5O38: Human Brd2(BD2) mutant in free form

Human Brd2(BD2) mutant in free form. Determined by X-ray diffraction at 1.2 Å resolution. Released 14 Feb 2018.

Method
X-ray diffraction
Resolution
1.2 Å
Organism
Homo sapiens
Chains
1
Atoms
1,259
Mol. weight
13.84 kDa
Ligands
9JB, DQW
Released
14 Feb 2018

Explore 5O38 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5O38 contains 10 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: 10 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix345-3473
α-helix348-36013
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 2Aprotein114Homo sapiensP25440 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5O38_1 Bromodomain-containing protein 2 (chains A)
SMGKLSEQLKHCNGILKELLSKKHAAYAWPFYKPVDASALGVHDYHDIIKHPMDLSTVKR
KMENRDYRDAQEFAADVRLMFSNCYKYNPPDHDVVAMARKLQDVFEFRYAKMPD

Ligands and cofactors

IDNameFormulaCopies
9JB3-[(2~{R})-2-oxidanylpropoxy]-2-[[(2~{R})-2-oxidanylpropoxy]methyl]-2-[[(2~{S})…C14 H30 O71
DQW(2~{S})-1-[(2~{S})-2-oxidanylpropoxy]propan-2-olC6 H14 O31

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

Primary citation

Optimization of a "bump-and-hole" approach to allele-selective BET bromodomain inhibition. Runcie, A.C., Zengerle, M., Chan, K.H. et al. Chem Sci (2018) 9:2452-2468. DOI 10.1039/c7sc02536j · PubMed

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

Browse structure collections

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