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Reduced thiol peroxidase (tpx) from yersinia pseudotuberculosis

Analyse Reduced thiol peroxidase (tpx) from yersinia pseudotuberculosis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2XPD
Type
protein
Length
1,002 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thiol peroxidase
EC
1.11.1.15
UniProt
Q66A71
Pockets
7 · best druggability 0.84

Structure

x-ray diffraction · 4 distinct chains · 24% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThiol peroxidase (EC 1.11.1.15)protein16623% helix, 31% strandQ66A71
B, D, EThiol peroxidase (EC 1.11.1.15)protein16725% helix, 31% strandQ66A71
CThiol peroxidase (EC 1.11.1.15)protein17024% helix, 31% strandQ66A71
FThiol peroxidase (EC 1.11.1.15)protein16521% helix, 32% strandQ66A71

Ligands and binding sites

  • DTU · (2R,3S)-1,4-dimercaptobutane-2,3-diol · additive · chains A, B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111120.840.85127DTU
211370.810.82116empty
31240.490.8023empty
41210.460.7816empty
5660.420.8116empty

Interfaces

10 interfaces between chains.

  • C–D · 775 Ų buried · 6 hydrogen bonds · protein-protein
  • A–B · 738 Ų buried · 4 hydrogen bonds · protein-protein
  • E–F · 736 Ų buried · 4 hydrogen bonds · protein-protein
  • B–F · 387 Ų buried · 7 hydrogen bonds · protein-protein
  • A–E · 373 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 2XPD · Reduced Thiol peroxidase (Tpx) from yersinia Pseudotuberculosis · the same entry in another collection · chain A against A, TM-score 1.00

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