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7LPK

Crystal structure of BPTF bromodomain in complex with inhibitor HZ-03-112

Summary for 7LPK
Entry DOI10.2210/pdb7lpk/pdb
Related7LP0
DescriptorNucleosome-remodeling factor subunit BPTF, 4-chloranyl-2-methyl-5-[[(3~{R})-pyrrolidin-3-yl]amino]pyridazin-3-one, 1,2-ETHANEDIOL, ... (4 entities in total)
Functional Keywordsbptf, bromodomain, inhibitor, gene regulation, gene regulation-inhibitor complex, gene regulation/inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight30050.94
Authors
Chan, A.,Schonbrunn, E. (deposition date: 2021-02-12, release date: 2022-08-10, Last modification date: 2024-02-21)
Primary citationZahid, H.,Buchholz, C.R.,Singh, M.,Ciccone, M.F.,Chan, A.,Nithianantham, S.,Shi, K.,Aihara, H.,Fischer, M.,Schonbrunn, E.,Dos Santos, C.O.,Landry, J.W.,Pomerantz, W.C.K.
New Design Rules for Developing Potent Cell-Active Inhibitors of the Nucleosome Remodeling Factor (NURF) via BPTF Bromodomain Inhibition.
J.Med.Chem., 64:13902-13917, 2021
Cited by
PubMed: 34515477
DOI: 10.1021/acs.jmedchem.1c01294
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.39 Å)
Structure validation

221051

数据于2024-06-12公开中

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