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Structure of the reduced form of human thioredoxin 2

Analyse Structure of the reduced form of human thioredoxin 2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1W89
Type
protein
Length
654 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thioredoxin
UniProt
Q99757
Pockets
3 · best druggability 0.67

Structure

x-ray diffraction · 4 distinct chains · 38% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, EThioredoxinprotein11039% helix, 25% strandQ99757
CThioredoxinprotein10738% helix, 26% strandQ99757
DThioredoxinprotein10937% helix, 26% strandQ99757
FThioredoxinprotein10837% helix, 26% strandQ99757

Pockets

3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15920.670.7763empty
25060.650.7763empty
3540.270.7314empty

Interfaces

9 interfaces between chains.

  • C–D · 515 Ų buried · 3 hydrogen bonds · protein-protein
  • E–F · 495 Ų buried · 4 hydrogen bonds · protein-protein
  • A–B · 479 Ų buried · 5 hydrogen bonds · protein-protein
  • A–F · 420 Ų buried · 7 hydrogen bonds · protein-protein
  • A–D · 412 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 1W89 · Structure of the reduced form of human thioredoxin 2 · the same entry in another collection · chain F against F, TM-score 1.00
  • Q99757 · AlphaFold monomer V2.0 prediction for thioredoxin, mitochondrial (Q99757) · a predicted model of the same protein · chain C against A, TM-score 0.99

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