7WN5
Crystal Structure of the second bromodomain of human BRD2 in complex with the inhibitor Y13142
7WN5 の概要
エントリーDOI | 10.2210/pdb7wn5/pdb |
分子名称 | Isoform 4 of Bromodomain-containing protein 2, ~{N}-[4-[2,4-bis(fluoranyl)phenoxy]-3-[2-(1~{H}-imidazol-5-yl)-5-methyl-4-oxidanylidene-furo[3,2-c]pyridin-7-yl]phenyl]ethanesulfonamide, 1,2-ETHANEDIOL, ... (5 entities in total) |
機能のキーワード | brd2-bd2, bromodomain, inhibitor, protein binding |
由来する生物種 | Homo sapiens (human) |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 33364.90 |
構造登録者 | |
主引用文献 | Li, J.,Zhang, C.,Xu, H.,Wang, C.,Dong, R.,Shen, H.,Zhuang, X.,Chen, X.,Li, Q.,Lu, J.,Zhang, M.,Wu, X.,Loomes, K.M.,Zhou, Y.,Zhang, Y.,Liu, J.,Xu, Y. Structure-Based Discovery and Optimization of Furo[3,2- c ]pyridin-4(5 H )-one Derivatives as Potent and Second Bromodomain (BD2)-Selective Bromo and Extra Terminal Domain (BET) Inhibitors. J.Med.Chem., 65:5760-5799, 2022 Cited by PubMed: 35333526DOI: 10.1021/acs.jmedchem.2c00100 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.7 Å) |
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