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5UF0

BRD4_BD2-A-35165

Summary for 5UF0
Entry DOI10.2210/pdb5uf0/pdb
Related5UEO 5UEP 5UEQ 5UER 5UES 5UET 5UEU 5UEV 5UEW 5UEX 5UEY 5UEZ
DescriptorBromodomain-containing protein 4, 2-methyl-5-(methylamino)-6-phenylpyridazin-3(2H)-one (3 entities in total)
Functional Keywordshelix bundle, signaling protein-inhibitor complex, signaling protein/inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationNucleus: O60885
Total number of polymer chains1
Total formula weight13022.18
Authors
Park, C.H. (deposition date: 2017-01-03, release date: 2017-06-28, Last modification date: 2024-03-06)
Primary citationWang, L.,Pratt, J.K.,Soltwedel, T.,Sheppard, G.S.,Fidanze, S.D.,Liu, D.,Hasvold, L.A.,Mantei, R.A.,Holms, J.H.,McClellan, W.J.,Wendt, M.D.,Wada, C.,Frey, R.,Hansen, T.M.,Hubbard, R.,Park, C.H.,Li, L.,Magoc, T.J.,Albert, D.H.,Lin, X.,Warder, S.E.,Kovar, P.,Huang, X.,Wilcox, D.,Wang, R.,Rajaraman, G.,Petros, A.M.,Hutchins, C.W.,Panchal, S.C.,Sun, C.,Elmore, S.W.,Shen, Y.,Kati, W.M.,McDaniel, K.F.
Fragment-Based, Structure-Enabled Discovery of Novel Pyridones and Pyridone Macrocycles as Potent Bromodomain and Extra-Terminal Domain (BET) Family Bromodomain Inhibitors.
J. Med. Chem., 60:3828-3850, 2017
Cited by
PubMed: 28368119
DOI: 10.1021/acs.jmedchem.7b00017
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.35 Å)
Structure validation

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