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Glutathione S-transferase complexed with sulfasalazine

Analyse Glutathione S-transferase complexed with sulfasalazine in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
13GS
Type
protein
Length
418 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutathione S-transferase
EC
2.5.1.18
UniProt
P09211
Ligands
GSH, SAS
Pockets
4 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 60% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutathione S-transferase (EC 2.5.1.18)protein21060% helix, 8% strandP09211
BGlutathione S-transferase (EC 2.5.1.18)protein20861% helix, 9% strandP09211

Ligands and binding sites

  • GSH · Glutathione · ligand · 2 copies · chains A, B
  • SAS · 2-hydroxy-(5-([4-(2-pyridinylamino)sulfonyl]phenyl) azo)benzoic acid · ligand · 2 copies · chains A, B
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 3 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16980.730.7992GSH, SAS
2860.360.7514empty
3850.360.7517empty
4610.290.7415MES

Interfaces

1 interface between chains.

  • A–B · 1262 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 13GS · Glutathione S-transferase complexed with sulfasalazine · the same entry in another collection · chain A against A, TM-score 1.00
  • P09211 · AlphaFold monomer V2.0 prediction for glutathione S-transferase P (P09211) · a predicted model of the same protein · chain B against A, TM-score 1.00

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