The TIM-barrel fold: a versatile framework for efficient enzymes

FEBS Lett. 2001 Mar 16;492(3):193-8. doi: 10.1016/s0014-5793(01)02236-0.

Abstract

Recent studies on triosephosphate isomerase (TIM)-barrel enzymes highlight the remarkable versatility of the TIM-barrel scaffold. At least 15 distinct enzyme families use this framework to generate the appropriate active site geometry, always at the C-terminal end of the eight parallel beta-strands of the barrel. Sequence and structure comparisons now suggest that many of the TIM-barrel enzymes are evolutionarily related. Common structural properties of TIM-barrel enzymes are discussed.

Publication types

  • Review

MeSH terms

  • Binding Sites
  • Escherichia coli / chemistry
  • Escherichia coli / enzymology
  • Evolution, Molecular
  • Models, Molecular
  • Protein Conformation
  • Triose-Phosphate Isomerase / chemistry*
  • Triose-Phosphate Isomerase / metabolism

Substances

  • Triose-Phosphate Isomerase