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4Z6I

Crystal structure of BRD9 bromodomain in complex with a substituted valerolactam quinolone ligand

Summary for 4Z6I
Entry DOI10.2210/pdb4z6i/pdb
DescriptorBromodomain-containing protein 9, tert-butyl [(2R,3S)-1-(1,4-dimethyl-2-oxo-1,2-dihydroquinolin-7-yl)-6-oxo-2-phenylpiperidin-3-yl]carbamate (3 entities in total)
Functional Keywordslysine-acetylated histone binding, chromatin regulator, transcription, bromodomain, structural genomics, structural genomics consortium, sgc
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight29422.63
Authors
Primary citationClark, P.G.,Vieira, L.C.,Tallant, C.,Fedorov, O.,Singleton, D.C.,Rogers, C.M.,Monteiro, O.P.,Bennett, J.M.,Baronio, R.,Muller, S.,Daniels, D.L.,Mendez, J.,Knapp, S.,Brennan, P.E.,Dixon, D.J.
LP99: Discovery and Synthesis of the First Selective BRD7/9 Bromodomain Inhibitor.
Angew.Chem.Int.Ed.Engl., 54:6217-6221, 2015
Cited by
PubMed: 25864491
DOI: 10.1002/anie.201501394
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.95 Å)
Structure validation

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