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Structure of glutathione S-TRANSFERASE(PP0183) from pseudomonas putida in complex with gsh

Analyse Structure of glutathione S-TRANSFERASE(PP0183) from pseudomonas putida in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3PR8
Type
protein
Length
871 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutathione S-transferase family protein
UniProt
Q88RE7
Ligands
GSH
Pockets
13 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 62% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, DGlutathione S-transferase family proteinprotein21862% helix, 8% strandQ88RE7
BGlutathione S-transferase family proteinprotein21761% helix, 8% strandQ88RE7

Ligands and binding sites

  • GSH · Glutathione · ligand · 4 copies · chains A, B, C, D
  • EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · chains B

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

Pockets

13 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18040.790.8282GSH
21000.760.9617empty
35700.640.7564GSH
4500.630.9419empty
53470.580.7644GSH

Interfaces

3 interfaces between chains.

  • C–D · 1709 Ų buried · 22 hydrogen bonds · protein-protein
  • B–C · 584 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 564 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 32 modified (engineered).

Compared structures

  • 3PR8 · Structure of Glutathione S-transferase(PP0183) from Pseudomonas putida in complex with GSH · the same entry in another collection · chain D against D, TM-score 1.00

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