A glycyl radical site in the crystal structure of a class III ribonucleotide reductase

Science. 1999 Mar 5;283(5407):1499-504. doi: 10.1126/science.283.5407.1499.

Abstract

Ribonucleotide reductases catalyze the reduction of ribonucleotides to deoxyribonucleotides. Three classes have been identified, all using free-radical chemistry but based on different cofactors. Classes I and II have been shown to be evolutionarily related, whereas the origin of anaerobic class III has remained elusive. The structure of a class III enzyme suggests a common origin for the three classes but shows differences in the active site that can be understood on the basis of the radical-initiation system and source of reductive electrons, as well as a unique protein glycyl radical site. A possible evolutionary relationship between early deoxyribonucleotide metabolism and primary anaerobic metabolism is suggested.

Publication types

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

MeSH terms

  • Acetyltransferases / chemistry
  • Acetyltransferases / metabolism
  • Amino Acid Sequence
  • Anaerobiosis
  • Binding Sites
  • Crystallography, X-Ray
  • Dimerization
  • Evolution, Molecular
  • Glycine / chemistry*
  • Hydrogen Bonding
  • Models, Molecular
  • Molecular Sequence Data
  • Mutation
  • Protein Conformation
  • Protein Folding
  • Protein Structure, Secondary
  • Ribonucleotide Reductases / chemistry*
  • Ribonucleotide Reductases / genetics
  • Ribonucleotide Reductases / metabolism
  • Viral Proteins / chemistry

Substances

  • Viral Proteins
  • Ribonucleotide Reductases
  • anaerobic ribonucleotide reductase
  • Acetyltransferases
  • formate C-acetyltransferase
  • Glycine

Associated data

  • PDB/1B8B