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MolNFT v1 · #116630 · protein

Structure of wt human glutathione transferase in complex with cisplatin in the presence of glutathione.

5DJL · Glutathione S-transferase P: “Structure of wt human glutathione transferase in complex with cisplatin in the presence of glutathione.”. X-ray diffraction, 5 ligands (GSH, PT, CA), 4 pockets (best druggability 0.72). MolNFT v1…

PDB
5DJL
Type
protein
Length
419 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutathione S-transferase P
EC
2.5.1.18
UniProt
P09211
Ligands
GSH, PT, CA, CO3, SO4
Pockets
4 · best druggability 0.72

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutathione S-transferase P (EC 2.5.1.18)protein21062% helix, 8% strandP09211
BGlutathione S-transferase P (EC 2.5.1.18)protein20961% helix, 9% strandP09211

Ligands and binding sites

  • GSH · Glutathione · ligand · 2 copies · chains A, B
  • PT · Platinum (II) ion · metal · 3 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains B
  • CO3 · Carbonate ion · ion · chains B
  • SO4 · Sulfate ion · ion · chains 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
16900.720.7988PT, GSH
21010.380.7518empty
3640.320.7514empty
4630.290.7419empty

Interfaces

1 interface between chains.

  • A–B · 1300 Ų buried · 20 hydrogen bonds · protein-protein

Compared structures

  • 5DJL · Structure of WT Human Glutathione Transferase in complex with cisplatin in the presence… · the same entry in another collection · chain A against A, TM-score 1.00

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