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Structure of WT Human Glutathione Transferase in complex with cisplatin in the absence of glutathione.

Analyse Structure of WT Human Glutathione Transferase in complex with cisplatin in the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5DJM
Type
protein
Length
396 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.9
Source
Homo sapiens
Molecule
Glutathione S-transferase P
EC
2.5.1.18
UniProt
P09211
Ligands
PT
Pockets
3 · best druggability 0.74

Structure

x-ray diffraction · resolution 1.9 · 2 distinct chains · 59% helix, 9% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutathione S-transferase P (EC 2.5.1.18)protein19959% helix, 9% strandP09211
BGlutathione S-transferase P (EC 2.5.1.18)protein19759% helix, 9% strandP09211

Ligands and binding sites

  • PT · Platinum (II) ion · metal · 3 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16200.740.8172PT
2930.380.7619empty
3520.290.7413empty

Interfaces

1 interface between chains.

  • A–B · 1298 Ų buried · 21 hydrogen bonds · protein-protein

Compared structures

  • 5DJM · Structure of wt human glutathione transferase in complex with cisplatin in the absence of… · 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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