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Crystal structure of the bromodomain of human BRD9 bound to TP472

Analyse Crystal structure of the bromodomain of human BRD9 bound to TP472 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6V14
Type
protein
Length
102 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.7
Source
Homo sapiens
Molecule
Bromodomain-containing protein 9
UniProt
Q9H8M2
Ligands
QMG
Pockets
1 · best druggability 0.53

Structure

x-ray diffraction · resolution 1.7 · 1 distinct chain · 61% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABromodomain-containing protein 9protein10261% helix, 0% strandQ9H8M2

Ligands and binding sites

  • QMG · 3-(6-acetylpyrrolo[1,2-a]pyrimidin-8-yl)-N-cyclopropyl-4-methylbenzamide · ligand · chains A
  • EDO · 1,2-ethanediol · additive · chains A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1780.530.8518QMG

Compared structures

  • 6V14 · Crystal structure of the bromodomain of human BRD9 bound to TP472 · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9H8M2 · AlphaFold monomer V2.0 prediction for bromodomain-containing protein 9 (Q9H8M2) · a predicted model of the same protein · chain A against A, TM-score 0.99

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