Active sites of transition-metal enzymes with a focus on nickel

Curr Opin Struct Biol. 1998 Dec;8(6):749-58. doi: 10.1016/s0959-440x(98)80095-x.

Abstract

Since 1995, crystal structures have been determined for many transition-metal enzymes, in particular those containing the rarely used transition metals vanadium, molybdenum, tungsten, manganese, cobalt and nickel. Accordingly, our understanding of how an enzyme uses the unique properties of a specific transition metal has been substantially increased in the past few years. The different functions of nickel in catalysis are highlighted by describing the active sites of six nickel enzymes - methyl-coenyzme M reductase, urease, hydrogenase, superoxide dismutase, carbon monoxide dehydrogenase and acetyl-coenzyme A synthase.

Publication types

  • Review

MeSH terms

  • Binding Sites
  • Enzymes / chemistry
  • Enzymes / metabolism*
  • Models, Molecular
  • Nickel / chemistry*
  • Protein Conformation

Substances

  • Enzymes
  • Nickel