| Hits from PDB |
Structure Title |
| 101M | SPERM WHALE MYOGLOBIN F46V N-BUTYL ISOCYANIDE AT PH 9.0 |
| 102L | HOW AMINO-ACID INSERTIONS ARE ALLOWED IN AN ALPHA-HELIX OF T4 LYSOZYME |
| 102M | SPERM WHALE MYOGLOBIN H64A AQUOMET AT PH 9.0 |
| 103L | HOW AMINO-ACID INSERTIONS ARE ALLOWED IN AN ALPHA-HELIX OF T4 LYSOZYME |
| 103M | SPERM WHALE MYOGLOBIN H64A N-BUTYL ISOCYANIDE AT PH 9.0 |
| 104L | HOW AMINO-ACID INSERTIONS ARE ALLOWED IN AN ALPHA-HELIX OF T4 LYSOZYME |
| 104M | SPERM WHALE MYOGLOBIN N-BUTYL ISOCYANIDE AT PH 7.0 |
| 105M | SPERM WHALE MYOGLOBIN N-BUTYL ISOCYANIDE AT PH 9.0 |
| 106M | SPERM WHALE MYOGLOBIN V68F ETHYL ISOCYANIDE AT PH 9.0 |
| 107L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 107M | SPERM WHALE MYOGLOBIN V68F N-BUTYL ISOCYANIDE AT PH 9.0 |
| 108L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 108M | SPERM WHALE MYOGLOBIN V68F N-BUTYL ISOCYANIDE AT PH 7.0 |
| 109L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 109M | SPERM WHALE MYOGLOBIN D122N ETHYL ISOCYANIDE AT PH 9.0 |
| 10GS | HUMAN GLUTATHIONE S-TRANSFERASE P1-1, COMPLEX WITH TER117 |
| 10MH | TERNARY STRUCTURE OF HHAI METHYLTRANSFERASE WITH ADOHCY AND HEMIMETHYLATED DNA CONTAINING 5,6-DIHYDRO-5-AZACYTOSINE AT THE TARGET |
| 110L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 110M | SPERM WHALE MYOGLOBIN D122N METHYL ISOCYANIDE AT PH 9.0 |
| 111L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 111M | SPERM WHALE MYOGLOBIN D122N N-BUTYL ISOCYANIDE AT PH 9.0 |
| 112L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 112M | SPERM WHALE MYOGLOBIN D122N N-PROPYL ISOCYANIDE AT PH 9.0 |
| 113L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 114L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 115L | STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME |
| 117E | THE R78K AND D117E ACTIVE SITE VARIANTS OF SACCHAROMYCES CEREVISIAE SOLUBLE INORGANIC PYROPHOSPHATASE: STRUCTURAL STUDIES AND MECHANISTIC IMPLICATIONS |
| 118L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 119L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 11AS | ASPARAGINE SYNTHETASE MUTANT C51A, C315A COMPLEXED WITH L-ASPARAGINE |
| 11BA | BINDING OF A SUBSTRATE ANALOGUE TO A DOMAIN SWAPPING PROTEIN IN THE COMPLEX OF BOVINE SEMINAL RIBONUCLEASE WITH URIDYLYL-2',5'-ADENOSINE |
| 11BG | A POTENTIAL ALLOSTERIC SUBSITE GENERATED BY DOMAIN SWAPPING IN BOVINE SEMINAL RIBONUCLEASE |
| 11GS | GLUTATHIONE S-TRANSFERASE COMPLEXED WITH ETHACRYNIC ACID-GLUTATHIONE CONJUGATE (FORM II) |
| 120L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 121P | STRUKTUR UND GUANOSINTRIPHOSPHAT-HYDROLYSEMECHANISMUS DES C-TERMINAL VERKUERZTEN MENSCHLICHEN KREBSPROTEINS P21-H-RAS |
| 122L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 123L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 125L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 126L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 127L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 128L | THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME |
| 129L | STRUCTURES OF RANDOMLY GENERATED MUTANTS OF T4 LYSOZYME SHOW THAT PROTEIN STABILITY CAN BE ENHANCED BY RELAXATION OF STRAIN AND BY IMPROVED HYDROGEN BONDING VIA BOUND SOLVENT |
| 12AS | ASPARAGINE SYNTHETASE MUTANT C51A, C315A COMPLEXED WITH L-ASPARAGINE AND AMP |
| 12CA | ALTERING THE MOUTH OF A HYDROPHOBIC POCKET. STRUCTURE AND KINETICS OF HUMAN CARBONIC ANHYDRASE II MUTANTS AT RESIDUE VAL-121 |
| 12E8 | 2E8 FAB FRAGMENT |
| 12GS | GLUTATHIONE S-TRANSFERASE COMPLEXED WITH S-NONYL-GLUTATHIONE |
| 130L | STRUCTURES OF RANDOMLY GENERATED MUTANTS OF T4 LYSOZYME SHOW THAT PROTEIN STABILITY CAN BE ENHANCED BY RELAXATION OF STRAIN AND BY IMPROVED HYDROGEN BONDING VIA BOUND SOLVENT |
| 131L | STRUCTURES OF RANDOMLY GENERATED MUTANTS OF T4 LYSOZYME SHOW THAT PROTEIN STABILITY CAN BE ENHANCED BY RELAXATION OF STRAIN AND BY IMPROVED HYDROGEN BONDING VIA BOUND SOLVENT |
| 132L | STRUCTURAL CONSEQUENCES OF REDUCTIVE METHYLATION OF LYSINE RESIDUES IN HEN EGG WHITE LYSOZYME: AN X-RAY ANALYSIS AT 1.8 ANGSTROMS RESOLUTION |
| 133L | ROLE OF ARG 115 IN THE CATALYTIC ACTION OF HUMAN LYSOZYME. X-RAY STRUCTURE OF HIS 115 AND GLU 115 MUTANTS |
| 134L | ROLE OF ARG 115 IN THE CATALYTIC ACTION OF HUMAN LYSOZYME. X-RAY STRUCTURE OF HIS 115 AND GLU 115 MUTANTS |
| 135L | X-RAY STRUCTURE OF MONOCLINIC TURKEY EGG LYSOZYME AT 1.3 ANGSTROMS RESOLUTION |
| 137L | STRUCTURAL BASIS OF AMINO ACID ALPHA HELIX PROPENSITY |
| 138L | RAPID CRYSTALLIZATION OF T4 LYSOZYME BY INTERMOLECULAR DISULFIDE CROSSLINKING |
| 139L | RAPID CRYSTALLIZATION OF T4 LYSOZYME BY INTERMOLECULAR DISULFIDE CROSSLINKING |
| 13GS | GLUTATHIONE S-TRANSFERASE COMPLEXED WITH SULFASALAZINE |
| 13PK | TERNARY COMPLEX OF PHOSPHOGLYCERATE KINASE FROM TRYPANOSOMA BRUCEI |
| 140L | ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
| 141L | ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
| 142L | ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
| 143L | ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
| 144L | ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
| 145L | ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
| 146L | ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
| 147L | ROLE OF BACKBONE FLEXIBILITY IN THE ACCOMMODATION OF VARIANTS THAT REPACK THE CORE OF T4 LYSOZYME |
| 148L | A COVALENT ENZYME-SUBSTRATE INTERMEDIATE WITH SACCHARIDE DISTORTION IN A MUTANT T4 LYSOZYME |
| 149L | CONSERVATION OF SOLVENT-BINDING SITES IN 10 CRYSTAL FORMS OF T4 LYSOZYME |
| 14GS | GLUTATHIONE S-TRANSFERASE P1-1 APO FORM 1 |
| 150L | CONSERVATION OF SOLVENT-BINDING SITES IN 10 CRYSTAL FORMS OF T4 LYSOZYME |
| 151L | CONSERVATION OF SOLVENT-BINDING SITES IN 10 CRYSTAL FORMS OF T4 LYSOZYME |
| 152L | CONSERVATION OF SOLVENT-BINDING SITES IN 10 CRYSTAL FORMS OF T4 LYSOZYME |
| 153L | THE REFINED STRUCTURES OF GOOSE LYSOZYME AND ITS COMPLEX WITH A BOUND TRISACCHARIDE SHOW THAT THE GOOSE-TYPE LYSOZYMES LACK A CATALYTIC ASPARTATE" |
| 154L | THE REFINED STRUCTURES OF GOOSE LYSOZYME AND ITS COMPLEX WITH A BOUND TRISACCHARIDE SHOW THAT THE GOOSE-TYPE LYSOZYMES LACK A CATALYTIC ASPARTATE" |
| 155C | THE STRUCTURE OF PARACOCCUS DENITRIFICANS CYTOCHROME C550 |
| 155L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 156L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 157L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 158L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 159L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 15C8 | CATALYTIC ANTIBODY 5C8, FREE FAB |
| 160L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 161L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 162L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 163L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 164L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 165L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 166L | CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
| 167L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 168L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 169L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 16GS | GLUTATHIONE S-TRANSFERASE P1-1 APO FORM 3 |
| 16PK | PHOSPHOGLYCERATE KINASE FROM TRYPANOSOMA BRUCEI BISUBSTRATE ANALOG |
| 16VP | CONSERVED CORE OF THE HERPES SIMPLEX VIRUS TRANSCRIPTIONAL REGULATORY PROTEIN VP16 |
| 170L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 171L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 172L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 173L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 174L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 175L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 176L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 177L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 178L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 17GS | GLUTATHIONE S-TRANSFERASE P1-1 |
| 180L | PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
| 181L | SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
| 182L | SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
| 183L | SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
| 184L | SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
| 185L | SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
| 186L | SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
| 187L | SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
| 188L | SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
| 189L | ENHANCEMENT OF PROTEIN STABILITY BY THE COMBINATION OF POINT MUTATIONS IN T4 LYSOZYME IS ADDITIVE |
| 18GS | GLUTATHIONE S-TRANSFERASE P1-1 COMPLEXED WITH 1-(S-GLUTATHIONYL)-2,4-DINITROBENZENE |
| 190L | A HELIX INITIATION SIGNAL IN T4 LYSOZYME IDENTIFIED BY POLYALANINE MUTAGENESIS |
| 1914 | SIGNAL RECOGNITION PARTICLE ALU RNA BINDING HETERODIMER, SRP9/14 |
| 191L | A HELIX INITIATION SIGNAL IN T4 LYSOZYME IDENTIFIED BY POLYALANINE MUTAGENESIS |
| 192L | A HELIX INITIATION SIGNAL IN T4 LYSOZYME IDENTIFIED BY POLYALANINE MUTAGENESIS |
| 193L | THE 1.33 A STRUCTURE OF TETRAGONAL HEN EGG WHITE LYSOZYME |
| 194L | THE 1.40 A STRUCTURE OF SPACEHAB-01 HEN EGG WHITE LYSOZYME |
| 195L | THERMODYNAMIC AND STRUCTURAL COMPENSATION IN SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME" |
| 196L | THERMODYNAMIC AND STRUCTURAL COMPENSATION IN SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME" |
| 197L | THERMODYNAMIC AND STRUCTURAL COMPENSATION IN SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME" |
| 198L | THERMODYNAMIC AND STRUCTURAL COMPENSATION IN SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME" |
| 199L | THERMODYNAMIC AND STRUCTURAL COMPENSATION IN SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME" |
| 19GS | GLUTATHIONE S-TRANSFERASE P1-1 |
| 19HC | NINE-HAEM CYTOCHROME C FROM DESULFOVIBRIO DESULFURICANS ATCC 27774 |
| 1A00 | HEMOGLOBIN (VAL BETA1 MET, TRP BETA37 TYR) MUTANT |
| 1A01 | HEMOGLOBIN (VAL BETA1 MET, TRP BETA37 ALA) MUTANT |
| 1A02 | STRUCTURE OF THE DNA BINDING DOMAINS OF NFAT, FOS AND JUN BOUND TO DNA |
| 1A03 | THE THREE-DIMENSIONAL STRUCTURE OF CA2+-BOUND CALCYCLIN: IMPLICATIONS FOR CA2+-SIGNAL TRANSDUCTION BY S100 PROTEINS, NMR, 20 STRUCTURES |
| 1A04 | THE STRUCTURE OF THE NITRATE/NITRITE RESPONSE REGULATOR PROTEIN NARL IN THE MONOCLINIC C2 CRYSTAL FORM |
| 1A05 | CRYSTAL STRUCTURE OF THE COMPLEX OF 3-ISOPROPYLMALATE DEHYDROGENASE FROM THIOBACILLUS FERROOXIDANS WITH 3-ISOPROPYLMALATE |
| 1A06 | CALMODULIN-DEPENDENT PROTEIN KINASE FROM RAT |
| 1A07 | C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-MALONYL TYR-GLU-(N,N-DIPENTYL AMINE) |
| 1A08 | C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-DIFLUORO PHOSPHOTYR-GLU-(N,N-DIPENTYL AMINE) |
| 1A09 | C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-FORMYL PHOSPHOTYR-GLU-(N,N-DIPENTYL AMINE) |
| 1A0A | PHOSPHATE SYSTEM POSITIVE REGULATORY PROTEIN PHO4/DNA COMPLEX |
| 1A0B | HISTIDINE-CONTAINING PHOSPHOTRANSFER DOMAIN OF ARCB FROM ESCHERICHIA COLI |
| 1A0C | XYLOSE ISOMERASE FROM THERMOANAEROBACTERIUM THERMOSULFURIGENES |
| 1A0D | XYLOSE ISOMERASE FROM BACILLUS STEAROTHERMOPHILUS |
| 1A0E | XYLOSE ISOMERASE FROM THERMOTOGA NEAPOLITANA |
| 1A0F | CRYSTAL STRUCTURE OF GLUTATHIONE S-TRANSFERASE FROM ESCHERICHIA COLI COMPLEXED WITH GLUTATHIONESULFONIC ACID |
| 1A0G | L201A MUTANT OF D-AMINO ACID AMINOTRANSFERASE COMPLEXED WITH PYRIDOXAMINE-5'-PHOSPHATE |
| 1A0H | THE X-RAY CRYSTAL STRUCTURE OF PPACK-MEIZOTHROMBIN DESF1: KRINGLE/THROMBIN AND CARBOHYDRATE/KRINGLE/THROMBIN INTERACTIONS AND LOCATION OF THE LINKER CHAIN |
| 1A0I | ATP-DEPENDENT DNA LIGASE FROM BACTERIOPHAGE T7 COMPLEX WITH ATP |
| 1A0J | CRYSTAL STRUCTURE OF A NON-PSYCHROPHILIC TRYPSIN FROM A COLD-ADAPTED FISH SPECIES. |
| 1A0K | PROFILIN I FROM ARABIDOPSIS THALIANA |
| 1A0L | HUMAN BETA-TRYPTASE: A RING-LIKE TETRAMER WITH ACTIVE SITES FACING A CENTRAL PORE |
| 1A0M | 1.1 ANGSTROM CRYSTAL STRUCTURE OF A-CONOTOXIN [TYR15]-EPI |
| 1A0N | NMR STUDY OF THE SH3 DOMAIN FROM FYN PROTO-ONCOGENE TYROSINE KINASE COMPLEXED WITH THE SYNTHETIC PEPTIDE P2L CORRESPONDING TO RESIDUES 91-104 OF THE P85 SUBUNIT OF PI3-KINASE, FAMILY OF 25 STRUCTURES |
| 1A0O | CHEY-BINDING DOMAIN OF CHEA IN COMPLEX WITH CHEY |
| 1A0P | SITE-SPECIFIC RECOMBINASE, XERD |
| 1A0Q | 29G11 COMPLEXED WITH PHENYL [1-(1-N-SUCCINYLAMINO)PENTYL] PHOSPHONATE |
| 1A0R | HETEROTRIMERIC COMPLEX OF PHOSDUCIN/TRANSDUCIN BETA-GAMMA |
| 1A0S | SUCROSE-SPECIFIC PORIN |
| 1A0T | SUCROSE-SPECIFIC PORIN, WITH BOUND SUCROSE MOLECULES |
| 1A0U | HEMOGLOBIN (VAL BETA1 MET) MUTANT |
| 1A0Z | HEMOGLOBIN (VAL BETA1 MET) MUTANT |
| 1A11 | NMR STRUCTURE OF MEMBRANE SPANNING SEGMENT 2 OF THE ACETYLCHOLINE RECEPTOR IN DPC MICELLES, 10 STRUCTURES |
| 1A12 | REGULATOR OF CHROMOSOME CONDENSATION (RCC1) OF HUMAN |
| 1A13 | G PROTEIN-BOUND CONFORMATION OF MASTOPARAN-X, NMR, 14 STRUCTURES |
| 1A14 | COMPLEX BETWEEN NC10 ANTI-INFLUENZA VIRUS NEURAMINIDASE SINGLE CHAIN ANTIBODY WITH A 5 RESIDUE LINKER AND INFLUENZA VIRUS NEURAMINIDASE |
| 1A15 | SDF-1ALPHA |
| 1A16 | AMINOPEPTIDASE P FROM E. COLI WITH THE INHIBITOR PRO-LEU |
| 1A17 | TETRATRICOPEPTIDE REPEATS OF PROTEIN PHOSPHATASE 5 |
| 1A18 | PHENANTHROLINE MODIFIED MURINE ADIPOCYTE LIPID BINDING PROTEIN |
| 1A19 | BARSTAR (FREE), C82A MUTANT |
| 1A1A | C-SRC (SH2 DOMAIN WITH C188A MUTATION) COMPLEXED WITH ACE-FORMYL PHOSPHOTYR-GLU-(N,N-DIPENTYL AMINE) |
| 1A1B | C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-PHOSPHOTYR-GLU-(N,N-DIPENTYL AMINE) |
| 1A1C | C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-PHOSPHOTYR-GLU-(N-ME(-(CH2)3-CYCLOPENTYL)) |
| 1A1E | C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-PHOSPHOTYR-GLU-(3-BUTYLPIPERIDINE) |
| 1A1F | DSNR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GACC SITE) |
| 1A1G | DSNR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GCGT SITE) |
| 1A1H | QGSR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GCAC SITE) |
| 1A1I | RADR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GCAC SITE) |
| 1A1J | RADR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GCGT SITE) |
| 1A1K | RADR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GACC SITE) |
| 1A1L | ZIF268 ZINC FINGER-DNA COMPLEX (GCAC SITE) |
| 1A1M | MHC CLASS I MOLECULE B*5301 COMPLEXED WITH PEPTIDE TPYDINQML FROM GAG PROTEIN OF HIV2 |
| 1A1N | MHC CLASS I MOLECULE B*3501 COMPLEXED WITH PEPTIDE VPLRPMTY FROM THE NEF PROTEIN (75-82) OF HIV1 |
| 1A1O | MHC CLASS I MOLECULE B*5301 COMPLEXED WITH PEPTIDE LS6 (KPIVQYDNF) FROM THE MALARIA PARASITE P. FALCIPARUM |
| 1A1P | COMPSTATIN, NMR, 21 STRUCTURES |
| 1A1Q | HEPATITIS C VIRUS NS3 PROTEINASE |
| 1A1R | HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX |
| 1A1S | ORNITHINE CARBAMOYLTRANSFERASE FROM PYROCOCCUS FURIOSUS |
| 1A1T | STRUCTURE OF THE HIV-1 NUCLEOCAPSID PROTEIN BOUND TO THE SL3 PSI-RNA RECOGNITION ELEMENT, NMR, 25 STRUCTURES |
| 1A1U | SOLUTION STRUCTURE DETERMINATION OF A P53 MUTANT DIMERIZATION DOMAIN, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1A1V | HEPATITIS C VIRUS NS3 HELICASE DOMAIN COMPLEXED WITH SINGLE STRANDED SDNA |
| 1A1W | FADD DEATH EFFECTOR DOMAIN, F25Y MUTANT, NMR MINIMIZED AVERAGE STRUCTURE |
| 1A1X | CRYSTAL STRUCTURE OF MTCP-1 INVOLVED IN T CELL MALIGNANCIES |
| 1A1Z | FADD DEATH EFFECTOR DOMAIN, F25G MUTANT, NMR MINIMIZED AVERAGE STRUCTURE |
| 1A21 | TISSUE FACTOR (TF) FROM RABBIT |
| 1A22 | HUMAN GROWTH HORMONE BOUND TO SINGLE RECEPTOR |
| 1A23 | SOLUTION NMR STRUCTURE OF REDUCED DSBA FROM ESCHERICHIA COLI, MINIMIZED AVERAGE STRUCTURE |
| 1A24 | SOLUTION NMR STRUCTURE OF REDUCED DSBA FROM ESCHERICHIA COLI, FAMILY OF 20 STRUCTURES |
| 1A25 | C2 DOMAIN FROM PROTEIN KINASE C (BETA) |
| 1A26 | THE CATALYTIC FRAGMENT OF POLY(ADP-RIBOSE) POLYMERASE COMPLEXED WITH CARBA-NAD |
| 1A27 | HUMAN 17-BETA-HYDROXYSTEROID-DEHYDROGENASE TYPE 1 C-TERMINAL DELETION MUTANT COMPLEXED WITH ESTRADIOL AND NADP+ |
| 1A28 | HORMONE-BOUND HUMAN PROGESTERONE RECEPTOR LIGAND-BINDING DOMAIN |
| 1A29 | CALMODULIN COMPLEXED WITH TRIFLUOPERAZINE (1:2 COMPLEX) |
| 1A2A | AGKISTROTOXIN, A PHOSPHOLIPASE A2-TYPE PRESYNAPTIC NEUROTOXIN FROM AGKISTRODON HALYS PALLAS |
| 1A2B | HUMAN RHOA COMPLEXED WITH GTP ANALOGUE |
| 1A2C | STRUCTURE OF THROMBIN INHIBITED BY AERUGINOSIN298-A FROM A BLUE-GREEN ALGA |
| 1A2D | PYRIDOXAMINE MODIFIED MURINE ADIPOCYTE LIPID BINDING PROTEIN |
| 1A2F | PROBING THE STRENGTH AND CHARACTER OF AN ASP-HIS-X HYDROGEN BOND BY INTRODUCING BURIED CHARGES |
| 1A2G | PROBING THE STRENGTH AND CHARACTER OF AN ASP-HIS-X HYDROGEN BOND BY INTRODUCING BURIED CHARGES |
| 1A2I | SOLUTION STRUCTURE OF DESULFOVIBRIO VULGARIS (HILDENBOROUGH) FERROCYTOCHROME C3, NMR, 20 STRUCTURES |
| 1A2J | OXIDIZED DSBA CRYSTAL FORM II |
| 1A2K | GDPRAN-NTF2 COMPLEX |
| 1A2L | REDUCED DSBA AT 2.7 ANGSTROMS RESOLUTION |
| 1A2M | OXIDIZED DSBA AT 2.7 ANGSTROMS RESOLUTION, CRYSTAL FORM III |
| 1A2N | STRUCTURE OF THE C115A MUTANT OF MURA COMPLEXED WITH THE FLUORINATED ANALOG OF THE REACTION TETRAHEDRAL INTERMEDIATE |
| 1A2O | STRUCTURAL BASIS FOR METHYLESTERASE CHEB REGULATION BY A PHOSPHORYLATION-ACTIVATED DOMAIN |
| 1A2P | BARNASE WILDTYPE STRUCTURE AT 1.5 ANGSTROMS RESOLUTION |
| 1A2Q | SUBTILISIN BPN' MUTANT 7186 |
| 1A2S | THE SOLUTION NMR STRUCTURE OF OXIDIZED CYTOCHROME C6 FROM THE GREEN ALGA MONORAPHIDIUM BRAUNII, MINIMIZED AVERAGE STRUCTURE |
| 1A2T | STAPHYLOCOCCAL NUCLEASE, B-MERCAPTOETHANOL DISULFIDE TO V23C VARIANT |
| 1A2U | STAPHYLOCOCCAL NUCLEASE, V23C VARIANT, COMPLEX WITH 1-N-BUTANE THIOL AND 3',5'-THYMIDINE DIPHOSPHATE |
| 1A2V | COPPER AMINE OXIDASE FROM HANSENULA POLYMORPHA |
| 1A2W | CRYSTAL STRUCTURE OF A 3D DOMAIN-SWAPPED DIMER OF BOVINE PANCREATIC RIBONUCLEASE A |
| 1A2X | COMPLEX OF TROPONIN C WITH A 47 RESIDUE (1-47) FRAGMENT OF TROPONIN I |
| 1A2Y | HEN EGG WHITE LYSOZYME, D18A MUTANT, IN COMPLEX WITH MOUSE MONOCLONAL ANTIBODY D1.3 |
| 1A2Z | PYRROLIDONE CARBOXYL PEPTIDASE FROM THERMOCOCCUS LITORALIS |
| 1A30 | HIV-1 PROTEASE COMPLEXED WITH A TRIPEPTIDE INHIBITOR |
| 1A31 | HUMAN RECONSTITUTED DNA TOPOISOMERASE I IN COVALENT COMPLEX WITH A 22 BASE PAIR DNA DUPLEX |
| 1A32 | RIBOSOMAL PROTEIN S15 FROM BACILLUS STEAROTHERMOPHILUS |
| 1A33 | PEPTIDYLPROLYL ISOMERASE, CYCLOPHILIN-LIKE DOMAIN FROM BRUGIA MALAYI |
| 1A34 | SATELLITE TOBACCO MOSAIC VIRUS/RNA COMPLEX |
| 1A35 | HUMAN TOPOISOMERASE I/DNA COMPLEX |
| 1A36 | TOPOISOMERASE I/DNA COMPLEX |
| 1A37 | 14-3-3 PROTEIN ZETA BOUND TO PS-RAF259 PEPTIDE |
| 1A38 | 14-3-3 PROTEIN ZETA BOUND TO R18 PEPTIDE |
| 1A39 | HUMICOLA INSOLENS ENDOCELLULASE EGI S37W, P39W DOUBLE-MUTANT |
| 1A3A | CRYSTAL STRUCTURE OF IIA MANNITOL FROM ESCHERICHIA COLI |
| 1A3B | COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG1 |
| 1A3C | PYRR, THE BACILLUS SUBTILIS PYRIMIDINE BIOSYNTHETIC OPERON REPRESSOR, DIMERIC FORM |
| 1A3D | PHOSPHOLIPASE A2 (PLA2) FROM NAJA NAJA VENOM |
| 1A3E | COMPLEX OF HUMAN ALPHA-THROMBIN WITH THE BIFUNCTIONAL BORONATE INHIBITOR BOROLOG2 |
| 1A3F | PHOSPHOLIPASE A2 (PLA2) FROM NAJA NAJA VENOM |
| 1A3G | BRANCHED-CHAIN AMINO ACID AMINOTRANSFERASE FROM ESCHERICHIA COLI |
| 1A3H | ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHERANS AT 1.6A RESOLUTION |
| 1A3I | X-RAY CRYSTALLOGRAPHIC DETERMINATION OF A COLLAGEN-LIKE PEPTIDE WITH THE REPEATING SEQUENCE (PRO-PRO-GLY) |
| 1A3K | X-RAY CRYSTAL STRUCTURE OF THE HUMAN GALECTIN-3 CARBOHYDRATE RECOGNITION DOMAIN (CRD) AT 2.1 ANGSTROM RESOLUTION |
| 1A3L | CATALYSIS OF A DISFAVORED REACTION: AN ANTIBODY EXO DIELS-ALDERASE-TSA-INHIBITOR COMPLEX AT 1.95 A RESOLUTION |
| 1A3N | DEOXY HUMAN HEMOGLOBIN |
| 1A3O | ARTIFICIAL MUTANT (ALPHA Y42H) OF DEOXY HEMOGLOBIN |
| 1A3P | ROLE OF THE 6-20 DISULFIDE BRIDGE IN THE STRUCTURE AND ACTIVITY OF EPIDERMAL GROWTH FACTOR, NMR, 20 STRUCTURES |
| 1A3Q | HUMAN NF-KAPPA-B P52 BOUND TO DNA |
| 1A3R | FAB FRAGMENT (ANTIBODY 8F5) COMPLEXED WITH PEPTIDE FROM HUMAN RHINOVIRUS (SEROTYPE 2) VIRAL CAPSID PROTEIN VP2 (RESIDUES 156-170) |
| 1A3S | HUMAN UBC9 |
| 1A3T | STAPHYLOCOCCAL NUCLEASE, V23C VARIANT, COMPLEX WITH 2-FLUOROETHANE THIOL AND 3',5'-THYMIDINE DIPHOSPHATE |
| 1A3U | STAPHYLOCOCCAL NUCLEASE, CYCLOHEXANE THIOL DISULFIDE TO V23C VARIANT |
| 1A3V | STAPHYLOCOCCAL NUCLEASE, CYCLOPENTANE THIOL DISULFIDE TO V23C VARIANT |
| 1A3W | PYRUVATE KINASE FROM SACCHAROMYCES CEREVISIAE COMPLEXED WITH FBP, PG, MN2+ AND K+ |
| 1A3X | PYRUVATE KINASE FROM SACCHAROMYCES CEREVISIAE COMPLEXED WITH PG, MN2+ AND K+ |
| 1A3Y | ODORANT BINDING PROTEIN FROM NASAL MUCOSA OF PIG |
| 1A3Z | REDUCED RUSTICYANIN AT 1.9 ANGSTROMS |
| 1A40 | PHOSPHATE-BINDING PROTEIN WITH ALA 197 REPLACED WITH TRP |
| 1A41 | TYPE 1-TOPOISOMERASE CATALYTIC FRAGMENT FROM VACCINIA VIRUS |
| 1A42 | HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH BRINZOLAMIDE |
| 1A43 | STRUCTURE OF THE HIV-1 CAPSID PROTEIN DIMERIZATION DOMAIN AT 2.6A RESOLUTION |
| 1A44 | PHOSPHATIDYLETHANOLAMINE BINDING PROTEIN FROM CALF BRAIN |
| 1A45 | GAMMAF CRYSTALLIN FROM BOVINE LENS |
| 1A46 | THROMBIN COMPLEXED WITH HIRUGEN AND A BETA-STRAND MIMETIC INHIBITOR |
| 1A47 | CGTASE FROM THERMOANAEROBACTERIUM THERMOSULFURIGENES EM1 IN COMPLEX WITH A MALTOHEXAOSE INHIBITOR |
| 1A48 | SAICAR SYNTHASE |
| 1A4A | AZURIN MUTANT WITH MET 121 REPLACED BY HIS, PH 6.5 CRYSTAL FORM, DATA COLLECTED AT 16 DEGREES CELSIUS |
| 1A4B | AZURIN MUTANT WITH MET 121 REPLACED BY HIS, PH 6.5 CRYSTAL FORM, DATA COLLECTED AT-180 DEGREES CELSIUS |
| 1A4C | AZURIN MUTANT WITH MET 121 REPLACED BY HIS, PH 3.5 CRYSTAL FORM, DATA COLLECTED AT-180 DEGREES CELSIUS |
| 1A4E | CATALASE A FROM SACCHAROMYCES CEREVISIAE |
| 1A4F | BAR-HEADED GOOSE HEMOGLOBIN (OXY FORM) |
| 1A4G | INFLUENZA VIRUS B/BEIJING/1/87 NEURAMINIDASE COMPLEXED WITH ZANAMIVIR |
| 1A4H | STRUCTURE OF THE N-TERMINAL DOMAIN OF THE YEAST HSP90 CHAPERONE IN COMPLEX WITH GELDANAMYCIN |
| 1A4I | HUMAN TETRAHYDROFOLATE DEHYDROGENASE / CYCLOHYDROLASE |
| 1A4J | DIELS ALDER CATALYTIC ANTIBODY GERMLINE PRECURSOR |
| 1A4K | DIELS ALDER CATALYTIC ANTIBODY WITH TRANSITION STATE ANALOGUE |
| 1A4L | ADA STRUCTURE COMPLEXED WITH DEOXYCOFORMYCIN AT PH 7.0 |
| 1A4M | ADA STRUCTURE COMPLEXED WITH PURINE RIBOSIDE AT PH 7.0 |
| 1A4O | 14-3-3 PROTEIN ZETA ISOFORM |
| 1A4P | P11 (S100A10), LIGAND OF ANNEXIN II |
| 1A4Q | INFLUENZA VIRUS B/BEIJING/1/87 NEURAMINIDASE COMPLEXED WITH DIHYDROPYRAN-PHENETHYL-PROPYL-CARBOXAMIDE |
| 1A4R | G12V MUTANT OF HUMAN PLACENTAL CDC42 GTPASE IN THE GDP FORM |
| 1A4S | BETAINE ALDEHYDE DEHYDROGENASE FROM COD LIVER |
| 1A4T | SOLUTION STRUCTURE OF PHAGE P22 N PEPTIDE-BOX B RNA COMPLEX, NMR, 20 STRUCTURES |
| 1A4U | ALCOHOL DEHYDROGENASE FROM DROSOPHILA LEBANONENSIS |
| 1A4V | ALPHA-LACTALBUMIN |
| 1A4W | CRYSTAL STRUCTURES OF THROMBIN WITH THIAZOLE-CONTAINING INHIBITORS: PROBES OF THE S1' BINDING SITE |
| 1A4X | PYRR, THE BACILLUS SUBTILIS PYRIMIDINE BIOSYNTHETIC OPERON REPRESSOR, HEXAMERIC FORM |
| 1A4Y | RIBONUCLEASE INHIBITOR-ANGIOGENIN COMPLEX |
| 1A4Z | ALDEHYDE DEHYDROGENASE FROM BOVINE MITOCHONDRIA COMPLEX WITH NAD (REDUCED) AND SAMARIUM (III) |
| 1A50 | CRYSTAL STRUCTURE OF WILD-TYPE TRYPTOPHAN SYNTHASE COMPLEXED WITH 5-FLUOROINDOLE PROPANOL PHOSPHATE |
| 1A52 | ESTROGEN RECEPTOR ALPHA LIGAND-BINDING DOMAIN COMPLEXED TO ESTRADIOL |
| 1A53 | COMPLEX OF INDOLE-3-GLYCEROLPHOSPHATE SYNTHASE FROM SULFOLOBUS SOLFATARICUS WITH INDOLE-3-GLYCEROLPHOSPHATE AT 2.0 A RESOLUTION |
| 1A54 | PHOSPHATE-BINDING PROTEIN MUTANT A197C LABELLED WITH A COUMARIN FLUOROPHORE AND BOUND TO DIHYDROGENPHOSPHATE ION |
| 1A55 | PHOSPHATE-BINDING PROTEIN MUTANT A197C |
| 1A56 | PRIMARY SEQUENCE AND SOLUTION CONFORMATION OF FERRICYTOCHROME C-552 FROM NITROSOMONAS EUROPAEA, NMR, MEAN STRUCTURE REFINED WITH EXPLICIT HYDROGEN BOND CONSTRAINTS |
| 1A57 | THE THREE-DIMENSIONAL STRUCTURE OF A HELIX-LESS VARIANT OF INTESTINAL FATTY ACID BINDING PROTEIN, NMR, 20 STRUCTURES |
| 1A58 | CYCLOPHILIN FROM BRUGIA MALAYI |
| 1A59 | COLD-ACTIVE CITRATE SYNTHASE |
| 1A5A | CRYO-CRYSTALLOGRAPHY OF A TRUE SUBSTRATE, INDOLE-3-GLYCEROL PHOSPHATE, BOUND TO A MUTANT (ALPHAD60N) TRYPTOPHAN SYNTHASE ALPHA2BETA2 COMPLEX REVEALS THE CORRECT ORIENTATION OF ACTIVE SITE ALPHA GLU 49 |
| 1A5B | CRYO-CRYSTALLOGRAPHY OF A TRUE SUBSTRATE, INDOLE-3-GLYCEROL PHOSPHATE, BOUND TO A MUTANT (ALPHA D60N) TRYPTOPHAN SYNTHASE ALPHA2BETA2 COMPLEX REVEALS THE CORRECT ORIENTATION OF ACTIVE SITE ALPHA GLU 49 |
| 1A5C | FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE FROM PLASMODIUM FALCIPARUM |
| 1A5D | GAMMAE CRYSTALLIN FROM RAT LENS |
| 1A5E | SOLUTION NMR STRUCTURE OF TUMOR SUPPRESSOR P16INK4A, 18 STRUCTURES |
| 1A5F | FAB FRAGMENT OF A MONOCLONAL ANTI-E-SELECTIN ANTIBODY |
| 1A5G | HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN |
| 1A5H | CATALYTIC DOMAIN OF HUMAN TWO-CHAIN TISSUE PLASMINOGEN ACTIVATOR COMPLEX OF A BIS-BENZAMIDINE |
| 1A5I | CATALYTIC DOMAIN OF VAMPIRE BAT (DESMODUS ROTUNDUS) SALIVA PLASMINOGEN ACTIVATOR IN COMPLEX WITH EGR-CMK (GLU-GLY-ARG CHLOROMETHYL KETONE) |
| 1A5J | CHICKEN B-MYB DNA BINDING DOMAIN, REPEAT 2 AND REPEAT3, NMR, 32 STRUCTURES |
| 1A5K | K217E VARIANT OF KLEBSIELLA AEROGENES UREASE |
| 1A5L | K217C VARIANT OF KLEBSIELLA AEROGENES UREASE |
| 1A5M | K217A VARIANT OF KLEBSIELLA AEROGENES UREASE |
| 1A5N | K217A VARIANT OF KLEBSIELLA AEROGENES UREASE, CHEMICALLY RESCUED BY FORMATE AND NICKEL |
| 1A5O | K217C VARIANT OF KLEBSIELLA AEROGENES UREASE, CHEMICALLY RESCUED BY FORMATE AND NICKEL |
| 1A5P | C[40,95]A VARIANT OF BOVINE PANCREATIC RIBONUCLEASE A |
| 1A5Q | P93A VARIANT OF BOVINE PANCREATIC RIBONUCLEASE A |
| 1A5R | STRUCTURE DETERMINATION OF THE SMALL UBIQUITIN-RELATED MODIFIER SUMO-1, NMR, 10 STRUCTURES |
| 1A5S | CRYSTAL STRUCTURE OF WILD-TYPE TRYPTOPHAN SYNTHASE COMPLEXED WITH 5-FLUOROINDOLE PROPANOL PHOSPHATE AND L-SER BOUND AS AMINO ACRYLATE TO THE BETA SITE |
| 1A5T | CRYSTAL STRUCTURE OF THE DELTA PRIME SUBUNIT OF THE CLAMP-LOADER COMPLEX OF ESCHERICHIA COLI DNA POLYMERASE III |
| 1A5V | ASV INTEGRASE CORE DOMAIN WITH HIV-1 INTEGRASE INHIBITOR Y3 AND MN CATION |
| 1A5W | ASV INTEGRASE CORE DOMAIN WITH HIV-1 INTEGRASE INHIBITOR Y3 |
| 1A5X | ASV INTEGRASE CORE DOMAIN WITH HIV-1 INTEGRASE INHIBITOR Y3 |
| 1A5Y | PROTEIN TYROSINE PHOSPHATASE 1B CYSTEINYL-PHOSPHATE INTERMEDIATE |
| 1A5Z | LACTATE DEHYDROGENASE FROM THERMOTOGA MARITIMA (TMLDH) |
| 1A61 | THROMBIN COMPLEXED WITH A BETA-MIMETIC THIAZOLE-CONTAINING INHIBITOR |
| 1A62 | CRYSTAL STRUCTURE OF THE RNA-BINDING DOMAIN OF THE TRANSCRIPTIONAL TERMINATOR PROTEIN RHO |
| 1A63 | THE NMR STRUCTURE OF THE RNA BINDING DOMAIN OF E.COLI RHO FACTOR SUGGESTS POSSIBLE RNA-PROTEIN INTERACTIONS, 10 STRUCTURES |
| 1A64 | ENGINEERING A MISFOLDED FORM OF RAT CD2 |
| 1A65 | TYPE-2 CU-DEPLETED LACCASE FROM COPRINUS CINEREUS |
| 1A66 | SOLUTION NMR STRUCTURE OF THE CORE NFATC1/DNA COMPLEX, 18 STRUCTURES |
| 1A67 | CHICKEN EGG WHITE CYSTATIN WILDTYPE, NMR, 16 STRUCTURES |
| 1A68 | CRYSTAL STRUCTURE OF THE TETRAMERIZATION DOMAIN OF THE SHAKER POTASSIUM CHANNEL |
| 1A69 | PURINE NUCLEOSIDE PHOSPHORYLASE IN COMPLEX WITH FORMYCIN B AND SULPHATE (PHOSPHATE) |
| 1A6A | THE STRUCTURE OF AN INTERMEDIATE IN CLASS II MHC MATURATION: CLIP BOUND TO HLA-DR3 |
| 1A6B | NMR STRUCTURE OF THE COMPLEX BETWEEN THE ZINC FINGER PROTEIN NCP10 OF MOLONEY MURINE LEUKEMIA VIRUS AND A SEQUENCE OF THE PSI-PACKAGING DOMAIN OF HIV-1, 20 STRUCTURES |
| 1A6C | STRUCTURE OF TOBACCO RINGSPOT VIRUS |
| 1A6D | THERMOSOME FROM T. ACIDOPHILUM |
| 1A6E | THERMOSOME-MG-ADP-ALF3 COMPLEX |
| 1A6F | RNASE P PROTEIN FROM BACILLUS SUBTILIS |
| 1A6G | CARBONMONOXY-MYOGLOBIN, ATOMIC RESOLUTION |
| 1A6I | TET REPRESSOR, CLASS D VARIANT |
| 1A6J | NITROGEN REGULATORY BACTERIAL PROTEIN IIA-NITROGEN |
| 1A6K | AQUOMET-MYOGLOBIN, ATOMIC RESOLUTION |
| 1A6L | T14C MUTANT OF AZOTOBACTER VINELANDII FDI |
| 1A6M | OXY-MYOGLOBIN, ATOMIC RESOLUTION |
| 1A6N | DEOXY-MYOGLOBIN, ATOMIC RESOLUTION |
| 1A6P | ENGINEERING OF A MISFOLDED FORM OF CD2 |
| 1A6Q | CRYSTAL STRUCTURE OF THE PROTEIN SERINE/THREONINE PHOSPHATASE 2C AT 2 A RESOLUTION |
| 1A6R | GAL6 (YEAST BLEOMYCIN HYDROLASE) MUTANT C73A |
| 1A6S | M-DOMAIN FROM GAG POLYPROTEIN OF ROUS SARCOMA VIRUS, NMR, 20 STRUCTURES |
| 1A6T | FAB FRAGMENT OF MAB1-IA MONOCLONAL ANTIBODY TO HUMAN RHINOVIRUS 14 NIM-IA SITE |
| 1A6U | B1-8 FV FRAGMENT |
| 1A6V | B1-8 FV FRAGMENT COMPLEXED WITH A (4-HYDROXY-3-NITROPHENYL) ACETATE COMPOUND |
| 1A6W | B1-8 FV FRAGMENT COMPLEXED WITH A (4-HYDROXY-5-IODO-3-NITROPHENYL) ACETATE COMPOUND |
| 1A6X | STRUCTURE OF THE APO-BIOTIN CARBOXYL CARRIER PROTEIN (APO-BCCP87) OF ESCHERICHIA COLI ACETYL-COA CARBOXYLASE, NMR, 49 STRUCTURES |
| 1A6Y | REVERBA ORPHAN NUCLEAR RECEPTOR/DNA COMPLEX |
| 1A6Z | HFE (HUMAN) HEMOCHROMATOSIS PROTEIN |
| 1A70 | SPINACH FERREDOXIN |
| 1A71 | TERNARY COMPLEX OF AN ACTIVE SITE DOUBLE MUTANT OF HORSE LIVER ALCOHOL DEHYDROGENASE, PHE93=>TRP, VAL203=>ALA WITH NAD AND TRIFLUOROETHANOL |
| 1A72 | AN ACTIVE-SITE DOUBLE MUTANT (PHE93->TRP, VAL203->ALA) OF HORSE LIVER ALCOHOL DEHYDROGENASE IN COMPLEX WITH THE ISOSTERIC NAD ANALOG CPAD |
| 1A73 | INTRON-ENCODED ENDONUCLEASE I-PPOI COMPLEXED WITH DNA |
| 1A74 | I-PPOL HOMING ENDONUCLEASE/DNA COMPLEX |
| 1A75 | WHITING PARVALBUMIN |
| 1A76 | FLAP ENDONUCLEASE-1 FROM METHANOCOCCUS JANNASCHII |
| 1A77 | FLAP ENDONUCLEASE-1 FROM METHANOCOCCUS JANNASCHII |
| 1A78 | COMPLEX OF TOAD OVARY GALECTIN WITH THIO-DIGALACTOSE |
| 1A79 | CRYSTAL STRUCTURE OF THE TRNA SPLICING ENDONUCLEASE FROM METHANOCOCCUS JANNASCHII |
| 1A7A | STRUCTURE OF HUMAN PLACENTAL S-ADENOSYLHOMOCYSTEINE HYDROLASE: DETERMINATION OF A 30 SELENIUM ATOM SUBSTRUCTURE FROM DATA AT A SINGLE WAVELENGTH |
| 1A7B | ENGINEERING A MISFOLDED FORM OF CD2 |
| 1A7C | HUMAN PLASMINOGEN ACTIVATOR INHIBITOR TYPE-1 IN COMPLEX WITH A PENTAPEPTIDE |
| 1A7D | CHLOROMET MYOHEMERYTHRIN FROM THEMISTE ZOSTERICOLA |
| 1A7E | HYDROXOMET MYOHEMERYTHRIN FROM THEMISTE ZOSTERICOLA |
| 1A7F | INSULIN MUTANT B16 GLU, B24 GLY, DES-B30, NMR, 20 STRUCTURES |
| 1A7G | THE CRYSTAL STRUCTURE OF THE E2 DNA-BINDING DOMAIN FROM HUMAN PAPILLOMAVIRUS AT 2.4 ANGSTROMS |
| 1A7H | GAMMA S CRYSTALLIN C-TERMINAL DOMAIN |
| 1A7I | AMINO-TERMINAL LIM DOMAIN FROM QUAIL CYSTEINE AND GLYCINE-RICH PROTEIN, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1A7J | PHOSPHORIBULOKINASE FROM RHODOBACTER SPHEROIDES |
| 1A7K | GLYCOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE IN A MONOCLINIC CRYSTAL FORM |
| 1A7L | DOMINANT B-CELL EPITOPE FROM THE PRES2 REGION OF HEPATITIS B VIRUS IN THE FORM OF AN INSERTED PEPTIDE SEGMENT IN MALTODEXTRIN-BINDING PROTEIN |
| 1A7M | LEUKAEMIA INHIBITORY FACTOR CHIMERA (MH35-LIF), NMR, 20 STRUCTURES |
| 1A7N | FV FRAGMENT OF MOUSE MONOCLONAL ANTIBODY D1.3 (BALB/C, IGG1, K) VARIANT FOR CHAIN L GLU81->ASP AND CHAIN H LEU312->VAL |
| 1A7O | FV FRAGMENT OF MOUSE MONOCLONAL ANTIBODY D1.3 (BALB/C, IGG1, K) R96L DELETION MUTANT ON VARIANT FOR CHAIN L GLU81->ASP AND CHAIN H LEU312->VAL |
| 1A7P | FV FRAGMENT OF MOUSE MONOCLONAL ANTIBODY D1.3 (BALB/C, IGG1, K) ENGINEERED MUTANT PRO95L->SER ON VARIANT CHAIN L GLU81->ASP AND CHAIN H LEU312->VAL |
| 1A7Q | FV FRAGMENT OF MOUSE MONOCLONAL ANTIBODY D1.3 (BALB/C, IGG1, K) HIGH AFFINITY EXPRESSED VARIANT CONTAINING SER26L->GLY, ILE29L->THR, GLU81L->ASP, THR97L->SER, PRO240H->LEU, ASP258H->ALA, LYS281H->GLU, ASN283H->ASP AND LEU312H->VAL |
| 1A7R | FV FRAGMENT OF MOUSE MONOCLONAL ANTIBODY D1.3 (BALB/C, IGG1, K) VARIANT CHAIN L GLU81->ASP |
| 1A7S | ATOMIC RESOLUTION STRUCTURE OF HBP |
| 1A7T | METALLO-BETA-LACTAMASE WITH MES |
| 1A7U | CHLOROPEROXIDASE T |
| 1A7V | CYTOCHROME C' FROM RHODOPSEUDOMONAS PALUSTRIS |
| 1A7W | CRYSTAL STRUCTURE OF THE HISTONE HMFB FROM METHANOTHERMUS FERVIDUS |
| 1A7X | FKBP12-FK1012 COMPLEX |
| 1A80 | NATIVE 2,5-DIKETO-D-GLUCONIC ACID REDUCTASE A FROM CORYNBACTERIUM SP. COMPLEXED WITH NADPH |
| 1A81 | CRYSTAL STRUCTURE OF THE TANDEM SH2 DOMAIN OF THE SYK KINASE BOUND TO A DUALLY TYROSINE-PHOSPHORYLATED ITAM |
| 1A82 | DETHIOBIOTIN SYNTHETASE FROM ESCHERICHIA COLI, COMPLEX WITH SUBSTRATES ATP AND DIAMINOPELARGONIC ACID |
| 1A85 | MMP8 WITH MALONIC AND ASPARAGINE BASED INHIBITOR |
| 1A86 | MMP8 WITH MALONIC AND ASPARTIC ACID BASED INHIBITOR |
| 1A87 | COLICIN N |
| 1A88 | CHLOROPEROXIDASE L |
| 1A8A | RAT ANNEXIN V COMPLEXED WITH GLYCEROPHOSPHOSERINE |
| 1A8B | RAT ANNEXIN V COMPLEXED WITH GLYCEROPHOSPHOETHANOLAMINE |
| 1A8C | PRIMARY SEQUENCE AND SOLUTION CONFORMATION OF FERROCYTOCHROME C-552 FROM NITROSOMONAS EUROPAEA, NMR, MEAN STRUCTURE REFINED WITHOUT HYDROGEN BOND CONSTRAINTS |
| 1A8D | TETANUS TOXIN C FRAGMENT |
| 1A8E | HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE |
| 1A8F | HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE |
| 1A8G | HIV-1 PROTEASE IN COMPLEX WITH SDZ283-910 |
| 1A8H | METHIONYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS |
| 1A8I | SPIROHYDANTOIN INHIBITOR OF GLYCOGEN PHOSPHORYLASE |
| 1A8J | IMMUNOGLOBULIN LAMBDA LIGHT CHAIN DIMER (MCG) COMPLEX WITH ASPARTAME |
| 1A8K | CRYSTALLOGRAPHIC ANALYSIS OF HUMAN IMMUNODEFICIENCY VIRUS 1 PROTEASE WITH AN ANALOG OF THE CONSERVED CA-P2 SUBSTRATE: INTERACTIONS WITH FREQUENTLY OCCURRING GLUTAMIC ACID RESIDUE AT P2' POSITION OF SUBSTRATES |
| 1A8L | PROTEIN DISULFIDE OXIDOREDUCTASE FROM ARCHAEON PYROCOCCUS FURIOSUS |
| 1A8M | TUMOR NECROSIS FACTOR ALPHA, R31D MUTANT |
| 1A8O | HIV CAPSID C-TERMINAL DOMAIN |
| 1A8P | FERREDOXIN REDUCTASE FROM AZOTOBACTER VINELANDII |
| 1A8Q | BROMOPEROXIDASE A1 |
| 1A8R | GTP CYCLOHYDROLASE I (H112S MUTANT) IN COMPLEX WITH GTP |
| 1A8S | CHLOROPEROXIDASE F/PROPIONATE COMPLEX |
| 1A8T | METALLO-BETA-LACTAMASE IN COMPLEX WITH L-159,061 |
| 1A8U | CHLOROPEROXIDASE T/BENZOATE COMPLEX |
| 1A8V | STRUCTURE OF THE RNA-BINDING DOMAIN OF THE RHO TRANSCRIPTION TERMINATOR |
| 1A8Y | CRYSTAL STRUCTURE OF CALSEQUESTRIN FROM RABBIT SKELETAL MUSCLE SARCOPLASMIC RETICULUM AT 2.4 A RESOLUTION |
| 1A8Z | STRUCTURE DETERMINATION OF A 16.8KDA COPPER PROTEIN RUSTICYANIN AT 2.1A RESOLUTION USING ANOMALOUS SCATTERING DATA WITH DIRECT METHODS |
| 1A90 | RECOMBINANT MUTANT CHICKEN EGG WHITE CYSTATIN, NMR, 31 STRUCTURES |
| 1A91 | SUBUNIT C OF THE F1FO ATP SYNTHASE OF ESCHERICHIA COLI; NMR, 10 STRUCTURES |
| 1A93 | NMR SOLUTION STRUCTURE OF THE C-MYC-MAX HETERODIMERIC LEUCINE ZIPPER, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1A94 | STRUCTURAL BASIS FOR SPECIFICITY OF RETROVIRAL PROTEASES |
| 1A95 | XPRTASE FROM E. COLI COMPLEXED WITH MG:CPRPP AND GUANINE |
| 1A96 | XPRTASE FROM E. COLI WITH BOUND CPRPP AND XANTHINE |
| 1A97 | XPRTASE FROM E. COLI COMPLEXED WITH GMP |
| 1A98 | XPRTASE FROM E. COLI COMPLEXED WITH GMP |
| 1A99 | PUTRESCINE RECEPTOR (POTF) FROM E. COLI |
| 1A9B | DECAMER-LIKE CONFORMATION OF A NANO-PEPTIDE BOUND TO HLA-B3501 DUE TO NONSTANDARD POSITIONING OF THE C-TERMINUS |
| 1A9E | DECAMER-LIKE CONFORMATION OF A NANO-PEPTIDE BOUND TO HLA-B3501 DUE TO NONSTANDARD POSITIONING OF THE C-TERMINUS |
| 1A9M | G48H MUTANT OF HIV-1 PROTEASE IN COMPLEX WITH A PEPTIDIC INHIBITOR U-89360E |
| 1A9N | CRYSTAL STRUCTURE OF THE SPLICEOSOMAL U2B''-U2A' PROTEIN COMPLEX BOUND TO A FRAGMENT OF U2 SMALL NUCLEAR RNA |
| 1A9O | BOVINE PURINE NUCLEOSIDE PHOSPHORYLASE COMPLEXED WITH PHOSPHATE |
| 1A9P | BOVINE PURINE NUCLEOSIDE PHOSPHORYLASE COMPLEXED WITH 9-DEAZAINOSINE AND PHOSPHATE |
| 1A9Q | BOVINE PURINE NUCLEOSIDE PHOSPHORYLASE COMPLEXED WITH INOSINE |
| 1A9R | BOVINE PURINE NUCLEOSIDE PHOSPHORYLASE COMPLEXED WITH HYPOXANTHINE AND SULFATE |
| 1A9S | BOVINE PURINE NUCLEOSIDE PHOSPHORYLASE COMPLEXED WITH INOSINE AND SULFATE |
| 1A9T | BOVINE PURINE NUCLEOSIDE PHOSPHORYLASE COMPLEXED WITH 9-DEAZAINOSINE AND PHOSPHATE |
| 1A9U | THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB203580 |
| 1A9V | TERTIARY STRUCTURE OF THE MAJOR HOUSE DUST MITE ALLERGEN DER P 2, NMR, 10 STRUCTURES |
| 1A9W | HUMAN EMBRYONIC GOWER II CARBONMONOXY HEMOGLOBIN |
| 1A9Y | UDP-GALACTOSE 4-EPIMERASE MUTANT S124A/Y149F COMPLEXED WITH UDP-GLUCOSE |
| 1A9Z | UDP-GALACTOSE 4-EPIMERASE MUTANT S124A/Y149F COMPLEXED WITH UDP-GALACTOSE |
| 1AA0 | FIBRITIN DELETION MUTANT E (BACTERIOPHAGE T4) |
| 1AA1 | ACTIVATED SPINACH RUBISCO IN COMPLEX WITH THE PRODUCT 3-PHOSPHOGLYCERATE |
| 1AA2 | CALPONIN HOMOLOGY (CH) DOMAIN FROM HUMAN BETA-SPECTRIN |
| 1AA3 | C-TERMINAL DOMAIN OF THE E. COLI RECA, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AA4 | SPECIFICITY OF LIGAND BINDING IN A BURIED POLAR CAVITY OF CYTOCHROME C PEROXIDASE |
| 1AA6 | REDUCED FORM OF FORMATE DEHYDROGENASE H FROM E. COLI |
| 1AA7 | INFLUENZA VIRUS MATRIX PROTEIN CRYSTAL STRUCTURE AT PH 4.0 |
| 1AA9 | HUMAN C-HA-RAS(1-171)(DOT)GDP, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AAB | NMR STRUCTURE OF RAT HMG1 HMGA FRAGMENT |
| 1AAC | AMICYANIN OXIDIZED, 1.31 ANGSTROMS |
| 1AAF | NUCLEOCAPSID ZINC FINGERS DETECTED IN RETROVIRUSES: EXAFS STUDIES ON INTACT VIRUSES AND THE SOLUTION-STATE STRUCTURE OF THE NUCLEOCAPSID PROTEIN FROM HIV-1 |
| 1AAJ | CRYSTAL STRUCTURE ANALYSIS OF AMICYANIN AND APOAMICYANIN FROM PARACOCCUS DENITRIFICANS AT 2.0 ANGSTROMS AND 1.8 ANGSTROMS RESOLUTION |
| 1AAL | STRUCTURAL EFFECTS INDUCED BY MUTAGENESIS AFFECTED BY CRYSTAL PACKING FACTORS: THE STRUCTURE OF A 30-51 DISULFIDE MUTANT OF BASIC PANCREATIC TRYPSIN INHIBITOR |
| 1AAM | THE STRUCTURAL BASIS FOR THE ALTERED SUBSTRATE SPECIFICITY OF THE R292D ACTIVE SITE MUTANT OF ASPARTATE AMINOTRANSFERASE FROM E. COLI |
| 1AAN | CRYSTAL STRUCTURE ANALYSIS OF AMICYANIN AND APOAMICYANIN FROM PARACOCCUS DENITRIFICANS AT 2.0 ANGSTROMS AND 1.8 ANGSTROMS RESOLUTION |
| 1AAP | X-RAY CRYSTAL STRUCTURE OF THE PROTEASE INHIBITOR DOMAIN OF ALZHEIMER'S AMYLOID BETA-PROTEIN PRECURSOR |
| 1AAQ | HYDROXYETHYLENE ISOSTERE INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS-1 PROTEASE: STRUCTURE-ACTIVITY ANALYSIS USING ENZYME KINETICS, X-RAY CRYSTALLOGRAPHY, AND INFECTED T-CELL ASSAYS |
| 1AAR | STRUCTURE OF A DIUBIQUITIN CONJUGATE AND A MODEL FOR INTERACTION WITH UBIQUITIN CONJUGATING ENZYME (E2) |
| 1AAT | OXOGLUTARATE-INDUCED CONFORMATIONAL CHANGES IN CYTOSOLIC ASPARTATE AMINOTRANSFERASE |
| 1AAW | THE STRUCTURAL BASIS FOR THE ALTERED SUBSTRATE SPECIFICITY OF THE R292D ACTIVE SITE MUTANT OF ASPARTATE AMINOTRANSFERASE FROM E. COLI |
| 1AAX | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH TWO BIS(PARA-PHOSPHOPHENYL)METHANE (BPPM) MOLECULES |
| 1AAY | ZIF268 ZINC FINGER-DNA COMPLEX |
| 1AAZ | THE STRUCTURE OF OXIDIZED BACTERIOPHAGE T4 GLUTAREDOXIN (THIOREDOXIN) |
| 1AB0 | C1G/V32D/F57H MUTANT OF MURINE ADIPOCYTE LIPID BINDING PROTEIN AT PH 4.5 |
| 1AB1 | SI FORM CRAMBIN |
| 1AB2 | THREE-DIMENSIONAL SOLUTION STRUCTURE OF THE SRC HOMOLOGY 2 DOMAIN OF C-ABL |
| 1AB3 | RIBOSOMAL PROTEIN S15 FROM THERMUS THERMOPHILUS, NMR, 26 STRUCTURES |
| 1AB4 | 59KDA FRAGMENT OF GYRASE A FROM E. COLI |
| 1AB5 | STRUCTURE OF CHEY MUTANT F14N, V21T |
| 1AB6 | STRUCTURE OF CHEY MUTANT F14N, V86T |
| 1AB7 | NMR 15N RELAXATION AND STRUCTURAL STUDIES REVEAL CONFORMATIONAL EXCHANGE IN BARSTAR C40/82A, 30 STRUCTURES |
| 1AB8 | RAT TYPE II ADENYLYL CYCLASE C2 DOMAIN/FORSKOLIN COMPLEX |
| 1AB9 | CRYSTAL STRUCTURE OF BOVINE GAMMA-CHYMOTRYPSIN |
| 1ABA | THE STRUCTURE OF OXIDIZED BACTERIOPHAGE T4 GLUTAREDOXIN (THIOREDOXIN). REFINEMENT OF NATIVE AND MUTANT PROTEINS |
| 1ABE | NOVEL STEREOSPECIFICITY OF THE L-ARABINOSE-BINDING PROTEIN |
| 1ABF | SUBSTRATE SPECIFICITY AND AFFINITY OF A PROTEIN MODULATED BY BOUND WATER MOLECULES |
| 1ABI | STRUCTURE OF THE HIRULOG 3-THROMBIN COMPLEX AND NATURE OF THE S' SUBSITES OF SUBSTRATES AND INHIBITORS |
| 1ABJ | STRUCTURE OF THE HIRULOG 3-THROMBIN COMPLEX AND NATURE OF THE S' SUBSITES OF SUBSTRATES AND INHIBITORS |
| 1ABO | CRYSTAL STRUCTURE OF THE COMPLEX OF THE ABL TYROSINE KINASE SH3 DOMAIN WITH 3BP-1 SYNTHETIC PEPTIDE |
| 1ABQ | CRYSTAL STRUCTURE OF THE UNLIGANDED ABL TYROSINE KINASE SH3 DOMAIN |
| 1ABR | CRYSTAL STRUCTURE OF ABRIN-A |
| 1ABS | PHOTOLYSED CARBONMONOXY-MYOGLOBIN AT 20 K |
| 1ABT | NMR SOLUTION STRUCTURE OF AN ALPHA-BUNGAROTOXIN(SLASH)NICOTINIC RECEPTOR PEPTIDE COMPLEX |
| 1ABV | N-TERMINAL DOMAIN OF THE DELTA SUBUNIT OF THE F1F0-ATP SYNTHASE FROM ESCHERICHIA COLI, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1ABW | DEOXY RHB1.1 (RECOMBINANT HEMOGLOBIN) |
| 1ABY | CYANOMET RHB1.1 (RECOMBINANT HEMOGLOBIN) |
| 1ABZ | ALPHA-T-ALPHA, A DE NOVO DESIGNED PEPTIDE, NMR, 23 STRUCTURES |
| 1AC0 | GLUCOAMYLASE, GRANULAR STARCH-BINDING DOMAIN COMPLEX WITH CYCLODEXTRIN, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AC1 | DSBA MUTANT H32L |
| 1AC4 | VARIATION IN THE STRENGTH OF A CH TO O HYDROGEN BOND IN AN ARTIFICIAL PROTEIN CAVITY (2,3,4-TRIMETHYL-1,3-THIAZOLE) |
| 1AC5 | CRYSTAL STRUCTURE OF KEX1(DELTA)P, A PROHORMONE-PROCESSING CARBOXYPEPTIDASE FROM SACCHAROMYCES CEREVISIAE |
| 1AC6 | CRYSTAL STRUCTURE OF A VARIABLE DOMAIN MUTANT OF A T-CELL RECEPTOR ALPHA CHAIN |
| 1AC8 | VARIATION IN THE STRENGTH OF A CH TO O HYDROGEN BOND IN AN ARTIFICIAL PROTEIN CAVITY (3,4,5-TRIMETHYLTHIAZOLE) |
| 1ACA | THREE-DIMENSIONAL STRUCTURE OF THE COMPLEX BETWEEN ACYL-COENZYME A BINDING PROTEIN AND PALMITOYL-COENZYME A |
| 1ACB | CRYSTAL AND MOLECULAR STRUCTURE OF THE BOVINE ALPHA-CHYMOTRYPSIN-EGLIN C COMPLEX AT 2.0 ANGSTROMS RESOLUTION |
| 1ACC | ANTHRAX PROTECTIVE ANTIGEN |
| 1ACD | V32D/F57H MUTANT OF MURINE ADIPOCYTE LIPID BINDING PROTEIN |
| 1ACF | ACANTHAMOEBA CASTELLANII PROFILIN IB |
| 1ACI | L11 RIBOSOMAL PROTEIN RNA BINDING DOMAIN, NMR, 20 STRUCTURES |
| 1ACJ | QUATERNARY LIGAND BINDING TO AROMATIC RESIDUES IN THE ACTIVE-SITE GORGE OF ACETYLCHOLINESTERASE |
| 1ACL | QUATERNARY LIGAND BINDING TO AROMATIC RESIDUES IN THE ACTIVE-SITE GORGE OF ACETYLCHOLINESTERASE |
| 1ACM | ARGININE 54 IN THE ACTIVE SITE OF ESCHERICHIA COLI ASPARTATE TRANSCARBAMOYLASE IS CRITICAL FOR CATALYSIS: A SITE-SPECIFIC MUTAGENESIS, NMR AND X-RAY CRYSTALLOGRAPHY STUDY |
| 1ACO | CRYSTAL STRUCTURE OF ACONITASE WITH TRANSACONITATE BOUND |
| 1ACP | REFINEMENT OF THE NMR STRUCTURES FOR ACYL CARRIER PROTEIN WITH SCALAR COUPLING DATA |
| 1ACV | DSBA MUTANT H32S |
| 1ACW | SOLUTION NMR STRUCTURE OF P01, A NATURAL SCORPION PEPTIDE STRUCTURALLY ANALOGOUS TO SCORPION TOXINS SPECIFIC FOR APAMIN-SENSITIVE POTASSIUM CHANNEL, 25 STRUCTURES |
| 1ACX | ACTINOXANTHIN STRUCTURE AT THE ATOMIC LEVEL (RUSSIAN) |
| 1ACY | CRYSTAL STRUCTURE OF THE PRINCIPAL NEUTRALIZING SITE OF HIV-1 |
| 1ACZ | GLUCOAMYLASE, GRANULAR STARCH-BINDING DOMAIN COMPLEX WITH CYCLODEXTRIN, NMR, 5 STRUCTURES |
| 1AD0 | FAB FRAGMENT OF ENGINEERED HUMAN MONOCLONAL ANTIBODY A5B7 |
| 1AD1 | DIHYDROPTEROATE SYNTHETASE (APO FORM) FROM STAPHYLOCOCCUS AUREUS |
| 1AD2 | RIBOSOMAL PROTEIN L1 MUTANT WITH SERINE 179 REPLACED BY CYSTEINE |
| 1AD3 | CLASS 3 ALDEHYDE DEHYDROGENASE COMPLEX WITH NICOTINAMIDE-ADENINE-DINUCLEOTIDE |
| 1AD4 | DIHYDROPTEROATE SYNTHETASE COMPLEXED WITH OH-CH2-PTERIN-PYROPHOSPHATE FROM STAPHYLOCOCCUS AUREUS |
| 1AD5 | SRC FAMILY KINASE HCK-AMP-PNP COMPLEX |
| 1AD6 | DOMAIN A OF HUMAN RETINOBLASTOMA TUMOR SUPPRESSOR |
| 1AD8 | COMPLEX OF THROMBIN WITH AND INHIBITOR CONTAINING A NOVEL P1 MOIETY |
| 1AD9 | IGG-FAB FRAGMENT OF ENGINEERED HUMAN MONOCLONAL ANTIBODY CTM01 |
| 1ADB | CRYSTALLOGRAPHIC STUDIES OF ISOSTERIC NAD ANALOGUES BOUND TO ALCOHOL DEHYDROGENASE: SPECIFICITY AND SUBSTRATE BINDING IN TWO TERNARY COMPLEXES |
| 1ADC | CRYSTALLOGRAPHIC STUDIES OF ISOSTERIC NAD ANALOGUES BOUND TO ALCOHOL DEHYDROGENASE: SPECIFICITY AND SUBSTRATE BINDING IN TWO TERNARY COMPLEXES |
| 1ADD | A PRE-TRANSITION STATE MIMIC OF AN ENZYME: X-RAY STRUCTURE OF ADENOSINE DEAMINASE WITH BOUND 1-DEAZA-ADENOSINE AND ZINC-ACTIVATED WATER |
| 1ADE | STRUCTURE OF ADENYLOSUCCINATE SYNTHETASE PH 7 AT 25 DEGREES CELSIUS |
| 1ADF | CRYSTALLOGRAPHIC STUDIES OF TWO ALCOHOL DEHYDROGENASE-BOUND ANALOGS OF THIAZOLE-4-CARBOXAMIDE ADENINE DINUCLEOTIDE (TAD), THE ACTIVE ANABOLITE OF THE ANTITUMOR AGENT TIAZOFURIN |
| 1ADG | CRYSTALLOGRAPHIC STUDIES OF TWO ALCOHOL DEHYDROGENASE-BOUND ANALOGS OF THIAZOLE-4-CARBOXAMIDE ADENINE DINUCLEOTIDE (TAD), THE ACTIVE ANABOLITE OF THE ANTITUMOR AGENT TIAZOFURIN |
| 1ADI | STRUCTURE OF ADENYLOSUCCINATE SYNTHETASE AT PH 6.5 AND 25 DEGREES CELSIUS |
| 1ADJ | HISTIDYL-TRNA SYNTHETASE IN COMPLEX WITH HISTIDINE |
| 1ADL | ADIPOCYTE LIPID BINDING PROTEIN COMPLEXED WITH ARACHIDONIC ACID: X-RAY CRYSTALLOGRAPHIC AND TITRATION CALORIMETRY STUDIES |
| 1ADN | SOLUTION STRUCTURE OF THE DNA METHYLPHOSPHOTRIESTER REPAIR DOMAIN OF ESCHERICHIA COLI ADA |
| 1ADO | FRUCTOSE 1,6-BISPHOSPHATE ALDOLASE FROM RABBIT MUSCLE |
| 1ADQ | CRYSTAL STRUCTURE OF A HUMAN IGM RHEUMATOID FACTOR FAB IN COMPLEX WITH ITS AUTOANTIGEN IGG FC |
| 1ADR | DETERMINATION OF THE NUCLEAR MAGNETIC RESONANCE STRUCTURE OF THE DNA-BINDING DOMAIN OF THE P22 C2 REPRESSOR (1-76) IN SOLUTION AND COMPARISON WITH THE DNA-BINDING DOMAIN OF THE 434 REPRESSOR |
| 1ADS | AN UNLIKELY SUGAR SUBSTRATE SITE IN THE 1.65 ANGSTROMS STRUCTURE OF THE HUMAN ALDOSE REDUCTASE HOLOENZYME IMPLICATED IN DIABETIC COMPLICATIONS |
| 1ADU | EARLY E2A DNA-BINDING PROTEIN |
| 1ADV | EARLY E2A DNA-BINDING PROTEIN |
| 1ADW | PSEUDOAZURIN |
| 1ADX | FIFTH EGF-LIKE DOMAIN OF THROMBOMODULIN (TMEGF5), NMR, 14 STRUCTURES |
| 1ADY | HISTIDYL-TRNA SYNTHETASE IN COMPLEX WITH HISTIDYL-ADENYLATE |
| 1ADZ | THE SOLUTION STRUCTURE OF THE SECOND KUNITZ DOMAIN OF TISSUE FACTOR PATHWAY INHIBITOR, NMR, 30 STRUCTURES |
| 1AE1 | TROPINONE REDUCTASE-I COMPLEX WITH NADP |
| 1AE2 | MUTANT L32R OF GENE V PROTEIN (SINGLE-STRANDED DNA BINDING PROTEIN) |
| 1AE3 | MUTANT R82C OF GENE V PROTEIN (SINGLE-STRANDED DNA BINDING PROTEIN) |
| 1AE5 | HUMAN HEPARIN BINDING PROTEIN |
| 1AE6 | IGG-FAB FRAGMENT OF MOUSE MONOCLONAL ANTIBODY CTM01 |
| 1AE7 | NOTEXIN, A PRESYNAPTIC NEUROTOXIC PHOSPHOLIPASE A2 |
| 1AE8 | HUMAN ALPHA-THROMBIN INHIBITION BY EOC-D-PHE-PRO-AZALYS-ONP |
| 1AE9 | STRUCTURE OF THE LAMBDA INTEGRASE CATALYTIC CORE |
| 1AEB | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (3-METHYLTHIAZOLE) |
| 1AEC | CRYSTAL STRUCTURE OF ACTINIDIN-E-64 COMPLEX+ |
| 1AED | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (3,4-DIMETHYLTHIAZOLE) |
| 1AEE | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (ANILINE) |
| 1AEF | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (3-AMINOPYRIDINE) |
| 1AEG | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (4-AMINOPYRIDINE) |
| 1AEH | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (2-AMINO-4-METHYLTHIAZOLE) |
| 1AEI | CRYSTAL STRUCTURE OF THE ANNEXIN XII HEXAMER |
| 1AEJ | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (1-VINYLIMIDAZOLE) |
| 1AEK | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (INDOLINE) |
| 1AEL | NMR STRUCTURE OF APO INTESTINAL FATTY ACID-BINDING PROTEIN, 20 STRUCTURES |
| 1AEM | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (IMIDAZO[1,2-A]PYRIDINE) |
| 1AEN | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (2-AMINO-5-METHYLTHIAZOLE) |
| 1AEO | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (2-AMINOPYRIDINE) |
| 1AEP | MOLECULAR STRUCTURE OF AN APOLIPOPROTEIN DETERMINED AT 2.5-ANGSTROMS RESOLUTION |
| 1AEQ | VARIATION IN THE STRENGTH OF A CH TO O HYDROGEN BOND IN AN ARTIFICIAL PROTEIN CAVITY (2-ETHYLIMIDAZOLE) |
| 1AER | DOMAIN III OF PSEUDOMONAS AERUGINOSA EXOTOXIN COMPLEXED WITH BETA-TAD |
| 1AES | SPECIFICITY OF LIGAND BINDING TO A BURIED POLAR CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE (IMIDAZOLE) |
| 1AET | VARIATION IN THE STRENGTH OF A CH TO O HYDROGEN BOND IN AN ARTIFICIAL PROTEIN CAVITY (1-METHYLIMIDAZOLE) |
| 1AEU | SPECIFICITY OF LIGAND BINDING IN A POLAR CAVITY OF CYTOCHROME C PEROXIDASE (2-METHYLIMIDAZOLE) |
| 1AEV | INTRODUCTION OF NOVEL SUBSTRATE OXIDATION INTO CYTOCHROME C PEROXIDASE BY CAVITY COMPLEMENTATION: OXIDATION OF 2-AMINOTHIAZOLE AND COVALENT MODIFICATION OF THE ENZYME (2-AMINOTHIAZOLE) |
| 1AEW | L-CHAIN HORSE APOFERRITIN |
| 1AEX | STAPHYLOCOCCAL NUCLEASE, METHANE THIOL DISULFIDE TO V23C VARIANT |
| 1AEY | ALPHA-SPECTRIN SRC HOMOLOGY 3 DOMAIN, SOLUTION NMR, 15 STRUCTURES |
| 1AF0 | SERRATIA PROTEASE IN COMPLEX WITH INHIBITOR |
| 1AF2 | CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE COMPLEXED WITH URIDINE |
| 1AF3 | RAT BCL-XL AN APOPTOSIS INHIBITORY PROTEIN |
| 1AF4 | CRYSTAL STRUCTURE OF SUBTILISIN CARLSBERG IN ANHYDROUS DIOXANE |
| 1AF5 | GROUP I MOBILE INTRON ENDONUCLEASE |
| 1AF6 | MALTOPORIN SUCROSE COMPLEX |
| 1AF7 | CHER FROM SALMONELLA TYPHIMURIUM |
| 1AF8 | ACTINORHODIN POLYKETIDE SYNTHASE ACYL CARRIER PROTEIN FROM STREPTOMYCES COELICOLOR A3(2), NMR, 24 STRUCTURES |
| 1AF9 | TETANUS NEUROTOXIN C FRAGMENT |
| 1AFA | STRUCTURAL BASIS OF GALACTOSE RECOGNITION IN C-TYPE ANIMAL LECTINS |
| 1AFB | STRUCTURAL BASIS OF GALACTOSE RECOGNITION IN C-TYPE ANIMAL LECTINS |
| 1AFC | STRUCTURAL STUDIES OF THE BINDING OF THE ANTI-ULCER DRUG SUCROSE OCTASULFATE TO ACIDIC FIBROBLAST GROWTH FACTOR |
| 1AFD | STRUCTURAL BASIS OF GALACTOSE RECOGNITION IN C-TYPE ANIMAL LECTINS |
| 1AFE | HUMAN ALPHA-THROMBIN INHIBITION BY CBZ-PRO-AZALYS-ONP |
| 1AFH | LIPID TRANSFER PROTEIN FROM MAIZE SEEDLINGS, NMR, 15 STRUCTURES |
| 1AFI | STRUCTURE OF THE REDUCED FORM OF MERP, THE PERIPLASMIC PROTEIN FROM THE BACTERIAL MERCURY DETOXIFICATION SYSTEM, NMR, 20 STRUCTURES |
| 1AFJ | STRUCTURE OF THE MERCURY-BOUND FORM OF MERP, THE PERIPLASMIC PROTEIN FROM THE BACTERIAL MERCURY DETOXIFICATION SYSTEM, NMR, 20 STRUCTURES |
| 1AFK | CRYSTAL STRUCTURE OF RIBONUCLEASE A IN COMPLEX WITH 5'-DIPHOSPHOADENOSINE-3'-PHOSPHATE |
| 1AFL | RIBONUCLEASE A IN COMPLEX WITH 5'-DIPHOSPHOADENOSINE 2'-PHOSPHATE AT 1.7 ANGSTROM RESOLUTION |
| 1AFO | DIMERIC TRANSMEMBRANE DOMAIN OF HUMAN GLYCOPHORIN A, NMR, 20 STRUCTURES |
| 1AFP | SOLUTION STRUCTURE OF THE ANTIFUNGAL PROTEIN FROM ASPERGILLUS GIGANTEUS. EVIDENCE FOR DISULPHIDE CONFIGURATIONAL ISOMERISM |
| 1AFQ | CRYSTAL STRUCTURE OF BOVINE GAMMA-CHYMOTRYPSIN COMPLEXED WITH A SYNTHETIC INHIBITOR |
| 1AFR | STEAROYL-ACYL CARRIER PROTEIN DESATURASE FROM CASTOR SEEDS |
| 1AFS | RECOMBINANT RAT LIVER 3-ALPHA-HYDROXYSTEROID DEHYDROGENASE (3-ALPHA-HSD) COMPLEXED WITH NADP AND TESTOSTERONE |
| 1AFT | SMALL SUBUNIT C-TERMINAL INHIBITORY PEPTIDE OF MOUSE RIBONUCLEOTIDE REDUCTASE AS BOUND TO THE LARGE SUBUNIT, NMR, 26 STRUCTURES |
| 1AFU | STRUCTURE OF RIBONUCLEASE A AT 2.0 ANGSTROMS FROM MONOCLINIC CRYSTALS |
| 1AFV | HIV-1 CAPSID PROTEIN (P24) COMPLEX WITH FAB25.3 |
| 1AFW | THE 1.8 ANGSTROM CRYSTAL STRUCTURE OF THE DIMERIC PEROXISOMAL THIOLASE OF SACCHAROMYCES CEREVISIAE |
| 1AG0 | STRUCTURE OF CYS 112 ASP AZURIN FROM PSEUDOMONAS AERUGINOSA |
| 1AG1 | MONOHYDROGEN PHOSPHATE BINDING TO TRYPANOSOMAL TRIOSEPHOSPHATE ISOMERASE |
| 1AG2 | PRION PROTEIN DOMAIN PRP(121-231) FROM MOUSE, NMR, 2 MINIMIZED AVERAGE STRUCTURE |
| 1AG4 | NMR STRUCTURE OF SPHERULIN 3A (S3A) FROM PHYSARUM POLYCEPHALUM, MINIMIZED AVERAGE STRUCTURE |
| 1AG6 | PLASTOCYANIN FROM SPINACH |
| 1AG7 | CONOTOXIN GS, NMR, 20 STRUCTURES |
| 1AG8 | ALDEHYDE DEHYDROGENASE FROM BOVINE MITOCHONDRIA |
| 1AG9 | FLAVODOXINS THAT ARE REQUIRED FOR ENZYME ACTIVATION: THE STRUCTURE OF OXIDIZED FLAVODOXIN FROM ESCHERICHIA COLI AT 1.8 ANGSTROMS RESOLUTION. |
| 1AGB | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGRKKYKL-3R MUTATION) |
| 1AGC | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYQL-7Q MUTATION) |
| 1AGD | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYKL-INDEX PEPTIDE) |
| 1AGE | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYRL-7R MUTATION) |
| 1AGF | ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKRYKL-5R MUTATION) |
| 1AGG | THE SOLUTION STRUCTURE OF OMEGA-AGA-IVB, A P-TYPE CALCIUM CHANNEL ANTAGONIST FROM THE VENOM OF AGELENOPSIS APERTA |
| 1AGI | CRYSTAL STRUCTURE OF BOVINE ANGIOGENIN AT 1.5 ANGSTROMS RESOLUTION |
| 1AGJ | EPIDERMOLYTIC TOXIN A FROM STAPHYLOCOCCUS AUREUS |
| 1AGM | REFINED STRUCTURE FOR THE COMPLEX OF ACARBOSE WITH GLUCOAMYLASE FROM ASPERGILLUS AWAMORI VAR. X100 TO 2.4 ANGSTROMS RESOLUTION |
| 1AGN | X-RAY STRUCTURE OF HUMAN SIGMA ALCOHOL DEHYDROGENASE |
| 1AGP | THREE-DIMENSIONAL STRUCTURES AND PROPERTIES OF A TRANSFORMING AND A NONTRANSFORMING GLY-12 MUTANT OF P21-H-RAS |
| 1AGQ | GLIAL CELL-DERIVED NEUROTROPHIC FACTOR FROM RAT |
| 1AGR | COMPLEX OF ALF4-ACTIVATED GI-ALPHA-1 WITH RGS4 |
| 1AGT | SOLUTION STRUCTURE OF THE POTASSIUM CHANNEL INHIBITOR AGITOXIN 2: CALIPER FOR PROBING CHANNEL GEOMETRY |
| 1AGW | CRYSTAL STRUCTURE OF THE TYROSINE KINASE DOMAIN OF FIBROBLAST GROWTH FACTOR RECEPTOR 1 IN COMPLEX WITH SU4984 INHIBITOR |
| 1AGX | REFINED CRYSTAL STRUCTURE OF ACINETOBACTER GLUTAMINASIFICANS GLUTAMINASE-ASPARAGINASE |
| 1AGY | THE 1.15 ANGSTROM REFINED STRUCTURE OF FUSARIUM SOLANI PISI CUTINASE |
| 1AH0 | PIG ALDOSE REDUCTASE COMPLEXED WITH SORBINIL |
| 1AH1 | CTLA-4, NMR, 20 STRUCTURES |
| 1AH2 | SERINE PROTEASE PB92 FROM BACILLUS ALCALOPHILUS, NMR, 18 STRUCTURES |
| 1AH3 | ALDOSE REDUCTASE COMPLEXED WITH TOLRESTAT INHIBITOR |
| 1AH4 | PIG ALDOSE REDUCTASE, HOLO FORM |
| 1AH5 | REDUCED FORM SELENOMETHIONINE-LABELLED HYDROXYMETHYLBILANE SYNTHASE DETERMINED BY MAD |
| 1AH6 | STRUCTURE OF THE TETRAGONAL FORM OF THE N-TERMINAL DOMAIN OF THE YEAST HSP90 CHAPERONE |
| 1AH7 | PHOSPHOLIPASE C FROM BACILLUS CEREUS |
| 1AH8 | STRUCTURE OF THE ORTHORHOMBIC FORM OF THE N-TERMINAL DOMAIN OF THE YEAST HSP90 CHAPERONE |
| 1AH9 | THE STRUCTURE OF THE TRANSLATIONAL INITIATION FACTOR IF1 FROM ESCHERICHIA COLI, NMR, 19 STRUCTURES |
| 1AHA | THE N-GLYCOSIDASE MECHANISM OF RIBOSOME-INACTIVATING PROTEINS IMPLIED BY CRYSTAL STRUCTURES OF ALPHA-MOMORCHARIN |
| 1AHB | THE N-GLYCOSIDASE MECHANISM OF RIBOSOME-INACTIVATING PROTEINS IMPLIED BY CRYSTAL STRUCTURES OF ALPHA-MOMORCHARIN |
| 1AHC | THE N-GLYCOSIDASE MECHANISM OF RIBOSOME-INACTIVATING PROTEINS IMPLIED BY CRYSTAL STRUCTURES OF ALPHA-MOMORCHARIN |
| 1AHD | DETERMINATION OF THE NMR SOLUTION STRUCTURE OF AN ANTENNAPEDIA HOMEODOMAIN-DNA COMPLEX |
| 1AHE | ASPARTATE AMINOTRANSFERASE HEXAMUTANT |
| 1AHF | ASPARTATE AMINOTRANSFERASE HEXAMUTANT |
| 1AHG | ASPARTATE AMINOTRANSFERASE HEXAMUTANT |
| 1AHH | 7 ALPHA-HYDROXYSTEROID DEHYDROGENASE COMPLEXED WITH NAD+ |
| 1AHI | 7 ALPHA-HYDROXYSTEROID DEHYDROGENASE COMPLEXED WITH NADH AND 7-OXO GLYCOCHENODEOXYCHOLIC ACID |
| 1AHJ | NITRILE HYDRATASE |
| 1AHK | DER F 2, THE MAJOR MITE ALLERGEN FROM DERMATOPHAGOIDES FARINAE, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AHL | ANTHOPLEURIN-A,NMR, 20 STRUCTURES |
| 1AHM | DER F 2, THE MAJOR MITE ALLERGEN FROM DERMATOPHAGOIDES FARINAE, NMR, 10 STRUCTURES |
| 1AHN | E. COLI FLAVODOXIN AT 2.6 ANGSTROMS RESOLUTION |
| 1AHO | THE AB INITIO STRUCTURE DETERMINATION AND REFINEMENT OF A SCORPION PROTEIN TOXIN |
| 1AHP | OLIGOSACCHARIDE SUBSTRATE BINDING IN ESCHERICHIA COLI MALTODEXTRIN PHSPHORYLASE |
| 1AHQ | RECOMBINANT ACTOPHORIN |
| 1AHR | CALMODULIN MUTANT WITH A TWO RESIDUE DELETION IN THE CENTRAL HELIX |
| 1AHS | CRYSTAL STRUCTURE OF THE TOP DOMAIN OF AFRICAN HORSE SICKNESS VIRUS VP7 |
| 1AHT | CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH HIRUGEN AND P-AMIDINOPHENYLPYRUVATE AT 1.6 ANGSTROMS RESOLUTION |
| 1AHU | STRUCTURE OF THE OCTAMERIC FLAVOENZYME VANILLYL-ALCOHOL OXIDASE IN COMPLEX WITH P-CRESOL |
| 1AHV | STRUCTURE OF THE OCTAMERIC FLAVOENZYME VANILLYL-ALCOHOL OXIDASE IN COMPLEX WITH 2-NITRO-P-CRESOL |
| 1AHW | A COMPLEX OF EXTRACELLULAR DOMAIN OF TISSUE FACTOR WITH AN INHIBITORY FAB (5G9) |
| 1AHX | ASPARTATE AMINOTRANSFERASE HEXAMUTANT |
| 1AHY | ASPARTATE AMINOTRANSFERASE HEXAMUTANT |
| 1AHZ | STRUCTURE OF THE OCTAMERIC FLAVOENZYME VANILLYL-ALCOHOL OXIDASE IN COMPLEX WITH 4-(1-HEPTENYL)PHENOL |
| 1AI0 | R6 HUMAN INSULIN HEXAMER (NON-SYMMETRIC), NMR, 10 STRUCTURES |
| 1AI1 | HIV-1 V3 LOOP MIMIC |
| 1AI2 | ISOCITRATE DEHYDROGENASE COMPLEXED WITH ISOCITRATE, NADP+, AND CALCIUM (FLASH-COOLED) |
| 1AI3 | ORBITAL STEERING IN THE CATALYTIC POWER OF ENZYMES: SMALL STRUCTURAL CHANGES WITH LARGE CATALYTIC CONSEQUENCES |
| 1AI4 | PENICILLIN ACYLASE COMPLEXED WITH 3,4-DIHYDROXYPHENYLACETIC ACID |
| 1AI5 | PENICILLIN ACYLASE COMPLEXED WITH M-NITROPHENYLACETIC ACID |
| 1AI6 | PENICILLIN ACYLASE WITH P-HYDROXYPHENYLACETIC ACID |
| 1AI7 | PENICILLIN ACYLASE COMPLEXED WITH PHENOL |
| 1AI8 | HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG |
| 1AI9 | CANDIDA ALBICANS DIHYDROFOLATE REDUCTASE |
| 1AIA | STRUCTURAL BASIS FOR THE CATALYTIC ACTIVITY OF ASPARTATE AMINOTRANSFERASE K258H LACKING THE PYRIDOXAL-5'-PHOSPHATE BINDING LYSINE RESIDUE |
| 1AIB | STRUCTURAL BASIS FOR THE CATALYTIC ACTIVITY OF ASPARTATE AMINOTRANSFERASE K258H LACKING THE PYRIDOXAL-5'-PHOSPHATE BINDING LYSINE RESIDUE |
| 1AIC | STRUCTURAL BASIS FOR THE CATALYTIC ACTIVITY OF ASPARTATE AMINOTRANSFERASE K258H LACKING THE PYRIDOXAL-5'-PHOSPHATE BINDING LYSINE RESIDUE |
| 1AID | STRUCTURE OF A NON-PEPTIDE INHIBITOR COMPLEXED WITH HIV-1 PROTEASE: DEVELOPING A CYCLE OF STRUCTURE-BASED DRUG DESIGN |
| 1AIE | P53 TETRAMERIZATION DOMAIN CRYSTAL STRUCTURE |
| 1AIF | ANTI-IDIOTYPIC FAB 409.5.3 (IGG2A) FAB FROM MOUSE |
| 1AIG | PHOTOSYNTHETIC REACTION CENTER FROM RHODOBACTER SPHAEROIDES IN THE D+QB-CHARGE SEPARATED STATE |
| 1AIH | CATALYTIC DOMAIN OF BACTERIOPHAGE HP1 INTEGRASE |
| 1AII | ANNEXIN III |
| 1AIJ | PHOTOSYNTHETIC REACTION CENTER FROM RHODOBACTER SPHAEROIDES IN THE CHARGE-NEUTRAL DQAQB STATE |
| 1AIK | HIV GP41 CORE STRUCTURE |
| 1AIL | N-TERMINAL FRAGMENT OF NS1 PROTEIN FROM INFLUENZA A VIRUS |
| 1AIM | CRUZAIN INHIBITED BY BENZOYL-TYROSINE-ALANINE-FLUOROMETHYLKETONE |
| 1AIP | EF-TU EF-TS COMPLEX FROM THERMUS THERMOPHILUS |
| 1AIQ | CRYSTAL STRUCTURE OF THYMIDYLATE SYNTHASE R126E MUTANT |
| 1AIR | PECTATE LYASE C FROM ERWINIA CHRYSANTHEMI (EC16) TO A RESOLUTION OF 2.2 ANGSTROMS WITH 128 WATERS |
| 1AIS | TATA-BINDING PROTEIN/TRANSCRIPTION FACTOR (II)B/TATA-BOX COMPLEX FROM PYROCOCCUS WOESEI |
| 1AIU | HUMAN THIOREDOXIN (D60N MUTANT, REDUCED FORM) |
| 1AIV | APO OVOTRANSFERRIN |
| 1AIW | NMR STRUCTURES OF THE CELLULOSE-BINDING DOMAIN OF THE ENDOGLUCANASE Z FROM ERWINIA CHRYSANTHEMI, 23 STRUCTURES |
| 1AIX | HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROVAL |
| 1AIY | R6 HUMAN INSULIN HEXAMER (SYMMETRIC), NMR, 10 STRUCTURES |
| 1AIZ | STRUCTURE OF APO-AZURIN FROM ALCALIGENES DENITRIFICANS AT 1.8 ANGSTROMS RESOLUTION |
| 1AJ0 | CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF E. COLI DIHYDROPTEROATE SYNTHASE |
| 1AJ1 | NMR STRUCTURE OF THE LANTIBIOTIC ACTAGARDINE |
| 1AJ2 | CRYSTAL STRUCTURE OF A BINARY COMPLEX OF E. COLI DIHYDROPTEROATE SYNTHASE |
| 1AJ3 | SOLUTION STRUCTURE OF THE SPECTRIN REPEAT, NMR, 20 STRUCTURES |
| 1AJ4 | STRUCTURE OF CALCIUM-SATURATED CARDIAC TROPONIN C, NMR, 1 STRUCTURE |
| 1AJ5 | CALPAIN DOMAIN VI APO |
| 1AJ6 | NOVOBIOCIN-RESISTANT MUTANT (R136H) OF THE N-TERMINAL 24 KDA FRAGMENT OF DNA GYRASE B COMPLEXED WITH NOVOBIOCIN AT 2.3 ANGSTROMS RESOLUTION |
| 1AJ7 | IMMUNOGLOBULIN 48G7 GERMLINE FAB ANTIBODY COMPLEXED WITH HAPTEN 5-(PARA-NITROPHENYL PHOSPHONATE)-PENTANOIC ACID. AFFINITY MATURATION OF AN ESTEROLYTIC ANTIBODY |
| 1AJ8 | CITRATE SYNTHASE FROM PYROCOCCUS FURIOSUS |
| 1AJ9 | R-STATE HUMAN CARBONMONOXYHEMOGLOBIN ALPHA-A53S |
| 1AJA | THREE-DIMENSIONAL STRUCTURE OF THE D153G MUTANT OF E. COLI ALKALINE PHOSPHATASE: A MUTANT WITH WEAKER MAGNESIUM BINDING AND INCREASED CATALYTIC ACTIVITY |
| 1AJB | THREE-DIMENSIONAL STRUCTURE OF THE D153G MUTANT OF E. COLI ALKALINE PHOSPHATASE: A MUTANT WITH WEAKER MAGNESIUM BINDING AND INCREASED CATALYTIC ACTIVITY |
| 1AJC | THREE-DIMENSIONAL STRUCTURE OF THE D153G MUTANT OF E. COLI ALKALINE PHOSPHATASE: A MUTANT WITH WEAKER MAGNESIUM BINDING AND INCREASED CATALYTIC ACTIVITY |
| 1AJD | THREE-DIMENSIONAL STRUCTURE OF THE D153G MUTANT OF E. COLI ALKALINE PHOSPHATASE: A MUTANT WITH WEAKER MAGNESIUM BINDING AND INCREASED CATALYTIC ACTIVITY |
| 1AJE | CDC42 FROM HUMAN, NMR, 20 STRUCTURES |
| 1AJG | CARBONMONOXY MYOGLOBIN AT 40 K |
| 1AJH | PHOTOPRODUCT OF CARBONMONOXY MYOGLOBIN AT 40 K |
| 1AJJ | LDL RECEPTOR LIGAND-BINDING MODULE 5, CALCIUM-COORDINATING |
| 1AJK | CIRCULARLY PERMUTED (1-3,1-4)-BETA-D-GLUCAN 4-GLUCANOHYDROLASE CPA16M-84 |
| 1AJM | CRYSTAL STRUCTURE OF THYMIDYLATE SYNTHASE R126E MUTANT |
| 1AJN | PENICILLIN ACYLASE COMPLEXED WITH P-NITROPHENYLACETIC ACID |
| 1AJO | CIRCULARLY PERMUTED (1-3,1-4)-BETA-D-GLUCAN 4-GLUCANOHYDROLASE CPA16M-127 |
| 1AJP | PENICILLIN ACYLASE COMPLEXED WITH 2,5-DIHYDROXYPHENYLACETIC ACID |
| 1AJQ | PENICILLIN ACYLASE COMPLEXED WITH THIOPHENEACETIC ACID |
| 1AJR | REFINEMENT AND COMPARISON OF THE CRYSTAL STRUCTURES OF PIG CYTOSOLIC ASPARTATE AMINOTRANSFERASE AND ITS COMPLEX WITH 2-METHYLASPARTATE |
| 1AJS | REFINEMENT AND COMPARISON OF THE CRYSTAL STRUCTURES OF PIG CYTOSOLIC ASPARTATE AMINOTRANSFERASE AND ITS COMPLEX WITH 2-METHYLASPARTATE |
| 1AJV | HIV-1 PROTEASE IN COMPLEX WITH THE CYCLIC SULFAMIDE INHIBITOR AHA006 |
| 1AJW | STRUCTURE OF RHOGDI: A C-TERMINAL BINDING DOMAIN TARGETS AN N-TERMINAL INHIBITORY PEPTIDE TO GTPASES, NMR, 20 STRUCTURES |
| 1AJX | HIV-1 PROTEASE IN COMPLEX WITH THE CYCLIC UREA INHIBITOR AHA001 |
| 1AJY | STRUCTURE AND MOBILITY OF THE PUT3 DIMER: A DNA PINCER, NMR, 13 STRUCTURES |
| 1AJZ | STRUCTURE OF DIHYDROPTEROATE PYROPHOSPHORYLASE |
| 1AK0 | P1 NUCLEASE IN COMPLEX WITH A SUBSTRATE ANALOG |
| 1AK1 | FERROCHELATASE FROM BACILLUS SUBTILIS |
| 1AK2 | ADENYLATE KINASE ISOENZYME-2 |
| 1AK4 | HUMAN CYCLOPHILIN A BOUND TO THE AMINO-TERMINAL DOMAIN OF HIV-1 CAPSID |
| 1AK5 | INOSINE MONOPHOSPHATE DEHYDROGENASE (IMPDH) FROM TRITRICHOMONAS FOETUS |
| 1AK6 | DESTRIN, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AK7 | DESTRIN, NMR, 20 STRUCTURES |
| 1AK8 | NMR SOLUTION STRUCTURE OF CERIUM-LOADED CALMODULIN AMINO-TERMINAL DOMAIN (CE2-TR1C), 23 STRUCTURES |
| 1AK9 | SUBTILISIN MUTANT 8321 |
| 1AKA | STRUCTURAL BASIS FOR THE CATALYTIC ACTIVITY OF ASPARTATE AMINOTRANSFERASE K258H LACKING ITS PYRIDOXAL-5'-PHOSPHATE-BINDING LYSINE RESIDUE |
| 1AKB | STRUCTURAL BASIS FOR THE CATALYTIC ACTIVITY OF ASPARTATE AMINOTRANSFERASE K258H LACKING ITS PYRIDOXAL-5'-PHOSPHATE-BINDING LYSINE RESIDUE |
| 1AKC | STRUCTURAL BASIS FOR THE CATALYTIC ACTIVITY OF ASPARTATE AMINOTRANSFERASE K258H LACKING ITS PYRIDOXAL-5'-PHOSPHATE-BINDING LYSINE RESIDUE |
| 1AKD | CYTOCHROME P450CAM FROM PSEUDOMONAS PUTIDA, COMPLEXED WITH 1S-CAMPHOR |
| 1AKE | STRUCTURE OF THE COMPLEX BETWEEN ADENYLATE KINASE FROM ESCHERICHIA COLI AND THE INHIBITOR AP5A REFINED AT 1.9 ANGSTROMS RESOLUTION: A MODEL FOR A CATALYTIC TRANSITION STATE |
| 1AKG | ALPHA-CONOTOXIN PNIB FROM CONUS PENNACEUS |
| 1AKH | MAT A1/ALPHA2/DNA TERNARY COMPLEX |
| 1AKI | THE STRUCTURE OF THE ORTHORHOMBIC FORM OF HEN EGG-WHITE LYSOZYME AT 1.5 ANGSTROMS RESOLUTION |
| 1AKJ | COMPLEX OF THE HUMAN MHC CLASS I GLYCOPROTEIN HLA-A2 AND THE T CELL CORECEPTOR CD8 |
| 1AKK | SOLUTION STRUCTURE OF OXIDIZED HORSE HEART CYTOCHROME C, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AKL | ALKALINE PROTEASE FROM PSEUDOMONAS AERUGINOSA IFO3080 |
| 1AKM | ORNITHINE TRANSCARBAMYLASE FROM ESCHERICHIA COLI |
| 1AKN | STRUCTURE OF BILE-SALT ACTIVATED LIPASE |
| 1AKO | EXONUCLEASE III FROM ESCHERICHIA COLI |
| 1AKP | SEQUENTIAL 1H,13C AND 15N NMR ASSIGNMENTS AND SOLUTION CONFORMATION OF APOKEDARCIDIN |
| 1AKQ | D95A OXIDIZED FLAVODOXIN MUTANT FROM D. VULGARIS |
| 1AKR | G61A OXIDIZED FLAVODOXIN MUTANT |
| 1AKS | CRYSTAL STRUCTURE OF THE FIRST ACTIVE AUTOLYSATE FORM OF THE PORCINE ALPHA TRYPSIN |
| 1AKT | G61N OXIDIZED FLAVODOXIN MUTANT |
| 1AKU | D95A HYDROQUINONE FLAVODOXIN MUTANT FROM D. VULGARIS |
| 1AKV | D95A SEMIQUINONE FLAVODOXIN MUTANT FROM D. VULGARIS |
| 1AKW | G61L OXIDIZED FLAVODOXIN MUTANT |
| 1AKY | HIGH-RESOLUTION STRUCTURES OF ADENYLATE KINASE FROM YEAST LIGATED WITH INHIBITOR AP5A, SHOWING THE PATHWAY OF PHOSPHORYL TRANSFER |
| 1AKZ | HUMAN URACIL-DNA GLYCOSYLASE |
| 1AL0 | PROCAPSID OF BACTERIOPHAGE PHIX174 |
| 1AL1 | CRYSTAL STRUCTURE OF ALPHA1: IMPLICATIONS FOR PROTEIN DESIGN |
| 1AL2 | P1/MAHONEY POLIOVIRUS, SINGLE SITE MUTANT V1160I |
| 1AL3 | COFACTOR BINDING FRAGMENT OF CYSB FROM KLEBSIELLA AEROGENES |
| 1AL6 | CHICKEN CITRATE SYNTHASE COMPLEX WITH N-HYDROXYAMIDO-COA AND OXALOACETATE |
| 1AL7 | THREE-DIMENSIONAL STRUCTURES OF GLYCOLATE OXIDASE WITH BOUND ACTIVE-SITE INHIBITORS |
| 1AL8 | THREE-DIMENSIONAL STRUCTURE OF GLYCOLATE OXIDASE WITH BOUND ACTIVE-SITE INHIBITORS |
| 1ALA | STRUCTURE OF CHICKEN ANNEXIN V AT 2.25-ANGSTROMS RESOLUTION |
| 1ALB | CRYSTAL STRUCTURE OF RECOMBINANT MURINE ADIPOCYTE LIPID-BINDING PROTEIN |
| 1ALC | REFINED STRUCTURE OF BABOON ALPHA-LACTALBUMIN AT 1.7 ANGSTROMS RESOLUTION. COMPARISON WITH C-TYPE LYSOZYME |
| 1ALD | ACTIVITY AND SPECIFICITY OF HUMAN ALDOLASES |
| 1ALE | CONFORMATION OF TWO PEPTIDES CORRESPONDING TO HUMAN APOLIPOPROTEIN C-I RESIDUES 7-24 AND 35-53 IN THE PRESENCE OF SODIUM DODECYLSULFATE BY CD AND NMR SPECTROSCOPY |
| 1ALF | CONFORMATION OF TWO PEPTIDES CORRESPONDING TO HUMAN APOLIPOPROTEIN C-I RESIDUES 7-24 AND 35-53 IN THE PRESENCE OF SODIUM DODECYLSULFATE BY CD AND NMR SPECTROSCOPY |
| 1ALG | SOLUTION STRUCTURE OF AN HGR INHIBITOR, NMR, 10 STRUCTURES |
| 1ALH | KINETICS AND CRYSTAL STRUCTURE OF A MUTANT E. COLI ALKALINE PHOSPHATASE (ASP-369-->ASN): A MECHANISM INVOLVING ONE ZINC PER ACTIVE SITE |
| 1ALI | ALKALINE PHOSPHATASE MUTANT (H412N) |
| 1ALJ | ALKALINE PHOSPHATASE MUTANT (H412N) |
| 1ALK | REACTION MECHANISM OF ALKALINE PHOSPHATASE BASED ON CRYSTAL STRUCTURES. TWO METAL ION CATALYSIS |
| 1ALL | ALLOPHYCOCYANIN |
| 1ALN | CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE COMPLEXED WITH 3-DEAZACYTIDINE |
| 1ALQ | CIRCULARLY PERMUTED BETA-LACTAMASE FROM STAPHYLOCOCCUS AUREUS PC1 |
| 1ALU | HUMAN INTERLEUKIN-6 |
| 1ALV | CALCIUM BOUND DOMAIN VI OF PORCINE CALPAIN |
| 1ALW | INHIBITOR AND CALCIUM BOUND DOMAIN VI OF PORCINE CALPAIN |
| 1ALY | CRYSTAL STRUCTURE OF HUMAN CD40 LIGAND |
| 1AM1 | ATP BINDING SITE IN THE HSP90 MOLECULAR CHAPERONE |
| 1AM2 | GYRA INTEIN FROM MYCOBACTERIUM XENOPI |
| 1AM4 | COMPLEX BETWEEN CDC42HS.GMPPNP AND P50 RHOGAP (H. SAPIENS) |
| 1AM5 | THE CRYSTAL STRUCTURE AND PROPOSED AMINO ACID SEQUENCE OF A PEPSIN FROM ATLANTIC COD (GADUS MORHUA) |
| 1AM6 | CARBONIC ANHYDRASE II INHIBITOR: ACETOHYDROXAMATE |
| 1AM7 | LYSOZYME FROM BACTERIOPHAGE LAMBDA |
| 1AM9 | HUMAN SREBP-1A BOUND TO LDL RECEPTOR PROMOTER |
| 1AMA | DOMAIN CLOSURE IN MITOCHONDRIAL ASPARTATE AMINOTRANSFERASE |
| 1AMB | SOLUTION STRUCTURE OF RESIDUES 1-28 OF THE AMYLOID BETA-PEPTIDE |
| 1AMC | SOLUTION STRUCTURE OF RESIDUES 1-28 OF THE AMYLOID BETA-PEPTIDE |
| 1AME | CRYSTAL STRUCTURE OF TYPE III ANTIFREEZE PROTEIN AT 4 C |
| 1AMF | CRYSTAL STRUCTURE OF MODA, A MOLYBDATE TRANSPORT PROTEIN, COMPLEXED WITH MOLYBDATE |
| 1AMH | UNCOMPLEXED RAT TRYPSIN MUTANT WITH ASP 189 REPLACED WITH SER (D189S) |
| 1AMI | STERIC AND CONFORMATIONAL FEATURES OF THE ACONITASE MECHANISM |
| 1AMJ | STERIC AND CONFORMATIONAL FEATURES OF THE ACONITASE MECHANISM |
| 1AMK | LEISHMANIA MEXICANA TRIOSE PHOSPHATE ISOMERASE |
| 1AMM | 1.2 ANGSTROM STRUCTURE OF GAMMA-B CRYSTALLIN AT 150K |
| 1AMN | TRANSITION STATE ANALOG: ACETYLCHOLINESTERASE COMPLEXED WITH M-(N,N,N-TRIMETHYLAMMONIO)TRIFLUOROACETOPHENONE |
| 1AMO | THREE-DIMENSIONAL STRUCTURE OF NADPH-CYTOCHROME P450 REDUCTASE: PROTOTYPE FOR FMN-AND FAD-CONTAINING ENZYMES |
| 1AMP | CRYSTAL STRUCTURE OF AEROMONAS PROTEOLYTICA AMINOPEPTIDASE: A PROTOTYPICAL MEMBER OF THE CO-CATALYTIC ZINC ENZYME FAMILY |
| 1AMQ | X-RAY CRYSTALLOGRAPHIC STUDY OF PYRIDOXAMINE 5'-PHOSPHATE-TYPE ASPARTATE AMINOTRANSFERASES FROM ESCHERICHIA COLI IN THREE FORMS |
| 1AMR | X-RAY CRYSTALLOGRAPHIC STUDY OF PYRIDOXAMINE 5'-PHOSPHATE-TYPE ASPARTATE AMINOTRANSFERASES FROM ESCHERICHIA COLI IN THREE FORMS |
| 1AMS | X-RAY CRYSTALLOGRAPHIC STUDY OF PYRIDOXAMINE 5'-PHOSPHATE-TYPE ASPARTATE AMINOTRANSFERASES FROM ESCHERICHIA COLI IN THREE FORMS |
| 1AMT | CRYSTAL STRUCTURE OF ALAMETHICIN AT 1.5 ANGSTROM RESOLUTION |
| 1AMU | PHENYLALANINE ACTIVATING DOMAIN OF GRAMICIDIN SYNTHETASE 1 IN A COMPLEX WITH AMP AND PHENYLALANINE |
| 1AMW | ADP BINDING SITE IN THE HSP90 MOLECULAR CHAPERONE |
| 1AMX | COLLAGEN-BINDING DOMAIN FROM A STAPHYLOCOCCUS AUREUS ADHESIN |
| 1AMY | CRYSTAL AND MOLECULAR STRUCTURE OF BARLEY ALPHA-AMYLASE |
| 1AMZ | CHICKEN CITRATE SYNTHASE COMPLEX WITH NITROMETHYLDE-COA AND MALATE |
| 1AN0 | CDC42HS-GDP COMPLEX |
| 1AN1 | LEECH-DERIVED TRYPTASE INHIBITOR/TRYPSIN COMPLEX |
| 1AN2 | RECOGNITION BY MAX OF ITS COGNATE DNA THROUGH A DIMERIC B/HLH/Z DOMAIN |
| 1AN4 | STRUCTURE AND FUNCTION OF THE B/HLH/Z DOMAIN OF USF |
| 1AN5 | E. COLI THYMIDYLATE SYNTHASE IN COMPLEX WITH CB3717 |
| 1AN7 | RIBOSOMAL PROTEIN S8 FROM THERMUS THERMOPHILUS |
| 1AN8 | CRYSTAL STRUCTURE OF THE STREPTOCOCCAL SUPERANTIGEN SPE-C |
| 1AN9 | D-AMINO ACID OXIDASE COMPLEX WITH O-AMINOBENZOATE |
| 1ANB | ANIONIC TRYPSIN MUTANT WITH SER 214 REPLACED BY GLU |
| 1ANC | ANIONIC TRYPSIN MUTANT WITH SER 214 REPLACED BY LYS |
| 1AND | ANIONIC TRYPSIN MUTANT WITH ARG 96 REPLACED BY HIS |
| 1ANE | ANIONIC TRYPSIN WILD TYPE |
| 1ANF | MALTODEXTRIN BINDING PROTEIN WITH BOUND MALTOSE |
| 1ANG | CRYSTAL STRUCTURE OF HUMAN ANGIOGENIN REVEALS THE STRUCTURAL BASIS FOR ITS FUNCTIONAL DIVERGENCE FROM RIBONUCLEASE |
| 1ANI | ALKALINE PHOSPHATASE (D153H, K328H) |
| 1ANJ | ALKALINE PHOSPHATASE (K328H) |
| 1ANK | THE CLOSED CONFORMATION OF A HIGHLY FLEXIBLE PROTEIN: THE STRUCTURE OF E. COLI ADENYLATE KINASE WITH BOUND AMP AND AMPPNP |
| 1ANN | ANNEXIN IV |
| 1ANS | THREE-DIMENSIONAL STRUCTURE IN SOLUTION OF NEUROTOXIN III FROM THE SEA ANEMONE ANEMONIA SULCATA |
| 1ANT | BIOLOGICAL IMPLICATIONS OF A 3 ANGSTROMS STRUCTURE OF DIMERIC ANTITHROMBIN |
| 1ANU | COHESIN-2 DOMAIN OF THE CELLULOSOME FROM CLOSTRIDIUM THERMOCELLUM |
| 1ANV | ADENOVIRUS 5 DBP/URANYL FLUORIDE SOAK |
| 1ANW | THE EFFECT OF METAL BINDING ON THE STRUCTURE OF ANNEXIN V AND IMPLICATIONS FOR MEMBRANE BINDING |
| 1ANX | THE CRYSTAL STRUCTURE OF A NEW HIGH-CALCIUM FORM OF ANNEXIN V |
| 1AO0 | GLUTAMINE PHOSPHORIBOSYLPYROPHOSPHATE (PRPP) AMIDOTRANSFERASE FROM B. SUBTILIS COMPLEXED WITH ADP AND GMP |
| 1AO3 | A3 DOMAIN OF VON WILLEBRAND FACTOR |
| 1AO5 | MOUSE GLANDULAR KALLIKREIN-13 (PRORENIN CONVERTING ENZYME) |
| 1AO6 | CRYSTAL STRUCTURE OF HUMAN SERUM ALBUMIN |
| 1AO7 | COMPLEX BETWEEN HUMAN T-CELL RECEPTOR, VIRAL PEPTIDE (TAX), AND HLA-A 0201 |
| 1AO8 | DIHYDROFOLATE REDUCTASE COMPLEXED WITH METHOTREXATE, NMR, 21 STRUCTURES |
| 1AOA | N-TERMINAL ACTIN-CROSSLINKING DOMAIN FROM HUMAN FIMBRIN |
| 1AOB | E. COLI THYMIDYLATE SYNTHASE COMPLEXED WITH DDURD |
| 1AOC | JAPANESE HORSESHOE CRAB COAGULOGEN |
| 1AOD | PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C FROM LISTERIA MONOCYTOGENES |
| 1AOE | CANDIDA ALBICANS DIHYDROFOLATE REDUCTASE COMPLEXED WITH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE (NADPH) AND 1,3-DIAMINO-7-(1-ETHYEPROPYE)-7H-PYRRALO-[3,2-F]QUINAZOLINE (GW345) |
| 1AOF | CYTOCHROME CD1 NITRITE REDUCTASE, REDUCED FORM |
| 1AOG | TRYPANOSOMA CRUZI TRYPANOTHIONE REDUCTASE (OXIDIZED FORM) |
| 1AOH | SINGLE COHESIN DOMAIN FROM THE SCAFFOLDING PROTEIN CIPA OF THE CLOSTRIDIUM THERMOCELLUM CELLULOSOME |
| 1AOI | COMPLEX BETWEEN NUCLEOSOME CORE PARTICLE (H3,H4,H2A,H2B) AND 146 BP LONG DNA FRAGMENT |
| 1AOJ | THE SH3 DOMAIN OF EPS8 EXISTS AS A NOVEL INTERTWINED DIMER |
| 1AOK | VIPOXIN COMPLEX |
| 1AOL | FRIEND MURINE LEUKEMIA VIRUS RECEPTOR-BINDING DOMAIN |
| 1AOM | SUBSTRATE AND PRODUCT BOUND TO CYTOCHROME CD1 NITRITE REDUCTASE |
| 1AOO | AG-SUBSTITUTED METALLOTHIONEIN FROM SACCHAROMYCES CEREVISIAE, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AOP | SULFITE REDUCTASE STRUCTURE AT 1.6 ANGSTROM RESOLUTION |
| 1AOQ | CYTOCHROME CD1 NITRITE REDUCTASE WITH SUBSTRATE AND PRODUCT BOUND |
| 1AOR | STRUCTURE OF A HYPERTHERMOPHILIC TUNGSTOPTERIN ENZYME, ALDEHYDE FERREDOXIN OXIDOREDUCTASE |
| 1AOS | HUMAN ARGININOSUCCINATE LYASE |
| 1AOT | NMR STRUCTURE OF THE FYN SH2 DOMAIN COMPLEXED WITH A PHOSPHOTYROSYL PEPTIDE, MINIMIZED AVERAGE STRUCTURE |
| 1AOU | NMR STRUCTURE OF THE FYN SH2 DOMAIN COMPLEXED WITH A PHOSPHOTYROSYL PEPTIDE, 22 STRUCTURES |
| 1AOV | APO DUCK OVOTRANSFERRIN |
| 1AOW | ANNEXIN IV |
| 1AOX | I DOMAIN FROM INTEGRIN ALPHA2-BETA1 |
| 1AOY | N-TERMINAL DOMAIN OF ESCHERICHIA COLI ARGININE REPRESSOR NMR, 23 STRUCTURES |
| 1AOZ | REFINED CRYSTAL STRUCTURE OF ASCORBATE OXIDASE AT 1.9 ANGSTROMS RESOLUTION |
| 1AP0 | STRUCTURE OF THE CHROMATIN BINDING (CHROMO) DOMAIN FROM MOUSE MODIFIER PROTEIN 1, NMR, 26 STRUCTURES |
| 1AP2 | SINGLE CHAIN FV OF C219 |
| 1AP4 | REGULATORY DOMAIN OF HUMAN CARDIAC TROPONIN C IN THE CALCIUM-SATURATED STATE, NMR, 40 STRUCTURES |
| 1AP5 | TYR34->PHE MUTANT OF HUMAN MITOCHONDRIAL MANGANESE SUPEROXIDE DISMUTASE |
| 1AP6 | TYR34->PHE MUTANT OF HUMAN MITOCHONDRIAL MANGANESE SUPEROXIDE DISMUTASE |
| 1AP7 | P19-INK4D FROM MOUSE, NMR, 20 STRUCTURES |
| 1AP8 | TRANSLATION INITIATION FACTOR EIF4E IN COMPLEX WITH M7GDP, NMR, 20 STRUCTURES |
| 1AP9 | X-RAY STRUCTURE OF BACTERIORHODOPSIN FROM MICROCRYSTALS GROWN IN LIPIDIC CUBIC PHASES |
| 1APA | X-RAY STRUCTURE OF A POKEWEED ANTIVIRAL PROTEIN, CODED BY A NEW GENOMIC CLONE, AT 0.23 NM RESOLUTION. A MODEL STRUCTURE PROVIDES A SUITABLE ELECTROSTATIC FIELD FOR SUBSTRATE BINDING. |
| 1APB | A PRO TO GLY MUTATION IN THE HINGE OF THE ARABINOSE-BINDING PROTEIN ENHANCES BINDING AND ALTERS SPECIFICITY: SUGAR-BINDING AND CRYSTALLOGRAPHIC STUDIES |
| 1APC | SOLUTION STRUCTURE OF APOCYTOCHROME B562 |
| 1APF | ANTHOPLEURIN-B, NMR, 20 STRUCTURES |
| 1APH | CONFORMATIONAL CHANGES IN CUBIC INSULIN CRYSTALS IN THE PH RANGE 7-11 |
| 1APJ | NMR STUDY OF THE TRANSFORMING GROWTH FACTOR BETA BINDING PROTEIN-LIKE DOMAIN (TB MODULE/8-CYS DOMAIN), NMR, 21 STRUCTURES |
| 1APL | CRYSTAL STRUCTURE OF A MAT-ALPHA2 HOMEODOMAIN-OPERATOR COMPLEX SUGGESTS A GENERAL MODEL FOR HOMEODOMAIN-DNA INTERACTIONS |
| 1APM | 2.0 ANGSTROM REFINED CRYSTAL STRUCTURE OF THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH A PEPTIDE INHIBITOR AND DETERGENT |
| 1APN | THE CRYSTALLOGRAPHIC STRUCTURE OF METAL-FREE CONCANAVALIN A AT 2.5 ANGSTROMS RESOLUTION |
| 1APO | THREE-DIMENSIONAL STRUCTURE OF THE APO FORM OF THE N-TERMINAL EGF-LIKE MODULE OF BLOOD COAGULATION FACTOR X AS DETERMINED BY NMR SPECTROSCOPY AND SIMULATED FOLDING |
| 1APQ | STRUCTURE OF THE EGF-LIKE MODULE OF HUMAN C1R, NMR, 19 STRUCTURES |
| 1APS | THREE-DIMENSIONAL STRUCTURE OF ACYLPHOSPHATASE. REFINEMENT AND STRUCTURE ANALYSIS |
| 1APT | CRYSTALLOGRAPHIC ANALYSIS OF A PEPSTATIN ANALOGUE BINDING TO THE ASPARTYL PROTEINASE PENICILLOPEPSIN AT 1.8 ANGSTROMS RESOLUTION |
| 1APU | CRYSTALLOGRAPHIC ANALYSIS OF A PEPSTATIN ANALOGUE BINDING TO THE ASPARTYL PROTEINASE PENICILLOPEPSIN AT 1.8 ANGSTROMS RESOLUTION |
| 1APV | CRYSTALLOGRAPHIC ANALYSIS OF TRANSITION STATE MIMICS BOUND TO PENICILLOPEPSIN: DIFLUOROSTATINE-AND DIFLUOROSTATONE-CONTAINING PEPTIDES |
| 1APW | CRYSTALLOGRAPHIC ANALYSIS OF TRANSITION STATE MIMICS BOUND TO PENICILLOPEPSIN: DIFLUOROSTATINE-AND DIFLUOROSTATONE-CONTAINING PEPTIDES |
| 1APX | CRYSTAL STRUCTURE OF RECOMBINANT ASCORBATE PEROXIDASE |
| 1APY | HUMAN ASPARTYLGLUCOSAMINIDASE |
| 1APZ | HUMAN ASPARTYLGLUCOSAMINIDASE COMPLEX WITH REACTION PRODUCT |
| 1AQ0 | BARLEY 1,3-1,4-BETA-GLUCANASE IN MONOCLINIC SPACE GROUP |
| 1AQ1 | HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR STAUROSPORINE |
| 1AQ2 | PHOSPHOENOLPYRUVATE CARBOXYKINASE |
| 1AQ3 | BACTERIOPHAGE MS2 CAPSID PROTEIN/RNA COMPLEX |
| 1AQ4 | STRUCTURE OF A MS2 COAT PROTEIN MUTANT IN COMPLEX WITH AN RNA OPERATOR |
| 1AQ5 | HIGH-RESOLUTION SOLUTION NMR STRUCTURE OF THE TRIMERIC COILED-COIL DOMAIN OF CHICKEN CARTILAGE MATRIX PROTEIN, 20 STRUCTURES |
| 1AQ6 | STRUCTURE OF L-2-HALOACID DEHALOGENASE FROM XANTHOBACTER AUTOTROPHICUS |
| 1AQ7 | TRYPSIN WITH INHIBITOR AERUGINOSIN 98-B |
| 1AQ8 | STRUCTURE OF ALCALIGENES FAECALIS NITRITE REDUCTASE REDUCED WITH ASCORBATE |
| 1AQA | SOLUTION STRUCTURE OF REDUCED MICROSOMAL RAT CYTOCHROME B5, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AQB | RETINOL-BINDING PROTEIN (RBP) FROM PIG PLASMA |
| 1AQC | X11 PTB DOMAIN-10MER PEPTIDE COMPLEX |
| 1AQD | HLA-DR1 (DRA, DRB1 0101) HUMAN CLASS II HISTOCOMPATIBILITY PROTEIN (EXTRACELLULAR DOMAIN) COMPLEXED WITH ENDOGENOUS PEPTIDE |
| 1AQE | CRYSTAL STRUCTURE OF THE Y73E MUTANT OF CYTOCHROME C OF CLASS III (AMBLER) 26 KD |
| 1AQG | NMR STRUCTURE OF THE RHODOPSIN-BOUND C-TERMINAL PEPTIDE OF THE TRANSDUCIN ALPHA-SUBUNIT, 20 STRUCTURES |
| 1AQH | ALPHA-AMYLASE FROM ALTEROMONAS HALOPLANCTIS |
| 1AQI | STRUCTURE OF ADENINE-N6-DNA-METHYLTRANSFERASE TAQI |
| 1AQJ | STRUCTURE OF ADENINE-N6-DNA-METHYLTRANSFERASE TAQI |
| 1AQK | THREE-DIMENSIONAL STRUCTURE OF A HUMAN FAB WITH HIGH AFFINITY FOR TETANUS TOXOID |
| 1AQL | CRYSTAL STRUCTURE OF BOVINE BILE-SALT ACTIVATED LIPASE COMPLEXED WITH TAUROCHOLATE |
| 1AQM | ALPHA-AMYLASE FROM ALTEROMONAS HALOPLANCTIS COMPLEXED WITH TRIS |
| 1AQN | SUBTILISIN MUTANT 8324 |
| 1AQP | RIBONUCLEASE A COPPER COMPLEX |
| 1AQQ | AG-SUBSTITUTED METALLOTHIONEIN FROM SACCHAROMYCES CEREVISIAE, NMR, 10 STRUCTURES |
| 1AQR | CU-METALLOTHIONEIN FROM SACCHAROMYCES CEREVISIAE, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AQS | CU-METALLOTHIONEIN FROM SACCHAROMYCES CEREVISIAE, NMR, 10 STRUCTURES |
| 1AQT | EPSILON SUBUNIT OF F1F0-ATP SYNTHASE FROM ESCHERICHIA COLI |
| 1AQU | ESTROGEN SULFOTRANSFERASE WITH BOUND INACTIVE COFACTOR PAP AND 17-BETA ESTRADIOL |
| 1AQV | GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH P-BROMOBENZYLGLUTATHIONE |
| 1AQW | GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH GLUTATHIONE |
| 1AQX | GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH MEISENHEIMER COMPLEX |
| 1AQY | ESTROGEN SULFOTRANSFERASE WITH PAP |
| 1AQZ | CRYSTAL STRUCTURE OF A HIGHLY SPECIFIC ASPERGILLUS RIBOTOXIN, RESTRICTOCIN |
| 1AR0 | NUCLEAR TRANSPORT FACTOR 2 (NTF2) E42K MUTANT |
| 1AR1 | STRUCTURE AT 2.7 ANGSTROM RESOLUTION OF THE PARACOCCUS DENITRIFICANS TWO-SUBUNIT CYTOCHROME C OXIDASE COMPLEXED WITH AN ANTIBODY FV FRAGMENT |
| 1AR2 | DISULFIDE-FREE IMMUNOGLOBULIN FRAGMENT |
| 1AR4 | X-RAY STRUCTURE ANALYSIS OF THE CAMBIALISTIC SUPEROXIDE DISMUTASE FROM PROPIONIBACTERIUM SHERMANII ACTIVE WITH FE OR MN |
| 1AR5 | X-RAY STRUCTURE OF THE CAMBIALISTIC SUPEROXIDE DISMUTASE FROM PROPIONIBACTERIUM SHERMANII ACTIVE WITH FE OR MN |
| 1AR6 | P1/MAHONEY POLIOVIRUS, DOUBLE MUTANT V1160I +P1095S |
| 1AR7 | P1/MAHONEY POLIOVIRUS, DOUBLE MUTANT P1095S + H2142Y |
| 1AR8 | P1/MAHONEY POLIOVIRUS, MUTANT P1095S |
| 1AR9 | P1/MAHONEY POLIOVIRUS, SINGLE SITE MUTANT H2142Y |
| 1ARB | THE PRIMARY STRUCTURE AND STRUCTURAL CHARACTERISTICS OF ACHROMOBACTER LYTICUS PROTEASE I, A LYSINE-SPECIFIC SERINE PROTEASE |
| 1ARC | THE PRIMARY STRUCTURE AND STRUCTURAL CHARACTERISTICS OF ACHROMOBACTER LYTICUS PROTEASE I, A LYSINE-SPECIFIC SERINE PROTEASE |
| 1ARD | STRUCTURES OF DNA-BINDING MUTANT ZINC FINGER DOMAINS: IMPLICATIONS FOR DNA BINDING |
| 1ARE | STRUCTURES OF DNA-BINDING MUTANT ZINC FINGER DOMAINS: IMPLICATIONS FOR DNA BINDING |
| 1ARF | STRUCTURES OF DNA-BINDING MUTANT ZINC FINGER DOMAINS: IMPLICATIONS FOR DNA BINDING |
| 1ARG | ASPARTATE AMINOTRANSFERASE, PHOSPHO-5'-PYRIDOXYL ASPARTATE COMPLEX |
| 1ARH | ASPARTATE AMINOTRANSFERASE, Y225R/R386A MUTANT |
| 1ARI | ASPARTATE AMINOTRANSFERASE, W140H MUTANT, MALEATE COMPLEX |
| 1ARK | SH3 DOMAIN FROM HUMAN NEBULIN, NMR, 15 STRUCTURES |
| 1ARL | CARBOXYPEPTIDASE A WITH ZN REMOVED |
| 1ARM | CARBOXYPEPTIDASE A WITH ZN REPLACED BY HG |
| 1ARO | T7 RNA POLYMERASE COMPLEXED WITH T7 LYSOZYME |
| 1ARP | CRYSTAL STRUCTURE OF THE FUNGAL PEROXIDASE FROM ARTHROMYCES RAMOSUS AT 1.9 ANGSTROMS RESOLUTION: STRUCTURAL COMPARISONS WITH THE LIGNIN AND CYTOCHROME C PEROXIDASES |
| 1ARQ | RELAXATION MATRIX REFINEMENT OF THE SOLUTION STRUCTURE OF THE ARC REPRESSOR |
| 1ARR | RELAXATION MATRIX REFINEMENT OF THE SOLUTION STRUCTURE OF THE ARC REPRESSOR |
| 1ARS | X-RAY CRYSTALLOGRAPHIC STUDY OF PYRIDOXAL 5'-PHOSPHATE-TYPE ASPARTATE AMINOTRANSFERASES FROM ESCHERICHIA COLI IN OPEN AND CLOSED FORM |
| 1ART | X-RAY CRYSTALLOGRAPHIC STUDY OF PYRIDOXAL 5'-PHOSPHATE-TYPE ASPARTATE AMINOTRANSFERASES FROM ESCHERICHIA COLI IN OPEN AND CLOSED FORM |
| 1ARU | CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS |
| 1ARV | CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS |
| 1ARW | CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS |
| 1ARX | CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS |
| 1ARY | CRYSTAL STRUCTURES OF CYANIDE-AND TRIIODIDE-BOUND FORMS OF ARTHROMYCES RAMOSUS PEROXIDASE AT DIFFERENT PH VALUES. PERTURBATIONS OF ACTIVE SITE RESIDUES AND THEIR IMPLICATION IN ENZYME CATALYSIS |
| 1ARZ | ESCHERICHIA COLI DIHYDRODIPICOLINATE REDUCTASE IN COMPLEX WITH NADH AND 2,6 PYRIDINE DICARBOXYLATE |
| 1AS0 | GTP-GAMMA-S BOUND G42V GIA1 |
| 1AS2 | GDP+PI BOUND G42V GIA1 |
| 1AS3 | GDP BOUND G42V GIA1 |
| 1AS4 | CLEAVED ANTICHYMOTRYPSIN A349R |
| 1AS5 | SOLUTION STRUCTURE OF CONOTOXIN Y-PIIIE FROM CONUS PURPURASCENS, NMR, 14 STRUCTURES |
| 1AS6 | STRUCTURE OF NITRITE BOUND TO OXIDIZED ALCALIGENES FAECALIS NITRITE REDUCTASE AT CRYO TEMPERATURE |
| 1AS7 | STRUCTURE OF ALCALIGENES FAECALIS NITRITE REDUCTASE AT CRYO TEMPERATURE |
| 1AS8 | STRUCTURE OF NITRITE BOUND TO REDUCED ALCALIGENES FAECALIS NITRITE REDUCTASE AT CRYO TEMPERATURE |
| 1ASA | THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE Y226F(Y225F) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
| 1ASB | THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE D223A(D222A) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
| 1ASC | THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE D223A(D222A) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
| 1ASD | THE STRUCTURE OF WILD TYPE E. COLI ASPARTATE AMINOTRANSFERASE RECONSTITUTED WITH N-MEPLP |
| 1ASE | THE STRUCTURE OF WILD TYPE E. COLI ASPARTATE AMINOTRANSFERASE RECONSTITUTED WITH PLP-N-OXIDE |
| 1ASF | THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE Y226F(Y225F) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
| 1ASG | THE STRUCTURAL BASIS FOR THE REDUCED ACTIVITY OF THE Y226F(Y225F) ACTIVE SITE MUTANT OF E. COLI ASPARTATE AMINOTRANSFERASE |
| 1ASH | THE STRUCTURE OF ASCARIS HEMOGLOBIN DOMAIN I AT 2.2 ANGSTROMS RESOLUTION: MOLECULAR FEATURES OF OXYGEN AVIDITY |
| 1ASJ | P1/MAHONEY POLIOVIRUS, AT CRYOGENIC TEMPERATURE |
| 1ASK | NUCLEAR TRANSPORT FACTOR 2 (NTF2) H66A MUTANT |
| 1ASL | CRYSTAL STRUCTURES OF ESCHERICHIA COLI ASPARTATE AMINOTRANSFERASE IN TWO CONFORMATIONS: COMPARISON OF AN UNLIGANDED OPEN AND TWO LIGANDED CLOSED FORMS |
| 1ASM | CRYSTAL STRUCTURES OF ESCHERICHIA COLI ASPARTATE AMINOTRANSFERASE IN TWO CONFORMATIONS: COMPARISON OF AN UNLIGANDED OPEN AND TWO LIGANDED CLOSED FORMS |
| 1ASN | CRYSTAL STRUCTURES OF ESCHERICHIA COLI ASPARTATE AMINOTRANSFERASE IN TWO CONFORMATIONS: COMPARISON OF AN UNLIGANDED OPEN AND TWO LIGANDED CLOSED FORMS |
| 1ASO | X-RAY STRUCTURES AND MECHANISTIC IMPLICATIONS OF THREE FUNCTIONAL DERIVATIVES OF ASCORBATE OXIDASE FROM ZUCCHINI: REDUCED-, PEROXIDE-, AND AZIDE-FORMS |
| 1ASP | X-RAY STRUCTURES AND MECHANISTIC IMPLICATIONS OF THREE FUNCTIONAL DERIVATIVES OF ASCORBATE OXIDASE FROM ZUCCHINI: REDUCED-, PEROXIDE-, AND AZIDE-FORMS |
| 1ASQ | X-RAY STRUCTURES AND MECHANISTIC IMPLICATIONS OF THREE FUNCTIONAL DERIVATIVES OF ASCORBATE OXIDASE FROM ZUCCHINI: REDUCED-, PEROXIDE-, AND AZIDE-FORMS |
| 1ASS | APICAL DOMAIN OF THE CHAPERONIN FROM THERMOPLASMA ACIDOPHILUM |
| 1AST | STRUCTURE OF ASTACIN AND IMPLICATIONS FOR ACTIVATION OF ASTACINS AND ZINC-LIGATION OF COLLAGENASES |
| 1ASU | AVIAN SARCOMA VIRUS INTEGRASE CATALYTIC CORE DOMAIN CRYSTALLIZED FROM 2% PEG 400, 2M AMMONIUM SULFATE, HEPES PH 7.5 |
| 1ASV | AVIAN SARCOMA VIRUS INTEGRASE CATALYTIC CORE DOMAIN |
| 1ASW | AVIAN SARCOMA VIRUS INTEGRASE CATALYTIC CORE DOMAIN CRYSTALLIZED FROM 20% PEG 4000, 10% ISOPROPANOL, HEPES PH 7.5 USING SELENOMETHIONINE SUBSTITUTED PROTEIN; DATA COLLECTED AT-165 DEGREES C |
| 1ASX | APICAL DOMAIN OF THE CHAPERONIN FROM THERMOPLASMA ACIDOPHILUM |
| 1ASY | CLASS II AMINOACYL TRANSFER RNA SYNTHETASES: CRYSTAL STRUCTURE OF YEAST ASPARTYL-TRNA SYNTHETASE COMPLEXED WITH TRNA ASP |
| 1ASZ | THE ACTIVE SITE OF YEAST ASPARTYL-TRNA SYNTHETASE: STRUCTURAL AND FUNCTIONAL ASPECTS OF THE AMINOACYLATION REACTION |
| 1AT0 | 17-KDA FRAGMENT OF HEDGEHOG C-TERMINAL AUTOPROCESSING DOMAIN |
| 1AT1 | CRYSTAL STRUCTURES OF PHOSPHONOACETAMIDE LIGATED T AND PHOSPHONOACETAMIDE AND MALONATE LIGATED R STATES OF ASPARTATE CARBAMOYLTRANSFERASE AT 2.8-ANGSTROMS RESOLUTION AND NEUTRAL P*H |
| 1AT3 | HERPES SIMPLEX VIRUS TYPE II PROTEASE |
| 1AT5 | HEN EGG WHITE LYSOZYME WITH A SUCCINIMIDE RESIDUE |
| 1AT6 | HEN EGG WHITE LYSOZYME WITH A ISOASPARTATE RESIDUE |
| 1AT9 | STRUCTURE OF BACTERIORHODOPSIN AT 3.0 ANGSTROM DETERMINED BY ELECTRON CRYSTALLOGRAPHY |
| 1ATA | HIGH-RESOLUTION STRUCTURE OF ASCARIS TRYPSIN INHIBITOR IN SOLUTION: DIRECT EVIDENCE FOR A PH INDUCED CONFORMATIONAL TRANSITION IN THE REACTIVE SITE |
| 1ATB | HIGH-RESOLUTION STRUCTURE OF ASCARIS TRYPSIN INHIBITOR IN SOLUTION: DIRECT EVIDENCE FOR A PH INDUCED CONFORMATIONAL TRANSITION IN THE REACTIVE SITE |
| 1ATD | HIGH-RESOLUTION STRUCTURE OF ASCARIS TRYPSIN INHIBITOR IN SOLUTION: DIRECT EVIDENCE FOR A PH INDUCED CONFORMATIONAL TRANSITION IN THE REACTIVE SITE |
| 1ATE | HIGH-RESOLUTION STRUCTURE OF ASCARIS TRYPSIN INHIBITOR IN SOLUTION: DIRECT EVIDENCE FOR A PH INDUCED CONFORMATIONAL TRANSITION IN THE REACTIVE SITE |
| 1ATG | AZOTOBACTER VINELANDII PERIPLASMIC MOLYBDATE-BINDING PROTEIN |
| 1ATH | THE INTACT AND CLEAVED HUMAN ANTITHROMBIN III COMPLEX AS A MODEL FOR SERPIN-PROTEINASE INTERACTIONS |
| 1ATI | CRYSTAL STRUCTURE OF GLYCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS |
| 1ATJ | RECOMBINANT HORSERADISH PEROXIDASE C1A |
| 1ATK | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH THE COVALENT INHIBITOR E-64 |
| 1ATL | STRUCTURAL INTERACTION OF NATURAL AND SYNTHETIC INHIBITORS WITH THE VENOM METALLOPROTEINASE, ATROLYSIN C (FORM-D) |
| 1ATN | ATOMIC STRUCTURE OF THE ACTIN:DNASE I COMPLEX |
| 1ATP | 2.2 ANGSTROM REFINED CRYSTAL STRUCTURE OF THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH MNATP AND A PEPTIDE INHIBITOR |
| 1ATR | THREONINE 204 OF THE CHAPERONE PROTEIN HSC70 INFLUENCES THE STRUCTURE OF THE ACTIVE SITE BUT IS NOT ESSENTIAL FOR ATP HYDROLYSIS |
| 1ATS | THREONINE 204 OF THE CHAPERONE PROTEIN HSC70 INFLUENCES THE STRUCTURE OF THE ACTIVE SITE BUT IS NOT ESSENTIAL FOR ATP HYDROLYSIS |
| 1ATT | CRYSTAL STRUCTURE OF CLEAVED BOVINE ANTITHROMBIN III AT 3.2 ANGSTROMS RESOLUTION |
| 1ATX | THREE-DIMENSIONAL STRUCTURE OF THE NEUROTOXIN ATX IA FROM ANEMONIA SULCATA IN AQUEOUS SOLUTION DETERMINED BY NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY |
| 1ATY | DETERMINATION OF LOCAL PROTEIN STRUCTURE BY SPIN LABEL DIFFERENCE 2D NMR: THE REGION NEIGHBORING ASP61 OF SUBUNIT C OF THE F1FO ATP SYNTHASE |
| 1ATZ | HUMAN VON WILLEBRAND FACTOR A3 DOMAIN |
| 1AU0 | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT SYMMETRIC DIACYLAMINOMETHYL KETONE INHIBITOR |
| 1AU1 | HUMAN INTERFERON-BETA CRYSTAL STRUCTURE |
| 1AU2 | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT PROPANONE INHIBITOR |
| 1AU3 | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT PYRROLIDINONE INHIBITOR |
| 1AU4 | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT PYRROLIDINONE INHIBITOR |
| 1AU7 | PIT-1 MUTANT/DNA COMPLEX |
| 1AU8 | HUMAN CATHEPSIN G |
| 1AU9 | SUBTILISIN BPN' MUTANT 8324 IN CITRATE |
| 1AUA | PHOSPHATIDYLINOSITOL TRANSFER PROTEIN SEC14P FROM SACCHAROMYCES CEREVISIAE |
| 1AUC | HUMAN THIOREDOXIN (OXIDIZED WITH DIAMIDE) |
| 1AUD | U1A-UTRRNA, NMR, 31 STRUCTURES |
| 1AUE | FKBP-RAPAMYCIN BINDING DOMAIN (FRB) OF THE FKBP-RAPAMYCIN ASSOCIATED PROTEIN |
| 1AUG | CRYSTAL STRUCTURE OF THE PYROGLUTAMYL PEPTIDASE I FROM BACILLUS AMYLOLIQUEFACIENS |
| 1AUI | HUMAN CALCINEURIN HETERODIMER |
| 1AUJ | BOVINE TRYPSIN COMPLEXED TO META-CYANO-BENZYLIC INHIBITOR |
| 1AUK | HUMAN ARYLSULFATASE A |
| 1AUM | HIV CAPSID C-TERMINAL DOMAIN (CAC146) |
| 1AUN | PATHOGENESIS-RELATED PROTEIN 5D FROM NICOTIANA TABACUM |
| 1AUO | CARBOXYLESTERASE FROM PSEUDOMONAS FLUORESCENS |
| 1AUP | GLUTAMATE DEHYDROGENASE |
| 1AUQ | A1 DOMAIN OF VON WILLEBRAND FACTOR |
| 1AUR | PMSF-INHIBITED CARBOXYLESTERASE FROM PSEUDOMONAS FLUORESCENS |
| 1AUT | HUMAN ACTIVATED PROTEIN C |
| 1AUU | SOLUTION STRUCTURE OF THE RNA-BINDING DOMAIN OF THE ANTITERMINATOR PROTEIN SACY, NMR, 10 STRUCTURES |
| 1AUV | STRUCTURE OF THE C DOMAIN OF SYNAPSIN IA FROM BOVINE BRAIN |
| 1AUW | H91N DELTA 2 CRYSTALLIN FROM DUCK |
| 1AUX | STRUCTURE OF THE C DOMAIN OF SYNAPSIN IA FROM BOVINE BRAIN WITH CALCIUM ATP-GAMMA-S BOUND |
| 1AUY | TURNIP YELLOW MOSAIC VIRUS |
| 1AUZ | SOLUTION STRUCTURE OF SPOIIAA, A PHOSPHORYLATABLE COMPONENT OF THE SYSTEM THAT REGULATES TRANSCRIPTION FACTOR SIGMA-F OF BACILLUS SUBTILIS, NMR, 24 STRUCTURES |
| 1AV1 | CRYSTAL STRUCTURE OF HUMAN APOLIPOPROTEIN A-I |
| 1AV3 | POTASSIUM CHANNEL BLOCKER KAPPA CONOTOXIN PVIIA FROM C. PURPURASCENS, NMR, 20 STRUCTURES |
| 1AV4 | CRYSTAL STRUCTURES OF THE COPPER-CONTAINING AMINE OXIDASE FROM ARTHROBACTER GLOBIFORMIS IN THE HOLO-AND APO-FORMS: IMPLICATIONS FOR THE BIOGENESIS OF TOPA QUINONE |
| 1AV5 | PKCI-SUBSTRATE ANALOG |
| 1AV6 | VACCINIA METHYLTRANSFERASE VP39 COMPLEXED WITH M7G CAPPED RNA HEXAMER AND S-ADENOSYLHOMOCYSTEINE |
| 1AV7 | SUBTILISIN CARLSBERG L-NAPHTHYL-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX |
| 1AV8 | RIBONUCLEOTIDE REDUCTASE R2 SUBUNIT FROM E. COLI |
| 1AVA | AMY2/BASI PROTEIN-PROTEIN COMPLEX FROM BARLEY SEED |
| 1AVB | ARCELIN-1 FROM PHASEOLUS VULGARIS L |
| 1AVC | BOVINE ANNEXIN VI (CALCIUM-BOUND) |
| 1AVD | THREE-DIMENSIONAL STRUCTURE OF THE TETRAGONAL CRYSTAL FORM OF EGG-WHITE AVIDIN IN ITS FUNCTIONAL COMPLEX WITH BIOTIN AT 2.7 ANGSTROMS RESOLUTION |
| 1AVE | CRYSTAL STRUCTURE OF HEN EGG-WHITE APO-AVIDIN IN RELATION TO ITS THERMAL STABILITY PROPERTIES |
| 1AVF | ACTIVATION INTERMEDIATE 2 OF HUMAN GASTRICSIN FROM HUMAN STOMACH |
| 1AVG | THROMBIN INHIBITOR FROM TRIATOMA PALLIDIPENNIS |
| 1AVH | CRYSTAL AND MOLECULAR STRUCTURE OF HUMAN ANNEXIN V AFTER REFINEMENT. IMPLICATIONS FOR STRUCTURE, MEMBRANE BINDING AND ION CHANNEL FORMATION OF THE ANNEXIN FAMILY OF PROTEINS |
| 1AVK | CRYSTAL STRUCTURES OF THE COPPER-CONTAINING AMINE OXIDASE FROM ARTHROBACTER GLOBIFORMIS IN THE HOLO-AND APO-FORMS: IMPLICATIONS FOR THE BIOGENESIS OF TOPA QUINONE |
| 1AVL | CRYSTAL STRUCTURES OF THE COPPER-CONTAINING AMINE OXIDASE FROM ARTHROBACTER GLOBIFORMIS IN THE HOLO-AND APO-FORMS: IMPLICATIONS FOR THE BIOGENESIS OF TOPA QUINONE |
| 1AVM | THE CAMBIALISTIC SUPEROXIDE DISMUTASE (FE-SOD) OF P. SHERMANII COORDINATED BY AZIDE |
| 1AVN | HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH THE HISTAMINE ACTIVATOR |
| 1AVO | PROTEASOME ACTIVATOR REG(ALPHA) |
| 1AVP | STRUCTURE OF HUMAN ADENOVIRUS 2 PROTEINASE WITH ITS 11 AMINO ACID COFACTOR |
| 1AVQ | TOROIDAL STRUCTURE OF LAMBDA EXONUCLEASE DETERMINED AT 2.4 ANGSTROMS |
| 1AVR | CRYSTAL AND MOLECULAR STRUCTURE OF HUMAN ANNEXIN V AFTER REFINEMENT. IMPLICATIONS FOR STRUCTURE, MEMBRANE BINDING AND ION CHANNEL FORMATION OF THE ANNEXIN FAMILY OF PROTEINS |
| 1AVS | X-RAY CRYSTALLOGRAPHIC STUDY OF CALCIUM-SATURATED N-TERMINAL DOMAIN OF TROPONIN C |
| 1AVT | SUBTILISIN CARLSBERG D-PARA-CHLOROPHENYL-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX |
| 1AVU | TRYPSIN INHIBITOR FROM SOYBEAN (STI) |
| 1AVV | HIV-1 NEF PROTEIN, UNLIGANDED CORE DOMAIN |
| 1AVW | COMPLEX PORCINE PANCREATIC TRYPSIN/SOYBEAN TRYPSIN INHIBITOR, ORTHORHOMBIC CRYSTAL FORM |
| 1AVX | COMPLEX PORCINE PANCREATIC TRYPSIN/SOYBEAN TRYPSIN INHIBITOR, TETRAGONAL CRYSTAL FORM |
| 1AVY | FIBRITIN DELETION MUTANT M (BACTERIOPHAGE T4) |
| 1AVZ | V-1 NEF PROTEIN IN COMPLEX WITH WILD TYPE FYN SH3 DOMAIN |
| 1AW0 | FOURTH METAL-BINDING DOMAIN OF THE MENKES COPPER-TRANSPORTING ATPASE, NMR, 20 STRUCTURES |
| 1AW1 | TRIOSEPHOSPHATE ISOMERASE OF VIBRIO MARINUS COMPLEXED WITH 2-PHOSPHOGLYCOLATE |
| 1AW2 | TRIOSEPHOSPHATE ISOMERASE OF VIBRIO MARINUS |
| 1AW3 | THE SOLUTION NMR STRUCTURE OF OXIDIZED RAT MICROSOMAL CYTOCHROME B5, MINIMIZED AVERAGE STRUCTURE |
| 1AW5 | 5-AMINOLEVULINATE DEHYDRATASE FROM SACCHAROMYCES CEREVISIAE |
| 1AW6 | GAL4 (CD), NMR, 24 STRUCTURES |
| 1AW7 | Q136A MUTANT OF TOXIC SHOCK SYNDROME TOXIN-1 FROM S. AUREUS |
| 1AW8 | PYRUVOYL DEPENDENT ASPARTATE DECARBOXYLASE |
| 1AW9 | STRUCTURE OF GLUTATHIONE S-TRANSFERASE III IN APO FORM |
| 1AWB | HUMAN MYO-INOSITOL MONOPHOSPHATASE IN COMPLEX WITH D-INOSITOL-1-PHOSPHATE AND CALCIUM |
| 1AWC | MOUSE GABP ALPHA/BETA DOMAIN BOUND TO DNA |
| 1AWD | FERREDOXIN [2FE-2S] OXIDIZED FORM FROM CHLORELLA FUSCA |
| 1AWE | HUMAN SOS1 PLECKSTRIN HOMOLOGY (PH) DOMAIN, NMR, 20 STRUCTURES |
| 1AWF | NOVEL COVALENT THROMBIN INHIBITOR FROM PLANT EXTRACT |
| 1AWH | NOVEL COVALENT THROMBIN INHIBITOR FROM PLANT EXTRACT |
| 1AWI | HUMAN PLATELET PROFILIN COMPLEXED WITH THE L-PRO10 PEPTIDE |
| 1AWJ | INTRAMOLECULAR ITK-PROLINE COMPLEX, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AWO | THE SOLUTION NMR STRUCTURE OF ABL SH3 AND ITS RELATIONSHIP TO SH2 IN THE SH(32) CONSTRUCT, 20 STRUCTURES |
| 1AWP | RAT OUTER MITOCHONDRIAL MEMBRANE CYTOCHROME B5 |
| 1AWQ | CYPA COMPLEXED WITH HAGPIA (PSEUDO-SYMMETRIC MONOMER) |
| 1AWR | CYPA COMPLEXED WITH HAGPIA |
| 1AWS | SECYPA COMPLEXED WITH HAGPIA (PSEUDO-SYMMETRIC MONOMER) |
| 1AWT | SECYPA COMPLEXED WITH HAGPIA |
| 1AWU | CYPA COMPLEXED WITH HVGPIA (PSEUDO-SYMMETRIC MONOMER) |
| 1AWV | CYPA COMPLEXED WITH HVGPIA |
| 1AWW | SH3 DOMAIN FROM BRUTON'S TYROSINE KINASE, NMR, 42 STRUCTURES |
| 1AWX | SH3 DOMAIN FROM BRUTON'S TYROSINE KINASE, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1AWZ | 3D SOLUTION STRUCTURE OF HUMAN ANGIOGENIN DETERMINED BY 1H, 15N NMR SPECTROSCOPY, 30 STRUCTURES |
| 1AX0 | ERYTHRINA CORALLODENDRON LECTIN IN COMPLEX WITH N-ACTYLGALACTOSAMINE |
| 1AX1 | ERYTHRINA CORALLODENDRON LECTIN IN COMPLEX WITH LACTOSE |
| 1AX2 | ERYTHRINA CORALLODENDRON LECTIN IN COMPLEX WITH N-ACETYLLACTOSAMINE |
| 1AX3 | SOLUTION NMR STRUCTURE OF B. SUBTILIS IIAGLC, 16 STRUCTURES |
| 1AX4 | TRYPTOPHANASE FROM PROTEUS VULGARIS |
| 1AX8 | HUMAN OBESITY PROTEIN, LEPTIN |
| 1AX9 | ACETYLCHOLINESTERASE COMPLEXED WITH EDROPHONIUM, LAUE DATA |
| 1AXA | ACTIVE-SITE MOBILITY IN HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 PROTEASE AS DEMONSTRATED BY CRYSTAL STRUCTURE OF A28S MUTANT |
| 1AXB | TEM-1 BETA-LACTAMASE FROM ESCHERICHIA COLI INHIBITED WITH AN ACYLATION TRANSITION STATE ANALOG |
| 1AXC | HUMAN PCNA |
| 1AXD | STRUCTURE OF GLUTATHIONE S-TRANSFERASE-I BOUND WITH THE LIGAND LACTOYLGLUTATHIONE |
| 1AXE | CRYSTAL STRUCTURE OF THE ACTIVE-SITE MUTANT PHE93->TRP OF HORSE LIVER ALCOHOL DEHYDROGENASE IN COMPLEX WITH NAD AND INHIBITOR TRIFLUOROETHANOL |
| 1AXG | CRYSTAL STRUCTURE OF THE VAL203->ALA MUTANT OF LIVER ALCOHOL DEHYDROGENASE COMPLEXED WITH COFACTOR NAD AND INHIBITOR TRIFLUOROETHANOL SOLVED TO 2.5 ANGSTROM RESOLUTION |
| 1AXH | ATRACOTOXIN-HVI FROM HADRONYCHE VERSUTA (AUSTRALIAN FUNNEL-WEB SPIDER, NMR, 20 STRUCTURES |
| 1AXI | STRUCTURAL PLASTICITY AT THE HGH:HGHBP INTERFACE |
| 1AXJ | FMN-BINDING PROTEIN FROM DESULFOVIBRIO VULGARIS (MIYAZAKI F), NMR, 20 STRUCTURES |
| 1AXK | ENGINEERED BACILLUS BIFUNCTIONAL ENZYME GLUXYN-1 |
| 1AXM | HEPARIN-LINKED BIOLOGICALLY-ACTIVE DIMER OF FIBROBLAST GROWTH FACTOR |
| 1AXN | THE HIGH RESOLUTION STRUCTURE OF ANNEXIN III SHOWS DIFFERENCES WITH ANNEXIN V |
| 1AXQ | FERRICYANIDE OXIDIZED FDI |
| 1AXR | COOPERATIVITY BETWEEN HYDROGEN-BONDING AND CHARGE-DIPOLE INTERACTIONS IN THE INHIBITION OF BETA-GLYCOSIDASES BY AZOLOPYRIDINES: EVIDENCE FROM A STUDY WITH GLYCOGEN PHOSPHORYLASE B |
| 1AXS | MATURE OXY-COPE CATALYTIC ANTIBODY WITH HAPTEN |
| 1AXT | IMMUNE VERSUS NATURAL SELECTION: ANTIBODY ALDOLASES WITH THE RATES OF NATURAL ENZYMES |
| 1AXW | E. COLI THYMIDYLATE SYNTHASE IN COMPLEX WITH METHOTREXATE (MTX) AND 2'-DEOXYURIDINE 5'-MONOPHOSPHATE (DUMP) |
| 1AXX | THE SOLUTION STRUCTURE OF OXIDIZED RAT MICROSOMAL CYTOCHROME B5, NMR, 19 STRUCTURES |
| 1AXY | ERYTHRINA CORALLODENDRON LECTIN |
| 1AXZ | ERYTHRINA CORALLODENDRON LECTIN IN COMPLEX WITH D-GALACTOSE |
| 1AY0 | IDENTIFICATION OF CATALYTICALLY IMPORTANT RESIDUES IN YEAST TRANSKETOLASE |
| 1AY1 | ANTI TAQ FAB TP7 |
| 1AY2 | STRUCTURE OF THE FIBER-FORMING PROTEIN PILIN AT 2.6 ANGSTROMS RESOLUTION |
| 1AY4 | AROMATIC AMINO ACID AMINOTRANSFERASE WITHOUT SUBSTRATE |
| 1AY5 | AROMATIC AMINO ACID AMINOTRANSFERASE COMPLEX WITH MALEATE |
| 1AY6 | THROMBIN INHIBITOR FROM THEONALLA, CYCLOTHEANAMIDE-BASED MACROCYCLIC TRIPEPTIDE MOTIF |
| 1AY7 | RIBONUCLEASE SA COMPLEX WITH BARSTAR |
| 1AY8 | AROMATIC AMINO ACID AMINOTRANSFERASE COMPLEX WITH 3-PHENYLPROPIONATE |
| 1AY9 | WILD-TYPE UMUD' FROM E. COLI |
| 1AYA | CRYSTAL STRUCTURES OF PEPTIDE COMPLEXES OF THE AMINO-TERMINAL SH2 DOMAIN OF THE SYP TYROSINE PHOSPHATASE |
| 1AYB | CRYSTAL STRUCTURES OF PEPTIDE COMPLEXES OF THE AMINO-TERMINAL SH2 DOMAIN OF THE SYP TYROSINE PHOSPHATASE |
| 1AYC | CRYSTAL STRUCTURES OF PEPTIDE COMPLEXES OF THE AMINO-TERMINAL SH2 DOMAIN OF THE SYP TYROSINE PHOSPHATASE |
| 1AYD | CRYSTAL STRUCTURES OF PEPTIDE COMPLEXES OF THE AMINO-TERMINAL SH2 DOMAIN OF THE SYP TYROSINE PHOSPHATASE |
| 1AYE | HUMAN PROCARBOXYPEPTIDASE A2 |
| 1AYF | BOVINE ADRENODOXIN (OXIDIZED) |
| 1AYG | SOLUTION STRUCTURE OF CYTOCHROME C-552, NMR, 20 STRUCTURES |
| 1AYI | COLICIN E7 IMMUNITY PROTEIN IM7 |
| 1AYJ | DETERMINATION OF THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF RAPHANUS SATIVUS ANTIFUNGAL PROTEIN 1 (RS-AFP1) BY 1H NMR, 20 STRUCTURES |
| 1AYK | INHIBITOR-FREE CATALYTIC FRAGMENT OF HUMAN FIBROBLAST COLLAGENASE, NMR, 30 STRUCTURES |
| 1AYL | PHOSPHOENOLPYRUVATE CARBOXYKINASE |
| 1AYM | HUMAN RHINOVIRUS 16 COAT PROTEIN AT HIGH RESOLUTION |
| 1AYN | HUMAN RHINOVIRUS 16 COAT PROTEIN |
| 1AYO | RECEPTOR BINDING DOMAIN OF BOVINE ALPHA-2-MACROGLOBULIN |
| 1AYP | A PROBE MOLECULE COMPOSED OF SEVENTEEN PERCENT OF TOTAL DIFFRACTING MATTER GIVES CORRECT SOLUTIONS IN MOLECULAR REPLACEMENT |
| 1AYR | ARRESTIN FROM BOVINE ROD OUTER SEGMENTS |
| 1AYU | CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT SYMMETRIC BISCARBOHYDRAZIDE INHIBITOR |
| 1AYV | CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT THIAZOLHYDRAZIDE INHIBITOR |
| 1AYW | CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT BENZYLOXYBENZOYLCARBOHYDRAZIDE INHIBITOR |
| 1AYX | CRYSTAL STRUCTURE OF GLUCOAMYLASE FROM SACCHAROMYCOPSIS FIBULIGERA AT 1.7 ANGSTROMS |
| 1AYY | GLYCOSYLASPARAGINASE |
| 1AYZ | CRYSTAL STRUCTURE OF THE SACCHAROMYCES CEREVISIAE UBIQUITIN-CONJUGATING ENZYME RAD6 (UBC2) AT 2.6A RESOLUTION |
| 1AZ0 | ECORV ENDONUCLEASE/DNA COMPLEX |
| 1AZ1 | ALRESTATIN BOUND TO C298A/W219Y MUTANT HUMAN ALDOSE REDUCTASE |
| 1AZ2 | CITRATE BOUND, C298A/W219Y MUTANT HUMAN ALDOSE REDUCTASE |
| 1AZ3 | ECORV ENDONUCLEASE, UNLIGANDED, FORM B |
| 1AZ4 | ECORV ENDONUCLEASE, UNLIGANDED, FORM B, T93A MUTANT |
| 1AZ5 | UNLIGANDED SIV PROTEASE STRUCTURE IN AN OPEN" CONFORMATION" |
| 1AZ6 | THREE-DIMENSIONAL STRUCTURES OF THREE ENGINEERED CELLULOSE-BINDING DOMAINS OF CELLOBIOHYDROLASE I FROM TRICHODERMA REESEI, NMR, 23 STRUCTURES |
| 1AZ8 | BOVINE TRYPSIN COMPLEXED TO BIS-PHENYLAMIDINE INHIBITOR |
| 1AZB | STRUCTURE OF APO-AZURIN FROM ALCALIGENES DENITRIFICANS AT 1.8 ANGSTROMS RESOLUTION |
| 1AZC | STRUCTURE OF APO-AZURIN FROM ALCALIGENES DENITRIFICANS AT 1.8 ANGSTROMS RESOLUTION |
| 1AZD | CONCANAVALIN FROM CANAVALIA BRASILIENSIS |
| 1AZE | NMR STRUCTURE OF THE COMPLEX BETWEEN THE C32S-Y7V MUTANT OF THE NSH3 DOMAIN OF GRB2 WITH A PEPTIDE FROM SOS, 10 STRUCTURES |
| 1AZF | CHICKEN EGG WHITE LYSOZYME CRYSTAL GROWN IN BROMIDE SOLUTION |
| 1AZG | NMR STUDY OF THE SH3 DOMAIN FROM FYN PROTO-ONCOGENE TYROSINE KINASE KINASE COMPLEXED WITH THE SYNTHETIC PEPTIDE P2L CORRESPONDING TO RESIDUES 91-104 OF THE P85 SUBUNIT OF PI3-KINASE, MINIMIZED AVERAGE (PROBMAP) STRUCTURE |
| 1AZH | THREE-DIMENSIONAL STRUCTURES OF THREE ENGINEERED CELLULOSE-BINDING DOMAINS OF CELLOBIOHYDROLASE I FROM TRICHODERMA REESEI, NMR, 14 STRUCTURES |
| 1AZI | MYOGLOBIN (HORSE HEART) RECOMBINANT WILD-TYPE COMPLEXED WITH AZIDE |
| 1AZK | THREE-DIMENSIONAL STRUCTURES OF THREE ENGINEERED CELLULOSE-BINDING DOMAINS OF CELLOBIOHYDROLASE I FROM TRICHODERMA REESEI, NMR, 19 STRUCTURES |
| 1AZL | G61V FLAVODOXIN MUTANT FROM DESULFOVIBRIO VULGARIS |
| 1AZM | DRUG-PROTEIN INTERACTIONS: STRUCTURE OF SULFONAMIDE DRUG COMPLEXED WITH HUMAN CARBONIC ANHYDRASE I |
| 1AZN | CRYSTAL STRUCTURE OF THE AZURIN MUTANT PHE114ALA FROM PSEUDOMONAS AERUGINOSA AT 2.6 ANGSTROMS RESOLUTION |
| 1AZO | DNA MISMATCH REPAIR PROTEIN MUTH FROM E. COLI |
| 1AZP | HYPERTHERMOPHILE CHROMOSOMAL PROTEIN SAC7D BOUND WITH KINKED DNA DUPLEX |
| 1AZQ | HYPERTHERMOPHILE CHROMOSOMAL PROTEIN SAC7D BOUND WITH KINKED DNA DUPLEX |
| 1AZR | CRYSTAL STRUCTURE OF PSEUDOMONAS AERUGINOSA ZINC AZURIN MUTANT ASP47ASP AT 2.4 ANGSTROMS RESOLUTION |
| 1AZS | COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE |
| 1AZT | GS-ALPHA COMPLEXED WITH GTP-GAMMA-S |
| 1AZU | STRUCTURAL FEATURES OF AZURIN AT 2.7 ANGSTROMS RESOLUTION |
| 1AZV | FAMILIAL ALS MUTANT G37R CUZNSOD (HUMAN) |
| 1AZW | PROLINE IMINOPEPTIDASE FROM XANTHOMONAS CAMPESTRIS PV. CITRI |
| 1AZX | ANTITHROMBIN/PENTASACCHARIDE COMPLEX |
| 1AZY | STRUCTURAL AND THEORETICAL STUDIES SUGGEST DOMAIN MOVEMENT PRODUCES AN ACTIVE CONFORMATION OF THYMIDINE PHOSPHORYLASE |
| 1AZZ | FIDDLER CRAB COLLAGENASE COMPLEXED TO ECOTIN |
| 1B00 | PHOB RECEIVER DOMAIN FROM ESCHERICHIA COLI |
| 1B01 | TRANSCRIPTIONAL REPRESSOR COPG/DNA COMPLEX |
| 1B02 | CRYSTAL STRUCTURE OF THYMIDYLATE SYNTHASE A FROM BACILLUS SUBTILIS |
| 1B03 | SOLUTION STRUCTURE OF THE ANTIBODY-BOUND HIV-1IIIB V3 PEPTIDE |
| 1B04 | STRUCTURE OF THE ADENYLATION DOMAIN OF AN NAD+ DEPENDENT LIGASE |
| 1B05 | STRUCTURE OF OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYS-CYS-LYS |
| 1B06 | SUPEROXIDE DISMUTASE FROM SULFOLOBUS ACIDOCALDARIUS |
| 1B07 | CRK SH3 DOMAIN COMPLEXED WITH PEPTOID INHIBITOR |
| 1B08 | LUNG SURFACTANT PROTEIN D (SP-D) (FRAGMENT) |
| 1B09 | HUMAN C-REACTIVE PROTEIN COMPLEXED WITH PHOSPHOCHOLINE |
| 1B0A | 5,10, METHYLENE-TETRAHYDROPHOLATE DEHYDROGENASE/CYCLOHYDROLASE FROM E COLI. |
| 1B0B | HEMOGLOBIN I FROM THE CLAM LUCINA PECTINATA, CYANIDE COMPLEX AT 100 KELVIN |
| 1B0C | EVIDENCE OF A COMMON DECAMER IN THREE CRYSTAL STRUCTURES OF BPTI, CRYSTALLIZED FROM THIOCYANATE, CHLORIDE OR SULFATE |
| 1B0D | STRUCTURAL EFFECTS OF MONOVALENT ANIONS ON POLYMORPHIC LYSOZYME CRYSTALS |
| 1B0E | CRYSTAL STRUCTURE OF PORCINE PANCREATIC ELASTASE WITH MDL 101,146 |
| 1B0F | CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL ELASTASE WITH MDL 101, 146 |
| 1B0G | CLASS I HISTOCOMPATIBILITY ANTIGEN (HLA-A2.1)/BETA 2-MICROGLOBULIN/PEPTIDE P1049 COMPLEX |
| 1B0H | OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYSYL-NAPTHYLALANYL-LYSINE |
| 1B0I | ALPHA-AMYLASE FROM ALTEROMONAS HALOPLANCTIS |
| 1B0J | CRYSTAL STRUCTURE OF ACONITASE WITH ISOCITRATE |
| 1B0K | S642A:FLUOROCITRATE COMPLEX OF ACONITASE |
| 1B0L | RECOMBINANT HUMAN DIFERRIC LACTOFERRIN |
| 1B0M | ACONITASE R644Q:FLUOROCITRATE COMPLEX |
| 1B0N | SINR PROTEIN/SINI PROTEIN COMPLEX |
| 1B0O | BOVINE BETA-LACTOGLOBULIN COMPLEXED WITH PALMITATE, LATTICE Z |
| 1B0R | CRYSTAL STRUCTURE OF HLA-A*0201 COMPLEXED WITH A PEPTIDE WITH THE CARBOXYL-TERMINAL GROUP SUBSTITUTED BY A METHYL GROUP |
| 1B0T | D15K/K84D MUTANT OF AZOTOBACTER VINELANDII FDI |
| 1B0U | ATP-BINDING SUBUNIT OF THE HISTIDINE PERMEASE FROM SALMONELLA TYPHIMURIUM |
| 1B0V | I40N MUTANT OF AZOTOBACTER VINELANDII FDI |
| 1B0W | STRUCTURAL COMPARISON OF AMYLOIDOGENIC LIGHT CHAIN DIMER IN TWO CRYSTAL FORMS WITH NONAMYLOIDOGENIC COUNTERPARTS |
| 1B0X | THE CRYSTAL STRUCTURE OF AN EPH RECEPTOR SAM DOMAIN REVEALS A MECHANISM FOR MODULAR DIMERIZATION. |
| 1B0Y | MUTANT H42Q OF HIPIP FROM CHROMATIUM VINOSUM AT 0.93A |
| 1B0Z | THE CRYSTAL STRUCTURE OF PHOSPHOGLUCOSE ISOMERASE-AN ENZYME WITH AUTOCRINE MOTILITY FACTOR ACTIVITY IN TUMOR CELLS |
| 1B10 | SOLUTION NMR STRUCTURE OF RECOMBINANT SYRIAN HAMSTER PRION PROTEIN RPRP(90-231) , 25 STRUCTURES |
| 1B11 | STRUCTURE OF FELINE IMMUNODEFICIENCY VIRUS PROTEASE COMPLEXED WITH TL-3-093 |
| 1B12 | CRYSTAL STRUCTURE OF TYPE 1 SIGNAL PEPTIDASE FROM ESCHERICHIA COLI IN COMPLEX WITH A BETA-LACTAM INHIBITOR |
| 1B13 | CLOSTRIDIUM PASTEURIANUM RUBREDOXIN G10A MUTANT |
| 1B14 | ALCOHOL DEHYDROGENASE FROM DROSOPHILA LEBANONENSIS BINARY COMPLEX WITH NAD+ |
| 1B15 | ALCOHOL DEHYDROGENASE FROM DROSOPHILA LEBANONENSIS TERNARY COMPLEX WITH NAD-ACETONE |
| 1B16 | ALCOHOL DEHYDROGENASE FROM DROSOPHILA LEBANONENSIS TERNARY COMPLEX WITH NAD-3-PENTANONE |
| 1B17 | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 5.00 COORDINATES) |
| 1B18 | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 5.53 COORDINATES) |
| 1B19 | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 5.80 COORDINATES) |
| 1B1A | GLUTAMATE MUTASE (B12-BINDING SUBUNIT), NMR, MINIMIZED AVERAGE STRUCTURE |
| 1B1B | IRON DEPENDENT REGULATOR |
| 1B1C | CRYSTAL STRUCTURE OF THE FMN-BINDING DOMAIN OF HUMAN CYTOCHROME P450 REDUCTASE AT 1.93A RESOLUTION |
| 1B1E | CRYSTAL STRUCTURE OF HUMAN ANGIOGENIN VARIANT K40Q |
| 1B1G | SOLVATED REFINEMENT OF CA-LOADED CALBINDIN D9K |
| 1B1H | OLIGO-PEPTIDE BINDING PROTEIN/TRIPEPTIDE (LYS HPE LYS) COMPLEX |
| 1B1I | CRYSTAL STRUCTURE OF HUMAN ANGIOGENIN |
| 1B1J | CRYSTAL STRUCTURE OF HUMAN ANGIOGENIN VARIANT H13A. |
| 1B1U | CRYSTAL STRUCTURE OF THE BIFUNCTIONAL INHIBITOR RAGI |
| 1B1V | NMR STRUCTURE OF PSP1, PLASMATOCYTE-SPREADING PEPTIDE FROM PSEUDOPLUSIA INCLUDENS |
| 1B1X | STRUCTURE OF DIFERRIC MARE LACTOFERRIN AT 2.62A RESOLUTION |
| 1B1Y | SEVENFOLD MUTANT OF BARLEY BETA-AMYLASE |
| 1B1Z | STREPTOCOCCAL PYROGENIC EXOTOXIN A1 |
| 1B20 | DELETION OF A BURIED SALT-BRIDGE IN BARNASE |
| 1B21 | DELETION OF A BURIED SALT BRIDGE IN BARNASE |
| 1B22 | RAD51 (N-TERMINAL DOMAIN) |
| 1B23 | E. COLI CYSTEINYL-TRNA AND T. AQUATICUS ELONGATION FACTOR EF-TU:GTP TERNARY COMPLEX |
| 1B24 | I-DMOI, INTRON-ENCODED ENDONUCLEASE |
| 1B25 | FORMALDEHYDE FERREDOXIN OXIDOREDUCTASE FROM PYROCOCCUS FURIOSUS |
| 1B26 | GLUTAMATE DEHYDROGENASE |
| 1B27 | STRUCTURAL RESPONSE TO MUTATION AT A PROTEIN-PROTEIN INTERFACE |
| 1B28 | ARC REPRESSOR MYL MUTANT FROM SALMONELLA BACTERIOPHAGE P22 |
| 1B2A | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 6.00 COORDINATES) |
| 1B2B | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 6.16 COORDINATES) |
| 1B2C | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 6.26 COORDINATES) |
| 1B2D | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 6.35 COORDINATES) |
| 1B2E | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 6.50 COORDINATES) |
| 1B2F | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 6.98 COORDINATES) |
| 1B2G | PH AFFECTS GLU B13 SWITCHING AND SULFATE BINDING IN CUBIC INSULIN CRYSTALS (PH 9.00 COORDINATES) |
| 1B2H | OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYSYL-ORNITHYL-LYSINE |
| 1B2I | KRINGLE 2 DOMAIN OF HUMAN PLASMINOGEN: NMR SOLUTION STRUCTURE OF TRANS-4-AMINOMETHYLCYCLOHEXANE-1-CARBOXYLIC ACID (AMCHA) COMPLEX |
| 1B2J | CLOSTRIDIUM PASTEURIANUM RUBREDOXIN G43A MUTANT |
| 1B2K | STRUCTURAL EFFECTS OF MONOVALENT ANIONS ON POLYMORPHIC LYSOZYME CRYSTALS |
| 1B2L | ALCOHOL DEHYDROGENASE FROM DROSOPHILA LEBANONENSIS: TERNARY COMPLEX WITH NAD-CYCLOHEXANONE |
| 1B2M | THREE-DIMENSIONAL STRUCTURE OF RIBONULCEASE T1 COMPLEXED WITH AN ISOSTERIC PHOSPHONATE ANALOGUE OF GPU: ALTERNATE SUBSTRATE BINDING MODES AND CATALYSIS. |
| 1B2O | CLOSTRIDIUM PASTEURIANUM RUBREDOXIN G10VG43A MUTANT |
| 1B2P | NATIVE MANNOSE-SPECIFIC BULB LECTIN FROM SCILLA CAMPANULATA (BLUEBELL) AT 1.7 ANGSTROMS RESOLUTION |
| 1B2R | FERREDOXIN-NADP+ REDUCTASE (MUTATION: E 301 A) |
| 1B2S | STRUCTURAL RESPONSE TO MUTATION AT A PROTEIN-PROTEIN INTERFACE |
| 1B2T | SOLUTION STRUCTURE OF THE CX3C CHEMOKINE DOMAIN OF FRACTALKINE |
| 1B2U | STRUCTURAL RESPONSE TO MUTATION AT A PROTEIN-PROTEIN INTERFACE |
| 1B2V | HEME-BINDING PROTEIN A |
| 1B2W | COMPARISON OF THE THREE-DIMENSIONAL STRUCTURES OF A HUMANIZED AND A CHIMERIC FAB OF AN ANTI-GAMMA-INTERFERON ANTIBODY |
| 1B2X | BARNASE WILDTYPE STRUCTURE AT PH 7.5 FROM A CRYO_COOLED CRYSTAL AT 100K |
| 1B2Y | STRUCTURE OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH THE CARBOHYDRATE INHIBITOR ACARBOSE |
| 1B2Z | DELETION OF A BURIED SALT BRIDGE IN BARNASE |
| 1B30 | XYLANASE FROM PENICILLIUM SIMPLICISSIMUM, COMPLEX WITH 1,2-(4-DEOXY-BETA-L-THREO-HEX-4-ENOPYRANOSYLURONIC ACID)-BETA-1,4-XYLOTRIOSE) |
| 1B31 | XYLANASE FROM PENICILLIUM SIMPLICISSIMUM, NATIVE WITH PEG200 AS CRYOPROTECTANT |
| 1B32 | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KMK |
| 1B33 | STRUCTURE OF LIGHT HARVESTING COMPLEX OF ALLOPHYCOCYANIN ALPHA AND BETA CHAINS/CORE-LINKER COMPLEX AP*LC7.8 |
| 1B34 | CRYSTAL STRUCTURE OF THE D1D2 SUB-COMPLEX FROM THE HUMAN SNRNP CORE DOMAIN |
| 1B35 | CRICKET PARALYSIS VIRUS (CRPV) |
| 1B37 | A 30 ANGSTROM U-SHAPED CATALYTIC TUNNEL IN THE CRYSTAL STRUCTURE OF POLYAMINE OXIDASE |
| 1B38 | HUMAN CYCLIN-DEPENDENT KINASE 2 |
| 1B39 | HUMAN CYCLIN-DEPENDENT KINASE 2 PHOSPHORYLATED ON THR 160 |
| 1B3A | TOTAL CHEMICAL SYNTHESIS AND HIGH-RESOLUTION CRYSTAL STRUCTURE OF THE POTENT ANTI-HIV PROTEIN AOP-RANTES |
| 1B3B | THERMOTOGA MARITIMA GLUTAMATE DEHYDROGENASE MUTANT N97D, G376K |
| 1B3C | SOLUTION STRUCTURE OF A BETA-NEUROTOXIN FROM THE NEW WORLD SCORPION CENTRUROIDES SCULPTURATUS EWING |
| 1B3D | STROMELYSIN-1 |
| 1B3E | HUMAN SERUM TRANSFERRIN, N-TERMINAL LOBE, EXPRESSED IN PICHIA PASTORIS |
| 1B3F | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KHK |
| 1B3G | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KIK |
| 1B3H | OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYSYL-CYCLOHEXYLALANYL-LYSINE |
| 1B3I | NMR SOLUTION STRUCTURE OF PLASTOCYANIN FROM THE PHOTOSYNTHETIC PROKARYOTE, PROCHLOROTHRIX HOLLANDICA (MINIMIZED AVERAGE STRUCTURE) |
| 1B3J | STRUCTURE OF THE MHC CLASS I HOMOLOG MIC-A, A GAMMADELTA T CELL LIGAND |
| 1B3K | PLASMINOGEN ACTIVATOR INHIBITOR-1 |
| 1B3L | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KGK |
| 1B3N | BETA-KETOACYL CARRIER PROTEIN SYNTHASE AS A DRUG TARGET, IMPLICATIONS FROM THE CRYSTAL STRUCTURE OF A COMPLEX WITH THE INHIBITOR CERULENIN. |
| 1B3O | TERNARY COMPLEX OF HUMAN TYPE-II INOSINE MONOPHOSPHATE DEHYDROGENASE WITH 6-CL-IMP AND SELENAZOLE ADENINE DINUCLEOTIDE |
| 1B3Q | CRYSTAL STRUCTURE OF CHEA-289, A SIGNAL TRANSDUCING HISTIDINE KINASE |
| 1B3R | RAT LIVER S-ADENOSYLHOMOCYSTEIN HYDROLASE |
| 1B3S | STRUCTURAL RESPONSE TO MUTATION AT A PROTEIN-PROTEIN INTERFACE |
| 1B3T | EBNA-1 NUCLEAR PROTEIN/DNA COMPLEX |
| 1B3U | CRYSTAL STRUCTURE OF CONSTANT REGULATORY DOMAIN OF HUMAN PP2A, PR65ALPHA |
| 1B3V | XYLANASE FROM PENICILLIUM SIMPLICISSIMUM, COMPLEX WITH XYLOSE |
| 1B3W | XYLANASE FROM PENICILLIUM SIMPLICISSIMUM, COMPLEX WITH XYLOBIOSE |
| 1B3X | XYLANASE FROM PENICILLIUM SIMPLICISSIMUM, COMPLEX WITH XYLOTRIOSE |
| 1B3Y | XYLANASE FROM PENICILLIUM SIMPLICISSIMUM, COMPLEX WITH XYLOTETRAOSE |
| 1B3Z | XYLANASE FROM PENICILLIUM SIMPLICISSIMUM, COMPLEX WITH XYLOPENTAOSE |
| 1B40 | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KFK |
| 1B42 | VACCINIA METHYLTRANSFERASE VP39 COMPLEXED WITH M1ADE AND S-ADENOSYLHOMOCYSTEINE |
| 1B43 | FEN-1 FROM P. FURIOSUS |
| 1B44 | CRYSTAL STRUCTURE OF THE B SUBUNIT OF HEAT-LABILE ENTEROTOXIN FROM E. COLI CARRYING A PEPTIDE WITH ANTI-HSV ACTIVITY |
| 1B45 | ALPHA-CNIA CONOTOXIN FROM CONUS CONSORS, NMR, 43 STRUCTURES |
| 1B46 | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KPK |
| 1B47 | STRUCTURE OF THE N-TERMINAL DOMAIN OF CBL IN COMPLEX WITH ITS BINDING SITE IN ZAP-70 |
| 1B48 | CRYSTAL STRUCTURE OF MGSTA4-4 IN COMPLEX WITH GSH CONJUGATE OF 4-HYDROXYNONENAL IN ONE SUBUNIT AND GSH IN THE OTHER: EVIDENCE OF SIGNALING ACROSS DIMER INTERFACE IN MGSTA4-4 |
| 1B49 | DCMP HYDROXYMETHYLASE FROM T4 (PHOSPHATE-BOUND) |
| 1B4A | STRUCTURE OF THE ARGININE REPRESSOR FROM BACILLUS STEAROTHERMOPHILUS |
| 1B4B | STRUCTURE OF THE OLIGOMERIZATION DOMAIN OF THE ARGININE REPRESSOR FROM BACILLUS STEAROTHERMOPHILUS |
| 1B4C | SOLUTION STRUCTURE OF RAT APO-S100B USING DIPOLAR COUPLINGS |
| 1B4D | AMIDOCARBAMATE INHIBITOR OF GLYCOGEN PHOSPHORYLASE |
| 1B4E | X-RAY STRUCTURE OF 5-AMINOLEVULINIC ACID DEHYDRATASE COMPLEXED WITH THE INHIBITOR LEVULINIC ACID |
| 1B4F | OLIGOMERIC STRUCTURE OF THE HUMAN EPHB2 RECEPTOR SAM DOMAIN |
| 1B4G | CONTROL OF K+ CHANNEL GATING BY PROTEIN PHOSPHORYLATION: STRUCTURAL SWITCHES OF THE INACTIVATION GATE, NMR, 22 STRUCTURES |
| 1B4H | OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYSYL-DIAMINOBUTYRIC ACID-LYSINE |
| 1B4I | CONTROL OF K+ CHANNEL GATING BY PROTEIN PHOSPHORYLATION: STRUCTURAL SWITCHES OF THE INACTIVATION GATE, NMR, 22 STRUCTURES |
| 1B4J | COMPARISON OF THE THREE-DIMENSIONAL STRUCTURES OF A HUMANIZED AND A CHIMERIC FAB OF AN ANTI-GAMMA-INTERFERON ANTIBODY |
| 1B4K | HIGH RESOLUTION CRYSTAL STRUCTURE OF A MG2-DEPENDENT 5-AMINOLEVULINIC ACID DEHYDRATASE |
| 1B4L | 15 ATMOSPHERE OXYGEN YEAST CU/ZN SUPEROXIDE DISMUTASE ROOM TEMPERATURE (298K) STRUCTURE |
| 1B4M | NMR STRUCTURE OF APO CELLULAR RETINOL-BINDING PROTEIN II, 24 STRUCTURES |
| 1B4N | FORMALDEHYDE FERREDOXIN OXIDOREDUCTASE FROM PYROCOCCUS FURIOSUS, COMPLEXED WITH GLUTARATE |
| 1B4O | NMR STUDY OF SSO7D MUTANT (F31A) MINIMIZED AVERAGE STRUCTURE |
| 1B4P | CRYSTAL STRUCTURES OF CLASS MU CHIMERIC GST ISOENZYMES M1-2 AND M2-1 |
| 1B4Q | SOLUTION STRUCTURE OF HUMAN THIOLTRANSFERASE COMPLEX WITH GLUTATHIONE |
| 1B4R | PKD DOMAIN 1 FROM HUMAN POLYCYSTEIN-1 |
| 1B4S | STRUCTURE OF NUCLEOSIDE DIPHOSPHATE KINASE H122G MUTANT |
| 1B4T | H48C YEAST CU(II)/ZN SUPEROXIDE DISMUTASE ROOM TEMPERATURE (298K) STRUCTURE |
| 1B4U | PROTOCATECHUATE 4,5-DIOXYGENASE (LIGAB) IN COMPLEX WITH PROTOCATECHUATE (PCA) |
| 1B4V | CHOLESTEROL OXIDASE FROM STREPTOMYCES |
| 1B4W | BASIC PHOSPHOLIPASE A2 FROM AGKISTRODON HALYS PALLAS-IMPLICATIONS FOR ITS ASSOCIATION AND ANTICOAGULANT ACTIVITIES BY X-RAY CRYSTALLOGRAPHY |
| 1B4X | ASPARTATE AMINOTRANSFERASE FROM E. COLI, C191S MUTATION, WITH BOUND MALEATE |
| 1B4Z | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KDK |
| 1B50 | NMR STRUCTURE OF HUMAN MIP-1A D26A, 10 STRUCTURES |
| 1B51 | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KSK |
| 1B52 | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KTK |
| 1B53 | NMR STRUCTURE OF HUMAN MIP-1A D26A, MINIMIZED AVERAGE STRUCTURE |
| 1B54 | CRYSTAL STRUCTURE OF A YEAST HYPOTHETICAL PROTEIN-A STRUCTURE FROM BNL'S HUMAN PROTEOME PROJECT |
| 1B55 | PH DOMAIN FROM BRUTON'S TYROSINE KINASE IN COMPLEX WITH INOSITOL 1,3,4,5-TETRAKISPHOSPHATE |
| 1B56 | HUMAN RECOMBINANT EPIDERMAL FATTY ACID BINDING PROTEIN |
| 1B57 | CLASS II FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE IN COMPLEX WITH PHOSPHOGLYCOLOHYDROXAMATE |
| 1B58 | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KYK |
| 1B59 | COMPLEX OF HUMAN METHIONINE AMINOPEPTIDASE-2 COMPLEXED WITH OVALICIN |
| 1B5A | RAT FERROCYTOCHROME B5 A CONFORMATION, NMR, 1 STRUCTURE |
| 1B5B | RAT FERROCYTOCHROME B5 B CONFORMATION, NMR, 1 STRUCTURE |
| 1B5D | DCMP HYDROXYMETHYLASE FROM T4 (INTACT) |
| 1B5E | DCMP HYDROXYMETHYLASE FROM T4 |
| 1B5F | NATIVE CARDOSIN A FROM CYNARA CARDUNCULUS L. |
| 1B5G | HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN |
| 1B5H | OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYSYL-DIAMINOPROPANOIC ACID-LYSINE |
| 1B5I | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KNK |
| 1B5J | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KQK |
| 1B5L | OVINE INTERFERON TAU |
| 1B5M | RAT OUTER MITOCHONDRIAL MEMBRANE CYTOCHROME B5 |
| 1B5N | NMR STRUCTURE OF PSP1, PLASMATOCYTE-SPREADING PEPTIDE FROM PSEUDOPLUSIA INCLUDENS |
| 1B5O | THERMUS THERMOPHILUS ASPARTATE AMINOTRANSFERASE SINGLE MUTANT 1 |
| 1B5P | THERMUS THERMOPHILUS ASPARTATE AMINOTRANSFERASE DOUBLE MUTANT 1 |
| 1B5Q | A 30 ANGSTROM U-SHAPED CATALYTIC TUNNEL IN THE CRYSTAL STRUCTURE OF POLYAMINE OXIDASE |
| 1B5S | DIHYDROLIPOYL TRANSACETYLASE (E.C.2.3.1.12) CATALYTIC DOMAIN (RESIDUES 184-425) FROM BACILLUS STEAROTHERMOPHILUS |
| 1B5T | ESCHERICHIA COLI METHYLENETETRAHYDROFOLATE REDUCTASE |
| 1B5U | CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME: CALORIMETRY AND X-RAY ANALYSIS OF SIX SER->ALA MUTANT |
| 1B5V | CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME: CALORIMETRY AND X-RAY ANALYSIS OF SIX SER->ALA MUTANTS |
| 1B5W | CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME: CALORIMETRY AND X-RAY ANALYSIS OF SIX SER->ALA MUTANTS |
| 1B5X | CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME: CALORIMETRY AND X-RAY ANALYSIS OF SIX SER->ALA MUTANTS |
| 1B5Y | CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME: CALORIMETRY AND X-RAY ANALYSIS OF SIX SER->ALA MUTANTS |
| 1B5Z | CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME: CALORIMETRY AND X-RAY ANALYSIS OF SIX SER->ALA MUTANTS |
| 1B62 | MUTL COMPLEXED WITH ADP |
| 1B63 | MUTL COMPLEXED WITH ADPNP |
| 1B64 | SOLUTION STRUCTURE OF THE GUANINE NUCLEOTIDE EXCHANGE FACTOR DOMAIN FROM HUMAN ELONGATION FACTOR-ONE BETA, NMR, 20 STRUCTURES |
| 1B65 | STRUCTURE OF L-AMINOPEPTIDASE D-ALA-ESTERASE/AMIDASE FROM OCHROBACTRUM ANTHROPI, A PROTOTYPE FOR THE SERINE AMINOPEPTIDASES, REVEALS A NEW VARIANT AMONG THE NTN HYDROLASE FOLD |
| 1B66 | 6-PYRUVOYL TETRAHYDROPTERIN SYNTHASE |
| 1B67 | CRYSTAL STRUCTURE OF THE HISTONE HMFA FROM METHANOTHERMUS FERVIDUS |
| 1B68 | APOLIPOPROTEIN E4 (APOE4), 22K FRAGMENT |
| 1B69 | THE SOLUTION STRUCTURE OF TN916 INTEGRASE N-TERMINAL DOMAIN/DNA COMPLEX |
| 1B6A | HUMAN METHIONINE AMINOPEPTIDASE 2 COMPLEXED WITH TNP-470 |
| 1B6B | MELATONIN BIOSYNTHESIS: THE STRUCTURE OF SEROTONIN N-ACETYLTRANSFERASE AT 2.5 A RESOLUTION SUGGESTS A CATALYTIC MECHANISM |
| 1B6C | CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF THE TYPE I TGF-BETA RECEPTOR IN COMPLEX WITH FKBP12 |
| 1B6D | BENCE JONES PROTEIN DEL: AN ENTIRE IMMUNOGLOBULIN KAPPA LIGHT-CHAIN DIMER |
| 1B6E | HUMAN CD94 |
| 1B6F | BIRCH POLLEN ALLERGEN BET V 1 |
| 1B6G | HALOALKANE DEHALOGENASE AT PH 5.0 CONTAINING CHLORIDE |
| 1B6H | OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYSYL-NORVALYL-LYSINE |
| 1B6I | T4 LYSOZYME MUTANT WITH CYS 54 REPLACED BY THR, CYS 97 REPLACED BY ALA, THR 21 REPLACED BY CYS AND LYS 124 REPLACED BY CYS (C54T,C97A,T21C,K124C) |
| 1B6J | HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 1 |
| 1B6K | HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 5 |
| 1B6L | HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 4 |
| 1B6M | HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 6 |
| 1B6P | HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 7 |
| 1B6Q | ALANINE 31 PROLINE MUTANT OF ROP PROTEIN |
| 1B6R | N5-CARBOXYAMINOIMIDAZOLE RIBONUCLEOTIDE SYNTHETASE FROM E. COLI |
| 1B6S | STRUCTURE OF N5-CARBOXYAMINOIMIDAZOLE RIBONUCLEOTIDE SYNTHETASE |
| 1B6T | PHOSPHOPANTETHEINE ADENYLYLTRANSFERASE IN COMPLEX WITH 3'-DEPHOSPHO-COA FROM ESCHERICHIA COLI |
| 1B6U | CRYSTAL STRUCTURE OF THE HUMAN KILLER CELL INHIBITORY RECEPTOR (KIR2DL3) SPECIFIC FOR HLA-CW3 RELATED ALLELES |
| 1B6V | CRYSTAL STRUCTURE OF A HYBRID BETWEEN RIBONUCLEASE A AND BOVINE SEMINAL RIBONUCLEASE |
| 1B6W | CRYSTAL STRUCTURE OF THE SELENOMETHIONINE VARIANT OF HISTONE HMFB FROM METHANOTHERMUS FERVIDUS |
| 1B6Z | 6-PYRUVOYL TETRAHYDROPTERIN SYNTHASE |
| 1B70 | PHENYLALANYL TRNA SYNTHETASE COMPLEXED WITH PHENYLALANINE |
| 1B71 | RUBRERYTHRIN |
| 1B72 | PBX1, HOMEOBOX PROTEIN HOX-B1/DNA TERNARY COMPLEX |
| 1B73 | GLUTAMATE RACEMASE FROM AQUIFEX PYROPHILUS |
| 1B74 | GLUTAMATE RACEMASE FROM AQUIFEX PYROPHILUS |
| 1B75 | SOLUTION STRUCTURE OF RIBOSOMAL PROTEIN L25 FROM ESCHERICHIA COLI |
| 1B76 | GLYCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS COMPLEXED WITH ATP |
| 1B77 | BUILDING A REPLISOME STRUCTURE FROM INTERACTING PIECES: A SLIDING CLAMP COMPLEXED WITH AN INTERACTION PEPTIDE FROM DNA POLYMERASE |
| 1B78 | STRUCTURE-BASED IDENTIFICATION OF THE BIOCHEMICAL FUNCTION OF A HYPOTHETICAL PROTEIN FROM METHANOCOCCUS JANNASCHII:MJ0226 |
| 1B79 | N-TERMINAL DOMAIN OF DNA REPLICATION PROTEIN DNAB |
| 1B7A | STRUCTURE OF THE PHOSPHATIDYLETHANOLAMINE-BINDING PROTEIN FROM BOVINE BRAIN |
| 1B7B | CARBAMATE KINASE FROM ENTEROCOCCUS FAECALIS |
| 1B7D | NEUROTOXIN (TS1) FROM BRAZILIAN SCORPION TITYUS SERRULATUS |
| 1B7E | TRANSPOSASE INHIBITOR |
| 1B7F | SXL-LETHAL PROTEIN/RNA COMPLEX |
| 1B7G | GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE |
| 1B7H | OLIGO-PEPTIDE BINDING PROTEIN COMPLEXED WITH LYSYL-NORLEUCYL-LYSINE |
| 1B7I | TYPE III ANTIFREEZE PROTEIN ISOFORM HPLC 12 K61R |
| 1B7J | TYPE III ANTIFREEZE PROTEIN ISOFORM HPLC 12 V20A |
| 1B7K | TYPE III ANTIFREEZE PROTEIN ISOFORM HPLC 12 R47H |
| 1B7L | VERIFICATION OF SPMP USING MUTANT HUMAN LYSOZYMES |
| 1B7M | VERIFICATION OF SPMP USING MUTANT HUMAN LYSOZYMES |
| 1B7N | VERIFICATION OF SPMP USING MUTANT HUMAN LYSOZYMES |
| 1B7O | VERIFICATION OF SPMP USING MUTANT HUMAN LYSOZYMES |
| 1B7P | VERIFICATION OF SPMP USING MUTANT HUMAN LYSOZYMES |
| 1B7Q | VERIFICATION OF SPMP USING MUTANT HUMAN LYSOZYMES |
| 1B7R | VERIFICATION OF SPMP USING MUTANT HUMAN LYSOZYMES |
| 1B7S | VERIFICATION OF SPMP USING MUTANT HUMAN LYSOZYMES |
| 1B7T | MYOSIN DIGESTED BY PAPAIN |
| 1B7U | STRUCTURE OF MARE APOLACTOFERRIN: THE N AND C LOBES ARE IN THE CLOSED FORM |
| 1B7V | STRUCTURE OF THE C-553 CYTOCHROME FROM BACILLUS PASTERUII TO 1.7 A RESOLUTION |
| 1B7X | STRUCTURE OF HUMAN ALPHA-THROMBIN Y225I MUTANT BOUND TO D-PHE-PRO-ARG-CHLOROMETHYLKETONE |
| 1B7Y | PHENYLALANYL TRNA SYNTHETASE COMPLEXED WITH PHENYLALANINYL-ADENYLATE |
| 1B7Z | STRUCTURE OF OXALATE SUBSTITUTED DIFERRIC MARE LACTOFERRIN FROM COLOSTRUM |
| 1B80 | REC. LIGNIN PEROXIDASE H8 OXIDATIVELY PROCESSED |
| 1B82 | PRISTINE RECOMB. LIGNIN PEROXIDASE H8 |
| 1B85 | LIGNIN PEROXIDASE |
| 1B86 | HUMAN DEOXYHAEMOGLOBIN-2,3-DIPHOSPHOGLYCERATE COMPLEX |
| 1B87 | CRYSTAL STRUCTURE OF AN AMINOGLYCOSIDE 6'-N-ACETYLTRANSFERASE |
| 1B88 | V-ALPHA 2.6 MOUSE T CELL RECEPTOR (TCR) DOMAIN |
| 1B89 | CLATHRIN HEAVY CHAIN PROXIMAL LEG SEGMENT (BOVINE) |
| 1B8A | ASPARTYL-TRNA SYNTHETASE |
| 1B8C | PARVALBUMIN |
| 1B8D | CRYSTAL STRUCTURE OF A PHYCOUROBILIN-CONTAINING PHYCOERYTHRIN |
| 1B8E | HIGH RESOLUTION CRYSTAL STRUCTURE OF THE BOVINE BETA-LACTOGLOBULIN (ISOFORMS A AND B) IN ORTHOROMBIC SPACE GROUP |
| 1B8F | HISTIDINE AMMONIA-LYASE (HAL) FROM PSEUDOMONAS PUTIDA |
| 1B8G | 1-AMINOCYCLOPROPANE-1-CARBOXYLATE SYNTHASE |
| 1B8H | SLIDING CLAMP, DNA POLYMERASE |
| 1B8I | STRUCTURE OF THE HOMEOTIC UBX/EXD/DNA TERNARY COMPLEX |
| 1B8J | ALKALINE PHOSPHATASE COMPLEXED WITH VANADATE |
| 1B8K | NEUROTROPHIN-3 FROM HUMAN |
| 1B8L | CALCIUM-BOUND D51A/E101D/F102W TRIPLE MUTANT OF BETA CARP PARVALBUMIN |
| 1B8M | BRAIN DERIVED NEUROTROPHIC FACTOR, NEUROTROPHIN-4 |
| 1B8N | PURINE NUCLEOSIDE PHOSPHORYLASE |
| 1B8O | PURINE NUCLEOSIDE PHOSPHORYLASE |
| 1B8P | MALATE DEHYDROGENASE FROM AQUASPIRILLUM ARCTICUM |
| 1B8Q | SOLUTION STRUCTURE OF THE EXTENDED NEURONAL NITRIC OXIDE SYNTHASE PDZ DOMAIN COMPLEXED WITH AN ASSOCIATED PEPTIDE |
| 1B8R | PARVALBUMIN |
| 1B8S | CHOLESTEROL OXIDASE FROM STREPTOMYCES GLU361GLN MUTANT |
| 1B8U | MALATE DEHYDROGENASE FROM AQUASPIRILLUM ARCTICUM |
| 1B8V | MALATE DEHYDROGENASE FROM AQUASPIRILLUM ARCTICUM |
| 1B8W | DEFENSIN-LIKE PEPTIDE 1 |
| 1B8X | GLUTATHIONE S-TRANSFERASE FUSED WITH THE NUCLEAR MATRIX TARGETING SIGNAL OF THE TRANSCRIPTION FACTOR AML-1 |
| 1B8Y | X-RAY STRUCTURE OF HUMAN STROMELYSIN CATALYTIC DOMAIN COMPLEXED WITH NON-PEPTIDE INHIBITORS: IMPLICATIONS FOR INHIBITOR SELECTIVITY |
| 1B8Z | HU FROM THERMOTOGA MARITIMA |
| 1B90 | BACILLUS CEREUS BETA-AMYLASE APO FORM |
| 1B92 | MOBILITY OF AN HIV-1 INTEGRASE ACTIVE SITE LOOP IS CORRELATED WITH CATALYTIC ACTIVITY |
| 1B93 | METHYLGLYOXAL SYNTHASE FROM ESCHERICHIA COLI |
| 1B94 | RESTRICTION ENDONUCLEASE ECORV WITH CALCIUM |
| 1B95 | ANALYSIS OF A MUTATIONAL HOT-SPOT IN THE ECORV RESTRICTION ENDONUCLEASE: A CATALYTIC ROLE FOR A MAIN CHAIN CARBONYL GROUP |
| 1B96 | ANALYSIS OF A MUTATIONAL HOT-SPOT IN THE ECORV RESTRICTION ENDONUCLEASE: A CATALYTIC ROLE FOR A MAIN CHAIN CARBONYL GROUP |
| 1B97 | ANALYSIS OF A MUTATIONAL HOT-SPOT IN THE ECORV RESTRICTION ENDONUCLEASE: A CATALYTIC ROLE FOR A MAIN CHAIN CARBONYL GROUP |
| 1B98 | NEUROTROPHIN 4 (HOMODIMER) |
| 1B99 | 3'-FLUORO-URIDINE DIPHOSPHATE BINDING TO NUCLEOSIDE DIPHOSPHATE KINASE |
| 1B9A | PARVALBUMIN (MUTATION;D51A, F102W) |
| 1B9B | TRIOSEPHOSPHATE ISOMERASE OF THERMOTOGA MARITIMA |
| 1B9C | GREEN FLUORESCENT PROTEIN MUTANT F99S, M153T AND V163A |
| 1B9D | MOBILITY OF AN HIV-1 INTEGRASE ACTIVE SITE LOOP IS CORRELATED WITH CATALYTIC ACTIVITY |
| 1B9E | HUMAN INSULIN MUTANT SERB9GLU |
| 1B9F | MOBILITY OF AN HIV-1 INTEGRASE ACTIVE SITE LOOP IS CORRELATED WITH CATALYTIC ACTIVITY |
| 1B9G | INSULIN-LIKE-GROWTH-FACTOR-1 |
| 1B9H | CRYSTAL STRUCTURE OF 3-AMINO-5-HYDROXYBENZOIC ACID (AHBA) SYNTHASE |
| 1B9I | CRYSTAL STRUCTURE OF 3-AMINO-5-HYDROXYBENZOIC ACID (AHBA) SYNTHASE |
| 1B9J | OLIGO-PEPTIDE BINDING PROTEIN (OPPA) COMPLEXED WITH KLK |
| 1B9K | ALPHA-ADAPTIN APPENDAGE DOMAIN, FROM CLATHRIN ADAPTOR AP2 |
| 1B9L | 7,8-DIHYDRONEOPTERIN TRIPHOSPHATE EPIMERASE |
| 1B9M | REGULATOR FROM ESCHERICHIA COLI |
| 1B9N | REGULATOR FROM ESCHERICHIA COLI |
| 1B9O | HUMAN ALPHA-LACTALBUMIN, LOW TEMPERATURE FORM |
| 1B9P | NMR STRUCTURE OF HEPARIN BINDING SITE OF NON COLLAGENOUS DOMAIN I (NC1) OF COLLAGEN FACIT XIV |
| 1B9Q | NMR STRUCTURE OF HEPARIN BINDING SITE OF NON COLLAGENOUS DOMAIN I (NC1) OF COLLAGEN FACIT XIV |
| 1B9R | TERPREDOXIN FROM PSEUDOMONAS SP. |
| 1B9S | NOVEL AROMATIC INHIBITORS OF INFLUENZA VIRUS NEURAMINIDASE MAKE SELECTIVE INTERACTIONS WITH CONSERVED RESIDUES AND WATER MOLECULES IN THE ACTIVE SITE |
| 1B9T | NOVEL AROMATIC INHIBITORS OF INFLUENZA VIRUS NEURAMINIDASE MAKE SELECTIVE INTERACTIONS WITH CONSERVED RESIDUES AND WATER MOLECULES IN THE ACTIVE SITE |
| 1B9U | MEMBRANE DOMAIN OF THE SUBUNIT B OF THE E.COLI ATP SYNTHASE |
| 1B9V | NOVEL AROMATIC INHIBITORS OF INFLUENZA VIRUS NEURAMINIDASE MAKE SELECTIVE INTERACTIONS WITH CONSERVED RESIDUES AND WATER MOLECULES IN TEH ACTIVE SITE |
| 1B9W | C-TERMINAL MEROZOITE SURFACE PROTEIN 1 FROM PLASMODIUM CYNOMOLGI |
| 1B9X | STRUCTURAL ANALYSIS OF PHOSDUCIN AND ITS PHOSPHORYLATION-REGULATED INTERACTION WITH TRANSDUCIN |
| 1B9Y | STRUCTURAL ANALYSIS OF PHOSDUCIN AND ITS PHOSPHORYLATION-REGULATED INTERACTION WITH TRANSDUCIN BETA-GAMMA |
| 1B9Z | BACILLUS CEREUS BETA-AMYLASE COMPLEXED WITH MALTOSE |
| 1BA0 | HEAT-SHOCK COGNATE 70KD PROTEIN 44KD ATPASE N-TERMINAL 1NGE 3 |
| 1BA1 | HEAT-SHOCK COGNATE 70KD PROTEIN 44KD ATPASE N-TERMINAL MUTANT WITH CYS 17 REPLACED BY LYS |
| 1BA2 | D67R MUTANT OF D-RIBOSE-BINDING PROTEIN FROM ESCHERICHIA COLI |
| 1BA3 | FIREFLY LUCIFERASE IN COMPLEX WITH BROMOFORM |
| 1BA4 | THE SOLUTION STRUCTURE OF AMYLOID BETA-PEPTIDE (1-40) IN A WATER-MICELLE ENVIRONMENT. IS THE MEMBRANE-SPANNING DOMAIN WHERE WE THINK IT IS? NMR, 10 STRUCTURES |
| 1BA5 | DNA-BINDING DOMAIN OF HUMAN TELOMERIC PROTEIN, HTRF1, NMR, 18 STRUCTURES |
| 1BA6 | SOLUTION STRUCTURE OF THE METHIONINE-OXIDIZED AMYLOID BETA-PEPTIDE (1-40). DOES OXIDATION AFFECT CONFORMATIONAL SWITCHING? NMR, 10 STRUCTURES |
| 1BA7 | SOYBEAN TRYPSIN INHIBITOR |
| 1BA8 | THROMBIN INHIBITOR WITH A RIGID TRIPEPTIDYL ALDEHYDES |
| 1BA9 | THE SOLUTION STRUCTURE OF REDUCED MONOMERIC SUPEROXIDE DISMUTASE, NMR, 36 STRUCTURES |
| 1BAB | HEMOGLOBIN THIONVILLE: AN ALPHA-CHAIN VARIANT WITH A SUBSTITUTION OF A GLUTAMATE FOR VALINE AT NA-1 AND HAVING AN ACETYLATED METHIONINE NH2 TERMINUS |
| 1BAF | 2.9 ANGSTROMS RESOLUTION STRUCTURE OF AN ANTI-DINITROPHENYL-SPIN-LABEL MONOCLONAL ANTIBODY FAB FRAGMENT WITH BOUND HAPTEN |
| 1BAG | ALPHA-AMYLASE FROM BACILLUS SUBTILIS COMPLEXED WITH MALTOPENTAOSE |
| 1BAH | A TWO DISULFIDE DERIVATIVE OF CHARYBDOTOXIN WITH DISULFIDE 13-33 REPLACED BY TWO ALPHA-AMINOBUTYRIC ACIDS, NMR, 30 STRUCTURES |
| 1BAI | CRYSTAL STRUCTURE OF ROUS SARCOMA VIRUS PROTEASE IN COMPLEX WITH INHIBITOR |
| 1BAJ | HIV-1 CAPSID PROTEIN C-TERMINAL FRAGMENT PLUS GAG P2 DOMAIN |
| 1BAK | SIGNAL TRANSDUCTION PLECKSTRIN HOMOLOGY DOMAIN OF G-PROTEIN COUPLED RECEPTOR KINASE 2 (BETA-ADRENERGIC RECEPTOR KINASE 1), C-TERMINAL EXTENDED, NMR, 20 STRUCTURES |
| 1BAL | THREE-DIMENSIONAL SOLUTION STRUCTURE OF THE E3-BINDING DOMAIN OF THE DIHYDROLIPOAMIDE SUCCINYLTRANSFERASE CORE FROM THE 2-OXOGLUTARATE DEHYDROGENASE MULTIENZYME COMPLEX OF (ESCHERICHIA COLI) |
| 1BAM | STRUCTURE OF RESTRICTION ENDONUCLEASE BAMHI PHASED AT 1.95 ANGSTROMS RESOLUTION BY MAD ANALYSIS |
| 1BAN | THE CONTRIBUTION OF BURIED HYDROGEN BONDS TO PROTEIN STABILITY: THE CRYSTAL STRUCTURES OF TWO BARNASE MUTANTS |
| 1BAO | THE CONTRIBUTION OF BURIED HYDROGEN BONDS TO PROTEIN STABILITY: THE CRYSTAL STRUCTURES OF TWO BARNASE MUTANTS |
| 1BAP | A PRO TO GLY MUTATION IN THE HINGE OF THE ARABINOSE-BINDING PROTEIN ENHANCES BINDING AND ALTERS SPECIFICITY: SUGAR-BINDING AND CRYSTALLOGRAPHIC STUDIES |
| 1BAR | THREE-DIMENSIONAL STRUCTURES OF ACIDIC AND BASIC FIBROBLAST GROWTH FACTORS |
| 1BAS | THREE-DIMENSIONAL STRUCTURES OF ACIDIC AND BASIC FIBROBLAST GROWTH FACTORS |
| 1BAV | CARBOXYPEPTIDASE A COMPLEXED WITH 2-BENZYL-3-IODO-PROPANOIC ACID (BIP) |
| 1BAW | PLASTOCYANIN FROM PHORMIDIUM LAMINOSUM |
| 1BAY | GLUTATHIONE S-TRANSFERASE YFYF CYS 47-CARBOXYMETHYLATED CLASS PI, FREE ENZYME |
| 1BAZ | ARC REPRESSOR MUTANT PHE10VAL |
| 1BB0 | THROMBIN INHIBITORS WITH RIGID TRIPEPTIDYL ALDEHYDES |
| 1BB3 | HUMAN LYSOZYME MUTANT A96L |
| 1BB4 | HUMAN LYSOZYME DOUBLE MUTANT A96L, W109H |
| 1BB5 | HUMAN LYSOZYME MUTANT A96L COMPLEXED WITH CHITOTRIOSE |
| 1BB6 | LYSOZYME COMPLEX WITH 4-METHYL-UMBELLIFERYL CHITOTRIOSE |
| 1BB7 | LYSOZYME COMPLEX WITH 4-METHYL-UMBELLIFERYL CHITOBIOSE |
| 1BB8 | N-TERMINAL DNA BINDING DOMAIN FROM TN916 INTEGRASE, NMR, 25 STRUCTURES |
| 1BB9 | CRYSTAL STRUCTURE OF THE SH3 DOMAIN FROM RAT AMPHIPHYSIN 2 |
| 1BBA | SEQUENCE-SPECIFIC 1H NMR ASSIGNMENTS AND SOLUTION STRUCTURE OF BOVINE PANCREATIC POLYPEPTIDE |
| 1BBB | A THIRD QUATERNARY STRUCTURE OF HUMAN HEMOGLOBIN A AT 1.7-ANGSTROMS RESOLUTION |
| 1BBC | STRUCTURE OF RECOMBINANT HUMAN RHEUMATOID ARTHRITIC SYNOVIAL FLUID PHOSPHOLIPASE A2 AT 2.2 ANGSTROMS RESOLUTION |
| 1BBD | THREE DIMENSIONAL STRUCTURE OF THE FAB FRAGMENT OF A NEUTRALIZING ANTIBODY TO HUMAN RHINOVIRUS SEROTYPE 2 |
| 1BBG | RAGWEED POLLEN ALLERGEN FROM AMBROSIA TRIFIDA V, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BBH | ATOMIC STRUCTURE OF A CYTOCHROME C' WITH AN UNUSUAL LIGAND-CONTROLLED DIMER DISSOCIATION AT 1.8 ANGSTROMS RESOLUTION |
| 1BBI | THREE-DIMENSIONAL STRUCTURE OF SOYBEAN TRYPSIN(SLASH)CHYMOTRYPSIN BOWMAN-BIRK INHIBITOR IN SOLUTION |
| 1BBJ | CRYSTAL STRUCTURE OF A CHIMERIC FAB' FRAGMENT OF AN ANTIBODY BINDING TUMOUR CELLS |
| 1BBL | THREE-DIMENSIONAL SOLUTION STRUCTURE OF THE E3-BINDING DOMAIN OF THE DIHYDROLIPOAMIDE SUCCINYLTRANSFERASE CORE FROM THE 2-OXOGLUTARATE DEHYDROGENASE MULTIENZYME COMPLEX OF ESCHERICHIA COLI |
| 1BBN | THREE-DIMENSIONAL SOLUTION STRUCTURE OF HUMAN INTERLEUKIN-4 BY MULTI-DIMENSIONAL HETERONUCLEAR MAGNETIC RESONANCE SPECTROSCOPY |
| 1BBO | HIGH-RESOLUTION SOLUTION STRUCTURE OF THE DOUBLE CYS2*HIS2 ZINC FINGER FROM THE HUMAN ENHANCER BINDING PROTEIN MBP-1 |
| 1BBP | MOLECULAR STRUCTURE OF THE BILIN BINDING PROTEIN (BBP) FROM PIERIS BRASSICAE AFTER REFINEMENT AT 2.0 ANGSTROMS RESOLUTION. |
| 1BBR | THE STRUCTURE OF RESIDUES 7-16 OF THE A ALPHA CHAIN OF HUMAN FIBRINOGEN BOUND TO BOVINE THROMBIN AT 2.3 ANGSTROMS RESOLUTION |
| 1BBS | X-RAY ANALYSES OF PEPTIDE INHIBITOR COMPLEXES DEFINE THE STRUCTURAL BASIS OF SPECIFICITY FOR HUMAN AND MOUSE RENINS |
| 1BBT | METHODS USED IN THE STRUCTURE DETERMINATION OF FOOT AND MOUTH DISEASE VIRUS |
| 1BBU | LYSYL-TRNA SYNTHETASE (LYSS) COMPLEXED WITH LYSINE |
| 1BBW | LYSYL-TRNA SYNTHETASE (LYSS) |
| 1BBX | NON-SPECIFIC PROTEIN-DNA INTERACTIONS IN THE SSO7D-DNA COMPLEX, NMR, 1 STRUCTURE |
| 1BBY | DNA-BINDING DOMAIN FROM HUMAN RAP30, NMR, MINIMIZED AVERAGE |
| 1BBZ | CRYSTAL STRUCTURE OF THE ABL-SH3 DOMAIN COMPLEXED WITH A DESIGNED HIGH-AFFINITY PEPTIDE LIGAND: IMPLICATIONS FOR SH3-LIGAND INTERACTIONS |
| 1BC0 | RECOMBINANT RAT ANNEXIN V, W185A MUTANT |
| 1BC1 | RECOMBINANT RAT ANNEXIN V, QUADRUPLE MUTANT (T72K, S144K, S228K, S303K) |
| 1BC2 | ZN-DEPENDENT METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS |
| 1BC3 | RECOMBINANT RAT ANNEXIN V, TRIPLE MUTANT (T72K, S144K, S228K) |
| 1BC4 | THE SOLUTION STRUCTURE OF A CYTOTOXIC RIBONUCLEASE FROM THE OOCYTES OF RANA CATESBEIANA (BULLFROG), NMR, 15 STRUCTURES |
| 1BC5 | CHEMOTAXIS RECEPTOR RECOGNITION BY PROTEIN METHYLTRANSFERASE CHER |
| 1BC6 | 7-FE FERREDOXIN FROM BACILLUS SCHLEGELII, NMR, 20 STRUCTURES |
| 1BC7 | SERUM RESPONSE FACTOR ACCESSORY PROTEIN 1A (SAP-1)/DNA COMPLEX |
| 1BC8 | STRUCTURES OF SAP-1 BOUND TO DNA SEQUENCES FROM THE E74 AND C-FOS PROMOTERS PROVIDE INSIGHTS INTO HOW ETS PROTEINS DISCRIMINATE BETWEEN RELATED DNA TARGETS |
| 1BC9 | CYTOHESIN-1/B2-1 SEC7 DOMAIN, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BCC | CYTOCHROME BC1 COMPLEX FROM CHICKEN |
| 1BCD | X-RAY CRYSTALLOGRAPHIC STRUCTURE OF A COMPLEX BETWEEN HUMAN CARBONIC ANHYDRASE II AND A NEW TOPICAL INHIBITOR, TRIFLUOROMETHANE SULPHONAMIDE |
| 1BCF | THE STRUCTURE OF A UNIQUE, TWO-FOLD SYMMETRIC, HAEM-BINDING SITE |
| 1BCG | SCORPION TOXIN BJXTR-IT |
| 1BCH | MANNOSE-BINDING PROTEIN-A MUTANT (QPDWGH) COMPLEXED WITH N-ACETYL-D-GALACTOSAMINE |
| 1BCI | C2 DOMAIN OF CYTOSOLIC PHOSPHOLIPASE A2, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BCJ | MANNOSE-BINDING PROTEIN-A MUTANT (QPDWGHV) COMPLEXED WITH N-ACETYL-D-GALACTOSAMINE |
| 1BCK | HUMAN CYCLOPHILIN A COMPLEXED WITH 2-THR CYCLOSPORIN |
| 1BCM | BACTERIOPHAGE MU TRANSPOSASE CORE DOMAIN WITH 2 MONOMERS PER ASYMMETRIC UNIT |
| 1BCN | THREE-DIMENSIONAL SOLUTION STRUCTURE OF HUMAN INTERLEUKIN-4 BY MULTI-DIMENSIONAL HETERONUCLEAR MAGNETIC RESONANCE SPECTROSCOPY |
| 1BCO | BACTERIOPHAGE MU TRANSPOSASE CORE DOMAIN |
| 1BCP | BINARY COMPLEX OF PERTUSSIS TOXIN AND ATP |
| 1BCR | COMPLEX OF THE WHEAT SERINE CARBOXYPEPTIDASE, CPDW-II, WITH THE MICROBIAL PEPTIDE ALDEHYDE INHIBITOR, ANTIPAIN, AND ARGININE AT ROOM TEMPERATURE |
| 1BCS | COMPLEX OF THE WHEAT SERINE CARBOXYPEPTIDASE, CPDW-II, WITH THE MICROBIAL PEPTIDE ALDEHYDE INHIBITOR, CHYMOSTATIN, AND ARGININE AT 100 DEGREES KELVIN |
| 1BCT | THREE-DIMENSIONAL STRUCTURE OF PROTEOLYTIC FRAGMENT 163-231 OF BACTERIOOPSIN DETERMINED FROM NUCLEAR MAGNETIC RESONANCE DATA IN SOLUTION |
| 1BCU | ALPHA-THROMBIN COMPLEXED WITH HIRUGEN AND PROFLAVIN |
| 1BCV | SYNTHETIC PEPTIDE CORRESPONDING TO THE MAJOR IMMUNOGEN SITE OF FMD VIRUS, NMR, 10 STRUCTURES |
| 1BCW | RECOMBINANT RAT ANNEXIN V, T72A MUTANT |
| 1BCX | MUTATIONAL AND CRYSTALLOGRAPHIC ANALYSES OF THE ACTIVE SITE RESIDUES OF THE BACILLUS CIRCULANS XYLANASE |
| 1BCY | RECOMBINANT RAT ANNEXIN V, T72K MUTANT |
| 1BCZ | RECOMBINANT RAT ANNEXIN V, T72S MUTANT |
| 1BD0 | ALANINE RACEMASE COMPLEXED WITH ALANINE PHOSPHONATE |
| 1BD2 | COMPLEX BETWEEN HUMAN T-CELL RECEPTOR B7, VIRAL PEPTIDE (TAX) AND MHC CLASS I MOLECULE HLA-A 0201 |
| 1BD3 | STRUCTURE OF THE APO URACIL PHOSPHORIBOSYLTRANSFERASE, 2 MUTANT C128V |
| 1BD4 | UPRT-URACIL COMPLEX |
| 1BD6 | 7-FE FERREDOXIN FROM BACILLUS SCHLEGELII, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BD7 | CIRCULARLY PERMUTED BB2-CRYSTALLIN |
| 1BD8 | STRUCTURE OF CDK INHIBITOR P19INK4D |
| 1BD9 | HUMAN PHOSPHATIDYLETHANOLAMINE BINDING PROTEIN |
| 1BDA | CATALYTIC DOMAIN OF HUMAN SINGLE CHAIN TISSUE PLASMINOGEN ACTIVATOR IN COMPLEX WITH DANSYL-EGR-CMK (DANSYL-GLU-GLY-ARG CHLOROMETHYL KETONE) |
| 1BDB | CIS-BIPHENYL-2,3-DIHYDRODIOL-2,3-DEHYDROGENASE FROM PSEUDOMONAS SP. LB400 |
| 1BDC | STAPHYLOCOCCUS AUREUS PROTEIN A, IMMUNOGLOBULIN-BINDING B DOMAIN, NMR, 10 STRUCTURES |
| 1BDD | STAPHYLOCOCCUS AUREUS PROTEIN A, IMMUNOGLOBULIN-BINDING B DOMAIN, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BDF | STRUCTURE OF ESCHERICHIA COLI RNA POLYMERASE ALPHA SUBUNIT N-TERMINAL DOMAIN |
| 1BDG | HEXOKINASE FROM SCHISTOSOMA MANSONI COMPLEXED WITH GLUCOSE |
| 1BDH | PURINE REPRESSOR MUTANT-HYPOXANTHINE-PALINDROMIC OPERATOR COMPLEX |
| 1BDI | PURINE REPRESSOR MUTANT-HYPOXANTHINE-PALINDROMIC OPERATOR COMPLEX |
| 1BDJ | COMPLEX STRUCTURE OF HPT DOMAIN AND CHEY |
| 1BDK | AN NMR, CD, MOLECULAR DYNAMICS, AND FLUOROMETRIC STUDY OF THE CONFORMATION OF THE BRADYKININ ANTAGONIST B-9340 IN WATER AND IN AQUEOUS MICELLAR SOLUTIONS |
| 1BDL | HIV-1 (2:31-37) PROTEASE COMPLEXED WITH INHIBITOR SB203386 |
| 1BDM | THE STRUCTURE AT 1.8 ANGSTROMS RESOLUTION OF A SINGLE SITE MUTANT (T189I) OF MALATE DEHYDROGENASE FROM THERMUS FLAVUS WITH INCREASED ENZYMATIC ACTIVITY |
| 1BDO | STRUCTURE OF THE BIOTINYL DOMAIN OF ACETYL-COENZYME A CARBOXYLASE DETERMINED BY MAD PHASING |
| 1BDQ | HIV-1 (2:31-37, 47, 82) PROTEASE COMPLEXED WITH INHIBITOR SB203386 |
| 1BDR | HIV-1 (2: 31, 33-37) PROTEASE COMPLEXED WITH INHIBITOR SB203386 |
| 1BDS | DETERMINATION OF THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF THE ANTIHYPERTENSIVE AND ANTIVIRAL PROTEIN BDS-I FROM THE SEA ANEMONE ANEMONIA SULCATA. A STUDY USING NUCLEAR MAGNETIC RESONANCE AND HYBRID DISTANCE GEOMETRY-DYNAMICAL SIMULATED ANNEALING |
| 1BDT | WILD TYPE GENE-REGULATING PROTEIN ARC/DNA COMPLEX |
| 1BDU | E. COLI THYMIDYLATE SYNTHASE COMPLEXED WITH DURD |
| 1BDV | ARC FV10 COCRYSTAL |
| 1BDX | E. COLI DNA HELICASE RUVA WITH BOUND DNA HOLLIDAY JUNCTION, ALPHA CARBONS AND PHOSPHATE ATOMS ONLY |
| 1BDY | C2 DOMAIN FROM PROTEIN KINASE C DELTA |
| 1BE0 | HALOALKANE DEHALOGENASE AT PH 5.0 CONTAINING ACETIC ACID |
| 1BE1 | GLUTAMATE MUTASE (B12-BINDING SUBUNIT), NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BE2 | LIPID TRANSFER PROTEIN COMPLEXED WITH PALMITATE, NMR, 10 STRUCTURES |
| 1BE3 | CYTOCHROME BC1 COMPLEX FROM BOVINE |
| 1BE4 | NUCLEOSIDE DIPHOSPHATE KINASE ISOFORM B FROM BOVINE RETINA |
| 1BE6 | TRANS-CINNAMOYL-SUBTILISIN IN ANHYDROUS ACETONITRILE |
| 1BE7 | CLOSTRIDIUM PASTEURIANUM RUBREDOXIN C42S MUTANT |
| 1BE8 | TRANS-CINNAMOYL-SUBTILISIN IN WATER |
| 1BE9 | THE THIRD PDZ DOMAIN FROM THE SYNAPTIC PROTEIN PSD-95 IN COMPLEX WITH A C-TERMINAL PEPTIDE DERIVED FROM CRIPT. |
| 1BEA | BIFUNCTIONAL HAGEMAN FACTOR/AMYLASE INHIBITOR FROM MAIZE |
| 1BEB | BOVINE BETA-LACTOGLOBULIN, LATTICE X |
| 1BEC | BETA CHAIN OF A T CELL ANTIGEN RECEPTOR |
| 1BED | STRUCTURE OF DISULFIDE OXIDOREDUCTASE |
| 1BEE | HALOALKANE DEHALOGENASE MUTANT WITH TRP 175 REPLACED BY TYR |
| 1BEG | STRUCTURE OF FUNGAL ELICITOR, NMR, 18 STRUCTURES |
| 1BEH | HUMAN PHOSPHATIDYLETHANOLAMINE BINDING PROTEIN IN COMPLEX WITH CACODYLATE |
| 1BEI | SHK-DNP22: A POTENT KV1.3-SPECIFIC IMMUNOSUPPRESSIVE POLYPEPTIDE, NMR, 20 STRUCTURES |
| 1BEJ | INTERACTION BETWEEN PROXIMAL AND DISTALS REGIONS OF CYTOCHROME C PEROXIDASE |
| 1BEK | EFFECT OF UNNATURAL HEME SUBSTITUTION ON KINETICS OF ELECTRON TRANSFER IN CYTOCHROME C PEROXIDASE |
| 1BEL | HYDROLASE PHOSPHORIC DIESTER, RNA |
| 1BEM | INTERACTION BETWEEN PROXIMAL AND DISTALS REGIONS OF CYTOCHROME C PEROXIDASE |
| 1BEN | INSULIN COMPLEXED WITH 4-HYDROXYBENZAMIDE |
| 1BEO | BETA-CRYPTOGEIN |
| 1BEP | EFFECT OF UNNATURAL HEME SUBSTITUTION ON KINETICS OF ELECTRON TRANSFER IN CYTOCHROME C PEROXIDASE |
| 1BEQ | INTERACTION BETWEEN PROXIMAL AND DISTALS REGIONS OF CYTOCHROME C PEROXIDASE |
| 1BES | INTERACTION BETWEEN PROXIMAL AND DISTALS REGIONS OF CYTOCHROME C PEROXIDASE |
| 1BET | NEW PROTEIN FOLD REVEALED BY A 2.3 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF NERVE GROWTH FACTOR |
| 1BEU | TRP SYNTHASE (D60N-IPP-SER) WITH K+ |
| 1BEV | BOVINE ENTEROVIRUS VG-5-27 |
| 1BEX | STRUCTURE OF RUTHENIUM-MODIFIED PSEUDOMONAS AERUGINOSA AZURIN |
| 1BEY | ANTIBODY TO CAMPATH-1H HUMANIZED FAB |
| 1BEZ | HALOALKANE DEHALOGENASE MUTANT WITH TRP 175 REPLACED BY TYR AT PH 5 |
| 1BF0 | CALCICLUDINE (CAC) FROM GREEN MAMBA DENDROASPIS ANGUSTICEPS, NMR, 15 STRUCTURES |
| 1BF2 | STRUCTURE OF PSEUDOMONAS ISOAMYLASE |
| 1BF3 | P-HYDROXYBENZOATE HYDROXYLASE (PHBH) MUTANT WITH CYS 116 REPLACED BY SER (C116S) AND ARG 42 REPLACED BY LYS (R42K), IN COMPLEX WITH FAD AND 4-HYDROXYBENZOIC ACID |
| 1BF4 | CHROMOSOMAL DNA-BINDING PROTEIN SSO7D/D(GCGAACGC) COMPLEX |
| 1BF5 | TYROSINE PHOSPHORYLATED STAT-1/DNA COMPLEX |
| 1BF6 | PHOSPHOTRIESTERASE HOMOLOGY PROTEIN FROM ESCHERICHIA COLI |
| 1BF8 | PERIPLASMIC CHAPERONE FIMC, NMR, 20 STRUCTURES |
| 1BF9 | N-TERMINAL EGF-LIKE DOMAIN FROM HUMAN FACTOR VII, NMR, 23 STRUCTURES |
| 1BFA | RECOMBINANT BIFUNCTIONAL HAGEMAN FACTOR/AMYLASE INHIBITOR FROM MAIZE |
| 1BFB | BASIC FIBROBLAST GROWTH FACTOR COMPLEXED WITH HEPARIN TETRAMER FRAGMENT |
| 1BFC | BASIC FIBROBLAST GROWTH FACTOR COMPLEXED WITH HEPARIN HEXAMER FRAGMENT |
| 1BFD | BENZOYLFORMATE DECARBOXYLASE FROM PSEUDOMONAS PUTIDA |
| 1BFE | THE THIRD PDZ DOMAIN FROM THE SYNAPTIC PROTEIN PSD-95 |
| 1BFF | THE 154 AMINO ACID FORM OF HUMAN BASIC FIBROBLAST GROWTH FACTOR |
| 1BFG | CRYSTAL STRUCTURE OF BASIC FIBROBLAST GROWTH FACTOR AT 1.6 ANGSTROMS RESOLUTION |
| 1BFI | SOLUTION STRUCTURE OF THE C-TERMINAL SH2 DOMAIN OF THE P85ALPHA REGULATORY SUBUNIT OF PHOSPHOINOSITIDE 3-KINASE, NMR, 30 STRUCTURES |
| 1BFJ | SOLUTION STRUCTURE OF THE C-TERMINAL SH2 DOMAIN OF THE P85ALPHA REGULATORY SUBUNIT OF PHOSPHOINOSITIDE 3-KINASE, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BFK | CRYSTAL STRUCTURE OF SUBTILISIN CARLSBERG IN 40% ACETONITRILE |
| 1BFM | HISTONE B FROM METHANOTHERMUS FERVIDUS |
| 1BFN | BETA-AMYLASE/BETA-CYCLODEXTRIN COMPLEX |
| 1BFO | CAMPATH-1G IGG2B RAT MONOCLONAL FAB |
| 1BFP | BLUE VARIANT OF GREEN FLUORESCENT PROTEIN |
| 1BFS | STRUCTURE OF NF-KB P50 HOMODIMER BOUND TO A KB SITE |
| 1BFT | STRUCTURE OF NF-KB P50 HOMODIMER BOUND TO A KB SITE |
| 1BFU | SUBTILISIN CARLSBERG IN 20% DIOXANE |
| 1BFV | MONOCLONAL ANTIBODY FRAGMENT FV4155 FROM E. COLI |
| 1BFX | THE SOLUTION NMR STRUCTURE OF THE B FORM OF OXIDIZED RAT MICROSOMAL CYTOCHROME B5, MINIMIZED AVERAGE STRUCTURE |
| 1BFY | SOLUTION STRUCTURE OF REDUCED CLOSTRIDIUM PASTEURIANUM RUBREDOXIN, NMR, 20 STRUCTURES |
| 1BG0 | TRANSITION STATE STRUCTURE OF ARGININE KINASE |
| 1BG1 | TRANSCRIPTION FACTOR STAT3B/DNA COMPLEX |
| 1BG2 | HUMAN UBIQUITOUS KINESIN MOTOR DOMAIN |
| 1BG3 | RAT BRAIN HEXOKINASE TYPE I COMPLEX WITH GLUCOSE AND INHIBITOR GLUCOSE-6-PHOSPHATE |
| 1BG4 | XYLANASE FROM PENICILLIUM SIMPLICISSIMUM |
| 1BG5 | CRYSTAL STRUCTURE OF THE ANKYRIN BINDING DOMAIN OF ALPHA-NA,K-ATPASE AS A FUSION PROTEIN WITH GLUTATHIONE S-TRANSFERASE |
| 1BG6 | CRYSTAL STRUCTURE OF THE N-(1-D-CARBOXYLETHYL)-L-NORVALINE DEHYDROGENASE FROM ARTHROBACTER SP. STRAIN 1C |
| 1BG7 | LOCALIZED UNFOLDING AT THE JUNCTION OF THREE FERRITIN SUBUNITS. A MECHANISM FOR IRON RELEASE? |
| 1BG8 | HDEA FROM ESCHERICHIA COLI |
| 1BG9 | BARLEY ALPHA-AMYLASE WITH SUBSTRATE ANALOGUE ACARBOSE |
| 1BGA | BETA-GLUCOSIDASE A FROM BACILLUS POLYMYXA |
| 1BGB | ECORV ENDONUCLEASE COMPLEX WITH 5'-CGGGATATCCC DNA |
| 1BGC | CRYSTAL STRUCTURE OF CANINE AND BOVINE GRANULOCYTE-COLONY STIMULATING FACTOR (G-CSF) |
| 1BGD | CRYSTAL STRUCTURE OF CANINE AND BOVINE GRANULOCYTE-COLONY STIMULATING FACTOR (G-CSF) |
| 1BGE | CRYSTAL STRUCTURE OF CANINE AND BOVINE GRANULOCYTE-COLONY STIMULATING FACTOR (G-CSF) |
| 1BGF | STAT-4 N-DOMAIN |
| 1BGG | GLUCOSIDASE A FROM BACILLUS POLYMYXA COMPLEXED WITH GLUCONATE |
| 1BGI | ORTHORHOMBIC LYSOZYME CRYSTALLIZED AT HIGH TEMPERATURE (310K) |
| 1BGJ | P-HYDROXYBENZOATE HYDROXYLASE (PHBH) MUTANT WITH CYS 116 REPLACED BY SER (C116S) AND HIS 162 REPLACED BY ARG (H162R), IN COMPLEX WITH FAD AND 4-HYDROXYBENZOIC ACID |
| 1BGK | SEA ANEMONE TOXIN (BGK) WITH HIGH AFFINITY FOR VOLTAGE DEPENDENT POTASSIUM CHANNEL, NMR, 15 STRUCTURES |
| 1BGN | P-HYDROXYBENZOATE HYDROXYLASE (PHBH) MUTANT WITH CYS 116 REPLACED BY SER (C116S) AND ARG 269 REPLACED BY THR (R269T), IN COMPLEX WITH FAD AND 4-HYDROXYBENZOIC ACID |
| 1BGO | CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT PEPTIDOMIMETIC INHIBITOR |
| 1BGP | CRYSTAL STRUCTURE OF BARLEY GRAIN PEROXIDASE 1 |
| 1BGQ | RADICICOL BOUND TO THE ATP BINDING SITE OF THE N-TERMINAL DOMAIN OF THE YEAST HSP90 CHAPERONE |
| 1BGS | RECOGNITION BETWEEN A BACTERIAL RIBONUCLEASE, BARNASE, AND ITS NATURAL INHIBITOR, BARSTAR |
| 1BGT | CRYSTAL STRUCTURE OF THE DNA MODIFYING ENZYME BETA-GLUCOSYLTRANSFERASE IN THE PRESENCE AND ABSENCE OF THE SUBSTRATE URIDINE DIPHOSPHOGLUCOSE |
| 1BGU | CRYSTAL STRUCTURE OF THE DNA MODIFYING ENZYME BETA-GLUCOSYLTRANSFERASE IN THE PRESENCE AND ABSENCE OF THE SUBSTRATE URIDINE DIPHOSPHOGLUCOSE |
| 1BGV | GLUTAMATE DEHYDROGENASE |
| 1BGW | TOPOISOMERASE RESIDUES 410-1202, |
| 1BGX | TAQ POLYMERASE IN COMPLEX WITH TP7, AN INHIBITORY FAB |
| 1BGY | CYTOCHROME BC1 COMPLEX FROM BOVINE |
| 1BH0 | STRUCTURE OF A GLUCAGON ANALOG |
| 1BH1 | STRUCTURAL STUDIES OF D-PRO MELITTIN, NMR, 20 STRUCTURES |
| 1BH2 | A326S MUTANT OF AN INHIBITORY ALPHA SUBUNIT |
| 1BH3 | E1M, A116K MUTANT OF RH. BLASTICA PORIN |
| 1BH4 | CIRCULIN A FROM CHASSALIA PARVIFLORA, NMR, 12 STRUCTURES |
| 1BH5 | HUMAN GLYOXALASE I Q33E, E172Q DOUBLE MUTANT |
| 1BH6 | SUBTILISIN DY IN COMPLEX WITH THE SYNTHETIC INHIBITOR N-BENZYLOXYCARBONYL-ALA-PRO-PHE-CHLOROMETHYL KETONE |
| 1BH7 | A LOW ENERGY STRUCTURE FOR THE FINAL CYTOPLASMIC LOOP OF BAND 3, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BH8 | HTAFII18/HTAFII28 HETERODIMER CRYSTAL STRUCTURE |
| 1BH9 | HTAFII18/HTAFII28 HETERODIMER CRYSTAL STRUCTURE WITH BOUND PCMBS |
| 1BHA | THREE-DIMENSIONAL STRUCTURE OF (1-71) BACTERIOOPSIN SOLUBILIZED IN METHANOL-CHLOROFORM AND SDS MICELLES DETERMINED BY 15N-1H HETERONUCLEAR NMR SPECTROSCOPY |
| 1BHB | THREE-DIMENSIONAL STRUCTURE OF (1-71) BACTERIOOPSIN SOLUBILIZED IN METHANOL-CHLOROFORM AND SDS MICELLES DETERMINED BY 15N-1H HETERONUCLEAR NMR SPECTROSCOPY |
| 1BHC | BOVINE PANCREATIC TRYPSIN INHIBITOR CRYSTALLIZED FROM THIOCYANATE |
| 1BHD | SECOND CALPONIN HOMOLOGY DOMAIN FROM UTROPHIN |
| 1BHE | POLYGALACTURONASE FROM ERWINIA CAROTOVORA SSP. CAROTOVORA |
| 1BHF | P56LCK SH2 DOMAIN INHIBITOR COMPLEX |
| 1BHG | HUMAN BETA-GLUCURONIDASE AT 2.6 A RESOLUTION |
| 1BHH | FREE P56LCK SH2 DOMAIN |
| 1BHI | STRUCTURE OF TRANSACTIVATION DOMAIN OF CRE-BP1/ATF-2, NMR, 20 STRUCTURES |
| 1BHJ | CRYSTAL STRUCTURE OF APO-GLYCINE N-METHYLTRANSFERASE (GNMT) |
| 1BHL | CACODYLATED CATALYTIC DOMAIN OF HIV-1 INTEGRASE |
| 1BHM | RESTRICTION ENDONUCLEASE BAMHI COMPLEX WITH DNA |
| 1BHN | NUCLEOSIDE DIPHOSPHATE KINASE ISOFORM A FROM BOVINE RETINA |
| 1BHO | MAC-1 I DOMAIN MAGNESIUM COMPLEX |
| 1BHP | STRUCTURE OF BETA-PUROTHIONIN AT ROOM TEMPERATURE AND 1.7 ANGSTROMS RESOLUTION |
| 1BHQ | MAC-1 I DOMAIN CADMIUM COMPLEX |
| 1BHS | HUMAN ESTROGENIC 17BETA-HYDROXYSTEROID DEHYDROGENASE |
| 1BHT | NK1 FRAGMENT OF HUMAN HEPATOCYTE GROWTH FACTOR |
| 1BHU | THE 3D STRUCTURE OF THE STREPTOMYCES METALLOPROTEINASE INHIBITOR, SMPI, ISOLATED FROM STREPTOMYCES NIGRESCENS TK-23, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BHW | LOW TEMPERATURE MIDDLE RESOLUTION STRUCTURE OF XYLOSE ISOMERASE FROM MASC DATA |
| 1BHX | X-RAY STRUCTURE OF THE COMPLEX OF HUMAN ALPHA THROMBIN WITH THE INHIBITOR SDZ 229-357 |
| 1BHY | LOW TEMPERATURE MIDDLE RESOLUTION STRUCTURE OF P64K FROM MASC DATA |
| 1BHZ | LOW TEMPERATURE MIDDLE RESOLUTION STRUCTURE OF HEN EGG WHITE LYSOZYME FROM MASC DATA |
| 1BI0 | STRUCTURE OF APO-AND HOLO-DIPHTHERIA TOXIN REPRESSOR |
| 1BI1 | STRUCTURE OF APO-AND HOLO-DIPHTHERIA TOXIN REPRESSOR |
| 1BI2 | STRUCTURE OF APO-AND HOLO-DIPHTHERIA TOXIN REPRESSOR |
| 1BI3 | STRUCTURE OF APO-AND HOLO-DIPHTHERIA TOXIN REPRESSOR |
| 1BI4 | CATALYTIC DOMAIN OF HIV-1 INTEGRASE |
| 1BI5 | CHALCONE SYNTHASE FROM ALFALFA |
| 1BI6 | NMR STRUCTURE OF BROMELAIN INHIBITOR VI FROM PINEAPPLE STEM |
| 1BI7 | MECHANISM OF G1 CYCLIN DEPENDENT KINASE INHIBITION FROM THE STRUCTURE OF THE CDK6-P16INK4A TUMOR SUPPRESSOR COMPLEX |
| 1BI8 | MECHANISM OF G1 CYCLIN DEPENDENT KINASE INHIBITION FROM THE STRUCTURES CDK6-P19INK4D INHIBITOR COMPLEX |
| 1BI9 | RETINAL DEHYDROGENASE TYPE TWO WITH NAD BOUND |
| 1BIA | THE E. COLI BIOTIN HOLOENZYME SYNTHETASE(SLASH)BIO REPRESSOR CRYSTAL STRUCTURE DELINEATES THE BIOTIN AND DNA-BINDING DOMAINS |
| 1BIB | THE E. COLI BIOTIN HOLOENZYME SYNTHETASE(SLASH)BIO REPRESSOR CRYSTAL STRUCTURE DELINEATES THE BIOTIN AND DNA-BINDING DOMAINS |
| 1BIC | CRYSTALLOGRAPHIC ANALYSIS OF THR-200-> HIS HUMAN CARBONIC ANHYDRASE II AND ITS COMPLEX WITH THE SUBSTRATE, HCO3- |
| 1BID | E. COLI THYMIDYLATE SYNTHASE COMPLEXED WITH DUMP |
| 1BIF | 6-PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE BIFUNCTIONAL ENZYME COMPLEXED WITH ATP-G-S AND PHOSPHATE |
| 1BIG | SCORPION TOXIN BMTX1 FROM BUTHUS MARTENSII KARSCH, NMR, 25 STRUCTURES |
| 1BIH | CRYSTAL STRUCTURE OF THE INSECT IMMUNE PROTEIN HEMOLIN: A NEW DOMAIN ARRANGEMENT WITH IMPLICATIONS FOR HOMOPHILIC ADHESION |
| 1BII | THE CRYSTAL STRUCTURE OF H-2DD MHC CLASS I IN COMPLEX WITH THE HIV-1 DERIVED PEPTIDE P18-110 |
| 1BIJ | CROSSLINKED, DEOXY HUMAN HEMOGLOBIN A |
| 1BIK | X-RAY STRUCTURE OF BIKUNIN FROM THE HUMAN INTER-ALPHA-INHIBITOR COMPLEX |
| 1BIL | CRYSTALLOGRAPHIC STUDIES ON THE BINDING MODES OF P2-P3 BUTANEDIAMIDE RENIN INHIBITORS |
| 1BIM | CRYSTALLOGRAPHIC STUDIES ON THE BINDING MODES OF P2-P3 BUTANEDIAMIDE RENIN INHIBITORS |
| 1BIN | LEGHEMOGLOBIN A (ACETOMET) |
| 1BIO | HUMAN COMPLEMENT FACTOR D IN COMPLEX WITH ISATOIC ANHYDRIDE INHIBITOR |
| 1BIP | BIFUNCTIONAL PROTEINASE INHIBITOR TRYPSIN/A-AMYLASE FROM SEEDS OF RAGI (ELEUSINE CORACANA GAERTNERI) |
| 1BIQ | RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE 1 BETA CHAIN MUTANT E238A |
| 1BIR | RIBONUCLEASE T1, PHE 100 TO ALA MUTANT COMPLEXED WITH 2' GMP |
| 1BIS | HIV-1 INTEGRASE CORE DOMAIN |
| 1BIT | THE CRYSTAL STRUCTURE OF ANIONIC SALMON TRYPSIN IN A SECOND CRYSTAL FORM |
| 1BIU | HIV-1 INTEGRASE CORE DOMAIN COMPLEXED WITH MG++ |
| 1BIV | BOVINE IMMUNODEFICIENCY VIRUS TAT-TAR COMPLEX, NMR, 5 STRUCTURES |
| 1BIW | DESIGN AND SYNTHESIS OF CONFORMATIONALLY-CONSTRAINED MMP INHIBITORS |
| 1BIX | THE CRYSTAL STRUCTURE OF THE HUMAN DNA REPAIR ENDONUCLEASE HAP1 SUGGESTS THE RECOGNITION OF EXTRA-HELICAL DEOXYRIBOSE AT DNA ABASIC SITES |
| 1BIY | STRUCTURE OF DIFERRIC BUFFALO LACTOFERRIN |
| 1BIZ | HIV-1 INTEGRASE CORE DOMAIN |
| 1BJ1 | VASCULAR ENDOTHELIAL GROWTH FACTOR IN COMPLEX WITH A NEUTRALIZING ANTIBODY |
| 1BJ3 | CRYSTAL STRUCTURE OF COAGULATION FACTOR IX-BINDING PROTEIN (IX-BP) FROM VENOM OF HABU SNAKE WITH A HETERODIMER OF C-TYPE LECTIN DOMAINS |
| 1BJ4 | RECOMBINANT SERINE HYDROXYMETHYLTRANSFERASE (HUMAN) |
| 1BJ5 | HUMAN SERUM ALBUMIN COMPLEXED WITH MYRISTIC ACID |
| 1BJ6 | 1H NMR OF (12-53) NCP7/D(ACGCC) COMPLEX, 10 STRUCTURES |
| 1BJ7 | BOVINE LIPOCALIN ALLERGEN BOS D 2 |
| 1BJ8 | THIRD N-TERMINAL DOMAIN OF GP130, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BJ9 | EFFECT OF UNNATURAL HEME SUBSTITUTION ON KINETICS OF ELECTRON TRANSFER IN CYTOCHROME C PEROXIDASE |
| 1BJA | ACTIVATION DOMAIN OF THE PHAGE T4 TRANSCRIPTION FACTOR MOTA |
| 1BJB | SOLUTION NMR STRUCTURE OF AMYLOID BETA[E16], RESIDUES 1-28, 14 STRUCTURES |
| 1BJC | SOLUTION NMR STRUCTURE OF AMYLOID BETA[F16], RESIDUES 1-28, 15 STRUCTURES |
| 1BJE | H64T VARIANT OF MYOGLOBIN (HORSE HEART) RECOMBINANT WILD-TYPE COMPLEXED WITH AZIDE |
| 1BJF | CRYSTAL STRUCTURE OF RECOMBINANT BOVINE NEUROCALCIN DELTA AT 2.4 ANGSTROMS |
| 1BJG | D221(169)N MUTANT DOES NOT PROMOTE OPENING OF THE COFACTOR IMIDAZOLIDINE RING |
| 1BJI | THE X-RAY STRUCTURE OF A COMPLEX OF TERN N9 INFLUENZA VIRUS NEURAMINIDASE COMPLEXED WITH THE GLAXO 6-CARBOXAMIDE SIALIC ACID ANALOGUE GR217029 |
| 1BJJ | AGKISTRODOTOXIN, A PHOSPHOLIPASE A2-TYPE PRESYNAPTIC NEUROTOXIN FROM AGKISTRODON HALYS PALLAS |
| 1BJK | FERREDOXIN:NADP+ REDUCTASE MUTANT WITH ARG 264 REPLACED BY GLU (R264E) |
| 1BJM | LOC NAKS, A LAMBDA 1 TYPE LIGHT-CHAIN DIMER (BENCE-JONES PROTEIN) CRYSTALLIZED IN NAKSO4 |
| 1BJN | STRUCTURE OF PHOSPHOSERINE AMINOTRANSFERASE FROM ESCHERICHIA COLI |
| 1BJO | THE STRUCTURE OF PHOSPHOSERINE AMINOTRANSFERASE FROM E. COLI IN COMPLEX WITH ALPHA-METHYL-L-GLUTAMATE |
| 1BJP | CRYSTAL STRUCTURE OF 4-OXALOCROTONATE TAUTOMERASE INACTIVATED BY 2-OXO-3-PENTYNOATE AT 2.4 ANGSTROMS RESOLUTION |
| 1BJQ | THE DOLICHOS BIFLORUS SEED LECTIN IN COMPLEX WITH ADENINE |
| 1BJR | COMPLEX FORMED BETWEEN PROTEOLYTICALLY GENERATED LACTOFERRIN FRAGMENT AND PROTEINASE K |
| 1BJT | TOPOISOMERASE II RESIDUES 409-1201 |
| 1BJU | BETA-TRYPSIN COMPLEXED WITH ACPU |
| 1BJV | BETA-TRYPSIN COMPLEXED WITH APPU |
| 1BJW | ASPARTATE AMINOTRANSFERASE FROM THERMUS THERMOPHILUS |
| 1BJX | HUMAN PROTEIN DISULFIDE ISOMERASE, NMR, 24 STRUCTURES |
| 1BJZ | TETRACYCLINE CHELATED MG2+-ION INITIATES HELIX UNWINDING FOR TET REPRESSOR INDUCTION |
| 1BK0 | ISOPENICILLIN N SYNTHASE FROM ASPERGILLUS NIDULANS (ACV-FE COMPLEX) |
| 1BK1 | ENDO-1,4-BETA-XYLANASE C |
| 1BK2 | A-SPECTRIN SH3 DOMAIN D48G MUTANT |
| 1BK4 | CRYSTAL STRUCTURE OF RABBIT LIVER FRUCTOSE-1,6-BISPHOSPHATASE AT 2.3 ANGSTROM RESOLUTION |
| 1BK5 | KARYOPHERIN ALPHA FROM SACCHAROMYCES CEREVISIAE |
| 1BK6 | KARYOPHERIN ALPHA (YEAST) + SV40 T ANTIGEN NLS |
| 1BK7 | RIBONUCLEASE MC1 FROM THE SEEDS OF BITTER GOURD |
| 1BK8 | DETERMINATION OF THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF AESCULUS HIPPOCASTANUM ANTIMICROBIAL PROTEIN 1 (AH-AMP1) BY 1H NMR, 25 STRUCTURES |
| 1BK9 | PHOSPHOLIPASE A2 MODIFIED BY PBPB |
| 1BKA | OXALATE-SUBSTITUTED DIFERRIC LACTOFERRIN |
| 1BKB | INITIATION FACTOR 5A FROM ARCHEBACTERIUM PYROBACULUM AEROPHILUM |
| 1BKC | CATALYTIC DOMAIN OF TNF-ALPHA CONVERTING ENZYME (TACE) |
| 1BKD | COMPLEX OF HUMAN H-RAS WITH HUMAN SOS-1 |
| 1BKE | HUMAN SERUM ALBUMIN IN A COMPLEX WITH MYRISTIC ACID AND TRI-IODOBENZOIC ACID |
| 1BKF | FK506 BINDING PROTEIN FKBP MUTANT R42K/H87V COMPLEX WITH IMMUNOSUPPRESSANT FK506 |
| 1BKG | ASPARTATE AMINOTRANSFERASE FROM THERMUS THERMOPHILUS WITH MALEATE |
| 1BKH | MUCONATE LACTONIZING ENZYME FROM PSEUDOMONAS PUTIDA |
| 1BKJ | NADPH:FMN OXIDOREDUCTASE FROM VIBRIO HARVEYI |
| 1BKL | SELF-ASSOCIATED APO SRC SH2 DOMAIN |
| 1BKM | COCRYSTAL STRUCTURE OF D-AMINO ACID SUBSTITUTED PHOSPHOPEPTIDE COMPLEX |
| 1BKN | CRYSTAL STRUCTURE OF AN N-TERMINAL 40KD FRAGMENT OF E. COLI DNA MISMATCH REPAIR PROTEIN MUTL |
| 1BKO | THERMOSTABLE THYMIDYLATE SYNTHASE A FROM BACILLUS SUBTILIS |
| 1BKP | THERMOSTABLE THYMIDYLATE SYNTHASE A FROM BACILLUS SUBTILIS |
| 1BKR | CALPONIN HOMOLOGY (CH) DOMAIN FROM HUMAN BETA-SPECTRIN AT 1.1 ANGSTROM RESOLUTION |
| 1BKS | TRYPTOPHAN SYNTHASE (E.C.4.2.1.20) FROM SALMONELLA TYPHIMURIUM |
| 1BKT | BMKTX TOXIN FROM SCORPION BUTHUS MARTENSII KARSCH, NMR, 25 STRUCTURES |
| 1BKU | EFFECTS OF GLYCOSYLATION ON THE STRUCTURE AND DYNAMICS OF EEL CALCITONIN, NMR, 10 STRUCTURES |
| 1BKV | COLLAGEN |
| 1BKW | P-HYDROXYBENZOATE HYDROXYLASE (PHBH) MUTANT WITH CYS116 REPLACED BY SER (C116S) AND ARG44 REPLACED BY LYS (R44K), IN COMPLEX WITH FAD AND 4-HYDROXYBENZOIC ACID |
| 1BKX | A BINARY COMPLEX OF THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE AND ADENOSINE FURTHER DEFINES CONFORMATIONAL FLEXIBILITY |
| 1BKY | VACCINIA METHYLTRANSFERASE VP39 COMPLEXED WITH M1CYT AND S-ADENOSYLHOMOCYSTEINE |
| 1BKZ | CRYSTAL STRUCTURE OF HUMAN GALECTIN-7 |
| 1BL0 | MULTIPLE ANTIBIOTIC RESISTANCE PROTEIN (MARA)/DNA COMPLEX |
| 1BL3 | CATALYTIC DOMAIN OF HIV-1 INTEGRASE |
| 1BL4 | FKBP MUTANT F36V COMPLEXED WITH REMODELED SYNTHETIC LIGAND |
| 1BL5 | ISOCITRATE DEHYDROGENASE FROM E. COLI SINGLE TURNOVER LAUE STRUCTURE OF RATE-LIMITED PRODUCT COMPLEX, 10 MSEC TIME RESOLUTION |
| 1BL6 | THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB216995 |
| 1BL7 | THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB220025 |
| 1BL8 | POTASSIUM CHANNEL (KCSA) FROM STREPTOMYCES LIVIDANS |
| 1BL9 | CONFORMATIONAL CHANGES OCCURRING UPON REDUCTION IN NITRITE REDUCTASE FROM PSEUDOMONAS AERUGINOSA |
| 1BLA | BASIC FIBROBLAST GROWTH FACTOR (FGF-2) MUTANT WITH CYS 78 REPLACED BY SER AND CYS 96 REPLACED BY SER, NMR |
| 1BLB | CLOSE PACKING OF AN OLIGOMERIC EYE LENS BETA-CRYSTALLIN INDUCES LOSS OF SYMMETRY AND ORDERING OF SEQUENCE EXTENSIONS |
| 1BLC | INHIBITION OF BETA-LACTAMASE BY CLAVULANATE: TRAPPED INTERMEDIATES IN CRYOCRYSTALLOGRAPHIC STUDIES |
| 1BLD | BASIC FIBROBLAST GROWTH FACTOR (FGF-2) MUTANT WITH CYS 78 REPLACED BY SER AND CYS 96 REPLACED BY SER, NMR |
| 1BLE | PHOSPHOENOLPYRUVATE-DEPENDENT PHOSPHOTRANSFERASE SYSTEM |
| 1BLF | STRUCTURE OF DIFERRIC BOVINE LACTOFERRIN AT 2.8 ANGSTROMS RESOLUTION |
| 1BLH | STRUCTURE OF A PHOSPHONATE-INHIBITED BETA-LACTAMASE. AN ANALOG OF THE TETRAHEDRAL TRANSITION STATE(SLASH)INTERMEDIATE OF BETA-LACTAM HYDROLYSIS |
| 1BLI | BACILLUS LICHENIFORMIS ALPHA-AMYLASE |
| 1BLJ | NMR ENSEMBLE OF BLK SH2 DOMAIN, 20 STRUCTURES |
| 1BLK | NMR ENSEMBLE OF BLK SH2 DOMAIN USING CHEMICAL SHIFT REFINEMENT, 20 STRUCTURES |
| 1BLL | X-RAY CRYSTALLOGRAPHIC DETERMINATION OF THE STRUCTURE OF BOVINE LENS LEUCINE AMINOPEPTIDASE COMPLEXED WITH AMASTATIN: FORMULATION OF A CATALYTIC MECHANISM FEATURING A GEM-DIOLATE TRANSITION STATE |
| 1BLN | ANTI-P-GLYCOPROTEIN FAB MRK-16 |
| 1BLP | STRUCTURAL BASIS FOR THE INACTIVATION OF THE P54 MUTANT OF BETA-LACTAMASE FROM STAPHYLOCOCCUS AUREUS PC1 |
| 1BLQ | STRUCTURE AND INTERACTION SITE OF THE REGULATORY DOMAIN OF TROPONIN-C WHEN COMPLEXED WITH THE 96-148 REGION OF TROPONIN-I, NMR, 29 STRUCTURES |
| 1BLR | NMR SOLUTION STRUCTURE OF HUMAN CELLULAR RETINOIC ACID BINDING PROTEIN-TYPE II, 22 STRUCTURES |
| 1BLS | CRYSTALLOGRAPHIC STRUCTURE OF A PHOSPHONATE DERIVATIVE OF THE ENTEROBACTER CLOACAE P99 CEPHALOSPORINASE: MECHANISTIC INTERPRETATION OF A BETA-LACTAMASE TRANSITION STATE ANALOG |
| 1BLU | STRUCTURE OF THE 2[4FE-4S] FERREDOXIN FROM CHROMATIUM VINOSUM |
| 1BLV | SOLUTION STRUCTURE OF OXIDIZED RAT MICROSOMAL CYTOCHROME B5 IN THE PRESENCE OF 2 M GUANIDINIUM CHLORIDE: MONITORING THE EARLY STEPS IN PROTEIN UNFOLDING |
| 1BLX | P19INK4D/CDK6 COMPLEX |
| 1BLZ | ISOPENICILLIN N SYNTHASE FROM ASPERGILLUS NIDULANS (ACV-FE-NO COMPLEX) |
| 1BM0 | CRYSTAL STRUCTURE OF HUMAN SERUM ALBUMIN |
| 1BM1 | CRYSTAL STRUCTURE OF BACTERIORHODOPSIN IN THE LIGHT-ADAPTED STATE |
| 1BM2 | GRB2-SH2 DOMAIN IN COMPLEX WITH CYCLO-[N-ALPHA-ACETYL-L-THI ALYSYL-O-PHOSPHOTYROSYL-VALYL-ASPARAGYL-VALYL-PROLYL] (PKF273-791) |
| 1BM3 | IMMUNOGLOBULIN OPG2 FAB-PEPTIDE COMPLEX |
| 1BM4 | MOMLV CAPSID PROTEIN MAJOR HOMOLOGY REGION PEPTIDE ANALOG |
| 1BM5 | THE SOLUTION STRUCTURE OF A SITE-DIRECTED MUTANT (R111M) OF HUMAN CELLULAR RETIONIC ACID BINDING PROTEIN-TYPE II, NMR, 31 STRUCTURES |
| 1BM6 | SOLUTION STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN STROMELYSIN-1 COMPLEXED TO A POTENT NON-PEPTIDIC INHIBITOR, NMR, 20 STRUCTURES |
| 1BM7 | HUMAN TRANSTHYRETIN (PREALBUMIN) COMPLEX WITH FLUFENAMIC ACID (2-[[3-(TRIFLUOROMETHYL)PHENYL]AMINO] BENZOIC ACID) |
| 1BM8 | DNA-BINDING DOMAIN OF MBP1 |
| 1BM9 | REPLICATION TERMINATOR PROTEIN FROM BACILLUS SUBTILIS |
| 1BMA | BENZYL METHYL AMINIMIDE INHIBITOR COMPLEXED TO PORCINE PANCREATIC ELASTASE |
| 1BMB | GRB2-SH2 DOMAIN IN COMPLEX WITH KPFY*VNVEF (PKF270-974) |
| 1BMC | STRUCTURE OF A ZINC METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS |
| 1BMD | DETERMINANTS OF PROTEIN THERMOSTABILITY OBSERVED IN THE 1.9 ANGSTROMS CRYSTAL STRUCTURE OF MALATE DEHYDROGENASE FROM THE THERMOPHILIC BACTERIUM THERMUS FLAVUS |
| 1BMF | BOVINE MITOCHONDRIAL F1-ATPASE |
| 1BMG | CRYSTAL STRUCTURE OF BOVINE BETA2-MICROGLOBULIN |
| 1BMK | THE COMPLEX STRUCTURE OF THE MAP KINASE P38/SB218655 |
| 1BML | COMPLEX OF THE CATALYTIC DOMAIN OF HUMAN PLASMIN AND STREPTOKINASE |
| 1BMM | HUMAN ALPHA-THROMBIN COMPLEXED WITH [S-(R*,R*)]-4-[(AMINOIMINOMETHYL)AMINO]-N-[[1-[3-HYDROXY-2-[(2-NAPHTHALENYLSULFONYL)AMINO]-1-OXOPROPYL]-2-PYRROLIDINYL] METHYL]BUTANAMIDE (BMS-186282) |
| 1BMN | HUMAN ALPHA-THROMBIN COMPLEXED WITH [S-(R*,R*)]-1-(AMINOIMINOMETHYL)-N-[[1-[N-[(2-NAPHTHALENYLSULFONYL)-L-SERYL]-PYRROLIDINYL]METHYL]-3-PIPERIDENECARBOXAMIDE (BMS-189090) |
| 1BMO | BM-40, FS/EC DOMAIN PAIR |
| 1BMP | BONE MORPHOGENETIC PROTEIN-7 |
| 1BMQ | CRYSTAL STRUCTURE OF THE COMPLEX OF INTERLEUKIN-1BETA CONVERTING ENZYME (ICE) WITH A PEPTIDE BASED INHIBITOR, (3S )-N-METHANESULFONYL-3-({1-[N-(2-NAPHTOYL)-L-VALYL]-L-PROLYL }AMINO)-4-OXOBUTANAMIDE |
| 1BMR | ALPHA-LIKE TOXIN LQH III FROM SCORPION LEIURUS QUINQUESTRIATUS HEBRAEUS, NMR, 25 STRUCTURES |
| 1BMS | CRYSTAL STRUCTURE OF MS2 CAPSIDS WITH MUTATIONS IN THE SUBUNIT FG LOOP |
| 1BMT | HOW A PROTEIN BINDS B12: A 3.O ANGSTROM X-RAY STRUCTURE OF THE B12-BINDING DOMAINS OF METHIONINE SYNTHASE |
| 1BMV | PROTEIN-RNA INTERACTIONS IN AN ICOSAHEDRAL VIRUS AT 3.0 ANGSTROMS RESOLUTION |
| 1BMW | A FIBRONECTIN TYPE III FOLD IN PLANT ALLERGENS: THE SOLUTION STRUCTURE OF PHL PII FROM TIMOTHY GRASS POLLEN, NMR, 38 STRUCTURES |
| 1BMX | HIV-1 CAPSID PROTEIN MAJOR HOMOLOGY REGION PEPTIDE ANALOG, NMR, 8 STRUCTURES |
| 1BMZ | HUMAN TRANSTHYRETIN (PREALBUMIN) |
| 1BN1 | CARBONIC ANHYDRASE II INHIBITOR |
| 1BN3 | CARBONIC ANHYDRASE II INHIBITOR |
| 1BN4 | CARBONIC ANHYDRASE II INHIBITOR |
| 1BN5 | HUMAN METHIONINE AMINOPEPTIDASE 2 |
| 1BN6 | HALOALKANE DEHALOGENASE FROM A RHODOCOCCUS SPECIES |
| 1BN7 | HALOALKANE DEHALOGENASE FROM A RHODOCOCCUS SPECIES |
| 1BN8 | BACILLUS SUBTILIS PECTATE LYASE |
| 1BNB | SOLUTION STRUCTURE OF BOVINE NEUTROPHIL BETA-DEFENSIN 12: THE PEPTIDE FOLD OF THE BETA-DEFENSINS IS IDENTICAL TO THAT OF THE CLASSICAL DEFENSINS |
| 1BNC | THREE-DIMENSIONAL STRUCTURE OF THE BIOTIN CARBOXYLASE SUBUNIT OF ACETYL-COA CARBOXYLASE |
| 1BND | STRUCTURE OF THE BRAIN-DERIVED NEUROTROPHIC FACTOR(SLASH)NEUROTROPHIN 3 HETERODIMER |
| 1BNE | BARNASE A43C/S80C DISULFIDE MUTANT |
| 1BNF | BARNASE T70C/S92C DISULFIDE MUTANT |
| 1BNG | BARNASE S85C/H102C DISULFIDE MUTANT |
| 1BNI | BARNASE WILDTYPE STRUCTURE AT PH 6.0 |
| 1BNJ | BARNASE WILDTYPE STRUCTURE AT PH 9.0 |
| 1BNK | HUMAN 3-METHYLADENINE DNA GLYCOSYLASE COMPLEXED TO DNA |
| 1BNL | ZINC DEPENDENT DIMERS OBSERVED IN CRYSTALS OF HUMAN ENDOSTATIN |
| 1BNM | CARBONIC ANHYDRASE II INHIBITOR |
| 1BNN | CARBONIC ANHYDRASE II INHIBITOR |
| 1BNO | NMR SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA, MINIMIZED AVERAGE STRUCTURE |
| 1BNP | NMR SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA, 55 STRUCTURES |
| 1BNQ | CARBONIC ANHYDRASE II INHIBITOR |
| 1BNR | BARNASE |
| 1BNS | STRUCTURAL STUDIES OF BARNASE MUTANTS |
| 1BNT | CARBONIC ANHYDRASE II INHIBITOR |
| 1BNU | CARBONIC ANHYDRASE II INHIBITOR |
| 1BNV | CARBONIC ANHYDRASE II INHIBITOR |
| 1BNW | CARBONIC ANHYDRASE II INHIBITOR |
| 1BNX | STRUCTURAL STUDIES ON THE EFFECTS OF THE DELETION IN THE RED CELL ANION EXCHANGER (BAND3, AE1) ASSOCIATED WITH SOUTH EAST ASIAN OVALOCYTOSIS. |
| 1BNZ | SSO7D HYPERTHERMOPHILE PROTEIN/DNA COMPLEX |
| 1BO0 | MONOCYTE CHEMOATTRACTANT PROTEIN-3, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BO1 | PHOSPHATIDYLINOSITOL PHOSPHATE KINASE TYPE II BETA |
| 1BO4 | CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE |
| 1BO5 | CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN ESCHERICHIA COLI GLYCEROL KINASE AND THE ALLOSTERIC REGULATOR FRUCTOSE 1,6-BISPHOSPHATE. |
| 1BO6 | ESTROGEN SULFOTRANSFERASE WITH INACTIVE COFACTOR PAP AND VANADATE |
| 1BO7 | THYMIDYLATE SYNTHASE R179T MUTANT |
| 1BO8 | THYMIDYLATE SYNTHASE R178T MUTANT |
| 1BO9 | NMR SOLUTION STRUCTURE OF DOMAIN 1 OF HUMAN ANNEXIN I |
| 1BOA | HUMAN METHIONINE AMINOPEPTIDASE 2 COMPLEXED WITH ANGIOGENESIS INHIBITOR FUMAGILLIN |
| 1BOB | HISTONE ACETYLTRANSFERASE HAT1 FROM SACCHAROMYCES CEREVISIAE IN COMPLEX WITH ACETYL COENZYME A |
| 1BOC | THE SOLUTION STRUCTURES OF MUTANT CALBINDIN D9K'S, AS DETERMINED BY NMR, SHOW THAT THE CALCIUM BINDING SITE CAN ADOPT DIFFERENT FOLDS |
| 1BOD | THE SOLUTION STRUCTURES OF MUTANT CALBINDIN D9K'S, AS DETERMINED BY NMR, SHOW THAT THE CALCIUM BINDING SITE CAN ADOPT DIFFERENT FOLDS |
| 1BOE | STRUCTURE OF THE IGF BINDING DOMAIN OF THE INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-5 (IGFBP-5): IMPLICATIONS FOR IGF AND IGF-I RECEPTOR INTERACTIONS |
| 1BOF | GI-ALPHA-1 BOUND TO GDP AND MAGNESIUM |
| 1BOG | ANTI-P24 (HIV-1) FAB FRAGMENT CB41 COMPLEXED WITH AN EPITOPE-HOMOLOGOUS PEPTIDE |
| 1BOH | SULFUR-SUBSTITUTED RHODANESE (ORTHORHOMBIC FORM) |
| 1BOI | N-TERMINALLY TRUNCATED RHODANESE |
| 1BOL | THE CRYSTAL STRUCTURE OF RIBONUCLEASE RH FROM RHIZOPUS NIVEUS AT 2.0 A RESOLUTION |
| 1BOM | THREE-DIMENSIONAL STRUCTURE OF BOMBYXIN-II, AN INSULIN-RELATED BRAIN-SECRETORY PEPTIDE OF THE SILKMOTH BOMBYX MORI: COMPARISON WITH INSULIN AND RELAXIN |
| 1BON | THREE-DIMENSIONAL STRUCTURE OF BOMBYXIN-II, AN INSULIN-RELATED BRAIN-SECRETORY PEPTIDE OF THE SILKMOTH BOMBYX MORI: COMPARISON WITH INSULIN AND RELAXIN |
| 1BOO | PVUII DNA METHYLTRANSFERASE (CYTOSINE-N4-SPECIFIC) |
| 1BOQ | PRO REGION C-TERMINUS: PROTEASE ACTIVE SITE INTERACTIONS ARE CRITICAL IN CATALYZING THE FOLDING OF ALPHA-LYTIC PROTEASE |
| 1BOR | TRANSCRIPTION FACTOR PML, A PROTO-ONCOPROTEIN, NMR, 1 REPRESENTATIVE STRUCTURE AT PH 7.5, 30 C, IN THE PRESENCE OF ZINC |
| 1BOS | SHIGA-LIKE TOXIN COMPLEXED WITH ITS RECEPTOR |
| 1BOT | CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN ESCHERICHIA COLI GLYCEROL KINASE AND THE ALLOSTERIC REGULATOR FRUCTOSE 1,6-BISPHOSPHATE. |
| 1BOU | THREE-DIMENSIONAL STRUCTURE OF LIGAB |
| 1BOW | MULTIDRUG-BINDING DOMAIN OF TRANSCRIPTION ACTIVATOR BMRR (APO FORM) |
| 1BOX | N39S MUTANT OF RNASE SA FROM STREPTOMYCES AUREOFACIENS |
| 1BOY | EXTRACELLULAR REGION OF HUMAN TISSUE FACTOR |
| 1BOZ | STRUCTURE-BASED DESIGN AND SYNTHESIS OF LIPOPHILIC 2,4-DIAMINO-6-SUBSTITUTED QUINAZOLINES AND THEIR EVALUATION AS INHIBITORS OF DIHYDROFOLATE REDUCTASE AND POTENTIAL ANTITUMOR AGENTS |
| 1BP0 | THYMIDYLATE SYNTHASE R23I MUTANT |
| 1BP1 | CRYSTAL STRUCTURE OF BPI, THE HUMAN BACTERICIDAL PERMEABILITY-INCREASING PROTEIN |
| 1BP2 | STRUCTURE OF BOVINE PANCREATIC PHOSPHOLIPASE A2 AT 1.7 ANGSTROMS RESOLUTION |
| 1BP3 | THE XRAY STRUCTURE OF A GROWTH HORMONE-PROLACTIN RECEPTOR COMPLEX |
| 1BP4 | USE OF PAPAIN AS A MODEL FOR THE STRUCTURE-BASED DESIGN OF CATHEPSIN K INHIBITORS. CRYSTAL STRUCTURES OF TWO PAPAIN INHIBITOR COMPLEXES DEMONSTRATE BINDING TO S'-SUBSITES. |
| 1BP5 | HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE, APO FORM |
| 1BP6 | THYMIDYLATE SYNTHASE R23I, R179T DOUBLE MUTANT |
| 1BP7 | GROUP I MOBILE INTRON ENDONUCLEASE I-CREI COMPLEXED WITH HOMING SITE DNA |
| 1BPB | CRYSTAL STRUCTURE OF RAT DNA POLYMERASE BETA: EVIDENCE FOR A COMMON POLYMERASE MECHANISM |
| 1BPD | CRYSTAL STRUCTURE OF RAT DNA POLYMERASE BETA: EVIDENCE FOR A COMMON POLYMERASE MECHANISM |
| 1BPE | CRYSTAL STRUCTURE OF RAT DNA POLYMERASE BETA; EVIDENCE FOR A COMMON POLYMERASE MECHANISM |
| 1BPH | CONFORMATIONAL CHANGES IN CUBIC INSULIN CRYSTALS IN THE PH RANGE 7-11 |
| 1BPI | THE STRUCTURE OF BOVINE PANCREATIC TRYPSIN INHIBITOR AT 125K: DEFINITION OF CARBOXYL-TERMINAL RESIDUES GLYCINE-57 AND ALANINE-58 |
| 1BPJ | THYMIDYLATE SYNTHASE R178T, R179T DOUBLE MUTANT |
| 1BPL | GLYCOSYLTRANSFERASE |
| 1BPM | DIFFERENTIATION AND IDENTIFICATION OF THE TWO CATALYTIC METAL BINDING SITES IN BOVINE LENS LEUCINE AMINOPEPTIDASE BY X-RAY CRYSTALLOGRAPHY |
| 1BPN | DIFFERENTIATION AND IDENTIFICATION OF THE TWO CATALYTIC METAL BINDING SITES IN BOVINE LENS LEUCINE AMINOPEPTIDASE BY X-RAY CRYSTALLOGRAPHY |
| 1BPO | CLATHRIN HEAVY-CHAIN TERMINAL DOMAIN AND LINKER |
| 1BPQ | PHOSPHOLIPASE A2 ENGINEERING. X-RAY STRUCTURAL AND FUNCTIONAL EVIDENCE FOR THE INTERACTION OF LYSINE-56 WITH SUBSTRATES |
| 1BPR | NMR STRUCTURE OF THE SUBSTRATE BINDING DOMAIN OF DNAK, MINIMIZED AVERAGE STRUCTURE |
| 1BPT | CREVICE-FORMING MUTANTS OF BPTI: CRYSTAL STRUCTURES OF F22A, Y23A, N43G, AND F45A |
| 1BPV | TITIN MODULE A71 FROM HUMAN CARDIAC MUSCLE, NMR, 50 STRUCTURES |
| 1BPW | BETAINE ALDEHYDE DEHYDROGENASE FROM COD LIVER |
| 1BPX | DNA POLYMERASE BETA/DNA COMPLEX |
| 1BPY | HUMAN DNA POLYMERASE BETA COMPLEXED WITH GAPPED DNA AND DDCTP |
| 1BPZ | HUMAN DNA POLYMERASE BETA COMPLEXED WITH NICKED DNA |
| 1BQ0 | J-DOMAIN (RESIDUES 1-77) OF THE ESCHERICHIA COLI N-TERMINAL FRAGMENT (RESIDUES 1-104) OF THE MOLECULAR CHAPERONE DNAJ, NMR, 20 STRUCTURES |
| 1BQ1 | E. COLI THYMIDYLATE SYNTHASE MUTANT N177A IN COMPLEX WITH CB3717 AND 2'-DEOXYURIDINE 5'-MONOPHOSPHATE (DUMP) |
| 1BQ2 | E. COLI THYMIDYLATE SYNTHASE MUTANT N177A |
| 1BQ3 | SACCHAROMYCES CEREVISIAE PHOSPHOGLYCERATE MUTASE IN COMPLEX WITH INOSITOL HEXAKISPHOSPHATE |
| 1BQ4 | SACCHAROMYCES CEREVISIAE PHOSPHOGLYCERATE MUTASE IN COMPLEX WITH BENZENE HEXACARBOXYLATE |
| 1BQ5 | NITRITE REDUCTASE FROM ALCALIGENES XYLOSOXIDANS GIFU 1051 |
| 1BQ6 | CHALCONE SYNTHASE FROM ALFALFA WITH COENZYME A |
| 1BQ7 | DSBA MUTANT P151A, ROLE OF THE CIS-PROLINE IN THE ACTIVE SITE OF DSBA |
| 1BQ8 | RUBREDOXIN (METHIONINE MUTANT) FROM PYROCOCCUS FURIOSUS |
| 1BQ9 | RUBREDOXIN (FORMYL METHIONINE MUTANT) FROM PYROCOCCUS FURIOSUS |
| 1BQA | ASPARTATE AMINOTRANSFERASE P195A MUTANT |
| 1BQB | AUREOLYSIN, STAPHYLOCOCCUS AUREUS METALLOPROTEINASE |
| 1BQC | BETA-MANNANASE FROM THERMOMONOSPORA FUSCA |
| 1BQD | ASPARTATE AMINOTRANSFERASE P138A/P195A DOUBLE MUTANT |
| 1BQE | FERREDOXIN:NADP+ REDUCTASE MUTANT WITH THR 155 REPLACED BY GLY (T155G) |
| 1BQF | GROWTH-BLOCKING PEPTIDE (GBP) FROM PSEUDALETIA SEPARATA |
| 1BQG | THE STRUCTURE OF THE D-GLUCARATE DEHYDRATASE PROTEIN FROM PSEUDOMONAS PUTIDA |
| 1BQH | MURINE CD8AA ECTODOMAIN FRAGMENT IN COMPLEX WITH H-2KB/VSV8 |
| 1BQI | USE OF PAPAIN AS A MODEL FOR THE STRUCTURE-BASED DESIGN OF CATHEPSIN K INHIBITORS. CRYSTAL STRUCTURES OF TWO PAPAIN INHIBITOR COMPLEXES DEMONSTRATE BINDING TO S'-SUBSITES. |
| 1BQK | OXIDIZED PSEUDOAZURIN |
| 1BQL | STRUCTURE OF AN ANTI-HEL FAB FRAGMENT COMPLEXED WITH BOBWHITE QUAIL LYSOZYME |
| 1BQM | HIV-1 RT/HBY 097 |
| 1BQN | TYR 188 LEU HIV-1 RT/HBY 097 |
| 1BQO | DISCOVERY OF POTENT, ACHIRAL MATRIX METALLOPROTEINASE INHIBITORS |
| 1BQP | THE STRUCTURE OF THE PEA LECTIN-D-MANNOPYRANOSE COMPLEX |
| 1BQQ | CRYSTAL STRUCTURE OF THE MT1-MMP--TIMP-2 COMPLEX |
| 1BQR | REDUCED PSEUDOAZURIN |
| 1BQS | THE CRYSTAL STRUCTURE OF MUCOSAL ADDRESSIN CELL ADHESION MOLECULE-1 (MADCAM-1) |
| 1BQT | THREE-DIMENSIONAL STRUCTURE OF HUMAN INSULIN-LIKE GROWTH FACTOR-I (IGF-I) DETERMINED BY 1H-NMR AND DISTANCE GEOMETRY, 6 STRUCTURES |
| 1BQU | CYTOKYNE-BINDING REGION OF GP130 |
| 1BQX | ARTIFICIAL FE8S8 FERREDOXIN: THE D13C VARIANT OF BACILLUS SCHLEGELII FE7S8 FERREDOXIN |
| 1BQY | PLASMINOGEN ACTIVATOR (TSV-PA) FROM SNAKE VENOM |
| 1BQZ | J-DOMAIN (RESIDUES 1-77) OF THE ESCHERICHIA COLI N-TERMINAL FRAGMENT (RESIDUES 1-78) OF THE MOLECULAR CHAPERONE DNAJ, NMR, 20 STRUCTURES |
| 1BR0 | THREE DIMENSIONAL STRUCTURE OF THE N-TERMINAL DOMAIN OF SYNTAXIN 1A |
| 1BR5 | RICIN A CHAIN (RECOMBINANT) COMPLEX WITH NEOPTERIN |
| 1BR6 | RICIN A CHAIN (RECOMBINANT) COMPLEX WITH PTEROIC ACID |
| 1BR8 | IMPLICATIONS FOR FUNCTION AND THERAPY OF A 2.9A STRUCTURE OF BINARY-COMPLEXED ANTITHROMBIN |
| 1BR9 | HUMAN TISSUE INHIBITOR OF METALLOPROTEINASE-2 |
| 1BRA | RELOCATING A NEGATIVE CHARGE IN THE BINDING POCKET OF TRYPSIN |
| 1BRC | RELOCATING A NEGATIVE CHARGE IN THE BINDING POCKET OF TRYPSIN |
| 1BRD | MODEL FOR THE STRUCTURE OF BACTERIORHODOPSIN BASED ON HIGH-RESOLUTION ELECTRON CRYO-MICROSCOPY |
| 1BRE | IMMUNOGLOBULIN LIGHT CHAIN PROTEIN |
| 1BRF | RUBREDOXIN (WILD TYPE) FROM PYROCOCCUS FURIOSUS |
| 1BRG | CRYSTALLOGRAPHIC ANALYSIS OF PHE->LEU SUBSTITUTION IN THE HYDROPHOBIC CORE OF BARNASE |
| 1BRH | BARNASE MUTANT WITH LEU 14 REPLACED BY ALA |
| 1BRI | BARNASE MUTANT WITH ILE 76 REPLACED BY ALA |
| 1BRJ | BARNASE MUTANT WITH ILE 88 REPLACED BY ALA |
| 1BRK | BARNASE MUTANT WITH ILE 96 REPLACED BY ALA |
| 1BRL | THREE-DIMENSIONAL STRUCTURE OF BACTERIAL LUCIFERASE FROM VIBRIO HARVEYI AT 2.4 ANGSTROMS RESOLUTION |
| 1BRM | ASPARTATE BETA-SEMIALDEHYDE DEHYDROGENASE FROM ESCHERICHIA COLI |
| 1BRN | SUBSITE BINDING IN AN RNASE: STRUCTURE OF A BARNASE-TETRANUCLEOTIDE COMPLEX AT 1.76 ANGSTROMS RESOLUTION |
| 1BRO | BROMOPEROXIDASE A2 |
| 1BRP | CRYSTAL STRUCTURE OF THE TRIGONAL FORM OF HUMAN PLASMA RETINOL-BINDING PROTEIN AT 2.5 ANGSTROMS RESOLUTION |
| 1BRQ | CRYSTAL STRUCTURE OF THE TRIGONAL FORM OF HUMAN PLASMA RETINOL-BINDING PROTEIN AT 2.5 ANGSTROMS RESOLUTION |
| 1BRR | X-RAY STRUCTURE OF THE BACTERIORHODOPSIN TRIMER/LIPID COMPLEX |
| 1BRS | PROTEIN-PROTEIN RECOGNITION: CRYSTAL STRUCTURAL ANALYSIS OF A BARNASE-BARSTAR COMPLEX AT 2.0-A RESOLUTION |
| 1BRT | BROMOPEROXIDASE A2 MUTANT M99T |
| 1BRU | STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH THE ELASTASE INHIBITOR GR143783 |
| 1BRV | SOLUTION NMR STRUCTURE OF THE IMMUNODOMINANT REGION OF PROTEIN G OF BOVINE RESPIRATORY SYNCYTIAL VIRUS, 48 STRUCTURES |
| 1BRW | THE CRYSTAL STRUCTURE OF PYRIMIDINE NUCLEOSIDE PHOSPHORYLASE IN A CLOSED CONFORMATION |
| 1BRX | BACTERIORHODOPSIN/LIPID COMPLEX |
| 1BRY | BRYODIN TYPE I RIP |
| 1BRZ | SOLUTION STRUCTURE OF THE SWEET PROTEIN BRAZZEIN, NMR, 43 STRUCTURES |
| 1BS0 | PLP-DEPENDENT ACYL-COA SYNTHASE |
| 1BS1 | DETHIOBIOTIN SYNTHETASE COMPLEXED WITH DETHIOBIOTIN, ADP , INORGANIC PHOSPHATE AND MAGNESIUM |
| 1BS2 | YEAST ARGINYL-TRNA SYNTHETASE |
| 1BS3 | P.SHERMANII SOD(FE+3) FLUORIDE |
| 1BS4 | PEPTIDE DEFORMYLASE AS ZN2+ CONTAINING FORM (NATIVE) IN COMPLEX WITH INHIBITOR POLYETHYLENE GLYCOL |
| 1BS5 | PEPTIDE DEFORMYLASE AS ZN2+ CONTAINING FORM |
| 1BS6 | PEPTIDE DEFORMYLASE AS NI2+ CONTAINING FORM IN COMPLEX WITH TRIPEPTIDE MET-ALA-SER |
| 1BS7 | PEPTIDE DEFORMYLASE AS NI2+ CONTAINING FORM |
| 1BS8 | PEPTIDE DEFORMYLASE AS ZN2+ CONTAINING FORM IN COMPLEX WITH TRIPEPTIDE MET-ALA-SER |
| 1BS9 | ACETYLXYLAN ESTERASE FROM P. PURPUROGENUM REFINED AT 1.10 ANGSTROMS |
| 1BSC | CRYSTAL STRUCTURAL ANALYSIS OF MUTATIONS IN THE HYDROPHOBIC CORES OF BARNASE |
| 1BSD | CRYSTAL STRUCTURAL ANALYSIS OF MUTATIONS IN THE HYDROPHOBIC CORES OF BARNASE |
| 1BSE | CRYSTAL STRUCTURAL ANALYSIS OF MUTATIONS IN THE HYDROPHOBIC CORES OF BARNASE |
| 1BSF | THERMOSTABLE THYMIDYLATE SYNTHASE A FROM BACILLUS SUBTILIS |
| 1BSG | BETA-LACTAMASE FROM STREPTOMYCES ALBUS G |
| 1BSH | SOLUTION STRUCTURE OF THE EPSILON SUBUNIT OF THE F1-ATPSYNTHASE FROM ESCHERICHIA COLI AND ORIENTATION OF THE SUBUNIT RELATIVE TO THE BETA SUBUNITS OF THE COMPLEX |
| 1BSI | HUMAN PANCREATIC ALPHA-AMYLASE FROM PICHIA PASTORIS, GLYCOSYLATED PROTEIN |
| 1BSJ | COBALT DEFORMYLASE INHIBITOR COMPLEX FROM E.COLI |
| 1BSK | ZINC DEFORMYLASE INHIBITOR COMPLEX FROM E.COLI |
| 1BSL | STRUCTURE OF ALKANAL MONOOXYGENASE BETA CHAIN |
| 1BSM | P.SHERMANII SOD(FE+3) 140K PH8 |
| 1BSN | SOLUTION STRUCTURE OF THE EPSILON SUBUNIT OF THE F1-ATPSYNTHASE FROM ESCHERICHIA COLI AND ORIENTATION OF THE SUBUNIT RELATIVE TO THE BETA SUBUNITS OF THE COMPLEX |
| 1BSO | 12-BROMODODECANOIC ACID BINDS INSIDE THE CALYX OF BOVINE BETA-LACTOGLOBULIN |
| 1BSP | THERMOSTABLE THYMIDYLATE SYNTHASE A FROM BACILLUS SUBTILIS |
| 1BSQ | STRUCTURAL AND FUNCTIONAL CONSEQUENCES OF POINT MUTATIONS OF VARIANTS A AND B OF BOVINE BETA-LACTOGLOBULIN |
| 1BSR | BOVINE SEMINAL RIBONUCLEASE STRUCTURE AT 1.9 ANGSTROMS RESOLUTION |
| 1BSS | ECORV-T93A/DNA/CA2+ |
| 1BSU | STRUCTURAL AND ENERGETIC ORIGINS OF INDIRECT READOUT IN SITE-SPECIFIC DNA CLEAVAGE BY A RESTRICTION ENDONUCLEASE |
| 1BSV | GDP-FUCOSE SYNTHETASE FROM ESCHERICHIA COLI COMPLEX WITH NADPH |
| 1BSW | ACUTOLYSIN A FROM SNAKE VENOM OF AGKISTRODON ACUTUS AT PH 7.5 |
| 1BSX | STRUCTURE AND SPECIFICITY OF NUCLEAR RECEPTOR-COACTIVATOR INTERACTIONS |
| 1BSY | STRUCTURAL BASIS OF THE TANFORD TRANSITION OF BOVINE BETA-LACTOGLOBULIN FROM CRYSTAL STRUCTURES AT THREE PH VALUES; PH 7.1 |
| 1BSZ | PEPTIDE DEFORMYLASE AS FE2+ CONTAINING FORM (NATIVE) IN COMPLEX WITH INHIBITOR POLYETHYLENE GLYCOL |
| 1BT0 | STRUCTURE OF UBIQUITIN-LIKE PROTEIN, RUB1 |
| 1BT1 | CATECHOL OXIDASE FROM IPOMOEA BATATAS (SWEET POTATOES) IN THE NATIVE CU(II)-CU(II) STATE |
| 1BT2 | CATECHOL OXIDASE FROM IPOMOEA BATATAS (SWEET POTATOES) IN THE REDUCED CU(I)-CU(I) STATE |
| 1BT3 | CATECHOL OXIDASE FROM IPOMOEA BATATAS (SWEET POTATOES) IN THE NATIVE CU(II)-CU(II) STATE |
| 1BT4 | PHOSPHOSERINE AMINOTRANSFERASE FROM BACILLUS CIRCULANS SUBSP. ALKALOPHILUS |
| 1BT5 | CRYSTAL STRUCTURE OF THE IMIPENEM INHIBITED TEM-1 BETA-LACTAMASE FROM ESCHERICHIA COLI |
| 1BT6 | P11 (S100A10), LIGAND OF ANNEXIN II IN COMPLEX WITH ANNEXIN II N-TERMINUS |
| 1BT7 | THE SOLUTION NMR STRUCTURE OF THE N-TERMINAL PROTEASE DOMAIN OF THE HEPATITIS C VIRUS (HCV) NS3-PROTEIN, FROM BK STRAIN, 20 STRUCTURES |
| 1BT8 | P.SHERMANII SOD(FE+3) PH 10.0 |
| 1BT9 | OMPF PORIN MUTANT D74A |
| 1BTA | THREE-DIMENSIONAL SOLUTION STRUCTURE AND 13C ASSIGNMENTS OF BARSTAR USING NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY |
| 1BTB | THREE-DIMENSIONAL SOLUTION STRUCTURE AND 13C ASSIGNMENTS OF BARSTAR USING NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY |
| 1BTC | THREE-DIMENSIONAL STRUCTURE OF SOYBEAN BETA-AMYLASE DETERMINED AT 3.0 ANGSTROMS RESOLUTION: PRELIMINARY CHAIN TRACING OF THE COMPLEX WITH ALPHA-CYCLODEXTRIN |
| 1BTE | CRYSTAL STRUCTURE OF THE EXTRACELLULAR DOMAIN OF THE TYPE II ACTIVIN RECEPTOR |
| 1BTG | CRYSTAL STRUCTURE OF BETA NERVE GROWTH FACTOR AT 2.5 A RESOLUTION IN C2 SPACE GROUP WITH ZN IONS BOUND |
| 1BTH | STRUCTURE OF THROMBIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR |
| 1BTI | CREVICE-FORMING MUTANTS IN THE RIGID CORE OF BOVINE PANCREATIC TRYPSIN INHIBITOR: CRYSTAL STRUCTURES OF F22A, Y23A, N43G, AND F45A |
| 1BTJ | HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE, APO FORM, CRYSTAL FORM 2 |
| 1BTK | PH DOMAIN AND BTK MOTIF FROM BRUTON'S TYROSINE KINASE MUTANT R28C |
| 1BTL | CRYSTAL STRUCTURE OF ESCHERICHIA COLI TEM1 BETA-LACTAMASE AT 1.8 ANGSTROMS RESOLUTION |
| 1BTM | TRIOSEPHOSPHATE ISOMERASE (TIM) COMPLEXED WITH 2-PHOSPHOGLYCOLIC ACID |
| 1BTN | STRUCTURE OF THE BINDING SITE FOR INOSITOL PHOSPHATES IN A PH DOMAIN |
| 1BTO | HORSE LIVER ALCOHOL DEHYDROGENASE COMPLEXED TO NADH AND (1S,3R)3-BUTYLTHIOLANE 1-OXIDE |
| 1BTP | UNIQUE BINDING OF A NOVEL SYNTHETIC INHIBITOR, N-[3-[4-[4-(AMIDINOPHENOXY)-CARBONYL]PHENYL]-2-METHYL-2-PROPENOYL]-N-ALLYLGLYCINE METHANESULFONATE TO BOVINE TRYPSIN, REVEALED BY THE CRYSTAL STRUCTURE OF THE COMPLEX |
| 1BTQ | THE SOLUTION STRUCTURES OF THE FIRST AND SECOND TRANSMEMBRANE-SPANNING SEGMENTS OF BAND 3 |
| 1BTU | PORCINE PANCREATIC ELASTASE COMPLEXED WITH (3S, 4R)-1-TOLUENESULPHONYL-3-ETHYL-AZETIDIN-2-ONE-4-CARBOXYLIC ACID |
| 1BTV | STRUCTURE OF BET V 1, NMR, 20 STRUCTURES |
| 1BTW | EPISELECTION: NOVEL KI ~NANOMOLAR INHIBITORS OF SERINE PROTEASES SELECTED BY BINDING OR CHEMISTRY ON AN ENZYME SURFACE |
| 1BTX | EPISELECTION: NOVEL KI ~NANOMOLAR INHIBITORS OF SERINE PROTEASES SELECTED BY BINDING OR CHEMISTRY ON AN ENZYME SURFACE |
| 1BTY | CRYSTAL STRUCTURE OF BETA-TRYPSIN IN COMPLEX WITH BENZAMIDINE |
| 1BTZ | EPISELECTION: NOVEL KI ~NANOMOLAR INHIBITORS OF SERINE PROTEASES SELECTED BY BINDING OR CHEMISTRY ON AN ENZYME SURFACE |
| 1BU1 | SRC FAMILY KINASE HCK SH3 DOMAIN |
| 1BU2 | X-RAY STRUCTURE OF A VIRAL CYCLIN FROM HERPESVIRUS SAIMIRI |
| 1BU3 | REFINED CRYSTAL STRUCTURE OF CALCIUM-BOUND SILVER HAKE (PI 4.2) PARVALBUMIN AT 1.65 A. |
| 1BU4 | RIBONUCLEASE 1 COMPLEX WITH 2'GMP |
| 1BU5 | X-RAY CRYSTAL STRUCTURE OF THE DESULFOVIBRIO VULGARIS (HILDENBOROUGH) APOFLAVODOXIN-RIBOFLAVIN COMPLEX |
| 1BU6 | CRYSTAL STRUCTURES OF ESCHERICHIA COLI GLYCEROL KINASE AND THE MUTANT A65T IN AN INACTIVE TETRAMER: CONFORMATIONAL CHANGES AND IMPLICATIONS FOR ALLOSTERIC REGULATION |
| 1BU7 | CRYOGENIC STRUCTURE OF CYTOCHROME P450BM-3 HEME DOMAIN |
| 1BU8 | RAT PANCREATIC LIPASE RELATED PROTEIN 2 |
| 1BU9 | SOLUTION STRUCTURE OF P18-INK4C, 21 STRUCTURES |
| 1BUA | STRUCTURAL AND ENERGETIC ORIGINS OF INDIRECT READOUT IN SITE-SPECIFIC DNA CLEAVAGE BY A RESTRICTION ENDONUCLEASE |
| 1BUC | THREE-DIMENSIONAL STRUCTURE OF BUTYRYL-COA DEHYDROGENASE FROM MEGASPHAERA ELSDENII |
| 1BUD | ACUTOLYSIN A FROM SNAKE VENOM OF AGKISTRODON ACUTUS AT PH 5.0 |
| 1BUE | NMC-A CARBAPENEMASE FROM ENTEROBACTER CLOACAE |
| 1BUG | CATECHOL OXIDASE FROM IPOMOEA BATATAS (SWEET POTATOES)-INHIBITOR COMPLEX WITH PHENYLTHIOUREA (PTU) |
| 1BUH | CRYSTAL STRUCTURE OF THE HUMAN CDK2 KINASE COMPLEX WITH CELL CYCLE-REGULATORY PROTEIN CKSHS1 |
| 1BUI | STRUCTURE OF THE TERNARY MICROPLASMIN-STAPHYLOKINASE-MICROPLASMIN COMPLEX: A PROTEINASE-COFACTOR-SUBSTRATE COMPLEX IN ACTION |
| 1BUJ | STRUCTURE OF BINASE IN SOLUTION |
| 1BUL | 6ALPHA-(HYDROXYPROPYL)PENICILLANATE ACYLATED ON NMC-A BETA-LACTAMASE FROM ENTEROBACTER CLOACAE |
| 1BUN | STRUCTURE OF BETA2-BUNGAROTOXIN: POTASSIUM CHANNEL BINDING BY KUNITZ MODULES AND TARGETED PHOSPHOLIPASE ACTION |
| 1BUO | BTB DOMAIN FROM PLZF |
| 1BUP | T13S MUTANT OF BOVINE 70 KILODALTON HEAT SHOCK PROTEIN |
| 1BUQ | SOLUTION STRUCTURE OF DELTA-5-3-KETOSTEROID ISOMERASE COMPLEXED WITH THE STEROID 19-NORTESTOSTERONE-HEMISUCCINATE |
| 1BUS | SOLUTION CONFORMATION OF PROTEINASE INHIBITOR IIA FROM BULL SEMINAL PLASMA BY 1H NUCLEAR MAGNETIC RESONANCE AND DISTANCE GEOMETRY |
| 1BUU | ONE HO3+ FORM OF RAT MANNOSE-BINDING PROTEIN A |
| 1BUV | CRYSTAL STRUCTURE OF THE MT1-MMP-TIMP-2 COMPLEX |
| 1BUW | CRYSTAL STRUCTURE OF S-NITROSO-NITROSYL HUMAN HEMOGLOBIN A |
| 1BUX | 3'-PHOSPHORYLATED NUCLEOTIDES BINDING TO NUCLEOSIDE DIPHOSPHATE KINASE |
| 1BUY | HUMAN ERYTHROPOIETIN, NMR MINIMIZED AVERAGE STRUCTURE |
| 1BUZ | SOLUTION STRUCTURE OF SPOIIAA, A PHOSPHORYLATABLE COMPONENT OF THE SYSTEM THAT REGULATES TRANSCRIPTION FACTOR SIGMA-F OF BACILLUS SUBTILIS NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BV1 | BIRCH POLLEN ALLERGEN BET V 1 |
| 1BV2 | LIPID TRANSFER PROTEIN FROM RICE SEEDS, NMR, 14 STRUCTURES |
| 1BV3 | HUMAN CARBONIC ANHYDRASE II COMPLEXED WITH UREA |
| 1BV4 | APO-MANNOSE-BINDING PROTEIN-C |
| 1BV7 | COUNTERACTING HIV-1 PROTEASE DRUG RESISTANCE: STRUCTURAL ANALYSIS OF MUTANT PROTEASES COMPLEXED WITH XV638 AND SD146, CYCLIC UREA AMIDES WITH BROAD SPECIFICITIES |
| 1BV8 | RECEPTOR DOMAIN FROM ALPHA-2-MACROGLOBULIN |
| 1BV9 | HIV-1 PROTEASE (I84V) COMPLEXED WITH XV638 OF DUPONT PHARMACEUTICALS |
| 1BVA | MANGANESE BINDING MUTANT IN CYTOCHROME C PEROXIDASE |
| 1BVB | HEME-PACKING MOTIFS REVEALED BY THE CRYSTAL STRUCTURE OF CYTOCHROME C554 FROM NITROSOMONAS EUROPAEA |
| 1BVC | STRUCTURE OF A BILIVERDIN APOMYOGLOBIN COMPLEX (FORM D) AT 118 K |
| 1BVD | STRUCTURE OF A BILIVERDIN APOMYOGLOBIN COMPLEX (FORM B) AT 98 K |
| 1BVE | HIV-1 PROTEASE-DMP323 COMPLEX IN SOLUTION, NMR, 28 STRUCTURES |
| 1BVG | HIV-1 PROTEASE-DMP323 COMPLEX IN SOLUTION, NMR MINIMIZED AVERAGE STRUCTURE |
| 1BVH | SOLUTION STRUCTURE OF A LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE |
| 1BVI | RIBONUCLEASE T1 (WILDTYPE) COMPLEXED WITH 2'GMP |
| 1BVK | HUMANIZED ANTI-LYSOZYME FV COMPLEXED WITH LYSOZYME |
| 1BVL | HUMANIZED ANTI-LYSOZYME FV |
| 1BVM | SOLUTION NMR STRUCTURE OF BOVINE PANCREATIC PHOSPHOLIPASE A2, 20 STRUCTURES |
| 1BVN | PIG PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH THE PROTEINACEOUS INHIBITOR TENDAMISTAT |
| 1BVO | DORSAL HOMOLOGUE GAMBIF1 BOUND TO DNA |
| 1BVP | THE CRYSTAL STRUCTURE OF BLUETONGUE VIRUS VP7 |
| 1BVQ | THREE-DIMENSIONAL STRUCTURE OF 4-HYDROXYBENZOYL COA THIOESTERASE FROM PSEUDOMONAS SP. STRAIN CBS-3. |
| 1BVR | M.TB. ENOYL-ACP REDUCTASE (INHA) IN COMPLEX WITH NAD+ AND C16-FATTY-ACYL-SUBSTRATE |
| 1BVS | RUVA COMPLEXED TO A HOLLIDAY JUNCTION. |
| 1BVT | METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS 569/H/9 |
| 1BVU | GLUTAMATE DEHYDROGENASE FROM THERMOCOCCUS LITORALIS |
| 1BVV | SUGAR RING DISTORTION IN THE GLYCOSYL-ENZYME INTERMEDIATE OF A FAMILY G/11 XYLANASE |
| 1BVW | CELLOBIOHYDROLASE II (CEL6A) FROM HUMICOLA INSOLENS |
| 1BVX | THE 1.8 A STRUCTURE OF GEL GROWN TETRAGONAL HEN EGG WHITE LYSOZYME |
| 1BVY | COMPLEX OF THE HEME AND FMN-BINDING DOMAINS OF THE CYTOCHROME P450(BM-3) |
| 1BVZ | ALPHA-AMYLASE II (TVAII) FROM THERMOACTINOMYCES VULGARIS R-47 |
| 1BW0 | CRYSTAL STRUCTURE OF TYROSINE AMINOTRANSFERASE FROM TRYPANOSOMA CRUZI |
| 1BW3 | THREE-DIMENSIONAL STRUCTURE IN SOLUTION OF BARWIN, A PROTEIN FROM BARLEY SEED |
| 1BW4 | THREE-DIMENSIONAL STRUCTURE IN SOLUTION OF BARWIN, A PROTEIN FROM BARLEY SEED |
| 1BW5 | THE NMR SOLUTION STRUCTURE OF THE HOMEODOMAIN OF THE RAT INSULIN GENE ENHANCER PROTEIN ISL-1, 50 STRUCTURES |
| 1BW6 | HUMAN CENTROMERE PROTEIN B (CENP-B) DNA BINDIGN DOMAIN RP1 |
| 1BW8 | MU2 ADAPTIN SUBUNIT (AP50) OF AP2 ADAPTOR (SECOND DOMAIN), COMPLEXED WITH EGFR INTERNALIZATION PEPTIDE FYRALM |
| 1BW9 | PHENYLALANINE DEHYDROGENASE STRUCTURE IN TERNARY COMPLEX WITH NAD+ AND PHENYLPYRUVATE |
| 1BWA | HIV-1 PROTEASE (V82F/I84V) DOUBLE MUTANT COMPLEXED WITH XV638 OF DUPONT PHARMACEUTICALS |
| 1BWB | HIV-1 PROTEASE (V82F/I84V) DOUBLE MUTANT COMPLEXED WITH SD146 OF DUPONT PHARMACEUTICALS |
| 1BWC | STRUCTURE OF HUMAN GLUTATHIONE REDUCTASE COMPLEXED WITH AJOENE INHIBITOR AND SUBVERSIVE SUBSTRATE |
| 1BWD | INOSAMINE-PHOSPHATE AMIDINOTRANSFERASE STRB1 FROM STREPTOMYCES GRISEUS |
| 1BWE | ARTIFICIAL FE8S8 FERREDOXIN: THE D13C VARIANT OF BACILLUS SCHLEGELII FE7S8 FERREDOXIN |
| 1BWF | ESCHERICHIA COLI GLYCEROL KINASE MUTANT WITH BOUND ATP ANALOG SHOWING SUBSTANTIAL DOMAIN MOTION |
| 1BWH | THE 1.8 A STRUCTURE OF GROUND CONTROL GROWN TETRAGONAL HEN EGG WHITE LYSOZYME |
| 1BWI | THE 1.8 A STRUCTURE OF MICROBATCH OIL DROP GROWN TETRAGONAL HEN EGG WHITE LYSOZYME |
| 1BWJ | THE 1.8 A STRUCTURE OF MICROGRAVITY GROWN TETRAGONAL HEN EGG WHITE LYSOZYME |
| 1BWK | OLD YELLOW ENZYME (OYE1) MUTANT H191N |
| 1BWL | OLD YELLOW ENZYME (OYE1) DOUBLE MUTANT H191N:N194H |
| 1BWM | A SINGLE-CHAIN T CELL RECEPTOR |
| 1BWN | PH DOMAIN AND BTK MOTIF FROM BRUTON'S TYROSINE KINASE MUTANT E41K IN COMPLEX WITH INS(1,3,4,5)P4 |
| 1BWO | THE CRYSTAL STRUCTURE OF WHEAT NON-SPECIFIC TRANSFER PROTEIN COMPLEXED WITH TWO MOLECULES OF PHOSPHOLIPID AT 2.1 A RESOLUTION |
| 1BWP | PROBING THE SUBSTRATE SPECIFICITY OF THE INTRACELLULAR BRAIN PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE |
| 1BWQ | PROBING THE SUBSTRATE SPECIFICITY OF THE INTRACELLULAR BRAIN PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE |
| 1BWR | PROBING THE SUBSTRATE SPECIFICITY OF THE INTRACELLULAR BRAIN PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE |
| 1BWU | MANNOSE-SPECIFIC AGGLUTININ (LECTIN) FROM GARLIC (ALLIUM SATIVUM) BULBS COMPLEXED WITH ALPHA-D-MANNOSE |
| 1BWV | ACTIVATED RIBULOSE 1,5-BISPHOSPHATE CARBOXYLASE/OXYGENASE (RUBISCO) COMPLEXED WITH THE REACTION INTERMEDIATE ANALOGUE 2-CARBOXYARABINITOL 1,5-BISPHOSPHATE |
| 1BWW | BENCE-JONES IMMUNOGLOBULIN REI VARIABLE PORTION, T39K MUTANT |
| 1BWX | THE SOLUTION STRUCTURE OF HUMAN PARATHYROID HORMONE FRAGMENT 1-39, NMR, 10 STRUCTURES |
| 1BWY | NMR STUDY OF BOVINE HEART FATTY ACID BINDING PROTEIN |
| 1BWZ | DIAMINOPIMELATE EPIMERASE FROM HEMOPHILUS INFLUENZAE |
| 1BX0 | FERREDOXIN:NADP+ OXIDOREDUCTASE (FERREDOXIN REDUCTASE) MUTANT E312L |
| 1BX1 | FERREDOXIN:NADP+ OXIDOREDUCTASE (FERREDOXIN REDUCTASE) MUTANT E312Q |
| 1BX2 | CRYSTAL STRUCTURE OF HLA-DR2 (DRA*0101,DRB1*1501) COMPLEXED WITH A PEPTIDE FROM HUMAN MYELIN BASIC PROTEIN |
| 1BX3 | EFFECTS OF COMMONLY USED CRYOPROTECTANTS ON GLYCOGEN PHOSPHORYLASE ACTIVITY AND STRUCTURE |
| 1BX4 | STRUCTURE OF HUMAN ADENOSINE KINASE AT 1.50 ANGSTROMS |
| 1BX6 | CRYSTAL STRUCTURE OF THE POTENT NATURAL PRODUCT INHIBITOR BALANOL IN COMPLEX WITH THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE |
| 1BX7 | HIRUSTASIN FROM HIRUDO MEDICINALIS AT 1.2 ANGSTROMS |
| 1BX8 | HIRUSTASIN FROM HIRUDO MEDICINALIS AT 1.4 ANGSTROMS |
| 1BX9 | GLUTATHIONE S-TRANSFERASE IN COMPLEX WITH HERBICIDE |
| 1BXA | AMICYANIN REDUCED, PH 4.4, 1.3 ANGSTROMS |
| 1BXD | NMR STRUCTURE OF THE HISTIDINE KINASE DOMAIN OF THE E. COLI OSMOSENSOR ENVZ |
| 1BXE | RIBOSOMAL PROTEIN L22 FROM THERMUS THERMOPHILUS |
| 1BXG | PHENYLALANINE DEHYDROGENASE STRUCTURE IN TERNARY COMPLEX WITH NAD+ AND BETA-PHENYLPROPIONATE |
| 1BXH | CONCANAVALIN A COMPLEXED TO METHYL ALPHA1-2 MANNOBIOSIDE |
| 1BXI | CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI COLICIN E9 DNASE DOMAIN WITH ITS COGNATE IMMUNITY PROTEIN IM9 |
| 1BXK | DTDP-GLUCOSE 4,6-DEHYDRATASE FROM E. COLI |
| 1BXL | STRUCTURE OF BCL-XL/BAK PEPTIDE COMPLEX, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BXM | ENGINEERED BETA-CRYPTOGEIN COMPLEXED WITH ERGOSTEROL |
| 1BXN | THE CRYSTAL STRUCTURE OF RUBISCO FROM ALCALIGENES EUTROPHUS TO 2.7 ANGSTROMS. |
| 1BXO | ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL CYCLO[(2S)-2-[[(1R)-1-(N-(L-N-(3-METHYLBUTANOYL)VALYL-L-ASPARTYL)AMINO)-3-METHYLBUT YL] HYDROXYPHOSPHINYLOXY]-3-(3-AMINOMETHYL) PHENYLPROPANOATE |
| 1BXP | SOLUTION NMR STRUCTURE OF THE COMPLEX OF ALPHA-BUNGAROTOXIN WITH A LIBRARY DERIVED PEPTIDE, 20 STRUCTURES |
| 1BXQ | ACID PROTEINASE (PENICILLOPEPSIN) COMPLEX WITH PHOSPHONATE INHIBITOR. |
| 1BXS | SHEEP LIVER CLASS 1 ALDEHYDE DEHYDROGENASE WITH NAD BOUND |
| 1BXT | STREPTOCOCCAL SUPERANTIGEN (SSA) FROM STREPTOCOCCUS PYOGENES |
| 1BXU | OXIDIZED PLASTOCYANIN FROM SYNECHOCOCCUS SP. |
| 1BXV | REDUCED PLASTOCYANIN FROM SYNECHOCOCCUS SP. |
| 1BXW | OUTER MEMBRANE PROTEIN A (OMPA) TRANSMEMBRANE DOMAIN |
| 1BXX | MU2 ADAPTIN SUBUNIT (AP50) OF AP2 ADAPTOR (SECOND DOMAIN), COMPLEXED WITH TGN38 INTERNALIZATION PEPTIDE DYQRLN |
| 1BXY | CRYSTAL STRUCTURE OF RIBOSOMAL PROTEIN L30 FROM THERMUS THERMOPHILUS AT 1.9 A RESOLUTION: CONFORMATIONAL FLEXIBILITY OF THE MOLECULE. |
| 1BXZ | CRYSTAL STRUCTURE OF A THERMOPHILIC ALCOHOL DEHYDROGENASE SUBSTRATE COMPLEX FROM THERMOANAEROBACTER BROCKII |
| 1BY0 | N-TERMINAL LEUCINE-REPEAT REGION OF HEPATITIS DELTA ANTIGEN |
| 1BY1 | DBL HOMOLOGY DOMAIN FROM BETA-PIX |
| 1BY2 | STRUCTURE OF M2BP SCAVENGER RECEPTOR CYSTEINE-RICH DOMAIN |
| 1BY3 | FHUA FROM E. COLI |
| 1BY4 | STRUCTURE AND MECHANISM OF THE HOMODIMERIC ASSEMBLY OF THE RXR ON DNA |
| 1BY5 | FHUA FROM E. COLI, WITH ITS LIGAND FERRICHROME |
| 1BY6 | PEPTIDE OF HUMAN APOLIPOPROTEIN C-II |
| 1BY7 | HUMAN PLASMINOGEN ACTIVATOR INHIBITOR-2. LOOP (66-98) DELETION MUTANT |
| 1BY8 | THE CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN K |
| 1BY9 | CRYSTAL STRUCTURE OF THE E2 DNA-BINDING DOMAIN FROM HUMAN PAPILLOMAVIRUS TYPE-16: IMPLICATIONS FOR ITS DNA BINDING-SITE SELECTION MECHANISM |
| 1BYA | CRYSTAL STRUCTURES OF SOYBEAN BETA-AMYLASE REACTED WITH BETA-MALTOSE AND MALTAL: ACTIVE SITE COMPONENTS AND THEIR APPARENT ROLE IN CATALYSIS |
| 1BYB | CRYSTAL STRUCTURES OF SOYBEAN BETA-AMYLASE REACTED WITH BETA-MALTOSE AND MALTAL: ACTIVE SITE COMPONENTS AND THEIR APPARENT ROLE IN CATALYSIS |
| 1BYC | CRYSTAL STRUCTURES OF SOYBEAN BETA-AMYLASE REACTED WITH BETA-MALTOSE AND MALTAL: ACTIVE SITE COMPONENTS AND THEIR APPARENT ROLE IN CATALYSIS |
| 1BYD | CRYSTAL STRUCTURES OF SOYBEAN BETA-AMYLASE REACTED WITH BETA-MALTOSE AND MALTAL: ACTIVE SITE COMPONENTS AND THEIR APPARENT ROLE IN CATALYSIS |
| 1BYE | GLUTATHIONE S-TRANSFERASE I FROM MAIS IN COMPLEX WITH ATRAZINE GLUTATHIONE CONJUGATE |
| 1BYF | STRUCTURE OF TC14; A C-TYPE LECTIN FROM THE TUNICATE POLYANDROCARPA MISAKIENSIS |
| 1BYG | KINASE DOMAIN OF HUMAN C-TERMINAL SRC KINASE (CSK) IN COMPLEX WITH INHIBITOR STAUROSPORINE |
| 1BYH | MOLECULAR AND ACTIVE-SITE STRUCTURE OF A BACILLUS (1-3,1-4)-BETA-GLUCANASE |
| 1BYI | STRUCTURE OF APO-DETHIOBIOTIN SYNTHASE AT 0.97 ANGSTROMS RESOLUTION |
| 1BYL | BLEOMYCIN RESISTANCE PROTEIN FROM STREPTOALLOTEICHUS HINDUSTANUS |
| 1BYM | SOLUTION STRUCTURES OF THE C-TERMINAL DOMAIN OF DIPHTHERIA TOXIN REPRESSOR |
| 1BYN | SOLUTION STRUCTURE OF THE CALCIUM-BOUND FIRST C2-DOMAIN OF SYNAPTOTAGMIN I |
| 1BYO | WILD-TYPE PLASTOCYANIN FROM SILENE |
| 1BYP | E43K,D44K DOUBLE MUTANT PLASTOCYANIN FROM SILENE |
| 1BYQ | HSP90 N-TERMINAL DOMAIN BOUND TO ADP-MG |
| 1BYR | CRYSTAL STRUCTURE OF A PHOSPHOLIPASE D FAMILY MEMBER, NUC FROM SALMONELLA TYPHIMURIUM |
| 1BYS | CRYSTAL STRUCTURE OF NUC COMPLEXED WITH TUNGSTATE |
| 1BYU | CANINE GDP-RAN |
| 1BYV | GLYCOSYLATED EEL CALCITONIN |
| 1BYW | STRUCTURE OF THE N-TERMINAL DOMAIN OF THE HUMAN-ERG POTASSIUM CHANNEL |
| 1BYY | SODIUM CHANNEL IIA INACTIVATION GATE |
| 1BYZ | DESIGNED PEPTIDE ALPHA-1, P1 FORM |
| 1BZ0 | HEMOGLOBIN A (HUMAN, DEOXY, HIGH SALT) |
| 1BZ1 | HEMOGLOBIN (ALPHA + MET) VARIANT |
| 1BZ4 | APOLIPOPROTEIN E3 (APO-E3), TRUNCATION MUTANT 165 |
| 1BZ5 | EVIDENCE OF A COMMON DECAMER IN THREE CRYSTAL STRUCTURES OF BPTI, CRYSTALLIZE FROM THIOCYANATE, CHLORIDE OR SULFATE |
| 1BZ6 | ATOMIC RESOLUTION CRYSTAL STRUCTURE AQUOMET-MYOGLOBIN FROM SPERM WHALE AT ROOM TEMPERATURE |
| 1BZ7 | FAB FRAGMENT FROM MURINE ASCITES |
| 1BZ8 | TRANSTHYRETIN (DEL VAL122) |
| 1BZ9 | CRYSTAL STRUCTURE OF MURINE CLASS I MHC H2-DB COMPLEXED WITH A SYNTHETIC PEPTIDE P1027 |
| 1BZA | BETA-LACTAMASE TOHO-1 FROM ESCHERICHIA COLI TUH12191 |
| 1BZB | GLYCOSYLATED EEL CALCITONIN |
| 1BZC | HUMAN PTP1B CATALYTIC DOMAIN COMPLEXED WITH TPI |
| 1BZD | TERTIARY STRUCTURES OF THREE AMYLOIDOGENIC TRANSTHYRETIN VARIANTS AND IMPLICATIONS FOR AMYLOID FIBRIL FORMATION |
| 1BZE | TERTIARY STRUCTURES OF THREE AMYLOIDOGENIC TRANSTHYRETIN VARIANTS AND IMPLICATIONS FOR AMYLOID FIBRIL FORMATION |
| 1BZF | NMR SOLUTION STRUCTURE AND DYNAMICS OF THE COMPLEX OF LACTOBACILLUS CASEI DIHYDROFOLATE REDUCTASE WITH THE NEW LIPOPHILIC ANTIFOLATE DRUG TRIMETREXATE, 22 STRUCTURES |
| 1BZG | THE SOLUTION STRUCTURE OF HUMAN PARATHYROID HORMONE-RELATED PROTEIN (1-34) IN NEAR-PHYSIOLOGICAL SOLUTION, NMR, 30 STRUCTURES |
| 1BZH | CYCLIC PEPTIDE INHIBITOR OF HUMAN PTP1B |
| 1BZJ | HUMAN PTP1B COMPLEXED WITH TPICOOH |
| 1BZK | STRUCTURAL STUDIES ON THE EFFECTS OF THE DELETION IN THE RED CELL ANION EXCHANGER (BAND3, AE1) ASSOCIATED WITH SOUTH EAST ASIAN OVALOCYTOSIS. |
| 1BZL | CRYSTAL STRUCTURE OF TRYPANOSOMA CRUZI TRYPANOTHIONE REDUCTASE IN COMPLEX WITH TRYPANOTHIONE, AND THE STRUCTURE-BASED DISCOVERY OF NEW NATURAL PRODUCT INHIBITORS |
| 1BZM | DRUG-PROTEIN INTERACTIONS: STRUCTURE OF SULFONAMIDE DRUG COMPLEXED WITH HUMAN CARBONIC ANHYDRASE I |
| 1BZO | THREE-DIMENSIONAL STRUCTURE OF PROKARYOTIC CU,ZN SUPEROXIDE DISMUTASE FROM P.LEIOGNATHI, SOLVED BY X-RAY CRYSTALLOGRAPHY. |
| 1BZP | ATOMIC RESOLUTION CRYSTAL STRUCTURE ANALYSIS OF NATIVE DEOXY AND CO MYOGLOBIN FROM SPERM WHALE AT ROOM TEMPERATURE |
| 1BZQ | COMPLEX OF A DROMEDARY SINGLE-DOMAIN VHH ANTIBODY FRAGMENT WITH RNASE A |
| 1BZR | ATOMIC RESOLUTION CRYSTAL STRUCTURE ANALYSIS OF NATIVE DEOXY AND CO MYOGLOBIN FROM SPERM WHALE AT ROOM TEMPERATURE |
| 1BZS | CRYSTAL STRUCTURE OF MMP8 COMPLEXED WITH HMR2909 |
| 1BZV | [D-ALAB26]-DES(B27-B30)-INSULIN-B26-AMIDE A SUPERPOTENT SINGLE-REPLACEMENT INSULIN ANALOGUE, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1BZW | PEANUT LECTIN COMPLEXED WITH C-LACTOSE |
| 1BZX | THE CRYSTAL STRUCTURE OF ANIONIC SALMON TRYPSIN IN COMPLEX WITH BOVINE PANCREATIC TRYPSIN INHIBITOR |
| 1BZY | HUMAN HGPRTASE WITH TRANSITION STATE INHIBITOR |
| 1BZZ | HEMOGLOBIN (ALPHA V1M) MUTANT |
| 1C01 | SOLUTION STRUCTURE OF MIAMP1, A PLANT ANTIMICROBIAL PROTEIN |
| 1C02 | CRYSTAL STRUCTURE OF YEAST YPD1P |
| 1C03 | CRYSTAL STRUCTURE OF YPD1P (TRICLINIC FORM) |
| 1C04 | IDENTIFICATION OF KNOWN PROTEIN AND RNA STRUCTURES IN A 5 A MAP OF THE LARGE RIBOSOMAL SUBUNIT FROM HALOARCULA MARISMORTUI |
| 1C05 | SOLUTION STRUCTURE OF RIBOSOMAL PROTEIN S4 DELTA 41, REFINED WITH DIPOLAR COUPLINGS (MINIMIZED AVERAGE STRUCTURE) |
| 1C06 | SOLUTION STRUCTURE OF RIBOSOMAL PROTEIN S4 DELTA 41, REFINED WITH DIPOLAR COUPLINGS (ENSEMBLE OF 16 STRUCTURES) |
| 1C07 | STRUCTURE OF THE THIRD EPS15 HOMOLOGY DOMAIN OF HUMAN EPS15 |
| 1C08 | CRYSTAL STRUCTURE OF HYHEL-10 FV-HEN LYSOZYME COMPLEX |
| 1C09 | RUBREDOXIN V44A CP |
| 1C0A | CRYSTAL STRUCTURE OF THE E. COLI ASPARTYL-TRNA SYNTHETASE : TRNAASP : ASPARTYL-ADENYLATE COMPLEX |
| 1C0B | BOVINE PANCREATIC RIBONUCLEASE A DESICCATED FOR 2.5 DAYS |
| 1C0C | BOVINE PANCREATIC RIBONUCLEASE A DESICCATED FOR 4.0 DAYS |
| 1C0E | ACTIVE SITE S19A MUTANT OF BOVINE HEART PHOSPHOTYROSYL PHOSPHATASE |
| 1C0F | CRYSTAL STRUCTURE OF DICTYOSTELIUM CAATP-ACTIN IN COMPLEX WITH GELSOLIN SEGMENT 1 |
| 1C0G | CRYSTAL STRUCTURE OF 1:1 COMPLEX BETWEEN GELSOLIN SEGMENT 1 AND A DICTYOSTELIUM/TETRAHYMENA CHIMERA ACTIN (MUTANT 228: Q228K/T229A/A230Y/E360H) |
| 1C0I | CRYSTAL STRUCTURE OF D-AMINO ACID OXIDASE IN COMPLEX WITH TWO ANTHRANYLATE MOLECULES |
| 1C0K | CRYSTAL STRUCTURE ANALYSIS OF D-AMINO ACID OXIDASE IN COMPLEX WITH L-LACTATE |
| 1C0L | D-AMINO ACID OXIDASE: STRUCTURE OF SUBSTRATE COMPLEXES AT VERY HIGH RESOLUTION REVEAL THE CHEMICAL REACTTION MECHANISM OF FLAVIN DEHYDROGENATION |
| 1C0M | CRYSTAL STRUCTURE OF RSV TWO-DOMAIN INTEGRASE |
| 1C0N | CSDB PROTEIN, NIFS HOMOLOGUE |
| 1C0P | D-AMINO ACIC OXIDASE IN COMPLEX WITH D-ALANINE AND A PARTIALLY OCCUPIED BIATOMIC SPECIES |
| 1C0T | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH BM+21.1326 |
| 1C0U | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH BM+50.0934 |
| 1C0V | SUBUNIT C OF THE F1FO ATP SYNTHASE OF ESCHERICHIA COLI; NMR, 10 STRUCTURES |
| 1C0W | CRYSTAL STRUCTURE OF THE COBALT-ACTIVATED DIPHTHERIA TOXIN REPRESSOR-DNA COMPLEX REVEALS A METAL BINDING SH-LIKE DOMAIN |
| 1C10 | CRYSTAL STRUCTURE OF HEW LYSOZYME UNDER PRESSURE OF XENON (8 BAR) |
| 1C12 | INSIGHT IN ODORANT PERCEPTION: THE CRYSTAL STRUCTURE AND BINDING CHARACTERISTICS OF ANTIBODY FRAGMENTS DIRECTED AGAINST THE MUSK ODORANT TRASEOLIDE |
| 1C14 | CRYSTAL STRUCTURE OF E COLI ENOYL REDUCTASE-NAD+-TRICLOSAN COMPLEX |
| 1C15 | SOLUTION STRUCTURE OF APAF-1 CARD |
| 1C16 | CRYSTAL STRUCTURE ANALYSIS OF THE GAMMA/DELTA T CELL LIGAND T22 |
| 1C17 | A1C12 SUBCOMPLEX OF F1FO ATP SYNTHASE |
| 1C1A | CRYSTAL STRUCTURE OF RSV TWO-DOMAIN INTEGRASE |
| 1C1B | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GCA-186 |
| 1C1C | CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH TNK-6123 |
| 1C1D | L-PHENYLALANINE DEHYDROGENASE STRUCTURE IN TERNARY COMPLEX WITH NADH AND L-PHENYLALANINE |
| 1C1E | CRYSTAL STRUCTURE OF A DIELS-ALDERASE CATALYTIC ANTIBODY 1E9 IN COMPLEX WITH ITS HAPTEN |
| 1C1F | LIGAND-FREE CONGERIN I |
| 1C1G | CRYSTAL STRUCTURE OF TROPOMYOSIN AT 7 ANGSTROMS RESOLUTION IN THE SPERMINE-INDUCED CRYSTAL FORM |
| 1C1H | CRYSTAL STRUCTURE OF BACILLUS SUBTILIS FERROCHELATASE IN COMPLEX WITH N-METHYL MESOPORPHYRIN |
| 1C1J | STRUCTURE OF CADMIUM-SUBSTITUTED PHOSPHOLIPASE A2 FROM AGKISTRONDON HALYS PALLAS AT 2.8 ANGSTROMS RESOLUTION |
| 1C1K | BACTERIOPHAGE T4 GENE 59 HELICASE ASSEMBLY PROTEIN |
| 1C1L | LACTOSE-LIGANDED CONGERIN I |
| 1C1M | PORCINE ELASTASE UNDER XENON PRESSURE (8 BAR) |
| 1C1N | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1O | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1P | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1Q | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1R | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1S | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1T | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1U | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1V | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1W | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C1X | L-PHENYLALANINE DEHYDROGENASE STRUCTURE IN TERNARY COMPLEX WITH NAD+ AND L-3-PHENYLLACTATE |
| 1C1Y | CRYSTAL STRUCTURE OF RAP.GMPPNP IN COMPLEX WITH THE RAS-BINDING-DOMAIN OF C-RAF1 KINASE (RAFRBD). |
| 1C1Z | CRYSTAL STRUCTURE OF HUMAN BETA-2-GLYCOPROTEIN-I (APOLIPOPROTEIN-H) |
| 1C20 | SOLUTION STRUCTURE OF THE DNA-BINDING DOMAIN FROM THE DEAD RINGER PROTEIN |
| 1C21 | E. COLI METHIONINE AMINOPEPTIDASE: METHIONINE COMPLEX |
| 1C22 | E. COLI METHIONINE AMINOPEPTIDASE: TRIFLUOROMETHIONINE COMPLEX |
| 1C23 | E. COLI METHIONINE AMINOPEPTIDASE: METHIONINE PHOSPHONATE COMPLEX |
| 1C24 | E. COLI METHIONINE AMINOPEPTIDASE: METHIONINE PHOSPHINATE COMPLEX |
| 1C25 | HUMAN CDC25A CATALYTIC DOMAIN |
| 1C26 | CRYSTAL STRUCTURE OF P53 TETRAMERIZATION DOMAIN |
| 1C27 | E. COLI METHIONINE AMINOPEPTIDASE:NORLEUCINE PHOSPHONATE COMPLEX |
| 1C28 | THE CRYSTAL STRUCTURE OF A COMPLMENT-1Q FAMILY PROTEIN SUGGESTS AN EVOLUTIONARY LINK TO TUMOR NECROSIS FACTOR |
| 1C29 | CRYSTAL STRUCTURE OF THE COMPLEX OF BACTERIAL TRYPTOPHAN SYNTHASE WITH THE TRANSITION STATE ANALOGUE INHIBITOR 4-(2-HYDROXYPHENYLTHIO)-1-BUTENYLPHOSPHONIC ACID |
| 1C2A | CRYSTAL STRUCTURE OF BARLEY BBI |
| 1C2B | ELECTROPHORUS ELECTRICUS ACETYLCHOLINESTERASE |
| 1C2D | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2E | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2F | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2G | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2H | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2I | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2J | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2K | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2L | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2M | RECRUITING ZINC TO MEDIATE POTENT, SPECIFIC INHIBITION OF SERINE PROTEASES |
| 1C2N | CYTOCHROME C2, NMR, 20 STRUCTURES |
| 1C2P | HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE |
| 1C2R | MOLECULAR STRUCTURE OF CYTOCHROME C2 ISOLATED FROM RHODOBACTER CAPSULATUS DETERMINED AT 2.5 ANGSTROMS RESOLUTION |
| 1C2T | NEW INSIGHTS INTO INHIBITOR DESIGN FROM THE CRYSTAL STRUCTURE AND NMR STUDIES OF E. COLI GAR TRANSFORMYLASE IN COMPLEX WITH BETA-GAR AND 10-FORMYL-5,8,10-TRIDEAZAFOLIC ACID. |
| 1C2U | SOLUTION STRUCTURE OF [ABU3,35]SHK12-28,17-32 |
| 1C39 | STRUCTURE OF CATION-DEPENDENT MANNOSE 6-PHOSPHATE RECEPTOR BOUND TO PENTAMANNOSYL PHOSPHATE |
| 1C3A | CRYSTAL STRUCTURE OF FLAVOCETIN-A FROM THE HABU SNAKE VENOM, A NOVEL CYCLIC TETRAMER OF C-TYPE LECTIN-LIKE HETERODIMERS |
| 1C3B | AMPC BETA-LACTAMASE FROM E. COLI COMPLEXED WITH INHIBITOR, BENZO(B)THIOPHENE-2-BORONIC ACID (BZB) |
| 1C3C | T. MARITIMA ADENYLOSUCCINATE LYASE |
| 1C3D | X-RAY CRYSTAL STRUCTURE OF C3D: A C3 FRAGMENT AND LIGAND FOR COMPLEMENT RECEPTOR 2 |
| 1C3E | NEW INSIGHTS INTO INHIBITOR DESIGN FROM THE CRYSTAL STRUCTURE AND NMR STUDIES OF E. COLI GAR TRANSFORMYLATE IN COMPLEX WITH BETA-GAR AND 10-FORMYL-5,8,10-TRIDEAZAFOLIC ACID. |
| 1C3F | ENDO-BETA-N-ACETYLGLUCOSAMINIDASE H, D130N MUTANT |
| 1C3G | S. CEREVISIAE HEAT SHOCK PROTEIN 40 SIS1 |
| 1C3H | ACRP30 CALCIUM COMPLEX |
| 1C3I | HUMAN STROMELYSIN-1 CATALYTIC DOMAIN COMPLEXED WITH RO-26-2812 |
| 1C3J | T4 PHAGE BETA-GLUCOSYLTRANSFERASE: SUBSTRATE BINDING AND PROPOSED CATALYTIC MECHANISM |
| 1C3K | CRYSTAL STRUCTURE OF HELIANTHUS TUBEROSUS LECTIN |
| 1C3L | SUBTILISIN-CARLSBERG COMPLEXED WITH XENON (8 BAR) |
| 1C3M | CRYSTAL STRUCTURE OF HELTUBA COMPLEXED TO MAN(1-3)MAN |
| 1C3N | CRYSTAL STRUCTURE OF HELIANTHUS TUBEROSUS LECTIN COMPLEXED TO MAN(1-2)MAN |
| 1C3P | CRYSTAL STRUCTURE OF AN HDAC HOMOLOG FROM AQUIFEX AEOLICUS |
| 1C3Q | CRYSTAL STRUCTURE OF NATIVE THIAZOLE KINASE IN THE MONOCLINIC FORM |
| 1C3R | CRYSTAL STRUCTURE OF AN HDAC HOMOLOG COMPLEXED WITH TRICHOSTATIN A |
| 1C3S | CRYSTAL STRUCTURE OF AN HDAC HOMOLOG COMPLEXED WITH SAHA |
| 1C3T | ROTAMER STRAIN AS A DETERMINANT OF PROTEIN STRUCTURAL SPECIFICITY |
| 1C3U | T. MARITIMA ADENYLOSUCCINATE LYASE |
| 1C3V | DIHYDRODIPICOLINATE REDUCTASE FROM MYCOBACTERIUM TUBERCULOSIS COMPLEXED WITH NADPH AND PDC |
| 1C3W | BACTERIORHODOPSIN/LIPID COMPLEX AT 1.55 A RESOLUTION |
| 1C3X | PURINE NUCLEOSIDE PHOSPHORYLASE FROM CELLULOMONAS SP. IN COMPLEX WITH 8-IODO-GUANINE |
| 1C3Y | THP12-CARRIER PROTEIN FROM YELLOW MEAL WORM |
| 1C3Z | THP12-CARRIER PROTEIN FROM YELLOW MEAL WORM |
| 1C40 | BAR-HEADED GOOSE HEMOGLOBIN (AQUOMET FORM) |
| 1C41 | CRYSTAL STRUCTURES OF A PENTAMERIC FUNGAL AND AN ICOSAHEDRAL PLANT LUMAZINE SYNTHASE REVEALS THE STRUCTURAL BASIS FOR DIFFERENCES IN ASSEMBLY |
| 1C43 | MUTANT HUMAN LYSOZYME WITH FOREIGN N-TERMINAL RESIDUES |
| 1C44 | STEROL CARRIER PROTEIN 2 (SCP2) FROM RABBIT |
| 1C45 | MUTANT HUMAN LYSOZYME WITH FOREIGN N-TERMINAL RESIDUES |
| 1C46 | MUTANT HUMAN LYSOZYME WITH FOREIGN N-TERMINAL RESIDUES |
| 1C47 | BINDING DRIVEN STRUCTURAL CHANGES IN CRYSTALINE PHOSPHOGLUCOMUTASE ASSOCIATED WITH CHEMICAL REACTION |
| 1C48 | MUTATED SHIGA-LIKE TOXIN B SUBUNIT (G62T) |
| 1C49 | STRUCTURAL AND FUNCTIONAL DIFFERENCES OF TWO TOXINS FROM THE SCORPION PANDINUS IMPERATOR |
| 1C4A | BINDING OF EXOGENOUSLY ADDED CARBON MONOXIDE AT THE ACTIVE SITE OF THE FE-ONLY HYDROGENASE (CPI) FROM CLOSTRIDIUM PASTEURIANUM |
| 1C4C | BINDING OF EXOGENOUSLY ADDED CARBON MONOXIDE AT THE ACTIVE SITE OF THE FE-ONLY HYDROGENASE (CPI) FROM CLOSTRIDIUM PASTEURIANUM |
| 1C4D | GRAMICIDIN CSCL COMPLEX |
| 1C4E | GURMARIN FROM GYMNEMA SYLVESTRE |
| 1C4F | GREEN FLUORESCENT PROTEIN S65T AT PH 4.6 |
| 1C4G | PHOSPHOGLUCOMUTASE VANADATE BASED TRANSITION STATE ANALOG COMPLEX |
| 1C4K | ORNITHINE DECARBOXYLASE MUTANT (GLY121TYR) |
| 1C4O | CRYSTAL STRUCTURE OF THE DNA NUCLEOTIDE EXCISION REPAIR ENZYME UVRB FROM THERMUS THERMOPHILUS |
| 1C4P | BETA DOMAIN OF STREPTOKINASE |
| 1C4Q | MUTATED SHIGA-LIKE TOXIN B SUBUNIT (F30A/W34A) COMPLEXED WITH RECEPTOR GB3 ANALOGUE |
| 1C4R | THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING |
| 1C4T | CATALYTIC DOMAIN FROM TRIMERIC DIHYDROLIPOAMIDE SUCCINYLTRANSFERASE |
| 1C4U | SELECTIVE NON ELECTROPHILIC THROMBIN INHIBITORS WITH CYCLOHEXYL MOIETIES. |
| 1C4V | SELECTIVE NON ELECTROPHILIC THROMBIN INHIBITORS WITH CYCLOHEXYL MOIETIES. |
| 1C4W | 1.9 A STRUCTURE OF A-THIOPHOSPHONATE MODIFIED CHEY D57C |
| 1C4X | 2-HYDROXY-6-OXO-6-PHENYLHEXA-2,4-DIENOATE HYDROLASE (BPHD) FROM RHODOCOCCUS SP. STRAIN RHA1 |
| 1C4Y | SELECTIVE NON-ELECTROPHILIC THROMBIN INHIBITORS |
| 1C4Z | STRUCTURE OF AN E6AP-UBCH7 COMPLEX: INSIGHTS INTO THE UBIQUITINATION PATHWAY |
| 1C50 | IDENTIFICATION AND STRUCTURAL CHARACTERIZATION OF A NOVEL ALLOSTERIC BINDING SITE OF GLYCOGEN PHOSPHORYLASE B |
| 1C52 | THERMUS THERMOPHILUS CYTOCHROME-C552: A NEW HIGHLY THERMOSTABLE CYTOCHROME-C STRUCTURE OBTAINED BY MAD PHASING |
| 1C53 | S-CLASS CYTOCHROMES C HAVE A VARIETY OF FOLDING PATTERNS: STRUCTURE OF CYTOCHROME C-553 FROM DESULFOVIBRIO VULGARIS DETERMINED BY THE MULTI-WAVELENGTH ANOMALOUS DISPERSION METHOD |
| 1C54 | SOLUTION STRUCTURE OF RIBONUCLEASE SA |
| 1C55 | NMR SOLUTION STRUCTURE OF BUTANTOXIN |
| 1C56 | NMR SOLUTION STRUCTURE OF BUTANTOXIN |
| 1C57 | DIRECT DETERMINATION OF THE POSITIONS OF DEUTERIUM ATOMS OF BOUND WATER IN CONCANAVALIN A BY NEUTRON LAUE CRYSTALLOGRAPHY |
| 1C5A | THREE-DIMENSIONAL STRUCTURE OF PORCINE C5ADES*ARG FROM 1H NUCLEAR MAGNETIC RESONANCE DATA |
| 1C5B | DECARBOXYLASE CATALYTIC ANTIBODY 21D8 UNLIGANDED FORM |
| 1C5C | DECARBOXYLASE CATALYTIC ANTIBODY 21D8-HAPTEN COMPLEX |
| 1C5D | THE CRYSTAL STRUCTURE OF THE FAB FRAGMENT OF A RAT MONOCLONAL ANTIBODY AGAINST THE MAIN IMMUNOGENIC REGION OF THE HUMAN MUSCLE ACETYLCHOLINE RECEPTOR |
| 1C5E | BACTERIOPHAGE LAMBDA HEAD PROTEIN D |
| 1C5F | CRYSTAL STRUCTURE OF THE CYCLOPHILIN-LIKE DOMAIN FROM BRUGIA MALAYI COMPLEXED WITH CYCLOSPORIN A |
| 1C5G | PLASMINOGEN ACTIVATOR INHIBITOR-1 |
| 1C5H | HYDROGEN BONDING AND CATALYSIS: AN UNEXPECTED EXPLANATION FOR HOW A SINGLE AMINO ACID SUBSTITUTION CAN CHANGE THE PH OPTIMUM OF A GLYCOSIDASE |
| 1C5I | HYDROGEN BONDING AND CATALYSIS: AN UNEXPECTED EXPLANATION FOR HOW A SINGLE AMINO ACID SUBSTITUTION CAN CHANGE THE PH OPTIMUM OF A GLYCOSIDASE |
| 1C5K | THE STRUCTURE OF TOLB, AN ESSENTIAL COMPONENT OF THE TOL-DEPENDENT TRANSLOCATION SYSTEM AND ITS INTERACTIONS WITH THE TRANSLOCATION DOMAIN OF COLICIN E9 |
| 1C5L | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5M | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5N | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5O | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5P | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5Q | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5R | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5S | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5T | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5U | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5V | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5W | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5X | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5Y | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C5Z | STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
| 1C60 | T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM ARGON |
| 1C61 | T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM KRYPTON |
| 1C62 | T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM XENON |
| 1C63 | T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM ARGON |
| 1C64 | T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM KRYPTON |
| 1C65 | T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM XENON |
| 1C66 | T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM ARGON |
| 1C67 | T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM KRYPTON |
| 1C68 | T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM XENON |
| 1C69 | T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM ARGON |
| 1C6A | T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM KRYPTON |
| 1C6B | T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM XENON |
| 1C6C | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 16 ATM ARGON |
| 1C6D | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 16 ATM KRYPTON |
| 1C6E | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 2 ATM XENON |
| 1C6F | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 32 ATM ARGON |
| 1C6G | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 4 ATM KRYPTON |
| 1C6H | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 4 ATM XENON |
| 1C6I | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM ARGON |
| 1C6J | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM KRYPTON |
| 1C6K | T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM XENON |
| 1C6L | T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM ARGON |
| 1C6M | T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM KRYPTON |
| 1C6N | T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM XENON |
| 1C6O | CRYSTAL STRUCTURE OF OXIDIZED CYTOCHROME C6 FROM THE GREEN ALGAE SCENEDESMUS OBLIQUUS |
| 1C6P | T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM ARGON |
| 1C6Q | T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM KRYPTON |
| 1C6R | CRYSTAL STRUCTURE OF REDUCED CYTOCHROME C6 FROM THE GREEN ALGAE SCENEDESMUS OBLIQUUS |
| 1C6S | THE SOLUTION STRUCTURE OF CYTOCHROME C6 FROM THE THERMOPHILIC CYANOBACTERIUM SYNECHOCOCCUS ELONGATUS, NMR, 20 STRUCTURES |
| 1C6T | T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM XENON |
| 1C6V | SIV INTEGRASE (CATALYTIC DOMAIN + DNA BIDING DOMAIN COMPRISING RESIDUES 50-293) MUTANT WITH PHE 185 REPLACED BY HIS (F185H) |
| 1C6W | MAUROCALCIN FROM SCORPIO MAURUS |
| 1C6X | ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. |
| 1C6Y | ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. |
| 1C6Z | ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. |
| 1C70 | ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. |
| 1C72 | TYR115, GLN165 AND TRP209 CONTRIBUTE TO THE 1,2-EPOXY-3-(P-NITROPHENOXY)PROPANE CONJUGATING ACTIVITIES OF GLUTATHIONE S-TRANSFERASE CGSTM1-1 |
| 1C74 | STRUCTURE OF THE DOUBLE MUTANT (K53,56M) OF PHOSPHOLIPASE A2 |
| 1C75 | 0.97 A AB INITIO" CRYSTAL STRUCTURE OF CYTOCHROME C-553 FROM BACILLUS PASTEURII" |
| 1C76 | STAPHYLOKINASE (SAK) MONOMER |
| 1C77 | STAPHYLOKINASE (SAK) DIMER |
| 1C78 | STAPHYLOKINASE (SAK) DIMER |
| 1C79 | STAPHYLOKINASE (SAK) DIMER |
| 1C7B | DEOXY RHB1.0 (RECOMBINANT HEMOGLOBIN) |
| 1C7C | DEOXY RHB1.1 (RECOMBINANT HEMOGLOBIN) |
| 1C7D | DEOXY RHB1.2 (RECOMBINANT HEMOGLOBIN) |
| 1C7E | D95E HYDROQUINONE FLAVODOXIN MUTANT FROM D. VULGARIS |
| 1C7F | D95E OXIDIZED FLAVODOXIN MUTANT FROM D. VULGARIS |
| 1C7G | TYROSINE PHENOL-LYASE FROM ERWINIA HERBICOLA |
| 1C7H | CRYSTAL STRUCTURE OF A MUTANT R75A IN KETOSTEROID ISOMERASE FROM PSEDOMONAS PUTIDA BIOTYPE B |
| 1C7I | THERMOPHYLIC PNB ESTERASE |
| 1C7J | PNB ESTERASE 56C8 |
| 1C7K | CRYSTAL STRUCTURE OF THE ZINC PROTEASE |
| 1C7M | SOLUTION STRUCTURE OF THE FUNCTIONAL DOMAIN OF PARACOCCUS DENITRIFICANS CYTOCHROME C552 IN THE REDUCED STATE |
| 1C7N | CRYSTAL STRUCTURE OF CYSTALYSIN FROM TREPONEMA DENTICOLA CONTAINS A PYRIDOXAL 5'-PHOSPHATE COFACTOR |
| 1C7P | CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME WITH FOUR EXTRA RESIDUES (EAEA) AT THE N-TERMINAL |
| 1C7Q | THE CRYSTAL STRUCTURE OF PHOSPHOGLUCOSE ISOMERASE/AUTOCRINE MOTILITY FACTOR/NEUROLEUKIN COMPLEXED WITH ITS CARBOHYDRATE PHOSPHATE INHIBITORS AND ITS SUBSTRATE RECOGNITION MECHANISM |
| 1C7R | THE CRYSTAL STRUCTURE OF PHOSPHOGLUCOSE ISOMERASE/AUTOCRINE MOTILITY FACTOR/NEUROLEUKIN COMPLEXED WITH ITS CARBOHYDRATE PHOSPHATE INHIBITORS AND ITS SUBSTRATE RECOGNITION MECHANISM |
| 1C7S | BETA-N-ACETYLHEXOSAMINIDASE MUTANT D539A COMPLEXED WITH DI-N-ACETYL-BETA-D-GLUCOSAMINE (CHITOBIASE) |
| 1C7T | BETA-N-ACETYLHEXOSAMINIDASE MUTANT E540D COMPLEXED WITH DI-N ACETYL-D-GLUCOSAMINE (CHITOBIASE) |
| 1C7U | COMPLEX OF THE DNA BINDING CORE DOMAIN OF THE TRANSCRIPTION FACTOR MEF2A WITH A 20MER OLIGONUCLEOTIDE |
| 1C7V | NMR SOLUTION STRUCTURE OF THE CALCIUM-BOUND C-TERMINAL DOMAIN (W81-S161) OF CALCIUM VECTOR PROTEIN FROM AMPHIOXUS |
| 1C7W | NMR SOLUTION STRUCTURE OF THE CALCIUM-BOUND C-TERMINAL DOMAIN (W81-S161) OF CALCIUM VECTOR PROTEIN FROM AMPHIOXUS |
| 1C7Y | E.COLI RUVA-HOLLIDAY JUNCTION COMPLEX |
| 1C7Z | REGULATORY COMPLEX OF FRUCTOSE-2,6-BISPHOSPHATASE |
| 1C80 | REGULATORY COMPLEX OF FRUCTOSE-2,6-BISPHOSPHATASE |
| 1C81 | MICHAELIS COMPLEX OF FRUCTOSE-2,6-BISPHOSPHATASE |
| 1C82 | MECHANISM OF HYALURONAN BINDING AND DEGRADATION: STRUCTURE OF STREPTOCOCCUS PNEUMONIAE HYALURONATE LYASE IN COMPLEX WITH HYALURONIC ACID DISACCHARIDE AT 1.7 A RESOLUTION |
| 1C83 | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH 6-(OXALYL-AMINO)-1H-INDOLE-5-CARBOXYLIC ACID |
| 1C84 | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH 3-(OXALYL-AMINO)-NAPHTHALENE-2-CARBOXLIC ACID |
| 1C85 | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH 2-(OXALYL-AMINO)-BENZOIC ACID |
| 1C86 | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B (R47V,D48N) COMPLEXED WITH 2-(OXALYL-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRAN-3-CARBOXYLIC ACID |
| 1C87 | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH 2-(OXALYL-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRAN-3-CARBOXYLIC ACID |
| 1C88 | CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH 2-(OXALYL-AMINO)-4,5,6,7-TETRAHYDRO-THIENO[2,3-C]PYRIDINE-3-CARBOXYLIC ACID |
| 1C89 | NMR STRUCTURE OF INTRAMOLECULAR DIMER ANTIFREEZE PROTEIN RD3, 40 SA STRUCTURES |
| 1C8A | NMR STRUCTURE OF INTRAMOLECULAR DIMER ANTIFREEZE PROTEIN RD3, 40 SA STRUCTURES |
| 1C8B | CRYSTAL STRUCTURE OF A NOVEL GERMINATION PROTEASE FROM SPORES OF BACILLUS MEGATERIUM: STRUCTURAL REARRANGEMENTS AND ZYMOGEN ACTIVATION |
| 1C8C | CRYSTAL STRUCTURES OF THE CHROMOSOMAL PROTEINS SSO7D/SAC7D BOUND TO DNA CONTAINING T-G MISMATCHED BASE PAIRS |
| 1C8D | CANINE PANLEUKOPENIA VIRUS EMPTY CAPSID STRUCTURE |
| 1C8E | FELINE PANLEUKOPENIA VIRUS EMPTY CAPSID STRUCTURE |
| 1C8F | FELINE PANLEUKOPENIA VIRUS EMPTY CAPSID STRUCTURE |
| 1C8G | FELINE PANLEUKOPENIA VIRUS EMPTY CAPSID STRUCTURE |
| 1C8H | CANINE PARVOVIRUS STRAIN D EMPTY CAPSID STRUCTURE AT PH 5.5 |
| 1C8I | BINDING MODE OF HYDROXYLAMINE TO ARTHROMYCES RAMOSUS PEROXIDASE |
| 1C8K | FLAVOPIRIDOL INHIBITS GLYCOGEN PHOSPHORYLASE BY BINDING AT THE INHIBITOR SITE |
| 1C8L | SYNERGISTIC INHIBITION OF GLYCOGEN PHOSPHORYLASE A BY A POTENTIAL ANTIDIABETIC DRUG AND CAFFEINE |
| 1C8M | REFINED CRYSTAL STRUCTURE OF HUMAN RHINOVIRUS 16 COMPLEXED WITH VP63843 (PLECONARIL), AN ANTI-PICORNAVIRAL DRUG CURRENTLY IN CLINICAL TRIALS |
| 1C8N | TOBACCO NECROSIS VIRUS |
| 1C8O | 2.9 A STRUCTURE OF CLEAVED VIRAL SERPIN CRMA |
| 1C8P | NMR STRUCTURE OF THE LIGAND BINDING DOMAIN OF THE COMMON BETA-CHAIN IN THE GM-CSF, IL-3 AND IL-5 RECEPTORS |
| 1C8Q | STRUCTURE SOLUTION AND REFINEMENT OF THE RECOMBINANT HUMAN SALIVARY AMYLASE |
| 1C8R | BACTERIORHODOPSIN D96N BR STATE AT 2.0 A RESOLUTION |
| 1C8S | BACTERIORHODOPSIN D96N LATE M STATE INTERMEDIATE |
| 1C8T | HUMAN STROMELYSIN-1 (E202Q) CATALYTIC DOMAIN COMPLEXED WITH RO-26-2812 |
| 1C8U | CRYSTAL STRUCTURE OF THE E.COLI THIOESTERASE II, A HOMOLOGUE OF THE HUMAN NEF-BINDING ENZYME |
| 1C8V | CRYSTAL STRUCTURE OF THE COMPLEX OF BACTERIAL TRYPTOPHAN SYNTHASE WITH THE TRANSITION STATE ANALOGUE INHIBITOR 4-(2-HYDROXYPHENYLTHIO)-BUTYLPHOSPHONIC ACID |
| 1C8W | THR45GLY VARIANT OF RIBONUCLEASE A |
| 1C8X | ENDO-BETA-N-ACETYLGLUCOSAMINIDASE H, D130E MUTANT |
| 1C8Y | ENDO-BETA-N-ACETYLGLUCOSAMINIDASE H, D130A MUTANT |
| 1C8Z | C-TERMINAL DOMAIN OF MOUSE BRAIN TUBBY PROTEIN |
| 1C90 | ENDO-BETA-N-ACETYLGLUCOSAMINIDASE H, E132Q MUTANT |
| 1C91 | ENDO-BETA-N-ACETYLGLUCOSAMINIDASE H, E132D |
| 1C92 | ENDO-BETA-N-ACETYLGLUCOSAMINIDASE H, E132A MUTANT |
| 1C93 | ENDO-BETA-N-ACETYLGLUCOSAMINIDASE H, D130N/E132Q DOUBLE MUTANT |
| 1C94 | REVERSING THE SEQUENCE OF THE GCN4 LEUCINE ZIPPER DOES NOT AFFECT ITS FOLD. |
| 1C96 | S642A:CITRATE COMPLEX OF ACONITASE |
| 1C97 | S642A:ISOCITRATE COMPLEX OF ACONITASE |
| 1C98 | SOLUTION STRUCTURE OF NEUROMEDIN B |
| 1C99 | ASP61 DEPROTONATED FORM OF SUBUNIT C OF THE F1FO ATP SYNTHASE OF ESCHERICHIA COLI |
| 1C9A | SOLUTION STRUCTURE OF NEUROMEDIN B |
| 1C9B | CRYSTAL STRUCTURE OF A HUMAN TBP CORE DOMAIN-HUMAN TFIIB CORE DOMAIN COMPLEX BOUND TO AN EXTENDED, MODIFIED ADENOVIRAL MAJOR LATE PROMOTER (ADMLP) |
| 1C9C | ASPARTATE AMINOTRANSFERASE COMPLEXED WITH C3-PYRIDOXAL-5'-PHOSPHATE |
| 1C9D | CRYSTAL STRUCTURE OF THE COMPLEX OF BACTERIAL TRYPTOPHAN SYNTHASE WITH THE TRANSITION STATE ANALOGUE INHIBITOR 4-(2-HYDROXY-4-FLUOROPHENYLTHIO)-BUTYLPHOSPHONIC ACID |
| 1C9E | STRUCTURE OF FERROCHELATASE WITH COPPER(II) N-METHYLMESOPORPHYRIN COMPLEX BOUND AT THE ACTIVE SITE |
| 1C9F | NMR STRUCTURE OF THE CAD DOMAIN OF CASPASE-ACTIVATED DNASE |
| 1C9H | CRYSTAL STRUCTURE OF FKBP12.6 IN COMPLEX WITH RAPAMYCIN |
| 1C9I | PEPTIDE-IN-GROOVE INTERACTIONS LINK TARGET PROTEINS TO THE B-PROPELLER OF CLATHRIN |
| 1C9J | BACILLUS LENTUS SUBTILISIN K27R/N87S/V104Y/N123S/T274A VARIANT |
| 1C9K | THE THREE DIMENSIONAL STRUCTURE OF ADENOSYLCOBINAMIDE KINASE/ ADENOSYLCOBINAMIDE PHOSPHATE GUALYLYLTRANSFERASE (COBU) COMPLEXED WITH GMP: EVIDENCE FOR A SUBSTRATE INDUCED TRANSFERASE ACTIVE SITE |
| 1C9L | PEPTIDE-IN-GROOVE INTERACTIONS LINK TARGET PROTEINS TO THE B-PROPELLER OF CLATHRIN |
| 1C9M | BACILLUS LENTUS SUBTILSIN (SER 87) N76D/S103A/V104I |
| 1C9N | BACILLUS LENTUS SUBSTILISIN VARIANT (SER 87) K27R/V104Y/N123S/T274A |
| 1C9O | CRYSTAL STRUCTURE ANALYSIS OF THE BACILLUS CALDOLYTICUS COLD SHOCK PROTEIN BC-CSP |
| 1C9P | COMPLEX OF BDELLASTASIN WITH PORCINE TRYPSIN |
| 1C9Q | AVERAGE NMR SOLUTION STRUCTURE OF THE BIR-2 DOMAIN OF XIAP |
| 1C9S | CRYSTAL STRUCTURE OF A COMPLEX OF TRP RNA-BINDING ATTENUATION PROTEIN WITH A 53-BASE SINGLE STRANDED RNA CONTAINING ELEVEN GAG TRIPLETS SEPARATED BY AU DINUCLEOTIDES |
| 1C9T | COMPLEX OF BDELLASTASIN WITH BOVINE TRYPSIN |
| 1C9U | CRYSTAL STRUCTURE OF THE SOLUBLE QUINOPROTEIN GLUCOSE DEHYDROGENASE IN COMPLEX WITH PQQ |
| 1C9V | H12A VARIANT OF RIBONUCLEASE A |
| 1C9W | CHO REDUCTASE WITH NADP+ |
| 1C9X | H119A VARIANT OF RIBONUCLEASE A |
| 1C9Y | HUMAN ORNITHINE TRANSCARBAMYLASE: CRYSTALLOGRAPHIC INSIGHTS INTO SUBSTRATE RECOGNITION AND CATALYTIC MECHANISM |
| 1CA0 | BOVINE CHYMOTRYPSIN COMPLEXED TO APPI |
| 1CA1 | ALPHA-TOXIN FROM CLOSTRIDIUM PERFRINGENS |
| 1CA2 | REFINED STRUCTURE OF HUMAN CARBONIC ANHYDRASE II AT 2.0 ANGSTROMS RESOLUTION |
| 1CA3 | UNEXPECTED PH-DEPENDENT CONFORMATION OF HIS-64, THE PROTON SHUTTLE OF CARBONIC ANHYDRASE II. |
| 1CA4 | STRUCTURE OF TNF RECEPTOR ASSOCIATED FACTOR 2 (TRAF2) |
| 1CA5 | INTERCALATION SITE OF HYPERTHERMOPHILE CHROMOSOMAL PROTEIN SSO7D/SAC7D BOUND TO DNA |
| 1CA6 | INTERCALATION SITE OF HYPERTHERMOPHILE CHROMOSOMAL PROTEIN SSO7D/SAC7D BOUND TO DNA |
| 1CA7 | MACROPHAGE MIGRATION INHIBITORY FACTOR (MIF) WITH HYDROXPHENYLPYRUVATE |
| 1CA8 | THROMBIN INHIBITORS WITH RIGID TRIPEPTIDYL ALDEHYDES |
| 1CA9 | STRUCTURE OF TNF RECEPTOR ASSOCIATED FACTOR 2 IN COMPLEX WITH A PEPTIDE FROM TNF-R2 |
| 1CAA | X-RAY CRYSTAL STRUCTURES OF THE OXIDIZED AND REDUCED FORMS OF THE RUBREDOXIN FROM THE MARINE HYPERTHERMOPHILIC ARCHAEBACTERIUM PYROCOCCUS FURIOSUS |
| 1CAD | X-RAY CRYSTAL STRUCTURES OF THE OXIDIZED AND REDUCED FORMS OF THE RUBREDOXIN FROM THE MARINE HYPERTHERMOPHILIC ARCHAEBACTERIUM PYROCOCCUS FURIOSUS |
| 1CAG | CRYSTAL AND MOLECULAR STRUCTURE OF A COLLAGEN-LIKE PEPTIDE AT 1.9 ANGSTROM RESOLUTION |
| 1CAH | STRUCTURE OF COBALT CARBONIC ANHYDRASE COMPLEXED WITH BICARBONATE |
| 1CAI | STRUCTURAL ANALYSIS OF THE ZINC HYDROXIDE-THR 199-GLU 106 HYDROGEN BONDING NETWORK IN HUMAN CARBONIC ANHYDRASE II |
| 1CAJ | STRUCTURAL ANALYSIS OF THE ZINC HYDROXIDE-THR 199-GLU 106 HYDROGEN BONDING NETWORK IN HUMAN CARBONIC ANHYDRASE II |
| 1CAK | STRUCTURAL ANALYSIS OF THE ZINC HYDROXIDE-THR 199-GLU 106 HYDROGEN BONDING NETWORK IN HUMAN CARBONIC ANHYDRASE II |
| 1CAL | STRUCTURAL ANALYSIS OF THE ZINC HYDROXIDE-THR 199-GLU 106 HYDROGEN BONDING NETWORK IN HUMAN CARBONIC ANHYDRASE II |
| 1CAM | STRUCTURAL ANALYSIS OF THE ZINC HYDROXIDE-THR 199-GLU 106 HYDROGEN BONDING NETWORK IN HUMAN CARBONIC ANHYDRASE II |
| 1CAN | CRYSTALLOGRAPHIC STUDIES OF THE BINDING OF PROTONATED AND UNPROTONATED INHIBITORS TO CARBONIC ANHYDRASE USING HYDROGEN SULPHIDE AND NITRATE ANIONS |
| 1CAO | CRYSTALLOGRAPHIC STUDIES OF THE BINDING OF PROTONATED AND UNPROTONATED INHIBITORS TO CARBONIC ANHYDRASE USING HYDROGEN SULPHIDE AND NITRATE ANIONS |
| 1CAQ | X-RAY STRUCTURE OF HUMAN STROMELYSIN CATALYTIC DOMAIN COMPLEXES WITH NON-PEPTIDE INHIBITORS: IMPLICATION FOR INHIBITOR SELECTIVITY |
| 1CAU | DETERMINATION OF THREE CRYSTAL STRUCTURES OF CANAVALIN BY MOLECULAR REPLACEMENT |
| 1CAV | THE THREE-DIMENSIONAL STRUCTURE OF CANAVALIN FROM JACK BEAN (CANAVALIA ENSIFORMIS) |
| 1CAW | DETERMINATION OF THREE CRYSTAL STRUCTURES OF CANAVALIN BY MOLECULAR REPLACEMENT |
| 1CAX | DETERMINATION OF THREE CRYSTAL STRUCTURES OF CANAVALIN BY MOLECULAR REPLACEMENT |
| 1CAY | WILD-TYPE AND E106Q MUTANT CARBONIC ANHYDRASE COMPLEXED WITH ACETATE |
| 1CAZ | WILD-TYPE AND E106Q MUTANT CARBONIC ANHYDRASE COMPLEXED WITH ACETATE |
| 1CB0 | STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE AT 1.7 A RESOLUTION |
| 1CB1 | THREE-DIMENSIONAL SOLUTION STRUCTURE OF CA2+-LOADED PORCINE CALBINDIN D9K DETERMINED BY NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY |
| 1CB2 | CELLOBIOHYDROLASE II, CATALYTIC DOMAIN, MUTANT Y169F |
| 1CB3 | LOCAL INTERACTIONS DRIVE THE FORMATION OF NON-NATIVE STRUCTURE IN THE DENATURED STATE OF HUMAN ALPHA-LACTALBUMIN: A HIGH RESOLUTION STRUCTURAL CHARACTERIZATION OF A PEPTIDE MODEL IN AQUEOUS SOLUTION |
| 1CB4 | CRYSTAL STRUCTURE OF COPPER, ZINC SUPEROXIDE DISMUTASE |
| 1CB5 | HUMAN BLEOMYCIN HYDROLASE. |
| 1CB6 | STRUCTURE OF HUMAN APOLACTOFERRIN AT 2.0 A RESOLUTION. |
| 1CB7 | GLUTAMATE MUTASE FROM CLOSTRIDIUM COCHLEARIUM RECONSTITUTED WITH METHYL-COBALAMIN |
| 1CB8 | CHONDROITINASE AC LYASE FROM FLAVOBACTERIUM HEPARINUM |
| 1CB9 | NMR STRUCTURE WITH TIGHTLY BOUND WATER MOLECULES OF CYTOTOXIN II (CARDIOTOXIN) FROM NAJA NAJA OXIANA IN AQUEOUS SOLUTION (MAJOR FORM). |
| 1CBF | THE X-RAY STRUCTURE OF A COBALAMIN BIOSYNTHETIC ENZYME, COBALT PRECORRIN-4 METHYLTRANSFERASE, CBIF |
| 1CBG | THE CRYSTAL STRUCTURE OF A CYANOGENIC BETA-GLUCOSIDASE FROM WHITE CLOVER (TRIFOLIUM REPENS L.), A FAMILY 1 GLYCOSYL-HYDROLASE |
| 1CBH | DETERMINATION OF THE THREE-DIMENSIONAL STRUCTURE OF THE C-TERMINAL DOMAIN OF CELLOBIOHYDROLASE I FROM TRICHODERMA REESEI. A STUDY USING NUCLEAR MAGNETIC RESONANCE AND HYBRID DISTANCE GEOMETRY-DYNAMICAL SIMULATED ANNEALING |
| 1CBI | APO-CELLULAR RETINOIC ACID BINDING PROTEIN I |
| 1CBJ | CRYSTAL STRUCTURE OF BOVINE SUPEROXIDE DISMUTASE CRYSTAL. |
| 1CBK | 7,8-DIHYDRO-6-HYDROXYMETHYLPTERIN-PYROPHOSPHOKINASE FROM HAEMOPHILUS INFLUENZAE |
| 1CBL | THE 1.9 ANGSTROM STRUCTURE OF DEOXY-BETA4 HEMOGLOBIN: ANALYSIS OF THE PARTITIONING OF QUATERNARY-ASSOCIATED AND LIGAND-INDUCED CHANGES IN TERTIARY STRUCTURE |
| 1CBM | THE 1.8 ANGSTROM STRUCTURE OF CARBONMONOXY-BETA4 HEMOGLOBIN: ANALYSIS OF A HOMOTETRAMER WITH THE R QUATERNARY STRUCTURE OF LIGANDED ALPHA2BETA2 HEMOGLOBIN |
| 1CBN | ATOMIC RESOLUTION (0.83 ANGSTROMS) CRYSTAL STRUCTURE OF THE HYDROPHOBIC PROTEIN CRAMBIN AT 130 K |
| 1CBO | CHOLESTEROL OXIDASE FROM STREPTOMYCES HIS447ASN MUTANT |
| 1CBQ | CRYSTAL STRUCTURE OF CELLULAR RETINOIC-ACID-BINDING PROTEINS I AND II IN COMPLEX WITH ALL-TRANS-RETINOIC ACID AND A SYNTHETIC RETINOID |
| 1CBR | CRYSTAL STRUCTURE OF CELLULAR RETINOIC-ACID-BINDING PROTEINS I AND II IN COMPLEX WITH ALL-TRANS-RETINOIC ACID AND A SYNTHETIC RETINOID |
| 1CBS | CRYSTAL STRUCTURE OF CELLULAR RETINOIC-ACID-BINDING PROTEINS I AND II IN COMPLEX WITH ALL-TRANS-RETINOIC ACID AND A SYNTHETIC RETINOID |
| 1CBU | ADENOSYLCOBINAMIDE KINASE/ADENOSYLCOBINAMIDE PHOSPHATE GUANYLYLTRANSFERASE (COBU) FROM SALMONELLA TYPHIMURIUM |
| 1CBV | AN AUTOANTIBODY TO SINGLE-STRANDED DNA: COMPARISON OF THE THREE-DIMENSIONAL STRUCTURES OF THE UNLIGANDED FAB AND A DEOXYNUCLEOTIDE-FAB COMPLEX |
| 1CBW | BOVINE CHYMOTRYPSIN COMPLEXED TO BPTI |
| 1CBX | CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN CARBOXYPEPTIDASE A AND THE BIPRODUCT ANALOG INHIBITOR L-BENZYLSUCCINATE AT 2.0 ANGSTROMS RESOLUTION |
| 1CBY | DELTA-ENDOTOXIN |
| 1CC0 | CRYSTAL STRUCTURE OF THE RHOA.GDP-RHOGDI COMPLEX |
| 1CC1 | CRYSTAL STRUCTURE OF A REDUCED, ACTIVE FORM OF THE NI-FE-SE HYDROGENASE FROM DESULFOMICROBIUM BACULATUM |
| 1CC2 | CHOLESTEROL OXIDASE FROM STREPTOMYCES HIS447GLN MUTANT |
| 1CC3 | PURPLE CUA CENTER |
| 1CC4 | PHE161 AND ARG166 VARIANTS OF P-HYDROXYBENZOATE HYDROXYLASE. IMPLICATIONS FOR NADPH RECOGNITION AND STRUCTURAL STABILITY. |
| 1CC5 | CRYSTAL STRUCTURE OF AZOTOBACTER CYTOCHROME C5 AT 2.5 ANGSTROMS RESOLUTION |
| 1CC6 | PHE161 AND ARG166 VARIANTS OF P-HYDROXYBENZOATE HYDROXYLASE. IMPLICATIONS FOR NADPH RECOGNITION AND STRUCTURAL STABILITY. |
| 1CC7 | CRYSTAL STRUCTURE OF THE ATX1 METALLOCHAPERONE PROTEIN |
| 1CC8 | CRYSTAL STRUCTURE OF THE ATX1 METALLOCHAPERONE PROTEIN |
| 1CCA | THE ASP-HIS-FE TRIAD OF CYTOCHROME C PEROXIDASE CONTROLS THE REDUCTION POTENTIAL, ELECTRONIC STRUCTURE, AND COUPLING OF THE TRYPTOPHAN FREE-RADICAL TO THE HEME |
| 1CCB | THE ASP-HIS-FE TRIAD OF CYTOCHROME C PEROXIDASE CONTROLS THE REDUCTION POTENTIAL, ELECTRONIC STRUCTURE, AND COUPLING OF THE TRYPTOPHAN FREE-RADICAL TO THE HEME |
| 1CCC | THE ASP-HIS-FE TRIAD OF CYTOCHROME C PEROXIDASE CONTROLS THE REDUCTION POTENTIAL, ELECTRONIC STRUCTURE, AND COUPLING OF THE TRYPTOPHAN FREE-RADICAL TO THE HEME |
| 1CCD | REFINED STRUCTURE OF RAT CLARA CELL 17 KDA PROTEIN AT 3.0 ANGSTROMS RESOLUTION |
| 1CCE | CONSTRUCTION OF A BIS-AQUO HEME ENZYME AND REPLACEMENT WITH EXOGENOUS LIGAND |
| 1CCF | HOW AN EPIDERMAL GROWTH FACTOR (EGF)-LIKE DOMAIN BINDS CALCIUM-HIGH RESOLUTION NMR STRUCTURE OF THE CALCIUM FORM OF THE NH2-TERMINAL EGF-LIKE DOMAIN IN COAGULATION FACTOR X |
| 1CCG | CONSTRUCTION OF A BIS-AQUO HEME ENZYME AND REPLACEMENT WITH EXOGENOUS LIGAND |
| 1CCH | THE SOLUTION CONFORMATION OF CYTOCHROME C-551 FROM P.STUTZERI ZOBELL DETERMINED BY NMR+ |
| 1CCI | HOW FLEXIBLE ARE PROTEINS? TRAPPING OF A FLEXIBLE LOOP |
| 1CCJ | CONFORMER SELECTION BY LIGAND BINDING OBSERVED WITH PROTEIN CRYSTALLOGRAPHY |
| 1CCK | ALTERING SUBSTRATE SPECIFICITY OF CYTOCHROME C PEROXIDASE TOWARDS A SMALL MOLECULAR SUBSTRATE PEROXIDASE BY SUBSTITUTING TYROSINE FOR PHE 202 |
| 1CCL | PROBING THE STRENGTH AND CHARACTER OF AN ASP-HIS-X HYDROGEN BOND BY INTRODUCING BURIED CHARGES |
| 1CCM | DIRECT NOE REFINEMENT OF CRAMBIN FROM 2D NMR DATA USING A SLOW-COOLING ANNEALING PROTOCOL |
| 1CCN | DIRECT NOE REFINEMENT OF CRAMBIN FROM 2D NMR DATA USING A SLOW-COOLING ANNEALING PROTOCOL |
| 1CCP | X-RAY STRUCTURES OF RECOMBINANT YEAST CYTOCHROME C PEROXIDASE AND THREE HEME-CLEFT MUTANTS PREPARED BY SITE-DIRECTED MUTAGENESIS |
| 1CCQ | NMR STRUCTURE WITH TIGHTLY BOUND WATER MOLECULES OF CYTOTOXIN II (CARDIOTOXIN) FROM NAJA NAJA OXIANA IN AQUEOUS SOLUTION (MINOR FORM). |
| 1CCR | STRUCTURE OF RICE FERRICYTOCHROME C AT 2.0 ANGSTROMS RESOLUTION |
| 1CCS | STRUCTURE-ASSISTED REDESIGN OF A PROTEIN-ZINC BINDING SITE WITH FEMTOMOLAR AFFINITY |
| 1CCT | STRUCTURE-ASSISTED REDESIGN OF A PROTEIN-ZINC BINDING SITE WITH FEMTOMOLAR AFFINITY |
| 1CCU | STRUCTURE-ASSISTED REDESIGN OF A PROTEIN-ZINC BINDING SITE WITH FEMTOMOLAR AFFINITY |
| 1CCV | NMR SOLUTION STRUCTURE OF APIS MELLIFERA CHYMOTRYPSIN INHIBITOR (AMCI). |
| 1CCW | STRUCTURE OF THE COENZYME B12 DEPENDENT ENZYME GLUTAMATE MUTASE FROM CLOSTRIDIUM COCHLEARIUM |
| 1CCZ | CRYSTAL STRUCTURE OF THE CD2-BINDING DOMAIN OF CD58 (LYMPHOCYTE FUNCTION-ASSOCIATED ANTIGEN 3) AT 1.8-A RESOLUTION |
| 1CD0 | STRUCTURE OF HUMAN LAMDA-6 LIGHT CHAIN DIMER JTO |
| 1CD1 | CD1(MOUSE) ANTIGEN PRESENTING MOLECULE |
| 1CD2 | LIGAND INDUCED CONFORMATIONAL CHANGES IN THE CRYSTAL STRUCTURES OF PNEUMOCYSTIS CARINII DIHYDROFOLATE REDUCTASE COMPLEXES WITH FOLATE AND NADP+ |
| 1CD3 | PROCAPSID OF BACTERIOPHAGE PHIX174 |
| 1CD5 | GLUCOSAMINE-6-PHOSPHATE DEAMINASE FROM E.COLI, T CONFORMER |
| 1CD8 | CRYSTAL STRUCTURE OF A SOLUBLE FORM OF THE HUMAN T CELL CO-RECEPTOR CD8 AT 2.6 ANGSTROMS RESOLUTION |
| 1CD9 | 2:2 COMPLEX OF G-CSF WITH ITS RECEPTOR |
| 1CDB | STRUCTURE OF THE GLYCOSYLATED ADHESION DOMAIN OF HUMAN T LYMPHOCYTE GLYCOPROTEIN CD2 |
| 1CDC | CD2, N-TERMINAL DOMAIN (1-99), TRUNCATED FORM |
| 1CDD | STRUCTURES OF APO AND COMPLEXED ESCHERICHIA COLI GLYCINAMIDE RIBONUCLEOTIDE TRANSFORMYLASE |
| 1CDE | STRUCTURES OF APO AND COMPLEXED ESCHERICHIA COLI GLYCINAMIDE RIBONUCLEOTIDE TRANSFORMYLASE |
| 1CDG | NUCLEOTIDE SEQUENCE AND X-RAY STRUCTURE OF CYCLODEXTRIN GLYCOSYLTRANSFERASE FROM BACILLUS CIRCULANS STRAIN 251 IN A MALTOSE-DEPENDENT CRYSTAL FORM |
| 1CDH | STRUCTURES OF AN HIV AND MHC BINDING FRAGMENT FROM HUMAN CD4 AS REFINED IN TWO CRYSTAL LATTICES |
| 1CDI | STRUCTURES OF AN HIV AND MHC BINDING FRAGMENT FROM HUMAN CD4 AS REFINED IN TWO CRYSTAL LATTICES |
| 1CDJ | STRUCTURE OF T-CELL SURFACE GLYCOPROTEIN CD4 |
| 1CDK | CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT (E.C.2.7.1.37) (PROTEIN KINASE A) COMPLEXED WITH PROTEIN KINASE INHIBITOR PEPTIDE FRAGMENT 5-24 (PKI(5-24) ISOELECTRIC VARIANT CA) AND MN2+ ADENYLYL IMIDODIPHOSPHATE (MNAMP-PNP) AT PH 5.6 AND 7C AND 4C |
| 1CDL | TARGET ENZYME RECOGNITION BY CALMODULIN: 2.4 ANGSTROMS STRUCTURE OF A CALMODULIN-PEPTIDE COMPLEX |
| 1CDM | MODULATION OF CALMODULIN PLASTICITY IN MOLECULAR RECOGNITION ON THE BASIS OF X-RAY STRUCTURES |
| 1CDN | SOLUTION STRUCTURE OF (CD2+)1-CALBINDIN D9K REVEALS DETAILS OF THE STEPWISE STRUCTURAL CHANGES ALONG THE APO--> (CA2+)II1--> (CA2+)I,II2 BINDING PATHWAY |
| 1CDO | ALCOHOL DEHYDROGENASE (E.C.1.1.1.1) (EE ISOZYME) COMPLEXED WITH NICOTINAMIDE ADENINE DINUCLEOTIDE (NAD), AND ZINC |
| 1CDP | RESTRAINED LEAST SQUARES REFINEMENT OF NATIVE (CALCIUM) AND CADMIUM-SUBSTITUTED CARP PARVALBUMIN USING X-RAY CRYSTALLOGRAPHIC DATA AT 1.6-ANGSTROMS RESOLUTION |
| 1CDQ | STRUCTURE OF A SOLUBLE, GLYCOSYLATED FORM OF THE HUMAN COMPLEMENT REGULATORY PROTEIN CD59 |
| 1CDR | STRUCTURE OF A SOLUBLE, GLYCOSYLATED FORM OF THE HUMAN COMPLEMENT REGULATORY PROTEIN CD59 |
| 1CDS | STRUCTURE OF A SOLUBLE, GLYCOSYLATED FORM OF THE HUMAN COMPLEMENT REGULATORY PROTEIN CD59 |
| 1CDT | CARDIOTOXIN V4/II FROM NAJA MOSSAMBICA MOSSAMBICA: THE REFINED CRYSTAL STRUCTURE |
| 1CDU | STRUCTURE OF T-CELL SURFACE GLYCOPROTEIN CD4 MUTANT WITH PHE 43 REPLACED BY VAL |
| 1CDW | HUMAN TBP CORE DOMAIN COMPLEXED WITH DNA |
| 1CDY | STRUCTURE OF T-CELL SURFACE GLYCOPROTEIN CD4 MUTANT WITH GLY 47 REPLACED BY SER |
| 1CDZ | BRCT DOMAIN FROM DNA-REPAIR PROTEIN XRCC1 |
| 1CE0 | TRIMERIZATION SPECIFICITY IN HIV-1 GP41: ANALYSIS WITH A GCN4 LEUCINE ZIPPER MODEL |
| 1CE1 | 1.9A STRUCTURE OF THE THERAPEUTIC ANTIBODY CAMPATH-1H FAB IN COMPLEX WITH A SYNTHETIC PEPTIDE ANTIGEN |
| 1CE2 | STRUCTURE OF DIFERRIC BUFFALO LACTOFERRIN AT 2.5A RESOLUTION |
| 1CE3 | PUTATIVE ANCESTRAL PROTEIN ENCODED BY A SINGLE SEQUENCE REPEAT OF THE MULTIDOMAIN PROTEINASE INHIBITOR FROM NICOTIANA ALATA |
| 1CE4 | CONFORMATIONAL MODEL FOR THE CONSENSUS V3 LOOP OF THE ENVELOPE PROTEIN GP120 OF HIV-1 |
| 1CE5 | BOVINE PANCREAS BETA-TRYPSIN IN COMPLEX WITH BENZAMIDINE |
| 1CE6 | MHC CLASS I H-2DB COMPLEXED WITH A SENDAI VIRUS NUCLEOPROTEIN PEPTIDE |
| 1CE7 | MISTLETOE LECTIN I FROM VISCUM ALBUM |
| 1CE9 | HELIX CAPPING IN THE GCN4 LEUCINE ZIPPER |
| 1CEA | THE STRUCTURE OF THE NON-COVALENT COMPLEX OF RECOMBINANT KRINGLE 1 DOMAIN OF HUMAN PLASMINOGEN WITH EACA (EPSILON-AMINOCAPROIC ACID) |
| 1CEB | THE STRUCTURE OF THE NON-COVALENT COMPLEX OF RECOMBINANT KRINGLE 1 DOMAIN OF HUMAN PLASMINOGEN WITH AMCHA (TRANS-4-AMINOMETHYLCYCLOHEXANE-1-CARBOXYLIC ACID) |
| 1CEC | A COMMON PROTEIN FOLD AND SIMILAR ACTIVE SITE IN TWO DISTINCT FAMILIES OF BETA-GLYCANASES |
| 1CED | THE STRUCTURE OF CYTOCHROME C6 FROM MONORAPHIDIUM BRAUNII, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1CEE | SOLUTION STRUCTURE OF CDC42 IN COMPLEX WITH THE GTPASE BINDING DOMAIN OF WASP |
| 1CEF | CEFOTAXIME COMPLEXED WITH THE STREPTOMYCES R61 DD-PEPTIDASE |
| 1CEG | CEPHALOTHIN COMPLEXED WITH DD-PEPTIDASE |
| 1CEH | STRUCTURE AND FUNCTION OF THE CATALYTIC SITE MUTANT ASP99ASN OF PHOSPHOLIPASE A2: ABSENCE OF CONSERVED STRUCTURAL WATER |
| 1CEI | STRUCTURE DETERMINATION OF THE COLICIN E7 IMMUNITY PROTEIN (IMME7) THAT BINDS SPECIFICALLY TO THE DNASE-TYPE COLICIN E7 AND INHIBITS ITS BACTERIOCIDAL ACTIVITY |
| 1CEJ | SOLUTION STRUCTURE OF AN EGF MODULE PAIR FROM THE PLASMODIUM FALCIPARUM MEROZOITE SURFACE PROTEIN 1 |
| 1CEL | THE THREE-DIMENSIONAL CRYSTAL STRUCTURE OF THE CATALYTIC CORE OF CELLOBIOHYDROLASE I FROM TRICHODERMA REESEI |
| 1CEM | ENDOGLUCANASE A (CELA) CATALYTIC CORE, RESIDUES 33-395 |
| 1CEN | CELLULASE (CELC) MUTANT WITH GLU 140 REPLACED BY GLN COMPLEXED WITH CELLOHEXAOSE |
| 1CEO | CELLULASE (CELC) MUTANT WITH GLU 140 REPLACED BY GLN |
| 1CEQ | CHLOROQUINE BINDS IN THE COFACTOR BINDING SITE OF PLASMODIUM FALCIPARUM LACTATE DEHYDROGENASE. |
| 1CES | CRYSTALS OF DEMETALLIZED CONCANAVALIN A SOAKED WITH ZINC HAVE A ZINC ION BOUND IN THE S1 SITE |
| 1CET | CHLOROQUINE BINDS IN THE COFACTOR BINDING SITE OF PLASMODIUM FALCIPARUM LACTATE DEHYDROGENASE. |
| 1CEU | NMR STRUCTURE OF THE (1-51) N-TERMINAL DOMAIN OF THE HIV-1 REGULATORY PROTEIN |
| 1CEV | ARGINASE FROM BACILLUS CALDOVELOX, NATIVE STRUCTURE AT PH 5.6 |
| 1CEW | THE 2.0 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF CHICKEN EGG WHITE CYSTATIN AND ITS POSSIBLE MODE OF INTERACTION WITH CYSTEINE PROTEINASES |
| 1CEX | STRUCTURE OF CUTINASE |
| 1CEY | ASSIGNMENTS, SECONDARY STRUCTURE, GLOBAL FOLD, AND DYNAMICS OF CHEMOTAXIS Y PROTEIN USING THREE-AND FOUR-DIMENSIONAL HETERONUCLEAR (13C,15N) NMR SPECTROSCOPY |
| 1CEZ | CRYSTAL STRUCTURE OF A T7 RNA POLYMERASE-T7 PROMOTER COMPLEX |
| 1CF0 | HUMAN PLATELET PROFILIN COMPLEXED WITH AN L-PRO10-IODOTYROSINE PEPTIDE |
| 1CF1 | ARRESTIN FROM BOVINE ROD OUTER SEGMENTS |
| 1CF2 | THREE-DIMENSIONAL STRUCTURE OF D-GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE FROM THE HYPERTHERMOPHILIC ARCHAEON METHANOTHERMUS FERVIDUS |
| 1CF3 | GLUCOSE OXIDASE FROM APERGILLUS NIGER |
| 1CF4 | CDC42/ACK GTPASE-BINDING DOMAIN COMPLEX |
| 1CF5 | BETA-MOMORCHARIN STRUCTURE AT 2.55 A |
| 1CF7 | STRUCTURAL BASIS OF DNA RECOGNITION BY THE HETERODIMERIC CELL CYCLE TRANSCRIPTION FACTOR E2F-DP |
| 1CF8 | CONVERGENCE OF CATALYTIC ANTIBODY AND TERPENE CYCLASE MECHANISMS: POLYENE CYCLIZATION DIRECTED BY CARBOCATION-PI INTERACTIONS |
| 1CF9 | STRUCTURE OF THE MUTANT VAL169CYS OF CATALASE HPII FROM ESCHERICHIA COLI |
| 1CFA | SOLUTION STRUCTURE OF A SEMI-SYNTHETIC C5A RECEPTOR ANTAGONIST AT PH 5.2, 303K, NMR, 20 STRUCTURES |
| 1CFB | CRYSTAL STRUCTURE OF TANDEM TYPE III FIBRONECTIN DOMAINS FROM DROSOPHILA NEUROGLIAN AT 2.0 ANGSTROMS |
| 1CFC | CALCIUM-FREE CALMODULIN |
| 1CFD | CALCIUM-FREE CALMODULIN |
| 1CFE | P14A, NMR, 20 STRUCTURES |
| 1CFF | NMR SOLUTION STRUCTURE OF A COMPLEX OF CALMODULIN WITH A BINDING PEPTIDE OF THE CA2+-PUMP |
| 1CFG | MEMBRANE-BINDING PEPTIDE FROM THE C2 DOMAIN OF FACTOR VIII FORMS AN AMPHIPATHIC STRUCTURE AS DETERMINED BY NMR SPECTROSCOPY |
| 1CFH | STRUCTURE OF THE METAL-FREE GAMMA-CARBOXYGLUTAMIC ACID-RICH MEMBRANE BINDING REGION OF FACTOR IX BY TWO-DIMENSIONAL NMR SPECTROSCOPY |
| 1CFI | NMR STRUCTURE OF CALCIUM ION-BOUND GAMMA-CARBOXY-GLUTAMIC ACID-RICH DOMAIN OF FACTOR IX |
| 1CFJ | METHYLPHOSPHONYLATED ACETYLCHOLINESTERASE (AGED) OBTAINED BY REACTION WITH O-ISOPROPYLMETHYLPHOSPHONOFLUORIDATE (GB, SARIN) |
| 1CFM | CYTOCHROME F FROM CHLAMYDOMONAS REINHARDTII |
| 1CFN | ANTI-P24 (HIV-1) FAB FRAGMENT CB41 COMPLEXED WITH AN EPITOPE-RELATED PEPTIDE |
| 1CFP | S100B (S100BETA) NMR DATA WAS COLLECTED FROM A SAMPLE OF CALCIUM FREE PROTEIN AT PH 6.3 AND A TEMPERATURE OF 311 K AND 1.7-6.9 MM CONCENTRATION, 25 STRUCTURES |
| 1CFQ | ANTI-P24 (HIV-1) FAB FRAGMENT CB41 |
| 1CFR | CRYSTAL STRUCTURE OF CITROBACTER FREUNDII RESTRICTION ENDONUCLEASE CFR10I AT 2.15 ANGSTROMS RESOLUTION. |
| 1CFS | ANTI-P24 (HIV-1) FAB FRAGMENT CB41 COMPLEXED WITH AN EPITOPE-UNRELATED PEPTIDE |
| 1CFT | ANTI-P24 (HIV-1) FAB FRAGMENT CB41 COMPLEXED WITH AN EPITOPE-UNRELATED D-PEPTIDE |
| 1CFV | MONOCLONAL ANTIBODY FRAGMENT FV4155 FROM E. COLI |
| 1CFW | GA-SUBSTITUTED DESULFOREDOXIN |
| 1CFY | YEAST COFILIN, MONOCLINIC CRYSTAL FORM |
| 1CFZ | HYDROGENASE MATURATING ENDOPEPTIDASE HYBD FROM E. COLI |
| 1CG0 | STRUCTURE OF ADENYLOSUCCINATE SYNTHETASE FROM E. COLI COMPLEXED WITH HADACIDIN, GDP, 6-PHOSPHORYL-IMP, AND MG2+ |
| 1CG1 | STRUCTURE OF THE MUTANT (K16Q) OF ADENYLOSUCCINATE SYNTHETASE FROM E. COLI COMPLEXED WITH HADACIDIN, GDP, 6-PHOSPHORYL-IMP, AND MG2+ |
| 1CG2 | CARBOXYPEPTIDASE G2 |
| 1CG3 | STRUCTURE OF THE MUTANT (R143L) OF ADENYLOSUCCINATE SYNTHETASE FROM E. COLI COMPLEXED WITH HADACIDIN, GDP, 6-PHOSPHORYL-IMP, AND MG2+ |
| 1CG4 | STRUCTURE OF THE MUTANT (R303L) OF ADENYLOSUCCINATE SYNTHETASE FROM E. COLI COMPLEXED WITH, GDP, 6-PHOSPHORYL-IMP, AND MG2+ |
| 1CG5 | DEOXY FORM HEMOGLOBIN FROM DASYATIS AKAJEI |
| 1CG6 | STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE COMPLEXED WITH 5'-DEOXY-5'-METHYLTHIOADENOSINE AND SULFATE AT 1.7 A RESOLUTION |
| 1CG7 | HMG PROTEIN NHP6A FROM SACCHAROMYCES CEREVISIAE |
| 1CG8 | CO FORM HEMOGLOBIN FROM DASYATIS AKAJEI |
| 1CG9 | COMPLEX RECOGNITION OF THE SUPERTYPIC BW6-DETERMINANT ON HLA-B AND-C MOLECULES BY THE MONOCLONAL ANTIBODY SFR8-B6 |
| 1CGD | HYDRATION STRUCTURE OF A COLLAGEN PEPTIDE |
| 1CGE | CRYSTAL STRUCTURES OF RECOMBINANT 19-KDA HUMAN FIBROBLAST COLLAGENASE COMPLEXED TO ITSELF |
| 1CGF | CRYSTAL STRUCTURES OF RECOMBINANT 19-KDA HUMAN FIBROBLAST COLLAGENASE COMPLEXED TO ITSELF |
| 1CGH | HUMAN CATHEPSIN G |
| 1CGI | THREE-DIMENSIONAL STRUCTURE OF THE COMPLEXES BETWEEN BOVINE CHYMOTRYPSINOGEN*A AND TWO RECOMBINANT VARIANTS OF HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR (KAZAL-TYPE) |
| 1CGJ | THREE-DIMENSIONAL STRUCTURE OF THE COMPLEXES BETWEEN BOVINE CHYMOTRYPSINOGEN*A AND TWO RECOMBINANT VARIANTS OF HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR (KAZAL-TYPE) |
| 1CGK | CHALCONE SYNTHASE FROM ALFALFA COMPLEXED WITH NARINGENIN |
| 1CGL | STRUCTURE OF THE CATALYTIC DOMAIN OF FIBROBLAST COLLAGENASE COMPLEXED WITH AN INHIBITOR |
| 1CGM | STRUCTURE DETERMINATION OF CUCUMBER GREEN MOTTLE MOSAIC VIRUS BY X-RAY FIBER DIFFRACTION. SIGNIFICANCE FOR THE EVOLUTION OF TOBAMOVIRUSES |
| 1CGN | CYTOCHROME C' |
| 1CGO | CYTOCHROME C' |
| 1CGP | CATABOLITE GENE ACTIVATOR PROTEIN (CAP)/DNA COMPLEX + ADENOSINE-3',5'-CYCLIC-MONOPHOSPHATE |
| 1CGQ | MACROPHAGE MIGRATION INHIBITORY FACTOR (MIF) WITH ALANINE INSERTED BETWEEN PRO-1 AND MET-2 |
| 1CGS | LOCAL AND TRANSMITTED CONFORMATIONAL CHANGES ON COMPLEXATION OF AN ANTI-SWEETENER FAB |
| 1CGT | STRUCTURE OF CYCLODEXTRIN GLYCOSYLTRANSFERASE REFINED AT 2.0 ANGSTROMS RESOLUTION |
| 1CGU | CATALYTIC CENTER OF CYCLODEXTRIN GLYCOSYLTRANSFERASE DERIVED FROM X-RAY STRUCTURE ANALYSIS COMBINED WITH SITE-DIRECTED MUTAGENESIS |
| 1CGV | SITE DIRECTED MUTATIONS OF THE ACTIVE SITE RESIDUE TYROSINE 195 OF CYCLODEXTRIN GLYCOSYLTRANSFERASE FROM BACILLUS CIRCULANS STRAIN 251 AFFECTING ACTIVITY AND PRODUCT SPECIFICITY |
| 1CGW | SITE DIRECTED MUTATIONS OF THE ACTIVE SITE RESIDUE TYROSINE 195 OF CYCLODEXTRIN GLYCOSYLTRANSFERASE FROM BACILLUS CIRCULANS STRAIN 251 AFFECTING ACTIVITY AND PRODUCT SPECIFICITY |
| 1CGX | SITE DIRECTED MUTATIONS OF THE ACTIVE SITE RESIDUE TYROSINE 195 OF CYCLODEXTRIN GLYXOSYLTRANSFERASE FROM BACILLUS CIRCULANS STRAIN 251 AFFECTING ACTIVITY AND PRODUCT SPECIFICITY |
| 1CGY | SITE DIRECTED MUTATIONS OF THE ACTIVE SITE RESIDUE TYROSINE 195 OF CYCLODEXTRIN GLYXOSYLTRANSFERASE FROM BACILLUS CIRCULANS STRAIN 251 AFFECTING ACTIVITY AND PRODUCT SPECIFICITY |
| 1CGZ | CHALCONE SYNTHASE FROM ALFALFA COMPLEXED WITH RESVERATROL |
| 1CH0 | RNASE T1 VARIANT WITH ALTERED GUANINE BINDING SEGMENT |
| 1CH1 | RECOMBINANT SPERM WHALE MYOGLOBIN L89G MUTATNT (MET) |
| 1CH2 | RECOMBINANT SPERM WHALE MYOGLOBIN L89F MUTANT (MET) |
| 1CH3 | RECOMBINANT SPERM WHALE MYOGLOBIN L89W MUTANT (MET) |
| 1CH4 | MODULE-SUBSTITUTED CHIMERA HEMOGLOBIN BETA-ALPHA (F133V) |
| 1CH5 | RECOMBINANT SPERM WHALE MYOGLOBIN H97V MUTANT (MET) |
| 1CH7 | RECOMBINANT SPERM WHALE MYOGLOBIN H97F MUTANT (MET) |
| 1CH8 | STRUCTURE OF ADENYLOSUCCINATE SYNTHETASE FROM E. COLI COMPLEXED WITH A STRINGENT EFFECTOR, PPG2':3'P |
| 1CH9 | RECOMBINANT SPERM WHALE MYOGLOBIN H97Q MUTANT (MET) |
| 1CHC | STRUCTURE OF THE C3HC4 DOMAIN BY 1H-NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; A NEW STRUCTURAL CLASS OF ZINC-FINGER |
| 1CHD | CHEB METHYLESTERASE DOMAIN |
| 1CHG | CHYMOTRYPSINOGEN,2.5 ANGSTROMS CRYSTAL STRUCTURE, COMPARISON WITH ALPHA-CHYMOTRYPSIN,AND IMPLICATIONS FOR ZYMOGEN ACTIVATION |
| 1CHH | STRUCTURAL STUDIES OF THE ROLES OF RESIDUES 82 AND 85 AT THE INTERACTIVE FACE OF CYTOCHROME C |
| 1CHI | STRUCTURAL STUDIES OF THE ROLES OF RESIDUES 82 AND 85 AT THE INTERACTIVE FACE OF CYTOCHROME C |
| 1CHJ | STRUCTURAL STUDIES OF THE ROLES OF RESIDUES 82 AND 85 AT THE INTERACTIVE FACE OF CYTOCHROME C |
| 1CHK | STREPTOMYCES N174 CHITOSANASE PH5.5 298K |
| 1CHL | NMR SEQUENTIAL ASSIGNMENTS AND SOLUTION STRUCTURE OF CHLOROTOXIN, A SMALL SCORPION TOXIN THAT BLOCKS CHLORIDE CHANNELS |
| 1CHM | ENZYMATIC MECHANISM OF CREATINE AMIDINOHYDROLASE AS DEDUCED FROM CRYSTAL STRUCTURES |
| 1CHN | MAGNESIUM BINDING TO THE BACTERIAL CHEMOTAXIS PROTEIN CHEY RESULTS IN LARGE CONFORMATIONAL CHANGES INVOLVING ITS FUNCTIONAL SURFACE |
| 1CHO | CRYSTAL AND MOLECULAR STRUCTURES OF THE COMPLEX OF ALPHA-*CHYMOTRYPSIN WITH ITS INHIBITOR TURKEY OVOMUCOID THIRD DOMAIN AT 1.8 ANGSTROMS RESOLUTION |
| 1CHP | SURPRISING LEADS FOR A CHOLERA TOXIN RECEPTOR BINDING ANTAGONIST; CRYSTALLOGRAPHIC STUDIES OF CTB MUTANTS |
| 1CHQ | SURPRISING LEADS FOR A CHOLERA TOXIN RECEPTOR BINDING ANTAGONIST; CRYSTALLOGRAPHIC STUDIES OF CTB MUTANTS |
| 1CHU | STRUCTURE OF L-ASPARTATE OXIDASE: IMPLICATIONS FOR THE SUCCINATE DEHYDROGENASE/ FUMARATE REDUCATSE FAMILY |
| 1CHV | ELUCIDATION OF THE SOLUTION STRUCTURE OF CARDIOTOXIN ANALOGUE V FROM THE TAIWAN COBRA (NAJA NAJA ATRA) VENOM |
| 1CHW | CHALCONE SYNTHASE FROM ALFALFA COMPLEXED WITH HEXANOYL-COA |
| 1CHZ | A NEW NEUROTOXIN FROM BUTHUS MARTENSII KARSCH |
| 1CI0 | PNP OXIDASE FROM SACCHAROMYCES CEREVISIAE |
| 1CI1 | CRYSTAL STRUCTURE OF TRIOSEPHOSPHATE ISOMERASE FROM TRYPANOSOMA CRUZI IN HEXANE |
| 1CI3 | CYTOCHROME F FROM THE B6F COMPLEX OF PHORMIDIUM LAMINOSUM |
| 1CI4 | THE CRYSTAL STRUCTURE OF HUMAN BARRIER-TO-AUTOINTEGRATION FACTOR (BAF) |
| 1CI5 | GLYCAN-FREE MUTANT ADHESION DOMAIN OF HUMAN CD58 (LFA-3) |
| 1CI6 | TRANSCRIPTION FACTOR ATF4-C/EBP BETA BZIP HETERODIMER |
| 1CI7 | TERNARY COMPLEX OF THYMIDYLATE SYNTHASE FROM PNEUMOCYSTIS CARINII |
| 1CI8 | ESTERASE ESTB FROM BURKHOLDERIA GLADIOLI: AN ESTERASE WITH (BETA)-LACTAMASE FOLD. |
| 1CI9 | DFP-INHIBITED ESTERASE ESTB FROM BURKHOLDERIA GLADIOLI |
| 1CIA | REPLACEMENT OF CATALYTIC HISTIDINE-195 OF CHLORAMPHENICOL ACETYLTRANSFERASE: EVIDENCE FOR A GENERAL BASE ROLE FOR GLUTAMATE |
| 1CIB | STRUCTURE OF ADENYLOSUCCINATE SYNTHETASE FROM E. COLI COMPLEXED WITH GDP, IMP, HADACIDIN, AND NO3 |
| 1CIC | IDIOTOPE-ANTI-IDIOTOPE FAB-FAB COMPLEX; D1.3-E225 |
| 1CID | CRYSTAL STRUCTURE OF DOMAINS 3 & 4 OF RAT CD4 AND THEIR RELATIONSHIP TO THE NH2-TERMINAL DOMAINS |
| 1CIE | STRUCTURAL AND FUNCTIONAL EFFECTS OF MULTIPLE MUTATIONS AT DISTAL SITES IN CYTOCHROME C |
| 1CIF | STRUCTURAL AND FUNCTIONAL EFFECTS OF MULTIPLE MUTATIONS AT DISTAL SITES IN CYTOCHROME C |
| 1CIG | STRUCTURAL AND FUNCTIONAL EFFECTS OF MULTIPLE MUTATIONS AT DISTAL SITES IN CYTOCHROME C |
| 1CIH | STRUCTURAL AND FUNCTIONAL EFFECTS OF MULTIPLE MUTATIONS AT DISTAL SITES IN CYTOCHROME C |
| 1CII | COLICIN IA |
| 1CIJ | HALOALKANE DEHALOGENASE SOAKED WITH HIGH CONCENTRATION OF BROMIDE |
| 1CIK | RECOMBINANT SPERM WHALE MYOGLOBIN I99A MUTANT (MET) |
| 1CIL | THE POSITIONS OF HIS-64 AND A BOUND WATER IN HUMAN CARBONIC ANHYDRASE II UPON BINDING THREE STRUCTURALLY RELATED INHIBITORS |
| 1CIM | THE POSITIONS OF HIS-64 AND A BOUND WATER IN HUMAN CARBONIC ANHYDRASE II UPON BINDING THREE STRUCTURALLY RELATED INHIBITORS |
| 1CIN | THE POSITIONS OF HIS-64 AND A BOUND WATER IN HUMAN CARBONIC ANHYDRASE II UPON BINDING THREE STRUCTURALLY RELATED INHIBITORS |
| 1CIO | RECOMBINANT SPERM WHALE MYOGLOBIN I99V MUTANT (MET) |
| 1CIP | GI-ALPHA-1 SUBUNIT OF GUANINE NUCLEOTIDE-BINDING PROTEIN COMPLEXED WITH A GTP ANALOGUE |
| 1CIQ | COMPLEX OF TWO FRAGMENTS OF CI2, RESIDUES 1-40 AND 41-64 |
| 1CIR | COMPLEX OF TWO FRAGMENTS OF CI2 [(1-40)(DOT)(41-64)] |
| 1CIS | CONTEXT DEPENDENCE OF PROTEIN SECONDARY STRUCTURE FORMATION. THE THREE-DIMENSIONAL STRUCTURE AND STABILITY OF A HYBRID BETWEEN CHYMOTRYPSIN INHIBITOR 2 AND HELIX E FROM SUBTILISIN CARLSBERG |
| 1CIT | DNA-BINDING MECHANISM OF THE MONOMERIC ORPHAN NUCLEAR RECEPTOR NGFI-B |
| 1CIU | THERMOSTABLE CGTASE FROM THERMOANAEROBACTERIUM THERMOSULFURIGENES EM1 AT PH 8.0. |
| 1CIV | CHLOROPLAST NADP-DEPENDENT MALATE DEHYDROGENASE FROM FLAVERIA BIDENTIS |
| 1CIW | PEANUT LECTIN COMPLEXED WITH N-ACETYLLACTOSAMINE |
| 1CIX | THREE-DIMENSIONAL STRUCTURE OF ANTIMICROBIAL PEPTIDE TACHYSTATIN A ISOLATED FROM HORSESHOE CRAB |
| 1CIY | INSECTICIDAL TOXIN: STRUCTURE AND CHANNEL FORMATION |
| 1CIZ | X-RAY STRUCTURE OF HUMAN STROMELYSIN CATALYTIC DOMAIN COMPLEXES WITH NON-PEPTIDE INHIBITORS: IMPLICATION FOR INHIBITOR SELECTIVITY |
| 1CJ0 | CRYSTAL STRUCTURE OF RABBIT CYTOSOLIC SERINE HYDROXYMETHYLTRANSFERASE AT 2.8 ANGSTROM RESOLUTION |
| 1CJ1 | GROWTH FACTOR RECEPTOR BINDING PROTEIN SH2 DOMAIN (HUMAN) COMPLEXED WITH A PHOSPHOTYROSYL DERIVATIVE |
| 1CJ2 | MUTANT GLN34ARG OF PARA-HYDROXYBENZOATE HYDROXYLASE |
| 1CJ3 | MUTANT TYR38GLU OF PARA-HYDROXYBENZOATE HYDROXYLASE |
| 1CJ4 | MUTANT Q34T OF PARA-HYDROXYBENZOATE HYDROXYLASE |
| 1CJ5 | BOVINE BETA-LACTOGLOBULIN A |
| 1CJ6 | T11A MUTANT HUMAN LYSOZYME |
| 1CJ7 | T11V MUTANT HUMAN LYSOZYME |
| 1CJ8 | T40A MUTANT HUMAN LYSOZYME |
| 1CJ9 | T40V MUTANT HUMAN LYSOZYME |
| 1CJA | ACTIN-FRAGMIN KINASE, CATALYTIC DOMAIN FROM PHYSARUM POLYCEPHALUM |
| 1CJB | MALARIAL PURINE PHOSPHORIBOSYLTRANSFERASE |
| 1CJC | STRUCTURE OF ADRENODOXIN REDUCTASE OF MITOCHONDRIAL P450 SYSTEMS |
| 1CJD | THE BACTERIOPHAGE PRD1 COAT PROTEIN, P3, IS STRUCTURALLY SIMILAR TO HUMAN ADENOVIRUS HEXON |
| 1CJE | ADRENODOXIN FROM BOVINE |
| 1CJF | PROFILIN BINDS PROLINE-RICH LIGANDS IN TWO DISTINCT AMIDE BACKBONE ORIENTATIONS |
| 1CJG | NMR STRUCTURE OF LAC REPRESSOR HP62-DNA COMPLEX |
| 1CJK | COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH ADENOSINE 5'-(ALPHA THIO)-TRIPHOSPHATE (RP), MG, AND MN |
| 1CJL | CRYSTAL STRUCTURE OF A CYSTEINE PROTEASE PROFORM |
| 1CJM | HUMAN SULT1A3 WITH SULFATE BOUND |
| 1CJP | CONCANAVALIN A COMPLEX WITH 4'-METHYLUMBELLIFERYL-ALPHA-D-GLUCOPYRANOSIDE |
| 1CJQ | X-RAY CRYSTALLOGRAPHIC STUDIES OF THE DENATURATION OF THE DENATURATION OF RIBONUCLEASE S. |
| 1CJR | X-RAY CRYSTALLOGRAPHIC STUDIES OF DENATURATION IN RIBONUCLEASE S |
| 1CJS | CRYSTAL STRUCTURE OF RIBOSOMAL PROTEIN L1 FROM METHANOCOCCUS JANNASCHII |
| 1CJT | COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH BETA-L-2',3'-DIDEOXYATP, MN, AND MG |
| 1CJU | COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH BETA-L-2',3'-DIDEOXYATP AND MG |
| 1CJV | COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH BETA-L-2',3'-DIDEOXYATP, MG, AND ZN |
| 1CJW | SEROTONIN N-ACETYLTRANSFERASE COMPLEXED WITH A BISUBSTRATE ANALOG |
| 1CJX | CRYSTAL STRUCTURE OF PSEUDOMONAS FLUORESCENS HPPD |
| 1CJY | HUMAN CYTOSOLIC PHOSPHOLIPASE A2 |
| 1CK0 | ANTI-ANTI-IDIOTYPIC ANTIBODY AGAINST HUMAN ANGIOTENSIN II, UNLIGANDED FORM |
| 1CK1 | STRUCTURE OF STAPHYLOCOCCAL ENTEROTOXIN C3 |
| 1CK2 | YEAST (SACCHAROMYCES CEREVISIAE) RIBOSOMAL PROTEIN L30 |
| 1CK3 | N276D MUTANT OF ESCHERICHIA COLI TEM-1 BETA-LACTAMASE |
| 1CK4 | CRYSTAL STRUCTURE OF RAT A1B1 INTEGRIN I-DOMAIN. |
| 1CK6 | BINDING MODE OF SALICYLHYDROXAMIC ACID TO ARTHROMYCES RAMOSUS PEROXIDASE |
| 1CK7 | GELATINASE A (FULL-LENGTH) |
| 1CKA | STRUCTURAL BASIS FOR THE SPECIFIC INTERACTION OF LYSINE-CONTAINING PROLINE-RICH PEPTIDES WITH THE N-TERMINAL SH3 DOMAIN OF C-CRK |
| 1CKB | STRUCTURAL BASIS FOR THE SPECIFIC INTERACTION OF LYSINE-CONTAINING PROLINE-RICH PEPTIDES WITH THE N-TERMINAL SH3 DOMAIN OF C-CRK |
| 1CKC | T43A MUTANT HUMAN LYSOZYME |
| 1CKD | T43V MUTANT HUMAN LYSOZYME |
| 1CKE | CMP KINASE FROM ESCHERICHIA COLI FREE ENZYME STRUCTURE |
| 1CKF | T52A MUTANT HUMAN LYSOZYME |
| 1CKG | T52V MUTANT HUMAN LYSOZYME |
| 1CKH | T70V MUTANT HUMAN LYSOZYME |
| 1CKI | RECOMBINANT CASEIN KINASE I DELTA TRUNCATION MUTANT CONTAINING RESIDUES 1-317 |
| 1CKJ | CASEIN KINASE I DELTA TRUNCATION MUTANT CONTAINING RESIDUES 1-317 COMPLEX WITH BOUND TUNGSTATE |
| 1CKK | CALMODULIN/RAT CA2+/CALMODULIN DEPENDENT PROTEIN KINASE FRAGMENT |
| 1CKL | N-TERMINAL TWO DOMAINS OF HUMAN CD46 (MEMBRANE COFACTOR PROTEIN, MCP) |
| 1CKM | STRUCTURE OF TWO DIFFERENT CONFORMATIONS OF MRNA CAPPING ENZYME IN COMPLEX WITH GTP |
| 1CKN | STRUCTURE OF GUANYLYLATED MRNA CAPPING ENZYME COMPLEXED WITH GTP |
| 1CKO | STRUCTURE OF MRNA CAPPING ENZYME IN COMPLEX WITH THE CAP ANALOG GPPPG |
| 1CKP | HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR PURVALANOL B |
| 1CKQ | PRE-TRANSITION STATE ECO RI ENDONUCLEASE/COGNATE DNA (TCGCGAATTCGCG) COMPLEX |
| 1CKR | HIGH RESOLUTION SOLUTION STRUCTURE OF THE HEAT SHOCK COGNATE-70 KD SUBSTRATE BINDING DOMAIN OBTAINED BY MULTIDIMENSIONAL NMR TECHNIQUES |
| 1CKS | HUMAN CKSHS2 ATOMIC STRUCTURE: A ROLE FOR ITS HEXAMERIC ASSEMBLY IN CELL CYCLE CONTROL |
| 1CKT | CRYSTAL STRUCTURE OF HMG1 DOMAIN A BOUND TO A CISPLATIN-MODIFIED DNA DUPLEX |
| 1CKU | AB INITIO SOLUTION AND REFINEMENT OF TWO HIGH POTENTIAL IRON PROTEIN STRUCTURES AT ATOMIC RESOLUTION |
| 1CKV | STRUCTURE OF THE SOLUBLE METHANE MONOOXYGENASE REGULATORY PROTEIN B |
| 1CKW | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR: SOLUTION STRUCTURES OF PEPTIDES BASED ON THE PHE508 REGION, THE MOST COMMON SITE OF DISEASE-CAUSING DELTA-F508 MUTATION |
| 1CKY | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR: SOLUTION STRUCTURES OF PEPTIDES BASED ON THE PHE508 REGION, THE MOST COMMON SITE OF DISEASE-CAUSING DELTA-F508 MUTATION |
| 1CKZ | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR: SOLUTION STRUCTURES OF PEPTIDES BASED ON THE PHE508 REGION, THE MOST COMMON SITE OF DISEASE-CAUSING DELTA-F508 MUTATION |
| 1CL0 | CRYSTAL STRUCTURE OF REDUCED THIOREDOXIN REDUCTASE FROM ESCHERICHIA COLI. |
| 1CL1 | CYSTATHIONINE BETA-LYASE (CBL) FROM ESCHERICHIA COLI |
| 1CL2 | CYSTATHIONINE BETA-LYASE (CBL) FROM ESCHERICHIA COLI IN COMPLEX WITH AMINOETHOXYVINYLGLYCINE |
| 1CL3 | MOLECULAR INSIGHTS INTO PEBP2/CBF-SMMHC ASSOCIATED ACUTE LEUKEMIA REVEALED FROM THE THREE-DIMENSIONAL STRUCTURE OF PEBP2/CBF BETA |
| 1CL4 | NUCLEOCAPSID PROTEIN FROM MASON-PFIZER MONKEY VIRUS (MPMV) |
| 1CL5 | CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 FROM DABOIA RUSSELLI PULCHELLA |
| 1CL6 | CRYSTAL STRUCTURES OF FERRIC-NO COMPLEXES OF FUNGAL NITRIC OXIDE REDUCTASE AND ITS SER286 MUTANTS AT CRYOGENIC TEMPERATURE |
| 1CL7 | ANTI HIV1 PROTEASE FAB |
| 1CL8 | A PRE-TRANSITION STATE ECO RI ENDONUCLEASE/COGNATE DNA (TCGCGAPTTCGCG) COMPLEX WITH DNA BASE ANALOG PURINE (P) |
| 1CLA | EVIDENCE FOR TRANSITION-STATE STABILIZATION BY SERINE-148 IN THE CATALYTIC MECHANISM OF CHLORAMPHENICOL ACETYLTRANSFERASE |
| 1CLB | DETERMINATION OF THE SOLUTION STRUCTURE OF APO CALBINDIN D9K BY NMR SPECTROSCOPY |
| 1CLC | THREE-DIMENSIONAL STRUCTURE OF ENDOGLUCANASE D AT 1.9 ANGSTROMS RESOLUTION |
| 1CLD | DNA-BINDING PROTEIN |
| 1CLE | STRUCTURE OF UNCOMPLEXED AND LINOLEATE-BOUND CANDIDA CYLINDRACEA CHOLESTEROL ESTERASE |
| 1CLF | CLOSTRIDIUM PASTEURIANUM FERREDOXIN |
| 1CLH | THREE-DIMENSIONAL SOLUTION STRUCTURE OF ESCHERICHIA COLI PERIPLASMIC CYCLOPHILIN |
| 1CLI | X-RAY CRYSTAL STRUCTURE OF AMINOIMIDAZOLE RIBONUCLEOTIDE SYNTHETASE (PURM), FROM THE E. COLI PURINE BIOSYNTHETIC PATHWAY, AT 2.5 A RESOLUTION |
| 1CLK | CRYSTAL STRUCTURE OF STREPTOMYCES DIASTATICUS NO.7 STRAIN M1033 XYLOSE ISOMERASE AT 1.9 A RESOLUTION WITH PSEUDO-I222 SPACE GROUP |
| 1CLL | CALMODULIN STRUCTURE REFINED AT 1.7 ANGSTROMS RESOLUTION |
| 1CLM | STRUCTURE OF PARAMECIUM TETRAURELIA CALMODULIN AT 1.8 ANGSTROMS RESOLUTION |
| 1CLO | ANTI-CARCINOEMBRYONIC ANTIGEN MONOCLONAL ANTIBODY A5B7 |
| 1CLP | CRYSTAL STRUCTURE OF A CALCIUM-INDEPENDENT PHOSPHOLIPASELIKE MYOTOXIC PROTEIN FROM BOTHROPS ASPER VENOM |
| 1CLQ | CRYSTAL STRUCTURE OF A REPLICATION FORK DNA POLYMERASE EDITING COMPLEX AT 2.7 A RESOLUTION |
| 1CLS | CROSS-LINKED HUMAN HEMOGLOBIN DEOXY |
| 1CLU | H-RAS COMPLEXED WITH DIAMINOBENZOPHENONE-BETA,GAMMA-IMIDO-GTP |
| 1CLV | YELLOW MEAL WORM ALPHA-AMYLASE IN COMPLEX WITH THE AMARANTH ALPHA-AMYLASE INHIBITOR |
| 1CLW | TAILSPIKE PROTEIN FROM PHAGE P22, V331A MUTANT |
| 1CLX | CATALYTIC CORE OF XYLANASE A |
| 1CLY | IGG FAB (HUMAN IGG1, KAPPA) CHIMERIC FRAGMENT (CBR96) COMPLEXED WITH LEWIS Y NONOATE METHYL ESTER |
| 1CLZ | IGG FAB (IGG3, KAPPA) FRAGMENT (MBR96) COMPLEXED WITH LEWIS Y NONOATE METHYL ESTER |
| 1CM0 | CRYSTAL STRUCTURE OF THE PCAF/COENZYME-A COMPLEX |
| 1CM1 | MOTIONS OF CALMODULIN-SINGLE-CONFORMER REFINEMENT |
| 1CM2 | STRUCTURE OF HIS15ASP HPR AFTER HYDROLYSIS OF RINGED SPECIES. |
| 1CM3 | HIS15ASP HPR FROM E. COLI |
| 1CM5 | CRYSTAL STRUCTURE OF C418A,C419A MUTANT OF PFL FROM E.COLI |
| 1CM7 | 3-ISOPROPYLMALATE DEHYDROGENASE FROM ESCHERICHIA COLI |
| 1CM8 | PHOSPHORYLATED MAP KINASE P38-GAMMA |
| 1CM9 | CRYSTAL STRUCTURE OF VIRAL MACROPHAGE INFLAMMATORY PROTEIN-II |
| 1CMA | MET REPRESSOR/DNA COMPLEX + S-ADENOSYL-METHIONINE |
| 1CMB | THREE DIMENSIONAL CRYSTAL STRUCTURES OF ESCHERICHIA COLI MET REPRESSOR WITH AND WITHOUT COREPRESSOR |
| 1CMC | THREE DIMENSIONAL CRYSTAL STRUCTURES OF E. COLI MET REPRESSOR WITH AND WITHOUT COREPRESSOR |
| 1CMF | NMR SOLUTION STRUCTURE OF APO CALMODULIN CARBOXY-TERMINAL DOMAIN |
| 1CMG | NMR SOLUTION STRUCTURE OF CALCIUM-LOADED CALMODULIN CARBOXY-TERMINAL DOMAIN |
| 1CMI | STRUCTURE OF THE HUMAN PIN/LC8 DIMER WITH A BOUND PEPTIDE |
| 1CMJ | CRYSTAL STRUCTURES OF FERRIC-NO COMPLEXES OF FUNGAL NITRIC OXIDE REDUCTASE AND THEIR SER286 MUTANTS AT CRYOGENIC TEMPERATURE |
| 1CMK | CRYSTAL STRUCTURES OF THE MYRISTYLATED CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE REVEAL OPEN AND CLOSED CONFORMATIONS |
| 1CML | CHALCONE SYNTHASE FROM ALFALFA COMPLEXED WITH MALONYL-COA |
| 1CMN | CRYSTAL STRUCTURES OF FERRIC-NO COMPLEXES OF FUNGAL NITRIC OXIDE REDUCTASE AND THEIR SER286 MUTANTS AT CRYOGENIC TEMPERATURE |
| 1CMO | IMMUNOGLOBULIN MOTIF DNA-RECOGNITION AND HETERODIMERIZATION FOR THE PEBP2/CBF RUNT-DOMAIN |
| 1CMP | SMALL MOLECULE BINDING TO AN ARTIFICIALLY CREATED CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE |
| 1CMQ | SMALL MOLECULE BINDING TO AN ARTIFICIALLY CREATED CAVITY AT THE ACTIVE SITE OF CYTOCHROME C PEROXIDASE |
| 1CMR | NMR SOLUTION STRUCTURE OF A CHIMERIC PROTEIN, DESIGNED BY TRANSFERRING A FUNCTIONAL SNAKE BETA-HAIRPIN INTO A SCORPION ALPHA/BETA SCAFFOLD (PH 3.5, 20C), NMR, 18 STRUCTURES |
| 1CMS | THE THREE-DIMENSIONAL STRUCTURE OF RECOMBINANT BOVINE CHYMOSIN AT 2.3 ANGSTROMS RESOLUTION |
| 1CMT | THE ROLE OF ASPARTATE-235 IN THE BINDING OF CATIONS TO AN ARTIFICIAL CAVITY AT THE RADICAL SITE OF CYTOCHROME C PEROXIDASE |
| 1CMU | THE ROLE OF ASPARTATE-235 IN THE BINDING OF CATIONS TO AN ARTIFICIAL CAVITY AT THE RADICAL SITE OF CYTOCHROME C PEROXIDASE |
| 1CMV | HUMAN CYTOMEGALOVIRUS PROTEASE |
| 1CMX | STRUCTURAL BASIS FOR THE SPECIFICITY OF UBIQUITIN C-TERMINAL HYDROLASES |
| 1CMY | THE MUTATION BETA99 ASP-TYR STABILIZES Y-A NEW, COMPOSITE QUATERNARY STATE OF HUMAN HEMOGLOBIN |
| 1CMZ | SOLUTION STRUCTURE OF GAIP (GALPHA INTERACTING PROTEIN): A REGULATOR OF G PROTEIN SIGNALING |
| 1CN1 | CRYSTAL STRUCTURE OF DEMETALLIZED CONCANAVALIN A. THE METAL-BINDING REGION |
| 1CN2 | SOLUTION STRUCTURE OF TOXIN 2 FROM CENTRUROIDES NOXIUS HOFFMANN, A BETA SCORPION NEUROTOXIN ACTING ON SODIUM CHANNELS, NMR, 15 STRUCTURES |
| 1CN3 | INTERACTION OF POLYOMAVIRUS INTERNAL PROTEIN VP2 WITH MAJOR CAPSID PROTEIN VP1 AND IMPLICATIONS FOR PARTICIPATION OF VP2 IN VIRAL ENTRY |
| 1CN4 | ERYTHROPOIETIN COMPLEXED WITH EXTRACELLULAR DOMAINS OF ERYTHROPOIETIN RECEPTOR |
| 1CN7 | YEAST RIBOSOMAL PROTEIN L30 |
| 1CNB | COMPENSATORY PLASTIC EFFECTS IN THE REDESIGN OF PROTEIN-ZINC BINDING SITES |
| 1CNC | COMPENSATORY PLASTIC EFFECTS IN THE REDESIGN OF PROTEIN-ZINC BINDING SITES |
| 1CNE | STRUCTURAL STUDIES ON CORN NITRATE REDUCTASE: REFINED STRUCTURE OF THE CYTOCHROME B REDUCTASE FRAGMENT AT 2.5 ANGSTROMS, ITS ADP COMPLEX AND AN ACTIVE SITE MUTANT AND MODELING OF THE CYTOCHROME B DOMAIN |
| 1CNF | STRUCTURAL STUDIES ON CORN NITRATE REDUCTASE: REFINED STRUCTURE OF THE CYTOCHROME B REDUCTASE FRAGMENT AT 2.5 ANGSTROMS, ITS ADP COMPLEX AND AN ACTIVE SITE MUTANT AND MODELING OF THE CYTOCHROME B DOMAIN |
| 1CNG | X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE |
| 1CNH | X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE |
| 1CNI | X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE |
| 1CNJ | X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE |
| 1CNK | X-RAY CRYSTALLOGRAPHIC STUDIES OF ENGINEERED HYDROGEN BOND NETWORKS IN A PROTEIN-ZINC BINDING SITE |
| 1CNL | ALPHA-CONOTOXIN IMI |
| 1CNM | ENHANCEMENT OF CATALYTIC EFFICIENCY OF PROTEINASE K THROUGH EXPOSURE TO ANHYDROUS ORGANIC SOLVENT AT 70 DEGREES CELSIUS |
| 1CNN | OMEGA-CONOTOXIN MVIIC FROM CONUS MAGUS |
| 1CNO | STRUCTURE OF PSEUDOMONAS NAUTICA CYTOCHROME C552, BY MAD METHOD |
| 1CNP | THE STRUCTURE OF CALCYCLIN REVEALS A NOVEL HOMODIMERIC FOLD FOR S100 CA2+-BINDING PROTEINS, NMR, 22 STRUCTURES |
| 1CNQ | FRUCTOSE-1,6-BISPHOSPHATASE COMPLEXED WITH FRUCTOSE-6-PHOSPHATE AND ZINC IONS |
| 1CNR | CORRELATED DISORDER OF THE PURE PRO22(SLASH)LEU25 FORM OF CRAMBIN AT 150K REFINED TO 1.05 ANGSTROMS RESOLUTION |
| 1CNS | CRYSTAL STRUCTURE OF CHITINASE AT 1.91A RESOLUTION |
| 1CNT | CILIARY NEUROTROPHIC FACTOR |
| 1CNU | PHOSPHORYLATED ACTOPHORIN FROM ACANTAMOEBA POLYPHAGA |
| 1CNV | CRYSTAL STRUCTURE OF CONCANAVALIN B AT 1.65 A RESOLUTION |
| 1CNW | SECONDARY INTERACTIONS SIGNIFICANTLY REMOVED FROM THE SULFONAMIDE BINDING POCKET OF CARBONIC ANHYDRASE II INFLUENCE BINDING CONSTANTS |
| 1CNX | SECONDARY INTERACTIONS SIGNIFICANTLY REMOVED FROM THE SULFONAMIDE BINDING POCKET OF CARBONIC ANHYDRASE II INFLUENCE BINDING CONSTANTS |
| 1CNY | SECONDARY INTERACTIONS SIGNIFICANTLY REMOVED FROM THE SULFONAMIDE BINDING POCKET OF CARBONIC ANHYDRASE II INFLUENCE BINDING CONSTANTS |
| 1CNZ | 3-ISOPROPYLMALATE DEHYDROGENASE (IPMDH) FROM SALMONELLA TYPHIMURIUM |
| 1CO0 | NMR STUDY OF TRP REPRESSOR-MTR OPERATOR DNA COMPLEX |
| 1CO1 | FOLD OF THE CBFA |
| 1CO4 | SOLUTION STRUCTURE OF A ZINC DOMAIN CONSERVED IN YEAST COPPER-REGULATED TRANSCRIPTION FACTORS |
| 1CO6 | CRYSTAL STRUCTURE OF FERROCYTOCHROME C2 FROM RHODOPSEUDOMONAS VIRIDIS |
| 1CO8 | RECOMBINANT SPERM WHALE MYOGLOBIN L104A MUTANT (MET) |
| 1CO9 | RECOMBINANT SPERM WHALE MYOGLOBIN L104V MUTANT (MET) |
| 1COA | THE EFFECT OF CAVITY CREATING MUTATIONS IN THE HYDROPHOBIC CORE OF CHYMOTRYPSIN INHIBITOR 2 |
| 1COB | CRYSTAL STRUCTURE SOLUTION AND REFINEMENT OF THE SEMISYNTHETIC COBALT SUBSTITUTED BOVINE ERYTHROCYTE ENZYME SUPEROXIDE DISMUTASE AT 2.0 ANGSTROMS RESOLUTION |
| 1COD | SOLUTION CONFORMATION OF COBROTOXIN: A NUCLEAR MAGNETIC RESONANCE AND HYBRID DISTANCE GEOMETRY-DYNAMICAL SIMULATED ANNEALING STUDY |
| 1COE | SOLUTION CONFORMATION OF COBROTOXIN: A NUCLEAR MAGNETIC RESONANCE AND HYBRID DISTANCE GEOMETRY-DYNAMICAL SIMULATED ANNEALING STUDY |
| 1COF | YEAST COFILIN, ORTHORHOMBIC CRYSTAL FORM |
| 1COH | STRUCTURE OF HAEMOGLOBIN IN THE DEOXY QUATERNARY STATE WITH LIGAND BOUND AT THE ALPHA HAEMS |
| 1COJ | FE-SOD FROM AQUIFEX PYROPHILUS, A HYPERTHERMOPHILIC BACTERIUM |
| 1COK | STRUCTURE OF THE C-TERMINAL DOMAIN OF P73 |
| 1COL | REFINED STRUCTURE OF THE PORE-FORMING DOMAIN OF COLICIN A AT 2.4 ANGSTROMS RESOLUTION |
| 1COM | THE MONOFUNCTIONAL CHORISMATE MUTASE FROM BACILLUS SUBTILIS: STRUCTURE DETERMINATION OF CHORISMATE MUTASE AND ITS COMPLEXES WITH A TRANSITION STATE ANALOG AND PREPHENATE, AND IMPLICATIONS ON THE MECHANISM OF ENZYMATIC REACTION |
| 1CON | THE REFINED STRUCTURE OF CADMIUM SUBSTITUTED CONCANAVALIN A AT 2.0 ANGSTROMS RESOLUTION |
| 1COO | THE COOH-TERMINAL DOMAIN OF RNA POLYMERASE ALPHA SUBUNIT |
| 1COP | THREE-DIMENSIONAL DIMER STRUCTURE OF THE LAMBDA-CRO REPRESSOR IN SOLUTION AS DETERMINED BY HETERONUCLEAR MULTIDIMENSIONAL NMR |
| 1COR | INVESTIGATION OF THE SOLUTION CONFORMATION OF CYTOCHROME C-551 FROM PSEUDOMONAS STUTZERI |
| 1COT | X-RAY STRUCTURE OF THE CYTOCHROME C2 ISOLATED FROM PARACOCCUS DENITRIFICANS REFINED TO 1.7 ANGSTROMS RESOLUTION |
| 1COU | ANTICOAGULANT PROTEIN FROM THE NEMATODE ANCYLOSTOMA CANINUM |
| 1COV | COXSACKIEVIRUS B3 COAT PROTEIN |
| 1COW | BOVINE MITOCHONDRIAL F1-ATPASE COMPLEXED WITH AUROVERTIN B |
| 1COY | CRYSTAL STRUCTURE OF CHOLESTEROL OXIDASE COMPLEXED WITH A STEROID SUBSTRATE. IMPLICATIONS FOR FAD DEPENDENT ALCOHOL OXIDASES |
| 1COZ | CTP:GLYCEROL-3-PHOSPHATE CYTIDYLYLTRANSFERASE FROM BACILLUS SUBTILIS |
| 1CP0 | RECOMBINANT SPERM WHALE MYOGLOBIN L104N MUTANT (MET) |
| 1CP2 | NITROGENASE IRON PROTEIN FROM CLOSTRIDIUM PASTEURIANUM |
| 1CP3 | CRYSTAL STRUCTURE OF THE COMPLEX OF APOPAIN WITH THE TETRAPEPTIDE INHIBITOR ACE-DVAD-FMC |
| 1CP4 | FORMATION, CRYSTAL STRUCTURE, AND REARRANGEMENT OF A CYTOCHROME P450-CAM IRON-PHENYL COMPLEX |
| 1CP5 | RECOMBINANT SPERM WHALE MYOGLOBIN L104F MUTANT (MET) |
| 1CP6 | 1-BUTANEBORONIC ACID BINDING TO AEROMONAS PROTEOLYTICA AMINOPEPTIDASE |
| 1CP7 | AMINOPEPTIDASE FROM STREPTOMYCES GRISEUS |
| 1CP9 | CRYSTAL STRUCTURE OF PENICILLIN G ACYLASE FROM THE BRO1 MUTANT STRAIN OF PROVIDENCIA RETTGERI |
| 1CPB | STRUCTURE OF CARBOXYPEPTIDASE B AT 2.8 ANGSTROMS RESOLUTION |
| 1CPC | ISOLATION, CRYSTALLIZATION, CRYSTAL STRUCTURE ANALYSIS AND REFINEMENT OF CONSTITUTIVE C-PHYCOCYANIN FROM THE CHROMATICALLY ADAPTING CYANOBACTERIUM FREMYELLA DIPLOSIPHON AT 1.66 ANGSTROMS RESOLUTION |
| 1CPD | A CATION BINDING MOTIF STABILIZES THE COMPOUND I RADICAL OF CYTOCHROME C PEROXIDASE |
| 1CPE | A CATION BINDING MOTIF STABILIZES THE COMPOUND I RADICAL OF CYTOCHROME C PEROXIDASE |
| 1CPF | A CATION BINDING MOTIF STABILIZES THE COMPOUND I RADICAL OF CYTOCHROME C PEROXIDASE |
| 1CPG | A CATION BINDING MOTIF STABILIZES THE COMPOUND I RADICAL OF CYTOCHROME C PEROXIDASE |
| 1CPH | CONFORMATIONAL CHANGES IN CUBIC INSULIN CRYSTALS IN THE PH RANGE 7-11 |
| 1CPI | REGIOSELECTIVE STRUCTURAL AND FUNCTIONAL MIMICRY OF PEPTIDES. DESIGN OF HYDROLYTICALLY STABLE CYCLIC PEPTIDOMIMETIC INHIBITORS OF HIV-1 PROTEASE |
| 1CPJ | CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE-BASED INHIBITOR DESIGN |
| 1CPM | NATIVE-LIKE IN VIVO FOLDING OF A CIRCULARLY PERMUTED JELLYROLL PROTEIN SHOWN BY CRYSTAL STRUCTURE ANALYSIS |
| 1CPN | NATIVE-LIKE IN VIVO FOLDING OF A CIRCULARLY PERMUTED JELLYROLL PROTEIN SHOWN BY CRYSTAL STRUCTURE ANALYSIS |
| 1CPO | CHLOROPEROXIDASE |
| 1CPQ | CYTOCHROME C' FROM RHODOPSEUDOMONAS CAPSULATA |
| 1CPR | ST. LOUIS CYTOCHROME C' FROM THE PURPLE PHOTOTROPIC BACTERIUM, RHODOBACTER CAPSULATUS |
| 1CPS | STRUCTURAL COMPARISON OF SULFODIIMINE AND SULFONAMIDE INHIBITORS IN THEIR COMPLEXES WITH ZINC ENZYMES |
| 1CPT | CRYSTAL STRUCTURE AND REFINEMENT OF CYTOCHROME P450-TERP AT 2.3 ANGSTROMS RESOLUTION |
| 1CPU | SUBSITE MAPPING OF THE ACTIVE SITE OF HUMAN PANCREATIC ALPHA-AMYLASE USING SUBSTRATES, THE PHARMACOLOGICAL INHIBITOR ACARBOSE, AND AN ACTIVE SITE VARIANT |
| 1CPW | RECOMBINANT SPERM WHALE MYOGLOBIN L104W MUTANT (MET) |
| 1CPX | BETA FORM OF CARBOXYPEPTIDASE A (RESIDUES 3-307) FROM BOVINE PANCREAS IN AN ORTHORHOMBIC CRYSTAL FORM WITH TWO ZINC IONS IN THE ACTIVE SITE. |
| 1CPY | SITE-DIRECTED MUTAGENESIS ON (SERINE) CARBOXYPEPTIDASE Y FROM YEAST. THE SIGNIFICANCE OF THR 60 AND MET 398 IN HYDROLYSIS AND AMINOLYSIS REACTIONS |
| 1CPZ | COPPER CHAPERONE OF ENTEROCOCCUS HIRAE (APO-FORM) |
| 1CQ0 | SOLUTION STRUCTURE OF A HUMAN HYPOCRETIN-2/OREXIN-B'SOLUTION STRUCTURE OF A HUMAN HYPOCRETIN-2/OREXIN-B ' |
| 1CQ1 | SOLUBLE QUINOPROTEIN GLUCOSE DEHYDROGENASE FROM ACINETOBACTER CALCOACETICUS IN COMPLEX WITH PQQH2 AND GLUCOSE |
| 1CQ2 | NEUTRON STRUCTURE OF FULLY DEUTERATED SPERM WHALE MYOGLOBIN AT 2.0 ANGSTROM |
| 1CQ3 | STRUCTURE OF A SOLUBLE SECRETED CHEMOKINE INHIBITOR, VCCI, FROM COWPOX VIRUS |
| 1CQ4 | CI2 MUTANT WITH TETRAGLUTAMINE (MGQQQQGM) REPLACING MET59 |
| 1CQ6 | ASPARTATE AMINOTRANSFERASE COMPLEX WITH C4-PYRIDOXAL-5P-PHOSPHATE |
| 1CQ7 | ASPARTATE AMINOTRANSFERASE (E.C. 2.6.1.1) COMPLEXED WITH C5-PYRIDOXAL-5P-PHOSPHATE |
| 1CQ8 | ASPARTATE AMINOTRANSFERASE (E.C. 2.6.1.1) COMPLEXED WITH C6-PYRIDOXAL-5P-PHOSPHATE |
| 1CQ9 | PEANUT LECTIN-TRICLINIC FORM |
| 1CQA | BIRCH POLLEN PROFILIN |
| 1CQD | THE 2.1 ANGSTROM STRUCTURE OF A CYSTEINE PROTEASE WITH PROLINE SPECIFICITY FROM GINGER RHIZOME, ZINGIBER OFFICINALE |
| 1CQE | PROSTAGLANDIN H2 SYNTHASE-1 COMPLEX WITH FLURBIPROFEN |
| 1CQF | THE COMPLEX OF THE MUTATED SHIGA TOXIN B SUBUNIT AND GB3 TRISACCHARIDE |
| 1CQG | HIGH RESOLUTION SOLUTION NMR STRUCTURE OF MIXED DISULFIDE INTERMEDIATE BETWEEN HUMAN THIOREDOXIN (C35A, C62A, C69A, C73A) MUTANT AND A 13 RESIDUE PEPTIDE COMPRISING ITS TARGET SITE IN HUMAN REF-1 (RESIDUES 59-71 OF THE P50 SUBUNIT OF NFKB), NMR, 31 STRUCTURES |
| 1CQH | HIGH RESOLUTION SOLUTION NMR STRUCTURE OF MIXED DISULFIDE INTERMEDIATE BETWEEN HUMAN THIOREDOXIN (C35A, C62A, C69A, C73A) MUTANT AND A 13 RESIDUE PEPTIDE COMPRISING ITS TARGET SITE IN HUMAN REF-1 (RESIDUES 59-71 OF THE P50 SUBUNIT OF NFKB), NMR, MINIMIZED AVERAGE STRUCTURE |
| 1CQI | CRYSTAL STRUCTURE OF THE COMPLEX OF ADP AND MG2+ WITH DEPHOSPHORYLATED E. COLI SUCCINYL-COA SYNTHETASE |
| 1CQJ | CRYSTAL STRUCTURE OF DEPHOSPHORYLATED E. COLI SUCCINYL-COA SYNTHETASE |
| 1CQK | CRYSTAL STRUCTURE OF THE CH3 DOMAIN FROM THE MAK33 ANTIBODY |
| 1CQM | PROTEIN AGGREGATION AND ALZHEIMER'S DISEASE: CRYSTALLOGRAPHIC ANALYSIS OF THE PHENOMENON. ENGINEERED VERSION OF THE RIBOSOMAL PROTEIN S6 USED AS A STABLE SCAFFOLD TO STUDY OLIGOMERIZATION. |
| 1CQN | PROTEIN AGGREGATION AND ALZHEIMER'S DISEASE: CRYSTALLOGRAPHIC ANALYSIS OF THE PHENOMENON. ENGINEERED VERSION OF THE RIBOSOMAL PROTEIN S6 USED AS A STABLE SCAFFOLD TO STUDY OLIGOMERIZATION. |
| 1CQP | CRYSTAL STRUCTURE ANALYSIS OF THE COMPLEX LFA-1 (CD11A) I-DOMAIN / LOVASTATIN AT 2.6 A RESOLUTION |
| 1CQQ | TYPE 2 RHINOVIRUS 3C PROTEASE WITH AG7088 INHIBITOR |
| 1CQR | CRYSTAL STRUCTURE OF THE STROMELYSIN CATALYTIC DOMAIN AT 2.0 A RESOLUTION |
| 1CQS | CRYSTAL STRUCTURE OF D103E MUTANT WITH EQUILENINEOF KSI IN PSEUDOMONAS PUTIDA |
| 1CQT | CRYSTAL STRUCTURE OF A TERNARY COMPLEX CONTAINING AN OCA-B PEPTIDE, THE OCT-1 POU DOMAIN, AND AN OCTAMER ELEMENT |
| 1CQU | SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF RIBOSOMAL PROTEIN L9 |
| 1CQV | CRYSTAL STRUCTURE OF STAPHYLOCOCCAL ENTEROTOXIN C2 AT 100K CRYSTALLIZED AT PH 5.0 |
| 1CQW | NAI COCRYSTALLISED WITH HALOALKANE DEHALOGENASE FROM A RHODOCOCCUS SPECIES |
| 1CQX | CRYSTAL STRUCTURE OF THE FLAVOHEMOGLOBIN FROM ALCALIGENES EUTROPHUS AT 1.75 A RESOLUTION |
| 1CQY | STARCH BINDING DOMAIN OF BACILLUS CEREUS BETA-AMYLASE |
| 1CR0 | CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF THE GENE4 PROTEIN OF BACTERIOPHAGE T7 |
| 1CR1 | CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF THE GENE 4 PROTEIN OF BACTERIOPHAGE T7: COMPLEX WITH DTTP |
| 1CR2 | CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF THE GENE 4 PROTEIN OF BACTERIOPHAGE T7: COMPLEX WITH DATP |
| 1CR4 | CRYSTAL STRUCTURE OF THE HELICASE DOMAIN OF THE GENE 4 PROTEIN OF BACTERIOPHAGE T7: COMPLEX WITH DTDP |
| 1CR5 | N-TERMINAL DOMAIN OF SEC18P |
| 1CR7 | PEANUT LECTIN-LACTOSE COMPLEX MONOCLINIC FORM |
| 1CR8 | LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN COMPLEMENT REPEAT 8 |
| 1CR9 | CRYSTAL STRUCTURE OF THE ANTI-PRION FAB 3F4 |
| 1CRA | THE COMPLEX BETWEEN HUMAN CARBONIC ANHYDRASE II AND THE AROMATIC INHIBITOR 1,2,4-TRIAZOLE |
| 1CRB | CRYSTALLOGRAPHIC STUDIES ON A FAMILY OF CELLULAR LIPOPHILIC TRANSPORT PROTEINS. REFINEMENT OF P2 MYELIN PROTEIN AND THE STRUCTURE DETERMINATION AND REFINEMENT OF CELLULAR RETINOL-BINDING PROTEIN IN COMPLEX WITH ALL-TRANS-RETINOL |
| 1CRC | CYTOCHROME C AT LOW IONIC STRENGTH |
| 1CRE | CARDIOTOXIN II FROM TAIWAN COBRA VENOM, NAJA NAJA ATRA: STRUCTURE IN SOLUTION AND COMPARISION AMONG HOMOLOGOUS CARDIOTOXINS |
| 1CRF | CARDIOTOXIN II FROM TAIWAN COBRA VENOM, NAJA NAJA ATRA: STRUCTURE IN SOLUTION AND COMPARISION AMONG HOMOLOGOUS CARDIOTOXINS |
| 1CRG | THE ROLE OF A CONSERVED INTERNAL WATER MOLECULE AND ITS ASSOCIATED HYDROGEN BOND NETWORK IN CYTOCHROME C |
| 1CRH | THE ROLE OF A CONSERVED INTERNAL WATER MOLECULE AND ITS ASSOCIATED HYDROGEN BOND NETWORK IN CYTOCHROME C |
| 1CRI | THE ROLE OF A CONSERVED INTERNAL WATER MOLECULE AND ITS ASSOCIATED HYDROGEN BOND NETWORK IN CYTOCHROME C |
| 1CRJ | THE ROLE OF A CONSERVED INTERNAL WATER MOLECULE AND ITS ASSOCIATED HYDROGEN BOND NETWORK IN CYTOCHROME C |
| 1CRK | MITOCHONDRIAL CREATINE KINASE |
| 1CRL | INSIGHTS INTO INTERFACIAL ACTIVATION FROM AN 'OPEN' STRUCTURE OF CANDIDA RUGOSA LIPASE |
| 1CRM | STRUCTURE AND FUNCTION OF CARBONIC ANHYDRASES |
| 1CRN | WATER STRUCTURE OF A HYDROPHOBIC PROTEIN AT ATOMIC RESOLUTION. PENTAGON RINGS OF WATER MOLECULES IN CRYSTALS OF CRAMBIN |
| 1CRP | THE SOLUTION STRUCTURE AND DYNAMICS OF RAS P21. GDP DETERMINED BY HETERONUCLEAR THREE AND FOUR DIMENSIONAL NMR SPECTROSCOPY |
| 1CRQ | THE SOLUTION STRUCTURE AND DYNAMICS OF RAS P21. GDP DETERMINED BY HETERONUCLEAR THREE AND FOUR DIMENSIONAL NMR SPECTROSCOPY |
| 1CRU | SOLUBLE QUINOPROTEIN GLUCOSE DEHYDROGENASE FROM ACINETOBACTER CALCOACETICUS IN COMPLEX WITH PQQ AND METHYLHYDRAZINE |
| 1CRW | CRYSTAL STRUCTURE OF APO-GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE FROM PALINURUS VERSICOLOR AT 2.0A RESOLUTION |
| 1CRX | CRE RECOMBINASE/DNA COMPLEX REACTION INTERMEDIATE I |
| 1CRY | APPLICATION OF AN AUTOMATIC MOLECULAR REPLACEMENT PROCEDURE TO CRYSTAL STRUCTURE OF CYTOCHROME C2 FROM RHODOPSEUDOMONAS VIRIDIS |
| 1CRZ | CRYSTAL STRUCTURE OF THE E. COLI TOLB PROTEIN |
| 1CS1 | CYSTATHIONINE GAMMA-SYNTHASE (CGS) FROM ESCHERICHIA COLI |
| 1CS3 | STRUCTURE OF BTB/POZ TRANSCRIPTION REPRESSION DOMAIN FROM PROMELOCYTIC LEUKEMIA ZINC FINGER ONCOPROTEIN |
| 1CS4 | COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH 2'-DEOXY-ADENOSINE 3'-MONOPHOSPHATE, PYROPHOSPHATE AND MG |
| 1CS6 | N-TERMINAL FRAGMENT OF AXONIN-1 FROM CHICKEN |
| 1CS8 | CRYSTAL STRUCTURE OF PROCATHEPSIN L |
| 1CS9 | SOLUTION STRUCTURE OF CGGIRGERA IN CONTACT WITH THE MONOCLONAL ANTIBODY MAB 4X11, NMR, 7 STRUCTURES |
| 1CSB | CRYSTAL STRUCTURE OF CATHEPSIN B INHIBITED WITH CA030 AT 2.1 ANGSTROMS RESOLUTION: A BASIS FOR THE DESIGN OF SPECIFIC EPOXYSUCCINYL INHIBITORS |
| 1CSC | STRUCTURE OF TERNARY COMPLEXES OF CITRATE SYNTHASE WITH D-AND L-MALATE: MECHANISTIC IMPLICATIONS |
| 1CSE | THE HIGH-RESOLUTION X-RAY CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN SUBTILISIN CARLSBERG AND EGLIN C, AN ELASTASE INHIBITOR FROM THE LEECH HIRUDO MEDICINALIS. STRUCTURAL ANALYSIS, SUBTILISIN STRUCTURE AND INTERFACE GEOMETRY |
| 1CSG | THREE-DIMENSIONAL STRUCTURE OF RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR |
| 1CSH | A VERY SHORT HYDROGEN BOND PROVIDES ONLY MODERATE STABILIZATION OF AN ENZYME: INHIBITOR COMPLEX OF CITRATE SYNTHASE |
| 1CSI | A VERY SHORT HYDROGEN BOND PROVIDES ONLY MODERATE STABILIZATION OF AN ENZYME: INHIBITOR COMPLEX OF CITRATE SYNTHASE |
| 1CSJ | CRYSTAL STRUCTURE OF THE RNA-DEPENDENT RNA POLYMERASE OF HEPATITIS C VIRUS |
| 1CSK | THE CRYSTAL STRUCTURE OF HUMAN CSKSH3: STRUCTURAL DIVERSITY NEAR THE RT-SRC AND N-SRC LOOP |
| 1CSM | THE CRYSTAL STRUCTURE OF ALLOSTERIC CHORISMATE MUTASE AT 2.2 ANGSTROMS RESOLUTION |
| 1CSN | BINARY COMPLEX OF CASEIN KINASE-1 WITH MGATP |
| 1CSO | CRYSTAL STRUCTURE OF THE OMTKY3 P1 VARIANT OMTKY3-ILE18I IN COMPLEX WITH SGPB |
| 1CSP | CRYSTAL STRUCTURE OF THE BACILLUS SUBTILIS MAJOR COLD SHOCK PROTEIN, CSPB: A UNIVERSAL NUCLEIC-ACID BINDING DOMAIN |
| 1CSQ | CRYSTAL STRUCTURE OF THE BACILLUS SUBTILIS MAJOR COLD SHOCK PROTEIN, CSPB: A UNIVERSAL NUCLEIC-ACID BINDING DOMAIN |
| 1CSR | ALPHA-FLUORO ACID AND ALPHA-FLUORO AMIDE ANALOGS OF ACETYL-COA AS INHIBITORS OF OF CITRATE SYNTHASE: EFFECT OF PKA MATCHING ON BINDING AFFINITY AND HYDROGEN BOND LENGTH |
| 1CSS | ALPHA-FLUORO ACID AND ALPHA-FLUORO AMIDE ANALOGS OF ACETYL-COA AS INHIBITORS OF OF CITRATE SYNTHASE: EFFECT OF PKA MATCHING ON BINDING AFFINITY AND HYDROGEN BOND LENGTH |
| 1CSU | REPLACEMENTS IN A CONSERVED LEUCINE CLUSTER IN THE HYDROPHOBIC HEME POCKET OF CYTOCHROME C |
| 1CSV | REPLACEMENTS IN A CONSERVED LEUCINE CLUSTER IN THE HYDROPHOBIC HEME POCKET OF CYTOCHROME C |
| 1CSW | REPLACEMENTS IN A CONSERVED LEUCINE CLUSTER IN THE HYDROPHOBIC HEME POCKET OF CYTOCHROME C |
| 1CSX | REPLACEMENTS IN A CONSERVED LEUCINE CLUSTER IN THE HYDROPHOBIC HEME POCKET OF CYTOCHROME C |
| 1CSY | SYK TYROSINE KINASE C-TERMINAL SH2 DOMAIN COMPLEXED WITH A PHOSPHOPEPTIDEFROM THE GAMMA CHAIN OF THE HIGH AFFINITY IMMUNOGLOBIN G RECEPTOR, NMR |
| 1CSZ | SYK TYROSINE KINASE C-TERMINAL SH2 DOMAIN COMPLEXED WITH A PHOSPHOPEPTIDEFROM THE GAMMA CHAIN OF THE HIGH AFFINITY IMMUNOGLOBIN G RECEPTOR, NMR |
| 1CT0 | CRYSTAL STRUCTURE OF THE OMTKY3 P1 VARIANT OMTKY3-SER18I IN COMPLEX WITH SGPB |
| 1CT1 | CHOLERA TOXIN B-PENTAMER MUTANT G33R BOUND TO RECEPTOR PENTASACCHARIDE |
| 1CT2 | CRYSTAL STRUCTURE OF THE OMTKY3 P1 VARIANT OMTKY3-THR18I IN COMPLEX WITH SGPB |
| 1CT4 | CRYSTAL STRUCTURE OF THE OMTKY3 P1 VARIANT OMTKY3-VAL18I IN COMPLEX WITH SGPB |
| 1CT5 | CRYSTAL STRUCTURE OF YEAST HYPOTHETICAL PROTEIN YBL036C-SELENOMET CRYSTAL |
| 1CT8 | CATALYTIC ANTIBODY 7C8 COMPLEX |
| 1CT9 | CRYSTAL STRUCTURE OF ASPARAGINE SYNTHETASE B FROM ESCHERICHIA COLI |
| 1CTA | DETERMINATION OF THE SOLUTION STRUCTURE OF A SYNTHETIC TWO-SITE CALCIUM-BINDING HOMODIMERIC PROTEIN DOMAIN BY NMR SPECTROSCOPY |
| 1CTD | DETERMINATION OF THE SOLUTION STRUCTURE OF A SYNTHETIC TWO-SITE CALCIUM-BINDING HOMODIMERIC PROTEIN DOMAIN BY NMR SPECTROSCOPY |
| 1CTE | CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE-BASED INHIBITOR DESIGN |
| 1CTF | STRUCTURE OF THE C-TERMINAL DOMAIN OF THE RIBOSOMAL PROTEIN L7/L12 FROM ESCHERICHIA COLI AT 1.7 ANGSTROMS |
| 1CTI | DETERMINATION OF THE COMPLETE THREE-DIMENSIONAL STRUCTURE OF THE TRYPSIN INHIBITOR FROM SQUASH SEEDS IN AQUEOUS SOLUTION BY NUCLEAR MAGNETIC RESONANCE AND A COMBINATION OF DISTANCE GEOMETRY AND DYNAMICAL SIMULATED ANNEALING |
| 1CTJ | CRYSTAL STRUCTURE OF CYTOCHROME C6 |
| 1CTL | STRUCTURE OF THE CARBOXY-TERMINAL LIM DOMAIN FROM THE CYSTEINE RICH PROTEIN CRP |
| 1CTM | CRYSTAL STRUCTURE OF CHLOROPLAST CYTOCHROME F REVEALS A NOVEL CYTOCHROME FOLD AND UNEXPECTED HEME LIGATION |
| 1CTN | CRYSTAL STRUCTURE OF A BACTERIAL CHITINASE AT 2.3 ANGSTROMS RESOLUTION |
| 1CTO | NMR STRUCTURE OF THE C-TERMINAL DOMAIN OF THE LIGAND-BINDING REGION OF MURINE GRANULOCYTE COLONY-STIMULATING FACTOR RECEPTOR, MINIMIZED AVERAGE STRUCTURE |
| 1CTP | STRUCTURE OF THE MAMMALIAN CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE AND AN INHIBITOR PEPTIDE DISPLAYS AN OPEN CONFORMATION |
| 1CTQ | STRUCTURE OF P21RAS IN COMPLEX WITH GPPNHP AT 100 K |
| 1CTR | DRUG BINDING BY CALMODULIN: CRYSTAL STRUCTURE OF A CALMODULIN-TRIFLUOPERAZINE COMPLEX |
| 1CTS | CRYSTALLOGRAPHIC REFINEMENT AND ATOMIC MODELS OF TWO DIFFERENT FORMS OF CITRATE SYNTHASE AT 2.7 AND 1.7 ANGSTROMS RESOLUTION |
| 1CTT | TRANSITION-STATE SELECTIVITY FOR A SINGLE OH GROUP DURING CATALYSIS BY CYTIDINE DEAMINASE |
| 1CTU | TRANSITION-STATE SELECTIVITY FOR A SINGLE OH GROUP DURING CATALYSIS BY CYTIDINE DEAMINASE |
| 1CTW | T4 LYSOZYME MUTANT I78A |
| 1CTX | THREE-DIMENSIONAL STRUCTURE OF THE-LONG-NEUROTOXIN FROM COBRA VENOM |
| 1CTY | MUTATION OF TYROSINE-67 IN CYTOCHROME C SIGNIFICANTLY ALTERS THE LOCAL HEME ENVIRONMENT |
| 1CTZ | MUTATION OF TYROSINE-67 IN CYTOCHROME C SIGNIFICANTLY ALTERS THE LOCAL HEME ENVIRONMENT |
| 1CU0 | T4 LYSOZYME MUTANT I78M |
| 1CU1 | CRYSTAL STRUCTURE OF AN ENZYME COMPLEX FROM HEPATITIS C VIRUS |
| 1CU2 | T4 LYSOZYME MUTANT L84M |
| 1CU3 | T4 LYSOZYME MUTANT V87M |
| 1CU4 | CRYSTAL STRUCTURE OF THE ANTI-PRION FAB 3F4 IN COMPLEX WITH ITS PEPTIDE EPITOPE |
| 1CU5 | T4 LYSOZYME MUTANT L91M |
| 1CU6 | T4 LYSOZYME MUTANT L91A |
| 1CUA | CUTINASE, N172K MUTANT |
| 1CUB | CUTINASE, N172K, R196D MUTANT, MONOCLINIC CRYSTAL FORM |
| 1CUC | CUTINASE, N172K, R196D MUTANT, ORTHORHOMBIC CRYSTAL FORM |
| 1CUD | CUTINASE, N172K, R196D MUTANT, MONOCLINIC CRYSTAL FORM WITH THREE MOLECULES PER ASYMMETRIC UNIT |
| 1CUE | CUTINASE, Q121L MUTANT |
| 1CUF | CUTINASE, R156L MUTANT |
| 1CUG | CUTINASE, R17E, N172K MUTANT |
| 1CUH | CUTINASE, R196E MUTANT |
| 1CUI | CUTINASE, S120A MUTANT |
| 1CUJ | CUTINASE, S120C MUTANT |
| 1CUK | ESCHERICHIA COLI RUVA PROTEIN AT PH 4.9 AND ROOM TEMPERATURE |
| 1CUL | COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH 2',5'-DIDEOXY-ADENOSINE 3'-TRIPHOSPHATE AND MG |
| 1CUN | CRYSTAL STRUCTURE OF REPEATS 16 AND 17 OF CHICKEN BRAIN ALPHA SPECTRIN |
| 1CUO | CRYSTAL STRUCTURE ANALYSIS OF ISOMER-2 AZURIN FROM METHYLOMONAS J |
| 1CUP | METHIONINE CORE MUTANT OF T4 LYSOZYME |
| 1CUQ | T4 LYSOZYME MUTANT V103M |
| 1CUR | REDUCED RUSTICYANIN, NMR |
| 1CUS | FUSARIUM SOLANI CUTINASE IS A LIPOLYTIC ENZYME WITH A CATALYTIC SERINE ACCESSIBLE TO SOLVENT |
| 1CUU | CUTINASE, A199C MUTANT |
| 1CUV | CUTINASE, A85F MUTANT |
| 1CUW | CUTINASE, G82A, A85F, V184I, A185L, L189F MUTANT |
| 1CUX | CUTINASE, L114Y MUTANT |
| 1CUY | CUTINASE, L189F MUTANT |
| 1CUZ | CUTINASE, L81G, L182G MUTANT |
| 1CV0 | T4 LYSOZYME MUTANT F104M |
| 1CV1 | T4 LYSOZYME MUTANT V111M |
| 1CV2 | HYDROLYTIC HALOALKANE DEHALOGENASE LINB FROM SPHINGOMONAS PAUCIMOBILIS UT26 AT 1.6 A RESOLUTION |
| 1CV3 | T4 LYSOZYME MUTANT L121M |
| 1CV4 | T4 LYSOZYME MUTANT L118M |
| 1CV5 | T4 LYSOZYME MUTANT L133M |
| 1CV6 | T4 LYSOZYME MUTANT V149M |
| 1CV7 | CRYSTAL STRUCTURE OF ENHANCED CYAN-EMISSION VARIANT OF GFP |
| 1CV8 | STAPHOPAIN, CYSTEINE PROTEINASE FROM STAPHYLOCOCCUS AUREUS V8 |
| 1CV9 | NMR STUDY OF ITAM PEPTIDE SUBSTRATE |
| 1CVA | STRUCTURAL AND FUNCTIONAL IMPORTANCE OF A CONSERVED HYDROGEN BOND NETWORK IN HUMAN CARBONIC ANHYDRASE II |
| 1CVB | STRUCTURAL AND FUNCTIONAL IMPORTANCE OF A CONSERVED HYDROGEN BOND NETWORK IN HUMAN CARBONIC ANHYDRASE II |
| 1CVC | REDESIGNING THE ZINC BINDING SITE OF HUMAN CARBONIC ANHYDRASE II: STRUCTURE OF A HIS2ASP-ZN2+ METAL COORDINATION POLYHEDRON |
| 1CVD | STRUCTURAL CONSEQUENCES OF REDESIGNING A PROTEIN-ZINC BINDING SITE |
| 1CVE | STRUCTURAL CONSEQUENCES OF REDESIGNING A PROTEIN-ZINC BINDING SITE |
| 1CVF | STRUCTURAL CONSEQUENCES OF REDESIGNING A PROTEIN-ZINC BINDING SITE |
| 1CVH | STRUCTURAL CONSEQUENCES OF REDESIGNING A PROTEIN-ZINC BINDING SITE |
| 1CVI | CRYSTAL STRUCTURE OF HUMAN PROSTATIC ACID PHOSPHATASE |
| 1CVJ | X-RAY CRYSTAL STRUCTURE OF THE POLY(A)-BINDING PROTEIN IN COMPLEX WITH POLYADENYLATE RNA |
| 1CVK | T4 LYSOZYME MUTANT L118A |
| 1CVL | CRYSTAL STRUCTURE OF BACTERIAL LIPASE FROM CHROMOBACTERIUM VISCOSUM ATCC 6918 |
| 1CVM | CADMIUM INHIBITED CRYSTAL STRUCTURE OF PHYTASE FROM BACILLUS AMYLOLIQUEFACIENS |
| 1CVN | CONCANAVALIN A COMPLEXED TO TRIMANNOSIDE |
| 1CVO | THE SOLUTION STRUCTURE OF CARDIOTOXIN V FROM NAJA NAJA ATRA |
| 1CVR | CRYSTAL STRUCTURE OF THE ARG SPECIFIC CYSTEINE PROTEINASE GINGIPAIN R (RGPB) |
| 1CVS | CRYSTAL STRUCTURE OF A DIMERIC FGF2-FGFR1 COMPLEX |
| 1CVU | CRYSTAL STRUCTURE OF ARACHIDONIC ACID BOUND TO THE CYCLOOXYGENASE ACTIVE SITE OF COX-2 |
| 1CVW | CRYSTAL STRUCTURE OF ACTIVE SITE-INHIBITED HUMAN COAGULATION FACTOR VIIA (DES-GLA) |
| 1CVZ | CRYSTAL STRUCTURE ANALYSIS OF PAPAIN WITH CLIK148(CATHEPSIN L SPECIFIC INHIBITOR) |
| 1CW0 | CRYSTAL STRUCTURE ANALYSIS OF VERY SHORT PATCH REPAIR (VSR) ENDONUCLEASE IN COMPLEX WITH A DUPLEX DNA |
| 1CW1 | CRYSTAL STRUCTURE OF ISOCITRATE DEHYDROGENASE MUTANT K230M BOUND TO ISOCITRATE AND MN2+ |
| 1CW2 | CRYSTAL STRUCTURE OF THE COMPLEX OF BACTERIAL TRYPTOPHAN SYNTHASE WITH THE TRANSITION STATE ANALOGUE INHIBITOR 4-(2-HYDROXYPHENYLSULFINYL)-BUTYLPHOSPHONIC ACID |
| 1CW4 | CRYSTAL STRUCTURE OF K230M ISOCITRATE DEHYDROGENASE IN COMPLEX WITH ALPHA-KETOGLUTARATE |
| 1CW5 | SOLUTION STRUCTURE OF CARNOBACTERIOCIN B2 |
| 1CW6 | REFINED SOLUTION STRUCTURE OF LEUCOCIN A |
| 1CW7 | LOW TEMPERATURE STRUCTURE OF WILD-TYPE IDH COMPLEXED WITH MG-ISOCITRATE |
| 1CWA | X-RAY STRUCTURE OF A MONOMERIC CYCLOPHILIN A-CYCLOSPORIN A CRYSTAL COMPLEX AT 2.1 ANGSTROMS RESOLUTION |
| 1CWB | THE X-RAY STRUCTURE OF (MEBM2T)1-CYCLOSPORIN COMPLEXED WITH CYCLOPHILIN A PROVIDES AN EXPLANATION FOR ITS ANOMALOUSLY HIGH IMMUNOSUPPRESSIVE ACTIVITY |
| 1CWC | IMPROVED BINDING AFFINITY FOR CYCLOPHILIN A BY A CYCLOSPORIN DERIVATIVE SINGLY MODIFIED AT ITS EFFECTOR DOMAIN |
| 1CWD | HUMAN P56LCK TYROSINE KINASE COMPLEXED WITH PHOSPHOPEPTIDE |
| 1CWE | HUMAN P56LCK TYROSINE KINASE COMPLEXED WITH PHOSPHOPEPTIDE |
| 1CWF | HUMAN CYCLOPHILIN A COMPLEXED WITH 2-VAL CYCLOSPORIN |
| 1CWH | HUMAN CYCLOPHILIN A COMPLEXED WITH 3-D-SER CYCLOSPORIN |
| 1CWI | HUMAN CYCLOPHILIN A COMPLEXED WITH 2-VAL 3-(N-METHYL)-D-ALANINE CYCLOSPORIN |
| 1CWJ | HUMAN CYCLOPHILIN A COMPLEXED WITH 2-VAL 3-S-METHYL-SARCOSINE CYCLOSPORIN |
| 1CWK | HUMAN CYCLOPHILIN A COMPLEXED WITH 1-(6,7-DIHYDRO)MEBMT 2-VAL 3-D-(2-S-METHYL)SARCOSINE CYCLOSPORIN |
| 1CWL | HUMAN CYCLOPHILIN A COMPLEXED WITH 4 4-HYDROXY-MELEU CYCLOSPORIN |
| 1CWM | HUMAN CYCLOPHILIN A COMPLEXED WITH 4 MEILE CYCLOSPORIN |
| 1CWO | HUMAN CYCLOPHILIN A COMPLEXED WITH THR2, LEU5, D-HIV8, LEU10 CYCLOSPORIN |
| 1CWP | STRUCTURES OF THE NATIVE AND SWOLLEN FORMS OF COWPEA CHLOROTIC MOTTLE VIRUS DETERMINED BY X-RAY CRYSTALLOGRAPHY AND CRYO-ELECTRON MICROSCOPY |
| 1CWQ | M INTERMEDIATE STRUCTURE OF THE WILD TYPE BACTERIORHODOPSIN IN COMBINATION WITH THE GROUND STATE STRUCTURE |
| 1CWR | HUMAN CDC25B CATALYTIC DOMAIN WITHOUT ION IN CATALYTIC SITE |
| 1CWS | HUMAN CDC25B CATALYTIC DOMAIN WITH TUNGSTATE |
| 1CWT | HUMAN CDC25B CATALYTIC DOMAIN WITH METHYL MERCURY |
| 1CWU | BRASSICA NAPUS ENOYL ACP REDUCTASE A138G MUTANT COMPLEXED WITH NAD+ AND THIENODIAZABORINE |
| 1CWV | CRYSTAL STRUCTURE OF INVASIN: A BACTERIAL INTEGRIN-BINDING PROTEIN |
| 1CWW | SOLUTION STRUCTURE OF THE CASPASE RECRUITMENT DOMAIN (CARD) FROM APAF-1 |
| 1CWX | SOLUTION STRUCTURE OF THE HEPATITIS C VIRUS N-TERMINAL CAPSID PROTEIN 2-45 [C-HCV(2-45)] |
| 1CWY | CRYSTAL STRUCTURE OF AMYLOMALTASE FROM THERMUS AQUATICUS, A GLYCOSYLTRANSFERASE CATALYSING THE PRODUCTION OF LARGE CYCLIC GLUCANS |
| 1CX1 | SECOND N-TERMINAL CELLULOSE-BINDING DOMAIN FROM CELLULOMONAS FIMI BETA-1,4-GLUCANASE C, NMR, 22 STRUCTURES |
| 1CX2 | CYCLOOXYGENASE-2 (PROSTAGLANDIN SYNTHASE-2) COMPLEXED WITH A SELECTIVE INHIBITOR, SC-558 |
| 1CX4 | CRYSTAL STRUCTURE OF A DELETION MUTANT OF THE TYPE II BETA REGULATORY SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE |
| 1CX6 | T4 LYSOZYME SUBSTITUTED WITH SELENOMETHIONINE |
| 1CX7 | T4 LYSOZYME METHIONINE CORE MUTANT |
| 1CX9 | CRYSTAL STRUCTURE OF THE COMPLEX OF BACTERIAL TRYPTOPHAN SYNTHASE WITH THE TRANSITION STATE ANALOGUE INHIBITOR 4-(2-AMINOPHENYLTHIO)-BUTYLPHOSPHONIC ACID |
| 1CXA | CRYSTALLIZATION AND X-RAY STRUCTURE DETERMINATION OF CYTOCHROME C2 FROM RHODOBACTER SPHAEROIDES IN THREE CRYSTAL FORMS |
| 1CXC | CRYSTALLIZATION AND X-RAY STRUCTURE DETERMINATION OF CYTOCHROME C2 FROM RHODOBACTER SPHAEROIDES IN THREE CRYSTAL FORMS |
| 1CXE | COMPLEX OF CGTASE WITH MALTOTETRAOSE AT ROOM TEMPERATURE AND PH 9.1 BASED ON DIFFRACTION DATA OF A CRYSTAL SOAKED WITH ALPHA-CYCLODEXTRIN |
| 1CXF | COMPLEX OF A (D229N/E257Q) DOUBLE MUTANT CGTASE FROM BACILLUS CIRCULANS STRAIN 251 WITH MALTOTETRAOSE AT 120 K AND PH 9.1 OBTAINED AFTER SOAKING THE CRYSTAL WITH ALPHA-CYCLODEXTRIN |
| 1CXH | COMPLEX OF CGTASE WITH MALTOTETRAOSE AT ROOM TEMPERATURE AND PH 9.6 BASED ON DIFFRACTION DATA OF A CRYSTAL SOAKED WITH MALTOHEPTAOSE |
| 1CXI | WILD-TYPE CGTASE FROM BACILLUS CIRCULANS STRAIN 251 AT 120 K AND PH 7.55 |
| 1CXK | COMPLEX BETWEEN A MALTONONAOSE SUBSTRATE AND BACILLUS CIRCULANS STRAIN 251 CGTASE E257Q/D229N |
| 1CXL | COMPLEX BETWEEN A COVALENT INTERMEDIATE AND BACILLUS CIRCULANS STRAIN 251 CGTASE E257Q |
| 1CXN | REFINED THREE-DIMENSIONAL SOLUTION STRUCTURE OF A SNAKE CARDIOTOXIN: ANALYSIS OF THE SIDE-CHAIN ORGANISATION SUGGESTS THE EXISTENCE OF A POSSIBLE PHOSPHOLIPID BINDING SITE |
| 1CXO | REFINED THREE-DIMENSIONAL SOLUTION STRUCTURE OF A SNAKE CARDIOTOXIN: ANALYSIS OF THE SIDE-CHAIN ORGANISATION SUGGESTS THE EXISTENCE OF A POSSIBLE PHOSPHOLIPID BINDING SITE |
| 1CXP | CRYOGENIC CRYSTAL STRUCTURE OF HUMAN MYELOPEROXIDASE ISOFORM C |
| 1CXQ | ATOMIC RESOLUTION ASV INTEGRASE CORE DOMAIN FROM AMMONIUM SULFATE |
| 1CXR | AUTOMATED 2D NOESY ASSIGNMENT AND STRUCTURE CALCULATION OF CRAMBIN(S22/I25) WITH SELF-CORRECTING DISTANCE GEOMETRY BASED NOAH/DIAMOD PROGRAMS |
| 1CXU | 1.42A RESOLUTION ASV INTEGRASE CORE DOMAIN FROM CITRATE |
| 1CXV | STRUCTURE OF RECOMBINANT MOUSE COLLAGENASE-3 (MMP-13) |
| 1CXW | THE SECOND TYPE II MODULE FROM HUMAN MATRIX METALLOPROTEINASE 2 |
| 1CXX | MUTANT R122A OF QUAIL CYSTEINE AND GLYCINE-RICH PROTEIN, NMR, MINIMIZED STRUCTURE |
| 1CXY | STRUCTURE AND CHARACTERIZATION OF ECTOTHIORHODOSPIRA VACUOLATA CYTOCHROME B558, A PROKARYOTIC HOMOLOGUE OF CYTOCHROME B5 |
| 1CXZ | CRYSTAL STRUCTURE OF HUMAN RHOA COMPLEXED WITH THE EFFECTOR DOMAIN OF THE PROTEIN KINASE PKN/PRK1 |
| 1CY0 | COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 3'-5'-ADENOSINE DIPHOSPHATE |
| 1CY1 | COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 5'PTPTPT |
| 1CY2 | COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH TPTPTP3' |
| 1CY4 | COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 5'PTPTPTP3' |
| 1CY5 | CRYSTAL STRUCTURE OF THE APAF-1 CARD |
| 1CY6 | COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 3' THYMIDINE MONOPHOSPHATE |
| 1CY7 | COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 5'-THYMIDINE MONOPHOSPHATE |
| 1CY8 | COMPLEX OF E.COLI DNA TOPOISOMERASE I WITH 5'-THYMIDINE MONOPHOSPHATE AND 3'-THYMIDINE MONOPHOSPHATE |
| 1CY9 | CRYSTAL STRUCTURE OF THE 30 KDA FRAGMENT OF E. COLI DNA TOPOISOMERASE I. MONOCLINIC FORM |
| 1CYC | THE CRYSTAL STRUCTURE OF BONITO (KATSUO) FERROCYTOCHROME C AT 2.3 ANGSTROMS RESOLUTION. II. STRUCTURE AND FUNCTION |
| 1CYD | CARBONYL REDUCTASE COMPLEXED WITH NADPH AND 2-PROPANOL |
| 1CYE | THREE DIMENSIONAL STRUCTURE OF CHEMOTACTIC CHE Y PROTEIN IN AQUEOUS SOLUTION BY NUCLEAR MAGNETIC RESONANCE METHODS |
| 1CYF | IDENTIFYING THE PHYSIOLOGICAL ELECTRON TRANSFER SITE OF CYTOCHROME C PEROXIDASE BY STRUCTURE-BASED ENGINEERING |
| 1CYG | CYCLODEXTRIN GLUCANOTRANSFERASE (E.C.2.4.1.19) (CGTASE) |
| 1CYI | CYTOCHROME C6 |
| 1CYJ | CYTOCHROME C6 |
| 1CYL | ASPECTS OF RECEPTOR BINDING AND SIGNALLING OF INTERLEUKIN-4 INVESTIGATED BY SITE-DIRECTED MUTAGENESIS AND NMR SPECTROSCOPY |
| 1CYN | CYCLOPHILIN B COMPLEXED WITH [D-(CHOLINYLESTER)SER8]-CYCLOSPORIN |
| 1CYO | BOVINE CYTOCHROME B(5) |
| 1CYQ | INTRON ENCODED HOMING ENDONUCLEASE I-PPOI (H98A)/DNA HOMING SITE COMPLEX |
| 1CYU | SOLUTION NMR STRUCTURE OF RECOMBINANT HUMAN CYSTATIN A UNDER THE CONDITION OF PH 3.8 AND 310K |
| 1CYV | SOLUTION NMR STRUCTURE OF RECOMBINANT HUMAN CYSTATIN A UNDER THE CONDITION OF PH 3.8 AND 310K |
| 1CYW | QUINOL OXIDASE (PERIPLASMIC FRAGMENT OF SUBUNIT II) (CYOA) |
| 1CYX | QUINOL OXIDASE (PERIPLASMIC FRAGMENT OF SUBUNIT II WITH ENGINEERED CU-A BINDING SITE)(CYOA) |
| 1CYY | CRYSTAL STRUCTURE OF THE 30 KDA FRAGMENT OF E. COLI DNA TOPOISOMERASE I. HEXAGONAL FORM |
| 1CZ0 | INTRON ENCODED HOMING ENDONUCLEASE I-PPOI/DNA COMPLEX LACKING CATALYTIC METAL ION |
| 1CZ1 | EXO-B-(1,3)-GLUCANASE FROM CANDIDA ALBICANS AT 1.85 A RESOLUTION |
| 1CZ2 | SOLUTION STRUCTURE OF WHEAT NS-LTP COMPLEXED WITH PROSTAGLANDIN B2. |
| 1CZ3 | DIHYDROFOLATE REDUCTASE FROM THERMOTOGA MARITIMA |
| 1CZ4 | NMR STRUCTURE OF VAT-N: THE N-TERMINAL DOMAIN OF VAT (VCP-LIKE ATPASE OF THERMOPLASMA) |
| 1CZ5 | NMR STRUCTURE OF VAT-N: THE N-TERMINAL DOMAIN OF VAT (VCP-LIKE ATPASE OF THERMOPLASMA) |
| 1CZ6 | SOLUTION STRUCTURE OF ANDROCTONIN |
| 1CZ7 | THE CRYSTAL STRUCTURE OF A MINUS-END DIRECTED MICROTUBULE MOTOR PROTEIN NCD REVEALS VARIABLE DIMER CONFORMATIONS |
| 1CZ8 | VASCULAR ENDOTHELIAL GROWTH FACTOR IN COMPLEX WITH AN AFFINITY MATURED ANTIBODY |
| 1CZ9 | ATOMIC RESOLUTION ASV INTEGRASE CORE DOMAIN (D64N) FROM CITRATE |
| 1CZA | MUTANT MONOMER OF RECOMBINANT HUMAN HEXOKINASE TYPE I COMPLEXED WITH GLUCOSE, GLUCOSE-6-PHOSPHATE, AND ADP |
| 1CZB | ATOMIC RESOLUTION ASV INTEGRASE CORE DOMAIN FROM HEPES |
| 1CZC | ASPARTATE AMINOTRANSFERASE MUTANT ATB17/139S/142N WITH GLUTARIC ACID |
| 1CZD | CRYSTAL STRUCTURE OF THE PROCESSIVITY CLAMP GP45 FROM BACTERIOPHAGE T4 |
| 1CZE | ASPARTATE AMINOTRANSFERASE MUTANT ATB17/139S/142N WITH SUCCINIC ACID |
| 1CZF | ENDO-POLYGALACTURONASE II FROM ASPERGILLUS NIGER |
| 1CZG | STRUCTURE OF THE G62T MUTANT OF SHIGA-LIKE TOXIN I B SUBUNIT |
| 1CZH | COMPARISONS OF WILD TYPE AND MUTANT FLAVODOXINS FROM ANACYSTIS NIDULANS. STRUCTURAL DETERMINANTS OF THE REDOX POTENTIALS. |
| 1CZI | CHYMOSIN COMPLEX WITH THE INHIBITOR CP-113972 |
| 1CZJ | CYTOCHROME C OF CLASS III (AMBLER) 26 KD |
| 1CZK | COMPARISONS OF WILD TYPE AND MUTANT FLAVODOXINS FROM ANACYSTIS NIDULANS. STRUCTURAL DETERMINANTS OF THE REDOX POTENTIALS. |
| 1CZL | COMPARISONS OF WILD TYPE AND MUTANT FLAVODOXINS FROM ANACYSTIS NIDULANS. STRUCTURAL DETERMINANTS OF THE REDOX POTENTIALS. |
| 1CZM | DRUG-PROTEIN INTERACTIONS: STRUCTURE OF SULFONAMIDE DRUG COMPLEXED WITH HUMAN CARBONIC ANHYDRASE I |
| 1CZN | REFINED STRUCTURES OF OXIDIZED FLAVODOXIN FROM ANACYSTIS NIDULANS |
| 1CZO | COMPARISONS OF WILD TYPE AND MUTANT FLAVODOXINS FROM ANACYSTIS NIDULANS. STRUCTURAL DETERMINANTS OF THE REDOX POTENTIALS. |
| 1CZP | ANABAENA PCC7119 [2FE-2S] FERREDOXIN IN THE REDUCED AND OXIXIZED STATE AT 1.17 A |
| 1CZQ | CRYSTAL STRUCTURE OF THE D10-P1/IQN17 COMPLEX: A D-PEPTIDE INHIBITOR OF HIV-1 ENTRY BOUND TO THE GP41 COILED-COIL POCKET. |
| 1CZR | COMPARISONS OF WILD TYPE AND MUTANT FLAVODOXINS FROM ANACYSTIS NIDULANS. STRUCTURAL DETERMINANTS OF THE REDOX POTENTIALS. |
| 1CZS | CRYSTAL STRUCTURE OF THE C2 DOMAIN OF HUMAN COAGULATION FACTOR V: COMPLEX WITH PHENYLMERCURY |
| 1CZT | CRYSTAL STRUCTURE OF THE C2 DOMAIN OF HUMAN COAGULATION FACTOR V |
| 1CZU | REFINED STRUCTURES OF OXIDIZED FLAVODOXIN FROM ANACYSTIS NIDULANS |
| 1CZV | CRYSTAL STRUCTURE OF THE C2 DOMAIN OF HUMAN COAGULATION FACTOR V: DIMERIC CRYSTAL FORM |
| 1CZW | STRUCTURE OF THE W34A MUTANT OF SHIGA-LIKE TOXIN I B SUBUNIT |
| 1CZY | CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE TRAF DOMAIN OF HUMAN TRAF2 AND AN LMP1 BINDING PEPTIDE |
| 1CZZ | STRUCTURE OF TNF RECEPTOR ASSOCIATED FACTOR 2 IN COMPLEX WITH A 17-RESIDUE CD40 PEPTIDE |
| 1D00 | STRUCTURE OF TNF RECEPTOR ASSOCIATED FACTOR 2 IN COMPLEX WITH A 5-RESIDUE CD40 PEPTIDE |
| 1D01 | STRUCTURE OF TNF RECEPTOR ASSOCIATED FACTOR 2 IN COMPLEX WITH A HUMAN CD30 PEPTIDE |
| 1D02 | CRYSTAL STRUCTURE OF MUNI RESTRICTION ENDONUCLEASE IN COMPLEX WITH COGNATE DNA |
| 1D03 | REFINED STRUCTURES OF OXIDIZED FLAVODOXIN FROM ANACYSTIS NIDULANS |
| 1D04 | COMPARISONS OF WILD TYPE AND MUTANT FLAVODOXINS FROM ANACYSTIS NIDULANS. STRUCTURAL DETERMINANTS OF THE REDOX POTENTIALS. |
| 1D06 | STRUCTURAL BASIS OF DIMERIZATION AND SENSORY MECHANISMS OF OXYGEN-SENSING DOMAIN OF RHIZOBIUM MELILOTI FIXL DETERMINED AT 1.4A RESOLUTION |
| 1D07 | HYDROLYTIC HALOALKANE DEHALOGENASE LINB FROM SPHINGOMONAS PAUCIMOBILIS UT26 WITH 1,3-PROPANEDIOL, A PRODUCT OF DEBROMIDATION OF DIBROMPROPANE, AT 2.0A RESOLUTION |
| 1D09 | ASPARTATE TRANSCARBAMOYLASE COMPLEXED WITH N-PHOSPHONACETYL-L-ASPARTATE (PALA) |
| 1D0A | STRUCTURE OF TNF RECEPTOR ASSOCIATED FACTOR 2 (TRAF2) IN COMPLEX WITH A HUMAN OX40 PEPTIDE |
| 1D0B | INTERNALIN B LEUCINE RICH REPEAT DOMAIN |
| 1D0C | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 3-BROMO-7-NITROINDAZOLE (H4B FREE) |
| 1D0D | CRYSTAL STRUCTURE OF TICK ANTICOAGULANT PROTEIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR |
| 1D0E | CRYSTAL STRUCTURES OF THE N-TERMINAL FRAGMENT FROM MOLONEY MURINE LEUKEMIA VIRUS REVERSE TRANSCRIPTASE COMPLEXED WITH NUCLEIC ACID: FUNCTIONAL IMPLICATIONS FOR TEMPLATE-PRIMER BINDING TO THE FINGERS DOMAIN |
| 1D0G | CRYSTAL STRUCTURE OF DEATH RECEPTOR 5 (DR5) BOUND TO APO2L/TRAIL |
| 1D0H | THE HC FRAGMENT OF TETANUS TOXIN COMPLEXED WITH N-ACETYL-GALACTOSAMINE |
| 1D0I | CRYSTAL STRUCTURE OF TYPE II DEHYDROQUINASE FROM STREPTOMYCES COELICOLOR COMPLEXED WITH PHOSPHATE IONS |
| 1D0J | STRUCTURE OF TNF RECEPTOR ASSOCIATED FACTOR 2 IN COMPLEX WITH A M4-1BB PEPTIDE |
| 1D0K | THE ESCHERICHIA COLI LYTIC TRANSGLYCOSYLASE SLT35 IN COMPLEX WITH TWO MURODIPEPTIDES (GLCNAC-MURNAC-L-ALA-D-GLU) |
| 1D0L | THE ESCHERICHIA COLI LYTIC TRANSGLYCOSYLASE SLT35 IN COMPLEX WITH BULGECIN A |
| 1D0M | THE ESCHERICHIA COLI LYTIC TRANSGLYCOSYLASE SLT35 IN COMPLEX WITH BULGECIN A AND (GLCNAC)2 |
| 1D0N | THE CRYSTAL STRUCTURE OF CALCIUM-FREE EQUINE PLASMA GELSOLIN. |
| 1D0O | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 3-BROMO-7-NITROINDAZOLE (H4B PRESENT) |
| 1D0Q | STRUCTURE OF THE ZINC-BINDING DOMAIN OF BACILLUS STEAROTHERMOPHILUS DNA PRIMASE |
| 1D0R | SOLUTION STRUCTURE OF GLUCAGON-LIKE PEPTIDE-1-(7-36)-AMIDE IN TRIFLUOROETHANOL/WATER |
| 1D0S | CRYSTAL STRUCTURE OF NICOTINATE MONONUCLEOTIDE : 5,6-DIMETHYLBENZIMIDAZOLE PHOSPHORIBOSYLTRANSFERASE (COBT) FROM SALMONELLA TYPHIMURIUM COMPLEXED WITH 5, 6-DIMETHYLBENZIMIDAZOLE |
| 1D0V | CRYSTAL STRUCTURE OF NICOTINATE MONONUCLEOTIDE:5,6-DIMETHYLBENZIMIDAZOLE PHOSPHORIBOSYLTRANSFERASE (COBT) FROM SALMONELLA TYPHIMURIUM COMPLEXED WITH ITS REACTION PRODUCTS DETERMINED TO 1.9 A RESOLUTION |
| 1D0X | DICTYOSTELIUM MYOSIN S1DC (MOTOR DOMAIN FRAGMENT) COMPLEXED WITH M-NITROPHENYL AMINOETHYLDIPHOSPHATE BERYLLIUM TRIFLUORIDE. |
| 1D0Y | DICTYOSTELIUM MYOSIN S1DC (MOTOR DOMAIN FRAGMENT) COMPLEXED WITH O-NITROPHENYL AMINOETHYLDIPHOSPHATE BERYLLIUM FLUORIDE. |
| 1D0Z | DICTYOSTELIUM MYOSIN S1DC (MOTOR DOMAIN FRAGMENT) COMPLEXED WITH P-NITROPHENYL AMINOETHYLDIPHOSPHATE BERYLLIUM TRIFLUORIDE. |
| 1D1A | DICTYOSTELIUM MYOSIN S1DC (MOTOR DOMAIN FRAGMENT) COMPLEXED WITH O,P-DINITROPHENYL AMINOETHYLDIPHOSPHATE BERYLLIUM TRIFLUORIDE. |
| 1D1B | DICTYOSTELIUM MYOSIN S1DC (MOTOR DOMAIN FRAGMENT) COMPLEXED WITH O,P-DINITROPHENYL AMINOPROPYLDIPHOSPHATE BERYLLIUM TRIFLUORIDE. |
| 1D1C | DICTYOSTELIUM MYOSIN S1DC (MOTOR DOMAIN FRAGMENT) COMPLEXED WITH N-METHYL-O-NITROPHENYL AMINOETHYLDIPHOSPHATE BERYLLIUM TRIFLUORIDE. |
| 1D1D | NMR SOLUTION STRUCTURE OF THE CAPSID PROTEIN FROM ROUS SARCOMA VIRUS |
| 1D1E | SOLUTION STRUCTURE OF LACTAM-BRIDGED C-TERMINAL ANALOGUE-II OF NEUROPEPTIDE Y |
| 1D1F | SOLUTION STRUCTURE OF LACTAM-BRIDGED C-TERMINAL ANALOGUE-III OF NEUROPEPTIDE Y |
| 1D1G | DIHYDROFOLATE REDUCTASE FROM THERMOTOGA MARITIMA |
| 1D1H | SOLUTION STRUCTURE OF HANATOXIN 1 |
| 1D1I | MUTATED SHIGA-LIKE TOXIN B SUBUNIT (W34A) COMPLEXED WITH RECEPTOR GB3 ANALOGUE |
| 1D1J | CRYSTAL STRUCTURE OF HUMAN PROFILIN II |
| 1D1K | MUTATED SHIGA-LIKE TOXIN B SUBUNIT (D17E/W34A) COMPLEXED WITH RECEPTOR GB3 ANALOGUE |
| 1D1L | CRYSTAL STRUCTURE OF CRO-F58W MUTANT |
| 1D1M | CRYSTAL STRUCTURE OF CRO K56-[DGEVK]-F58W MUTANT |
| 1D1N | SOLUTION STRUCTURE OF THE FMET-TRNAFMET BINDING DOMAIN OF BECILLUS STEAROTHERMOPHILLUS TRANSLATION INITIATION FACTOR IF2 |
| 1D1O | COOPERATIVITY IN EF-HAND CA2+-BINDING PROTEINS: EVIDENCE OF SITE-SITE COMMUNICATION FROM BINDING-INDUCED CHANGES IN STRUCTURE AND DYNAMICS OF N56A CALBINDIN D9K |
| 1D1P | CRYSTAL STRUCTURE OF A YEAST LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE (LTP1) |
| 1D1Q | CRYSTAL STRUCTURE OF A YEAST LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE (LTP1) COMPLEXED WITH THE SUBSTRATE PNPP |
| 1D1R | NMR SOLUTION STRUCTURE OF THE PRODUCT OF THE E. COLI YCIH GENE. |
| 1D1S | WILD-TYPE HUMAN SIGMA (CLASS IV) ALCOHOL DEHYDROGENASE |
| 1D1T | MUTANT OF HUMAN SIGMA ALCOHOL DEHYDROGENASE WITH LEUCINE AT POSITION 141 |
| 1D1U | USE OF AN N-TERMINAL FRAGMENT FROM MOLONEY MURINE LEUKEMIA VIRUS REVERSE TRANSCRIPTASE TO FACILITATE CRYSTALLIZATION AND ANALYSIS OF A PSEUDO-16-MER DNA MOLECULE CONTAINING G-A MISPAIRS |
| 1D1V | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH S-ETHYL-N-PHENYL-ISOTHIOUREA (H4B BOUND) |
| 1D1W | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 2-AMINOTHIAZOLINE (H4B BOUND) |
| 1D1X | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 1,4-PBITU (H4B BOUND) |
| 1D1Y | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 1,3-PBITU (H4B FREE) |
| 1D1Z | CRYSTAL STRUCTURE OF THE XLP PROTEIN SAP |
| 1D2A | CRYSTAL STRUCTURE OF A YEAST LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE (LTP1) COMPLEXED WITH THE ACTIVATOR ADENINE |
| 1D2B | THE MMP-INHIBITORY, N-TERMINAL DOMAIN OF HUMAN TISSUE INHIBITOR OF METALLOPROTEINASES-1 (N-TIMP-1), SOLUTION NMR, 29 STRUCTURES |
| 1D2C | METHYLTRANSFERASE |
| 1D2D | HAMSTER EPRS SECOND REPEATED ELEMENT. NMR, 5 STRUCTURES |
| 1D2E | CRYSTAL STRUCTURE OF MITOCHONDRIAL EF-TU IN COMPLEX WITH GDP |
| 1D2F | X-RAY STRUCTURE OF MALY FROM ESCHERICHIA COLI: A PYRIDOXAL-5'-PHOSPHATE-DEPENDENT ENZYME ACTING AS A MODULATOR IN MAL GENE EXPRESSION |
| 1D2G | CRYSTAL STRUCTURE OF R175K MUTANT GLYCINE N-METHYLTRANSFERASE FROM RAT LIVER |
| 1D2H | CRYSTAL STRUCTURE OF R175K MUTANT GLYCINE N-METHYLTRANSFERASE COMPLEXED WITH S-ADENOSYLHOMOCYSTEINE |
| 1D2I | CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE BGLII COMPLEXED WITH DNA 16-MER |
| 1D2J | LDL RECEPTOR LIGAND-BINDING MODULE 6 |
| 1D2K | C. IMMITIS CHITINASE 1 AT 2.2 ANGSTROMS RESOLUTION |
| 1D2L | NMR SOLUTION STRUCTURE OF COMPLEMENT-LIKE REPEAT CR3 FROM THE LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN (LRP). EVIDENCE FOR SPECIFIC BINDING TO THE RECEPTOR BINDING DOMAIN OF HUMAN ALPHA-2 MACROGLOBULIN |
| 1D2M | UVRB PROTEIN OF THERMUS THERMOPHILUS HB8; A NUCLEOTIDE EXCISION REPAIR ENZYME |
| 1D2N | D2 DOMAIN OF N-ETHYLMALEIMIDE-SENSITIVE FUSION PROTEIN |
| 1D2O | CRYSTAL STRUCTURE OF A SINGLE B REPEAT UNIT (B1) OF COLLAGEN BINDING SURFACE PROTEIN (CNA) OF STAPHYLOCOCCUS AUREUS. |
| 1D2P | CRYSTAL STRUCTURE OF TWO B REPEAT UNITS (B1B2) OF THE COLLAGEN BINDING PROTEIN (CNA) OF STAPHYLOCOCCUS AUREUS |
| 1D2Q | CRYSTAL STRUCTURE OF HUMAN TRAIL |
| 1D2R | 2.9 A CRYSTAL STRUCTURE OF LIGAND-FREE TRYPTOPHANYL-TRNA SYNTHETASE: DOMAIN MOVEMENTS FRAGMENT THE ADENINE NUCLEOTIDE BINDING SITE. |
| 1D2S | CRYSTAL STRUCTURE OF THE N-TERMINAL LAMININ G-LIKE DOMAIN OF SHBG IN COMPLEX WITH DIHYDROTESTOSTERONE |
| 1D2T | CRYSTAL STRUCTURE OF ACID PHOSPHATASE FROM ESCHERICHIA BLATTAE |
| 1D2U | 1.15 A CRYSTAL STRUCTURE OF NITROPHORIN 4 FROM RHODNIUS PROLIXUS |
| 1D2V | CRYSTAL STRUCTURE OF BROMIDE-BOUND HUMAN MYELOPEROXIDASE ISOFORM C AT PH 5.5 |
| 1D2W | N-TERMINAL DOMAIN CORE METHIONINE MUTATION |
| 1D2Y | N-TERMINAL DOMAIN CORE METHIONINE MUTATION |
| 1D2Z | THREE-DIMENSIONAL STRUCTURE OF A COMPLEX BETWEEN THE DEATH DOMAINS OF PELLE AND TUBE |
| 1D3A | CRYSTAL STRUCTURE OF THE WILD TYPE HALOPHILIC MALATE DEHYDROGENASE IN THE APO FORM |
| 1D3B | CRYSTAL STRUCTURE OF THE D3B SUBCOMPLEX OF THE HUMAN CORE SNRNP DOMAIN AT 2.0A RESOLUTION |
| 1D3C | MICHAELIS COMPLEX OF BACILLUS CIRCULANS STRAIN 251 CYCLODEXTRIN GLYCOSYLTRANSFERASE WITH GAMMA-CYCLODEXTRIN |
| 1D3D | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZOTHIOPHENE INHIBITOR 4 |
| 1D3F | N-TERMINAL DOMAIN CORE METHIONINE MUTATION |
| 1D3G | HUMAN DIHYDROOROTATE DEHYDROGENASE COMPLEXED WITH BREQUINAR ANALOG |
| 1D3H | HUMAN DIHYDROOROTATE DEHYDROGENASE COMPLEXED WITH ANTIPROLIFERATIVE AGENT A771726 |
| 1D3J | N-TERMINAL DOMAIN CORE METHIONINE MUTATION |
| 1D3K | HUMAN SERUM TRANSFERRIN |
| 1D3M | METHIONINE CORE MUTATION |
| 1D3N | METHIONINE CORE MUTATION |
| 1D3P | CRYSTAL STRUCTURE OF HUMAN APLHA-THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 3 |
| 1D3Q | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 2 |
| 1D3S | 1.4 A CRYSTAL STRUCTURE OF NITROPHORIN 4 FROM RHODNIUS PROLIXIS AT PH=5.6. |
| 1D3T | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH BENZO[B]THIOPHENE INHIBITOR 1 |
| 1D3U | TATA-BINDING PROTEIN/TRANSCRIPTION FACTOR (II)B/BRE+TATA-BOX COMPLEX FROM PYROCOCCUS WOESEI |
| 1D3V | CRYSTAL STRUCTURE OF THE BINUCLEAR MANGANESE METALLOENZYME ARGINASE COMPLEXED WITH 2(S)-AMINO-6-BORONOHEXANOIC ACID, AN L-ARGININE ANALOG |
| 1D3W | CRYSTAL STRUCTURE OF FERREDOXIN 1 D15E MUTANT FROM AZOTOBACTER VINELANDII AT 1.7 ANGSTROM RESOLUTION. |
| 1D3Y | STRUCTURE OF THE DNA TOPOISOMERASE VI A SUBUNIT |
| 1D3Z | UBIQUITIN NMR STRUCTURE |
| 1D4A | CRYSTAL STRUCTURE OF HUMAN NAD[P]H-QUINONE OXIDOREDUCTASE AT 1.7 A RESOLUTION |
| 1D4B | CIDE-N DOMAIN OF HUMAN CIDE-B |
| 1D4C | CRYSTAL STRUCTURE OF THE UNCOMPLEXED FORM OF THE FLAVOCYTOCHROME C FUMARATE REDUCTASE OF SHEWANELLA PUTREFACIENS STRAIN MR-1 |
| 1D4D | CRYSTAL STRUCTURE OF THE SUCCINATE COMPLEXED FORM OF THE FLAVOCYTOCHROME C FUMARATE REDUCTASE OF SHEWANELLA PUTREFACIENS STRAIN MR-1 |
| 1D4E | CRYSTAL STRUCTURE OF THE FLAVOCYTOCHROME C FUMARATE REDUCTASE OF SHEWANELLA PUTREFACIENS STRAIN MR-1 COMPLEXED WITH FUMARATE |
| 1D4F | CRYSTAL STRUCTURE OF RECOMBINANT RAT-LIVER D244E MUTANT S-ADENOSYLHOMOCYSTEINE HYDROLASE |
| 1D4H | HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA435 |
| 1D4I | HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA425 |
| 1D4J | HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR MSL370 |
| 1D4K | HIV-1 PROTEASE COMPLEXED WITH A MACROCYCLIC PEPTIDOMIMETIC INHIBITOR |
| 1D4L | HIV-1 PROTEASE COMPLEXED WITH A MACROCYCLIC PEPTIDOMIMETIC INHIBITOR |
| 1D4M | THE CRYSTAL STRUCTURE OF COXSACKIEVIRUS A9 TO 2.9 A RESOLUTION |
| 1D4N | HUMAN SERUM TRANSFERRIN |
| 1D4O | CRYSTAL STRUCTURE OF TRANSHYDROGENASE DOMAIN III AT 1.2 ANGSTROMS RESOLUTION |
| 1D4P | CRYSTAL STRUCTURE OF HUMAN ALPHA THROMBIN IN COMPLEX WITH 5-AMIDINOINDOLE-4-BENZYLPIPERIDINE INHIBITOR |
| 1D4S | HIV-1 PROTEASE V82F/I84V DOUBLE MUTANT/TIPRANAVIR COMPLEX |
| 1D4T | CRYSTAL STRUCTURE OF THE XLP PROTEIN SAP IN COMPLEX WITH A SLAM PEPTIDE |
| 1D4U | INTERACTIONS OF HUMAN NUCLEOTIDE EXCISION REPAIR PROTEIN XPA WITH RPA70 AND DNA: CHEMICAL SHIFT MAPPING AND 15N NMR RELAXATION STUDIES |
| 1D4V | CRYSTAL STRUCTURE OF TRAIL-DR5 COMPLEX |
| 1D4W | CRYSTAL STRUCTURE OF THE XLP PROTEIN SAP IN COMPLEX WITH SLAM PHOSPHOPEPTIDE |
| 1D4X | CRYSTAL STRUCTURE OF CAENORHABDITIS ELEGANS MG-ATP ACTIN COMPLEXED WITH HUMAN GELSOLIN SEGMENT 1 AT 1.75 A RESOLUTION. |
| 1D4Y | HIV-1 PROTEASE TRIPLE MUTANT/TIPRANAVIR COMPLEX |
| 1D4Z | CRYSTAL STRUCTURE OF CHEY-95IV, A HYPERACTIVE CHEY MUTANT |
| 1D5A | CRYSTAL STRUCTURE OF AN ARCHAEBACTERIAL DNA POLYMERASE D.TOK. DEPOSITION OF SECOND NATIVE STRUCTURE AT 2.4 ANGSTROM |
| 1D5B | UNLIGANDED MATURE OXY-COPE CATALYTIC ANTIBODY |
| 1D5C | CRYSTAL STRUCTURE OF PLASMODIUM FALCIPARUM RAB6 COMPLEXED WITH GDP |
| 1D5D | THE ROLE OF PHENYLALANINE 8 IN THE STABILIZATION OF THE S PROTEIN-S PEPTIDE INTERACTION: PACKING AND CAVITIES |
| 1D5E | THE ROLE OF PHENYLALANINE 8 IN THE STABILIZATION OF THE S PROTEIN-S PEPTIDE INTERACTION: PACKING AND CAVITIES |
| 1D5F | STRUCTURE OF E6AP: INSIGHTS INTO UBIQUITINATION PATHWAY |
| 1D5G | SOLUTION STRUCTURE OF THE PDZ2 DOMAIN FROM HUMAN PHOSPHATASE HPTP1E COMPLEXED WITH A PEPTIDE |
| 1D5H | RNASE S(F8A). MUTANT RIBONUCLEASE S. |
| 1D5I | UNLIGANDED GERMLINE PRECURSOR OF AN OXY-COPE CATALYTIC ANTIBODY |
| 1D5J | CRYSTAL STRUCTURE OF MMP3 COMPLEXED WITH A THIAZEPINE BASED INHIBITOR. |
| 1D5L | CRYSTAL STRUCTURE OF CYANIDE-BOUND HUMAN MYELOPEROXIDASE ISOFORM C AT PH 5.5 |
| 1D5M | X-RAY CRYSTAL STRUCTURE OF HLA-DR4 COMPLEXED WITH PEPTIDE AND SEB |
| 1D5N | CRYSTAL STRUCTURE OF E. COLI MNSOD AT 100K |
| 1D5Q | SOLUTION STRUCTURE OF A MINI-PROTEIN REPRODUCING THE CORE OF THE CD4 SURFACE INTERACTING WITH THE HIV-1 ENVELOPE GLYCOPROTEIN |
| 1D5R | CRYSTAL STRUCTURE OF THE PTEN TUMOR SUPPRESSOR |
| 1D5S | CRYSTAL STRUCTURE OF CLEAVED ANTITRYPSIN POLYMER |
| 1D5T | GUANINE NUCLEOTIDE DISSOCIATION INHIBITOR, ALPHA-ISOFORM |
| 1D5V | SOLUTION STRUCTURE OF THE FORKHEAD DOMAIN OF THE ADIPOCYTE-TRANSCRIPTION FACTOR FREAC-11 (S12) |
| 1D5W | PHOSPHORYLATED FIXJ RECEIVER DOMAIN |
| 1D5X | X-RAY CRYSTAL STRUCTURE OF HLA-DR4 COMPLEXED WITH DIPEPTIDE MIMETIC AND SEB |
| 1D5Y | CRYSTAL STRUCTURE OF THE E. COLI ROB TRANSCRIPTION FACTOR IN COMPLEX WITH DNA |
| 1D5Z | X-RAY CRYSTAL STRUCTURE OF HLA-DR4 COMPLEXED WITH PEPTIDOMIMETIC AND SEB |
| 1D66 | DNA RECOGNITION BY GAL4: STRUCTURE OF A PROTEIN/DNA COMPLEX |
| 1D6A | STRUCTURE OF POKEWEED ANTIVIRAL PROTEIN COMPLEXED WITH GUANINE |
| 1D6B | SOLUTION STRUCTURE OF DEFENSIN-LIKE PEPTIDE-2 (DLP-2) FROM PLATYPUS VENOM |
| 1D6E | CRYSTAL STRUCTURE OF HLA-DR4 COMPLEX WITH PEPTIDOMIMETIC AND SEB |
| 1D6F | CHALCONE SYNTHASE C164A MUTANT |
| 1D6G | MOLECULAR COMPLEX OF CHOLECYSTOKININ-8 AND N-TERMINUS OF THE CHOLECYSTOKININ A RECEPTOR BY NMR SPECTROSCOPY |
| 1D6H | CHALONE SYNTHASE (N336A MUTANT COMPLEXED WITH COA) |
| 1D6I | CHALCONE SYNTHASE (H303Q MUTANT) |
| 1D6J | CRYSTAL STRUCTURE OF ADENOSINE 5'-PHOSPHOSULFATE (APS) KINASE FROM PENICILLIUM CHRYSOGENUM |
| 1D6K | NMR SOLUTION STRUCTURE OF THE 5S RRNA E-LOOP/L25 COMPLEX |
| 1D6M | CRYSTAL STRUCTURE OF E. COLI DNA TOPOISOMERASE III |
| 1D6N | TERNARY COMPLEX STRUCTURE OF HUMAN HGPRTASE, PRPP, MG2+, AND THE INHIBITOR HPP REVEALS THE INVOLVEMENT OF THE FLEXIBLE LOOP IN SUBSTRATE BINDING |
| 1D6O | NATIVE FKBP |
| 1D6P | HUMAN LYSOZYME L63 MUTANT LABELLED WITH 2',3'-EPOXYPROPYL N,N'-DIACETYLCHITOBIOSE |
| 1D6Q | HUMAN LYSOZYME E102 MUTANT LABELLED WITH 2',3'-EPOXYPROPYL GLYCOSIDE OF N-ACETYLLACTOSAMINE |
| 1D6R | CRYSTAL STRUCTURE OF CANCER CHEMOPREVENTIVE BOWMAN-BIRK INHIBITOR IN TERNARY COMPLEX WITH BOVINE TRYPSIN AT 2.3 A RESOLUTION. STRUCTURAL BASIS OF JANUS-FACED SERINE PROTEASE INHIBITOR SPECIFICITY |
| 1D6S | CRYSTAL STRUCTURE OF THE K41A MUTANT OF O-ACETYLSERINE SULFHYDRYLASE COMPLEXED IN EXTERNAL ALDIMINE LINKAGE WITH METHIONINE |
| 1D6T | RNASE P PROTEIN FROM STAPHYLOCOCCUS AUREUS |
| 1D6U | CRYSTAL STRUCTURE OF E. COLI AMINE OXIDASE ANAEROBICALLY REDUCED WITH BETA-PHENYLETHYLAMINE |
| 1D6V | CONFORMATION EFFECTS IN BIOLOGICAL CATALYSIS INTRODUCED BY OXY-COPE ANTIBODY MATURATION |
| 1D6W | STRUCTURE OF THROMBIN COMPLEXED WITH SELECTIVE NON-ELECTROPHILIC INHIBITORS HAVING CYCLOHEXYL MOIETIES AT P1 |
| 1D6Y | CRYSTAL STRUCTURE OF E. COLI COPPER-CONTAINING AMINE OXIDASE ANAEROBICALLY REDUCED WITH BETA-PHENYLETHYLAMINE AND COMPLEXED WITH NITRIC OXIDE. |
| 1D6Z | CRYSTAL STRUCTURE OF THE AEROBICALLY FREEZE TRAPPED RATE-DETERMINING CATALYTIC INTERMEDIATE OF E. COLI COPPER-CONTAINING AMINE OXIDASE. |
| 1D7A | CRYSTAL STRUCTURE OF E. COLI PURE-MONONUCLEOTIDE COMPLEX. |
| 1D7B | CYTOCHROME DOMAIN OF CELLOBIOSE DEHYDROGENASE, PH 7.5 |
| 1D7C | CYTOCHROME DOMAIN OF CELLOBIOSE DEHYDROGENASE, PH 4.6 |
| 1D7D | CYTOCHROME DOMAIN OF CELLOBIOSE DEHYDROGENASE, HP3 FRAGMENT, PH 7.5 |
| 1D7E | CRYSTAL STRUCTURE OF THE P65 CRYSTAL FORM OF PHOTOACTIVE YELLOW PROTEIN |
| 1D7F | CRYSTAL STRUCTURE OF ASPARAGINE 233-REPLACED CYCLODEXTRIN GLUCANOTRANSFERASE FROM ALKALOPHILIC BACILLUS SP. 1011 DETERMINED AT 1.9 A RESOLUTION |
| 1D7H | FKBP COMPLEXED WITH DMSO |
| 1D7I | FKBP COMPLEXED WITH METHYL METHYLSULFINYLMETHYL SULFIDE (DSS) |
| 1D7J | FKBP COMPLEXED WITH 4-HYDROXY-2-BUTANONE |
| 1D7K | CRYSTAL STRUCTURE OF HUMAN ORNITHINE DECARBOXYLASE AT 2.1 ANGSTROMS RESOLUTION |
| 1D7L | STRUCTURE-FUNCTION CORRELATIONS OF THE REACTION OF REDUCED NICOTINAMIDE ANALOGS WITH P-HYDROXYBENZOATE HYDROXYLASE SUBSTITUTED WITH A SERIES OF 8-SUBSTITUTED FLAVINS |
| 1D7M | COILED-COIL DIMERIZATION DOMAIN FROM CORTEXILLIN I |
| 1D7N | SOLUTION STRUCTURE ANALYSIS OF THE MASTOPARAN WITH DETERGENTS |
| 1D7O | CRYSTAL STRUCTURE OF BRASSICA NAPUS ENOYL ACYL CARRIER PROTEIN REDUCTASE COMPLEXED WITH NAD AND TRICLOSAN |
| 1D7P | CRYSTAL STRUCTURE OF THE C2 DOMAIN OF HUMAN FACTOR VIII AT 1.5 A RESOLUTION AT 1.5 A |
| 1D7Q | HUMAN TRANSLATION INITIATION FACTOR EIF1A |
| 1D7R | CRYSTAL STRUCTURE OF THE COMPLEX OF 2,2-DIALKYLGLYCINE DECARBOXYLASE WITH 5PA |
| 1D7S | CRYSTAL STRUCTURE OF THE COMPLEX OF 2,2-DIALKYLGLYCINE DECARBOXYLASE WITH DCS |
| 1D7U | CRYSTAL STRUCTURE OF THE COMPLEX OF 2,2-DIALKYLGLYCINE DECARBOXYLASE WITH LCS |
| 1D7V | CRYSTAL STRUCTURE OF THE COMPLEX OF 2,2-DIALKYLGLYCINE DECARBOXYLASE WITH NMA |
| 1D7W | CRYSTAL STRUCTURE OF HUMAN MYELOPEROXIDASE ISOFORM C COMPLEXED WITH CYANIDE AND BROMIDE AT PH 4.0 |
| 1D7X | CRYSTAL STRUCTURE OF MMP3 COMPLEXED WITH A MODIFIED PROLINE SCAFFOLD BASED INHIBITOR. |
| 1D7Y | CRYSTAL STRUCTURE OF NADH-DEPENDENT FERREDOXIN REDUCTASE, BPHA4 |
| 1D8A | E. COLI ENOYL REDUCTASE/NAD+/TRICLOSAN COMPLEX |
| 1D8B | NMR STRUCTURE OF THE HRDC DOMAIN FROM SACCHAROMYCES CEREVISIAE RECQ HELICASE |
| 1D8C | MALATE SYNTHASE G COMPLEXED WITH MAGNESIUM AND GLYOXYLATE |
| 1D8D | CO-CRYSTAL STRUCTURE OF RAT PROTEIN FARNESYLTRANSFERASE COMPLEXED WITH A K-RAS4B PEPTIDE SUBSTRATE AND FPP ANALOG AT 2.0A RESOLUTION |
| 1D8E | ZINC-DEPLETED FTASE COMPLEXED WITH K-RAS4B PEPTIDE SUBSTRATE AND FPP ANALOG. |
| 1D8F | CRYSTAL STRUCTURE OF MMP3 COMPLEXED WITH A PIPERAZINE BASED INHIBITOR. |
| 1D8H | X-RAY CRYSTAL STRUCTURE OF YEAST RNA TRIPHOSPHATASE IN COMPLEX WITH SULFATE AND MANGANESE IONS. |
| 1D8I | X-RAY CRYSTAL STRUCTURE OF YEAST RNA TRIPHOSPHATASE IN COMPLEX WITH A SULFATE ION. |
| 1D8J | SOLUTION STRUCTURE OF THE CENTRAL CORE DOMAIN OF TFIIE BETA |
| 1D8K | SOLUTION STRUCTURE OF THE CENTRAL CORE DOMAIN OF TFIIE BETA |
| 1D8L | E. COLI HOLLIDAY JUNCTION BINDING PROTEIN RUVA NH2 REGION LACKING DOMAIN III |
| 1D8M | CRYSTAL STRUCTURE OF MMP3 COMPLEXED WITH A HETEROCYCLE-BASED INHIBITOR |
| 1D8T | CRYSTAL STRUCTURE OF ELONGATION FACTOR, TU (EF-TU-MGGDP) COMPLEXED WITH GE2270A, A THIAZOLYL PEPTIDE ANTIBIOTIC |
| 1D8U | CRYSTAL STRUCTURE OF NON-SYMBIOTIC PLANT HEMOGLOBIN FROM RICE |
| 1D8V | THE RESTRAINED AND MINIMIZED AVERAGE NMR STRUCTURE OF MAP30. |
| 1D8W | L-RHAMNOSE ISOMERASE |
| 1D8Y | CRYSTAL STRUCTURE OF THE COMPLEX OF DNA POLYMERASE I KLENOW FRAGMENT WITH DNA |
| 1D8Z | SOLUTION STRUCTURE OF THE FIRST RNA-BINDING DOMAIN (RBD1) OF HU ANTIGEN C (HUC) |
| 1D9A | SOLUTION STRUCTURE OF THE SECOND RNA-BINDING DOMAIN (RBD2) OF HU ANTIGEN C (HUC) |
| 1D9C | BOVINE INTERFERON-GAMMA AT 2.0 ANGSTROMS |
| 1D9D | CRYSTALL STRUCTURE OF THE COMPLEX OF DNA POLYMERASE I KLENOW FRAGMENT WITH SHORT DNA FRAGMENT CARRYING 2'-0-AMINOPROPYL-RNA MODIFICATIONS 5'-D(TCG)-AP(AUC)-3' |
| 1D9E | STRUCTURE OF E. COLI KDO8P SYNTHASE |
| 1D9F | CRYSTAL STRUCTURE OF THE COMPLEX OF DNA POLYMERASE I KLENOW FRAGMENT WITH DNA TETRAMER CARRYING 2'-O-(3-AMINOPROPYL)-RNA MODIFICATION 5'-D(TT)-AP(U)-D(T)-3' |
| 1D9G | BOVINE INTERFERON-GAMMA AT 2.9 ANGSTROMS |
| 1D9I | STRUCTURE OF THROMBIN COMPLEXED WITH SELECTIVE NON-ELECTOPHILIC INHIBITORS HAVING CYCLOHEXYL MOIETIES AT P1 |
| 1D9J | SOLUTION STRUCTURE OF CECROPIN A(1-8)-MAGAININ 2(1-12) HYBRID PEPTIDE |
| 1D9K | CRYSTAL STRUCTURE OF COMPLEX BETWEEN D10 TCR AND PMHC I-AK/CA |
| 1D9L | SOLUTION STRUCTURE OF CECROPIN A(1-8)-MAGAININ 2 HYBRID PEPTIDE ANALOGUE(P1) |
| 1D9M | SOLUTION STRUCTURE OF CECROPIN A(1-8)-MAGAININ 2 HYBRID PEPTIDE ANALOGUE(P2) |
| 1D9N | SOLUTION STRUCTURE OF THE METHYL-CPG-BINDING DOMAIN OF THE METHYLATION-DEPENDENT TRANSCRIPTIONAL REPRESSOR MBD1/PCM1 |
| 1D9P | SOLUTION STRUCTURE OF CECROPIN A(1-8)-MAGAININ 2(1-12) HYBRID PEPTIDE ANALOGUE(P4) |
| 1D9Q | OXIDIZED PEA FRUCTOSE-1,6-BISPHOSPHATASE FORM 1 |
| 1D9S | TUMOR SUPPRESSOR P15(INK4B) STRUCTURE BY COMPARATIVE MODELING AND NMR DATA |
| 1D9U | BACTERIOPHAGE LAMBDA LYSOZYME COMPLEXED WITH A CHITOHEXASACHARIDE |
| 1D9V | HAEMOPHILUS INFLUENZAE FERRIC-BINDING PROTEIN APO FORM |
| 1D9W | BACTERIOPHAGE T4 LYSOZYME MUTANT |
| 1D9X | CRYSTAL STRUCTURE OF THE DNA REPAIR PROTEIN UVRB |
| 1D9Y | NEISSERIA GONORRHOEAE FERRIC BINDING PROTEIN |
| 1D9Z | CRYSTAL STRUCTURE OF THE DNA REPAIR PROTEIN UVRB IN COMPLEX WITH ATP |
| 1DAA | CRYSTALLOGRAPHIC STRUCTURE OF D-AMINO ACID AMINOTRANSFERASE COMPLEXED WITH PYRIDOXAL-5'-PHOSPHATE |
| 1DAB | THE STRUCTURE OF BORDETELLA PERTUSSIS VIRULENCE FACTOR P.69 PERTACTIN |
| 1DAD | DETHIOBIOTIN SYNTHETASE COMPLEXED WITH ADP |
| 1DAE | DETHIOBIOTIN SYNTHETASE COMPLEXED WITH 3-(1-AMINOETHYL) NONANEDIOIC ACID |
| 1DAF | DETHIOBIOTIN SYNTHETASE COMPLEXED WITH 7-(CARBOXYAMINO)-8-AMINO-NONANOIC ACID, ADP, AND CALCIUM |
| 1DAG | DETHIOBIOTIN SYNTHETASE COMPLEXED WITH 7-(CARBOXYAMINO)-8-AMINO-NONANOIC ACID AND 5'-ADENOSYL-METHYLENE-TRIPHOSPHATE |
| 1DAH | DETHIOBIOTIN SYNTHETASE COMPLEXED WITH 7,8-DIAMINO-NONANOIC ACID, 5'-ADENOSYL-METHYLENE-TRIPHOSPHATE, AND MANGANESE |
| 1DAI | DETHIOBIOTIN SYNTHETASE COMPLEXED WITH 7-(CARBOXYAMINO)-8-AMINO-NONANOIC ACID |
| 1DAJ | COMPARISON OF TERNARY COMPLEXES OF PNEUMOCYSTIS CARINII AND WILD TYPE HUMAN DIHYDROFOLATE REDUCTASE WITH COENZYME NADPH AND A NOVEL CLASSICAL ANTITUMOR FURO[2,3D]PYRIMIDINE ANTIFOLATE |
| 1DAK | DETHIOBIOTIN SYNTHETASE FROM ESCHERICHIA COLI, COMPLEX REACTION INTERMEDIATE ADP AND MIXED ANHYDRIDE |
| 1DAM | DETHIOBIOTIN SYNTHETASE COMPLEXED WITH DETHIOBIOTIN, ADP, INORGANIC PHOSPHATE AND MAGNESIUM |
| 1DAN | COMPLEX OF ACTIVE SITE INHIBITED HUMAN BLOOD COAGULATION FACTOR VIIA WITH HUMAN RECOMBINANT SOLUBLE TISSUE FACTOR |
| 1DAP | C. GLUTAMICUM DAP DEHYDROGENASE IN COMPLEX WITH NADP+ |
| 1DAQ | SOLUTION STRUCTURE OF THE TYPE I DOCKERIN DOMAIN FROM THE CLOSTRIDIUM THERMOCELLUM CELLULOSOME (MINIMIZED AVERAGE STRUCTURE) |
| 1DAR | ELONGATION FACTOR G IN COMPLEX WITH GDP |
| 1DAT | CUBIC CRYSTAL STRUCTURE RECOMBINANT HORSE L APOFERRITIN |
| 1DAV | SOLUTION STRUCTURE OF THE TYPE I DOCKERIN DOMAIN FROM THE CLOSTRIDIUM THERMOCELLUM CELLULOSOME (20 STRUCTURES) |
| 1DAW | CRYSTAL STRUCTURE OF A BINARY COMPLEX OF PROTEIN KINASE CK2 (ALPHA-SUBUNIT) AND MG-AMPPNP |
| 1DAX | OXIDISED DESULFOVIBRIO AFRICANUS FERREDOXIN I, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1DAY | CRYSTAL STRUCTURE OF A BINARY COMPLEX OF PROTEIN KINASE CK2 (ALPHA-SUBUNIT) AND MG-GMPPNP |
| 1DAZ | STRUCTURAL AND KINETIC ANALYSIS OF DRUG RESISTANT MUTANTS OF HIV-1 PROTEASE |
| 1DB1 | CRYSTAL STRUCTURE OF THE NUCLEAR RECEPTOR FOR VITAMIN D COMPLEXED TO VITAMIN D |
| 1DB2 | CRYSTAL STRUCTURE OF NATIVE PLASMINOGEN ACTIVATOR INHIBITOR-1 |
| 1DB3 | E.COLI GDP-MANNOSE 4,6-DEHYDRATASE |
| 1DB4 | HUMAN S-PLA2 IN COMPLEX WITH INDOLE 8 |
| 1DB5 | HUMAN S-PLA2 IN COMPLEX WITH INDOLE 6 |
| 1DBA | THREE-DIMENSIONAL STRUCTURE OF AN ANTI-STEROID FAB' AND PROGESTERONE-FAB' COMPLEX |
| 1DBB | THREE-DIMENSIONAL STRUCTURE OF AN ANTI-STEROID FAB' AND PROGESTERONE-FAB' COMPLEX |
| 1DBD | E2 DNA-BINDING DOMAIN FROM PAPILLOMAVIRUS BPV-1 |
| 1DBF | CHORISMATE MUTASE FROM BACILLUS SUBTILIS AT 1.30 ANGSTROM |
| 1DBG | CRYSTAL STRUCTURE OF CHONDROITINASE B |
| 1DBH | DBL AND PLECKSTRIN HOMOLOGY DOMAINS FROM HSOS1 |
| 1DBI | CRYSTAL STRUCTURE OF A THERMOSTABLE SERINE PROTEASE |
| 1DBJ | MOLECULAR BASIS OF CROSS-REACTIVITY AND THE LIMITS OF ANTIBODY-ANTIGEN COMPLEMENTARITY |
| 1DBK | MOLECULAR BASIS OF CROSS-REACTIVITY AND THE LIMITS OF ANTIBODY-ANTIGEN COMPLEMENTARITY |
| 1DBM | MOLECULAR BASIS OF CROSS-REACTIVITY AND THE LIMITS OF ANTIBODY-ANTIGEN COMPLEMENTARITY |
| 1DBN | MAACKIA AMURENSIS LEUKOAGGLUTININ (LECTIN) WITH SIALYLLACTOSE |
| 1DBO | CRYSTAL STRUCTURE OF CHONDROITINASE B |
| 1DBP | IDENTICAL MUTATIONS AT CORRESPONDING POSITIONS IN TWO HOMOLOGOUS PROTEINS WITH NON-IDENTICAL EFFECTS |
| 1DBQ | DNA-BINDING REGULATORY PROTEIN |
| 1DBR | HYPOXANTHINE GUANINE XANTHINE |
| 1DBS | MECHANISTIC IMPLICATIONS AND FAMILY RELATIONSHIPS FROM THE STRUCTURE OF DETHIOBIOTIN SYNTHETASE |
| 1DBT | CRYSTAL STRUCTURE OF OROTIDINE 5'-MONOPHOSPHATE DECARBOXYLASE FROM BACILLUS SUBTILIS COMPLEXED WITH UMP |
| 1DBU | CRYSTAL STRUCTURE OF CYSTEINYL-TRNA(PRO) DEACYLASE PROTEIN FROM H. INFLUENZAE (HI1434) |
| 1DBV | GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE MUTANT WITH ASP 32 REPLACED BY GLY, LEU 187 REPLACED BY ALA, AND PRO 188 REPLACED BY SER COMPLEXED WITH NAD+ |
| 1DBW | CRYSTAL STRUCTURE OF FIXJ-N |
| 1DBX | CRYSTAL STRUCTURE OF CYSTEINYL-TRNA(PRO) DEACYLASE FROM H. INFLUENZAE (HI1434) |
| 1DBY | NMR STRUCTURES OF CHLOROPLAST THIOREDOXIN M CH2 FROM THE GREEN ALGA CHLAMYDOMONAS REINHARDTII |
| 1DBZ | C153S MUTANT OF PEA FRUCTOSE-1,6-BISPHOSPHATASE |
| 1DC1 | RESTRICTION ENZYME BSOBI/DNA COMPLEX STRUCTURE: ENCIRCLEMENT OF THE DNA AND HISTIDINE-CATALYZED HYDROLYSIS WITHIN A CANONICAL RESTRICTION ENZYME FOLD |
| 1DC2 | SOLUTION NMR STRUCTURE OF TUMOR SUPPRESSOR P16INK4A, 20 STRUCTURES |
| 1DC3 | STRUCTURAL ANALYSIS OF GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE FROM ESCHERICHIA COLI: DIRECT EVIDENCE FOR SUBSTRATE BINDING AND COFACTOR-INDUCED CONFORMATIONAL CHANGES |
| 1DC4 | STRUCTURAL ANALYSIS OF GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE FROM ESCHERICHIA COLI: DIRECT EVIDENCE FOR SUBSTRATE BINDING AND COFACTOR-INDUCED CONFORMATIONAL CHANGES |
| 1DC5 | STRUCTURAL ANALYSIS OF GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE FROM ESCHERICHIA COLI: DIRECT EVIDENCE FOR SUBSTRATE BINDING AND COFACTOR-INDUCED CONFORMATIONAL CHANGES |
| 1DC6 | STRUCTURAL ANALYSIS OF GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE FROM ESCHERICHIA COLI: DIRECT EVIDENCE FOR SUBSTRATE BINDING AND COFACTOR-INDUCED CONFORMATIONAL CHANGES. |
| 1DC7 | STRUCTURE OF A TRANSIENTLY PHOSPHORYLATED SWITCH" IN BACTERIAL SIGNAL TRANSDUCTION" |
| 1DC8 | STRUCTURE OF A TRANSIENTLY PHOSPHORYLATED SWITCH" IN BACTERIAL SIGNAL TRANSDUCTION" |
| 1DC9 | PROPERTIES AND CRYSTAL STRUCTURE OF A BETA-BARREL FOLDING MUTANT, V60N INTESTINAL FATTY ACID BINDING PROTEIN (IFABP) |
| 1DCA | STRUCTURE OF AN ENGINEERED METAL BINDING SITE IN HUMAN CARBONIC ANHYDRASE II REVEALS THE ARCHITECTURE OF A REGULATORY CYSTEINE SWITCH |
| 1DCB | STRUCTURE OF AN ENGINEERED METAL BINDING SITE IN HUMAN CARBONIC ANHYDRASE II REVEALS THE ARCHITECTURE OF A REGULATORY CYSTEINE SWITCH |
| 1DCC | 2.2 ANGSTROM STRUCTURE OF OXYPEROXIDASE: A MODEL FOR THE ENZYME:PEROXIDE COMPLEX |
| 1DCD | DESULFOREDOXIN COMPLEXED WITH CD2+ |
| 1DCE | CRYSTAL STRUCTURE OF RAB GERANYLGERANYLTRANSFERASE FROM RAT BRAIN |
| 1DCF | CRYSTAL STRUCTURE OF THE RECEIVER DOMAIN OF THE ETHYLENE RECEPTOR OF ARABIDOPSIS THALIANA |
| 1DCH | CRYSTAL STRUCTURE OF DCOH, A BIFUNCTIONAL, PROTEIN-BINDING TRANSCRIPTION COACTIVATOR |
| 1DCI | DIENOYL-COA ISOMERASE |
| 1DCJ | SOLUTION STRUCTURE OF YHHP, A NOVEL ESCHERICHIA COLI PROTEIN IMPLICATED IN THE CELL DIVISION |
| 1DCK | STRUCTURE OF UNPHOSPHORYLATED FIXJ-N COMPLEXED WITH MN2+ |
| 1DCL | MCG, A LAMBDA V TYPE LIGHT-CHAIN DIMER (BENCE-JONES PROTEIN), CRYSTALLIZED FROM AMMONIUM SULFATE |
| 1DCM | STRUCTURE OF UNPHOSPHORYLATED FIXJ-N WITH AN ATYPICAL CONFORMER (MONOMER A) |
| 1DCN | INACTIVE MUTANT H162N OF DELTA 2 CRYSTALLIN WITH BOUND ARGININOSUCCINATE |
| 1DCO | DCOH, A BIFUNCTIONAL PROTEIN-BINDING TRANSCRIPTIONAL COACTIVATOR |
| 1DCP | DCOH, A BIFUNCTIONAL PROTEIN-BINDING TRANSCRIPTIONAL COACTIVATOR, COMPLEXED WITH BIOPTERIN |
| 1DCQ | CRYSTAL STRUCTURE OF THE ARF-GAP DOMAIN AND ANKYRIN REPEATS OF PAPBETA. |
| 1DCS | DEACETOXYCEPHALOSPORIN C SYNTHASE FROM S. CLAVULIGERUS |
| 1DCT | DNA (CYTOSINE-5) METHYLASE FROM HAEIII COVALENTLY BOUND TO DNA |
| 1DCU | REDOX SIGNALING IN THE CHLOROPLAST: STRUCTURE OF OXIDIZED PEA FRUCTOSE-1,6-BISPHOSPHATE PHOSPHATASE |
| 1DCY | CRYSTAL STRUCTURE OF HUMAN S-PLA2 IN COMPLEX WITH INDOLE 3 ACTIVE SITE INHIBITOR |
| 1DCZ | BIOTIN CARBOXYL CARRIER DOMAIN OF TRANSCARBOXYLASE (TC 1.3S) |
| 1DD1 | CRYSTAL STRUCTURE ANALYSIS OF THE SMAD4 ACTIVE FRAGMENT |
| 1DD2 | BIOTIN CARBOXYL CARRIER DOMAIN OF TRANSCARBOXYLASE (TC 1.3S) |
| 1DD3 | CRYSTAL STRUCTURE OF RIBOSOMAL PROTEIN L12 FROM THERMOTOGA MARITIMA |
| 1DD4 | CRYSTAL STRUCTURE OF RIBOSOMAL PROTEIN L12 FROM THERMOTOGA MARITIM |
| 1DD5 | CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA RIBOSOME RECYCLING FACTOR, RRF |
| 1DD6 | IMP-1 METALLO BETA-LACTAMASE FROM PSEUDOMONAS AERUGINOSA IN COMPLEX WITH A MERCAPTOCARBOXYLATE INHIBITOR |
| 1DD7 | MURINE INDUCIBLE NITRIC OXIDE SYNTHASE OXYGENASE DOMAIN (DELTA 114) (N-[(1,3-BENZODIOXOL-5-YL)METHYL]-1-[2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL]-4-(METHOXYCARBONYL)-PIPERAZINE-2-ACETAMIDE COMPLEX |
| 1DD8 | CRYSTAL STRUCTURE OF BETA-KETOACYL-[ACYL CARRIER PROTEIN] SYNTHASE I FROM ESCHERICHIA COLI |
| 1DD9 | STRUCTURE OF THE DNAG CATALYTIC CORE |
| 1DDB | STRUCTURE OF MOUSE BID, NMR, 20 STRUCTURES |
| 1DDE | STRUCTURE OF THE DNAG CATALYTIC CORE |
| 1DDF | FAS DEATH DOMAIN, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1DDG | CRYSTAL STRUCTURE OF SIR-FP60 |
| 1DDH | MHC CLASS I H-2DD HEAVY CHAIN COMPLEXED WITH BETA-2 MICROGLOBULIN AND AN IMMUNODOMINANT PEPTIDE P18-I10 FROM THE HUMAN IMMUNODEFICIENCY VIRUS ENVELOPE GLYCOPROTEIN 120 |
| 1DDI | CRYSTAL STRUCTURE OF SIR-FP60 |
| 1DDJ | CRYSTAL STRUCTURE OF HUMAN PLASMINOGEN CATALYTIC DOMAIN |
| 1DDK | CRYSTAL STRUCTURE OF IMP-1 METALLO BETA-LACTAMASE FROM PSEUDOMONAS AERUGINOSA |
| 1DDL | DESMODIUM YELLOW MOTTLE TYMOVIRUS |
| 1DDM | SOLUTION STRUCTURE OF THE NUMB PTB DOMAIN COMPLEXED TO A NAK PEPTIDE |
| 1DDN | DIPHTHERIA TOX REPRESSOR (C102D MUTANT)/TOX DNA OPERATOR COMPLEX |
| 1DDO | REDUCED D-AMINO ACID OXIDASE FROM PIG KIDNEY IN COMPLEX WITH IMINO-TRP |
| 1DDR | MOLECULE: DIHYDROFOLATE REDUCTASE (E.C.1.5.1.3) COMPLEXED WITH METHOTREXATE AND UREA |
| 1DDS | MOLECULE: DIHYDROFOLATE REDUCTASE (E.C.1.5.1.3) COMPLEXED WITH METHOTREXATE |
| 1DDT | THE REFINED STRUCTURE OF DIMERIC DIPHTHERIA TOXIN AT 2.0 ANGSTROMS RESOLUTION |
| 1DDU | E. COLI THYMIDYLATE SYNTHASE IN COMPLEX WITH CB3717 AND 2',5'-DIDEOXYURIDINE (DDURD) |
| 1DDV | CRYSTAL STRUCTURE OF THE HOMER EVH1 DOMAIN WITH BOUND MGLUR PEPTIDE |
| 1DDW | HOMER EVH1 DOMAIN UNLIGANDED |
| 1DDX | CRYSTAL STRUCTURE OF A MIXTURE OF ARACHIDONIC ACID AND PROSTAGLANDIN BOUND TO THE CYCLOOXYGENASE ACTIVE SITE OF COX-2: PROSTAGLANDIN STRUCTURE |
| 1DDZ | X-RAY STRUCTURE OF A BETA-CARBONIC ANHYDRASE FROM THE RED ALGA, PORPHYRIDIUM PURPUREUM R-1 |
| 1DE0 | MODULATING THE MIDPOINT POTENTIAL OF THE [4FE-4S] CLUSTER OF THE NITROGENASE FE PROTEIN |
| 1DE1 | NMR STRUCTURES OF OXIDIZED BACTERIOPHAGE T4 GLUTAREDOXIN |
| 1DE2 | NMR STRUCTURES OF REDUCED BACTERIOPHAGE T4 GLUTAREDOXIN |
| 1DE3 | SOLUTION STRUCTURE OF THE CYTOTOXIC RIBONUCLEASE ALPHA-SARCIN |
| 1DE5 | L-RHAMNOSE ISOMERASE |
| 1DE6 | L-RHAMNOSE ISOMERASE |
| 1DE7 | INTERACTION OF FACTOR XIII ACTIVATION PEPTIDE WITH ALPHA-THROMBIN: CRYSTAL STRUCTURE OF THE ENZYME-SUBSTRATE COMPLEX |
| 1DE8 | HUMAN APURINIC/APYRIMIDINIC ENDONUCLEASE-1 (APE1) BOUND TO ABASIC DNA |
| 1DE9 | HUMAN APE1 ENDONUCLEASE WITH BOUND ABASIC DNA AND MN2+ ION |
| 1DEA | STRUCTURE AND CATALYTIC MECHANISM OF GLUCOSAMINE 6-PHOSPHATE DEAMINASE FROM ESCHERICHIA COLI AT 2.1 ANGSTROMS RESOLUTION |
| 1DEB | CRYSTAL STRUCTURE OF THE N-TERMINAL COILED COIL DOMAIN FROM APC |
| 1DEC | STRUCTURE OF THE RGD PROTEIN DECORSIN: CONSERVED MOTIF AND DISTINCT FUNCTION IN LEECH PROTEINS THAT AFFECT BLOOD CLOTTING |
| 1DED | CRYSTAL STRUCTURE OF ALKALOPHILIC ASPARAGINE 233-REPLACED CYCLODEXTRIN GLUCANOTRANSFERASE COMPLEXED WITH AN INHIBITOR, ACARBOSE, AT 2.0 A RESOLUTION |
| 1DEE | STRUCTURE OF S. AUREUS PROTEIN A BOUND TO A HUMAN IGM FAB |
| 1DEF | PEPTIDE DEFORMYLASE CATALYTIC CORE (RESIDUES 1-147), NMR, 9 STRUCTURES |
| 1DEH | CRYSTALLIZATION OF HUMAN BETA1 ALCOHOL DEHYDROGENASE (15 MG/ML) IN 50 MM SODIUM PHOSPHATE (PH 7.5), 2.0 MM NAD+ AND 1 MM 4-IODOPYRAZOLE AT 25 OC, 13% (W/V) PEG 8000 |
| 1DEI | DESHEPTAPEPTIDE (B24-B30) INSULIN |
| 1DEJ | CRYSTAL STRUCTURE OF A DICTYOSTELIUM/TETRAHYMENA CHIMERA ACTIN (MUTANT 646: Q228K/T229A/A230Y/A231K/S232E/E360H) IN COMPLEX WITH HUMAN GELSOLIN SEGMENT 1 |
| 1DEK | DEOXYNUCLEOSIDE MONOPHOSPHATE KINASE COMPLEXED WITH DEOXY-GMP |
| 1DEL | DEOXYNUCLEOSIDE MONOPHOSPHATE KINASE COMPLEXED WITH DEOXY-GMP AND AMP |
| 1DEM | PROTEINASE INHIBITOR HOMOLOGUES AS POTASSIUM CHANNEL BLOCKERS |
| 1DEN | PROTEINASE INHIBITOR HOMOLOGUES AS POTASSIUM CHANNEL BLOCKERS |
| 1DEO | RHAMNOGALACTURONAN ACETYLESTERASE FROM ASPERGILLUS ACULEATUS AT 1.55 A RESOLUTION WITH SO4 IN THE ACTIVE SITE |
| 1DEP | MEMBRANE PROTEIN, NMR, 1 STRUCTURE |
| 1DET | RIBONUCLEASE T1 CARBOXYMETHYLATED AT GLU 58 IN COMPLEX WITH 2'GMP |
| 1DEU | CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN X: A CYSTEINE PROTEASE WITH THE PROREGION COVALENTLY LINKED TO THE ACTIVE SITE CYSTEINE |
| 1DEV | CRYSTAL STRUCTURE OF SMAD2 MH2 DOMAIN BOUND TO THE SMAD-BINDING DOMAIN OF SARA |
| 1DEW | CRYSTAL STRUCTURE OF HUMAN APE1 BOUND TO ABASIC DNA |
| 1DEX | RHAMNOGALACTURONAN ACETYLESTERASE FROM ASPERGILLUS ACULEATUS AT 1.9 A RESOLUTION |
| 1DF0 | CRYSTAL STRUCTURE OF M-CALPAIN |
| 1DF1 | MURINE INOSOXY DIMER WITH ISOTHIOUREA BOUND IN THE ACTIVE SITE |
| 1DF3 | SOLUTION STRUCTURE OF A RECOMBINANT MOUSE MAJOR URINARY PROTEIN |
| 1DF4 | INTERACTIONS BETWEEN HIV-1 GP41 CORE AND DETERGENTS AND THEIR IMPLICATIONS FOR MEMBRANE FUSION |
| 1DF5 | INTERACTIONS BETWEEN HIV-1 GP41 CORE AND DETERGENTS AND THEIR IMPLICATIONS FOR MEMBRANE FUSION |
| 1DF6 | 1H NMR SOLUTION STRUCTURE OF CYCLOVIOLACIN O1 |
| 1DF7 | DIHYDROFOLATE REDUCTASE OF MYCOBACTERIUM TUBERCULOSIS COMPLEXED WITH NADPH AND METHOTREXATE |
| 1DF8 | S45A MUTANT OF STREPTAVIDIN IN COMPLEX WITH BIOTIN |
| 1DFA | CRYSTAL STRUCTURE OF PI-SCEI IN C2 SPACE GROUP |
| 1DFB | STRUCTURE OF A HUMAN MONOCLONAL ANTIBODY FAB FRAGMENT AGAINST GP41 OF HUMAN IMMUNODEFICIENCY VIRUS TYPE I |
| 1DFC | CRYSTAL STRUCTURE OF HUMAN FASCIN, AN ACTIN-CROSSLINKING PROTEIN |
| 1DFD | OXIDISED DESULFOVIBRIO AFRICANUS FERREDOXIN I, NMR, 19 STRUCTURES |
| 1DFE | NMR STRUCTURE OF RIBOSOMAL PROTEIN L36 FROM THERMUS THERMOPHILUS |
| 1DFF | PEPTIDE DEFORMYLASE |
| 1DFG | X-RAY STRUCTURE OF ESCHERICHIA COLI ENOYL REDUCTASE WITH BOUND NAD AND BENZO-DIAZABORINE |
| 1DFH | X-RAY STRUCTURE OF ESCHERICHIA COLI ENOYL REDUCTASE WITH BOUND NAD AND THIENO-DIAZABORINE |
| 1DFI | X-RAY STRUCTURE OF ESCHERICHIA COLI ENOYL REDUCTASE WITH BOUND NAD |
| 1DFJ | RIBONUCLEASE INHIBITOR COMPLEXED WITH RIBONUCLEASE A |
| 1DFK | NUCLEOTIDE-FREE SCALLOP MYOSIN S1-NEAR RIGOR STATE |
| 1DFM | CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE BGLII COMPLEXED WITH DNA 16-MER |
| 1DFN | CRYSTAL STRUCTURE OF DEFENSIN HNP-3, AN AMPHIPHILIC DIMER: MECHANISMS OF MEMBRANE PERMEABILIZATION |
| 1DFO | CRYSTAL STRUCTURE AT 2.4 ANGSTROM RESOLUTION OF E. COLI SERINE HYDROXYMETHYLTRANSFERASE IN COMPLEX WITH GLYCINE AND 5-FORMYL TETRAHYDROFOLATE |
| 1DFP | FACTOR D INHIBITED BY DIISOPROPYL FLUOROPHOSPHATE |
| 1DFQ | THE HC FRAGMENT OF TETANUS TOXIN COMPLEXED WITH SIALIC ACID |
| 1DFS | SOLUTION STRUCTURE OF THE ALPHA-DOMAIN OF MOUSE METALLOTHIONEIN-1 |
| 1DFT | SOLUTION STRUCTURE OF THE BETA-DOMAIN OF MOUSE METALLOTHIONEIN-1 |
| 1DFU | CRYSTAL STRUCTURE OF E.COLI RIBOSOMAL PROTEIN L25 COMPLEXED WITH A 5S RRNA FRAGMENT AT 1.8 A RESOLUTION |
| 1DFV | CRYSTAL STRUCTURE OF HUMAN NEUTROPHIL GELATINASE ASSOCIATED LIPOCALIN MONOMER |
| 1DFW | CONFORMATIONAL MAPPING OF THE N-TERMINAL SEGMENT OF SURFACTANT PROTEIN B IN LIPID USING 13C-ENHANCED FOURIER TRANSFORM INFRARED SPECTROSCOPY (FTIR) |
| 1DFX | DESULFOFERRODOXIN FROM DESULFOVIBRIO DESULFURICANS, ATCC 27774 |
| 1DG1 | WHOLE, UNMODIFIED, EF-TU(ELONGATION FACTOR TU). |
| 1DG2 | SOLUTION CONFORMATION OF A-CONOTOXIN AUIB |
| 1DG3 | STRUCTURE OF HUMAN GUANYLATE BINDING PROTEIN-1 IN NUCLEOTIDE FREE FORM |
| 1DG4 | NMR STRUCTURE OF THE SUBSTRATE BINDING DOMAIN OF DNAK IN THE APO FORM |
| 1DG5 | DIHYDROFOLATE REDUCTASE OF MYCOBACTERIUM TUBERCULOSIS COMPLEXED WITH NADPH AND TRIMETHOPRIM |
| 1DG6 | CRYSTAL STRUCTURE OF APO2L/TRAIL |
| 1DG7 | DIHYDROFOLATE REDUCTASE OF MYCOBACTERIUM TUBERCULOSIS COMPLEXED WITH NADPH AND 4-BROMO WR99210 |
| 1DG8 | DIHYDROFOLATE REDUCTASE OF MYCOBACTERIUM TUBERCULOSIS COMPLEXED WITH NADPH |
| 1DG9 | CRYSTAL STRUCTURE OF BOVINE LOW MOLECULAR WEIGHT PTPASE COMPLEXED WITH HEPES |
| 1DGB | HUMAN ERYTHROCYTE CATALASE |
| 1DGC | THE X-RAY STRUCTURE OF THE GCN4-BZIP BOUND TO ATF/CREB SITE DNA SHOWS THE COMPLEX DEPENDS ON DNA FLEXIBILITY |
| 1DGD | AN ALKALI METAL ION SIZE-DEPENDENT SWITCH IN THE ACTIVE SITE STRUCTURE OF DIALKYLGLYCINE DECARBOXYLASE |
| 1DGE | AN ALKALI METAL ION SIZE-DEPENDENT SWITCH IN THE ACTIVE SITE STRUCTURE OF DIALKYLGLYCINE DECARBOXYLASE |
| 1DGF | HUMAN ERYTHROCYTE CATALASE |
| 1DGG | HUMAN ERYTHROCYTE CATALSE CYANIDE COMPLEX |
| 1DGH | HUMAN ERYTHROCYTE CATALASE 3-AMINO-1,2,4-TRIAZOLE COMPLEX |
| 1DGI | CRYO-EM STRUCTURE OF HUMAN POLIOVIRUS(SEROTYPE 1)COMPLEXED WITH THREE DOMAIN CD155 |
| 1DGJ | CRYSTAL STRUCTURE OF THE ALDEHYDE OXIDOREDUCTASE FROM DESULFOVIBRIO DESULFURICANS ATCC 27774 |
| 1DGK | MUTANT MONOMER OF RECOMBINANT HUMAN HEXOKINASE TYPE I WITH GLUCOSE AND ADP IN THE ACTIVE SITE |
| 1DGL | LECTIN FROM DIOCLEA GRANDIFLORA COMPLEXED TO TRIMANNOSIDE |
| 1DGM | CRYSTAL STRUCTURE OF ADENOSINE KINASE FROM TOXOPLASMA GONDII |
| 1DGN | SOLUTION STRUCTURE OF ICEBERG, AN INHIBITOR OF INTERLEUKIN-1BETA GENERATION |
| 1DGP | ARISTOLOCHENE SYNTHASE FARNESOL COMPLEX |
| 1DGQ | NMR SOLUTION STRUCTURE OF THE INSERTED DOMAIN OF HUMAN LEUKOCYTE FUNCTION ASSOCIATED ANTIGEN-1 |
| 1DGR | REFINED CRYSTAL STRUCTURE OF CANAVALIN FROM JACK BEAN |
| 1DGS | CRYSTAL STRUCTURE OF NAD+-DEPENDENT DNA LIGASE FROM T. FILIFORMIS |
| 1DGU | HOMOLOGY-BASED MODEL OF CALCIUM-SATURATED CIB (CALCIUM-AND INTEGRIN-BINDING PROTEIN) |
| 1DGV | HOMOLOGY-BASED MODEL OF APO CIB (CALCIUM-AND INTEGRIN-BINDING PROTEIN) |
| 1DGW | STRUCTURE OF THE RHOMBOHEDRAL CRYSTAL OF CANAVALIN FROM JACK BEAN |
| 1DGZ | RIBOSMAL PROTEIN L36 FROM THERMUS THERMOPHILUS: NMR STRUCTURE ENSEMBLE |
| 1DH3 | CRYSTAL STRUCTURE OF A CREB BZIP-CRE COMPLEX REVEALS THE BASIS FOR CREB FAIMLY SELECTIVE DIMERIZATION AND DNA BINDING |
| 1DHF | CRYSTAL STRUCTURES OF RECOMBINANT HUMAN DIHYDROFOLATE REDUCTASE COMPLEXED WITH FOLATE AND 5-DEAZOFOLATE |
| 1DHG | HG-SUBSTITUTED DESULFOREDOXIN |
| 1DHI | LONG-RANGE STRUCTURAL EFFECTS IN A SECOND-SITE REVERTANT OF A MUTANT DIHYDROFOLATE REDUCTASE |
| 1DHJ | LONG-RANGE STRUCTURAL EFFECTS IN A SECOND-SITE REVERTANT OF A MUTANT DIHYDROFOLATE REDUCTASE |
| 1DHK | STRUCTURE OF PORCINE PANCREATIC ALPHA-AMYLASE |
| 1DHM | DNA-BINDING DOMAIN OF E2 FROM HUMAN PAPILLOMAVIRUS-31, NMR, MINIMIZED AVERAGE STRUCTURE |
| 1DHN | 1.65 ANGSTROM RESOLUTION STRUCTURE OF 7,8-DIHYDRONEOPTERIN ALDOLASE FROM STAPHYLOCOCCUS AUREUS |
| 1DHP | DIHYDRODIPICOLINATE SYNTHASE |
| 1DHR | CRYSTAL STRUCTURE OF RAT LIVER DIHYDROPTERIDINE REDUCTASE |
| 1DHS | CRYSTAL STRUCTURE OF THE NAD COMPLEX OF HUMAN DEOXYHYPUSINE SYNTHASE |
| 1DHT | ESTROGENIC 17-BETA HYDROXYSTEROID DEHYDROGENASE COMPLEXED DIHYDROTESTOSTERONE |
| 1DHY | KKS102 BPHC ENZYME |
| 1DI0 | CRYSTAL STRUCTURE OF LUMAZINE SYNTHASE FROM BRUCELLA ABORTUS |
| 1DI1 | CRYSTAL STRUCTURE OF ARISTOLOCHENE SYNTHASE FROM PENICILLIUM ROQUEFORTI |
| 1DI2 | CRYSTAL STRUCTURE OF A DSRNA-BINDING DOMAIN COMPLEXED WITH DSRNA: MOLECULAR BASIS OF DOUBLE-STRANDED RNA-PROTEIN INTERACTIONS |
| 1DI3 | ROLE OF AMINO ACID RESIDUES AT TURNS IN THE CONFORMATIONAL STABILITY AND FOLDING OF HUMAN LYSOZYME |
| 1DI4 | ROLE OF AMINO ACID RESIDUES AT TURNS IN THE CONFORMATIONAL STABILITY AND FOLDING OF HUMAN LYSOZYME |
| 1DI5 | ROLE OF AMINO ACID RESIDUES AT TURNS IN THE CONFORMATIONAL STABILITY AND FOLDING OF HUMAN LYSOZYME |
| 1DI6 | 1.45 A CRYSTAL STRUCTURE OF THE MOLYBDENUMM COFACTOR BIOSYNTHESIS PROTEIN MOGA FROM ESCHERICHIA COLI |
| 1DI7 | 1.60 ANGSTROM CRYSTAL STRUCTURE OF THE MOLYBDENUM COFACTOR BIOSYNTHESIS PROTEIN MOGA FROM ESCHERICHIA COLI |
| 1DI8 | THE STRUCTURE OF CYCLIN-DEPENDENT KINASE 2 (CDK2) IN COMPLEX WITH 4-[3-HYDROXYANILINO]-6,7-DIMETHOXYQUINAZOLINE |
| 1DI9 | THE STRUCTURE OF P38 MITOGEN-ACTIVATED PROTEIN KINASE IN COMPLEX WITH 4-[3-METHYLSULFANYLANILINO]-6,7-DIMETHOXYQUINAZOLINE |
| 1DIA | HUMAN METHYLENETETRAHYDROFOLATE DEHYDROGENASE / CYCLOHYDROLASE COMPLEXED WITH NADP AND INHIBITOR LY249543 |
| 1DIB | HUMAN METHYLENETETRAHYDROFOLATE DEHYDROGENASE / CYCLOHYDROLASE COMPLEXED WITH NADP AND INHIBITOR LY345899 |
| 1DIC | STRUCTURE OF 3,4-DICHLOROISOCOUMARIN-INHIBITED FACTOR D |
| 1DID | OBSERVATIONS OF REACTION INTERMEDIATES AND THE MECHANISM OF ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE |
| 1DIE | OBSERVATIONS OF REACTION INTERMEDIATES AND THE MECHANISM OF ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE |
| 1DIF | HIV-1 PROTEASE IN COMPLEX WITH A DIFLUOROKETONE CONTAINING INHIBITOR A79285 |
| 1DIG | HUMAN METHYLENETETRAHYDROFOLATE DEHYDROGENASE / CYCLOHYDROLASE COMPLEXED WITH NADP AND INHIBITOR LY374571 |
| 1DIH | THREE-DIMENSIONAL STRUCTURE OF E. COLI DIHYDRODIPICOLINATE REDUCTASE |
| 1DII | CRYSTAL STRUCTURE OF P-CRESOL METHYLHYDROXYLASE AT 2.5 A RESOLUTION |
| 1DIK | PYRUVATE PHOSPHATE DIKINASE |
| 1DIL | SIALIDASE FROM SALMONELLA TYPHIMURIUM COMPLEXED WITH APANA AND EPANA INHIBITORS |
| 1DIM | SIALIDASE FROM SALMONELLA TYPHIMURIUM COMPLEXED WITH EPANA INHIBITOR |
| 1DIN | DIENELACTONE HYDROLASE AT 2.8 ANGSTROMS |
| 1DIO | DIOL DEHYDRATASE-CYANOCOBALAMIN COMPLEX FROM KLEBSIELLA OXYTOCA |
| 1DIP | THE SOLUTION STRUCTURE OF PORCINE DELTA-SLEEP-INDUCING PEPTIDE IMMUNOREACTIVE PEPTIDE, NMR, 10 STRUCTURES |
| 1DIQ | CRYSTAL STRUCTURE OF P-CRESOL METHYLHYDROXYLASE WITH SUBSTRATE BOUND |
| 1DIR | CRYSTAL STRUCTURE OF A MONOCLINIC FORM OF DIHYDROPTERIDINE REDUCTASE FROM RAT LIVER |
| 1DIS | DIHYDROFOLATE REDUCTASE (E.C.1.5.1.3) COMPLEX WITH BRODIMOPRIM-4,6-DICARBOXYLATE |
| 1DIT | COMPLEX OF A DIVALENT INHIBITOR WITH THROMBIN |
| 1DIU | DIHYDROFOLATE REDUCTASE (E.C.1.5.1.3) COMPLEX WITH BRODIMOPRIM-4,6-DICARBOXYLATE |
| 1DIV | RIBOSOMAL PROTEIN L9 |
| 1DIW | THE HC FRAGMENT OF TETANUS TOXIN COMPLEXED WITH GALACTOSE |
| 1DIX | CRYSTAL STRUCTURE OF RNASE LE |
| 1DIY | CRYSTAL STRUCTURE OF ARACHIDONIC ACID BOUND IN THE CYCLOOXYGENASE ACTIVE SITE OF PGHS-1 |
| 1DIZ | CRYSTAL STRUCTURE OF E. COLI 3-METHYLADENINE DNA GLYCOSYLASE (ALKA) COMPLEXED WITH DNA |
| 1DJ0 | THE CRYSTAL STRUCTURE OF E. COLI PSEUDOURIDINE SYNTHASE I AT 1.5 ANGSTROM RESOLUTION |
| 1DJ1 | CRYSTAL STRUCTURE OF R48A MUTANT OF CYTOCHROME C PEROXIDASE |
| 1DJ2 | STRUCTURES OF ADENYLOSUCCINATE SYNTHETASE FROM TRITICUM AESTIVUM AND ARABIDOPSIS THALIANA |
| 1DJ3 | STRUCTURES OF ADENYLOSUCCINATE SYNTHETASE FROM TRITICUM AESTIVUM AND ARABIDOPSIS THALIANA |
| 1DJ5 | CRYSTAL STRUCTURE OF R48A MUTANT OF CYTOCHROME C PEROXIDASE WITH N-HYDROXYGUANIDINE BOUND |
| 1DJ7 | CRYSTAL STRUCTURE OF FERREDOXIN THIOREDOXIN REDUCTASE |
| 1DJ8 | CRYSTAL STRUCTURE OF E. COLI PERIPLASMIC PROTEIN HDEA |
| 1DJ9 | CRYSTAL STRUCTURE OF 8-AMINO-7-OXONANOATE SYNTHASE (OR 7-KETO-8AMINIPELARGONATE OR KAPA SYNTHASE) COMPLEXED WITH PLP AND THE PRODUCT 8(S)-AMINO-7-OXONANONOATE (OR KAPA). THE ENZYME OF BIOTIN BIOSYNTHETIC PATHWAY. |
| 1DJA | STRUCTURE OF BETA-LACTAMASE PRECURSOR, K73H MUTANT, AT 298K |
| 1DJB | STRUCTURE OF BETA-LACTAMASE PRECURSOR, S70A MUTANT, AT 298K |
| 1DJC | STRUCTURE OF BETA-LACTAMASE PRECURSOR, S70A MUTANT, AT 120K |
| 1DJE | CRYSTAL STRUCTURE OF THE PLP-BOUND FORM OF 8-AMINO-7-OXONANOATE SYNTHASE |
| 1DJF | NMR STRUCTURE OF A MODEL HYDROPHILIC AMPHIPATHIC HELICAL BASIC PEPTIDE |
| 1DJG | PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-DELTA1 FROM RAT COMPLEXED WITH LANTHANUM |
| 1DJH | PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-DELTA1 FROM RAT COMPLEXED WITH BARIUM |
| 1DJI | PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-DELTA1 FROM RAT COMPLEXED WITH CALCIUM |
| 1DJL | THE CRYSTAL STRUCTURE OF HUMAN TRANSHYDROGENASE DOMAIN III WITH BOUND NADP |
| 1DJM | SOLUTION STRUCTURE OF BEF3-ACTIVATED CHEY FROM ESCHERICHIA COLI |
| 1DJN | STRUCTURAL AND BIOCHEMICAL CHARACTERIZATION OF RECOMBINANT WILD TYPE TRIMETHYLAMINE DEHYDROGENASE FROM METHYLOPHILUS METHYLOTROPHUS (SP. W3A1) |
| 1DJO | CRYSTAL STRUCTURE OF PSEUDOMONAS 7A GLUTAMINASE-ASPARAGINASE WITH THE INHIBITOR DONV COVALENTLY BOUND IN THE ACTIVE SITE |
| 1DJP | CRYSTAL STRUCTURE OF PSEUDOMONAS 7A GLUTAMINASE-ASPARAGINASE WITH THE INHIBITOR DON COVALENTLY BOUND IN THE ACTIVE SITE |
| 1DJQ | STRUCTURAL AND BIOCHEMICAL CHARACTERIZATION OF RECOMBINANT C30A MUTANT OF TRIMETHYLAMINE DEHYDROGENASE FROM METHYLOPHILUS METHYLOTROPHUS (SP. W3A1) |
| 1DJR | HEAT-LABILE ENTEROTOXIN B-PENTAMER COMPLEXED WITH M-CARBOXYPHENYL-ALPHA-D-GALACTOSE |
| 1DJS | LIGAND-BINDING PORTION OF FIBROBLAST GROWTH FACTOR RECEPTOR 2 IN COMPLEX WITH FGF1 |
| 1DJT | ATOMIC RESOLUTION STRUCTURE OF SCORPION ALPHA-LIKE TOXIN BMK M1 IN A NEW CRYSTAL FORM |
| 1DJU | CRYSTAL STRUCTURE OF AROMATIC AMINOTRANSFERASE FROM PYROCOCCUS HORIKOSHII OT3 |
| 1DJW | PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-DELTA1 FROM RAT COMPLEXED WITH INOSITOL-2-METHYLENE-1,2-CYCLIC-MONOPHOSPHONATE |
| 1DJX | PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-DELTA1 FROM RAT COMPLEXED WITH INOSITOL-1,4,5-TRISPHOSPHATE |
| 1DJY | PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-DELTA1 FROM RAT COMPLEXED WITH INOSITOL-2,4,5-TRISPHOSPHATE |
| 1DJZ | PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-DELTA1 FROM RAT COMPLEXED WITH INOSITOL-4,5-BISPHOSPHATE |
| 1DK0 | CRYSTAL STRUCTURE OF THE HEMOPHORE HASA FROM SERRATIA MARCESCENS CRYSTAL FORM P2(1), PH8 |
| 1DK1 | DETAILED VIEW OF A KEY ELEMENT OF THE RIBOSOME ASSEMBLY: CRYSTAL STRUCTURE OF THE S15-RRNA COMPLEX |
| 1DK2 | REFINED SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA |
| 1DK3 | REFINED SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF DNA POLYMERASE BETA |
| 1DK4 | CRYSTAL STRUCTURE OF MJ0109 GENE PRODUCT INOSITOL MONOPHOSPHATASE |
| 1DK5 | CRYSTAL STRUCTURE OF ANNEXIN 24(CA32) FROM CAPSICUM ANNUUM |
| 1DK7 | CRYSTAL STRUCTURE OF AN ISOLATED APICAL DOMAIN OF GROEL |
| 1DK8 | CRYSTAL STRUCTURE OF THE RGS-HOMOLOGOUS DOMAIN OF AXIN |
| 1DKA | DIALKYLGLYCINE DECARBOXYLASE STRUCTURE: BIFUNCTIONAL ACTIVE SITE AND ALKALI METAL BINDING SITES |
| 1DKC | SOLUTION STRUCTURE OF PAFP-S, AN ANTIFUNGAL PEPTIDE FROM THE SEEDS OF PHYTOLACCA AMERICANA |
| 1DKD | CRYSTAL STRUCTURE OF A GROEL (APICAL DOMAIN) AND A DODECAMERIC PEPTIDE COMPLEX |
| 1DKE | NI BETA HEME HUMAN HEMOGLOBIN |
| 1DKF | CRYSTAL STRUCTURE OF A HETERODIMERIC COMPLEX OF RAR AND RXR LIGAND-BINDING DOMAINS |
| 1DKG | CRYSTAL STRUCTURE OF THE NUCLEOTIDE EXCHANGE FACTOR GRPE BOUND TO THE ATPASE DOMAIN OF THE MOLECULAR CHAPERONE DNAK |
| 1DKH | CRYSTAL STRUCTURE OF THE HEMOPHORE HASA, PH 6.5 |
| 1DKI | CRYSTAL STRUCTURE OF THE ZYMOGEN FORM OF STREPTOCOCCAL PYROGENIC EXOTOXIN B ACTIVE SITE (C47S) MUTANT |
| 1DKJ | BOBWHITE QUAIL LYSOZYME |
| 1DKK | BOBWHITE QUAIL LYSOZYME WITH NITRATE |
| 1DKL | CRYSTAL STRUCTURE OF ESCHERICHIA COLI PHYTASE AT PH 4.5 (NO LIGAND BOUND) |
| 1DKM | CRYSTAL STRUCTURE OF ESCHERICHIA COLI PHYTASE AT PH 6.6 WITH HG2+ CATION ACTING AS AN INTERMOLECULAR BRIDGE |
| 1DKN | CRYSTAL STRUCTURE OF ESCHERICHIA COLI PHYTASE AT PH 5.0 WITH HG2+ CATION ACTING AS AN INTERMOLECULAR BRIDGE |
| 1DKO | CRYSTAL STRUCTURE OF TUNGSTATE COMPLEX OF ESCHERICHIA COLI PHYTASE AT PH 6.6 WITH TUNGSTATE BOUND AT THE ACTIVE SITE AND WITH HG2+ CATION ACTING AS AN INTERMOLECULAR BRIDGE |
| 1DKP | CRYSTAL STRUCTURE OF PHYTATE COMPLEX OF ESCHERICHIA COLI PHYTASE AT PH 6.6. PHYTATE IS BOUND WITH ITS 3-PHOSPHATE IN THE ACTIVE SITE. HG2+ CATION ACTS AS AN INTERMOLECULAR BRIDGE |
| 1DKQ | CRYSTAL STRUCTURE OF PHYTATE COMPLEX ESCHERICHIA COLI PHYTASE AT PH 5.0. PHYTATE IS BOUND WITH ITS 3-PHOSPHATE IN THE ACTIVE SITE. HG2+ CATION ACTS AS AN INTERMOLECULAR BRIDGE |
| 1DKR | CRYSTAL STRUCTURES OF BACILLUS SUBTILIS PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE: MOLECULAR BASIS OF ALLOSTERIC INHIBITION AND ACTIVATION. |
| 1DKS | CKSHS1: HUMAN CYCLIN DEPENDENT KINASE SUBUNIT, TYPE 1 IN COMPLEX WITH PHOSPHATE |
| 1DKT | CKSHS1: HUMAN CYCLIN DEPENDENT KINASE SUBUNIT, TYPE 1 COMPLEX WITH METAVANADATE |
| 1DKU | CRYSTAL STRUCTURES OF BACILLUS SUBTILIS PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE: MOLECULAR BASIS OF ALLOSTERIC INHIBITION AND ACTIVATION. |
| 1DKW | CRYSTAL STRUCTURE OF TRIOSE-PHOSPHATE ISOMERASE WITH MODIFIED SUBSTRATE BINDING SITE |
| 1DKX | THE SUBSTRATE BINDING DOMAIN OF DNAK IN COMPLEX WITH A SUBSTRATE PEPTIDE, DETERMINED FROM TYPE 1 SELENOMETHIONYL CRYSTALS |
| 1DKY | THE SUBSTRATE BINDING DOMAIN OF DNAK IN COMPLEX WITH A SUBSTRATE PEPTIDE, DETERMINED FROM TYPE 2 NATIVE CRYSTALS |
| 1DKZ | THE SUBSTRATE BINDING DOMAIN OF DNAK IN COMPLEX WITH A SUBSTRATE PEPTIDE, DETERMINED FROM TYPE 1 NATIVE CRYSTALS |
| 1DL0 | SOLUTION STRUCTURE OF THE INSECTICIDAL NEUROTOXIN J-ATRACOTOXIN-HV1C |
| 1DL2 | CRYSTAL STRUCTURE OF CLASS I ALPHA-1,2-MANNOSIDASE FROM SACCHAROMYCES CEREVISIAE AT 1.54 ANGSTROM RESOLUTION |
| 1DL3 | CRYSTAL STRUCTURE OF MUTUALLY GENERATED MONOMERS OF DIMERIC PHOSPHORIBOSYLANTRANILATE ISOMERASE FROM THERMOTOGA MARITIMA |
| 1DL5 | PROTEIN-L-ISOASPARTATE O-METHYLTRANSFERASE |
| 1DL6 | SOLUTION STRUCTURE OF HUMAN TFIIB N-TERMINAL DOMAIN |
| 1DL7 | THE STRUCTURAL BASIS OF REPERTOIRE SHIFT IN AN IMMUNE RESPONSE TO PHOSPHOCHOLINE |
| 1DLB | HELICAL INTERACTIONS IN THE HIV-1 GP41 CORE REVEALS STRUCTURAL BASIS FOR THE INHIBITORY ACTIVITY OF GP41 PEPTIDES |
| 1DLC | CRYSTAL STRUCTURE OF INSECTICIDAL DELTA-ENDOTOXIN FROM BACILLUS THURINGIENSIS AT 2.5 ANGSTROMS RESOLUTION |
| 1DLE | FACTOR B SERINE PROTEASE DOMAIN |
| 1DLF | HIGH RESOLUTION CRYSTAL STRUCTURE OF THE FV FRAGMENT FROM AN ANTI-DANSYL SWITCH VARIANT ANTIBODY IGG2A(S) CRYSTALLIZED AT PH 5.25 |
| 1DLG | CRYSTAL STRUCTURE OF THE C115S ENTEROBACTER CLOACAE MURA IN THE UN-LIGANDED STATE |
| 1DLH | CRYSTAL STRUCTURE OF THE HUMAN CLASS II MHC PROTEIN HLA-DR1 COMPLEXED WITH AN INFLUENZA VIRUS PEPTIDE |
| 1DLI | THE FIRST STRUCTURE OF UDP-GLUCOSE DEHYDROGENASE (UDPGDH) REVEALS THE CATALYTIC RESIDUES NECESSARY FOR THE TWO-FOLD OXIDATION |
| 1DLJ | THE FIRST STRUCTURE OF UDP-GLUCOSE DEHYDROGENASE (UDPGDH) REVEALS THE CATALYTIC RESIDUES NECESSARY FOR THE TWO-FOLD OXIDATION |
| 1DLK | CRYSTAL STRUCTURE ANALYSIS OF DELTA-CHYMOTRYPSIN BOUND TO A PEPTIDYL CHLOROMETHYL KETONE INHIBITOR |
| 1DLL | THE HC FRAGEMENT OF TETANUS TOXIN COMPLEXED WITH LACTOSE |
| 1DLM | STRUCTURE OF CATECHOL 1,2-DIOXYGENASE FROM ACINETOBACTER CALCOACETICUS NATIVE DATA |
| 1DLO | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 |
| 1DLP | STRUCTURAL CHARACTERIZATION OF THE NATIVE FETUIN-BINDING PROTEIN SCILLA CAMPANULATA AGGLUTININ (SCAFET): A NOVEL TWO-DOMAIN LECTIN |
| 1DLQ | STRUCTURE OF CATECHOL 1,2-DIOXYGENASE FROM ACINETOBACTER SP. ADP1 INHIBITED BY BOUND MERCURY |
| 1DLR | METHOTREXATE-RESISTANT VARIANTS OF HUMAN DIHYDROFOLATE REDUCTASE WITH SUBSTITUTION OF LEUCINE 22: KINETICS, CRYSTALLOGRAPHY AND POTENTIAL AS SELECTABLE MARKERS |
| 1DLS | METHOTREXATE-RESISTANT VARIANTS OF HUMAN DIHYDROFOLATE REDUCTASE WITH SUBSTITUTION OF LEUCINE 22: KINETICS, CRYSTALLOGRAPHY AND POTENTIAL AS SELECTABLE MARKERS |
| 1DLT | STRUCTURE OF CATECHOL 1,2-DIOXYGENASE FROM ACINETOBACTER SP. ADP1 WITH BOUND CATECHOL |
| 1DLU | UNLIGANDED BIOSYNTHETIC THIOLASE FROM ZOOGLOEA RAMIGERA |
| 1DLV | BIOSYNTHETIC THIOLASE FROM ZOOGLOEA RAMIGERA IN COMPLEX WITH COA |
| 1DLW | X-RAY CRYSTAL STRUCTURE OF TRUNCATED HEMOGLOBIN FROM P.CAUDATUM. |
| 1DLY | X-RAY CRYSTAL STRUCTURE OF HEMOGLOBIN FROM THE GREEN UNICELLULAR ALGA CHLAMYDOMONAS EUGAMETOS |
| 1DM0 | SHIGA TOXIN |
| 1DM1 | 2.0 A CRYSTAL STRUCTURE OF THE DOUBLE MUTANT H(E7)V, T(E10)R OF MYOGLOBIN FROM APLYSIA LIMACINA |
| 1DM2 | HUMAN CYCLIN-DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR HYMENIALDISINE |
| 1DM3 | ACETYLATED BIOSYNTHETIC THIOLASE FROM ZOOGLOEA RAMIGERA IN COMPLEX WITH ACETYL-COA |
| 1DM4 | SER195ALA MUTANT OF HUMAN THROMBIN COMPLEXED WITH FIBRINOPEPTIDE A (7-16) |
| 1DM5 | ANNEXIN XII E105K HOMOHEXAMER CRYSTAL STRUCTURE |
| 1DM6 | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N-(4-CHLOROPHENYL)-N'-HYDROXYGUANIDINE (H4B FREE) |
| 1DM7 | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH HOMOARGININE (H4B FREE) |
| 1DM8 | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 1,2,4-TRIAZOLE-CARBOXAMIDINE (H4B BOUND) |
| 1DM9 | HEAT SHOCK PROTEIN 15 KD |
| 1DMA | DOMAIN III OF PSEUDOMONAS AERUGINOSA EXOTOXIN COMPLEXED WITH NICOTINAMIDE AND AMP |
| 1DMB | REFINED 1.8 ANGSTROMS STRUCTURE REVEALS THE MECHANISM OF BINDING OF A CYCLIC SUGAR, BETA-CYCLODEXTRIN, TO THE MALTODEXTRIN BINDING PROTEIN |
| 1DMC | THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF CALLINECTES SAPIDUS METALLOTHIONEIN-I DETERMINED BY HOMONUCLEAR AND HETERONUCLEAR MAGNETIC RESONANCE SPECTROSCOPY |
| 1DMD | THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF CALLINECTES SAPIDUS METALLOTHIONEIN-I DETERMINED BY HOMONUCLEAR AND HETERONUCLEAR MAGNETIC RESONANCE SPECTOSCOPY |
| 1DME | THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF CALLINECTES SAPIDUS METALLOTHIONEIN-I DETERMINED BY HOMONUCLEAR AND HETERONUCLEAR MAGNETIC RESONANCE SPECTOSCOPY |
| 1DMF | THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF CALLINECTES SAPIDUS METALLOTHIONEIN-I DETERMINED BY HOMONUCLEAR AND HETERONUCLEAR MAGNETIC RESONANCE SPECTOSCOPY |
| 1DMG | CRYSTAL STRUCTURE OF RIBOSOMAL PROTEIN L4 |
| 1DMH | STRUCTURE OF CATECHOL 1,2-DIOXYGENASE FROM ACINETOBACTER SP. ADP1 WITH BOUND 4-METHYLCATECHOL |
| 1DMI | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6S-H4B |
| 1DMJ | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 5,6-CYCLIC-TETRAHYDROPTERIDINE |
| 1DMK | BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-AMINO-6-PHENYL-TETRAHYDROPTERIDINE |
| 1DML | CRYSTAL STRUCTURE OF HERPES SIMPLEX UL42 BOUND TO THE C-TERMINUS OF HSV POL |
| 1DMM | CRYSTAL STRUCTURES OF MUTANT ENZYMES Y57F OF KETOSTEROID ISOMERASE FROM PSEUDOMONAS PUTIDA BIOTYPE B |
| 1DMN | CRYSTAL STRUCTURE OF MUTANT ENZYME Y32F/Y57F OF KETOSTEROID ISOMERASE FROM PSEUDOMONAS PUTIDA BIOTYPE B |
| 1DMO | CALMODULIN, NMR, 30 STRUCTURES |
| 1DMP | STRUCTURE OF HIV-1 PROTEASE COMPLEX |
| 1DMQ | CRYSTAL STRUCTURE OF MUTANT ENZYME Y32F OF KETOSTEROID ISOMERASE FROM PSEUDOMONAS PUTIDA BIOTYPE B |
| 1DMR | OXIDIZED DMSO REDUCTASE FROM RHODOBACTER CAPSULATUS |
| 1DMS | STRUCTURE OF DMSO REDUCTASE |
| 1DMT | STRUCTURE OF HUMAN NEUTRAL ENDOPEPTIDASE COMPLEXED WITH PHOSPHORAMIDON |
| 1DMU | CRYSTAL STRUCTURE OF THE RESTRICTION ENDONUCLEASE BGLI (E.C.3.1.21.4) BOUND TO ITS DNA RECOGNITION SEQUENCE |
| 1DMW | CRYSTAL STRUCTURE OF DOUBLE TRUNCATED HUMAN PHENYLALANINE HYDROXYLASE WITH BOUND 7,8-DIHYDRO-L-BIOPTERIN |
| 1DMX | MURINE MITOCHONDRIAL CARBONIC ANYHDRASE V AT 2.45 ANGSTROMS RESOLUTION |
| 1DMY | COMPLEX BETWEEN MURINE MITOCHONDRIAL CARBONIC ANYHDRASE V AND THE TRANSITION STATE ANALOGUE ACETAZOLAMIDE |
| 1DMZ | A REFINED NMR STRUCTURE OF A NEW PHOPHOPEPTIDE-BINDING DOMAIN CONTAINING THE FHA2 OF RAD53 |
| 1DN0 | STRUCTURE OF THE FAB FRAGMENT FROM A HUMAN IGM COLD AGGLUTININ |
| 1DN2 | FC FRAGMENT OF HUMAN IGG1 IN COMPLEX WITH AN ENGINEERED 13 RESIDUE PEPTIDE DCAWHLGELVWCT-NH2 |
| 1DN3 | NMR STRUCTURE OF A MODEL HYDROPHILIC AMPHIPATHIC HELICAL BASIC PEPTIDE |
| 1DNA | D221(169)N MUTANT DOES NOT PROMOTE OPENING OF THE COFACTOR IMIDAZOLIDINE RING |
| 1DNC | HUMAN GLUTATHIONE REDUCTASE MODIFIED BY DIGLUTATHIONE-DINITROSO-IRON |
| 1DNG | NMR STRUCTURE OF A MODEL HYDROPHILIC AMPHIPATHIC HELICAL ACIDIC PEPTIDE |
| 1DNK | THE X-RAY STRUCTURE OF THE DNASE I-D(GGTATACC)2 COMPLEX AT 2.3 ANGSTROMS RESOLUTION |
| 1DNL | X-RAY STRUCTURE OF ESCHERICHIA COLI PYRIDOXINE 5'-PHOSPHATE OXIDASE COMPLEXED WITH FMN AT 1.8 ANGSTROM RESOLUTION |
| 1DNP | STRUCTURE OF DEOXYRIBODIPYRIMIDINE PHOTOLYASE |
| 1DNU | STRUCTURAL ANALYSES OF HUMAN MYELOPEROXIDASE-THIOCYANATE COMPLEX |
| 1DNV | PARVOVIRUS (DENSOVIRUS) FROM GALLERIA MELLONELLA |
| 1DNW | HUMAN MYELOPEROXIDASE-CYANIDE-THIOCYANATE COMPLEX |
| 1DNY | SOLUTION STRUCTURE OF PCP, A PROTOTYPE FOR THE PEPTIDYL CARRIER DOMAINS OF MODULAR PEPTIDE SYNTHETASES |
| 1DO0 | ORTHORHOMBIC CRYSTAL FORM OF HEAT SHOCK LOCUS U (HSLU) FROM ESCHERICHIA COLI |
| 1DO1 | CARBONMONOXY-MYOGLOBIN MUTANT L29W AT 105K |
| 1DO2 | TRIGONAL CRYSTAL FORM OF HEAT SHOCK LOCUS U (HSLU) FROM ESCHERICHIA COLI |
| 1DO3 | CARBONMONOXY-MYOGLOBIN (MUTANT L29W) AFTER PHOTOLYSIS AT T>180K |
| 1DO4 | CARBONMONOXY-MYOGLOBIN (MUTANT L29W) AFTER PHOTOLYSIS AT T<180K |
| 1DO5 | HUMAN COPPER CHAPERONE FOR SUPEROXIDE DISMUTASE DOMAIN II |
| 1DO6 | CRYSTAL STRUCTURE OF SUPEROXIDE REDUCTASE IN THE OXIDIZED STATE AT 2.0 ANGSTROM RESOLUTION |
| 1DO7 | CARBONMONOXY-MYOGLOBIN (MUTANT L29W) REBINDING STRUCTURE AFTER PHOTOLYSIS AT T< 180K |
| 1DO8 | CRYSTAL STRUCTURE OF A CLOSED FORM OF HUMAN MITOCHONDRIAL NAD(P)+-DEPENDENT MALIC ENZYME |
| 1DO9 | SOLUTION STRUCTURE OF OXIDIZED MICROSOMAL RABBIT CYTOCHROME B5. FACTORS DETERMINING THE HETEROGENEOUS BINDING OF THE HEME. |
| 1DOA | STRUCTURE OF THE RHO FAMILY GTP-BINDING PROTEIN CDC42 IN COMPLEX WITH THE MULTIFUNCTIONAL REGULATOR RHOGDI |
| 1DOB | THE MOBIL FLAVIN OF 4-OH BENZOATE HYDROXYLASE: MOTION OF A PROSTHETIC GROUP REGULATES CATALYSIS |
| 1DOC | THE MOBIL FLAVIN OF 4-OH BENZOATE HYDROXYLASE: MOTION OF A PROSTHETIC GROUP REGULATES CATALYSIS |
| 1DOD | THE MOBIL FLAVIN OF 4-OH BENZOATE HYDROXYLASE: MOTION OF A PROSTHETIC GROUP REGULATES CATALYSIS |
| 1DOE | THE MOBIL FLAVIN OF 4-OH BENZOATE HYDROXYLASE: MOTION OF A PROSTHETIC GROUP REGULATES CATALYSIS |
| 1DOF | THE CRYSTAL STRUCTURE OF ADENYLOSUCCINATE LYASE FROM PYROBACULUM AEROPHILUM: INSIGHTS INTO THERMAL STABILITY AND HUMAN PATHOLOGY |
| 1DOG | REFINED STRUCTURE FOR THE COMPLEX OF 1-DEOXYNOJIRIMYCIN WITH GLUCOAMYLASE FROM (ASPERGILLUS AWAMORI) VAR. X100 TO 2.4 ANGSTROMS RESOLUTION |
| 1DOH | STRUCTURE OF TRIHYDROXYNAPHTHALENE REDUCTASE IN COMPLEX WITH NADPH AND 4-NITRO-INDEN-1-ONE |
| 1DOI | 2FE-2S FERREDOXIN FROM HALOARCULA MARISMORTUI |
| 1DOJ | CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN*RWJ-51438 COMPLEX AT 1.7 A |