PDB ID: 5O5F
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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9LT | 1-ethyl-~{N}-[(~{R})-(3-fluorophenyl)-(1-methylimidazol-2-yl)methyl]-2,3-bis(oxidanylidene)-4~{H}-quinoxaline-6-carboxamide | PoSSuM | |||
NO3 | Nitrate ion | PoSSuM |
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Download interaction data: 5O5F
Structure summary
Code : | 5O5F PDBj RCSB PDB PDBe | ||||||||||||
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Header : | DNA BINDING PROTEIN | ||||||||||||
Title : | Crystal structure of the human BRPF1 bromodomain in complex with BZ038 | ||||||||||||
Release Data : | 2018-06-13 | ||||||||||||
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Authors : | Zhu, J., Caflisch, A. | ||||||||||||
Keywords : | Bromodomain and PHD finger-containing protein 1(BRPF1), monocytic leukemia zinc-finger (MOZ), Inhibitor, transcription, DNA binding protein | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.302 Å ) | ||||||||||||
Citation : |
Structure-based discovery of selective BRPF1 bromodomain inhibitors.
Zhu, J.,Zhou, C.,Caflisch, A.
PubMed: 29902720 |
Reaction
Chain : | A |
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UniProt : | P55201 (BRPF1_HUMAN) |
Reaction : | - |