Studies on the active site of yeast hexokinase. Specific phosphorylation of a serine residue induced by D-xylose and ATPMg

Eur J Biochem. 1976 May 17;65(1):41-7. doi: 10.1111/j.1432-1033.1976.tb10387.x.

Abstract

Yeast hexokinase A(ATP:D-hexose 6-phosphotransferase) is inactivated when incubated in the presence of xylose and ATPMg, or in the presence of D-lyxose in a reaction medium in which ATPMg is being continuously regenerated (phosphoenolpyruvate and pyruvate kinase). The inactivation is due to the phorphorylation of the protein. A linear relationship was observed between the inactivation and the incorporation of 32P from [gamma-32P] ATP. All hexokinase and ATPase activity of the enzyme is lost when one phosphoryl group is incorporated per enzyme subunit (molecular weight 51,000). The phosphoryl group is covalently bound by a ester linkage with a serine residue of the protein.

MeSH terms

  • Adenosine Triphosphate* / pharmacology
  • Binding Sites
  • Hexokinase / metabolism
  • Hydrogen-Ion Concentration
  • Kinetics
  • Magnesium / pharmacology
  • Protein Binding
  • Protein Conformation
  • Saccharomyces cerevisiae / enzymology*
  • Serine / analysis
  • Xylose / pharmacology*

Substances

  • Serine
  • Adenosine Triphosphate
  • Xylose
  • Hexokinase
  • Magnesium