6S56

Crystal structure of human ATAD2 bromodomain in complex with N-(4-chloro-3-(N,N-dimethylsulfamoyl)phenyl)-2-(2,5-dioxo-3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphthalen]-1-yl)acetamide

6S56 の概要

• エントリーDOI: 10.2210/pdb6s56/pdb
• 分子名称: ATPase family AAA domain-containing protein 2, 1,2-ETHANEDIOL, SULFATE ION, ... (5 entities in total)
• 機能のキーワード: inhibitor, atad2, bromodomain, epigenetics, atpase family aaa domain-containing protein 2, transcription
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 16260.74

構造登録者

Chung, C. (登録日: 2019-06-30, 公開日: 2019-08-21, 最終更新日: 2024-05-15)

• 主引用文献: Bamborough, P.,Chung, C.W.,Demont, E.H.,Bridges, A.M.,Craggs, P.D.,Dixon, D.P.,Francis, P.,Furze, R.C.,Grandi, P.,Jones, E.J.,Karamshi, B.,Locke, K.,Lucas, S.C.C.,Michon, A.M.,Mitchell, D.J.,Pogany, P.,Prinjha, R.K.,Rau, C.,Roa, A.M.,Roberts, A.D.,Sheppard, R.J.,Watson, R.J.; A Qualified Success: Discovery of a New Series of ATAD2 Bromodomain Inhibitors with a Novel Binding Mode Using High-Throughput Screening and Hit Qualification.; J.Med.Chem., 62:7506-7525, 2019; PubMed: 31398032; DOI: 10.1021/acs.jmedchem.9b00673

実験手法

X-RAY DIFFRACTION (2.01 Å)