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5I29

TAF1(2) bound to a pyrrolopyridone compound

Summary for 5I29
Entry DOI10.2210/pdb5i29/pdb
Related5I1Q
DescriptorTranscription initiation factor TFIID subunit 1, N,N-dimethyl-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)benzamide, CALCIUM ION, ... (4 entities in total)
Functional Keywordstaf1(2), second bromodomain of taf1, inhibitor-bound, protein binding-inhibitor complex, protein binding/inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationNucleus : P21675
Total number of polymer chains1
Total formula weight16912.02
Authors
Tang, Y.,Poy, F.,Bellon, S.F. (deposition date: 2016-02-08, release date: 2016-06-08, Last modification date: 2023-09-27)
Primary citationCrawford, T.D.,Tsui, V.,Flynn, E.M.,Wang, S.,Taylor, A.M.,Cote, A.,Audia, J.E.,Beresini, M.H.,Burdick, D.J.,Cummings, R.,Dakin, L.A.,Duplessis, M.,Good, A.C.,Hewitt, M.C.,Huang, H.R.,Jayaram, H.,Kiefer, J.R.,Jiang, Y.,Murray, J.,Nasveschuk, C.G.,Pardo, E.,Poy, F.,Romero, F.A.,Tang, Y.,Wang, J.,Xu, Z.,Zawadzke, L.E.,Zhu, X.,Albrecht, B.K.,Magnuson, S.R.,Bellon, S.,Cochran, A.G.
Diving into the Water: Inducible Binding Conformations for BRD4, TAF1(2), BRD9, and CECR2 Bromodomains.
J.Med.Chem., 59:5391-5402, 2016
Cited by
PubMed: 27219867
DOI: 10.1021/acs.jmedchem.6b00264
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.21 Å)
Structure validation

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