4HUA: Thioredoxin-1

E. coli thioredoxin variant with (4R)-FluoroPro76 as single proline residue. Determined by X-ray diffraction at 1.1 Å resolution. Released 29 May 2013.

Method
X-ray diffraction
Resolution
1.1 Å
Organism
Escherichia coli
Chains
1
Atoms
1,058
Mol. weight
11.66 kDa
Ligands
CU
Released
29 May 2013

Explore 4HUA in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4HUA contains 5 α-helices and 5 β-strands across 1 chain. 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-strand4-741
α-helix121
α-helix13-175
β-strand22-2871
α-helix33-4816
β-strand54-5961
α-helix64-696
β-strand77-8261
β-strand85-9171
α-helix96-10510

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Thioredoxin-1Aprotein108Escherichia coliP0AA25 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>4HUA_1 Thioredoxin-1 (chains A)
SDKIIHLTDDSFDTDVLKADGAILVDFWAEWCGACKMIAAILDEIADEYQGKLTVAKLNI
DQNAGTAAKYGIRGIPTLLLFKNGEVAATKVGALSKGQLKEFLDANLA

Ligands and cofactors

IDNameFormulaCopies
CUCopper (II) ionCu1

Primary citation

(4R)- and (4S)-Fluoroproline in the Conserved cis-Prolyl Peptide Bond of the Thioredoxin Fold: Tertiary Structure Context Dictates Ring Puckering. Rubini, M., Scharer, M.A., Capitani, G. et al. Chembiochem (2013) 14:1053-1057. DOI 10.1002/cbic.201300178 · PubMed

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

Browse structure collections

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