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Crystal structure of Glutathione transferase dmGSTD1 from Drosophila melanogaster, in complex with glutathione

Analyse Crystal structure of Glutathione transferase dmGSTD1 from Drosophila… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3MAK
Type
protein
Length
208 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.8
Source
Drosophila melanogaster
Molecule
Glutathione S-transferase 1-1
EC
2.5.1.18
UniProt
P20432
Ligands
GSH
Pockets
1 · best druggability 0.56

Structure

x-ray diffraction · resolution 1.8 · 1 distinct chain · 63% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlutathione S-transferase 1-1 (EC 2.5.1.18)protein20863% helix, 8% strandP20432

Ligands and binding sites

  • GSH · Glutathione · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12770.560.7636GSH

Compared structures

  • 3MAK · Crystal structure of glutathione transferase DMGSTD1 from drosophila melanogaster, in… · the same entry in another collection · chain A against A, TM-score 1.00
  • P20432 · AlphaFold monomer V2.0 prediction for glutathione S-transferase D1 (P20432) · a predicted model of the same protein · chain A against A, TM-score 0.99

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