5IGM: Bromodomain of human BRD9

Crystal structure of the bromodomain of human BRD9 in complex with bromosporine (BSP). Determined by X-ray diffraction at 1.6 Å resolution. Released 19 Oct 2016.

Method
X-ray diffraction
Resolution
1.6 Å
Organism
Homo sapiens
Chains
2
Atoms
1,997
Mol. weight
29.31 kDa
Ligands
BMF
Released
19 Oct 2016

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

Secondary structure: helices and β-sheets

5IGM 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-helix140-15314
α-helix164-1663
α-helix173-1764
α-helix183-1919
α-helix198-21518
α-helix221-23616
α-helix239-24810
Chain B: 7 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix140-15415
α-helix164-1663
α-helix173-1764
α-helix183-1919
α-helix198-21518
α-helix221-23616
α-helix239-2479

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Bromodomain-containing protein 9A, Bprotein123Homo sapiensQ9H8M2 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5IGM_1 Bromodomain-containing protein 9 (chains A, B)
SMLKLSAENESTPIQQLLEHFLRQLQRKDPHGFFAFPVTDAIAPGYSMIIKHPMDFGTMK
DKIVANEYKSVTEFKADFKLMCDNAMTYNRPDTVYYKLAKKILHAGFKMMSKERLLALKR
SMS

Ligands and cofactors

IDNameFormulaCopies
BMFBromosporineC17 H20 N6 O4 S2

Primary citation

Promiscuous targeting of bromodomains by bromosporine identifies BET proteins as master regulators of primary transcription response in leukemia. Picaud, S., Leonards, K., Lambert, J.P. et al. Sci Adv (2016) 2:e1600760-e1600760. DOI 10.1126/sciadv.1600760 · 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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