1A4L
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1A4M
| ADA STRUCTURE COMPLEXED WITH PURINE RIBOSIDE AT PH 7.0 | 分子名称: | 6-HYDROXY-1,6-DIHYDRO PURINE NUCLEOSIDE, ADENOSINE DEAMINASE, ZINC ION | 著者 | Wang, Z, Quiocho, F.A. | 登録日 | 1998-01-31 | 公開日 | 1998-10-14 | 最終更新日 | 2024-05-22 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Complexes of adenosine deaminase with two potent inhibitors: X-ray structures in four independent molecules at pH of maximum activity. Biochemistry, 37, 1998
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1ADD
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1FKW
| MURINE ADENOSINE DEAMINASE (D295E) | 分子名称: | ADENOSINE DEAMINASE, PURINE RIBOSIDE, ZINC ION | 著者 | Wilson, D.K, Quiocho, F.A. | 登録日 | 1996-02-29 | 公開日 | 1996-08-01 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Probing the functional role of two conserved active site aspartates in mouse adenosine deaminase. Biochemistry, 35, 1996
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1FKX
| MURINE ADENOSINE DEAMINASE (D296A) | 分子名称: | 6-HYDROXY-1,6-DIHYDRO PURINE NUCLEOSIDE, ADENOSINE DEAMINASE, ZINC ION | 著者 | Wilson, D.K, Quiocho, F.A. | 登録日 | 1996-02-29 | 公開日 | 1996-08-01 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Probing the functional role of two conserved active site aspartates in mouse adenosine deaminase. Biochemistry, 35, 1996
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1KRM
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1NDV
| Crystal Structure of Adenosine Deaminase complexed with FR117016 | 分子名称: | Adenosine deaminase, N''-(4-(5-((1H-BENZIMIDAZOL-2-YLAMINO)METHYL)-2-THIENYL)-1,3-THIAZOL-2-YL)GUANIDINE, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2002-12-09 | 公開日 | 2003-12-09 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | A highly potent non-nucleoside adenosine deaminase inhibitor: efficient drug discovery by intentional lead hybridization J.Am.Chem.Soc., 126, 2004
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1NDW
| Crystal Structure of Adenosine Deaminase Complexed with FR221647 | 分子名称: | 1-((1R)-1-(HYDROXYMETHYL)-3-PHENYLPROPYL)-1H-IMIDAZOLE-4-CARBOXAMIDE, Adenosine Deaminase, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2002-12-09 | 公開日 | 2003-12-09 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | A highly potent non-nucleoside adenosine deaminase inhibitor: efficient drug discovery by intentional lead hybridization J.Am.Chem.Soc., 126, 2004
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1NDY
| Crystal Structure of Adenosine Deaminase Complexed with FR230513 | 分子名称: | 1-((1R)-1-(HYDROXYMETHYL)-3-(1-NAPHTHYL)PROPYL)-1H-IMIDAZOLE-4-CARBOXAMIDE, Adenosine Deaminase, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2002-12-09 | 公開日 | 2003-12-09 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | A highly potent non-nucleoside adenosine deaminase inhibitor: efficient drug discovery by intentional lead hybridization J.Am.Chem.Soc., 126, 2004
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1NDZ
| Crystal Structure of Adenosine Deaminase Complexed with FR235999 | 分子名称: | 1-((1R)-1-(HYDROXYMETHYL)-3-(6-((3-(1-METHYL-1H-BENZIMIDAZOL-2-YL)PROPANOYL)AMINO)-1H-INDOL-1-YL)PROPYL)-1H-IMIDAZOLE-4-CARBOXAMIDE, Adenosine Deaminase, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2002-12-09 | 公開日 | 2003-12-09 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | A highly potent non-nucleoside adenosine deaminase inhibitor: efficient drug discovery by intentional lead hybridization J.Am.Chem.Soc., 126, 2004
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1O5R
| Crystal structure of adenosine deaminase complexed with a potent inhibitor | 分子名称: | 1-[(1R)-3-(6-{[(BENZYLAMINO)CARBONYL]AMINO}-1H-INDOL-1-YL)-1-(HYDROXYMETHYL)PROPYL]-1H-IMIDAZOLE-4-CARBOXAMIDE, Adenosine deaminase, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2003-10-05 | 公開日 | 2004-09-21 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.35 Å) | 主引用文献 | Structure-based design, synthesis, and structure-activity relationship studies of novel non-nucleoside adenosine deaminase inhibitors J.Med.Chem., 47, 2004
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1QXL
| Crystal structure of Adenosine deaminase complexed with FR235380 | 分子名称: | 1-((1R)-1-(HYDROXYMETHYL)-3-{6-[(5-PHENYLPENTANOYL)AMINO]-1H-INDOL-1-YL}PROPYL)-1H-IMIDAZOLE-4-CARBOXAMIDE, Adenosine deaminase, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2003-09-08 | 公開日 | 2004-09-21 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Structure-based design, synthesis, and structure-activity relationship studies of novel non-nucleoside adenosine deaminase inhibitors J.Med.Chem., 47, 2004
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1UIO
| ADENOSINE DEAMINASE (HIS 238 ALA MUTANT) | 分子名称: | 6-HYDROXY-7,8-DIHYDRO PURINE NUCLEOSIDE, ADENOSINE DEAMINASE, ZINC ION | 著者 | Wilson, D.K, Quiocho, F.A. | 登録日 | 1996-08-30 | 公開日 | 1997-06-24 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Site-directed mutagenesis of histidine 238 in mouse adenosine deaminase: substitution of histidine 238 does not impede hydroxylate formation. Biochemistry, 35, 1996
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1UIP
| ADENOSINE DEAMINASE (HIS 238 GLU MUTANT) | 分子名称: | ADENOSINE DEAMINASE, PURINE RIBOSIDE, ZINC ION | 著者 | Wilson, D.K, Quiocho, F.A. | 登録日 | 1996-08-30 | 公開日 | 1997-06-24 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Site-directed mutagenesis of histidine 238 in mouse adenosine deaminase: substitution of histidine 238 does not impede hydroxylate formation. Biochemistry, 35, 1996
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1UML
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1V79
| Crystal structures of adenosine deaminase complexed with potent inhibitors | 分子名称: | 1-{(1R,2S)-1-[2-(2,3,-DICHLOROPHENYL)ETHYL]-2-HYDROXYPROPYL}-1H-IMIDAZOLE-4-CARBOXAMIDE, Adenosine deaminase, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2003-12-14 | 公開日 | 2004-12-21 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structure-based design and synthesis of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors J.Med.Chem., 47, 2004
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1V7A
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1VFL
| Adenosine deaminase | 分子名称: | Adenosine deaminase, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2004-04-16 | 公開日 | 2005-08-16 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Structural Basis of Compound Recognition by Adenosine Deaminase Biochemistry, 44, 2005
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1W1I
| Crystal structure of dipeptidyl peptidase IV (DPPIV or CD26) in complex with adenosine deaminase | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Weihofen, W.A, Liu, J, Reutter, W, Saenger, W, Fan, H. | 登録日 | 2004-06-22 | 公開日 | 2004-09-02 | 最終更新日 | 2023-12-13 | 実験手法 | X-RAY DIFFRACTION (3.03 Å) | 主引用文献 | Crystal structure of CD26/dipeptidyl-peptidase IV in complex with adenosine deaminase reveals a highly amphiphilic interface. J. Biol. Chem., 279, 2004
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1WXY
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1WXZ
| Crystal structure of adenosine deaminase ligated with a potent inhibitor | 分子名称: | 1-((1R,2S)-1-{2-[2-(4-CHLOROPHENYL)-1,3-BENZOXAZOL-7-YL]ETHYL}-2-HYDROXYPROPYL)-1H-IMIDAZOLE-4-CARBOXAMIDE, Adenosine deaminase, ZINC ION | 著者 | Kinoshita, T. | 登録日 | 2005-02-02 | 公開日 | 2005-08-16 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Rational design of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors: predicting enzyme conformational change and metabolism J.Med.Chem., 48, 2005
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2ADA
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2AMX
| Crystal structure of Plasmodium Yoelii Adenosine deaminase (PY02076) | 分子名称: | COBALT (II) ION, UNKNOWN ATOM OR ION, adenosine deaminase | 著者 | Dong, A, Vedadi, M, Wasney, G, Zhao, Y, Lew, J, Alam, Z, Melone, M, Koeieradzki, I, Edwards, A.M, Arrowsmith, C.H, Weigelt, J, Sundstrom, M, Bochkarev, A, Hui, R, Amani, M, Structural Genomics Consortium (SGC) | 登録日 | 2005-08-10 | 公開日 | 2005-09-20 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.02 Å) | 主引用文献 | Genome-scale protein expression and structural biology of Plasmodium falciparum and related Apicomplexan organisms. Mol.Biochem.Parasitol., 151, 2007
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2BGN
| HIV-1 Tat protein derived N-terminal nonapeptide Trp2-Tat(1-9) bound to the active site of Dipeptidyl peptidase IV (CD26) | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[beta-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Weihofen, W.A, Liu, J, Reutter, W, Saenger, W, Fan, H. | 登録日 | 2005-01-03 | 公開日 | 2005-01-27 | 最終更新日 | 2023-12-13 | 実験手法 | X-RAY DIFFRACTION (3.15 Å) | 主引用文献 | Crystal Structures of HIV-1 Tat-Derived Nonapeptides Tat-(1-9) and Trp2-Tat-(1-9) Bound to the Active Site of Dipeptidyl-Peptidase Iv (Cd26) J.Biol.Chem., 280, 2005
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2E1W
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