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Pyrrolidone carboxyl peptidase from thermococcus litoralis

Analyse Pyrrolidone carboxyl peptidase from thermococcus litoralis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1A2Z
Type
protein
Length
880 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pyrrolidone carboxyl peptidase
EC
3.4.19.3
UniProt
O07883
Ligands
SO4
Pockets
9 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DPyrrolidone carboxyl peptidase (EC 3.4.19.3)protein22034% helix, 24% strandO07883

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 4 copies · chains A, B, C, D

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
110260.840.8582empty
29690.840.8588empty
31020.350.7419empty
4950.350.7422empty
5800.350.7514empty

Interfaces

6 interfaces between chains.

  • A–B · 1099 Ų buried · 14 hydrogen bonds · protein-protein
  • C–D · 1071 Ų buried · 19 hydrogen bonds · protein-protein
  • A–C · 926 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 921 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 348 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 1A2Z · Pyrrolidone carboxyl peptidase from thermococcus litoralis · the same entry in another collection · chain A against A, TM-score 1.00
  • O07883 · AlphaFold monomer V2.0 prediction for pyrrolidone-carboxylate peptidase (O07883) · a predicted model of the same protein · chain A against A, TM-score 0.97

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