.2.1.17
3LZU	CRYSTAL STRUCTURE OF A NELFINAVIR RESISTANT HIV-1 CRF01_AE PROTEASE VARIANT (N88S) IN COMPLEX WITH THE PROTEASE INHIBITOR DARUNAVIR.	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
3LZV	STRUCTURE OF NELFINAVIR-RESISTANT HIV-1 PROTEASE (D30N/N88D) IN COMPLEX WITH DARUNAVIR.	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
3LZY	CRYSTAL STRUCTURE OF ENDOTHIAPESIN IN COMPLEX WITH XENON	3.4.23.22
3M07	1.4 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF PUTATIVE ALPHA AMYLASE FROM SALMONELLA TYPHIMURIUM.	3.2.1.141
3M0E	CRYSTAL STRUCTURE OF THE ATP-BOUND STATE OF WALKER B MUTANT OF NTRC1 ATPASE DOMAIN	3.6.1.3
3M0J	STRUCTURE OF OXALOACETATE ACETYLHYDROLASE IN COMPLEX WITH THE INHIBITOR 3,3-DIFLUOROOXALACETATE	3.7.1.1
3M0K	STRUCTURE OF OXALOACETATE ACETYLHYDROLASE IN COMPLEX WITH THE PRODUCT OXALATE	3.7.1.1
3M1H	CRYSTAL STRUCTURE ANALYSIS OF THE K3 CLEAVED ADHESIN DOMAIN OF LYS-GINGIPAIN (KGP) FROM PORPHYROMONAS GINGIVALIS W83	3.4.22.47
3M1R	THE CRYSTAL STRUCTURE OF FORMIMIDOYLGLUTAMASE FROM BACILLUS SUBTILIS SUBSP. SUBTILIS STR. 168	3.5.3.8
3M1Y	CRYSTAL STRUCTURE OF A PHOSPHOSERINE PHOSPHATASE (SERB) FROM HELICOBACTER PYLORI	3.1.3.3
3M2J	CRYSTAL STRUCTURE OF FLUORESCEIN-LABELED CLASS A -LACTAMASE PENP	3.5.2.6
3M2K	CRYSTAL STRUCTURE OF FLUORESCEIN-LABELED CLASS A -BETA LACTAMASE PENP IN COMPLEX WITH CEFOTAXIME	3.5.2.6
3M35	TRYPSIN IN COMPLEX WITH THE INHIBITOR 1-[3-(AMINOMETHYL)PHENYL]-N-[3-FLUORO-2'-(METHYLSULFONYL)BIPHENYL-4-YL]-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-5-CARBOXAMIDE (DPC423)	3.4.21.4
3M36	FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-[3-(AMINOMETHYL)PHENYL]-N-[3-FLUORO-2'-(METHYLSULFONYL)BIPHENYL-4-YL]-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-5-CARBOXAMIDE (DPC423)	3.4.21.6
3M37	FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-[2-(AMINOMETHYL)PHENYL]-N-(3-FLUORO-2'-SULFAMOYLBIPHENYL-4-YL)-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-5-CARBOXAMIDE (DPC602)	3.4.21.6
3M3C	CRYSTAL STRUCTURE OF AGROCYBE AEGERITA LECTIN AAL COMPLEXED WITH P-NITROPHENYL TF DISACCHARIDE	3.1.21
3M3D	CRYSTAL STRUCTURE OF ACETYLCHOLINESTERASE IN COMPLEX WITH XENON	3.1.1.7
3M3E	CRYSTAL STRUCTURE OF AGROCYBE AEGERITA LECTIN AAL MUTANT E66A COMPLEXED WITH P-NITROPHENYL THOMSEN-FRIEDENREICH DISACCHARIDE	3.1.21
3M3O	CRYSTAL STRUCTURE OF AGROCYBE AEGERITA LECTIN AAL MUTANT R85A COMPLEXED WITH P-NITROPHENYL TF DISACCHARIDE	3.1.21
3M3Q	CRYSTAL STRUCTURE OF AGROCYBE AEGERITA LECTIN AAL COMPLEXED WITH GANGLOSIDES GM1 PENTASACCHARIDE	3.1.21
3M3S	CRYSTAL STRUCTURE OF SARS-COV MAIN PROTEASE ASN214ALA MUTANT WITH AUTHORIZE N-TERMINUS	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
3M3T	SARS-COV MAIN PROTEASE MONOMERIC ARG298ALA MUTANT WITH N-TERMINAL ADDITIONAL RESIDUES (GLY-SER)	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
3M3U	EFFECT OF TEMPERATURE ON TRYPTOPHAN FLUORESCENCE IN LYSOZYME CRYSTALS	3.2.1.17
3M3V	SARS-COV MAIN PROTEASE TRIPLE MUTANT STI/A WITH TWO N-TERMINAL ADDITIONAL RESIDUE (GLY-SER)	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
3M46	THE CRYSTAL STRUCTURE OF THE D73A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174	3.2.1
3M4F	STRUCTURAL INSIGHTS INTO THE ACIDOPHILIC PH ADAPTATION OF A NOVEL ENDO-1,4-BETA-XYLANASE FROM SCYTALIDIUM ACIDOPHILUM	3.2.1.8
3M4U	CRYSTAL STRUCTURE OF TRYPANOSOMA BRUCEI PROTEIN TYROSINE PHOSPHATASE TBPTP1	3.1.3.48
3M4Y	STRUCTURAL CHARACTERIZATION OF THE SUBUNIT A MUTANT P235A OF THE A-ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3M5L	CRYSTAL STRUCTURE OF HCV NS3/4A PROTEASE IN COMPLEX WITH ITMN-191	3.4.21.98 2.7.7.48 3.6.1.15 3.6.4.13
3M5M	AVOIDING DRUG RESISTANCE AGAINST HCV NS3/4A PROTEASE INHIBITORS	3.4.21.98 2.7.7.48 3.6.1.15 3.6.4.13
3M5N	CRYSTAL STRUCTURE OF HCV NS3/4A PROTEASE IN COMPLEX WITH N-TERMINAL PRODUCT 4B5A	3.4.21.98 2.7.7.48 3.6.1.15 3.6.4.13
3M5O	CRYSTAL STRUCTURE OF HCV NS3/4A PROTEASE IN COMPLEX WITH N-TERMINAL PRODUCT 5A5B	3.4.21.98 2.7.7.48 3.6.1.15 3.6.4.13
3M65	CRYSTAL STRUCTURE OF BACILLUS SUBTILIS LON N-TERMINAL DOMAIN	3.4.21.53
3M6A	CRYSTAL STRUCTURE OF BACILLUS SUBTILIS LON C-TERMINAL DOMAIN	3.4.21.53
3M6B	CRYSTAL STRUCTURE OF THE ERTAPENEM PRE-ISOMERIZED COVALENT ADDUCT WITH TB B-LACTAMASE	3.5.2.6
3M6D	THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174	3.2.1
3M6H	CRYSTAL STRUCTURE OF POST-ISOMERIZED ERTAPENEM COVALENT ADDUCT WITH TB B-LACTAMASE	3.5.2.6
3M6O	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PEPTIDE DEFORMYLASE 1B (ATPDF1B)	3.5.1.88
3M6P	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PEPTIDE DEFORMYLASE 1B (ATPDF1B) IN COMPLEX WITH ACTINONIN	3.5.1.88
3M6Q	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PEPTIDE DEFORMYLASE 1B (ATPDF1B) G41Q MUTANT IN COMPLEX WITH ACTINONIN	3.5.1.88
3M7Q	CRYSTAL STRUCTURE OF RECOMBINANT KUNITZ TYPE SERINE PROTEASE INHIBITOR-1 FROM THE CARIBBEAN SEA ANEMONE STICHODACTYLA HELIANTHUS IN COMPLEX WITH BOVINE PANCREATIC TRYPSIN	3.4.21.4
3M7T	CRYSTAL STRUCTURE OF ALPHA-LYTIC PROTEASE SB2+3 E8A/R105S MUTANT	3.4.21.12
3M7U	CRYSTAL STRUCTURE OF ALPHA-LYTIC PROTEASE SB1+2 R64A/E182Q MUTANT	3.4.21.12
3M81	CRYSTAL STRUCTURE OF ACETYL XYLAN ESTERASE (TM0077) FROM THERMOTOGA MARITIMA AT 2.50 A RESOLUTION (NATIVE APO STRUCTURE)	3.1.1.41 3.1.1.72
3M82	CRYSTAL STRUCTURE OF ACETYL XYLAN ESTERASE (TM0077) FROM THERMOTOGA MARITIMA AT 2.40 A RESOLUTION (PMSF INHIBITOR COMPLEX STRUCTURE)	3.1.1.41 3.1.1.72
3M83	CRYSTAL STRUCTURE OF ACETYL XYLAN ESTERASE (TM0077) FROM THERMOTOGA MARITIMA AT 2.12 A RESOLUTION (PARAOXON INHIBITOR COMPLEX STRUCTURE)	3.1.1.41 3.1.1.72
3M89	STRUCTURE OF TUBZ-GTP-G-S	3.6.5
3M8K	PROTEIN STRUCTURE OF TYPE III PLASMID SEGREGATION TUBZ	3.6.5
3M8P	HIV-1 RT WITH NNRTI TMC-125	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
3M8Q	HIV-1 RT WITH AMINOPYRIMIDINE NNRTI	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
3M99	STRUCTURE OF THE UBP8-SGF11-SGF73-SUS1 SAGA DUB MODULE	3.1.2.15 3.4.19.12
3MA2	COMPLEX MEMBRANE TYPE-1 MATRIX METALLOPROTEINASE (MT1-MMP) WITH TISSUE INHIBITOR OF METALLOPROTEINASE-1 (TIMP-1)	3.4.24.80
3MAN	MANNOHEXAOSE COMPLEX OF THERMOMONOSPORA FUSCA BETA-MANNANASE	3.2.1.78
3MAT	E.COLI METHIONINE AMINOPEPTIDASE TRANSITION-STATE INHIBITOR COMPLEX	3.4.11.18
3MAX	CRYSTAL STRUCTURE OF HUMAN HDAC2 COMPLEXED WITH AN N-(2-AMINOPHENYL)BENZAMIDE	3.5.1.98
3MBK	THE 1.35 A STRUCTURE OF THE PHOSPHATASE DOMAIN OF THE SUPPRESSOR OF T CELL RECEPTOR SIGNALLING PROTEIN IN COMPLEX WITH SULPHATE	3.1.3.48
3MBQ	CRYSTAL STRUCTURE OF DEOXYURIDINE 5-TRIPHOSPHATE NUCLEOTIDOHYDROLASE FROM BRUCELLA MELITENSIS, ORTHORHOMBIC CRYSTAL FORM	3.6.1.23
3MBZ	OXA-24 BETA-LACTAMASE COMPLEX SOAKED WITH 10MM SA4-17 INHIBITOR FOR 15MIN	3.5.2.6
3MCF	CRYSTAL STRUCTURE OF HUMAN DIPHOSPHOINOSITOL POLYPHOSPHATE PHOSPHOHYDROLASE 3-ALPHA	3.6.1.52 3.6.1 3.6.1.60
3MD0	CRYSTAL STRUCTURE OF ARGININE/ORNITHINE TRANSPORT SYSTEM ATPASE FROM MYCOBACTERIUM TUBERCULOSIS BOUND TO GDP (A RAS-LIKE GTPASE SUPERFAMILY PROTEIN)	3.6
3MDQ	CRYSTAL STRUCTURE OF AN EXOPOLYPHOSPHATASE (CHU_0316) FROM CYTOPHAGA HUTCHINSONII ATCC 33406 AT 1.50 A RESOLUTION	3.6.1.11
3MDX	CRYSTAL STRUCTURE OF DEOXYURIDINE 5-TRIPHOSPHATE NUCLEOTIDOHYDROLASE FROM BRUCELLA MELITENSIS, RHOMBOHEDRAL CRYSTAL FORM	3.6.1.23
3MEC	HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH TMC125	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
3MED	HIV-1 K103N REVERSE TRANSCRIPTASE IN COMPLEX WITH TMC125	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
3MEE	HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH TMC278	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
3MEG	HIV-1 K103N REVERSE TRANSCRIPTASE IN COMPLEX WITH TMC278	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
3MEH	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS I92A AT CRYOGENIC TEMPERATURE	3.1.31.1
3MEN	CRYSTAL STRUCTURE OF ACETYLPOLYAMINE AMINOHYDROLASE FROM BURKHOLDERIA PSEUDOMALLEI, IODIDE SOAK	3.5.1 3.5.1.62
3MF0	CRYSTAL STRUCTURE OF PDE5A GAF DOMAIN (89-518)	3.1.4.35
3MF5	HEPATITIS C VIRUS POLYMERASE NS5B (BK) WITH AMIDE BIOISOSTERE THUMB SITE INHIBITOR	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3MF6	COMPUTATIONALLY DESIGNED ENDO-1,4-BETA-XYLANASE	3.2.1.8
3MF7	CRYSTAL STRUCTURE OF (R)-OXIRANE-2-CARBOXYLATE INHIBITED CIS-CAAD	3.8.1
3MF8	CRYSTAL STRUCTURE OF NATIVE CIS-CAAD	3.8.1
3MF9	COMPUTATIONALLY DESIGNED ENDO-1,4-BETA-XYLANASE	3.2.1.8
3MFA	COMPUTATIONALLY DESIGNED ENDO-1,4-BETA-XYLANASE	3.2.1.8
3MFC	COMPUTATIONALLY DESIGNED END0-1,4-BETA,XYLANASE	3.2.1.8
3MFD	THE STRUCTURE OF THE BETA-LACTAMASE SUPERFAMILY DOMAIN OF D-ALANYL-D-ALANINE CARBOXYPEPTIDASE FROM BACILLUS SUBTILIS	3.4.16.4
3MFJ	BOVINE TRYPSIN AT 0.8 A RESOLUTION, RESTRAINED REFINEMENT	3.4.21.4
3MFV	CRYSTAL STRUCTURE OF HUMAN ARGINASE I IN COMPLEX WITH 2-AMINOHOMOHISTIDINE	3.5.3.1
3MFW	CRYSTAL STRUCTURE OF HUMAN ARGINASE I IN COMPLEX WITH L-2-AMINOHISTIDINE AND SULPHATE	3.5.3.1
3MFY	STRUCTURAL CHARACTERIZATION OF THE SUBUNIT A MUTANT F236A OF THE A-ATP SYNTHASE FROM PYROCOCCUS HORIKOSHII	3.6.3.14 7.1.2.2 3.1
3MGE	X-RAY STRUCTURE OF HEXAMERIC 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
3MGM	CRYSTAL STRUCTURE OF HUMAN NUDT16	3.6.1 3.6.1.62 3.6.1.64
3MGW	THERMODYNAMICS AND STRUCTURE OF A SALMON COLD-ACTIVE GOOSE-TYPE LYSOZYME	3.2.1.17
3MGZ	CRYSTAL STRUCTURE OF DHBPS DOMAIN OF BI-FUNCTIONAL DHBPS/GTP CYCLOHYDROLASE II FROM MYCOBACTERIUM TUBERCULOSIS AT PH 4.0	4.1.99.12 3.5.4.25
3MH4	HTRA PROTEASES ARE ACTIVATED BY A CONSERVED MECHANISM THAT CAN BE TRIGGERED BY DISTINCT MOLECULAR CUES	3.4.21 3.4.21.107
3MH5	HTRA PROTEASES ARE ACTIVATED BY A CONSERVED MECHANISM THAT CAN BE TRIGGERED BY DISTINCT MOLECULAR CUES	3.4.21 3.4.21.107
3MH6	HTRA PROTEASES ARE ACTIVATED BY A CONSERVED MECHANISM THAT CAN BE TRIGGERED BY DISTINCT MOLECULAR CUES	3.4.21 3.4.21.107
3MH7	HTRA PROTEASES ARE ACTIVATED BY A CONSERVED MECHANISM THAT CAN BE TRIGGERED BY DISTINCT MOLECULAR CUES	3.4.21 3.4.21.107
3MHB	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L38A AT CRYOGENIC TEMPERATURE	3.1.31.1
3MHH	STRUCTURE OF THE SAGA UBP8/SGF11/SUS1/SGF73 DUB MODULE	3.1.2.15 3.4.19.12
3MHS	STRUCTURE OF THE SAGA UBP8/SGF11/SUS1/SGF73 DUB MODULE BOUND TO UBIQUITIN ALDEHYDE	3.1.2.15 3.4.19.12
3MHW	THE COMPLEX CRYSTAL STRUCTURE OF UROKIANSE AND 2-AMINOBENZOTHIAZOLE	3.4.21.73
3MI4	BOVINE TRYPSIN AT 0.8 A RESOLUTION, NON-RESTRAINED REFINEMENT	3.4.21.4
3MI6	CRYSTAL STRUCTURE OF THE ALPHA-GALACTOSIDASE FROM LACTOBACILLUS BREVIS, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET LBR11.	3.2.1.22
3MII	CRYSTAL STRUCTURE OF Y0R391CP/HSP33 FROM SACCHAROMYCES CEREVISIAE	3.2 4.2.1.130
3MIL	CRYSTAL STRUCTURE OF ISOAMYL ACETATE-HYDROLYZING ESTERASE FROM SACCHAROMYCES CEREVISIAE	3.1 3.1.1.112
3MIO	CRYSTAL STRUCTURE OF 3,4-DIHYDROXY-2-BUTANONE 4-PHOSPHATE SYNTHASE DOMAIN FROM MYCOBACTERIUM TUBERCULOSIS AT PH 6.00	4.1.99.12 3.5.4.25
3MJ5	SEVERE ACUTE RESPIRATORY SYNDROME-CORONAVIRUS PAPAIN-LIKE PROTEASE INHIBITORS: DESIGN, SYNTHESIS, PROTEIN-LIGAND X-RAY STRUCTURE AND BIOLOGICAL EVALUATION	3.4.22 3.4.19.12 3.4.22.69
3MJH	CRYSTAL STRUCTURE OF HUMAN RAB5A IN COMPLEX WITH THE C2H2 ZINC FINGER OF EEA1	3.6.5.2
3MJI	ACTIVATION OF CATALYTIC CYSTEINE WITHOUT A BASE IN A MUTANT PENICILLIN ACYLASE PRECURSOR	3.5.1.11
3MJL	CRYSTAL STRUCTURE OF HUMAN ARGINASE I IN COMPLEX WITH 2-AMINOIMIDAZOLE. RESOLUTION 1.90 A.	3.5.3.1
3MJM	HIS257ALA MUTANT OF DIHYDROOROTASE FROM E. COLI	3.5.2.3
3MJN	CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF LACTOFERRIN WITH ISOPROPYLAMINO-3-(1-NAPHTHYLOXY)PROPAN-2-OL AT 2.38 A RESOLUTION	3.4.21
3MK0	REFINEMENT OF PLACENTAL ALKALINE PHOSPHATASE COMPLEXED WITH NITROPHENYL	3.1.3.1
3MK1	REFINEMENT OF PLACENTAL ALKALINE PHOSPHATASE COMPLEXED WITH NITROPHENYL	3.1.3.1
3MK2	PLACENTAL ALKALINE PHOSPHATASE COMPLEXED WITH PHE	3.1.3.1
3MK5	CRYSTAL STRUCTURE OF 3,4-DIHYDROXY-2-BUTANONE 4-PHOSPHATE SYNTHASE DOMAIN FROM MYCOBACTERIUM TUBERCULOSIS WITH SULFATE AND ZINC AT PH 4.00	4.1.99.12 3.5.4.25
3MK9	STABILIZED RICIN IMMUNOGEN 1-33/44-198	3.2.2.22
3MKD	CRYSTAL STRUCTURE OF MYOSIN-2 DICTYOSTELIUM DISCOIDEUM MOTOR DOMAIN S456Y MUTANT IN COMPLEX WITH ADP-ORTHOVANADATE	3.6.4.1
3MKE	SHV-1 BETA-LACTAMASE COMPLEX WITH LP06	3.5.2.6
3MKF	SHV-1 BETA-LACTAMASE COMPLEX WITH GB0301	3.5.2.6
3MKK	THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ISOMALTOSE	3.2.1
3MKM	CRYSTAL STRUCTURE OF THE E. COLI PYRIMIDINE NUCLEOSIDE HYDROLASE YEIK (APO-FORM)	3.2.2.8
3MKN	CRYSTAL STRUCTURE OF THE E. COLI PYRIMIDINE NUCLEOSIDASE YEIK BOUND TO A COMPETITIVE INHIBITOR	3.2.2.8
3ML0	THERMOSTABLE PENICILLIN G ACYLASE FROM ALCALIGENES FAECALIS IN TETRAGONAL FORM	3.5.1.11
3MLM	CRYSTAL STRUCTURE OF BN IV IN COMPLEX WITH MYRISTIC ACID: A LYS49 MYOTOXIC PHOSPHOLIPASE A2 FROM BOTHROPS NEUWIEDI VENOM	3.1.1.4
3MMG	CRYSTAL STRUCTURE OF TOBACCO VEIN MOTTLING VIRUS PROTEASE	3.4 3.4.22.45 3.6.4 3.4.22.44 2.7.7.48
3MML	ALLOPHANATE HYDROLASE COMPLEX FROM MYCOBACTERIUM SMEGMATIS, MSMEG0435-MSMEG0436	3.5.1.54
3MMR	STRUCTURE OF PLASMODIUM FALCIPARUM ARGINASE IN COMPLEX WITH ABH	3.5.3.1
3MN1	CRYSTAL STRUCTURE OF PROBABLE YRBI FAMILY PHOSPHATASE FROM PSEUDOMONAS SYRINGAE PV.PHASEOLICA 1448A	3.1.3.45
3MN8	STRUCTURE OF DROSOPHILA MELANOGASTER CARBOXYPEPTIDASE D ISOFORM 1B SHORT	3.4.17.22
3MNB	INVESTIGATION OF GLOBAL AND LOCAL EFFECTS OF RADIATION DAMAGE ON PORCINE PANCREATIC ELASTASE. FIRST STAGE OF RADIATION DAMAGE	3.4.21.36
3MNC	INVESTIGATION OF GLOBAL AND LOCAL EFFECTS OF RADIATION DAMAGE ON PORCINE PANCREATIC ELASTASE. SECOND STAGE OF RADIATION DAMAGE	3.4.21.36
3MNQ	CRYSTAL STRUCTURE OF MYOSIN-2 MOTOR DOMAIN IN COMPLEX WITH ADP-METAVANADATE AND RESVERATROL	3.6.4.1
3MNS	INVESTIGATION OF GLOBAL AND LOCAL EFFECTS OF RADIATION DAMAGE ON PORCINE PANCREATIC ELASTASE. THIRD STAGE OF RADIATION DAMAGE	3.4.21.36
3MNX	INVESTIGATION OF GLOBAL AND LOCAL EFFECTS OF RADIATION DAMAGE ON PORCINE PANCREATIC ELASTASE. FOURTH STAGE OF RADIATION DAMAGE	3.4.21.36
3MO3	INVESTIGATION OF GLOBAL AND LOCAL EFFECTS OF RADIATION DAMAGE ON PORCINE PANCREATIC ELASTASE. FIFTH STAGE OF RADIATION DAMAGE	3.4.21.36
3MO6	INVESTIGATION OF GLOBAL AND LOCAL EFFECTS OF RADIATION DAMAGE ON PORCINE PANCREATIC ELASTASE. SIXTH STAGE OF RADIATION DAMAGE	3.4.21.36
3MO9	INVESTIGATION OF GLOBAL AND LOCAL EFFECTS OF RADIATION DAMAGE ON PORCINE PANCREATIC ELASTASE. SEVENTH STAGE OF RADIATION DAMAGE	3.4.21.36
3MOC	INVESTIGATION OF GLOBAL AND LOCAL EFFECTS OF RADIATION DAMAGE ON PORCINE PANCREATIC ELASTASE. EIGHTH STAGE OF RADIATION DAMAGE	3.4.21.36
3MOR	CRYSTAL STRUCTURE OF CATHEPSIN B FROM TRYPANOSOMA BRUCEI	3.4.22
3MOW	CRYSTAL STRUCTURE OF SHP2 IN COMPLEX WITH A TAUTOMYCETIN ANALOG TTN D-1	3.1.3.48
3MP2	CRYSTAL STRUCTURE OF TRANSMISSIBLE GASTROENTERITIS VIRUS PAPAIN-LIKE PROTEASE 1	3.4.22 3.4.19.12
3MPG	DIHYDROOROTASE FROM BACILLUS ANTHRACIS	3.5.2.3
3MPP	BOTULINUM NEUROTOXIN TYPE G RECEPTOR BINDING DOMAIN	3.4.24.69
3MPZ	CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE FROM MYCOBACTERIUM SMEGMATIS	3.5.4.5
3MQ3	CRYSTAL STRUCTURE OF NATIVE BOVINE PDP1C	3.1.3.43
3MQR	CRYSTAL STRUCTURE OF THE USP7:HDMX(AHSS) COMPLEX	3.1.2.15 3.4.19.12
3MQS	CRYSTAL STRUCTURE OF THE USP7:HDM2(PSTS) COMPLEX	3.1.2.15 3.4.19.12
3MQY	SGRAI WITH CLEAVED DNA AND MAGNESIUM BOUND	3.1.21.4
3MR1	CRYSTAL STRUCTURE OF METHIONINE AMINOPEPTIDASE FROM RICKETTSIA PROWAZEKII	3.4.11.18
3MRU	CRYSTAL STRUCTURE OF AMINOACYLHISTIDINE DIPEPTIDASE FROM VIBRIO ALGINOLYTICUS	3.4.13.3
3MRW	CRYSTAL STRUCTURE OF TYPE I RIBOSOME INACTIVATING PROTEIN FROM MOMORDICA BALSAMINA AT 1.7 A RESOLUTION	3.2.2.22
3MRY	CRYSTAL STRUCTURE OF TYPE I RIBOSOME INACTIVATING PROTEIN FROM MOMORDICA BALSAMINA WITH 6-AMINOPURINE AT 2.0A RESOLUTION	3.2.2.22
3MS3	CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH ANILINE	3.4.24.27
3MSA	CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH 3-BROMOPHENOL	3.4.24.27
3MSF	CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH UREA	3.4.24.27
3MSK	FRAGMENT BASED DISCOVERY AND OPTIMISATION OF BACE-1 INHIBITORS	3.4.23.46
3MSL	FRAGMENT BASED DISCOVERY AND OPTIMISATION OF BACE-1 INHIBITORS	3.4.23.46
3MSN	CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH N-METHYLUREA	3.4.24.27
3MSR	THE CRYSTAL STRUCTURE OF AN AMIDOHYDROLASE FROM MYCOPLASMA SYNOVIAE	3.1.1.25
3MSX	CRYSTAL STRUCTURE OF RHOA.GDP.MGF3 IN COMPLEX WITH GAP DOMAIN OF ARHGAP20	3.6.5.2
3MTC	CRYSTAL STRUCTURE OF INPP5B IN COMPLEX WITH PHOSPHATIDYLINOSITOL 4-PHOSPHATE	3.1.3.36
3MTG	CRYSTAL STRUCTURE OF HUMAN S-ADENOSYL HOMOCYSTEINE HYDROLASE-LIKE 1 PROTEIN	3.3.1.1
3MTN	USP21 IN COMPLEX WITH A UBIQUITIN-BASED, USP21-SPECIFIC INHIBITOR	3.1.2.15 3.4.19.12
3MTY	COMPARISON OF THE CHARACTER AND THE SPEED OF X-RAY-INDUCED STRUCTURAL CHANGES OF PORCINE PANCREATIC ELASTASE AT TWO TEMPERATURES, 100 AND 15K. THE DATA SET WAS COLLECTED FROM REGION A OF THE CRYSTAL. FIRST STEP OF RADIATION DAMAGE	3.4.21.36
3MU0	COMPARISON OF THE CHARACTER AND THE SPEED OF X-RAY-INDUCED STRUCTURAL CHANGES OF PORCINE PANCREATIC ELASTASE AT TWO TEMPERATURES, 100 AND 15K. THE DATA SET WAS COLLECTED FROM REGION A OF THE CRYSTAL. THIRD STEP OF RADIATION DAMAGE	3.4.21.36
3MU1	COMPARISON OF THE CHARACTER AND THE SPEED OF X-RAY-INDUCED STRUCTURAL CHANGES OF PORCINE PANCREATIC ELASTASE AT TWO TEMPERATURES, 100 AND 15K. THE DATA SET WAS COLLECTED FROM REGION A OF THE CRYSTAL. FIFTH STEP OF RADIATION DAMAGE	3.4.21.36
3MU4	COMPARISON OF THE CHARACTER AND THE SPEED OF X-RAY-INDUCED STRUCTURAL CHANGES OF PORCINE PANCREATIC ELASTASE AT TWO TEMPERATURES, 100 AND 15K. THE DATA SET WAS COLLECTED FROM REGION B OF THE CRYSTAL. FIRST STEP OF RADIATION DAMAGE	3.4.21.36
3MU5	COMPARISON OF THE CHARACTER AND THE SPEED OF X-RAY-INDUCED STRUCTURAL CHANGES OF PORCINE PANCREATIC ELASTASE AT TWO TEMPERATURES, 100 AND 15K. THE DATA SET WAS COLLECTED FROM REGION B OF THE CRYSTAL. THIRD STEP OF RADIATION DAMAGE	3.4.21.36
3MU8	COMPARISON OF THE CHARACTER AND THE SPEED OF X-RAY-INDUCED STRUCTURAL CHANGES OF PORCINE PANCREATIC ELASTASE AT TWO TEMPERATURES, 100 AND 15K. THE DATA SET WAS COLLECTED FROM REGION B OF THE CRYSTAL. FIFTH STEP OF RADIATION DAMAGE	3.4.21.36
3MUW	PSEUDO-ATOMIC STRUCTURE OF THE E2-E1 PROTEIN SHELL IN SINDBIS VIRUS	3.4.21 3.4.21.90
3MUY	E. COLI (LACZ) BETA-GALACTOSIDASE (R599A)	3.2.1.23
3MV0	E. COLI (LACZ) BETA-GALACTOSIDASE (R599A) IN COMPLEX WITH D-GALCTOPYRANOSYL-1-ONE	3.2.1.23
3MVE	CRYSTAL STRUCTURE OF A NOVEL PYRUVATE DECARBOXYLASE	3.1.1.1
3MVG	NATIVE STRUCTURE OF IRIP, A TYPE I RIBOSOME INACTIVATING PROTEIN FROM IRIS HOLLANDICA VAR. AT 1.25 A	3.2.2.22
3MVI	CRYSTAL STRUCTURE OF HOLO MADA AT 1.6 A RESOLUTION	3.5.4.4
3MVT	CRYSTAL STRUCTURE OF APO MADA AT 2.2A RESOLUTION	3.5.4.4
3MVU	CRYSTAL STRUCTURE OF A TENA FAMILY TRANSCRIPTION REGULATOR (TM1040_3656) FROM SILICIBACTER SP. TM1040 AT 1.80 A RESOLUTION	3.5.99.2
3MVV	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS F34A AT CRYOGENIC TEMPERATURE	3.1.31.1
3MVX	X-RAY STRUCTURE OF THE REDUCED NIKA/1 HYBRID, NIKA/1-RED	3.6.3.24
3MVY	X-RAY STRUCTURE OF THE DIATOMIC OXO-INTERMEDIATE NIKA/1-INT', PRIOR HYDROXYLATION	3.6.3.24
3MW0	X-RAY STRUCTURE OF THE DOUBLY HYDROXYLATED IRON COMPLEX-NIKA SPECIES, NIKA1/O2	3.6.3.24
3MWI	THE COMPLEX CRYSTAL STRUCTURE OF UROKIANSE AND 5-NITRO-1H-INDOLE-2-AMIDINE	3.4.21.73
3MWP	NUCLEOPROTEIN STRUCTURE OF LASSA FEVER VIRUS	3.1.13
3MWQ	CRYSTAL STRUCTURE OF RIBONUCLEASE A TANDEM ENZYMES AND THEIR INTERACTION WITH THE CYTOSOLIC RIBONUCLEASE INHIBITOR	3.1.27.5 4.6.1.18
3MWR	CRYSTAL STRUCTURE OF RIBONUCLEASE A TANDEM ENZYMES AND THEIR INTERACTION WITH THE CYTOSOLIC RIBONUCLEASE INHIBITOR	3.1.27.5 4.6.1.18
3MWS	CRYSTAL STRUCTURE OF GROUP N HIV-1 PROTEASE	3.4.23.16 2.7.7.49 3.1.13.2 3.1.26.13
3MWV	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3MWW	CRYSTAL STRUCTURE OF HCV NS5B POLYMERASE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3MWY	CRYSTAL STRUCTURE OF THE CHROMODOMAIN-ATPASE PORTION OF THE YEAST CHD1 CHROMATIN REMODELER	3.6.1 3.6.4
3MX1	THE STRUCTURE OF GIY-YIG ENDONUCLEASE R.ECO29KI	3.1.21.4
3MX4	DNA BINDING AND CLEAVAGE BY THE GIY-YIG ENDONUCLEASE R.ECO29KI INACTIVE VARIANT E142Q	3.1.21.4
3MX5	LASSA FEVER VIRUS NUCLEOPROTEIN COMPLEXED WITH UTP	3.1.13
3MX6	CRYSTAL STRUCTURE OF METHIONINE AMINOPEPTIDASE FROM RICKETTSIA PROWAZEKII BOUND TO METHIONINE	3.4.11.18
3MX8	CRYSTAL STRUCTURE OF RIBONUCLEASE A TANDEM ENZYMES AND THEIR INTERACTION WITH THE CYTOSOLIC RIBONUCLEASE INHIBITOR	3.1.27.5 4.6.1.18
3MXD	CRYSTAL STRUCTURE OF HIV-1 PROTEASE INHIBITOR KC53 IN COMPLEX WITH WILD-TYPE 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
3MXE	CRYSTAL STRUCTURE OF HIV-1 PROTEASE INHIBITOR, KC32 COMPLEXED WITH WILD-TYPE 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
3MXI	TREX1 3' EXONUCLEASE D18N FAMILIAL CHILBLAIN LUPUS MUTANT	3.1.11.2
3MXJ	CRYSTAL STRUCTURE OF THE MTREX1 APOPROTEIN	3.1.11.2
3MXM	TREX1 3' EXONUCLEASE V201D AICARDI-GOUTIERES SYNDROME MUTANT	3.1.11.2
3MXO	CRYSTAL STRUCTURE OH HUMAN PHOSPHOGLYCERATE MUTASE FAMILY MEMBER 5 (PGAM5)	3.1.3.16
3MXP	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS T62A AT CRYOGENIC TEMPERATURE	3.1.31.1
3MXR	SHV-1 BETA-LACTAMASE COMPLEX WITH COMPOUND 1	3.5.2.6
3MXS	SHV-1 BETA-LACTAMASE COMPLEX WITH COMPOUND 2	3.5.2.6
3MY6	CRYSTAL STRUCTURE OF THE COMPLEX OF TYPE 1 RIBOSOME INACTIVATING PROTEIN WITH 7-METHYLGUANINE AT 2.65 A RESOLUTION	3.2.2.22
3MYW	THE BOWMAN-BIRK TYPE INHIBITOR FROM MUNG BEAN IN TERNARY COMPLEX WITH PORCINE TRYPSIN	3.4.21.4
3MZ3	CRYSTAL STRUCTURE OF CO2+ HDAC8 COMPLEXED WITH M344	3.5.1.98
3MZ4	CRYSTAL STRUCTURE OF D101L MN2+ HDAC8 COMPLEXED WITH M344	3.5.1.98
3MZ5	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L103A AT CRYOGENIC TEMPERATURE	3.1.31.1
3MZ6	CRYSTAL STRUCTURE OF D101L FE2+ HDAC8 COMPLEXED WITH M344	3.5.1.98
3MZ7	CRYSTAL STRUCTURE OF D101L CO2+ HDAC8 COMPLEXED WITH M344	3.5.1.98
3MZ9	X-RAY STRUCTURE OF NIKA IN COMPLEX WITH HBED	3.6.3.24
3MZB	X-RAY STRUCTURE OF NIKA IN COMPLEX WITH THE DOUBLY HYDROXYLATED IRON COMPLEX, 1-O2	3.6.3.24
3MZD	STRUCTURE OF PENICILLIN-BINDING PROTEIN 5 FROM E. COLI: CLOXACILLIN ACYL-ENZYME COMPLEX	3.4.16.4 3.5.2.6
3MZE	STRUCTURE OF PENICILLIN-BINDING PROTEIN 5 FROM E.COLI: CEFOXITIN ACYL-ENZYME COMPLEX	3.4.16.4 3.5.2.6
3MZF	STRUCTURE OF PENICILLIN-BINDING PROTEIN 5 FROM E. COLI: IMIPENEM ACYL-ENZYME COMPLEX	3.4.16.4 3.5.2.6
3MZQ	RNASE CRYSTALS GROWN BY THE HANGING DROP METHOD	3.1.27.5 4.6.1.18
3MZR	RNASE CRYSTALS GROWN IN LOOPS/MICROMOUNTS	3.1.27.5 4.6.1.18
3N04	THE CRYSTAL STRUCTURE OF THE ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174	3.2.1
3N07	STRUCTURE OF PUTATIVE 3-DEOXY-D-MANNO-OCTULOSONATE 8-PHOSPHATE PHOSPHATASE FROM VIBRIO CHOLERAE	3.1.3.45
3N0A	CRYSTAL STRUCTURE OF AUXILIN (40-400)	3.1.3.48
3N0T	HUMAN DIPEPTIDIL PEPTIDASE DPP7 COMPLEXED WITH INHIBITOR GSK237826A	3.4.14.2
3N0U	CRYSTAL STRUCTURE OF TM1821, THE 8-OXOGUANINE DNA GLYCOSYLASE OF THERMOTOGA MARITIMA	3.2.2 4.2.99.18
3N0V	CRYSTAL STRUCTURE OF A FORMYLTETRAHYDROFOLATE DEFORMYLASE (PP_0327) FROM PSEUDOMONAS PUTIDA KT2440 AT 2.25 A RESOLUTION	3.5.1.10
3N11	CRYSTAL STRICTURE OF WILD-TYPE CHITINASE FROM BACILLUS CEREUS NCTU2	3.2.1.14
3N12	CRYSTAL STRICTURE OF CHITINASE IN COMPLEX WITH ZINC ATOMS FROM BACILLUS CEREUS NCTU2	3.2.1.14
3N13	CRYSTAL STRICTURE OF D143A CHITINASE IN COMPLEX WITH NAG FROM BACILLUS CEREUS NCTU2	3.2.1.14
3N15	CRYSTAL STRICTURE OF E145Q CHITINASE IN COMPLEX WITH NAG FROM BACILLUS CEREUS NCTU2	3.2.1.14
3N17	CRYSTAL STRICTURE OF E145Q/Y227F CHITINASE IN COMPLEX WITH NAG FROM BACILLUS CEREUS NCTU2	3.2.1.14
3N18	CRYSTAL STRICTURE OF E145G/Y227F CHITINASE IN COMPLEX WITH NAG FROM BACILLUS CEREUS NCTU2	3.2.1.14
3N1A	CRYSTAL STRICTURE OF E145G/Y227F CHITINASE IN COMPLEX WITH CYCLO-(L-HIS-L-PRO) FROM BACILLUS CEREUS NCTU2	3.2.1.14
3N1D	CRYSTAL STRUCTURE OF THE COMPLEX OF TYPE I RIBOSOME INACTIVATING PROTEIN WITH RIBOSE AT 1.7A RESOLUTION	3.2.2.22
3N1N	CRYSTAL STRUCTURE OF THE COMPLEX OF TYPE I RIBOSOME INACTIVATING PROTEIN WITH GUANINE AT 2.2A RESOLUTION	3.2.2.22
3N1S	CRYSTAL STRUCTURE OF WILD TYPE ECHINT GMP COMPLEX	3.9.1
3N1T	CRYSTAL STRUCTURE OF THE H101A MUTANT ECHINT GMP COMPLEX	3.9.1
3N1U	STRUCTURE OF PUTATIVE HAD SUPERFAMILY (SUBFAMILY III A) HYDROLASE FROM LEGIONELLA PNEUMOPHILA	3.1.3.45
3N21	CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH S-1,2-PROPANDIOL	3.4.24.27
3N28	CRYSTAL STRUCTURE OF PROBABLE PHOSPHOSERINE PHOSPHATASE FROM VIBRIO CHOLERAE, UNLIGANDED FORM	3.1.3.3
3N2D	CRYSTAL STRUCTURE OF THE COMPLEX OF TYPE I RIBOSOME INACTIVATING PROTEIN WITH HEXAPEPTIDE SER-ASP-ASP-ASP-MET-GLY AT 2.2 A RESOLUTION	3.2.2.22
3N2U	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR N-HYDROXY-2-(4-METHOXY-N(2-(3,4,5-TRIHYDROXY-6-(HYDROXYMETHYL)TETRAHYDRO-2H-PYRAN-2-YLOXY)ETHYL)PHENYLSULFONAMIDO)ACETAMIDE	3.4.24.65
3N2V	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR N-HYDROXY-2-(N-HYDROXYETHYL)BIPHENYL-4-YLSULFONAMIDO)ACETAMIDE	3.4.24.65
3N2W	CRYSTAL STRUCTURE OF THE N-TERMINAL BETA-AMINOPEPTIDASE BAPA FROM SPHINGOSINICELLA XENOPEPTIDILYTICA	3.4.11.25
3N2Z	THE STRUCTURE OF HUMAN PROLYLCARBOXYPEPTIDASE AT 2.80 ANGSTROMS RESOLUTION	3.4.16.2
3N31	CRYSTAL STRUCTURE OF THE COMPLEX OF TYPE I RIBOSOME INACTIVATING PROTEIN WITH FUCOSE AT 2.1A RESOLUTION	3.2.2.22
3N33	CRYSTAL STRUCTURE OF THE N-TERMINAL BETA-AMINOPEPTIDASE BAPA IN COMPLEX WITH PEFABLOC SC (AEBSF)	3.4.11.25
3N3G	4-(3-TRIFLUOROMETHYLPHENYL)-PYRIMIDINE-2-CARBONITRILE AS CATHEPSIN S INHIBITORS: N3, NOT N1 IS CRITICALLY IMPORTANT	3.4.22.27
3N3I	CRYSTAL STRUCTURE OF G48V/C95F TETHERED HIV-1 PROTEASE/SAQUINAVIR 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
3N3K	THE CATALYTIC DOMAIN OF USP8 IN COMPLEX WITH A USP8 SPECIFIC INHIBITOR	3.1.2.15 3.4.19.12
3N3U	CRYSTAL STRUCTURE OF IBPAFIC2	2.7.7.1 2.7.7 3.4.22
3N3W	2.2 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF NUCLEASE DOMAIN OF RIBONUCLASE III (RNC) FROM CAMPYLOBACTER JEJUNI	3.1.26.3
3N3X	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN TYPE I RIBOSOME INACTIVATING PROTEIN AND HEXAPEPTIDE SER-ASP-ASP-ASP-MET-GLY AT 1.7 A RESOLUTION	3.2.2.22
3N3Z	CRYSTAL STRUCTURE OF PDE9A (E406A) MUTANT IN COMPLEX WITH IBMX	3.1.4.35
3N40	CRYSTAL STRUCTURE OF THE IMMATURE ENVELOPE GLYCOPROTEIN COMPLEX OF CHIKUNGUNYA VIRUS.	3.4.21.90
3N41	CRYSTAL STRUCTURE OF THE MATURE ENVELOPE GLYCOPROTEIN COMPLEX (SPONTANEOUS CLEAVAGE) OF CHIKUNGUNYA VIRUS.	3.4.21.90
3N42	CRYSTAL STRUCTURES OF THE MATURE ENVELOPE GLYCOPROTEIN COMPLEX (FURIN CLEAVAGE) OF CHIKUNGUNYA VIRUS.	3.4.21.90
3N43	CRYSTAL STRUCTURES OF THE MATURE ENVELOPE GLYCOPROTEIN COMPLEX (TRYPSIN CLEAVAGE) OF CHIKUNGUNYA VIRUS.	3.4.21.90
3N44	CRYSTAL STRUCTURE OF THE MATURE ENVELOPE GLYCOPROTEIN COMPLEX (TRYPSIN CLEAVAGE; OSMIUM SOAK) OF CHIKUNGUNYA VIRUS.	3.4.21.90
3N4C	6-PHENYL-1H-IMIDAZO[4,5-C]PYRIDINE-4-CARBONITRILE AS CATHEPSIN S INHIBITORS	3.4.22.27
3N4D	CRYSTAL STRUCTURE OF CG10062 INACTIVATED BY(R)-OXIRANE-2-CARBOXYLATE	3.8.1
3N4G	CRYSTAL STRUCTURE OF NATIVE CG10062	3.8.1
3N4H	CRYSTAL STRUCTURE OF CG10062 INACTIVATED BY (S)-OXIRANE-2-CARBOXYLATE	3.8.1
3N4I	CRYSTAL STRUCTURE OF THE SHV-1 D104E BETA-LACTAMASE/BETA-LACTAMASE INHIBITOR PROTEIN (BLIP) COMPLEX	3.5.2.6
3N4L	BACE-1 IN COMPLEX WITH ELN380842	3.4.23.46
3N4P	HUMAN CYTOMEGALOVIRUS TERMINASE NUCLEASE DOMAIN	3.1
3N4Q	HUMAN CYTOMEGALOVIRUS TERMINASE NUCLEASE DOMAIN, MN SOAKED	3.1
3N58	CRYSTAL STRUCTURE OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE FROM BRUCELLA MELITENSIS IN TERNARY COMPLEX WITH NAD AND ADENOSINE, ORTHORHOMBIC FORM	3.3.1.1
3N5D	CRYSTAL STRUCTURE OF THE COMPLEX OF TYPE I RIBOSOME INACTIVATING PROTEIN WITH GLUCOSE AT 1.9A RESOLUTION	3.2.2.22
3N5F	CRYSTAL STRUCTURE OF L-N-CARBAMOYLASE FROM GEOBACILLUS STEAROTHERMOPHILUS CECT43	3.5.1.87
3N5I	CRYSTAL STRUCTURE OF THE PRECURSOR (S250A MUTANT) OF THE N-TERMINAL BETA-AMINOPEPTIDASE BAPA	3.4.11.25
3N5K	STRUCTURE OF THE (SR)CA2+-ATPASE E2-ALF4- FORM	3.6.3.8 7.2.2.10
3N5N	CRYSTAL STRUCTURE ANALYSIS OF THE CATALYTIC DOMAIN AND INTERDOMAIN CONNECTOR OF HUMAN MUTY HOMOLOGUE	3.2.2 3.2.2.31
3N5U	CRYSTAL STRUCTURE OF AN RB C-TERMINAL PEPTIDE BOUND TO THE CATALYTIC SUBUNIT OF PP1	3.1.3.16
3N6I	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH 6-AMINOPENICILLIAN	3.5.2.6
3N6L	THE CRYSTAL STRUCTURE OF RNA-DEPENDENT RNA POLYMERASE OF EV71 VIRUS	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3N6M	CRYSTAL STRUCTURE OF EV71 RDRP IN COMPLEX WITH GTP	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3N6N	CRYSTAL STRUCTURE OF EV71 RDRP IN COMPLEX WITH BR-UTP	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
3N77	CRYSTAL STRUCTURE OF IDP01880, PUTATIVE NTP PYROPHOSPHOHYDROLASE OF SALMONELLA TYPHIMURIUM LT2	3.6.1 3.6.1.9 3.6.1.12 3.6.1.23
3N78	SGRAI BOUND TO SECONDARY SITE DNA AND MG(II)	3.1.21.4
3N7B	SGRAI BOUND TO SECONDARY SITE DNA AND CA(II)	3.1.21.4
3N7J	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN SEROTYPE D BINDING DOMAIN	3.4.24.69
3N7K	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN SEROTYPE C1 BINDING DOMAIN	3.4.24.69
3N7O	X-RAY STRUCTURE OF HUMAN CHYMASE IN COMPLEX WITH SMALL MOLECULE INHIBITOR.	3.4.21.39
3N7W	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH AMOXICILLIN	3.5.2.6
3N8G	STRUCTURE OF THE (SR)CA2+-ATPASE CA2-E1-CAAMPPCP FORM	3.6.3.8 7.2.2.10
3N8I	CRYSTAL STRUCTURE OF THE A ISOFORM OF HUMAN CYTOPLASMIC PROTEIN TYROSINE PHOSPHATASE (HCPTP-A) IN COMPLEX WITH 1-NAPHTYLACETIC ACID	3.1.3.48 3.1.3.2
3N8L	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH AMPICILLIN	3.5.2.6
3N8R	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH CARBENICILLIN	3.5.2.6
3N8S	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH CEFAMANDOLE	3.5.2.6
3N9A	MITE-Y LYSOZYME: VEGEMITE	3.2.1.17
3N9C	MITE-Y LYSOZYME: MARMITE	3.2.1.17
3N9E	MITE-Y LYSOZYME: PROMITE	3.2.1.17
3N9K	F229A/E292S DOUBLE MUTANT OF EXO-BETA-1,3-GLUCANASE FROM CANDIDA ALBICANS IN COMPLEX WITH LAMINARITRIOSE AT 1.7 A	3.2.1.58 2.4.1
3N9V	CRYSTAL STRUCTURE OF INPP5B	3.1.3.36
3NAE	RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DATP OPPOSITE GUANIDINOHYDANTOIN	2.7.7.7 3.1.11
3NAH	CRYSTAL STRUCTURES AND FUNCTIONAL ANALYSIS OF MURINE NOROVIRUS RNA-DEPENDENT RNA POLYMERASE	2.7.7.48 3.4.22.66 3.6.1.15
3NAI	CRYSTAL STRUCTURES AND FUNCTIONAL ANALYSIS OF MURINE NOROVIRUS RNA-DEPENDENT RNA POLYMERASE	2.7.7.48 3.4.22.66 3.6.1.15
3NAL	SR CA(2+)-ATPASE IN THE HNE2 STATE COMPLEXED WITH THE THAPSIGARGIN DERIVATIVE DTB	3.6.3.8 7.2.2.10
3NAM	SR CA(2+)-ATPASE IN THE HNE2 STATE COMPLEXED WITH THE THAPSIGARGIN DERIVATIVE DOTG	3.6.3.8 7.2.2.10
3NAN	SR CA(2+)-ATPASE IN THE HNE2 STATE COMPLEXED WITH A THAPSIGARGIN DERIVATIVE BOC-(PHI)TG	3.6.3.8 7.2.2.10
3NB6	CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS PEPTIDOGLYCAN GLYCOSYLTRANSFERASE IN COMPLEX WITH METHYLPHOSPHORYL NERYL MOENOMYCIN	2.4.2 2.4.1.129 3.4.16.4
3NB7	CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS PEPTIDOGLYCAN GLYCOSYLTRANSFERASE IN COMPLEX WITH DECARBOXYLATED NERYL MOENOMYCIN	2.4.2 2.4.1.129 3.4.16.4
3NBL	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH CEFUROXIME	3.5.2.6
3NBP	HIV-1 REVERSE TRANSCRIPTASE WITH AMINOPYRIMIDINE INHIBITOR 2	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
3NBX	CRYSTAL STRUCTURE OF E. COLI RAVA (REGULATORY ATPASE VARIANT A) IN COMPLEX WITH ADP	3.6.3
3NC8	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH MECILLINAM	3.5.2.6
3NCI	RB69 DNA POLYMERASE TERNARY COMPLEX WITH DCTP OPPOSITE DG AT 1.8 ANGSTROM RESOLUTION	2.7.7.7 3.1.11
3NCK	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH NAFCILLIN	3.5.2.6
3NCL	CRYSTAL STRUCTURE OF MT-SP1 BOUND TO BENZAMIDINE PHOSPHONATE INHIBITOR	3.4.21.109
3NCO	CRYSTAL STRUCTURE OF FNCEL5A FROM F. NODOSUM RT17-B1	3.2.1.4
3NCU	STRUCTURAL AND FUNCTIONAL INSIGHTS INTO PATTERN RECOGNITION BY THE INNATE IMMUNE RECEPTOR RIG-I	3.6.1 3.6.4.13
3ND8	STRUCTURAL CHARACTERIZATION FOR THE NUCLEOTIDE BINDING ABILITY OF SUBUNIT A OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3ND9	STRUCTURAL CHARACTERIZATION FOR THE NUCLEOTIDE BINDING ABILITY OF SUBUNIT A OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3NDE	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH CEPHALOTIN	3.5.2.6
3NDG	CRYSTAL STRUCTURE OF BLAC-E166A COVALENTLY BOUND WITH METHICILLIN	3.5.2.6
3NDK	RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE DG	2.7.7.7 3.1.11
3NDT	HIV-1 PROTEASE SAQUINAVIR:RITONAVIR 1:1 COMPLEX 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
3NDU	HIV-1 PROTEASE SAQUINAVIR:RITONAVIR 1:5 COMPLEX 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
3NDV	CRYSTAL STRUCTURE OF THE N-TERMINAL BETA-AMINOPEPTIDASE BAPA IN COMPLEX WITH AMPICILLIN	3.4.11.25
3NDW	HIV-1 PROTEASE SAQUINAVIR:RITONAVIR 1:15 COMPLEX 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
3NDX	HIV-1 PROTEASE SAQUINAVIR:RITONAVIR 1:50 COMPLEX 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
3NDY	THE STRUCTURE OF THE CATALYTIC AND CARBOHYDRATE BINDING DOMAIN OF ENDOGLUCANASE D FROM CLOSTRIDIUM CELLULOVORANS	3.2.1.4
3NDZ	THE STRUCTURE OF THE CATALYTIC AND CARBOHYDRATE BINDING DOMAIN OF ENDOGLUCANASE D FROM CLOSTRIDIUM CELLULOVORANS BOUND TO CELLOTRIOSE	3.2.1.4
3NE0	STRUCTURE AND FUNCTIONAL REGULATION OF RIPA, A MYCOBACTERIAL ENZYME ESSENTIAL FOR DAUGHTER CELL SEPARATION	3.4
3NE6	RB69 DNA POLYMERASE (S565G/Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE DG	2.7.7.7 3.1.11
3NE8	THE CRYSTAL STRUCTURE OF A DOMAIN FROM N-ACETYLMURAMOYL-L-ALANINE AMIDASE OF BARTONELLA HENSELAE STR. HOUSTON-1	3.5.1.28
3NEA	CRYSTAL STRUCTURE OF PEPTIDYL-TRNA HYDROLASE FROM FRANCISELLA TULARENSIS	3.1.1.29
3NEF	HIGH-RESOLUTION PYRABACTIN-BOUND PYL1 STRUCTURE	3.1.3.16
3NEG	PYRABACTIN-BOUND PYL1 STRUCTURE IN THE OPEN AND CLOSE FORMS	3.1.3.16
3NF3	CRYSTAL STRUCTURE OF BONT/A LC WITH JTH-NB-7239 PEPTIDE	3.4.24.69
3NF6	STRUCTURAL BASIS FOR A NEW MECHANISM OF INHIBITION OF HIV INTEGRASE IDENTIFIED BY FRAGMENT SCREENING AND STRUCTURE BASED DESIGN	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
3NF7	STRUCTURAL BASIS FOR A NEW MECHANISM OF INHIBITION OF HIV INTEGRASE IDENTIFIED BY FRAGMENT SCREENING AND STRUCTURE BASED DESIGN	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
3NF8	STRUCTURAL BASIS FOR A NEW MECHANISM OF INHIBITION OF HIV INTEGRASE IDENTIFIED BY FRAGMENT SCREENING AND STRUCTURE BASED DESIGN	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
3NF9	STRUCTURAL BASIS FOR A NEW MECHANISM OF INHIBITION OF HIV INTEGRASE IDENTIFIED BY FRAGMENT SCREENING AND STRUCTURE BASED DESIGN	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
3NFA	STRUCTURAL BASIS FOR A NEW MECHANISM OF INHIBITION OF HIV INTEGRASE IDENTIFIED BY FRAGMENT SCREENING AND STRUCTURE BASED DESIGN	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
3NFB	CRYSTAL STRUCTURE OF THE N-TERMINAL BETA-AMINOPEPTIDASE BAPA IN COMPLEX WITH HYDROLYZED AMPICILLIN	3.4.11.25
3NFC	CRYSTAL STRUCTURE OF E.COLI MAZF TOXIN	3.1.27
3NFK	CRYSTAL STRUCTURE OF THE PTPN4 PDZ DOMAIN COMPLEXED WITH THE C-TERMINUS OF A RABIES VIRUS G PROTEIN	3.1.3.48
3NFL	CRYSTAL STRUCTURE OF THE PTPN4 PDZ DOMAIN COMPLEXED WITH THE C-TERMINUS OF THE GLUN2A NMDA RECEPTOR SUBUNIT	3.1.3.48
3NFM	CRYSTAL STRUCTURE OF THE COMPLEX OF TYPE I RIBOSOME INACTIVATING PROTEIN WITH FRUCTOSE AT 2.5A RESOLUTION	3.2.2.22
3NFY	THE STRUCTURE OF HUMAN BISPHOSPHOGLYCERATE MUTASE TO 1.94A	5.4.2.4 5.4.2.1 3.1.3.13 5.4.2.11
3NFZ	CRYSTAL STRUCTURE OF MURINE AMINOACYLASE 3 IN COMPLEX WITH N-ACETYL-L-TYROSINE	3.5.1 3.5.1.114
3NGI	RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DTTP OPPOSITE DG	2.7.7.7 3.1.11
3NGL	CRYSTAL STRUCTURE OF BIFUNCTIONAL 5,10-METHYLENETETRAHYDROFOLATE DEHYDROGENASE / CYCLOHYDROLASE FROM THERMOPLASMA ACIDOPHILUM	1.5.1.5 3.5.4.9
3NGM	CRYSTAL STRUCTURE OF LIPASE FROM GIBBERELLA ZEAE	3.1.1.3
3NGN	CRYSTAL STRUCTURE OF THE HUMAN CNOT6L NUCLEASE DOMAIN IN COMPLEX WITH AMP	3.1 3.1.13.4
3NGO	CRYSTAL STRUCTURE OF THE HUMAN CNOT6L NUCLEASE DOMAIN IN COMPLEX WITH POLY(A) DNA	3.1 3.1.13.4
3NGQ	CRYSTAL STRUCTURE OF THE HUMAN CNOT6L NUCLEASE DOMAIN	3.1 3.1.13.4
3NGX	CRYSTAL STRUCTURE OF BIFUNCTIONAL 5,10-METHYLENETETRAHYDROFOLATE DEHYDROGENASE / CYCLOHYDROLASE FROM THERMOPLASMA ACIDOPHILUM	1.5.1.5 3.5.4.9
3NGY	CRYSTAL STRUCTURE OF RNASE T (E92G MUTANT)	3.1.13
3NGZ	CRYSTAL STRUCTURE OF RNASE T IN COMPLEX WITH A NON-PREFERRED SSDNA (GC) WITH ONE MG IN THE ACTIVE SITE	3.1.13
3NH0	CRYSTAL STRUCTURE OF RNASE T IN COMPLEX WITH A NON-PREFERRED SSDNA (AAC)	3.1.13
3NH1	CRYSTAL STRUCTURE OF RNASE T IN COMPLEX WITH A PREFERRED SSDNA (TAGG) WITH TWO MG IN THE ACTIVE SITE	3.1.13
3NH2	CRYSTAL STRUCTURE OF RNASE T IN COMPLEX WITH A STEM DNA WITH A 3' OVERHANG	3.1.13
3NH4	CRYSTAL STRUCTURE OF MURINE AMINOACYLASE 3	3.5.1 3.5.1.114
3NH5	CRYSTAL STRUCTURE OF E177A-MUTANT MURINE AMINOACYLASE 3	3.5.1 3.5.1.114
3NH8	CRYSTAL STRUCTURE OF MURINE AMINOACYLASE 3 IN COMPLEX WITH N-ACETYL-S-1,2-DICHLOROVINYL-L-CYSTEINE	3.5.1 3.5.1.114
3NHE	HIGH RESOLUTION STRUCTURE (1.26A) OF USP2A IN COMPLEX WITH UBIQUITIN	3.1.2.15 3.4.19.12
3NHG	RB69 DNA POLYMERASE (S565G/Y567A) TERNARY COMPLEX WITH DTTP OPPOSITE DG	2.7.7.7 3.1.11
3NHH	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT V23E-L36K AT CRYOGENIC TEMPERATURE	3.1.31.1
3NI9	GES-2 CARBAPENEMASE APO FORM	3.5.2.6
3NIA	GES-2 CARBAPENEMASE TAZOBACTAM COMPLEX	3.5.2.6
3NIC	DNA BINDING AND CLEAVAGE BY THE GIY-YIG ENDONUCLEASE R.ECO29KI INACTIVE VARIANT Y49F	3.1.21.4
3NIO	CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA GUANIDINOBUTYRASE	3.5.3.7
3NIP	CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA GUANIDINOPROPIONASE COMPLEXED WITH 1,6-DIAMINOHEXANE	3.5.3.17
3NIQ	CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA GUANIDINOPROPIONASE	3.5.3.17
3NIY	CRYSTAL STRUCTURE OF NATIVE XYLANASE 10B FROM THERMOTOGA PETROPHILA RKU-1	3.2.1.8
3NJ3	CRYSTAL STRUCTURE OF XYLANASE 10B FROM THERMOTOGA PETROPHILA RKU-1 IN COMPLEX WITH XYLOBIOSE	3.2.1.8
3NJ4	FLUORO-NEPLANOCIN A IN HUMAN S-ADENOSYLHOMOCYSTEINE HYDROLASE	3.3.1.1
3NJQ	CRYSTAL STRUCTURE OF KAPOSI'S SARCOMA-ASSOCIATED HERPESVIRUS PROTEASE IN COMPLEX WITH DIMER DISRUPTOR	3.4.21.97
3NJS	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN TYPEI RIBOSOME INACTIVATING PROTEIN AND LACTOSE AT 2.1A RESOLUTION	3.2.2.22
3NJU	CRYSTAL STRUCTURE OF THE COMPLEX OF GROUP I PHOSPHOLIPASE A2 WITH 4-METHOXY-BENZOICACID AT 1.4A RESOLUTION	3.1.1.4
3NK8	TRYPSIN IN COMPLEX WITH FLUORINE-CONTAINING FRAGMENT	3.4.21.4
3NK9	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS V74A AT CRYOGENIC TEMPERATURE	3.1.31.1
3NKD	STRUCTURE OF CRISP-ASSOCIATED PROTEIN CAS1 FROM ESCHERICHIA COLI STR. K-12	3.1
3NKE	HIGH RESOLUTION STRUCTURE OF THE C-TERMINAL DOMAIN CRISP-ASSOCIATED PROTEIN CAS1 FROM ESCHERICHIA COLI STR. K-12	3.1
3NKF	CRYSTAL STRUCTURE OF HUMAN LIGAND-FREE MATURE CASPASE-6 WITH INTERSUBUNIT LINKER ATTACHED	3.4.22.59
3NKK	TRYPSIN IN COMPLEX WITH FLUORINE CONTAINING FRAGMENT	3.4.21.4
3NKM	CRYSTAL STRUCTURE OF MOUSE AUTOTAXIN	3.1.4.39
3NKN	CRYSTAL STRUCTURE OF MOUSE AUTOTAXIN IN COMPLEX WITH 14:0-LPA	3.1.4.39
3NKO	CRYSTAL STRUCTURE OF MOUSE AUTOTAXIN IN COMPLEX WITH 16:0-LPA	3.1.4.39
3NKP	CRYSTAL STRUCTURE OF MOUSE AUTOTAXIN IN COMPLEX WITH 18:1-LPA	3.1.4.39
3NKQ	CRYSTAL STRUCTURE OF MOUSE AUTOTAXIN IN COMPLEX WITH 18:3-LPA	3.1.4.39
3NKR	CRYSTAL STRUCTURE OF MOUSE AUTOTAXIN IN COMPLEX WITH 22:6-LPA	3.1.4.39
3NKY	STRUCTURE OF A MUTANT P44S OF FOOT-AND-MOUTH DISEASE VIRUS RNA-DEPENDENT RNA POLYMERASE	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
3NL0	MUTANT P44S M296I OF FOOT-AND-MOUTH DISEASE VIRUS RNA-DEPENDENT RNA POLYMERASE	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
3NLS	CRYSTAL STRUCTURE OF HIV-1 PROTEASE IN COMPLEX WITH KNI-10772	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
3NM4	HELICOBACTER PYLORI MTAN	3.2.2.9 3.2.2.30
3NM5	HELICOBACTER PYLORI MTAN COMPLEXED WITH FORMYCIN A	3.2.2.9 3.2.2.30
3NM6	HELICOBACTER PYLORI MTAN COMPLEXED WITH ADENINE AND TRIS	3.2.2.9 3.2.2.30
3NMA	MUTANT P169S OF FOOT-AND-MOUTH DISEASE VIRUS RNA DEPENDENT RNA-POLYMERASE	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
3NME	STRUCTURE OF A PLANT PHOSPHATASE	3.1.3
3NN7	CRYSTAL STRUCTURE OF THERMOLYSIN IN COMPLEX WITH 2-BROMOACETATE	3.4.24.27
3NN9	REFINED ATOMIC STRUCTURES OF N9 SUBTYPE INFLUENZA VIRUS NEURAMINIDASE AND ESCAPE MUTANTS	3.2.1.18
3NNQ	CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF MOLONEY MURINE LEUKEMIA VIRUS INTEGRASE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET OR3	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
3NO6	CRYSTAL STRUCTURE OF A PUTATIVE THIAMINASE II (SE1693) FROM STAPHYLOCOCCUS EPIDERMIDIS ATCC 12228 AT 1.65 A RESOLUTION	3.5.99.2
3NOX	CRYSTAL STRUCTURE OF HUMAN DPP-IV IN COMPLEX WITH SA-(+)-(6-(AMINOMETHYL)-5-(2,4-DICHLOROPHENYL)-7-METHYLIMIDAZO[1,2-A]PYRIMIDIN-2-YL)(MORPHOLINO)METHANONE	3.4.14.5
3NP8	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L36A AT CRYOGENIC TEMPERATURE	3.1.31.1
3NPS	CRYSTAL STRUCTURE OF MEMBRANE-TYPE SERINE PROTEASE 1 (MT-SP1) IN COMPLEX WITH THE FAB INHIBITOR S4	3.4.21.109
3NQB	CRYSTAL STRUCTURE OF ADENINE DEAMINASE FROM AGROBACTERIUM TUMEFACIENS (STR. C 58)	3.5.4.2
3NQT	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS V66A AT CRYOGENIC TEMPERATURE	3.1.31.1
3NQW	A METAZOAN ORTHOLOG OF SPOT HYDROLYZES PPGPP AND PLAYS A ROLE IN STARVATION RESPONSES	3.1.7.2
3NQX	CRYSTAL STRUCTURE OF VIBRIOLYSIN MCP-02 MATURE ENZYME, A ZINC METALLOPROTEASE FROM M4 FAMILY	3.4.24.25
3NQY	CRYSTAL STRUCTURE OF THE AUTOPROCESSED COMPLEX OF VIBRIOLYSIN MCP-02 WITH A SINGLE POINT MUTATION E346A	3.4.24.25
3NQZ	CRYSTAL STRUCTURE OF THE AUTOPROCESSED VIBRIOLYSIN MCP-02 WITH E369A MUTATION	3.4.24.25
3NR1	A METAZOAN ORTHOLOG OF SPOT HYDROLYZES PPGPP AND PLAYS A ROLE IN STARVATION RESPONSES	3.1.7.2
3NR2	CRYSTAL STRUCTURE OF CASPASE-6 ZYMOGEN	3.4.22.59
3NR6	CRYSTAL STRUCTURE OF XENOTROPIC MURINE LEUKEMIA VIRUS-RELATED VIRUS (XMRV) PROTEASE	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
3NR8	CRYSTAL STRUCTURE OF HUMAN SHIP2	3.1.3.1 3.1.3.86
3NRB	CRYSTAL STRUCTURE OF A FORMYLTETRAHYDROFOLATE DEFORMYLASE (PURU, PP_1943) FROM PSEUDOMONAS PUTIDA KT2440 AT 2.05 A RESOLUTION	3.5.1.10
3NRJ	CRYSTAL STRUCTURE OF PROBABLE YRBI FAMILY PHOSPHATASE FROM PSEUDOMONAS SYRINGAE PV.PHASEOLICA 1448A COMPLEXED WITH MAGNESIUM	3.1.3.45
3NS7	SUCCINIC ACID AMIDES AS P2-P3 REPLACEMENTS FOR INHIBITORS OF INTERLEUKIN-1BETA CONVERTING ENZYME (ICE OR CASPASE 1)	3.4.22.36
3NSH	BACE-1 IN COMPLEX WITH ELN475957	3.4.23.46
3NSM	CRYSTAL STRUCTURE OF INSECT BETA-N-ACETYL-D-HEXOSAMINIDASE OFHEX1 FROM OSTRINIA FURNACALIS	3.2.1.52
3NSN	CRYSTAL STRUCTURE OF INSECT BETA-N-ACETYL-D-HEXOSAMINIDASE OFHEX1 COMPLEXED WITH TMG-CHITOTRIOMYCIN	3.2.1.52
3NSS	THE 2009 PANDEMIC H1N1 NEURAMINIDASE N1 LACKS THE 150-CAVITY IN ITS ACTIVE SITES	3.2.1.18
3NSX	THE CRYSTAL STRUCTURE OF THE THE CRYSTAL STRUCTURE OF THE D420A MUTANT OF THE ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174	3.2.1
3NT7	CRYSTAL STRUCTURE OF VACCINIA VIRUS URACIL DNA GLYCOSYLASE R187V MUTANT	3.2.2.27
3NTX	CRYSTAL STRUCTURE OF L-ASPARAGINASE I FROM YERSINIA PESTIS	3.5.1.1
3NU3	WILD TYPE HIV-1 PROTEASE WITH ANTIVIRAL DRUG AMPRENAVIR	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
3NU4	CRYSTAL STRUCTURE OF HIV-1 PROTEASE MUTANT V32I WITH ANTIVIRAL DRUG AMPRENAVIR	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
3NU5	CRYSTAL STRUCTURE OF HIV-1 PROTEASE MUTANT I50V WITH ANTIVIRAL DRUG AMPRENAVIR	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
3NU6	CRYSTAL STRUCTURE OF HIV-1 PROTEASE MUTANT I54M WITH ANTIVIRAL DRUG AMPRENAVIR	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
3NU9	CRYSTAL STRUCTURE OF HIV-1 PROTEASE MUTANT I84V WITH ANTIVIRAL DRUG AMPRENAVIR	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
3NUC	STAPHLOCOCCAL NUCLEASE, 1-N-PROPANE THIOL DISULFIDE TO V23C VARIANT	3.1.31.1
3NUJ	CRYSTAL STRUCTURE OF HIV-1 PROTEASE MUTANT I54V WITH ANTIVIRAL DRUG AMPRENAVIR	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
3NUK	THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174	3.2.1
3NUM	SUBSTRATE INDUCED REMODELING OF THE ACTIVE SITE REGULATES HTRA1 ACTIVITY	3.4.21
3NUO	CRYSTAL STRUCTURE OF HIV-1 PROTEASE MUTANT L90M WITH ANTIVIRAL DRUG AMPRENAVIR	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
3NUQ	STRUCTURE OF A PUTATIVE NUCLEOTIDE PHOSPHATASE FROM SACCHAROMYCES CEREVISIAE	3.1.3.5
3NUR	CRYSTAL STRUCTURE OF A PUTATIVE AMIDOHYDROLASE FROM STAPHYLOCOCCUS AUREUS	3.5.1
3NVD	STRUCTURE OF YBBD IN COMPLEX WITH PUGNAC	3.2.1.52
3NWO	CRYSTAL STRUCTURE OF PROLINE IMINOPEPTIDASE MYCOBACTERIUM SMEGMATIS	3.4.11.5
3NWP	CRYSTAL STRUCTURE OF A 6-PHOSPHOGLUCONOLACTONASE (SBAL_2240) FROM SHEWANELLA BALTICA OS155 AT 1.40 A RESOLUTION	3.1.1.31
3NWQ	X-RAY STRUCTURE OF ESTER CHEMICAL ANALOGUE [O-ILE50,O-ILE50']HIV-1 PROTEASE COMPLEXED WITH MVT-101	3.4.23.16
3NWU	SUBSTRATE INDUCED REMODELING OF THE ACTIVE SITE REGULATES HTRA1 ACTIVITY	3.4.21
3NWX	X-RAY STRUCTURE OF ESTER CHEMICAL ANALOGUE [O-ILE50,O-ILE50']HIV-1 PROTEASE COMPLEXED WITH KVS-1 INHIBITOR	3.4.23.16
3NX7	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR N-HYDROXY-2-(N-(2-HYDROXYETHYL)4-METHOXYPHENYLSULFONAMIDO)ACETAMIDE	3.4.24.65
3NX9	CRYSTAL STRUCTURE OF TYPE I RIBOSOME INACTIVATING PROTEIN IN COMPLEX WITH MALTOSE AT 1.7A RESOLUTION	3.2.2.22
3NXE	X-RAY STRUCTURE OF ESTER CHEMICAL ANALOGUE 'COVALENT DIMER' [ILE50,O-ILE50']HIV-1 PROTEASE COMPLEXED WITH MVT-101 INHIBITOR	3.4.23.16
3NXN	X-RAY STRUCTURE OF ESTER CHEMICAL ANALOGUE 'COVALENT DIMER' [ILE50,O-ILE50']HIV-1 PROTEASE COMPLEXED WITH KVS-1 INHIBITOR	3.4.23.16
3NXP	CRYSTAL STRUCTURE OF HUMAN PRETHROMBIN-1	3.4.21.5
3NXQ	ANGIOTENSIN CONVERTING ENZYME N DOMAIN GLYCSOYLATION MUTANT (NDOM389) IN COMPLEX WITH RXP407	3.4.15.1 3.2.1
3NXW	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L125A AT CRYOGENIC TEMPERATURE	3.1.31.1
3NY4	CRYSTAL STRUCTURE OF BLAC-K73A BOUND WITH CEFAMANDOLE	3.5.2.6
3NY8	CRYSTAL STRUCTURE OF THE HUMAN BETA2 ADRENERGIC RECEPTOR IN COMPLEX WITH THE INVERSE AGONIST ICI 118,551	3.2.1.17
3NY9	CRYSTAL STRUCTURE OF THE HUMAN BETA2 ADRENERGIC RECEPTOR IN COMPLEX WITH A NOVEL INVERSE AGONIST	3.2.1.17
3NYA	CRYSTAL STRUCTURE OF THE HUMAN BETA2 ADRENERGIC RECEPTOR IN COMPLEX WITH THE NEUTRAL ANTAGONIST ALPRENOLOL	3.2.1.17
3NYD	CRYSTAL STRUCTURE OF KEMP ELIMINASE HG-2 COMPLEXED WITH TRANSITION STATE ANALOG 5-NITRO BENZOTRIAZOLE	3.2.1.8
3NYG	X-RAY STRUCTURE OF ESTER CHEMICAL ANALOGUE [O-GLY51,O-GLY51']HIV-1 PROTEASE COMPLEXED WITH MVT-101 INHIBITOR	3.4.23.16
3NZI	SUBSTRATE INDUCED REMODELING OF THE ACTIVE SITE REGULATES HTRA1 ACTIVITY	3.4.21
3NZK	STRUCTURE OF LPXC FROM YERSINIA ENTEROCOLITICA COMPLEXED WITH CHIR090 INHIBITOR	3.5.1.33 3.5.1.108
3O0D	CRYSTAL STRUCTURE OF LIP2 LIPASE FROM YARROWIA LIPOLYTICA AT 1.7 A RESOLUTION	3.1.1.3
3O0J	PDE4B IN COMPLEX WITH LIGAND AN2898	3.1.4.17 3.1.4.53
3O0T	CRYSTAL STRUCTURE OF HUMAN PHOSPHOGLYCERATE MUTASE FAMILY MEMBER 5 (PGAM5) IN COMPLEX WITH PHOSPHATE	3.1.3.16
3O0U	CATHEPSIN K COVALENTLY BOUND TO A CYANO-PYRIMIDINE INHIBITOR WITH IMPROVED SELECTIVITY OVER HERG	3.4.22.38
3O1C	HIGH RESOLUTION CRYSTAL STRUCTURE OF HISTIDINE TRIAD NUCLEOTIDE-BINDING PROTEIN 1 (HINT1) C38A MUTANT FROM RABBIT COMPLEXED WITH ADENOSINE	3
3O1G	CATHEPSIN K COVALENTLY BOUND TO A 2-CYANO PYRIMIDINE INHIBITOR WITH A BENZYL P3 GROUP.	3.4.22.38
3O1L	CRYSTAL STRUCTURE OF A FORMYLTETRAHYDROFOLATE DEFORMYLASE (PSPTO_4314) FROM PSEUDOMONAS SYRINGAE PV. TOMATO STR. DC3000 AT 2.20 A RESOLUTION	3.5.1.10
3O1X	HIGH RESOLUTION CRYSTAL STRUCTURE OF HISTIDINE TRIAD NUCLEOTIDE-BINDING PROTEIN 1 (HINT1) C84A MUTANT FROM RABBIT COMPLEXED WITH ADENOSINE	3
3O1Z	HIGH RESOLUTION CRYSTAL STRUCTURE OF HISTIDINE TRIAD NUCLEOTIDE-BINDING PROTEIN 1 (HINT1) DOUBLE CYSTEINE MUTANT FROM RABBIT	3
3O2L	CRYSTAL STRUCTURE OF AN INACTIVE KEMP ELIMINATION DESIGN HG-1	3.2.1.8
3O2R	STRUCTURAL FLEXIBILITY IN REGION INVOLVED IN DIMER FORMATION OF NUCLEASE DOMAIN OF RIBONUCLASE III (RNC) FROM CAMPYLOBACTER JEJUNI	3.1.26.3
3O2X	MMP-13 IN COMPLEX WITH SELECTIVE TETRAZOLE CORE INHIBITOR	3.4.24
3O3F	T. MARITIMA RNASE H2 D107N IN COMPLEX WITH NUCLEIC ACID SUBSTRATE AND MAGNESIUM IONS	3.1.26.4
3O3G	T. MARITIMA RNASE H2 IN COMPLEX WITH NUCLEIC ACID SUBSTRATE AND CALCIUM IONS	3.1.26.4
3O3H	T. MARITIMA RNASE H2 D107N IN COMPLEX WITH NUCLEIC ACID SUBSTRATE AND MANGANESE IONS	3.1.26.4
3O3J	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PEPTIDE DEFORMYLASE 1B (ATPDF1B) IN COMPLEX WITH INHIBITOR 6B	3.5.1.88
3O3V	CRYSTAL STRUCTURE OF CLBP PEPTIDASE DOMAIN	3.5.2.6
3O4G	STRUCTURE AND CATALYSIS OF ACYLAMINOACYL PEPTIDASE	3.4.19.1
3O4H	STRUCTURE AND CATALYSIS OF ACYLAMINOACYL PEPTIDASE	3.4.19.1
3O4I	STRUCTURE AND CATALYSIS OF ACYLAMINOACYL PEPTIDASE	3.4.19.1
3O4J	STRUCTURE AND CATALYSIS OF ACYLAMINOACYL PEPTIDASE	3.4.19.1
3O4M	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH 1,2-DIHYDROXYBENZENE	3.1.1.4
3O4N	CRYSTAL STRUCTURE OF THE ROUS ASSOCIATED VIRUS INTEGRASE CATALYTIC DOMAIN IN MES BUFFER PH 6.0	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
3O4P	DFPASE AT 0.85 ANGSTROM RESOLUTION (H ATOMS INCLUDED)	3.1.8.2
3O4Q	CRYSTAL STRUCTURE OF THE ROUS ASSOCIATED VIRUS INTEGRASE CATALYTIC DOMAIN A182T IN CITRATE BUFFER PH 6.2	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
3O4S	CRYSTAL STRUCTURE OF HEPTP WITH A CLOSED WPD LOOP AND AN ORDERED E-LOOP	3.1.3.48
3O4T	CRYSTAL STRUCTURE OF HEPTP WITH AN OPEN WPD LOOP AND PARTIALLY DEPLETED ACTIVE SITE	3.1.3.48
3O4U	CRYSTAL STRUCTURE OF HEPTP WITH AN ATYPICALLY OPEN WPD LOOP	3.1.3.48
3O4V	CRYSTAL STRUCTURE OF E. COLI MTA/SAH NUCLEOSIDASE IN COMPLEX WITH (4-CHLOROPHENYL)THIO-DADME-IMMA	3.2.2.9 3.2.2.16
3O52	STRUCTURE OF THE E.COLI GDP-MANNOSE HYDROLASE (YFFH) IN COMPLEX WITH TARTRATE	3.6.1
3O56	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B2B IN COMPLEX WITH A 5-HETEROCYCLE PYRAZOLOPYRIDINE INHIBITOR	3.1.4.17 3.1.4.53
3O57	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B2B IN COMPLEX WITH A 5-HETEROCYCLE PYRAZOLOPYRIDINE INHIBITOR	3.1.4.17 3.1.4.53
3O59	DNA POLYMERASE D LARGE SUBUNIT DP2(1-300) FROM PYROCOCCUS HORIKOSHII	2.7.7.7 3.1.11.1
3O5S	CRYSTAL STRUCTURE OF THE ENDO-BETA-1,3-1,4 GLUCANASE FROM BACILLUS SUBTILIS (STRAIN 168)	3.2.1.73
3O5T	STRUCTURE OF DRAG-GLNZ COMPLEX WITH ADP	3.2.2.24
3O5V	THE CRYSTAL STRUCTURE OF THE CREATINASE/PROLIDASE N-TERMINAL DOMAIN OF AN X-PRO DIPEPTIDASE FROM STREPTOCOCCUS PYOGENES TO 1.85A	3.4.13.9
3O5W	BINDING OF KINETIN IN THE ACTIVE SITE OF MISTLETOE LECTIN I	3.2.2.22
3O5X	CRYSTAL STRUCTURE OF THE ONCOGENIC TYROSINE PHOSPHATASE SHP2 COMPLEXED WITH A SALICYLIC ACID-BASED SMALL MOLECULE INHIBITOR	3.1.3.48
3O61	STRUCTURE OF THE E100A E.COLI GDP-MANNOSE HYDROLASE (YFFH) IN COMPLEX WITH GDP-MANNOSE AND MG++	3.6.1
3O64	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH 2-(2-AMINOTHIAZOL-4-YL)PYRROLIDINE-BASED TARTRATE DIAMIDES	3.4.24.86
3O65	CRYSTAL STRUCTURE OF A JOSEPHIN-UBIQUITIN COMPLEX: EVOLUTIONARY RESTRAINTS ON ATAXIN-3 DEUBIQUITINATING ACTIVITY	3.1.2.15 3.4.19.12
3O69	STRUCTURE OF THE E100A E.COLI GDP-MANNOSE HYDROLASE (YFFH) IN COMPLEX WITH MG++	3.6.1
3O6A	F144Y/F258Y DOUBLE MUTANT OF EXO-BETA-1,3-GLUCANASE FROM CANDIDA ALBICANS AT 2 A	3.2.1.58 2.4.1
3O6Z	STRUCTURE OF THE D152A E.COLI GDP-MANNOSE HYDROLASE (YFFH) IN COMPLEX WITH MG++	3.6.1
3O7U	CRYSTAL STRUCTURE OF CYTOSINE DEAMINASE FROM ESCHERICHIA COLI COMPLEXED WITH ZINC AND PHOSPHONO-CYTOSINE	3.5.4.1 3.5.4
3O7X	CRYSTAL STRUCTURE OF HUMAN HILI PAZ DOMAIN	3.1.26
3O86	CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A SULFONAMIDE BORONIC ACID INHIBITOR	3.5.2.6
3O87	CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A SULFONAMIDE BORONIC ACID INHIBITOR	3.5.2.6
3O88	CRYSTAL STRUCTURE OF AMPC BETA-LACTAMASE IN COMPLEX WITH A SULFONAMIDE BORONIC ACID INHIBITOR	3.5.2.6
3O8B	VISUALIZING ATP-DEPENDENT RNA TRANSLOCATION BY THE NS3 HELICASE FROM HCV	3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3O8C	VISUALIZING ATP-DEPENDENT RNA TRANSLOCATION BY THE NS3 HELICASE FROM HCV	3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3O8D	VISUALIZING ATP-DEPENDENT RNA TRANSLOCATION BY THE NS3 HELICASE FROM HCV	3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3O8R	VISUALIZING ATP-DEPENDENT RNA TRANSLOCATION BY THE NS3 HELICASE FROM HCV	3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
3O95	CRYSTAL STRUCTURE OF HUMAN DPP4 BOUND TO TAK-100	3.4.14.5
3O97	CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF LACTOFERRIN WITH INDOLE ACETIC ACID AT 2.68 A RESOLUTION	3.4.21
3O98	GLUTATHIONYLSPERMIDINE SYNTHETASE/AMIDASE C59A COMPLEX WITH ADP AND GSP	6.3.1.8 3.5.1.78
3O99	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD13	2.7.7.49 3.1.26.13
3O9A	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD14	2.7.7.49 3.1.26.13
3O9B	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD25	2.7.7.49 3.1.26.13
3O9C	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD20	2.7.7.49 3.1.26.13
3O9D	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD19	2.7.7.49 3.1.26.13
3O9E	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH AF60	2.7.7.49 3.1.26.13
3O9F	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD27	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
3O9G	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH AF53	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
3O9H	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD26	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
3O9I	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH AF61	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
3O9J	INFLUENZA NA IN COMPLEX WITH COMPOUND 5	3.2.1.18
3O9K	INFLUENZA NA IN COMPLEX WITH COMPOUND 6	3.2.1.18
3O9L	DESIGN AND OPTIMISATION OF NEW PIPERIDINES AS RENIN INHIBITORS	3.4.23.15
3O9M	CO-CRYSTALLIZATION STUDIES OF FULL LENGTH RECOMBINANT BCHE WITH COCAINE OFFERS INSIGHTS INTO COCAINE DETOXIFICATION	3.1.1.8
3OA5	THE STRUCTURE OF CHI1, A CHITINASE FROM YERSINIA ENTOMOPHAGA	3.2.1.14
3OAD	DESIGN AND OPTIMIZATION OF NEW PIPERIDINES AS RENIN INHIBITORS	3.4.23.15
3OAG	DESIGN AND OPTIMIZATION OF NEW PIPERIDINES AS RENIN INHIBITORS	3.4.23.15
3OBI	CRYSTAL STRUCTURE OF A FORMYLTETRAHYDROFOLATE DEFORMYLASE (NP_949368) FROM RHODOPSEUDOMONAS PALUSTRIS CGA009 AT 1.95 A RESOLUTION	3.5.1.10
3OBR	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN SEROTYPE D BINDING DOMAIN	3.4.24.69
3OBT	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN SEROTYPE D LIGAND BINDING DOMAIN IN COMPLEX WITH N-ACETYLNEURAMINIC ACID	3.4.24.69
3OBW	CRYSTAL STRUCTURE OF TWO ARCHAEAL PELOTAS REVEAL INTER-DOMAIN STRUCTURAL PLASTICITY	3.1
3OBY	CRYSTAL STRUCTURE OF ARCHAEOGLOBUS FULGIDUS PELOTA REVEALS INTER-DOMAIN STRUCTURAL PLASTICITY	3.1
3OC0	STRUCTURE OF HUMAN DPP-IV WITH HTS HIT (2S,3S,11BS)-3-BUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-A]ISOQUINOLIN-2-YLAMINE	3.4.14.5
3OC2	CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN 3 FROM PSEUDOMONAS AERUGINOSA	3.4.16.4
3OC6	CRYSTAL STRUCTURE OF 6-PHOSPHOGLUCONOLACTONASE FROM MYCOBACTERIUM SMEGMATIS, APO FORM	3.1.1.31
3OCA	CRYSTAL STRUCTURE OF PEPTIDE DEFORMYLASE FROM EHRLICHIA CHAFFEENSIS	3.5.1.88
3OCL	CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN 3 FROM PSEUDOMONAS AERUGINOSA IN COMPLEX WITH CARBENICILLIN	3.4.16.4
3OCN	CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN 3 FROM PSEUDOMONAS AERUGINOSA IN COMPLEX WITH CEFTAZIDIME	3.4.16.4
3OCQ	CRYSTAL STRUCTURE OF TRNA-SPECIFIC ADENOSINE DEAMINASE FROM SALMONELLA ENTERICA	3.5.4.4 3.5.4.33
3OCU	STRUCTURE OF RECOMBINANT HAEMOPHILUS INFLUENZAE E(P4) ACID PHOSPHATASE MUTANT D66N COMPLEXED WITH NMN	3.1.3.2
3OCV	STRUCTURE OF RECOMBINANT HAEMOPHILUS INFLUENZAE E(P4) ACID PHOSPHATASE MUTANT D66N COMPLEXED WITH 5'-AMP	3.1.3.2
3OCW	STRUCTURE OF RECOMBINANT HAEMOPHILUS INFLUENZAE E(P4) ACID PHOSPHATASE MUTANT D66N COMPLEXED WITH 3'-AMP	3.1.3.2
3OCX	STRUCTURE OF RECOMBINANT HAEMOPHILUS INFLUENZAE E(P4) ACID PHOSPHATASE MUTANT D66N COMPLEXED WITH 2'-AMP	3.1.3.2
3OCY	STRUCTURE OF RECOMBINANT HAEMOPHILUS INFLUENZAE E(P4) ACID PHOSPHATASE COMPLEXED WITH INORGANIC PHOSPHATE	3.1.3.2
3OCZ	STRUCTURE OF RECOMBINANT HAEMOPHILUS INFLUENZAE E(P4) ACID PHOSPHATASE COMPLEXED WITH THE INHIBITOR ADENOSINE 5-O-THIOMONOPHOSPHATE	3.1.3.2
3OD5	CRYSTAL STRUCTURE OF ACTIVE CASPASE-6 BOUND WITH AC-VEID-CHO	3.4.22.59
3ODD	COMPARISON OF THE CHARACTER AND THE SPEED OF X-RAY-INDUCED STRUCTURAL CHANGES OF PORCINE PANCREATIC ELASTASE AT TWO TEMPERATURES, 100 AND 15K. THE DATA SET WAS COLLECTED FROM REGION B OF THE CRYSTAL. SECOND STEP OF RADIATION DAMAGE	3.4.21.36
3ODF	COMPARISON OF THE CHARACTER AND THE SPEED OF X-RAY-INDUCED STRUCTURAL CHANGES OF PORCINE PANCREATIC ELASTASE AT TWO TEMPERATURES, 100 AND 15K. THE DATA SET WAS COLLECTED FROM REGION A OF THE CRYSTAL. SECOND STEP OF RADIATION DAMAGE	3.4.21.36
3ODJ	CRYSTAL STRUCTURE OF H. INFLUENZAE RHOMBOID GLPG WITH DISORDERED LOOP 4, HELIX 5 AND LOOP 5	3.4.21.105
3ODU	THE 2.5 A STRUCTURE OF THE CXCR4 CHEMOKINE RECEPTOR IN COMPLEX WITH SMALL MOLECULE ANTAGONIST IT1T	3.2.1.17
3OE0	CRYSTAL STRUCTURE OF THE CXCR4 CHEMOKINE RECEPTOR IN COMPLEX WITH A CYCLIC PEPTIDE ANTAGONIST CVX15	3.2.1.17
3OE6	CRYSTAL STRUCTURE OF THE CXCR4 CHEMOKINE RECEPTOR IN COMPLEX WITH A SMALL MOLECULE ANTAGONIST IT1T IN I222 SPACEGROUP	3.2.1.17
3OE8	CRYSTAL STRUCTURE OF THE CXCR4 CHEMOKINE RECEPTOR IN COMPLEX WITH A SMALL MOLECULE ANTAGONIST IT1T IN P1 SPACEGROUP	3.2.1.17
3OE9	CRYSTAL STRUCTURE OF THE CHEMOKINE CXCR4 RECEPTOR IN COMPLEX WITH A SMALL MOLECULE ANTAGONIST IT1T IN P1 SPACEGROUP	3.2.1.17
3OF8	STRUCTURAL BASIS FOR REVERSIBLE AND IRREVERSIBLE INHIBITION OF HUMAN CATHEPSIN L BY THEIR RESPECTIVE DIPEPTIDYL GLYOXAL AND DIAZOMETHYLKETONE INHIBITORS	3.4.22.15
3OF9	STRUCTURAL BASIS FOR IRREVERSIBLE INHIBITION OF HUMAN CATHEPSIN L BY A DIAZOMETHYLKETONE INHIBITOR	3.4.22.15
3OFS	DYNAMIC CONFORMATIONS OF THE CD38-MEDIATED NAD CYCLIZATION CAPTURED USING MULTI-COPY CRYSTALLOGRAPHY	3.2.2.5 3.2.2.6 2.4.99.20
3OFV	CRYSTAL STRUCTURE OF PEPTIDYL-TRNA HYDROLASE FROM ESCHERICHIA COLI, I222 CRYSTAL FORM	3.1.1.29
3OG2	NATIVE CRYSTAL STRUCTURE OF TRICHODERMA REESEI BETA-GALACTOSIDASE	3.2.1.23
3OG8	CRYSTAL STRUCTURE OF HUMAN RIG-I CTD BOUND TO A 14-BP BLUNT-ENDED DSRNA	3.6.4.13
3OGA	1.75 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF A PUTATIVE NTP PYROPHOSPHOHYDROLASE (YFAO) FROM SALMONELLA TYPHIMURIUM LT2	3.6.1 3.6.1.9 3.6.1.12 3.6.1.23
3OGD	ALKA UNDAMAGED DNA COMPLEX: INTERROGATION OF A G*:C BASE PAIR	3.2.2.21
3OGG	CRYSTAL STRUCTURE OF THE RECEPTOR BINDING DOMAIN OF BOTULINUM NEUROTOXIN D	3.4.24.69
3OGP	CRYSTAL STRUCTURE OF 6S-98S FIV PROTEASE WITH DARUNAVIR BOUND	3.4.23 2.7.7.49 3.1.26.13 3.1.13.2 3.6.1.23 2.7.7 3.1
3OGQ	CRYSTAL STRUCTURE OF 6S-98S FIV PROTEASE WITH LOPINAVIR BOUND	3.4.23 2.7.7.49 3.1.26.13 3.1.13.2 3.6.1.23 2.7.7 3.1
3OGR	COMPLEX STRUCTURE OF BETA-GALACTOSIDASE FROM TRICHODERMA REESEI WITH GALACTOSE	3.2.1.23
3OGS	COMPLEX STRUCTURE OF BETA-GALACTOSIDASE FROM TRICHODERMA REESEI WITH IPTG	3.2.1.23
3OGV	COMPLEX STRUCTURE OF BETA-GALACTOSIDASE FROM TRICHODERMA REESEI WITH PETG	3.2.1.23
3OH6	ALKA UNDAMAGED DNA COMPLEX: INTERROGATION OF A C:G BASE PAIR	3.2.2.21
3OH9	ALKA UNDAMAGED DNA COMPLEX: INTERROGATION OF A T:A BASE PAIR	3.2.2.21
3OHF	CRYSTAL STRUCTURE OF BETA-SITE APP-CLEAVING ENZYME 1 (BACE-WT) COMPLEX WITH BMS-655295 AKA N~3~-((1S,2R)-1- BENZYL-2-HYDROXY-3-((3-METHOXYBENZYL)AMINO)PROPYL)-N~1~, N~1~-DIBUTYL-1H-INDOLE-1,3-DICARBOXAMIDE	3.4.23.46
3OHH	CRYSTAL STRUCTURE OF BETA-SITE APP-CLEAVING ENZYME 1 (BACE-WT) COMPLEX WITH BMS-681889 AKA N~1~-BUTYL-5-CYANO- N~3~-((1S,2R)-1-(3,5-DIFLUOROBENZYL)-2-HYDROXY-3-((3- METHOXYBENZYL)AMINO)PROPYL)-N~1~-METHYL-1H-INDOLE-1,3- DICARBOXAMIDE	3.4.23.46
3OHL	CATALYTIC DOMAIN OF STROMELYSIN-1 IN COMPLEX WITH N-HYDROXY-2-(4-METHOXY-N-(PYRIDINE-3-YLMETHYL)PHENYLSULFONAMIDO)ACETAMIDE	3.4.24.17
3OHO	CATALYTIC DOMAIN OF STROMELYSIN-1 IN COMPLEX WITH N-HYDROXY-2-(4-METHYLPHENYLSULFONAMIDO)ACETAMIDE	3.4.24.17
3OI7	STRUCTURE OF THE STRUCTURE OF THE H13A MUTANT OF YKR043C IN COMPLEX WITH SEDOHEPTULOSE-1,7-BISPHOSPHATE	3.1.3.11 3.1.3.37
3OIU	H-RASQ61L WITH ALLOSTERIC SWITCH IN THE ON" STATE"	3.6.5.2
3OIV	H-RASG12V WITH ALLOSTERIC SWITCH IN THE OFF" STATE"	3.6.5.2
3OIW	H-RASG12V WITH ALLOSTERIC SWITCH IN THE ON" STATE"	3.6.5.2
3OJ6	CRYSTAL STRUCTURE OF BLASTICIDIN S DEAMINASE FROM COCCIDIOIDES IMMITIS	3.5.4.23
3OJ7	CRYSTAL STRUCTURE OF A HISTIDINE TRIAD FAMILY PROTEIN FROM ENTAMOEBA HISTOLYTICA, BOUND TO SULFATE	3
3OJ8	ALPHA-KETOHETEROCYCLE INHIBITORS OF FATTY ACID AMIDE HYDROLASE CONTAINING ADDITIONAL CONFORMATIONAL CONTRAINTS IN THE ACYL SIDE CHAIN	3.5.1.99 3.1.1
3OJG	STRUCTURE OF AN INACTIVE LACTONASE FROM GEOBACILLUS KAUSTOPHILUS WITH BOUND N-BUTYRYL-DL-HOMOSERINE LACTONE	3.5
3OJP	D52N MUTANT OF HEN EGG WHITE LYSOZYME (HEWL)	3.2.1.17
3OK0	E35A MUTANT OF HEN EGG WHITE LYSOZYME (HEWL)	3.2.1.17
3OK9	CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE WITH NEW OXATRICYCLIC DESIGNED INHIBITOR GRL-0519A	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
3OL6	POLIOVIRUS POLYMERASE ELONGATION COMPLEX	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
3OL7	POLIOVIRUS POLYMERASE ELONGATION COMPLEX WITH CTP	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
3OL8	POLIOVIRUS POLYMERASE ELONGATION COMPLEX WITH CTP-MN	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
3OL9	POLIOVIRUS POLYMERASE ELONGATION COMPLEX WITH 3'-DEOXY-CTP	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
3OLA	POLIOVIRUS POLYMERASE ELONGATION COMPLEX WITH 2'-DEOXY-CTP	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
3OLB	POLIOVIRUS POLYMERASE ELONGATION COMPLEX WITH 2',3'-DIDEOXY-CTP	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
3OLD	CRYSTAL STRUCTURE OF ALPHA-AMYLASE IN COMPLEX WITH ACARVIOSTATIN I03	3.2.1.1
3OLE	STRUCTURES OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH ACARVIOSTATIN II03	3.2.1.1
3OLG	STRUCTURES OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH ACARVIOSTATIN III03	3.2.1.1
3OLI	STRUCTURES OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH ACARVIOSTATIN IV03	3.2.1.1
3OLR	PTPN22 IN COMPLEX WITH CONSENSUS PHOSPHO-TYROSINE PEPTIDE 1	3.1.3.48
3OMC	STRUCTURE OF HUMAN SND1 EXTENDED TUDOR DOMAIN IN COMPLEX WITH THE SYMMETRICALLY DIMETHYLATED ARGININE PIWIL1 PEPTIDE R4ME2S	3.1.31.1
3OMF	CRYSTAL STRUCTURE OF A HISTIDINE TRIAD FAMILY PROTEIN FROM ENTAMOEBA HISTOLYTICA, BOUND TO AMP	3
3OMG	STRUCTURE OF HUMAN SND1 EXTENDED TUDOR DOMAIN IN COMPLEX WITH THE SYMMETRICALLY DIMETHYLATED ARGININE PIWIL1 PEPTIDE R14ME2S	3.1.31.1
3OMH	CRYSTAL STRUCTURE OF PTPN22 IN COMPLEX WITH SKAP-HOM PTYR75 PEPTIDE	3.1.3.48
3OML	STRUCTURE OF FULL-LENGTH PEROXISOMAL MULTIFUNCTIONAL ENZYME TYPE 2 FROM DROSOPHILA MELANOGASTER	1.1.1.62 3.4.22 1.1.1 4.2.1.119
3OMW	CRYSTAL STRUCTURE OF SSU72, AN ESSENTIAL EUKARYOTIC PHOSPHATASE SPECIFIC FOR THE C-TERMINAL DOMAIN OF RNA POLYMERASE II	3.1.3.16
3OMX	CRYSTAL STRUCTURE OF SSU72 WITH VANADATE COMPLEX	3.1.3.16
3OND	CRYSTAL STRUCTURE OF LUPINUS LUTEUS S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE IN COMPLEX WITH ADENOSINE	3.3.1.1
3ONE	CRYSTAL STRUCTURE OF LUPINUS LUTEUS S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE IN COMPLEX WITH ADENINE	3.3.1.1
3ONF	CRYSTAL STRUCTURE OF LUPINUS LUTEUS S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE IN COMPLEX WITH CORDYCEPIN	3.3.1.1
3ONW	STRUCTURE OF A G-ALPHA-I1 MUTANT WITH ENHANCED AFFINITY FOR THE RGS14 GOLOCO MOTIF.	3.6.5.1
3OOD	STRUCTURE OF OPDA Y257F MUTANT SOAKED WITH DIETHYL 4-METHOXYPHENYL PHOSPHATE FOR 20 HOURS.	3.1.8.1
3OOL	I-SCEI COMPLEXED WITH C/G+4 DNA SUBSTRATE	3.1
3OOR	I-SCEI MUTANT (K86R/G100T)COMPLEXED WITH C/G+4 DNA SUBSTRATE	3.1
3OOT	CRYSTAL STRUCTURE ANALYSIS OF RENIN-INDOLE-PIPERAZIN INHIBITOR COMPLEXES	3.4.23.15
3OOZ	BACE1 IN COMPLEX WITH THE AMINOHYDANTOIN COMPOUND 102	3.4.23.46
3OP3	CRYSTAL STRUCTURE OF CELL DIVISION CYCLE 25C PROTEIN ISOFORM A FROM HOMO SAPIENS	3.1.3.48
3OPH	ESBL R164S MUTANT OF SHV-1 BETA-LACTAMASE	3.5.2.6
3OPL	ESBL R164H MUTANT SHV-1 BETA-LACTAMASE	3.5.2.6
3OPM	CRYSTAL STRUCTURE OF HUMAN DPP4 BOUND TO TAK-294	3.4.14.5
3OPP	ESBL R164S MUTANT OF SHV-1 BETA-LACTAMASE COMPLEXED WITH SA2-13	3.5.2.6
3OPR	ESBL R164H MUTANT OF SHV-1 BETA-LACTAMASE COMPLEXED TO SA2-13	3.5.2.6
3OQ2	STRUCTURE OF A CRISPR ASSOCIATED PROTEIN CAS2 FROM DESULFOVIBRIO VULGARIS	3.1
3OQ7	CRYSTAL STRUCTURES OF MULTIDRUG-RESISTANT CLINICAL ISOLATE 769 HIV-1 PROTEASE VARIANTS	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
3OQA	CRYSTAL STRUCTURES OF MULTIDRUG-RESISTANT CLINICAL ISOLATE 769 HIV-1 PROTEASE VARIANTS	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
3OQC	UBIQUITIN-FOLD MODIFIER 1 SPECIFIC PROTEASE, UFSP2	3.4.22
3OQD	CRYSTAL STRUCTURES OF MULTIDRUG-RESISTANT CLINICAL ISOLATE 769 HIV-1 PROTEASE VARIANTS	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
3OQE	STRUCTURE OF OPDA MUTANT Y257F	3.1.8.1
3OQF	CRYSTAL STRUCTURE ANALYSIS OF RENIN-INDOLE-PIPERAZINE INHIBITOR COMPLEXES	3.4.23.15
3OQK	CRYSTAL STRUCTURE ANALYSIS OF RENIN-INDOLE-PIPERAZIN INHIBITOR COMPLEXES	3.4.23.15
3OQY	SEMI-SYNTHETIC RIBONUCLEASE S: PARA-CYANO-PHENYLALANINE AT POSITION 8	3.1.27.5 4.6.1.18
3OQZ	SEMI-SYNTHETIC RIBONUCLEASE S: META-CYANO-PHENYLALANINE AT POSITION 8	3.1.27.5 4.6.1.18
3OR0	SEMI-SYNTHETIC RIBONUCLEASE S: CYANYLATED HOMOCYSTEINE AT POSITION 13	3.1.27.5 4.6.1.18
3ORW	CRYSTAL STRUCTURE OF THERMOPHILIC PHOSPHOTRIESTERASE FROM GEOBACILLUS KAUSTOPHILUS HTA426	3.5
3ORY	CRYSTAL STRUCTURE OF FLAP ENDONUCLEASE 1 FROM HYPERTHERMOPHILIC ARCHAEON DESULFUROCOCCUS AMYLOLYTICUS	3.1
3OS0	PFV STRAND TRANSFER COMPLEX (STC) AT 2.81 A RESOLUTION	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OS1	PFV TARGET CAPTURE COMPLEX (TCC) AT 2.97 A RESOLUTION	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OS2	PFV TARGET CAPTURE COMPLEX (TCC) AT 3.32 A RESOLUTION	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OSH	CRYSTAL STRUCTURE OF THE COMPLEX OF GROUP 1 PHOSPHOLIPASE A2 WITH ATROPIN AT 1.5 A RESOLUTION	3.1.1.4
3OSL	STRUCTURE OF BOVINE THROMBIN-ACTIVATABLE FIBRINOLYSIS INHIBITOR IN COMPLEX WITH TICK CARBOXYPEPTIDASE INHIBITOR	3.4.17.20
3OSO	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS L25A AT CRYOGENIC TEMPERATURE	3.1.31.1
3OSZ	CRYSTAL STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH AN ANTIMICROBIAL NONAPEPTIDE, AT 2.26 A RESOLUTION	3.4.21.64
3OT4	STRUCTURE AND CATALYTIC MECHANISM OF BORDETELLA BRONCHISEPTICA NICF	3.5.1.107
3OTJ	A CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH BPTI (BOVINE PANCREATIC TRYPSIN INHIBITOR) BY X-RAY/NEUTRON JOINT REFINEMENT	3.4.21.4
3OTQ	SOLUBLE EPOXIDE HYDROLASE IN COMPLEX WITH PYRAZOLE ANTAGONIST	3.3.2.10 3.1.3.76
3OTS	MDR769 HIV-1 PROTEASE COMPLEXED WITH MA/CA HEPTA-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
3OTY	MDR769 HIV-1 PROTEASE COMPLEXED WITH RT/RH HEPTA-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
3OU0	RE-REFINED 3CS0	3.4.21 3.4.21.107
3OU1	MDR769 HIV-1 PROTEASE COMPLEXED WITH RH/IN HEPTA-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
3OU3	MDR769 HIV-1 PROTEASE COMPLEXED WITH PR/RT HEPTA-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
3OU4	MDR769 HIV-1 PROTEASE COMPLEXED WITH TF/PR HEPTA-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
3OU8	THE CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE FROM PSEUDOMONAS AERUGINOSA	3.5.4.4 3.5.4.2
3OUA	MDR769 HIV-1 PROTEASE COMPLEXED WITH P1/P6 HEPTA-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
3OUB	MDR769 HIV-1 PROTEASE COMPLEXED WITH NC/P1 HEPTA-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
3OUC	MDR769 HIV-1 PROTEASE COMPLEXED WITH P2/NC HEPTA-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
3OUD	MDR769 HIV-1 PROTEASE COMPLEXED WITH CA/P2 HEPTA-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
3OUR	CRYSTAL STRUCTURE OF COMPLEX BETWEEN EIIA AND A NOVEL PYRUVATE DECARBOXYLASE	3.1.1.1
3OVG	THE CRYSTAL STRUCTURE OF AN AMIDOHYDROLASE FROM MYCOPLASMA SYNOVIAE WITH ZN ION BOUND	3.1.1.25
3OVK	CRYSTAL STRUCTURE OF AN XXA-PRO AMINOPEPTIDASE FROM STREPTOCOCCUS PYOGENES	3.4.13.9
3OVN	FRAGMENT-BASED APPROACH TO THE DESIGN OF LIGANDS TARGETING A NOVEL SITE ON HIV-1 INTEGRASE	2.7.7.49 3.1.13.2 3.1.26.13
3OVW	ENDOGLUCANASE I NATIVE STRUCTURE	3.2.1.4
3OVX	CATHEPSIN S IN COMPLEX WITH A COVALENT INHIBITOR WITH AN ALDEHYDE WARHEAD	3.4.22.27
3OVZ	CATHEPSIN K IN COMPLEX WITH A COVALENT INHIBITOR WITH A KETOAMIDE WARHEAD	3.4.22.38
3OWF	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS V66R AT CRYOGENIC TEMPERATURE	3.1.31.1
3OWN	POTENT MACROCYCLIC RENIN INHIBITORS	3.4.23.15
3OWV	STRUCTURAL INSIGHTS INTO CATALYTIC AND SUBSTRATE BINDING MECHANISMS OF THE STRATEGIC ENDA NUCLEASE FROM STREPTOCOCCUS PNEUMONIAE	3.1.30
3OXC	WILD TYPE HIV-1 PROTEASE WITH ANTIVIRAL DRUG SAQUINAVIR	3.4.23.16
3OXK	CRYSTAL STRUCTURE OF A HISTIDINE TRIAD FAMILY PROTEIN FROM ENTAMOEBA HISTOLYTICA, BOUND TO GMP	3
3OXV	CRYSTAL STRUCTURE OF HIV-1 I50V, A71 PROTEASE IN COMPLEX WITH THE PROTEASE INHIBITOR AMPRENAVIR.	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
3OXW	CRYSTAL STRUCTURE OF HIV-1 I50V, A71V PROTEASE IN COMPLEX WITH THE PROTEASE INHIBITOR DARUNAVIR	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
3OXX	CRYSTAL STRUCTURE OF HIV-1 I50V, A71V PROTEASE IN COMPLEX WITH THE PROTEASE INHIBITOR 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
3OY4	CRYSTAL STRUCTURE OF HIV-1 L76V PROTEASE IN COMPLEX WITH THE PROTEASE INHIBITOR DARUNAVIR.	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
3OY9	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MANGANESE AT 2.55 RESOLUTION	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYA	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND RALTEGRAVIR AT 2.65 RESOLUTION	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYB	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND THE INSTI MK2048	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYC	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND THE INSTI PICA	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYD	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND THE INSTI GS9160	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYE	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND THE INSTI COMPOUND2	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYF	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND THE INSTI L-870,810	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYG	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND THE INSTI COMPOUND1 (COMPOUNDG)	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYH	CRYSTAL STRUCTURE OF THE PROTOTYPE FOAMY VIRUS (PFV) INTASOME IN COMPLEX WITH MAGNESIUM AND THE INSTI MK0536	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYI	CRYSTAL STRUCTURE OF THE PFV S217Q MUTANT INTASOME IN COMPLEX WITH MANGANESE	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYJ	CRYSTAL STRUCTURE OF THE PFV S217Q MUTANT INTASOME IN COMPLEX WITH MAGNESIUM AND THE INSTI MK2048	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYK	CRYSTAL STRUCTURE OF THE PFV S217H MUTANT INTASOME BOUND TO MANGANESE	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYL	CRYSTAL STRUCTURE OF THE PFV S217H MUTANT INTASOME BOUND TO MAGNESIUM AND THE INSTI MK2048	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYM	CRYSTAL STRUCTURE OF THE PFV N224H MUTANT INTASOME BOUND TO MANGANESE	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYN	CRYSTAL STRUCTURE OF THE PFV N224H MUTANT INTASOME BOUND TO MAGNESIUM AND THE INSTI MK2048	2.7.7.49 2.7.7.7 3.1.26.4 3.4.23 2.7.7 3.1
3OYP	HCV NS3/4A IN COMPLEX WITH LIGAND 3	3.4.21.98 3.6.1.15 3.6.4.13 3.4.22 2.7.7.48
3OZI	CRYSTAL STRUCTURE OF THE TIR DOMAIN FROM THE FLAX DISEASE RESISTANCE PROTEIN L6	3.2.2.6
3OZO	CRYSTAL STRUCTURE OF INSECT BETA-N-ACETYL-D-HEXOSAMINIDASE OFHEX1 COMPLEXED WITH NGT	3.2.1.52
3OZP	CRYSTAL STRUCTURE OF INSECT BETA-N-ACETYL-D-HEXOSAMINIDASE OFHEX1 COMPLEXED WITH PUGNAC	3.2.1.52
3P05	X-RAY STRUCTURE OF PENTAMERIC 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
3P06	CRYSTAL STRUCTURE OF TELLINA VIRUS 1 VP4 PROTEASE IN THE FORM OF AN INTRA-MOLECULAR(CIS)ACYL-ENZYME COMPLEX.	3.4.21.115
3P09	CRYSTAL STRUCTURE OF BETA-LACTAMASE FROM FRANCISELLA TULARENSIS	3.5.2.6
3P0G	STRUCTURE OF A NANOBODY-STABILIZED ACTIVE STATE OF THE BETA2 ADRENOCEPTOR	3.2.1.17
3P17	THROMBIN INHIBITION BY PYRIDIN DERIVATIVES	3.4.21.5
3P1G	CRYSTAL STRUCTURE OF THE XENOTROPIC MURINE LEUKEMIA VIRUS-RELATED VIRUS (XMRV) RNASE H DOMAIN	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
3P1H	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS V23K/I92A AT CRYOGENIC TEMPERATURE	3.1.31.1
3P20	CRYSTAL STRUCTURE OF VANADATE BOUND SUBUNIT A OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3P23	CRYSTAL STRUCTURE OF THE HUMAN KINASE AND RNASE DOMAINS IN COMPLEX WITH ADP	2.7.11.1 3.1.26
3P24	STRUCTURE OF PROFRAGILYSIN-3 FROM BACTEROIDES FRAGILIS	3.4.24.74
3P2J	CRYSTAL STRUCTURE OF PEPTIDYL-TRNA HYDROLASE FROM MYCOBACTERIUM SMEGMATIS AT 2.2 A RESOLUTION	3.1.1.29
3P2L	CRYSTAL STRUCTURE OF ATP-DEPENDENT CLP PROTEASE SUBUNIT P FROM FRANCISELLA TULARENSIS	3.4.21.92
3P2M	CRYSTAL STRUCTURE OF A NOVEL ESTERASE RV0045C FROM MYCOBACTERIUM TUBERCULOSIS	3
3P2N	DISCOVERY AND STRUCTURAL CHARACTERIZATION OF A NEW GLYCOSIDE HYDROLASE FAMILY ABUNDANT IN COASTAL WATERS THAT WAS ANNOTATED AS 'HYPOTHETICAL PROTEIN'	3.2.1.159
3P2O	CRYSTAL STRUCTURE OF FOLD BIFUNCTIONAL PROTEIN FROM CAMPYLOBACTER JEJUNI	1.5.1.5 3.5.4.9
3P2P	ENHANCED ACTIVITY AND ALTERED SPECIFICITY OF PHOSPHOLIPASE A2 BY DELETION OF A SURFACE LOOP	3.1.1.4
3P2Q	CRYSTAL STRUCTURE OF THE FLUOROACETYL-COA-SPECIFIC THIOESTERASE, FLK	3.1.2.29
3P2R	CRYSTAL STRUCTURE OF THE FLUOROACETYL-COA-SPECIFIC THIOESTERASE FLK IN COMPLEX WITH FLUOROACETATE	3.1.2.29
3P2U	CRYSTAL STRUCTURE OF PHNP IN COMPLEX WITH ORTHOVANADATE	3.1.4.55
3P32	HYDROLYSIS OF GTP TO GDP BY AN MCM-ASSOCIATED AND MEAB- AND MMAA-LIKE G-PROTEIN FROM MYCOBACTERIUM TUBERCULOSIS	3.6
3P3C	CRYSTAL STRUCTURE OF THE AQUIFEX AEOLICUS LPXC/LPC-009 COMPLEX	3.5.1 3.5.1.108
3P3E	CRYSTAL STRUCTURE OF THE PSEUDOMONAS AERUGINOSA LPXC/LPC-009 COMPLEX	3.5.1 3.5.1.108
3P3F	CRYSTAL STRUCTURE OF THE F36A MUTANT OF THE FLUOROACETYL-COA-SPECIFIC THIOESTERASE FLK	3.1.2.29
3P3G	CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI LPXC/LPC-009 COMPLEX	3.5.1
3P3I	CRYSTAL STRUCTURE OF THE F36A MUTANT OF THE FLUOROACETYL-COA-SPECIFIC THIOESTERASE FLK IN COMPLEX WITH FLUOROACETATE AND COA	3.1.2.29
3P45	CRYSTAL STRUCTURE OF APO-CASPASE-6 AT PHYSIOLOGICAL PH	3.4.22.59
3P48	STRUCTURE OF THE YEAST DUTPASE DUT1 IN COMPLEX WITH DUMPNPP	3.6.1.23
3P4U	CRYSTAL STRUCTURE OF ACTIVE CASPASE-6 IN COMPLEX WITH AC-VEID-CHO INHIBITOR	3.4.22.59
3P4X	HELICASE DOMAIN OF REVERSE GYRASE FROM THERMOTOGA MARITIMA	3.6.4.12 5.6.2.2
3P4Y	HELICASE DOMAIN OF REVERSE GYRASE FROM THERMOTOGA MARITIMA - P2 FORM	3.6.4.12 5.6.2.2
3P4Z	TIME-DEPENDENT AND PROTEIN-DIRECTED IN SITU GROWTH OF GOLD NANOPARTICLES IN A SINGLE CRYSTAL OF LYSOZYME	3.2.1.17
3P54	CRYSTAL STRUCTURE OF THE JAPANESE ENCEPHALITIS VIRUS ENVELOPE PROTEIN, STRAIN SA-14-14-2.	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
3P56	THE STRUCTURE OF THE HUMAN RNASE H2 COMPLEX DEFINES KEY INTERACTION INTERFACES RELEVANT TO ENZYME FUNCTION AND HUMAN DISEASE	3.1.26.4
3P5B	THE STRUCTURE OF THE LDLR/PCSK9 COMPLEX REVEALS THE RECEPTOR IN AN EXTENDED CONFORMATION	3.4.21
3P5C	THE STRUCTURE OF THE LDLR/PCSK9 COMPLEX REVEALS THE RECEPTOR IN AN EXTENDED CONFORMATION	3.4.21
3P5J	THE STRUCTURE OF THE HUMAN RNASE H2 COMPLEX DEFINES KEY INTERACTION INTERFACES RELEVANT TO ENZYME FUNCTION AND HUMAN DISEASE	3.1.26.4
3P5S	STRUCTURAL INSIGHTS INTO THE CATALYTIC MECHANISM OF CD38: EVIDENCE FOR A CONFORMATIONALLY FLEXIBLE COVALENT ENZYME-SUBSTRATE COMPLEX	3.2.2.5 2.4.99.20 3.2.2.6
3P5U	ACTINIDIN FROM ACTINIDIA ARGUTA PLANCH (SARUSASHI)	3.4.22.14
3P5V	ACTINIDIN FROM ACTINIDIA ARGUTA PLANCH (SARUSASHI)	3.4.22.14
3P5W	ACTINIDIN FROM ACTINIDIA ARGUTA PLANCH (SARUSASHI)	3.4.22.14
3P5X	ACTINIDIN FROM ACTINIDIA ARGUTA PLANCH (SARUSASHI)	3.4.22.14
3P64	TIME-DEPENDENT AND PROTEIN-DIRECTED IN SITU GROWTH OF GOLD NANOPARTICLES IN A SINGLE CRYSTAL OF LYSOZYME	3.2.1.17
3P65	TIME-DEPENDENT AND PROTEIN-DIRECTED IN SITU GROWTH OF GOLD NANOPARTICLES IN A SINGLE CRYSTAL OF LYSOZYME	3.2.1.17
3P66	TIME-DEPENDENT AND PROTEIN-DIRECTED IN SITU GROWTH OF GOLD NANOPARTICLES IN A SINGLE CRYSTAL OF LYSOZYME	3.2.1.17
3P68	TIME-DEPENDENT AND PROTEIN-DIRECTED IN SITU GROWTH OF GOLD NANOPARTICLES IN A SINGLE CRYSTAL OF LYSOZYME	3.2.1.17
3P6B	THE CRYSTAL STRUCTURE OF CELK CBM4 FROM CLOSTRIDIUM THERMOCELLUM	3.2.1.91
3P6Z	STRUCTURAL BASIS OF THROMBIN MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION	3.4.21.5
3P70	STRUCTURAL BASIS OF THROMBIN-MEDIATED FACTOR V ACTIVATION: ESSENTIAL ROLE OF THE HIRUDIN-LIKE SEQUENCE GLU666-GLU672 FOR PROCESSING AT THE HEAVY CHAIN-B DOMAIN JUNCTION	3.4.21.5
3P71	CRYSTAL STRUCTURE OF THE COMPLEX OF LCMT-1 AND PP2A	3.1.3.16
3P75	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS V104D AT CRYOGENIC TEMPERATURE	3.1.31.1
3P76	X-RAY CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS LPXC COMPLEXED SCH1379777	3.5.1 3.5.1.108
3P7L	RAT INSULIN DEGRADING ENZYME (INSULYSIN)	3.4.24.56
3P7O	RAT INSULIN DEGRADING ENZYME (INSULYSIN) E111F MUTANT WITH TWO BOUND PEPTIDES	3.4.24.56
3P7P	RADIATION DAMAGE STUDY OF THERMOLYSIN - 100K STRUCTURE A (0.1 MGY)	3.4.24.27
3P7Q	RADIATION DAMAGE STUDY OF THERMOLYSIN - 100K STRUCTURE B (2.5 MGY)	3.4.24.27
3P7R	RADIATION DAMAGE STUDY OF THERMOLYSIN - 100K STRUCTURE C (4.9 MGY)	3.4.24.27
3P7S	RADIATION DAMAGE STUDY OF THERMOLYSIN - 100K STRUCTURE D (7.2 MGY)	3.4.24.27
3P7T	RADIATION DAMAGE STUDY OF THERMOLYSIN - 160K STRUCTURE A (0.1 MGY)	3.4.24.27
3P7U	RADIATION DAMAGE STUDY OF THERMOLYSIN - 160K STRUCTURE B (2.4 MGY)	3.4.24.27
3P7V	RADIATION DAMAGE STUDY OF THERMOLYSIN - 160K STRUCTURE C (4.8 MGY)	3.4.24.27
3P7W	RADIATION DAMAGE STUDY OF THERMOLYSIN - 160K STRUCTURE D (7.1 MGY)	3.4.24.27
3P8E	CRYSTAL STRUCTURE OF HUMAN DIMETHYLARGININE DIMETHYLAMINOHYDROLASE-1 (DDAH-1) COVALENTLY BOUND WITH N5-(1-IMINOPENTYL)-L-ORNITHINE	3.5.3.18
3P8F	CRYSTAL STRUCTURE OF MT-SP1 IN COMPLEX WITH SFTI-1	3.4.21.109
3P8G	CRYSTAL STRUCTURE OF MT-SP1 IN COMPLEX WITH BENZAMIDINE	3.4.21.109
3P8N	CRYSTAL STRUCTURE OF HCV NS3/NS4A PROTEASE COMPLEXED WITH BI 201335	3.4.21.98 3.4.22 3.6.1.15 3.6.4.13 2.7.7.48
3P8O	CRYSTAL STRUCTURE OF HCV NS3/NS4A PROTEASE COMPLEXED WITH DES-BROMINE ANALOGUE OF BI 201335	3.4.21.98 3.4.22 3.6.1.15 3.6.4.13 2.7.7.48
3P8P	CRYSTAL STRUCTURE OF HUMAN DIMETHYLARGININE DIMETHYLAMINOHYDROLASE-1 (DDAH-1) VARIANT C274S BOUND WITH N5-(1-IMINOPENTYL)-L-ORNITHINE	3.5.3.18
3P8Z	DENGUE METHYLTRANSFERASE BOUND TO A SAM-BASED INHIBITOR	2.1.1.56 2.1.1.57 3.4.21.91 3.6.1.15 3.6.4.13 2.7.7.48
3P92	HUMAN MESOTRYPSIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR VARIANT (BPTI-K15R/R17G)	3.4.21.4
3P95	HUMAN MESOTRYPSIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR VARIANT (BPTI-K15R/R17D)	3.4.21.4
3P96	CRYSTAL STRUCTURE OF PHOSPHOSERINE PHOSPHATASE SERB FROM MYCOBACTERIUM AVIUM, NATIVE FORM	3.1.3.3
3P97	DENGUE 3 NS5 METHYLTRANSFERASE BOUND TO THE SUBSTRATE S-ADENOSYL METHIONINE	2.1.1.56 2.1.1.57 3.4.21.91 3.6.1.15 3.6.4.13 2.7.7.48
3P98	THE CRYSTAL STRUCTURE OF THE EXTENDED SPECTRUM BETA-LACTAMASE TEM-72 REVEALS INHIBITION BY CITRATE	3.5.2.6
3P9Y	CRYSTAL STRUCTURE OF THE DROSOPHILA MELANOGASTER SSU72-PCTD COMPLEX	3.1.3.16
3PAE	CRYSTAL STRUCTURE OF THE K84D MUTANT OF OXA-24/40 IN COMPLEX WITH DORIPENEM	3.5.2.6
3PAG	CRYSTAL STRUCTURE OF THE V130D MUTANT OF OXA-24/40 IN COMPLEX WITH DORIPENEM	3.5.2.6
3PAN	THE CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE WITH HYPOXANTHINE BOUND FROM PSEUDOMONAS AERUGINOSA	3.5.4.4 3.5.4.2
3PAO	THE CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE WITH ADENINE BOUND FROM PSEUDOMONAS AERUGINOSA	3.5.4.4 3.5.4.2
3PB1	CRYSTAL STRUCTURE OF A MICHAELIS COMPLEX BETWEEN PLASMINOGEN ACTIVATOR INHIBITOR-1 AND UROKINASE-TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
3PB5	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PBC	PEPTIDASE MODULE OF THE PEPTIDOGLYCAN HYDROLASE RIPA (RV1477) FROM MYCOBACTERIUM TUBERCULOSIS AT 1.38 RESOLUTION	3.4
3PBD	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PBG	6-PHOSPHO-BETA-GALACTOSIDASE FORM-C	3.2.1.85
3PBH	REFINED CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN B AT 2.5 ANGSTROM RESOLUTION	3.4.22.1
3PBI	STRUCTURE OF THE PEPTIDOGLYCAN HYDROLASE RIPB (RV1478) FROM MYCOBACTERIUM TUBERCULOSIS AT 1.6 RESOLUTION	3.4
3PBL	STRUCTURE OF THE HUMAN DOPAMINE D3 RECEPTOR IN COMPLEX WITH ETICLOPRIDE	3.2.1.17
3PBM	THE CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE IN COMPLEX WITH CHLOROPURINE FROM PSEUDOMONAS AERUGINOSA	3.5.4.4 3.5.4.2
3PBN	CRYSTAL STRUCTURE OF APO PBP3 FROM PSEUDOMONAS AERUGINOSA	3.4.16.4
3PBO	CRYSTAL STRUCTURE OF PBP3 COMPLEXED WITH CEFTAZIDIME	3.4.16.4
3PBQ	CRYSTAL STRUCTURE OF PBP3 COMPLEXED WITH IMIPENEM	3.4.16.4
3PBR	CRYSTAL STRUCTURE OF PBP3 COMPLEXED WITH MEROPENEM	3.4.16.4
3PBS	CRYSTAL STRUCTURE OF PBP3 COMPLEXED WITH AZTREONAM	3.4.16.4
3PBT	CRYSTAL STRUCTURE OF PBP3 COMPLEXED WITH MC-1	3.4.16.4
3PBZ	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PCT	STRUCTURE OF THE CLASS C ACID PHOSPHATASE FROM PASTEURELLA MULTOCIDA	3.1.3.2
3PCW	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PCX	CASPASE-3 E246A, K242A DOUBLE MUTANT	3.4.22.56
3PCZ	ENDOTHIAPEPSIN IN COMPLEX WITH BENZAMIDINE	3.4.23.22
3PD0	CASPASE-3 E246A	3.4.22.56
3PD1	CASPASE-3 K242A	3.4.22.56
3PDC	CRYSTAL STRUCTURE OF HYDROLASE DOMAIN OF HUMAN SOLUBLE EPOXIDE HYDROLASE COMPLEXED WITH A BENZOXAZOLE INHIBITOR	3.3.2.10 3.1.3.76
3PDD	STRUCTURES OF CLOSTRIDIUM THERMOCELLUM CBHA FIBRONECTIN(III)-LIKE MODULES	3.2.1
3PDF	DISCOVERY OF NOVEL CYANAMIDE-BASED INHIBITORS OF CATHEPSIN C	3.4.14.1
3PDG	STRUCTURES OF CLOSTRIDIUM THERMOCELLUM CBHA FIBRONECTIN(III)-LIKE MODULES	3.2.1
3PDH	STRUCTURE OF SIR2TM BOUND TO A PROPIONYLATED PEPTIDE	3.5.1 2.3.1.286
3PDS	IRREVERSIBLE AGONIST-BETA2 ADRENOCEPTOR COMPLEX	3.2.1.17
3PDW	CRYSTAL STRUCTURE OF PUTATIVE P-NITROPHENYL PHOSPHATASE FROM BACILLUS SUBTILIS	3.1.3
3PDZ	SOLUTION STRUCTURE OF THE PDZ2 DOMAIN FROM HUMAN PHOSPHATASE HPTP1E	3.1.3.48
3PE6	CRYSTAL STRUCTURE OF A SOLUBLE FORM OF HUMAN MGLL IN COMPLEX WITH AN INHIBITOR	3.1.1.23
3PE9	STRUCTURES OF CLOSTRIDIUM THERMOCELLUM CBHA FIBRONECTIN(III)-LIKE MODULES	3.2.1
3PEI	CRYSTAL STRUCTURE OF CYTOSOL AMINOPEPTIDASE FROM FRANCISELLA TULARENSIS	3.4.11.1 3.4.11.10
3PEN	STRUCTURE OF ARCHAEAL INITIATION FACTOR AIF2GAMMA SUBUNIT DELTA 37-47 FROM SULFOLOBUS SOLFATARICUS IN THE GDP-BOUND FORM.	3.6.5.3
3PEP	REVISED 2.3 ANGSTROMS STRUCTURE OF PORCINE PEPSIN. EVIDENCE FOR A FLEXIBLE SUBDOMAIN	3.4.23.1
3PEU	S. CEREVISIAE DBP5 L327V C-TERMINAL DOMAIN BOUND TO GLE1 H337R AND IP6	3.6.4.13
3PEV	S. CEREVISIAE DBP5 L327V C-TERMINAL DOMAIN BOUND TO GLE1 AND IP6	3.6.4.13
3PEW	S. CEREVISIAE DBP5 L327V BOUND TO RNA AND ADP BEF3	3.6.4.13
3PEY	S. CEREVISIAE DBP5 BOUND TO RNA AND ADP BEF3	3.6.4.13
3PF8	CRYSTAL STRUCTURE OF THE LACTOBACILLUS JOHNSONII CINNAMOYL ESTERASE LJ0536	3.1.1
3PF9	CRYSTAL STRUCTURE OF THE LACTOBACILLUS JOHNSONII CINNAMOYL ESTERASE LJ0536 S106A MUTANT	3.1.1
3PFB	CRYSTAL STRUCTURE OF THE LACTOBACILLUS JOHNSONII CINNAMOYL ESTERASE LJ0536 S106A MUTANT IN COMPLEX WITH ETHYLFERULATE	3.1.1
3PFC	CRYSTAL STRUCTURE OF THE LACTOBACILLUS JOHNSONII CINNAMOYL ESTERASE LJ0536 S106A MUTANT IN COMPLEX WITH FERULIC ACID	3.1.1
3PFI	2.7 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF A PROBABLE HOLLIDAY JUNCTION DNA HELICASE (RUVB) FROM CAMPYLOBACTER JEJUNI SUBSP. JEJUNI NCTC 11168 IN COMPLEX WITH ADENOSINE-5'-DIPHOSPHATE	3.6.4.12
3PFJ	CRYSTAL STRUCTURE OF CEL7A FROM TALAROMYCES EMERSONII	3.2.1.91 3.2.1
3PFO	CRYSTAL STRUCTURE OF A PUTATIVE ACETYLORNITHINE DEACETYLASE (RPA2325) FROM RHODOPSEUDOMONAS PALUSTRIS CGA009 AT 1.90 A RESOLUTION	3.5.1.16
3PFX	CRYSTAL STRUCTURE OF CEL7A FROM TALAROMYCES EMERSONII IN COMPLEX WITH CELLOBIOSE	3.2.1.91 3.2.1
3PFY	THE CATALYTIC DOMAIN OF HUMAN OTUD5	3.4.19.12
3PFZ	CRYSTAL STRUCTURE OF CEL7A FROM TALAROMYCES EMERSONII IN COMPLEX WITH CELLOTETRAOSE	3.2.1.91 3.2.1
3PG4	THE CRYSTAL STRUCTURE OF NEW DELHI METALLO-BETA LACTAMASE (NDM-1)	3.5.2.6
3PGA	STRUCTURAL CHARACTERIZATION OF PSEUDOMONAS 7A GLUTAMINASE-ASPARAGINASE	3.5.1.1 3.5.1.38
3PGI	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PGL	CRYSTAL STRUCTURE OF HUMAN SMALL C-TERMINAL DOMAIN PHOSPHATASE 1 (SCP1) BOUND TO RABEPRAZOLE	3.1.3.16
3PHD	CRYSTAL STRUCTURE OF HUMAN HDAC6 IN COMPLEX WITH UBIQUITIN	3.5.1.98 3.5.1
3PHN	CRYSTAL STRUCTURE OF WILD-TYPE ONCONASE WITH RESOLUTION 1.46 A	3.1.27
3PHU	OTU DOMAIN OF CRIMEAN CONGO HEMORRHAGIC FEVER VIRUS	3.4.19.12 2.7.7.48
3PHV	X-RAY ANALYSIS OF HIV-1 PROTEINASE AT 2.7 ANGSTROMS RESOLUTION CONFIRMS STRUCTURAL HOMOLOGY AMONG RETROVIRAL ENZYMES	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
3PHW	OTU DOMAIN OF CRIMEAN CONGO HEMORRHAGIC FEVER VIRUS IN COMPLEX WITH UBIQUITIN	3.4.19.12 2.7.7.48
3PHX	OTU DOMAIN OF CRIMEAN CONGO HEMORRHAGIC FEVER VIRUS IN COMPLEX WITH ISG15	3.4.19.12 2.7.7.48
3PI0	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PI5	CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE IN COMPLEX WITH BFG356	3.4.23.46
3PIC	GLUCURONOYL ESTERASE CATALYTIC DOMAIN (CIP2_GE) FROM HYPOCREA JECORINA	3.1.1
3PIG	BETA-FRUCTOFURANOSIDASE FROM BIFIDOBACTERIUM LONGUM	3.2.1.26
3PIJ	BETA-FRUCTOFURANOSIDASE FROM BIFIDOBACTERIUM LONGUM - COMPLEX WITH FRUCTOSE	3.2.1.26
3PIR	CRYSTAL STRUCTURE OF M-RASD41E IN COMPLEX WITH GPPNHP (TYPE 1)	3.6.5.2
3PIT	CRYSTAL STRUCTURE OF M-RASD41E IN COMPLEX WITH GPPNHP (TYPE 2)	3.6.5.2
3PJ6	CRYSTAL STRUCTURES OF MULTIDRUG-RESISTANT CLINICAL ISOLATE 769 HIV-1 PROTEASE VARIANTS	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
3PJQ	TRYPANOSOMA CRUZI TRANS-SIALIDASE-LIKE INACTIVE ISOFORM (INCLUDING THE NATURAL MUTATION TYR342HIS) IN COMPLEX WITH LACTOSE	3.2.1.18
3PJR	HELICASE SUBSTRATE COMPLEX	3.6.1 3.6.4.12
3PKA	M. TUBERCULOSIS METAP WITH BENGAMIDE ANALOG Y02, IN MN FORM	3.4.11.18
3PKB	M. TUBERCULOSIS METAP WITH BENGAMIDE ANALOG Y16, IN MN FORM	3.4.11.18
3PKC	M. TUBERCULOSIS METAP WITH BENGAMIDE ANALOG Y08, IN MN FORM	3.4.11.18
3PKD	M. TUBERCULOSIS METAP WITH BENGAMIDE ANALOG Y10, IN MN FORM	3.4.11.18
3PKE	M. TUBERCULOSIS METAP WITH BENGAMIDE ANALOG Y10, IN NI FORM	3.4.11.18
3PKI	HUMAN SIRT6 CRYSTAL STRUCTURE IN COMPLEX WITH ADP RIBOSE	3.5.1 2.3.1.286
3PKJ	HUMAN SIRT6 CRYSTAL STRUCTURE IN COMPLEX WITH 2'-N-ACETYL ADP RIBOSE	3.5.1 2.3.1.286
3PKM	CRYSTAL STRUCTURE OF CAS6 WITH ITS SUBSTRATE RNA	3.1
3PL1	DETERMINATION OF THE CRYSTAL STRUCTURE OF THE PYRAZINAMIDASE FROM M.TUBERCULOSIS : A STRUCTURE-FUNCTION ANALYSIS FOR PREDICTION RESISTANCE TO PYRAZINAMIDE.	3.5.1.19 3.5.1
3PL3	CRYSTAL STRUCTURE OF CEL7A FROM TALAROMYCES EMERSONII IN COMPLEX WITH CELLOPENTAOSE	3.2.1.91 3.2.1
3PLB	BOVINE TRYPSIN VARIANT X(TRIPLEILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3PLD	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PLK	BOVINE TRYPSIN VARIANT X(TRIPLEILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3PLL	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PLP	BOVINE TRYPSIN VARIANT X(TRIPLEILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3PM3	BOVINE TRYPSIN VARIANT X(TRIPLEILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3PM4	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PMA	2.2 ANGSTROM CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN BOVINE THROMBIN AND SUCROSE OCTASULFATE	3.4.21.5
3PMB	2.9 ANGSTROM CRYSTAL STRUCTURE OF BOVINE THROMBIN IN TETRAGONAL SPACEGROUP	3.4.21.5
3PMF	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS V23A AT CRYOGENIC TEMPERATURE	3.1.31.1
3PMH	MECHANISM OF SULFOTYROSINE-MEDIATED GLYCOPROTEIN IB INTERACTION WITH TWO DISTINCT ALPHA-THROMBIN SITES	3.4.21.5
3PMJ	BOVINE TRYPSIN VARIANT X(TRIPLEILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3PMS	RECOMBINANT PEPTIDE: N-GLYCANASE F (PNGASE F)	3.5.1.52
3PMU	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PMY	ENDOTHIAPEPSIN IN COMPLEX WITH A FRAGMENT	3.4.23.22
3PN2	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PETIDE DEFORMYLASE 1B (ATPDF1B) (CRYSTALLIZED IN PEG-550-MME)	3.5.1.88
3PN3	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PETIDE DEFORMYLASE 1B (ATPDF1B) IN COMPLEX WITH INHIBITOR 21	3.5.1.88
3PN4	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PETIDE DEFORMYLASE 1B (ATPDF1B) IN COMPLEX WITH ACTINONIN (CRYSTALLIZED IN PEG-550-MME)	3.5.1.88
3PN5	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PETIDE DEFORMYLASE 1B (ATPDF1B) G41Q MUTANT	3.5.1.88
3PN6	CRYSTAL STRUCTURE OF ARABIDOPSIS THALIANA PETIDE DEFORMYLASE 1B (ATPDF1B) G41M MUTANT	3.5.1.88
3PN8	THE CRYSTAL STRUCTURE OF 6-PHOSPHO-BETA-GLUCOSIDASE FROM STREPTOCOCCUS MUTANS UA159	3.2.1.86
3PN9	CRYSTAL STRUCTURE OF A PROLINE DIPEPTIDASE FROM STREPTOCOCCUS PNEUMONIAE TIGR4	3.4.13.9
3PNR	STRUCTURE OF PBICP-C IN COMPLEX WITH FALCIPAIN-2	3.4.22
3PNT	CRYSTAL STRUCTURE OF THE STREPTOCOCCUS PYOGENES NAD+ GLYCOHYDROLASE SPN IN COMPLEX WITH IFS, THE IMMUNITY FACTOR FOR SPN	3.2.2.5
3PNU	2.4 ANGSTROM CRYSTAL STRUCTURE OF DIHYDROOROTASE (PYRC) FROM CAMPYLOBACTER JEJUNI.	3.5.2.3
3PO1	THROMBIN IN COMPLEX WITH BENZOTHIAZOLE GUANIDINE	3.4.21.5
3POB	CRYSTAL STRUCTURE OF MASP-1 CUB2 DOMAIN IN COMPLEX WITH THE COLLAGEN-LIKE DOMAIN OF MBL	3.4.21
3POC	THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE	3.2.1
3POE	CRYSTAL STRUCTURE OF THE MASP-1 CUB2 DOMAIN BOUND TO CA2+	3.4.21
3POF	CRYSTAL STRUCTURE OF MASP-1 CUB2 DOMAIN BOUND TO CA2+	3.4.21
3POG	CRYSTAL STRUCTURE OF THE MASP-1 CUB2 DOMAIN BOUND TO CA2+	3.4.21
3POI	CRYSTAL STRUCTURE OF MASP-1 CUB2 DOMAIN BOUND TO METHYLAMINE	3.4.21
3POJ	CRYSTAL STRUCTURE OF MASP-1 CUB2 DOMAIN BOUND TO ETHYLAMINE	3.4.21
3POV	CRYSTAL STRUCTURE OF A SOX-DNA COMPLEX	3.1
3PPA	STRUCTURE OF THE DUSP-UBL DOMAINS OF USP15	3.4.19.12
3PPM	CRYSTAL STRUCTURE OF A NONCOVALENTLY BOUND ALPHA-KETOHETEROCYCLE INHIBITOR (PHENHEXYL/OXADIAZOLE/PYRIDINE) TO A HUMANIZED VARIANT OF FATTY ACID AMIDE HYDROLASE	3.5.1.99 3.1.1
3PR0	CRYSTAL STRUCTURE OF A COVALENTLY BOUND ALPHA-KETOHETEROCYCLE INHIBITOR (PHENHEXYL/OXADIAZOLE/PYRIDINE) TO A HUMANIZED VARIANT OF FATTY ACID AMIDE HYDROLASE	3.5.1.4 3.5.1.99 3.1.1
3PRK	INHIBITION OF PROTEINASE K BY METHOXYSUCCINYL-ALA-ALA-PRO-ALA-CHLOROMETHYL KETONE. AN X-RAY STUDY AT 2.2-ANGSTROMS RESOLUTION	3.4.21.64
3PRO	ALPHA-LYTIC PROTEASE COMPLEXED WITH C-TERMINAL TRUNCATED PRO REGION	3.4.21.12
3PRS	ENDOTHIAPEPSIN IN COMPLEX WITH RITONAVIR	3.4.23.22
3PRT	MUTANT OF THE CARBOXYPEPTIDASE T	3.4.17.18
3PS1	CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI LPXC/LPC-011 COMPLEX	3.5.1
3PS2	CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI LPXC/LPC-012 COMPLEX	3.5.1
3PS3	CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI LPXC/LPC-053 COMPLEX	3.5.1
3PS5	CRYSTAL STRUCTURE OF THE FULL-LENGTH HUMAN PROTEIN TYROSINE PHOSPHATASE SHP-1	3.1.3.48
3PSG	THE HIGH RESOLUTION CRYSTAL STRUCTURE OF PORCINE PEPSINOGEN	3.4.23.1
3PSN	CRYSTAL STRUCTURE OF MOUSE VPS29 COMPLEXED WITH MN2+	3.1.3.3
3PSU	HIV-1 PROTEASE IN COMPLEX WITH AN ISOBUTYL DECORATED OLIGOAMINE (SYMMETRIC BINDING MODE)	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
3PSY	ENDOTHIAPEPSIN IN COMPLEX WITH AN INHIBITOR BASED ON THE GEWALD REACTION	3.4.23.22
3PT1	STRUCTURE OF DUF89 FROM SACCHAROMYCES CEREVISIAE CO-CRYSTALLIZED WITH F6P.	3.1.3
3PTB	THE GEOMETRY OF THE REACTIVE SITE AND OF THE PEPTIDE GROUPS IN TRYPSIN, TRYPSINOGEN AND ITS COMPLEXES WITH INHIBITORS	3.4.21.4
3PTD	PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C MUTANT D274S	3.1.4.10 4.6.1.13
3PTE	THE REFINED CRYSTALLOGRAPHIC STRUCTURE OF A DD-PEPTIDASE PENICILLIN-TARGET ENZYME AT 1.6 A RESOLUTION	3.4.16.4
3PTK	THE CRYSTAL STRUCTURE OF RICE (ORYZA SATIVA L.) OS4BGLU12	3.2.1.21
3PTL	CRYSTAL STRUCTURE OF PROTEINASE K INHIBITED BY A LACTOFERRIN NONAPEPTIDE, LYS-GLY-GLU-ALA-ASP-ALA-LEU-SER-LEU-ASP AT 1.3 A RESOLUTION.	3.4.21.64
3PTM	THE CRYSTAL STRUCTURE OF RICE (ORYZA SATIVA L.) OS4BGLU12 WITH 2-FLUOROGLUCOPYRANOSIDE	3.2.1.21
3PTN	ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY	3.4.21.4
3PTQ	THE CRYSTAL STRUCTURE OF RICE (ORYZA SATIVA L.) OS4BGLU12 WITH DINITROPHENYL 2-DEOXY-2-FLUORO-BETA-D-GLUCOPYRANOSIDE	3.2.1.21
3PUH	COCAINE ESTERASE, WILD-TYPE BIOLOGICALLY ACTIVE DIMER	3.1.1 3.1.1.84
3PUI	COCAINE ESTERASE WITH MUTATIONS G4C, S10C	3.1.1 3.1.1.84
3PUU	CRYSTAL STRUCTURE OF GLU121GLN MUTANT OF E. COLI AMINOPEPTIDASE N	3.4.11.2
3PUV	CRYSTAL STRUCTURE OF AN OUTWARD-FACING MBP-MALTOSE TRANSPORTER COMPLEX BOUND TO ADP-VO4	3.6.3.19 7.5.2.1
3PUW	CRYSTAL STRUCTURE OF AN OUTWARD-FACING MBP-MALTOSE TRANSPORTER COMPLEX BOUND TO ADP-ALF4	3.6.3.19 7.5.2.1
3PUX	CRYSTAL STRUCTURE OF AN OUTWARD-FACING MBP-MALTOSE TRANSPORTER COMPLEX BOUND TO ADP-BEF3	3.6.3.19 7.5.2.1
3PV1	CRYSTAL STRUCTURE OF THE USP15 DUSP-UBL DOMAINS	3.4.19.12
3PV2	STRUCTURE OF LEGIONELLA FALLONII DEGQ (WT)	3.4.21.107
3PV5	STRUCTURE OF LEGIONELLA FALLONII DEGQ (N189G/P190G VARIANT)	3.4.21.107
3PVI	D34G MUTANT OF PVUII ENDONUCLEASE COMPLEXED WITH COGNATE DNA SHOWS THAT ASP34 IS DIRECTLY INVOLVED IN DNA RECOGNITION AND INDIRECTLY INVOLVED IN CATALYSIS	3.1.21.4
3PVK	SECRETED ASPARTIC PROTEASE 2 IN COMPLEX WITH BENZAMIDINE	3.4.23.24
3PWB	BOVINE TRYPSIN VARIANT X(TRIPLEGLU217ILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3PWC	BOVINE TRYPSIN VARIANT X(TRIPLEGLU217ILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3PWM	HIV-1 PROTEASE MUTANT L76V WITH DARUNAVIR	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
3PWR	HIV-1 PROTEASE MUTANT L76V COMPLEXED WITH SAQUINAVIR	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
3PWW	ENDOTHIAPEPSIN IN COMPLEX WITH SAQUINAVIR	3.4.23.22
3PX8	RTA IN COMPLEX WITH 7-CARBOXY-PTERIN	3.2.2.22
3PX9	RTA IN COMPLEX WITH N-(FURANYLMETHYL)-7-CARBAMOYL-PTERIN	3.2.2.22
3PXH	TANDEM IG DOMAINS OF TYROSINE PHOSPHATASE LAR	3.1.3.48
3PXJ	TANDEM IG REPEATS OF DLAR	3.1.3.48
3PYH	BOVINE TRYPSIN VARIANT X(TRIPLEGLU217ILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3PZ9	NATIVE STRUCTURE OF ENDO-1,4-BETA-D-MANNANASE FROM THERMOTOGA PETROPHILA RKU-1	3.2.1.78
3PZG	I222 CRYSTAL FORM OF THE HYPERTHERMOSTABLE ENDO-1,4-BETA-D-MANNANASE FROM THERMOTOGA PETROPHILA RKU-1	3.2.1.78
3PZI	STRUCTURE OF THE HYPERTHERMOSTABLE ENDO-1,4-BETA-D-MANNANASE FROM THERMOTOGA PETROPHILA RKU-1 IN COMPLEX WITH BETA-D-GLUCOSE	3.2.1.78
3PZM	STRUCTURE OF THE HYPERTHERMOSTABLE ENDO-1,4-BETA-D-MANNANASE FROM THERMOTOGA PETROPHILA RKU-1 WITH THREE GLYCEROL MOLECULES	3.2.1.78
3PZN	STRUCTURE OF THE HYPERTHERMOSTABLE ENDO-1,4-BETA-D-MANNANASE FROM THERMOTOGA PETROPHILA RKU-1 WITH CITRATE AND GLYCEROL	3.2.1.78
3PZO	STRUCTURE OF THE HYPERTHERMOSTABLE ENDO-1,4-BETA-D-MANNANASE FROM THERMOTOGA PETROPHILA RKU-1 IN COMPLEX WITH THREE MALTOSE MOLECULES	3.2.1.78
3PZQ	STRUCTURE OF THE HYPERTHERMOSTABLE ENDO-1,4-BETA-D-MANNANASE FROM THERMOTOGA PETROPHILA RKU-1 WITH MALTOSE AND GLYCEROL	3.2.1.78
3PZT	STRUCTURE OF THE ENDO-1,4-BETA-GLUCANASE FROM BACILLUS SUBTILIS 168 WITH MANGANESE(II) ION	3.2.1.4
3PZU	P212121 CRYSTAL FORM OF THE ENDO-1,4-BETA-GLUCANASE FROM BACILLUS SUBTILIS 168	3.2.1.4
3PZV	C2 CRYSTAL FORM OF THE ENDO-1,4-BETA-GLUCANASE FROM BACILLUS SUBTILIS 168	3.2.1.4
3Q00	BOVINE TRYPSIN VARIANT X(TRIPLEGLU217ILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR	3.4.21.4
3Q07	CTX-M-9 S70G IN COMPLEX WITH PIPERACILLIN	3.5.2.6
3Q0T	CRYSTAL STRUCTURE OF HUMAN DPP-IV IN COMPLEX WITHSA-(+)- METHYL2-(3-(AMINOMETHYL)-4-(2,4-DICHLOROPHENYL)-2-METHYL- 7-OXO-5H-PYRROLO[3,4-B]PYRIDIN-6(7H)-YL)ACETATE	3.4.14.5
3Q0Z	CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE COMPLEX WITH (2E)-3-(4-{[(1-{[(13-CYCLOHEXYL-6-OXO-6,7-DIHYDRO-5H-INDOLO[1,2-D][1,4]BENZODIAZEPIN-10-YL)CARBONYL]AMINO}CYCLOPENTYL)CARBONYL]AMINO}PHENYL)PROP-2-ENOIC ACID	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3Q15	CRYSTAL STRUCTURE OF RAPH COMPLEXED WITH SPO0F	3.1
3Q1E	CRYSTAL STRUCTURE OF Y116T/I16A DOUBLE MUTANT OF 5-HYDROXYISOURATE HYDROLASE IN COMPLEX WITH T4	3.5.2.17
3Q1F	CTX-M-9 S70G IN COMPLEX WITH HYDROLYZED PIPERACILLIN	3.5.2.6
3Q1Q	STRUCTURE OF A BACTERIAL RIBONUCLEASE P HOLOENZYME IN COMPLEX WITH TRNA	3.1.26.5
3Q1R	CRYSTAL STRUCTURE OF A BACTERIAL RNASE P HOLOENZYME IN COMPLEX WITH TRNA AND IN THE PRESENCE OF 5' LEADER	3.1.26.5
3Q2G	ADAMTS1 IN COMPLEX WITH A NOVEL N-HYDROXYFORMAMIDE INHIBITORS	3.4.24
3Q2H	ADAMTS1 IN COMPLEX WITH N-HYDROXYFORMAMIDE INHIBITORS OF ADAM-TS4	3.4.24
3Q3F	ENGINEERING DOMAIN-SWAPPED BINDING INTERFACES BY MUTUALLY EXCLUSIVE FOLDING: INSERTION OF UBIQUITIN INTO POSITION 103 OF BARNASE	3.1.27
3Q3K	FACTOR XA IN COMPLEX WITH A PHENYLENEDIAMINE DERIVATIVE	3.4.21.6
3Q3L	THE NEUTRON CRYSTALLOGRAPHIC STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM THERMOCOCCUS THIOREDUCENS	3.6.1.1
3Q3Q	CRYSTAL STRUCTURE OF SPAP: AN NOVEL ALKALINE PHOSPHATASE FROM BACTERIUM SPHINGOMONAS SP. STRAIN BSAR-1	3.1.3.1
3Q3T	ALKYL AMINE RENIN INHIBITORS: FILLING S1 FROM S3	3.4.23.15
3Q3X	CRYSTAL STRUCTURE OF THE MAIN PROTEASE (3C) FROM HUMAN ENTEROVIRUS B EV93	3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48
3Q3Y	COMPLEX STRUCTURE OF HEVB EV93 MAIN PROTEASE 3C WITH COMPOUND 1 (AG7404)	3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48
3Q40	SULPHUR SAD STRUCTURE SOLUTION OF PROTEINASE K GROWN IN SO4-LESS SOLUTION.	3.4.21.64
3Q43	X-RAY CRYSTAL STRUCTURE OF PFA-M1 BOUND TO BESTATIN DERIVATIVE 15	3.4.11
3Q44	X-RAY CRYSTAL STRUCTURE OF PFA-M1 BOUND TO BESTATIN DERIVATIVE 16	3.4.11
3Q46	MAGNESIUM ACTIVATED INORGANIC PYROPHOSPHATASE FROM THERMOCOCCUS THIOREDUCENS BOUND TO HYDROLYZED PRODUCT AT 0.99 ANGSTROM RESOLUTION	3.6.1.1
3Q4B	CLINICALLY USEFUL ALKYL AMINE RENIN INHIBITORS	3.4.23.15
3Q4P	CRYSTAL STRUCTURE OF THE COMPLEX OF TYPE I RIBOSOME INACTIVATING PROTEIN WITH 7N-METHYL -8-HYDROGUANOSINE-5-P-DIPHOSPHATE AT 1.8 A RESOLUTION	3.2.2.22
3Q4W	THE STRUCTURE OF ARCHAEAL INORGANIC PYROPHOSPHATASE IN COMPLEX WITH SUBSTRATE	3.6.1.1
3Q4Y	CRYSTAL STRUCTURE OF GROUP I PHOSPHOLIPASE A2 AT 2.3 A RESOLUTION IN 40% ETHANOL REVEALED THE CRITICAL ELEMENTS OF HYDROPHOBICITY OF THE SUBSTRATE-BINDING SITE	3.1.1.4
3Q5D	CRYSTAL STRUCTURE OF HUMAN ATLASTIN-1 (RESIDUES 1-447) BOUND TO GDP, CRYSTAL FORM 1	3.6.5
3Q5E	CRYSTAL STRUCTURE OF HUMAN ATLASTIN-1 (RESIDUES 1-447) BOUND TO GDP, CRYSTAL FORM 2	3.6.5
3Q5G	SULPHUR SAD STRUCTURE SOLUTION OF PROTEINASE K GROWN IN SO4 SOLUTION	3.4.21.64
3Q5H	CLINICALLY USEFUL ALKYL AMINE RENIN INHIBITORS	3.4.23.15
3Q5V	THE STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM THERMOCOCCUS THIOREDUCENS IN COMPLEX WITH MAGNESIUM AND SULFATE	3.6.1.1
3Q6D	XAA-PRO DIPEPTIDASE FROM BACILLUS ANTHRACIS.	3.4.13.9
3Q6V	CRYSTAL STRUCTURE OF SERRATIA FONTICOLA SFH-I: GLYCEROL COMPLEX	3.5.2.6
3Q6Y	ENDOTHIAPEPSIN IN COMPLEX WITH A PYRROLIDINE BASED INHIBITOR	3.4.23.22
3Q70	SECRETED ASPARTIC PROTEASE IN COMPLEX WITH RITONAVIR	3.4.23.24
3Q76	STRUCTURE OF HUMAN NEUTROPHIL ELASTASE (UNCOMPLEXED)	3.4.21.37
3Q77	STRUCTURE OF HUMAN NEUTROPHIL ELASTASE IN COMPLEX WITH A DIHYDROPYRIMIDONE INHIBITOR	3.4.21.37
3Q7B	EXONUCLEASE DOMAIN OF LASSA VIRUS NUCLEOPROTEIN	3.1.13
3Q7C	EXONUCLEASE DOMAIN OF LASSA VIRUS NUCLEOPROTEIN BOUND TO MANGANESE	3.1.13
3Q7H	STRUCTURE OF THE CLPP SUBUNIT OF THE ATP-DEPENDENT CLP PROTEASE FROM COXIELLA BURNETII	3.4.21.92
3Q8K	CRYSTAL STRUCTURE OF HUMAN FLAP ENDONUCLEASE FEN1 (WT) IN COMPLEX WITH PRODUCT 5'-FLAP DNA, SM3+, AND K+	3.1
3Q8L	CRYSTAL STRUCTURE OF HUMAN FLAP ENDONUCLEASE FEN1 (WT) IN COMPLEX WITH SUBSTRATE 5'-FLAP DNA, SM3+, AND K+	3.1
3Q8M	CRYSTAL STRUCTURE OF HUMAN FLAP ENDONUCLEASE FEN1 (D181A) IN COMPLEX WITH SUBSTRATE 5'-FLAP DNA AND K+	3.1
3Q8W	A B-AMINOACYL CONTAINING THIAZOLIDINE DERIVATIVE AND DPPIV COMPLEX	3.4.14.5
3Q90	CRYSTAL STRUCTURE OF THE NTF2 DOMAIN OF RAS GTPASE-ACTIVATING PROTEIN-BINDING PROTEIN 1	3.6.4.12 3.6.4.13
3Q91	CRYSTAL STRUCTURE OF HUMAN URIDINE DIPHOSPHATE GLUCOSE PYROPHOSPHATASE (NUDT14)	3.6.1.45
3Q93	CRYSTAL STRUCTURE OF HUMAN 8-OXO-DGTPASE (MTH1)	3.6.1 3.6.1.55 3.6.1.56
3Q9B	CRYSTAL STRUCTURE OF APAH COMPLEXED WITH M344	3.5.1 3.5.1.62 3.5.1.48
3QAA	HIV-1 WILD TYPE PROTEASE WITH A SUBSTITUTED BIS-TETRAHYDROFURAN INHIBITOR, GRL-044-10A	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
3QAK	AGONIST BOUND STRUCTURE OF THE HUMAN ADENOSINE A2A RECEPTOR	3.2.1.17
3QB3	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT DELTA+PHS I92KL25A AT CRYOGENIC TEMPERATURE	3.1.31.1
3QB5	HUMAN C3PO COMPLEX IN THE PRESENCE OF MNSO4	3.1
3QBF	HIV-1 PROTEASE (MUTANT Q7K L33I L63I) IN COMPLEX WITH A THREE-ARMED 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
3QBH	STRUCTURE BASED DESIGN, SYNTHESIS AND SAR OF CYCLIC HYDROXYETHYLAMINE (HEA) BACE-1 INHIBITORS	3.4.23.46
3QBJ	CRYSTAL STRUCTURE OF DIPEPTIDYL PEPTIDASE IV IN COMPLEX WITH INHIBITOR	3.4.14.5
3QBU	CRYSTAL STRUCTURE OF PUTATIVE PEPTIDOGLYCAN DEACTELYASE (HP0310) FROM HELICOBACTER PYLORI	3.5.1 3.1.1.72
3QBV	STRUCTURE OF DESIGNED ORTHOGONAL INTERACTION BETWEEN CDC42 AND NUCLEOTIDE EXCHANGE DOMAINS OF INTERSECTIN	3.6.5.2
3QC8	CRYSTAL STRUCTURE OF FAF1 UBX DOMAIN IN COMPLEX WITH P97/VCP N DOMAIN REVEALS THE CONSERVED FCISP TOUCH-TURN MOTIF OF UBX DOMAIN SUFFERING CONFORMATIONAL CHANGE	3.6.4.6
3QCB	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, APO	3.1.3.48
3QCC	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH VANADATE, ORTHORHOMBIC CRYSTAL FORM	3.1.3.48
3QCD	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH VANADATE, TRIGONAL CRYSTAL FORM	3.1.3.48
3QCE	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH 3-[(3,4-DICHLOROBENZYL)SULFANYL]THIOPHENE-2-CARBOXYLIC ACID VIA SOAKING	3.1.3.48
3QCF	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH 3-[(3,4-DICHLOROBENZYL)SULFANYL]THIOPHENE-2-CARBOXYLIC ACID VIA CO-CRYSTALLIZATION	3.1.3.48
3QCG	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH 3-[(3-BROMO-4-CHLOROBENZYL)SULFANYL]THIOPHENE-2-CARBOXYLIC ACID	3.1.3.48
3QCH	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH 3-[(3,4-DICHLOROBENZYL)SULFANYL]-N-(METHYLSULFONYL)THIOPHENE-2-CARBOXAMIDE	3.1.3.48
3QCI	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH N-[(3-AMINOPHENYL)SULFONYL]-3-[(3,4-DICHLOROBENZYL)SULFANYL]THIOPHENE-2-CARBOXAMIDE	3.1.3.48
3QCJ	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH 5-[({3-[(3,4-DICHLOROBENZYL)SULFANYL]THIOPHEN-2-YL}CARBONYL)SULFAMOYL]-2-METHOXYBENZOIC ACID	3.1.3.48
3QCK	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH 2-[(3,4-DICHLOROBENZYL)SULFANYL]BENZOIC ACID	3.1.3.48
3QCL	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH 2-[(3,4-DICHLOROBENZYL)SULFANYL]-4-(4-HYDROXYBUT-1-YN-1-YL)BENZOIC ACID	3.1.3.48
3QCM	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, IN COMPLEX WITH 2-[(3,4-DICHLOROBENZYL)SULFANYL]-4-{[3-({N-[2-(METHYLAMINO)ETHYL]GLYCYL}AMINO)PHENYL]ETHYNYL}BENZOIC ACID	3.1.3.48
3QCN	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE GAMMA, DOMAIN 1, TRIGONAL CRYSTAL FORM	3.1.3.48
3QD7	CRYSTAL STRUCTURE OF YDAL, A STAND-ALONE SMALL MUTS-RELATED PROTEIN FROM ESCHERICHIA COLI	3.1
3QDZ	CRYSTAL STRUCTURE OF THE HUMAN THROMBIN MUTANT D102N IN COMPLEX WITH THE EXTRACELLULAR FRAGMENT OF HUMAN PAR4.	3.4.21.5
3QE0	A GALPHA-I1 P-LOOP MUTATION PREVENTS TRANSITION TO THE ACTIVATED STATE	3.6.5.1
3QE8	CRYSTAL STRUCTURE ANALYSIS OF LYSOZYME-BOUND FAC-[RE(CO)3(H2O)(IM)]+	3.2.1.17
3QED	THE STRUCTURE AND FUNCTION OF AN ARABINAN-SPECIFIC ALPHA-1,2-ARABINOFURANOSIDASE IDENTIFIED FROM SCREENING THE ACTIVITIES OF BACTERIAL GH43 GLYCOSIDE HYDROLASES	3.2.1
3QEE	THE STRUCTURE AND FUNCTION OF AN ARABINAN-SPECIFIC ALPHA-1,2-ARABINOFURANOSIDASE IDENTIFIED FROM SCREENING THE ACTIVITIES OF BACTERIAL GH43 GLYCOSIDE HYDROLASES	3.2.1
3QEF	THE STRUCTURE AND FUNCTION OF AN ARABINAN-SPECIFIC ALPHA-1,2-ARABINOFURANOSIDASE IDENTIFIED FROM SCREENING THE ACTIVITIES OF BACTERIAL GH43 GLYCOSIDE HYDROLASES	3.2.1
3QEI	RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE DIFLUOROTOLUENE NUCLEOSIDE	2.7.7.7 3.1.11
3QEP	RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DTTP OPPOSITE DIFLUOROTOLUENE NUCLEOSIDE	2.7.7.7 3.1.11
3QER	RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DATP OPPOSITE DIFLUOROTOLUENE NUCLEOSIDE	2.7.7.7 3.1.11
3QES	RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DGTP OPPOSITE DIFLUOROTOLUENE NUCLEOSIDE	2.7.7.7 3.1.11
3QET	RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DTTP OPPOSITE DT	2.7.7.7 3.1.11
3QEV	RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE DT	2.7.7.7 3.1.11
3QEW	RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DDTP OPPOSITE DT	2.7.7.7 3.1.11
3QEX	RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DGTP OPPOSITE DT	2.7.7.7 3.1.11
3QFP	CRYSTAL STRUCTURE OF YEAST HSP70 (BIP/KAR2) ATPASE DOMAIN	3.6.4.10
3QFU	CRYSTAL STRUCTURE OF YEAST HSP70 (BIP/KAR2) COMPLEXED WITH ADP	3.6.4.10
3QG1	CRYSTAL STRUCTURE OF P-LOOP G239A MUTANT OF SUBUNIT A OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3QGD	CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE COMPLEX WITH (2E)-3-(4-{[(1-{[(13-CYCLOHEXYL-6-OXO-6,7-DIHYDRO-5H-INDOLO[1,2-D][1,4]BENZODIAZEPIN-10-YL)CARBONYL]AMINO}CYCLOPENTYL)CARBONYL]AMINO}PHENYL)PROP-2-ENOIC ACID AND (2R)-4-(2,6-DIMETHOXYPYRIMIDIN-4-YL)-1-[(4-ETHYLPHENYL)SULFONYL]-N-(4-METHOXYBENZYL)PIPERAZINE-2-CARBOXAMIDE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3QGE	CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE COMPLEX WITH (2E)-3-(4-{[(1-{[(13-CYCLOHEXYL-6-OXO-6,7-DIHYDRO-5H-INDOLO[1,2-D][1,4]BENZODIAZEPIN-10-YL)CARBONYL]AMINO}CYCLOPENTYL)CARBONYL]AMINO}PHENYL)PROP-2-ENOIC ACID AND (2R)-4-(2,6-DIMETHOXYPYRIMIDIN-4-YL)-N-(4-METHOXYBENZYL)-1-{[4-(TRIFLUOROMETHOXY)PHENYL]SULFONYL}PIPERAZINE-2-CARBOXAMIDE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3QGF	CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE COMPLEX WITH (2E)-3-(4-{[(1-{[(13-CYCLOHEXYL-6-OXO-6,7-DIHYDRO-5H-INDOLO[1,2-D][1,4]BENZODIAZEPIN-10-YL)CARBONYL]AMINO}CYCLOPENTYL)CARBONYL]AMINO}PHENYL)PROP-2-ENOIC ACID AND (2R)-4-(6-CHLOROPYRIDAZIN-3-YL)-N-(4-METHOXYBENZYL)-1-{[4-(TRIFLUOROMETHOXY)PHENYL]SULFONYL}PIPERAZINE-2-CARBOXAMIDE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3QGG	CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE COMPLEX WITH (2E)-3-(4-{[(1-{[(13-CYCLOHEXYL-6-OXO-6,7-DIHYDRO-5H-INDOLO[1,2-D][1,4]BENZODIAZEPIN-10-YL)CARBONYL]AMINO}CYCLOPENTYL)CARBONYL]AMINO}PHENYL)PROP-2-ENOIC ACID AND N-CYCLOPROPYL-6-[(3R)-3-{[4-(TRIFLUOROMETHOXY)BENZYL]CARBAMOYL}-4-{[4-(TRIFLUOROMETHOXY)PHENYL]SULFONYL}PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXAMIDE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3QGH	CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE GENOTYPE 1A COMPLEX WITH N-CYCLOPROPYL-6-[(3R)-3-{[4-(TRIFLUOROMETHOXY)BENZYL]CARBAMOYL}-4-{[4-(TRIFLUOROMETHOXY)PHENYL]SULFONYL}PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXAMIDE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3QGI	CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE GENOTYPE 1A COMPLEX WITH N-[(2S)-BUTAN-2-YL]-6-[(3R)-3-{[4-(TRIFLUOROMETHOXY)BENZYL]CARBAMOYL}-4-{[4-(TRIFLUOROMETHOXY)PHENYL]SULFONYL}PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXAMIDE	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
3QGJ	1.3A STRUCTURE OF ALPHA-LYTIC PROTEASE BOUND TO AC-ALAALAPRO-ALANAL	3.4.21.12
3QGN	THE ALLOSTERIC E*-E EQUILIBRIUM IS A KEY PROPERTY OF THE TRYPSIN FOLD	3.4.21.5
3QGO	STRUCTURE OF THERMOLYSIN IN COMPLEX WITH L-PHENYLALANINE METHYLESTER	3.4.24.27
3QGV	CRYSTAL STRUCTURE OF A THERMOSTABLE AMYLASE VARIANT	3.2.1.1
3QGZ	RE-INVESTIGATED HIGH RESOLUTION CRYSTAL STRUCTURE OF HISTIDINE TRIAD NUCLEOTIDE-BINDING PROTEIN 1 (HINT1) FROM RABBIT COMPLEXED WITH ADENOSINE	3
3QH1	STRUCTURE OF THERMOLYSIN IN COMPLEX WITH N-BENZYLOXYCARBONYL-L-ASPARTIC ACID	3.4.24.27
3QH5	STRUCTURE OF THERMOLYSIN IN COMPLEX WITH N-CARBOBENZYLOXY-L-ASPARTIC ACID AND L-PHENYLALANINE METHYL ESTER	3.4.24.27
3QHM	CRYSTAL ANALYSIS OF THE COMPLEX STRUCTURE, E342A-CELLOTETRAOSE, OF ENDOCELLULASE FROM PYROCOCCUS HORIKOSHII	3.2.1.4
3QHN	CRYSTAL ANALYSIS OF THE COMPLEX STRUCTURE, E201A-CELLOTETRAOSE, OF ENDOCELLULASE FROM PYROCOCCUS HORIKOSHII	3.2.1.4
3QHO	CRYSTAL ANALYSIS OF THE COMPLEX STRUCTURE, Y299F-CELLOTETRAOSE, OF ENDOCELLULASE FROM PYROCOCCUS HORIKOSHII	3.2.1.4
3QHY	STRUCTURAL, THERMODYNAMIC AND KINETIC ANALYSIS OF THE PICOMOLAR BINDING AFFINITY INTERACTION OF THE BETA-LACTAMASE INHIBITOR PROTEIN-II (BLIP-II) WITH CLASS A BETA-LACTAMASES	3.5.2.6
3QI1	DESIGN AND SYNTHESIS OF HYDROXYETHYLAMINE (HEA) BACE-1 INHIBITORS: PRIME SIDE CHROMANE-CONTAINING INHIBITORS	3.4.23.46
3QI2	A GALPHA P-LOOP MUTATION PREVENTS TRANSITION TO THE ACTIVATED STATE: G42R BOUND TO RGS14 GOLOCO	3.6.5.1
3QI3	CRYSTAL STRUCTURE OF PDE9A(Q453E) IN COMPLEX WITH INHIBITOR BAY73-6691	3.1.4.35
3QI4	CRYSTAL STRUCTURE OF PDE9A(Q453E) IN COMPLEX WITH IBMX	3.1.4.35
3QI5	CRYSTAL STRUCTURE OF HUMAN ALKYLADENINE DNA GLYCOSYLASE IN COMPLEX WITH 3,N4-ETHENOCYSTOSINE CONTAINING DUPLEX DNA	3.2.2.21
3QIA	CRYSTAL STRUCTURE OF P-LOOP G237A MUTANT OF SUBUNIT A OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3QID	CRYSTAL STRUCTURES AND FUNCTIONAL ANALYSIS OF MURINE NOROVIRUS RNA-DEPENDENT RNA POLYMERASE	2.7.7.48 3.4.22.66 3.6.1.15
3QIH	HIV-1 PROTEASE (MUTANT Q7K L33I L63I) IN COMPLEX WITH A NOVEL 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
3QIN	CRYSTAL STRUCTURE OF HIV-1 RNASE H P15 WITH ENGINEERED E. COLI LOOP AND PYRIMIDINOL CARBOXYLIC ACID 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 3.1.26.4
3QIO	CRYSTAL STRUCTURE OF HIV-1 RNASE H WITH ENGINEERED E. COLI LOOP AND N-HYDROXY QUINAZOLINEDIONE 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 3.1.26.4
3QIP	STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH AN RNASE H INHIBITOR AND NEVIRAPINE	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
3QIR	CRYSTAL STRUCTURE OF PIWIL2 PAZ DOMAIN	3.1.26
3QIS	RECOGNITION OF THE F&H MOTIF BY THE LOWE SYNDROME PROTEIN OCRL	3.1.3.36 3.1.3.56 3.1.3.86
3QIT	THIOESTERASE DOMAIN FROM CURACIN BIOSYNTHETIC PATHWAY	3.1.2
3QIX	CRYSTAL STRUCTURE OF BONT/A LC WITH ZINC BOUND	3.4.24.69
3QIY	CRYSTAL STRUCTURE OF BONT/A LC COMPLEXED WITH HYDROXAMATE-BASED INHIBITOR PT-1	3.4.24.69
3QIZ	CRYSTAL STRUCTURE OF BONT/A LC COMPLEXED WITH HYDROXAMATE-BASED INHIBITOR PT-2	3.4.24.69
3QJ0	CRYSTAL STRUCTURE OF BONT/A LC COMPLEXED WITH HYDROXAMATE-BASED INHIBITOR PT-3	3.4.24.69
3QJ1	CRYSTAL STRUCTURE OF CAMEL PEPTIDOGLYCAN RECOGNITION PROTEIN, PGRP-S WITH A TRAPPED DIETHYLENE GLYCOL IN THE LIGAND DIFFUSION CHANNEL AT 3.2 A RESOLUTION	3.5.1.28
3QJ3	STRUCTURE OF DIGESTIVE PROCATHEPSIN L2 PROTEINASE FROM TENEBRIO MOLITOR LARVAL MIDGUT	3.4.22.15
3QJ8	CRYSTAL STRUCTURE OF FATTY ACID AMIDE HYDROLASE	3.5.1.99 3.1.1
3QJ9	CRYSTAL STRUCTURE OF FATTY ACID AMIDE HYDROLASE WITH SMALL MOLECULE INHIBITOR	3.5.1.99 3.1.1
3QJI	CRYSTAL STRUCTURE OF THE COMPLEX OF RIBOSOME INACTIVATING PROTEIN WITH 7-METHYLGUANOSINE TRIPHOSPHATE AT 1.75A RESOLUTION	3.2.2.22
3QJX	CRYSTAL STRUCTURE OF E. COLI AMINOPEPTIDASE N IN COMPLEX WITH L-SERINE	3.4.11.2
3QJY	CRYSTAL STRUCTURE OF P-LOOP G234A MUTANT OF SUBUNIT A OF THE A1AO ATP SYNTHASE	3.6.3.14 7.1.2.2 3.1
3QK1	CRYSTAL STRUCTURE OF ENTEROKINASE-LIKE TRYPSIN VARIANT	3.4.21.4
3QK2	STRUCTURE-BASED ANALYSIS OF THE INTERACTION BETWEEN THE SIMIAN VIRUS 40 T-ANTIGEN ORIGIN BINDING DOMAIN AND SINGLE-STRANDED DNA	3.6.4
3QK5	CRYSTAL STRUCTURE OF FATTY ACID AMIDE HYDROLASE WITH SMALL MOLECULE INHIBITOR	3.5.1.99 3.1.1
3QKP	PROTEIN TYROSINE PHOSPHATASE 1B - APO W179F MUTANT WITH OPEN WPD-LOOP	3.1.3.48
3QKQ	PROTEIN TYROSINE PHOSPHATASE 1B - W179F MUTANT BOUND WITH VANADATE	3.1.3.48
3QKR	MRE11 RAD50 BINDING DOMAIN BOUND TO RAD50	3.6
3QKS	MRE11 RAD50 BINDING DOMAIN BOUND TO RAD50	3.6
3QKT	RAD50 ABC-ATPASE WITH ADJACENT COILED-COIL REGION IN COMPLEX WITH AMP-PNP	3.6
3QKV	CRYSTAL STRUCTURE OF FATTY ACID AMIDE HYDROLASE WITH SMALL MOLECULE COMPOUND	3.5.1.99 3.1.1
3QL1	CRYSTAL STRUCTURE OF RIBONUCLEASE A VARIANT A4C/D83E/V118C	3.1.27.5 4.6.1.18
3QL2	CRYSTAL STRUCTURE OF RIBONUCLEASE A VARIANT A4C/D83E/V118C	3.1.27.5 4.6.1.18
3QL9	MONOCLINIC COMPLEX STRUCTURE OF ATRX ADD BOUND TO HISTONE H3K9ME3 PEPTIDE	3.6.4.12
3QLA	HEXAGONAL COMPLEX STRUCTURE OF ATRX ADD BOUND TO H3K9ME3 PEPTIDE	3.6.4.12
3QLC	COMPLEX STRUCTURE OF ATRX ADD DOMAIN BOUND TO UNMODIFIED H3 1-15 PEPTIDE	3.6.4.12
3QLH	HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH MANICOL AT THE RNASE H ACTIVE SITE AND TMC278 (RILPIVIRINE) AT THE NNRTI BINDING POCKET	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
3QLM	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH N-HEXADECANOIC ACID	3.1.1.4
3QLN	CRYSTAL STRUCTURE OF ATRX ADD DOMAIN IN FREE STATE	3.6.4.12
3QM1	CRYSTAL STRUCTURE OF THE LACTOBACILLUS JOHNSONII CINNAMOYL ESTERASE LJ0536 S106A MUTANT IN COMPLEX WITH ETHYLFERULATE, FORM II	3.1.1
3QMF	CRYSTAL STRUCUTURE OF AN INOSITOL MONOPHOSPHATASE FAMILY PROTEIN (SAS2203) FROM STAPHYLOCOCCUS AUREUS MSSA476	3.1.3.25
3QML	THE STRUCTURAL ANALYSIS OF SIL1-BIP COMPLEX REVEALS THE MECHANISM FOR SIL1 TO FUNCTION AS A NOVEL NUCLEOTIDE EXCHANGE FACTOR	3.6.4.10
3QMM	STRUCTURE OF 6B, A THERMOSTABLE MUTANT OF BACILLUS SUBTILIS LIPASE OBTAINED THROUGH DIRECTED EVOLUTION	3.1.1.3
3QMP	SELENIUM SAD STRUCTURE SOLUTION OF PROTEINASE K GROWN IN SO4-LESS SOLUTION AND SOAKED IN SELENATE.	3.4.21.64
3QMV	REDJ-THIOESTERASE FROM THE PRODIGININE BIOSYNTHETIC PATHWAY IN STREPTOMYCES COELICOLOR	3.1.2
3QMW	REDJ WITH PEG MOLECULE BOUND IN THE ACTIVE SITE	3.1.2
3QN2	STRUCTURE-BASED DESIGN OF A DISULFIDE-LINKED OLIGOMERIC FORM OF THE SIMIAN VIRUS 40 (SV40) LARGE T ANTIGEN DNA BINDING DOMAIN	3.6.4
3QN7	POTENT AND SELECTIVE BICYCLIC PEPTIDE INHIBITOR (UK18) OF HUMAN UROKINASE-TYPE PLASMINOGEN ACTIVATOR(UPA)	3.4.21.73
3QN8	HIV-1 PROTEASE (MUTANT Q7K L33I L63I) IN COMPLEX WITH A NOVEL 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
3QNB	CRYSTAL STRUCTURE OF AN ENGINEERED OXA-10 VARIANT WITH CARBAPENEMASE ACTIVITY, OXA-10LOOP24	3.5.2.6
3QNC	CRYSTAL STRUCTURE OF A RATIONALLY DESIGNED OXA-10 VARIANT SHOWING CARBAPENEMASE ACTIVITY, OXA-10LOOP48	3.5.2.6
3QNF	CRYSTAL STRUCTURE OF THE OPEN STATE OF HUMAN ENDOPLASMIC RETICULUM AMINOPEPTIDASE 1 ERAP1	3.4.11
3QNG	CRYSTAL STRUCTURE ANALYSIS OF LYSOZYME-BOUND FAC-[RE(CO)3(L-SERINE)]	3.2.1.17
3QNN	RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DGT OPPOSITE 3TCO	2.7.7.7 3.1.11
3QNO	RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DATP OPPOSITE 3TCO	2.7.7.7 3.1.11
3QNU	CRYSTAL STRUCTURE OF THE CYTOSOLIC DOMAIN OF HUMAN ATLASTIN-1 IN COMPLEX WITH GDP, HEXAGONAL FORM	3.6.5
3QNV	CARBOXYPEPTIDASE T	3.4.17.18
3QNW	CASPASE-6 IN COMPLEX WITH Z-VAD-FMK INHIBITOR	3.4.22.59
3QO6	CRYSTAL STRUCTURE ANALYSIS OF THE PLANT PROTEASE DEG1	3.4.21
3QO9	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH TSAO-T, 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
3QOF	CRYSTAL STRUCTURE OF THE CYTOSOLIC DOMAIN OF HUMAN ATLASTIN-1 IN COMPLEX WITH GDP, ORTHORHOMBIC FORM	3.6.5
3QOJ	CRYOGENIC STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT D+PHS/V23K	3.1.31.1
3QOL	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT D+PHS/V23E AT PH 6 DETERMINED AT 100 K	3.1.31.1
3QOM	CRYSTAL STRUCTURE OF 6-PHOSPHO-BETA-GLUCOSIDASE FROM LACTOBACILLUS PLANTARUM	3.2.1.86
3QP0	HIV-1 PROTEASE (MUTANT Q7K L33I L63I) IN COMPLEX WITH A NOVEL 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
3QPA	STRUCTURE OF FUSARIUM SOLANI CUTINASE EXPRESSED IN PICHIA PASTORIS	3.1.1.74
3QPC	STRUCTURE OF FUSARIUM SOLANI CUTINASE EXPRESSED IN PICHIA PASTORIS, CRYSTALLIZED IN THE PRESENCE OF PARAOXON	3.1.1.74
3QPD	STRUCTURE OF ASPERGILLUS ORYZAE CUTINASE EXPRESSED IN PICHIA PASTORIS, CRYSTALLIZED IN THE PRESENCE OF PARAOXON	3.1.1.74
3QPJ	HIV-1 PROTEASE (MUTANT Q7K L33I L63I) IN COMPLEX WITH A THREE-ARMED 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
3QPN	STRUCTURE OF PDE10-INHIBITOR COMPLEX	3.1.4.17 3.1.4.35
3QPO	STRUCTURE OF PDE10-INHIBITOR COMPLEX	3.1.4.17 3.1.4.35
3QPP	STRUCTURE OF PDE10-INHIBITOR COMPLEX	3.1.4.17 3.1.4.35
3QPU	PFKFB3 IN COMPLEX WITH PPI	2.7.1.105 3.1.3.46
3QPV	PFKFB3 TRAPPED IN A PHOSPHO-ENZYME INTERMEDIATE STATE	2.7.1.105 3.1.3.46
3QPW	PFKFB3 IN COMPLEX WITH ALUMINUM TETRAFLUORIDE	2.7.1.105 3.1.3.46
3QQ7	CRYSTAL STRUCTURE OF THE P97 N-TERMINAL DOMAIN	3.6.4.6
3QQ8	CRYSTAL STRUCTURE OF P97-N IN COMPLEX WITH FAF1-UBX	3.6.4.6
3QR0	CRYSTAL STRUCTURE OF S. OFFICINALIS PLC21	3.1.4.11
3QR1	CRYSTAL STRUCTURE OF L. PEALEI PLC21	3.1.4.11
3QR3	CRYSTAL STRUCTURE OF CEL5A (EG2) FROM HYPOCREA JECORINA (TRICHODERMA REESEI)	3.2.1.4
3QRM	HIV-1 PROTEASE (MUTANT Q7K L33I L63I) IN COMPLEX WITH A THREE-ARMED 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
3QRO	HIV-1 PROTEASE (MUTANT Q7K L33I L63I) IN COMPLEX WITH A THREE-ARMED 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
3QRP	STRUCTURE OF THERMUS THERMOPHILUS CSE3 BOUND TO AN RNA REPRESENTING A PRODUCT MIMIC COMPLEX	3.1
3QRQ	STRUCTURE OF THERMUS THERMOPHILUS CSE3 BOUND TO AN RNA REPRESENTING A PRE-CLEAVAGE COMPLEX	3.1
3QRR	STRUCTURE OF THERMUS THERMOPHILUS CSE3 BOUND TO AN RNA REPRESENTING A PRODUCT COMPLEX	3.1
3QRS	HIV-1 PROTEASE (MUTANT Q7K L33I L63I) IN COMPLEX WITH A THREE-ARMED 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
3QRV	CRYSTAL STRUCTURE OF PLASMEPSIN I (PMI) FROM PLASMODIUM FALCIPARUM	3.4.23.38
3QS1	CRYSTAL STRUCTURE OF KNI-10006 COMPLEX OF PLASMEPSIN I (PMI) FROM PLASMODIUM FALCIPARUM	3.4.23.38
3QSD	STRUCTURE OF CATHEPSIN B1 FROM SCHISTOSOMA MANSONI IN COMPLEX WITH CA074 INHIBITOR	3.4.22.1
3QSK	5 HISTIDINE VARIANT OF THE ANTI-RNASE A VHH IN COMPLEX WITH RNASE A	3.1.27.5 4.6.1.18
3QSY	RECOGNITION OF THE METHIONYLATED INITIATOR TRNA BY THE TRANSLATION INITIATION FACTOR 2 IN ARCHAEA	3.6.5.3
3QT4	STRUCTURE OF DIGESTIVE PROCATHEPSIN L 3 OF TENEBRIO MOLITOR LARVAL MIDGUT	3.4.22.15
3QTL	STRUCTURAL BASIS FOR DUAL-INHIBITION MECHANISM OF A NON-CLASSICAL KAZAL-TYPE SERINE PROTEASE INHIBITOR FROM HORSESHOE CRAB IN COMPLEX WITH SUBTILISIN	3.4.21.62
3QTO	THROMBIN INHIBITION BY PYRIDIN DERIVATIVES	3.4.21.5
3QTV	THROMBIN INHIBITION BY PYRIDIN DERIVATIVES	3.4.21.5
3QU1	PEPTIDE DEFORMYLASE FROM VIBRIO CHOLERAE	3.5.1.88
3QU2	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, A CLOSED CAP CONFORMATION	3.6.1.1
3QU4	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, ASP13ALA MUTANT	3.6.1.1
3QU5	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, ASP11ASN MUTANT	3.6.1.1
3QU7	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, ASP13ASN MUTANT COMPLEXED WITH CALCIUM AND PHOSPHATE	3.6.1.1
3QU9	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, ASP13ASN MUTANT COMPLEXED WITH MAGNESIUM AND TARTRATE	3.6.1.1
3QUA	CRYSTAL STRUCTURE OF A PUTATIVE UNCHARACTERIZED PROTEIN AND POSSIBLE MOLYBDENUM COFACTOR PROTEIN FROM MYCOBACTERIUM SMEGMATIS	3.2.2
3QUB	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, GLU47ALA MUTANT COMPLEXED WITH SULFATE	3.6.1.1
3QUC	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, GLU47ASN MUTANT COMPLEXED WITH SULFATE	3.6.1.1
3QUQ	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, AN OPEN CAP CONFORMATION	3.6.1.1
3QUT	CRYSTAL STRUCTURE OF PYROPHOSPHATASE FROM BACTEROIDES THETAIOTAOMICRON, ASP13ASN MUTANT, AN OPEN CAP CONFORMATION	3.6.1.1
3QVA	STRUCTURE OF KLEBSIELLA PNEUMONIAE 5-HYDROXYISOURATE HYDROLASE	3.5.2.17
3QVQ	THE STRUCTURE OF AN OLEISPIRA ANTARCTICA PHOSPHODIESTERASE OLEI02445 IN COMPLEX WITH THE PRODUCT SN-GLYCEROL-3-PHOSPHATE	3.1.4.2
3QW5	CRYSTAL STRUCTURE OF THE PROTEASE DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH A PEPTIDE INHIBITOR RRGF	3.4.24.69
3QW6	CRYSTAL STRUCTURE OF THE PROTEASE DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH A PEPTIDE INHIBITOR RYGC	3.4.24.69
3QW7	CRYSTAL STRUCTURE OF THE PROTEASE DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH A PEPTIDE INHIBITOR RRFC	3.4.24.69
3QW8	CRYSTAL STRUCTURE OF THE PROTEASE DOMAIN OF BOTULINUM NEUROTOXIN SEROTYPE A WITH A PEPTIDE INHIBITOR CRGC	3.4.24.69
3QWC	THROMBIN INHIBITION BY PYRIDIN DERIVATIVES	3.4.21.5
3QWZ	CRYSTAL STRUCTURE OF FAF1 UBX-P97N-DOMAIN COMPLEX	3.6.4.6
3QX5	THROMBIN INHIBITION BY PYRIDIN DERIVATIVES	3.4.21.5