5EU1: BRD9

Crystal structure of BRD9 in complex with bi-7273. Determined by X-ray diffraction at 1.6 Å resolution. Released 9 Mar 2016.

Method
X-ray diffraction
Resolution
1.6 Å
Organism
Homo sapiens
Chains
2
Atoms
2,255
Mol. weight
29.21 kDa
Ligands
5SW
Released
9 Mar 2016

Explore 5EU1 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5EU1 contains 14 α-helices and 0 β-strands across 2 chains. 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: 7 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix24-3815
α-helix48-503
α-helix57-604
α-helix67-759
α-helix82-9918
α-helix105-12016
α-helix123-13210
Chain B: 7 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix24-3714
α-helix48-503
α-helix57-604
α-helix67-759
α-helix82-9918
α-helix105-12016
α-helix123-13210

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
BRD9A, Bprotein123Homo sapiensQ9H8M2 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5EU1_1 BRD9 (chains A, B)
SMLKLSAENESTPIQQLLEHFLRQLQRKDPHGFFAFPVTDAIAPGYSMIIKHPMDFGTMK
DKIVANEYKSVTEFKADFKLMCDNAMTYNRPDTVYYKLAKKILHAGFKMMSKERLLALKR
SMS

Ligands and cofactors

IDNameFormulaCopies
5SW4-[4-[(dimethylamino)methyl]-3,5-dimethoxy-phenyl]-2-methyl-2,7-naphthyridin-1-…C20 H23 N3 O32

Primary citation

Structure-Based Design of an in Vivo Active Selective BRD9 Inhibitor. Martin, L.J., Koegl, M., Bader, G. et al. J Med Chem (2016) 59:4462-4475. DOI 10.1021/acs.jmedchem.5b01865 · PubMed

Other PDB entries of the same protein (UniProt Q9H8M2 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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