An equivalent metal ion in one- and two-metal-ion catalysis

Nat Struct Mol Biol. 2008 Nov;15(11):1228-31. doi: 10.1038/nsmb.1502. Epub 2008 Oct 26.

Abstract

Nucleotidyl-transfer enzymes, which synthesize, degrade and rearrange DNA and RNA, often depend on metal ions for catalysis. All DNA and RNA polymerases, MutH-like or RNase H-like nucleases and recombinases, and group I introns seem to require two divalent cations to form a complete active site. The two-metal-ion mechanism has been proposed to orient the substrate, facilitate acid-base catalysis and allow catalytic specificity to exceed substrate binding specificity attributable to the stringent metal-ion (Mg2+ in particular) coordination. Not all nucleotidyl-transfer enzymes use two metal ions for catalysis, however. The betabetaalpha-Me and HUH nucleases depend on a single metal ion in the active site for the catalysis. All of these one- and two metal ion-dependent enzymes generate 5'-phosphate and 3'-OH products. Structural and mechanistic comparisons show that these seemingly unrelated nucleotidyl-transferases share a functionally equivalent metal ion.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Catalysis
  • Catalytic Domain
  • Cations, Divalent / chemistry*
  • DNA Helicases / chemistry
  • DNA Helicases / metabolism
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / metabolism
  • Metals / chemistry*
  • Models, Molecular
  • Molecular Structure
  • Nucleotidyltransferases* / chemistry
  • Nucleotidyltransferases* / metabolism
  • Ribonuclease H / chemistry
  • Ribonuclease H / metabolism

Substances

  • Cations, Divalent
  • Escherichia coli Proteins
  • Metals
  • Nucleotidyltransferases
  • Ribonuclease H
  • TraI protein, E coli
  • DNA Helicases