タイトル | Novel Fragment Inhibitors of PYCR1 from Docking-Guided X-ray Crystallography. |
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ジャーナル・号・ページ | J. Chem. Inf. Model., Vol. 64, Page 1704-1718, Year 2024 |
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掲載日 | 2023年7月2日 (構造データの登録日) |
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著者 | Meeks, K.R. / Ji, J. / Protopopov, M.V. / Tarkhanova, O.O. / Moroz, Y.S. / Tanner, J.J. |
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リンク | J. Chem. Inf. Model. / PubMed:38411104 |
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手法 | X線回折 |
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解像度 | 1.72 - 2.2 Å |
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構造データ | PDB-8tcu: Structure of PYCR1 complexed with 2-chloro-5-(2-oxoimidazolidin-1-yl)benzoic acid 手法: X-RAY DIFFRACTION / 解像度: 2 Å PDB-8tcv: Structure of PYCR1 complexed with 4-bromobenzene-1,3-dicarboxylic acid 手法: X-RAY DIFFRACTION / 解像度: 1.74 Å PDB-8tcw: Structure of PYCR1 complexed with 2-methyl-3-(2-oxoimidazolidin-1-yl)benzoic acid 手法: X-RAY DIFFRACTION / 解像度: 1.94 Å PDB-8tcx: Structure of PYCR1 complexed with 2,4-dioxo-1,2,3,4-tetrahydroquinazoline-6-carboxylic acid 手法: X-RAY DIFFRACTION / 解像度: 1.72 Å PDB-8tcy: Structure of PYCR1 complexed with 7-fluoro-2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid 手法: X-RAY DIFFRACTION / 解像度: 1.95 Å PDB-8tcz: Structure of PYCR1 complexed with 2-(pyridin-2-yl)cyclopropane-1-carboxylic acid 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å PDB-8td0: Structure of PYCR1 complexed with 5-oxo-7a-phenyl-hexahydropyrrolo[2,1-b][1,3]thiazole-3-carboxylic acid 手法: X-RAY DIFFRACTION / 解像度: 2.2 Å PDB-8td1: Structure of PYCR1 complexed with 3-(6-Oxa-9-azaspiro(4.5)decane-9-carbonyl)benzoic acid 手法: X-RAY DIFFRACTION / 解像度: 1.88 Å |
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化合物 | |
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由来 | - homo sapiens (ヒト)
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キーワード | OXIDOREDUCTASE / AMINO-ACID BIOSYNTHESIS / PROLINE BIOSYNTHESIS |
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