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BRD3 second bromodomain in complex with histone H3 acetylation at K18

Analyse BRD3 second bromodomain in complex with histone H3 acetylation at K18 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5HJC
Type
protein
Length
119 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bromodomain-containing protein 3; Peptide of histone H3.1
UniProt
Q15059, P68431
Ligands
CL
Pockets
1 · best druggability 0.35

Structure

x-ray diffraction · 2 distinct chains · 61% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABromodomain-containing protein 3protein11065% helix, 0% strandQ15059
BPeptide of histone H3.1protein90% helix, 0% strandP68431

Ligands and binding sites

  • CL · Chloride ion · ion · 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, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1670.350.7713empty

Interfaces

1 interface between chains.

  • A–B · 508 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (acetylation).

Compared structures

  • 5HJC · BRD3 second bromodomain in complex with histone H3 acetylation at K18 · the same entry in another collection · chain A against A, TM-score 1.00
  • Q15059 · AlphaFold monomer V2.0 prediction for bromodomain-containing protein 3 (Q15059) · a predicted model of the same protein · chain A against A, TM-score 0.99

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