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Crystal structure of glutathione S transferase from pseudomonas fluorescens

Analyse Crystal structure of glutathione S transferase from pseudomonas fluorescens in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3LXT
Type
protein
Length
823 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutathione S transferase
UniProt
Q4KDJ6
Ligands
CL
Pockets
9 · best druggability 0.86

Structure

x-ray diffraction · 4 distinct chains · 60% helix, 6% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutathione S transferaseprotein20460% helix, 7% strandQ4KDJ6
BGlutathione S transferaseprotein20360% helix, 6% strandQ4KDJ6
CGlutathione S transferaseprotein21159% helix, 7% strandQ4KDJ6
DGlutathione S transferaseprotein20560% helix, 6% strandQ4KDJ6

Ligands and binding sites

  • CL · Chloride ion · ion · 7 copies · chains A, B, C, D
  • GOL · Glycerol · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19430.860.8781CL
29300.860.8780CL
33050.700.8434empty
43080.700.8436empty
55330.690.7950empty

Interfaces

4 interfaces between chains.

  • B–C · 2129 Ų buried · 36 hydrogen bonds · protein-protein
  • A–D · 2110 Ų buried · 33 hydrogen bonds · protein-protein
  • B–D · 464 Ų buried · 8 hydrogen bonds · protein-protein
  • C–D · 38 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 3LXT · Crystal structure of Glutathione S Transferase from Pseudomonas fluorescens · the same entry in another collection · chain A against A, TM-score 1.00

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