Thi20, a remarkable enzyme from Saccharomyces cerevisiae with dual thiamin biosynthetic and degradation activities

Bioorg Chem. 2005 Aug;33(4):338-44. doi: 10.1016/j.bioorg.2005.04.001.

Abstract

Saccharomyces cerevisiae Thi20 is a fusion protein with homology to Bacillus subtilis ThiD and TenA. The N-terminus of Thi20 has significant sequence homology to B. subtilis ThiD, while the C-terminus has homology to B. subtilis TenA. Incubation of Thi20 with thiamin reveals that it has thiaminase II activity, in addition, incubation of Thi20 with HMP (4-amino-2-methyl-5-hydroxymethylpyrimidine) and ATP reveals that it has HMP kinase and HMP-P (4-amino-2-methyl-5-hydroxymethylpyrimidine phosphate) kinase activity. This demonstrates that Thi20 is a trifunctional protein with thiamin biosynthetic and degradative activity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Catalysis
  • Chromatography, High Pressure Liquid
  • Hydrolases / chemistry
  • Hydrolases / metabolism*
  • Molecular Sequence Data
  • Phosphotransferases / metabolism
  • Pyrimidines / metabolism
  • Saccharomyces cerevisiae / enzymology*
  • Sequence Alignment
  • Thiamine / biosynthesis
  • Thiamine / metabolism*

Substances

  • Pyrimidines
  • Phosphotransferases
  • Hydrolases
  • thiaminase II
  • toxopyrimidine
  • Thiamine