4HXO

Brd4 Bromodomain 1 complex with 3-{[(3-METHYL-1,2-OXAZOL-5-YL)METHYL]SULFANYL}[1,2,4]TRIAZOLO[4,3-A]PYRIDINE inhibitor

Summary for 4HXO

Entry DOI	10.2210/pdb4hxo/pdb
Related	4HXK 4HXL 4HXM 4HXN 4HXP 4HXR 4HXS
Descriptor	Bromodomain-containing protein 4, 3-{[(3-methyl-1,2-oxazol-5-yl)methyl]sulfanyl}[1,2,4]triazolo[4,3-a]pyridine (3 entities in total)
Functional Keywords	brd4, bromodomain, four alpha helices, protein binding-inhibitor complex, protein binding/inhibitor
Biological source	Homo sapiens (human)
Total number of polymer chains	1
Total formula weight	15129.48
Authors	Chen, T.T.,Cao, D.Y.,Chen, W.Y.,Xiong, B.,Shen, J.K.,Xu, Y.C. (deposition date: 2012-11-12, release date: 2013-04-03, Last modification date: 2024-02-28)
Primary citation	Zhao, L.,Cao, D.,Chen, T.,Wang, Y.,Miao, Z.,Xu, Y.,Chen, W.,Wang, X.,Li, Y.,Du, Z.,Xiong, B.,Li, J.,Xu, C.,Zhang, N.,He, J.,Shen, J. Fragment-Based Drug Discovery of 2-Thiazolidinones as Inhibitors of the Histone Reader BRD4 Bromodomain. J.Med.Chem., 56:3833-3851, 2013 Cited by PubMed: 23530754 DOI: 10.1021/jm301793a PDB entries with the same primary citation
Experimental method	X-RAY DIFFRACTION (1.76 Å)

Structure validation