PDB ID: 6DDI
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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G7V | 4-{[(2s,4r)-1-acetyl-2-methyl-6-(1h-pyrazol-3-yl)-1,2,3,4-tetrahydroquinolin-4-yl]amino}benzonitrile | PoSSuM | |||
SO4 | Sulfate ion | PoSSuM | |||
EDO | 1,2-ethanediol | PoSSuM | |||
03S | Methanesulfonic acid | PoSSuM |
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Download interaction data: 6DDI
Structure summary
Code : | 6DDI PDBj RCSB PDB PDBe | ||||||||||||
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Header : | Transcription/Inhibitor | ||||||||||||
Title : | Crystal Structure of the human BRD2 BD1 bromodomain in complex with a Tetrahydroquinoline analogue | ||||||||||||
Release Data : | 2019-11-13 | ||||||||||||
Compound : |
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Source : |
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Authors : | White, S.W., Yun, M. | ||||||||||||
Keywords : | BET, BRD2, bromodomain, Inhibitor, Complex, Transcription, Transcription-Inhibitor complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.50 Å ) | ||||||||||||
Citation : |
Bromodomain-Selective BET Inhibitors Are Potent Antitumor Agents against MYC-Driven Pediatric Cancer.
Slavish, P.J.,Chi, L.,Yun, M.K.
et al.
PubMed: 32651255 |
Reaction
Chain : | A, B, C |
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UniProt : | P25440 (BRD2_HUMAN) |
Reaction : | - |