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Phosphotransacetylase from methanosarcina thermophila

Analyse Phosphotransacetylase from methanosarcina thermophila in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1QZT
Type
protein
Length
1,326 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phosphate acetyltransferase
EC
2.3.1.8
UniProt
P38503
Ligands
SO4
Pockets
12 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 47% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DPhosphate acetyltransferase (EC 2.3.1.8)protein33247% helix, 17% strandP38503
B, CPhosphate acetyltransferase (EC 2.3.1.8)protein33147% helix, 16% strandP38503

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 11 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15130.700.8051SO4
22310.660.8439SO4
34770.640.7745SO4
44380.640.7846SO4
52510.590.7928empty

Interfaces

2 interfaces between chains.

  • A–B · 1747 Ų buried · 7 hydrogen bonds · protein-protein
  • C–D · 1722 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 1QZT · Phosphotransacetylase from Methanosarcina thermophila · the same entry in another collection · chain A against A, TM-score 1.00
  • P38503 · AlphaFold monomer V2.0 prediction for phosphate acetyltransferase (P38503) · a predicted model of the same protein · chain B against A, TM-score 0.99

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