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7LP0

Crystal structure of BPTF bromodomain in complex with inhibitor Pdy-3-077

Summary for 7LP0
Entry DOI10.2210/pdb7lp0/pdb
DescriptorNucleosome-remodeling factor subunit BPTF, 4-chlorol-2-methyl-5-[[(3~{R})-1-methylpiperidin-3-yl]amino]pyridazin-3-one, DIMETHYL SULFOXIDE, ... (5 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 weight29626.56
Authors
Chan, A.,Schonbrunn, E. (deposition date: 2021-02-11, 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 (1.66 Å)
Structure validation

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