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Crystallographic structure of the tau class glutathione S-transferase migstu in complex with S-hexyl-glutathione

Analyse Crystallographic structure of the tau class glutathione S-transferase migstu in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5KEJ
Type
protein
Length
444 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tau class glutathione S-transferase
EC
2.5.1.18
Ligands
GTX
Pockets
5 · best druggability 0.77

Structure

x-ray diffraction · 1 distinct chain · 55% helix, 9% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BTau class glutathione S-transferase (EC 2.5.1.18)protein22255% helix, 9% strand—

Ligands and binding sites

  • GTX · S-hexylglutathione · ligand · 2 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · 6 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111430.770.7992GTX, PEG
22340.560.7839PEG
31330.460.7719PEG
4740.400.7925PEG
5800.330.7521empty

Interfaces

1 interface between chains.

  • A–B · 1149 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 5KEJ · Crystallographic structure of the Tau class glutathione S-transferase MiGSTU in complex… · the same entry in another collection · chain A against A, TM-score 1.00

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