7LAY
Crystal structure of the first bromodomain (BD1) of human BRD3 bound to SG3-179
Summary for 7LAY
Entry DOI | 10.2210/pdb7lay/pdb |
Descriptor | Bromodomain-containing protein 3, 4-[[4-[[3-(~{tert}-butylsulfonylamino)-4-chloranyl-phenyl]amino]-5-methyl-pyrimidin-2-yl]amino]-2-fluoranyl-~{N}-(1-methylpiperidin-4-yl)benzamide, 1,2-ETHANEDIOL, ... (5 entities in total) |
Functional Keywords | bet, erk5, dual brd-kinase inhibitor, gene regulation, gene regulation-inhibitor complex, gene regulation/inhibitor |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 2 |
Total formula weight | 30600.30 |
Authors | Karim, M.R.,Bikowitz, M.J.,Schonbrunn, E. (deposition date: 2021-01-07, release date: 2021-07-14, Last modification date: 2023-10-18) |
Primary citation | Karim, 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: 34710325DOI: 10.1021/acs.jmedchem.1c01096 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.45 Å) |
Structure validation
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