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.
Explore 3DYR in 3D Show helices and sheets RCSB PDB PDBe
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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 6-8 | 3 | 1 |
| α-helix | 13 | 1 | |
| α-helix | 14-18 | 5 | |
| β-strand | 24-29 | 6 | 1 |
| α-helix | 34-49 | 16 | |
| β-strand | 55-60 | 6 | 1 |
| α-helix | 67-70 | 4 | |
| β-strand | 78-83 | 6 | 1 |
| β-strand | 86-92 | 7 | 1 |
| α-helix | 97-109 | 13 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 5 | 1 | |
| β-strand | 6-7 | 2 | 2 |
| α-helix | 13 | 1 | |
| α-helix | 14-18 | 5 | |
| β-strand | 23-29 | 7 | 2 |
| α-helix | 34-49 | 16 | |
| β-strand | 54-60 | 7 | 2 |
| α-helix | 68-71 | 4 | |
| β-strand | 78-83 | 6 | 2 |
| β-strand | 86-92 | 7 | 2 |
| α-helix | 97-108 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Thioredoxin-1 | A, B | protein | 111 | Escherichia coli | P0AA25 (AlphaFold model) |
>3DYR_1 Thioredoxin-1 (chains A, B) GSDKIIHLTDDSFDTDVLKADGAILVDFWAEWCGPCKMIAPILDEIADEYQGKLTVAKLN IDQNPGTAPKYGIRGTPTLLLFKNGEVAATKVGALSKGQLKEFLDANLAAA
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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