Crystal structure of the first bromodomain (BD1) of human BRDT bound to GXH-II-082
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Crystal structure of the first bromodomain (BD1) of human BRDT bound to GXH-II-082 Descriptor: Bromodomain testis-specific protein, N,N'-[(1,16-dioxo-4,7,10,13-tetraoxahexadecane-1,16-diyl)di(piperidine-1,4-diyl)]bis{4-[(4-{4-chloro-3-[(2-methylpropane-2-sulfonyl)amino]anilino}-5-methylpyrimidin-2-yl)amino]-2-fluorobenzamide} Authors: Chan, A, Schonbrunn, E. Deposit date: 2021-05-07 Release date: 2022-05-18 Last modified: 2023-10-18 Method: X-RAY DIFFRACTION (1.39 Å) Cite: Bivalent BET Bromodomain Inhibitors Confer Increased Potency and Selectivity for BRDT via Protein Conformational Plasticity. J.Med.Chem., 65, 2022
人BRDT的首个溴结构域(bromodomain, BD1)与GXH-II-082结合的晶体结构
描述项:溴结构域睾丸特异性蛋白(BRDT),N,N'-[(1,16-二氧代-4,7,10,13-四氧杂十六烷-1,16-二基)二(哌啶-1,4-二基)]双{4-[(4-{4-氯-3-[(2-甲基丙烷-2-磺酰基)氨基]苯胺基}-5-甲基嘧啶-2-基)氨基]-2-氟苯甲酰胺}
作者:Chan, A、Schonbrunn, E.
沉积日期:2021-05-07
发布日期:2022-05-18
末次修改日期:2023-10-18
实验方法:X射线衍射(1.39 Å)
引用文献:《双价BET溴结构域抑制剂通过蛋白质构象可塑性增强对BRDT的效力与选择性》,J. Med. Chem., 65, 2022
创建时间:
2021-05-07



