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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1O5T
| Crystal structure of the aminoacylation catalytic fragment of human tryptophanyl-tRNA synthetase | 分子名称: | Tryptophanyl-tRNA synthetase | 著者 | Yu, Y, Liu, Y, Shen, N, Xu, X, Jia, J, Jin, Y, Arnold, E, Ding, J. | 登録日 | 2003-10-05 | 公開日 | 2004-07-06 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Crystal Structure of Human Tryptophanyl-tRNA Synthetase Catalytic Fragment J.BIOL.CHEM., 279, 2004
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1O5U
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1O5W
| The structure basis of specific recognitions for substrates and inhibitors of rat monoamine oxidase A | 分子名称: | Amine oxidase [flavin-containing] A, FLAVIN-ADENINE DINUCLEOTIDE, N-[3-(2,4-DICHLOROPHENOXY)PROPYL]-N-METHYL-N-PROP-2-YNYLAMINE | 著者 | Ma, J, Yoshimura, M, Yamashita, E, Nakagawa, A, Ito, A, Tsukihara, T. | 登録日 | 2003-10-06 | 公開日 | 2004-04-20 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | 主引用文献 | Structure of rat monoamine oxidase a and its specific recognitions for substrates and inhibitors. J.Mol.Biol., 338, 2004
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1O5X
| Plasmodium falciparum TIM complexed to 2-phosphoglycerate | 分子名称: | 2-PHOSPHOGLYCERIC ACID, 3-HYDROXYPYRUVIC ACID, PHOSPHITE ION, ... | 著者 | Parthasarathy, S, Eaazhisai, K, Balaram, H, Balaram, P, Murthy, M.R. | 登録日 | 2003-10-06 | 公開日 | 2004-01-13 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.1 Å) | 主引用文献 | Structure of Plasmodium falciparum Triose-phosphate Isomerase-2-Phosphoglycerate Complex at 1.1-A Resolution J.Biol.Chem., 278, 2003
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1O5Z
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1O60
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1O61
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1O62
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1O63
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1O64
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1O65
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1O66
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1O67
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1O68
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1O69
| Crystal structure of a PLP-dependent enzyme | 分子名称: | (2-AMINO-4-FORMYL-5-HYDROXY-6-METHYLPYRIDIN-3-YL)METHYL DIHYDROGEN PHOSPHATE, BETA-MERCAPTOETHANOL, aminotransferase | 著者 | Structural GenomiX | 登録日 | 2003-10-23 | 公開日 | 2003-11-11 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (1.84 Å) | 主引用文献 | Structural analysis of a set of proteins resulting from a bacterial genomics project Proteins, 60, 2005
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1O6A
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1O6B
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1O6C
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1O6D
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1O6E
| Epstein-Barr virus protease | 分子名称: | CAPSID PROTEIN P40, PHOSPHORYLISOPROPANE | 著者 | Buisson, M, Hernandez, J, Lascoux, D, Schoehn, G, Forest, E, Arlaud, G, Seigneurin, J, Ruigrok, R.W.H, Burmeister, W.P. | 登録日 | 2002-09-13 | 公開日 | 2002-11-14 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | The Crystal Structure of the Epstein-Barr Virus Protease Shows Rearrangement of the Processed C Terminus J.Mol.Biol., 324, 2002
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1O6F
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1O6G
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1O6H
| Squalene-Hopene Cyclase | 分子名称: | (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, N-(6-{[1-(4-BROMOPHENYL)ISOQUINOLIN-6-YL]OXY}HEXYL)-N-METHYLPROP-2-EN-1-AMINE, SQUALENE--HOPENE CYCLASE | 著者 | Lenhart, A, Reinert, D.J, Weihofen, W.A, Aebi, J.D, Dehmlow, H, Morand, O.H, Schulz, G.E. | 登録日 | 2002-10-03 | 公開日 | 2003-10-02 | 最終更新日 | 2024-05-08 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem., 46, 2003
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1O6I
| Chitinase B from Serratia marcescens complexed with the catalytic intermediate mimic cyclic dipeptide CI4. | 分子名称: | Chitinase, GLYCEROL, SULFATE ION, ... | 著者 | Houston, D.R, Eggleston, I, Synstad, B, Eijsink, V.G.H, van Aalten, D.M.F. | 登録日 | 2002-10-03 | 公開日 | 2003-03-30 | 最終更新日 | 2023-12-13 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | The cyclic dipeptide CI-4 [cyclo-(l-Arg-d-Pro)] inhibits family 18 chitinases by structural mimicry of a reaction intermediate. Biochem. J., 368, 2002
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