Brand  (β version)

  The number of atoms exceeds 100,000.
  So, it can not be displayed here.

Select unit:

Select hetatm:   

close
information
centroid:
interaction residue:

Select chain:   Sequence  

Data format:   

Color scheme of protein:

Ligands
Code Name Style Show Link
EDO 1,2-ethanediol
9U4 3-[7-(difluoromethyl)-6-(1-methyl-1h-pyrazol-4-yl)-3,4-dihydroquinolin-1(2h)-yl]-N-methyl-1-(oxan-4-yl)-1,4,6,7-tetrahydro-5h-pyrazolo[4,3-C]pyridine-5-carboxamide
Non-standard Residues
Code Name Show
Glycosylation
Code Name Emphasize
Modification
Code Name Show
Code : 5VZS   PDBj   RCSB PDB   PDBe
Header : TRANSCRIPTION REGULATOR/INHIBITOR
Title : BRD4-BD1 in complex with Cpd19 (3-(7-(difluoromethyl)-6-(1-methyl-1H-pyrazol-4-yl)-3,4-dihydroquinolin-1(2H)-yl)-N-methyl-1-(tetrahydro-2H-pyran-4-yl)-1,4,6,7-tetrahydro-5H-pyrazolo[4,3-C]pyridine-5-carboxamide)
Release Data : 2018-05-30
Compound :
mol_id molecule chains synonym
1 Bromodomain-containing protein 4 A,B Protein HUNK1
fragment: BRD4 Bromodomain-1, UNP residues 42-168
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: BRD4, HUNK1
Authors : Murray, J.M.
Keywords : BRD4, Bromodomain, small molecule inhibitor, TRANSCRIPTION REGULATOR-INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.7070 Å )
Citation :

GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of CBP/P300

Murray, J.M.
To be published 

Chain : A, B
UniProt : O60885 (BRD4_HUMAN)
Reaction : -