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Crystal structure of glutathione transferase omega 3S from trametes versicolor in complex with 2,4-dihydroxybenzophenone

Analyse Crystal structure of glutathione transferase omega 3S from trametes versicolor… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6F66
Type
protein
Length
482 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutathione transferase
Ligands
CUT, GSH, CA
Pockets
4 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 54% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BGlutathione transferaseprotein24154% helix, 8% strand—

Ligands and binding sites

  • CUT · [2,4-bis(oxidanyl)phenyl]-phenyl-methanone · ligand · 2 copies · chains A, B
  • GSH · Glutathione · ligand · 2 copies · chains A, B
  • CA · Calcium ion · metal · chains B
  • GOL · Glycerol · additive · 2 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110260.840.8486CUT, GSH
21790.510.7820PEG
32020.510.7622PEG
4970.360.7525GOL

Interfaces

1 interface between chains.

  • A–B · 1047 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 6F66 · Crystal structure of glutathione transferase Omega 3S from Trametes versicolor in complex… · the same entry in another collection · chain A against A, TM-score 1.00

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