8UN3
KRAS-G13D-GDP in complex with Cpd5 (1-((S)-10-(6-amino-4-methyl-3-(trifluoromethyl)pyridin-2-yl)-11-chloro-7-(((2S,4R)-4-fluoro-1-methylpyrrolidin-2-yl)methoxy)-3,4,13,13a-tetrahydropyrazino[2',1':3,4][1,4]oxazepino[5,6,7-de]quinazolin-2(1H)-yl)prop-2-en-1-one)
8UN3 の概要
エントリーDOI | 10.2210/pdb8un3/pdb |
分子名称 | GTPase KRas, 1-[(5M,8aS,13R)-5-[6-amino-4-methyl-3-(trifluoromethyl)pyridin-2-yl]-6-chloro-2-{[(2S,4R)-4-fluoro-1-methylpyrrolidin-2-yl]methoxy}-8a,9,11,12-tetrahydropyrazino[2',1':3,4][1,4]oxazepino[5,6,7-de]quinazolin-10(8H)-yl]prop-2-en-1-one, GUANOSINE-5'-DIPHOSPHATE, ... (7 entities in total) |
機能のキーワード | gtpase, kras, g13d, oncogenic, hydrolase, oncoprotein-inhibitor complex, oncoprotein/inhibitor |
由来する生物種 | Homo sapiens (human) |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 81330.42 |
構造登録者 | |
主引用文献 | Nilewski, C.,Labadie, S.,Wei, B.,Malhotra, S.,Do, S.,Gazzard, L.,Liu, L.,Shao, C.,Murray, J.,Izrayelit, Y.,Gustafson, A.,Endres, N.F.,Ma, F.,Ye, X.,Zou, J.,Evangelista, M. Structure-Based Design and Evaluation of Reversible KRAS G13D Inhibitors. Acs Med.Chem.Lett., 15:21-28, 2024 Cited by PubMed: 38229748DOI: 10.1021/acsmedchemlett.3c00478 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.07 Å) |
構造検証レポート
検証レポート(詳細版)をダウンロード