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Crystal structure of pcaf

Analyse Crystal structure of pcaf in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4NSQ
Type
protein
Length
628 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histone acetyltransferase KAT2B
EC
2.3.1.48
UniProt
Q92831
Ligands
COA
Pockets
6 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DHistone acetyltransferase KAT2B (EC 2.3.1.48)protein15734% helix, 31% strandQ92831

Ligands and binding sites

  • COA · Coenzyme A · ligand · 4 copies · chains A, B, C, D

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

Pockets

6 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111190.830.84116COA
22970.640.8034COA
32620.620.8035COA
41930.590.8131empty
51080.520.8219empty

Interfaces

4 interfaces between chains.

  • B–C · 697 Ų buried · 7 hydrogen bonds · protein-protein
  • A–D · 656 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 381 Ų buried · 0 hydrogen bonds · protein-protein
  • A–B · 356 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 4NSQ · Crystal structure of PCAF · 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 0.99

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