A Glycyl Radical Site in the Crystal Structure of a Class III Ribonucleotide Reductase
Derek T. Logan, Jessica Andersson, Britt‐Marie Sjöberg, P. Nordlund
Abstract
Derek T. Logan, Jessica Andersson, Britt‐Marie Sjöberg, P. Nordlund
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.
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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.
Key concepts: Ribonucleotide reductase, Deoxyribonucleotides, Ribonucleotide, Cofactor, Chemistry, Enzyme, Stereochemistry, Active site