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Crystal structures of thioredoxin with mesna at 1.85A resolution

Analyse Crystal structures of thioredoxin with mesna at 1.85A resolution in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4POM
Type
protein
Length
428 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.85
Source
Homo sapiens
Molecule
Thioredoxin
UniProt
P10599
Ligands
COM
Pockets
4 · best druggability 0.68

Structure

x-ray diffraction · resolution 1.85 · 1 distinct chain · 40% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DThioredoxinprotein10740% helix, 28% strandP10599

Ligands and binding sites

  • COM · 1-thioethanesulfonic acid · ligand · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16700.680.7765empty
21090.430.7721empty
3700.370.7715empty
4520.290.7616empty

Interfaces

5 interfaces between chains.

  • C–D · 819 Ų buried · 13 hydrogen bonds · protein-protein
  • A–C · 429 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 428 Ų buried · 5 hydrogen bonds · protein-protein
  • A–D · 240 Ų buried · 4 hydrogen bonds · protein-protein
  • B–C · 232 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 2 covalent (disulfide, covalent ligand).

Compared structures

  • 4POM · Crystal structures of thioredoxin with mesna at 1.85A resolution · the same entry in another collection · chain A against A, TM-score 1.00
  • P10599 · AlphaFold monomer V2.0 prediction for thioredoxin (P10599) · a predicted model of the same protein · chain A against A, TM-score 0.97

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