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Crystal structure of HGSTP1-1[V104] complexed with the gsh conjugate of (+)-anti-bpde

Analyse Crystal structure of HGSTP1-1[V104] complexed with the gsh conjugate of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PGT
Type
protein
Length
419 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein (glutathione S-transferase)
EC
2.5.1.18
UniProt
P09211
Ligands
GBX, SO4
Pockets
4 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 61% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein (glutathione S-transferase) (EC 2.5.1.18)protein21062% helix, 8% strandP09211
BProtein (glutathione S-transferase) (EC 2.5.1.18)protein20960% helix, 9% strandP09211

Ligands and binding sites

  • GBX · 2-amino-4-[1-(carboxymethyl-carbamoyl)-2-(9-hydroxy-7,8-dioxo-7,8,9,10-tetrahydro-benzo[def]chrysen-10-ylsulfanyl)-ethylcarbamoyl]-butyric acid · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 2 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
15990.720.8078GBX
2840.360.7516empty
3740.350.7512empty
4720.310.7416empty

Interfaces

1 interface between chains.

  • A–B · 1313 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (oxidation).

Compared structures

  • 4PGT · Crystal structure of HGSTP1-1[V104] complexed with the gsh conjugate of (+)-anti-bpde · the same entry in another collection · chain A against A, TM-score 1.00

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