Nuclear magnetic resonance studies of recombinant Escherichia coli glutaredoxin. Sequence-specific assignments and secondary structure determination of the oxidized form

Eur J Biochem. 1991 Sep 1;200(2):369-77. doi: 10.1111/j.1432-1033.1991.tb16194.x.

Abstract

Escherichia coli glutaredoxin (85 amino acid residues, Mr = 9100), the glutathione-dependent hydrogen donor for ribonucleotide reductase, was purified from an inducible lambda PL, expression system both with a natural isotope content and with uniform 15N labelling. This material was used for obtaining sequence-specific 1H magnetic resonance assignments and the identification of regular secondary structures in the oxidized form of the protein, which contains the redox-active disulfide Cys11-Pro-Tyr-Cys14. Oxidized glutaredoxin contains a four-stranded beta-sheet, with the peripheral strand 32-37 arranged parallel to the strand 2-7, which further combines with the two additional strands 61-64 and 67-69 in an antiparallel fashion. The protein further contains three helices extending approximately from residues 13-28, 45-54 and 72-84.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics
  • Escherichia coli* / genetics
  • Glutaredoxins
  • Magnetic Resonance Spectroscopy
  • Molecular Sequence Data
  • Oxidation-Reduction
  • Oxidoreductases*
  • Protein Conformation
  • Proteins / chemistry*
  • Proteins / genetics

Substances

  • Bacterial Proteins
  • Glutaredoxins
  • Proteins
  • Oxidoreductases