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Puromycin N-acetyltransferase in complex with acetylated puromycin and CoA

Analyse Puromycin N-acetyltransferase in complex with acetylated puromycin and CoA in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7K0A
Type
protein
Length
392 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Puromycin N-acetyltransferase
EC
2.3.-.-
UniProt
P13249
Ligands
VQ1, COA, SO4
Pockets
4 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 53% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPuromycin N-acetyltransferase (EC 2.3.-.-)protein19653% helix, 20% strandP13249

Ligands and binding sites

  • VQ1 · N-Acetylpuromycin · ligand · 2 copies · chains A, B
  • COA · Coenzyme A · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 6 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 3 copies · chains B
  • PEG · Di(hydroxyethyl)ether · additive · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16540.790.8359VQ1, EDO, COA
26670.780.8359VQ1, COA
3710.350.7614SO4
4740.330.7518SO4

Interfaces

1 interface between chains.

  • A–B · 482 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 7K0A · Puromycin N-acetyltransferase in complex with acetylated puromycin and CoA · the same entry in another collection · chain A against A, TM-score 1.00
  • P13249 · AlphaFold monomer V2.0 prediction for puromycin N-acetyltransferase (P13249) · a predicted model of the same protein · chain A against A, TM-score 0.99

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