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6BL1

Novel Modes of Inhibition of Wild-Type IDH1: Direct Covalent Modification of His315 with Cmpd13

6BL1 の概要
エントリーDOI10.2210/pdb6bl1/pdb
分子名称Isocitrate dehydrogenase [NADP] cytoplasmic, ISOCITRIC ACID, (6aS,7S,9S,10aS)-7-methyl-8-oxo-10a-phenyl-2-(phenylamino)-5,6,6a,7,8,9,10,10a-octahydrobenzo[h]quinazoline-9-carbonitrile, ... (5 entities in total)
機能のキーワードdehydrogenase, inhibitor, oxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数3
化学式量合計146386.28
構造登録者
Jakob, C.G.,Qiu, W. (登録日: 2017-11-09, 公開日: 2018-07-25, 最終更新日: 2023-10-04)
主引用文献Jakob, C.G.,Upadhyay, A.K.,Donner, P.L.,Nicholl, E.,Addo, S.N.,Qiu, W.,Ling, C.,Gopalakrishnan, S.M.,Torrent, M.,Cepa, S.P.,Shanley, J.,Shoemaker, A.R.,Sun, C.C.,Vasudevan, A.,Woller, K.R.,Shotwell, J.B.,Shaw, B.,Bian, Z.,Hutti, J.E.
Novel Modes of Inhibition of Wild-Type Isocitrate Dehydrogenase 1 (IDH1): Direct Covalent Modification of His315.
J. Med. Chem., 61:6647-6657, 2018
Cited by
PubMed: 30004704
DOI: 10.1021/acs.jmedchem.8b00305
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.02 Å)
構造検証レポート
Validation report summary of 6bl1
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-04-17に公開中

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