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MolNFT v1 · #125830 · protein

Crystal structure of the P300 acetyltransferase catalytic core with butyryl-coenzyme a.

5LKT · Histone acetyltransferase P300,HISTONE acetyltransferase…: “Crystal structure of the P300 acetyltransferase catalytic core with butyryl-coenzyme a.”. X-ray diffraction, 3 ligands (BCO, ZN, CL), 9 pockets (best druggability 0.73).…

PDB
5LKT
Type
protein
Length
551 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histone acetyltransferase P300,HISTONE acetyltransferase P300
EC
2.3.1.48
UniProt
Q09472
Ligands
BCO, ZN, CL
Pockets
9 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistone acetyltransferase P300,HISTONE acetyltransferase P300 (EC 2.3.1.48)protein55140% helix, 18% strandQ09472

Ligands and binding sites

  • BCO · Butyryl Coenzyme A · ligand · chains A
  • ZN · Zinc ion · metal · 4 copies · chains A
  • CL · Chloride ion · ion · chains A
  • GOL · Glycerol · additive · 3 copies · chains A
  • DMS · Dimethyl sulfoxide · additive · chains A

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

Pockets

9 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13670.730.8439BCO, GOL
22440.620.8134DMS
32250.480.7537empty
41670.470.7633GOL
5940.470.8017empty

Compared structures

  • 5LKT · Crystal structure of the p300 acetyltransferase catalytic core with butyryl-coenzyme A. · the same entry in another collection · chain A against A, TM-score 1.00
  • Q09472 · AlphaFold monomer V2.0 prediction for histone acetyltransferase P300 (Q09472) · a predicted model of the same protein · chain A against A, TM-score 0.98

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