Crystal Structure of Double Mutant M37L,P40S E.coli Thioredoxin. Determined by X-ray diffraction at 1.8 Å resolution. Released 13 Nov 2002.
Explore 1KEB in 3D Show helices and sheets RCSB PDB PDBe
1KEB contains 12 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 | 4-6 | 3 | 1 |
| α-helix | 12 | 1 | |
| α-helix | 13-17 | 5 | |
| β-strand | 22-28 | 7 | 1 |
| α-helix | 33-39 | 7 | |
| α-helix | 42-48 | 7 | |
| β-strand | 54-59 | 6 | 1 |
| α-helix | 67-70 | 4 | |
| β-strand | 77-82 | 6 | 1 |
| β-strand | 85-91 | 7 | 1 |
| α-helix | 96-106 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-6 | 3 | 2 |
| α-helix | 7 | 1 | |
| α-helix | 9-15 | 7 | |
| β-strand | 22-28 | 7 | 2 |
| α-helix | 33-39 | 7 | |
| α-helix | 42-48 | 7 | |
| β-strand | 54-59 | 6 | 2 |
| α-helix | 67-70 | 4 | |
| β-strand | 77-82 | 6 | 2 |
| β-strand | 85-91 | 7 | 2 |
| α-helix | 96-107 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Thioredoxin 1 | A, B | protein | 108 | Escherichia coli | P0AA25 (AlphaFold model) |
>1KEB_1 Thioredoxin 1 (chains A, B) SDKIIHLTDDSFDTDVLKADGAILVDFWAEWCGPCKLIASILDEIADEYQGKLTVAKLNI DQNPGTAPKYGIRGIPTLLLFKNGEVAATKVGALSKGQLKEFLDANLA
| ID | Name | Formula | Copies |
|---|---|---|---|
| CU | Copper (II) ion | Cu | 2 |
Structural Consequences of Replacement of an alpha-helical Pro Residue in E.coli Thioredoxin. Rudresh, Jain, R., Dani, V. et al. Protein Eng (2002) 15:627-633. DOI 10.1093/protein/15.8.627 · 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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