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7WN5

Crystal Structure of the second bromodomain of human BRD2 in complex with the inhibitor Y13142

Summary for 7WN5
Entry DOI10.2210/pdb7wn5/pdb
DescriptorIsoform 4 of Bromodomain-containing protein 2, ~{N}-[4-[2,4-bis(fluoranyl)phenoxy]-3-[2-(1~{H}-imidazol-5-yl)-5-methyl-4-oxidanylidene-furo[3,2-c]pyridin-7-yl]phenyl]ethanesulfonamide, 1,2-ETHANEDIOL, ... (5 entities in total)
Functional Keywordsbrd2-bd2, bromodomain, inhibitor, protein binding
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight33364.90
Authors
Li, J.,Zhang, C.,Xu, H.,Zhuang, X.,Wu, X.,Zhang, Y.,Xu, Y. (deposition date: 2022-01-17, release date: 2022-08-10, Last modification date: 2023-11-29)
Primary citationLi, J.,Zhang, C.,Xu, H.,Wang, C.,Dong, R.,Shen, H.,Zhuang, X.,Chen, X.,Li, Q.,Lu, J.,Zhang, M.,Wu, X.,Loomes, K.M.,Zhou, Y.,Zhang, Y.,Liu, J.,Xu, Y.
Structure-Based Discovery and Optimization of Furo[3,2- c ]pyridin-4(5 H )-one Derivatives as Potent and Second Bromodomain (BD2)-Selective Bromo and Extra Terminal Domain (BET) Inhibitors.
J.Med.Chem., 65:5760-5799, 2022
Cited by
PubMed: 35333526
DOI: 10.1021/acs.jmedchem.2c00100
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.7 Å)
Structure validation

221051

数据于2024-06-12公开中

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