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6P38

Crystal Structure Analysis of TAF1 Bromodomain

Summary for 6P38
Entry DOI10.2210/pdb6p38/pdb
DescriptorTranscription initiation factor TFIID subunit 1, 4-{[(3R)-4-cyclopentyl-1,3-dimethyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-6-yl]amino}-N-(1-methylpiperidin-4-yl)-3-[(propan-2-yl)oxy]benzamide (2 entities in total)
Functional Keywordskinase, bromodomain, inhibitor, transcription, transferase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight16417.51
Authors
Seo, H.-S.,Dhe-Paganon, S. (deposition date: 2019-05-23, release date: 2020-05-27, Last modification date: 2023-10-11)
Primary citationRemillard, D.,Buckley, D.L.,Seo, H.S.,Ferguson, F.M.,Dhe-Paganon, S.,Bradner, J.E.,Gray, N.S.
Dual Inhibition of TAF1 and BET Bromodomains from the BI-2536 Kinase Inhibitor Scaffold.
Acs Med.Chem.Lett., 10:1443-1449, 2019
Cited by
PubMed: 31620231
DOI: 10.1021/acsmedchemlett.9b00243
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.8 Å)
Structure validation

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