PDB ID: 6HDQ
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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EDO | 1,2-ethanediol | PoSSuM | |||
FZE | 8-(((1r,2r,3r,5s)-2-(2-(4,4-difluorocyclohexyl)ethyl)-8-azabicyclo[3.2.1]octan-3-yl)amino)-3-methyl-5-(5-methylpyridin-3-yl)-1,7-naphthyridin-2(1h)-one | PoSSuM |
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Download interaction data: 6HDQ
Structure summary
Code : | 6HDQ PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSCRIPTION | ||||||||||||
Title : | N-TERMINAL BROMODOMAIN OF HUMAN BRD4 WITH : 8-(((1R,2R,3R,5S)-2-(2-(4,4-difluorocyclohexyl)ethyl)-8-azabicyclo[3.2.1]octan-3-yl)amino)-3-methyl-5-(5-methylpyridin-3-yl)-1,7-naphthyridin-2(1H)-one | ||||||||||||
Release Data : | 2018-09-26 | ||||||||||||
Compound : |
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Source : |
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Authors : | Chung, C. | ||||||||||||
Keywords : | INHIBITOR, HISTONE, EPIGENETIC READER, BROMODOMAIN, BRD4, BROMODOMAIN CONTAINING PROTEIN 4, ANTAGONIST, TRANSCRIPTION | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.70 Å ) | ||||||||||||
Citation : |
Aiming to Miss a Moving Target: Bromo and Extra Terminal Domain (BET) Selectivity in Constrained ATAD2 Inhibitors.
Bamborough, P.,Chung, C.W.,Furze, R.C.
et al.
PubMed: 30226378 |
Reaction
Chain : | A |
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UniProt : | O60885 (BRD4_HUMAN) |
Reaction : | - |