PDB ID: 4E96
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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0NS | 2-methoxy-N-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)benzenesulfonamide | PoSSuM | |||
DMS | Dimethyl sulfoxide | PoSSuM | |||
EDO | 1,2-ethanediol | PoSSuM | |||
NA | Sodium ion | PoSSuM |
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Download interaction data: 4E96
Structure summary
Code : | 4E96 PDBj RCSB PDB PDBe | ||||||||||||
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Header : | PROTEIN BINDING/INHIBITOR | ||||||||||||
Title : | Crystal Structure of the first bromodomain of human BRD4 in complex with the inhibitor PFi-1 | ||||||||||||
Release Data : | 2012-04-18 | ||||||||||||
Compound : |
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Source : |
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Authors : | Filippakopoulos, P., Picaud, S., Felletar, I., Fedorov, O., von Delft, F., Arrowsmith, C.H., Edwards, A.M., Weigelt, J., Fish, P., Bunnage, M., Owen, D., Knapp, S., Cook, A., Structural Genomics Consortium (SGC) | ||||||||||||
Keywords : | BROMODOMAIN, CAP, HUNK1, MCAP, MITOTIC CHROMOSOME ASSOCIATED PROTEIN, JQ1, BETSOFF1, STRUCTURAL GENOMICS CONSORTIUM, SGC, CELL CYCLE, PROTEIN BINDING-INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.9200 Å ) | ||||||||||||
Citation : |
Identification of a chemical probe for bromo and extra C-terminal bromodomain inhibition through optimization of a fragment-derived hit.
Fish, P.V.,Filippakopoulos, P.,Bish, G.
et al.
PubMed: 23095041 |
Reaction
Chain : | A |
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UniProt : | O60885 (BRD4_HUMAN) |
Reaction : | - |