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Crystal structure of human pcaf bromodomain in complex with fragment ZB1916 (fragment 10)

Analyse Crystal structure of human pcaf bromodomain in complex with fragment ZB1916… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5FE6
Type
protein
Length
219 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histone acetyltransferase KAT2B
EC
2.3.1.48
UniProt
Q92831
Ligands
5WZ
Pockets
3 · best druggability 0.68

Structure

x-ray diffraction · 2 distinct chains · 66% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistone acetyltransferase KAT2B (EC 2.3.1.48)protein10965% helix, 0% strandQ92831
BHistone acetyltransferase KAT2B (EC 2.3.1.48)protein11067% helix, 0% strandQ92831

Ligands and binding sites

  • 5WZ · (4-azanylpiperidin-1-yl)-cyclopropyl-methanone · ligand · chains A
  • EDO · 1,2-ethanediol · additive · 10 copies · chains A, B
  • DMS · Dimethyl sulfoxide · additive · chains B

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

Pockets

3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14780.680.7937EDO
21350.530.8122DMS
31160.530.8219EDO, 5WZ

Interfaces

1 interface between chains.

  • A–B · 841 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 5FE6 · Crystal structure of human PCAF bromodomain in complex with fragment ZB1916 (fragment 10) · the same entry in another collection · chain A against A, TM-score 1.00
  • Q92831 · AlphaFold monomer V2.0 prediction for histone acetyltransferase KAT2B (Q92831) · a predicted model of the same protein · chain A against A, TM-score 0.96

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