Brand  (β version)

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Ligands
Code Name Style Show Link
G7V 4-{[(2s,4r)-1-acetyl-2-methyl-6-(1h-pyrazol-3-yl)-1,2,3,4-tetrahydroquinolin-4-yl]amino}benzonitrile
SO4 Sulfate ion
EDO 1,2-ethanediol
03S Methanesulfonic acid
Non-standard Residues
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Glycosylation
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Code : 6DDI   PDBj   RCSB PDB   PDBe
Header : Transcription/Inhibitor
Title : Crystal Structure of the human BRD2 BD1 bromodomain in complex with a Tetrahydroquinoline analogue
Release Data : 2019-11-13
Compound :
mol_id molecule chains synonym
1 Bromodomain-containing protein 2 A,B,C O27.1.1,Really interesting new gene 3 protein
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:469008)
gene: BRD2, KIAA9001, RING3
expression_system_strain: BL21(DE3)
expression_system_vector_type: PLASMID
expression_system_plasmid: pET28a(+)
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.
(2020)  Cancer Res.  80 : 3507 - 3518

PubMed: 32651255
DOI: 10.1158/0008-5472.CAN-19-3934

Chain : A, B, C
UniProt : P25440 (BRD2_HUMAN)
Reaction : -