8D4Z

Crystal structure of USP7 in complex with allosteric inhibitor FX1-3763

8D4Z の概要

• エントリーDOI: 10.2210/pdb8d4z/pdb
• 分子名称: Ubiquitin carboxyl-terminal hydrolase 7, 1-({(7M)-7-[1-(azetidin-3-yl)-6-chloro-1,2,3,4-tetrahydroquinolin-8-yl]thieno[3,2-b]pyridin-2-yl}methyl)pyrrolidine-2,5-dione, GLYCEROL, ... (4 entities in total)
• 機能のキーワード: usp7, allosteric, inhibitor, hydrolase, hydrolase-inhibitor complex, hydrolase/inhibitor
• 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: 85129.03

構造登録者

Bell, J.A. (登録日: 2022-06-03, 公開日: 2023-09-20)

• 主引用文献: Futran, A.S.,Lu, T.,Amberg-Johnson, K.,Xu, J.,Yang, X.,He, S.,Boyce, S.,Bell, J.,Pelletier, R.,Suzuki, T.,Huang, X.,Qian, H.,Fang, L.,Xing, L.,Xu, Z.,Kurtz, S.E.,Tyner, J.W.,Tang, W.,Guo, T.,Akinsanya, K.,Madge, D.,Jensen, K.; Novel USP7 inhibitors demonstrate potent anti-cancer activity in models of AML, synergy with BCL2 inhibition, and a differentiated mechanism of action; To Be Published,

実験手法

X-RAY DIFFRACTION (2.26 Å)