PDB ID: 4F3I
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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0S6 | Methyl [(6s)-4-(4-chlorophenyl)-2,3,9-trimethyl-6h-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl]acetate | PoSSuM | |||
EDO | 1,2-ethanediol | PoSSuM |
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Download interaction data: 4F3I
Structure summary
Code : | 4F3I PDBj RCSB PDB PDBe | ||||||||||||
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Header : | SIGNALING PROTEIN/INHIBITOR | ||||||||||||
Title : | Crystal structure of the first bromodomain of human BRD4 in complex with MS417 inhibitor | ||||||||||||
Release Data : | 2012-09-12 | ||||||||||||
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Authors : | Joshua, J., Zhou, M.-M., Plotnikov, A.N. | ||||||||||||
Keywords : | protein-inhibitor complex, acetyl-lysine binding, nucleus, SIGNALING PROTEIN-INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.40 Å ) | ||||||||||||
Citation : |
Down-regulation of NF-{kappa}B Transcriptional Activity in HIV-associated Kidney Disease by BRD4 Inhibition.
Zhang, G.,Liu, R.,Zhong, Y.
et al.
PubMed: 22645123 |
Reaction
Chain : | A |
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UniProt : | O60885 (BRD4_HUMAN) |
Reaction : | - |