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7LAJ

Crystal structure of the first bromodomain (BD1) of human BRD2 bound to Ro3280

Summary for 7LAJ
Entry DOI10.2210/pdb7laj/pdb
DescriptorBromodomain-containing protein 2, 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-N-(1-methylpiperidin-4-yl)benzamide (3 entities in total)
Functional Keywordsbet, erk5, dual brd-kinase inhibitor, gene regulation
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight15015.48
Authors
Karim, M.R.,Bikowitz, M.,Chan, A.,Schonbrunn, E. (deposition date: 2021-01-06, release date: 2021-08-11, Last modification date: 2023-10-18)
Primary citationKarim, R.M.,Bikowitz, M.J.,Chan, A.,Zhu, J.Y.,Grassie, D.,Becker, A.,Berndt, N.,Gunawan, S.,Lawrence, N.J.,Schonbrunn, E.
Differential BET Bromodomain Inhibition by Dihydropteridinone and Pyrimidodiazepinone Kinase Inhibitors.
J.Med.Chem., 64:15772-15786, 2021
Cited by
PubMed: 34710325
DOI: 10.1021/acs.jmedchem.1c01096
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.854 Å)
Structure validation

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