6DDJ: Human BRD2 BD2 bromodimain

Crystal Structure of the human BRD2 BD2 bromodimain in complex with a Tetrahydroquinoline analogue. Determined by X-ray diffraction at 1.05 Å resolution. Released 13 Nov 2019.

Method
X-ray diffraction
Resolution
1.05 Å
Organism
Homo sapiens
Chains
1
Atoms
1,157
Mol. weight
14.21 kDa
Ligands
G7V
Released
13 Nov 2019

Explore 6DDJ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6DDJ contains 9 α-helices and 0 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 9 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix346-36015
α-helix363-3653
α-helix366-3694
α-helix370-3723
α-helix378-3814
α-helix386-3894
α-helix396-4049
α-helix411-42818
α-helix434-45017

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Bromodomain-containing protein 2Aprotein115Homo sapiensP25440 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6DDJ_1 Bromodomain-containing protein 2 (chains A)
GSHMQDPEQLKHCNGILKELLSKKHAAYAWPFYKPVDASALGLHDYHDIIKHPMDLSTVK
RKMENRDYRDAQEFAADVRLMFSNCYKYNPPDHDVVAMARKLQDVFEFRYAKMPD

Ligands and cofactors

IDNameFormulaCopies
G7V4-{[(2S,4R)-1-acetyl-2-methyl-6-(1H-pyrazol-3-yl)-1,2,3,4-tetrahydroquinolin-4-…C22 H21 N5 O1

Water and common crystallization additives (EDO) are not listed.

Primary citation

Bromodomain-Selective BET Inhibitors Are Potent Antitumor Agents against MYC-Driven Pediatric Cancer. Slavish, P.J., Chi, L., Yun, M.K. et al. Cancer Res (2020) 80:3507-3518. DOI 10.1158/0008-5472.CAN-19-3934 · PubMed

Other PDB entries of the same protein (UniProt P25440 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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