1JP0
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1JQ9
| Crystal structure of a complex formed between phospholipase A2 from Daboia russelli pulchella and a designed pentapeptide Phe-Leu-Ser-Tyr-Lys at 1.8 resolution | 分子名称: | ACETIC ACID, Peptide inhibitor, Phospholipase A2 | 著者 | Chandra, V, Jasti, J, Kaur, P, Dey, S, Betzel, C, Singh, T.P. | 登録日 | 2001-08-04 | 公開日 | 2002-11-06 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Crystal Structure of a Complex Formed between a Snake Venom Phospholipase A2 and a Potent Peptide Inhibitor Phe-Leu-Ser-Tyr-Lys at 1.8 A Resolution J.BIOL.CHEM., 277, 2002
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1JQI
| Crystal Structure of Rat Short Chain Acyl-CoA Dehydrogenase Complexed With Acetoacetyl-CoA | 分子名称: | ACETOACETYL-COENZYME A, FLAVIN-ADENINE DINUCLEOTIDE, short chain acyl-CoA dehydrogenase | 著者 | Battaile, K.P, Molin-Case, J, Paschke, R, Wang, M, Bennett, D, Vockley, J, Kim, J.-J.P. | 登録日 | 2001-08-07 | 公開日 | 2002-02-13 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Crystal structure of rat short chain acyl-CoA dehydrogenase complexed with acetoacetyl-CoA: comparison with other acyl-CoA dehydrogenases. J.Biol.Chem., 277, 2002
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1JOA
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1YSL
| Crystal structure of HMG-CoA synthase from Enterococcus faecalis with AcetoAcetyl-CoA ligand. | 分子名称: | ACETOACETIC ACID, COENZYME A, GLYCEROL, ... | 著者 | Steussy, C.N, Vartia, A.A, Burgner II, J.W, Sutherlin, A, Rodwell, V.W, Stauffacher, C.V. | 登録日 | 2005-02-08 | 公開日 | 2005-11-08 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | X-ray Crystal Structures of HMG-CoA Synthase from Enterococcus faecalis and a Complex with Its Second Substrate/Inhibitor Acetoacetyl-CoA. Biochemistry, 44, 2005
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1YMU
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1JS3
| Crystal structure of dopa decarboxylase in complex with the inhibitor carbidopa | 分子名称: | CARBIDOPA, DOPA decarboxylase, PYRIDOXAL-5'-PHOSPHATE, ... | 著者 | Burkhard, P, Dominici, P, Borri-Voltattorni, C, Jansonius, J.N, Malashkevich, V.N. | 登録日 | 2001-08-16 | 公開日 | 2001-10-26 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Structural insight into Parkinson's disease treatment from drug-inhibited DOPA decarboxylase. Nat.Struct.Biol., 8, 2001
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1YTG
| SIV PROTEASE CRYSTALLIZED WITH PEPTIDE PRODUCT | 分子名称: | HIV PROTEASE, PEPTIDE PRODUCT | 著者 | Rose, R.B, Craik, C.S, Douglas, N.L, Stroud, R.M. | 登録日 | 1996-08-01 | 公開日 | 1997-03-12 | 最終更新日 | 2021-11-03 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Three-dimensional structures of HIV-1 and SIV protease product complexes. Biochemistry, 35, 1996
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1YBV
| STRUCTURE OF TRIHYDROXYNAPHTHALENE REDUCTASE IN COMPLEX WITH NADPH AND AN ACTIVE SITE INHIBITOR | 分子名称: | 5-METHYL-1,2,4-TRIAZOLO[3,4-B]BENZOTHIAZOLE, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, TRIHYDROXYNAPHTHALENE REDUCTASE | 著者 | Andersson, A, Schneider, G, Lindqvist, Y. | 登録日 | 1996-09-23 | 公開日 | 1997-10-15 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Crystal structure of the ternary complex of 1,3,8-trihydroxynaphthalene reductase from Magnaporthe grisea with NADPH and an active-site inhibitor. Structure, 4, 1996
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1JU2
| Crystal structure of the hydroxynitrile lyase from almond | 分子名称: | 2-acetamido-2-deoxy-alpha-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Dreveny, I, Gruber, K, Glieder, A, Thompson, A, Kratky, C. | 登録日 | 2001-08-23 | 公開日 | 2002-09-04 | 最終更新日 | 2020-07-29 | 実験手法 | X-RAY DIFFRACTION (1.47 Å) | 主引用文献 | The hydroxynitrile lyase from almond: a lyase that looks like an oxidoreductase. Structure, 9, 2001
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1YMV
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1YCP
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1YTJ
| SIV PROTEASE CRYSTALLIZED WITH PEPTIDE PRODUCT | 分子名称: | PEPTIDE PRODUCT, SIV PROTEASE | 著者 | Rose, R.B, Craik, C.S, Douglas, N.L, Stroud, R.M. | 登録日 | 1996-08-01 | 公開日 | 1997-03-12 | 最終更新日 | 2021-11-03 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Three-dimensional structures of HIV-1 and SIV protease product complexes. Biochemistry, 35, 1996
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1YJC
| SUBTILISIN BPN' 8397+1 (E.C. 3.4.21.14) (MUTANT WITH MET 50 REPLACED BY PHE, ASN 76 REPLACED BY ASP, GLY 169 REPLACED BY ALA, GLN 206 REPLACED BY CYS, ASN 218 REPLACED BY SER AND LYS 256 REPLACED BY TYR) (M50F, N76D, G169A, Q206C, N218S, AND K256Y) IN 50% DIMETHYLFORMAMIDE | 分子名称: | CALCIUM ION, SUBTILISIN 8397+1 | 著者 | Kidd, R.D, Farber, G.K. | 登録日 | 1996-01-16 | 公開日 | 1996-07-11 | 最終更新日 | 2021-11-03 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Breaking the low barrier hydrogen bond in a serine protease. Protein Sci., 8, 1999
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1YJA
| SUBTILISIN BPN' 8397+1 (E.C. 3.4.21.14) (MUTANT WITH MET 50 REPLACED BY PHE, ASN 76 REPLACED BY ASP, GLY 169 REPLACED BY ALA, GLN 206 REPLACED BY CYS, ASN 218 REPLACED BY SER AND LYS 256 REPLACED BY TYR) (M50F, N76D, G169A, Q206C, N218S, AND K256Y) IN 20% DIMETHYLFORMAMIDE | 分子名称: | CALCIUM ION, SUBTILISIN 8397+1 | 著者 | Kidd, R.D, Farber, G.K. | 登録日 | 1996-01-16 | 公開日 | 1996-07-11 | 最終更新日 | 2021-11-03 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Breaking the low barrier hydrogen bond in a serine protease. Protein Sci., 8, 1999
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1YPN
| REDUCED FORM HYDROXYMETHYLBILANE SYNTHASE (K59Q MUTANT) CRYSTAL STRUCTURE AFTER 2 HOURS IN A FLOW CELL DETERMINED BY TIME-RESOLVED LAUE DIFFRACTION | 分子名称: | 3-[5-{[3-(2-carboxyethyl)-4-(carboxymethyl)-5-methyl-1H-pyrrol-2-yl]methyl}-4-(carboxymethyl)-1H-pyrrol-3-yl]propanoic acid, HYDROXYMETHYLBILANE SYNTHASE | 著者 | Helliwell, J.R, Nieh, Y.P, Raftery, J, Cassetta, A, Habash, J, Carr, P.D, Ursby, T, Wulff, M, Thompson, A.W, Niemann, A.C, Haedener, A. | 登録日 | 1998-06-26 | 公開日 | 1999-03-02 | 最終更新日 | 2023-08-09 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Time-Resolved Structures of Hydroxymethylbilane Synthase (Lys59Gln Mutant) as It Isloaded with Substrate in the Crystal Determined by Laue Diffraction J.Chem.Soc.,Faraday Trans., 94, 1998
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1YTH
| SIV PROTEASE CRYSTALLIZED WITH PEPTIDE PRODUCT | 分子名称: | HIV PROTEASE, PEPTIDE PRODUCT | 著者 | Rose, R.B, Craik, C.S, Douglas, N.L, Stroud, R.M. | 登録日 | 1996-08-01 | 公開日 | 1997-03-12 | 最終更新日 | 2021-11-03 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Three-dimensional structures of HIV-1 and SIV protease product complexes. Biochemistry, 35, 1996
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1JVT
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1YFO
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1YAA
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1YER
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1YDV
| TRIOSEPHOSPHATE ISOMERASE (TIM) | 分子名称: | TRIOSEPHOSPHATE ISOMERASE | 著者 | Velankar, S.S, Murthy, M.R.N. | 登録日 | 1997-04-24 | 公開日 | 1997-10-15 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Triosephosphate isomerase from Plasmodium falciparum: the crystal structure provides insights into antimalarial drug design. Structure, 5, 1997
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1YPR
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1YST
| STRUCTURE OF THE PHOTOCHEMICAL REACTION CENTER OF A SPHEROIDENE CONTAINING PURPLE BACTERIUM, RHODOBACTER SPHAEROIDES Y, AT 3 ANGSTROMS RESOLUTION | 分子名称: | BACTERIOCHLOROPHYLL A, BACTERIOPHEOPHYTIN A, MANGANESE (II) ION, ... | 著者 | Arnoux, B, Gaucher, J.F, Ducruix, A, Reiss-Husson, F. | 登録日 | 1994-12-07 | 公開日 | 1995-02-27 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (3 Å) | 主引用文献 | Structure of the photochemical reaction centre of a spheroidene-containing purple-bacterium, Rhodobacter sphaeroides Y, at 3 A resolution. Acta Crystallogr.,Sect.D, 51, 1995
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1K1O
| BOVINE TRYPSIN-INHIBITOR COMPLEX | 分子名称: | CALCIUM ION, TRYPSIN, {[(1R)-2-((2S)-2-{[(3-{[AMINO(IMINO)METHYL]AMINO}PROPYL)AMINO]CARBONYL}PIPERIDINYL)-1-(CYCLOHEXYLMETHYL)-2-OXOETHYL]AMINO}ACETIC ACID | 著者 | Stubbs, M.T. | 登録日 | 2001-09-25 | 公開日 | 2001-11-28 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Factorising ligand affinity: a combined thermodynamic and crystallographic study of trypsin and thrombin inhibition. J.Mol.Biol., 313, 2001
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