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Crystal structure of thiol peroxidase from mycobacterium tuberculosis

Analyse Crystal structure of thiol peroxidase from mycobacterium tuberculosis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1XVQ
Type
protein
Length
160 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thiol peroxidase
EC
1.11.1.-
UniProt
P66952
Ligands
YT3, NH4
Pockets
2 · best druggability 0.42

Structure

x-ray diffraction · 1 distinct chain · 21% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThiol peroxidase (EC 1.11.1.-)protein16021% helix, 26% strandP66952

Ligands and binding sites

  • YT3 · Yttrium (III) ion · metal · 3 copies · chains A
  • NH4 · Ammonium ion · ion · 2 copies · chains A

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11370.420.7527empty
2650.400.8017empty

Modifications

Observed in the structure: 1 modified (oxidation).

Compared structures

  • 1XVQ · Crystal structure of thiol peroxidase from Mycobacterium tuberculosis · the same entry in another collection · chain A against A, TM-score 1.00

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