3DYR: Thioredoxin-1

Crystal structure of E. coli thioredoxin mutant I76T in its oxidized form. Determined by X-ray diffraction at 2.0 Å resolution. Released 27 Jan 2009.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
Escherichia coli
Chains
2
Atoms
1,733
Mol. weight
23.75 kDa
Released
27 Jan 2009

Explore 3DYR in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3DYR contains 11 α-helices and 10 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 5 helices, 5 β-strands

ElementResiduesLengthSheet
β-strand6-831
α-helix131
α-helix14-185
β-strand24-2961
α-helix34-4916
β-strand55-6061
α-helix67-704
β-strand78-8361
β-strand86-9271
α-helix97-10913
Chain B: 6 helices, 5 β-strands
ElementResiduesLengthSheet
α-helix51
β-strand6-722
α-helix131
α-helix14-185
β-strand23-2972
α-helix34-4916
β-strand54-6072
α-helix68-714
β-strand78-8362
β-strand86-9272
α-helix97-10812

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Thioredoxin-1A, Bprotein111Escherichia coliP0AA25 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>3DYR_1 Thioredoxin-1 (chains A, B)
GSDKIIHLTDDSFDTDVLKADGAILVDFWAEWCGPCKMIAPILDEIADEYQGKLTVAKLN
IDQNPGTAPKYGIRGTPTLLLFKNGEVAATKVGALSKGQLKEFLDANLAAA

Primary citation

Properties of the thioredoxin fold superfamily are modulated by a single amino acid residue. Ren, G., Stephan, D., Xu, Z. et al. J Biol Chem (2009) 284:10150-10159. DOI 10.1074/jbc.M809509200 · PubMed

Other PDB entries of the same protein (UniProt P0AA25 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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