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Trypanosoma brucei trypanothione reductase with bound NADP.

Analyse Trypanosoma brucei trypanothione reductase with bound NADP. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2WOV
Type
protein
Length
1,953 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Trypanothione reductase
EC
1.8.1.12
UniProt
Q389T8
Ligands
NDP, FAD, NA
Pockets
16 · best druggability 0.86

Structure

x-ray diffraction · 3 distinct chains · 33% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CTrypanothione reductase (EC 1.8.1.12)protein49033% helix, 27% strandQ389T8
BTrypanothione reductase (EC 1.8.1.12)protein48632% helix, 28% strandQ389T8
DTrypanothione reductase (EC 1.8.1.12)protein48733% helix, 27% strandQ389T8

Ligands and binding sites

  • NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · 4 copies · chains A, B, C, D
  • FAD · Flavin-adenine dinucleotide · ligand · 4 copies · chains A, B, C, D
  • NA · Sodium ion · metal · 7 copies · chains A, B, C, D

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

Pockets

16 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18610.860.8878empty
211360.850.86101NA
39090.810.8398NDP, FAD
48400.800.8395NDP, FAD
58460.800.83102NDP, FAD

Interfaces

3 interfaces between chains.

  • A–B · 3473 Ų buried · 33 hydrogen bonds · protein-protein
  • C–D · 3472 Ų buried · 30 hydrogen bonds · protein-protein
  • B–C · 505 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 2WOV · Trypanosoma brucei trypanothione reductase with bound NADP. · the same entry in another collection · chain A against A, TM-score 1.00

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