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7MRC

Crystal structure of the first bromodomain (BD1) of human BRDT bound to GXH-II-052

Summary for 7MRC
Entry DOI10.2210/pdb7mrc/pdb
DescriptorBromodomain testis-specific protein, 1,2-ETHANEDIOL, N,N'-{oxybis[(ethane-2,1-diyl)oxy(1-oxoethane-2,1-diyl)piperidine-1,4-diyl]}bis{4-[(4-{4-chloro-3-[(2-methylpropane-2-sulfonyl)amino]anilino}-5-methylpyrimidin-2-yl)amino]-2-fluorobenzamide}, ... (5 entities in total)
Functional Keywordsbrdt, brd, bet, gene regulation, contraceptive, cancer
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight28393.59
Authors
Chan, A.,Schonbrunn, E. (deposition date: 2021-05-07, release date: 2022-05-18, Last modification date: 2023-10-18)
Primary citationGuan, X.,Cheryala, N.,Karim, R.M.,Chan, A.,Berndt, N.,Qi, J.,Georg, G.I.,Schonbrunn, E.
Bivalent BET Bromodomain Inhibitors Confer Increased Potency and Selectivity for BRDT via Protein Conformational Plasticity.
J.Med.Chem., 65:10441-10458, 2022
Cited by
PubMed: 35867655
DOI: 10.1021/acs.jmedchem.2c00453
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.55 Å)
Structure validation

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