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Thioredoxin glutathione reductase from Schistosoma mansoni in complex with Indole-3-carbinol

Analyse Thioredoxin glutathione reductase from Schistosoma mansoni in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6ZLB
Type
protein
Length
587 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.9
Source
Schistosoma mansoni
Molecule
Thioredoxin glutathione reductase
EC
1.8.1.9
UniProt
G4V8J4
Ligands
FAD, FXK, K
Pockets
8 · best druggability 0.80

Structure

x-ray diffraction · resolution 1.9 · 1 distinct chain · 37% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThioredoxin glutathione reductase (EC 1.8.1.9)protein58737% helix, 25% strandG4V8J4

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · chains A
  • FXK · 1~{H}-indol-3-ylmethanol · ligand · chains A
  • K · Potassium ion · metal · 2 copies · chains A
  • DMS · Dimethyl sulfoxide · additive · chains A
  • PGE · Triethylene glycol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110160.800.81104FAD
21480.480.7821empty
3670.400.8022empty
4910.400.7716empty
5670.380.7816empty

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 6ZLB · Thioredoxin glutathione reductase from schistosoma mansoni in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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