Kinetic studies on rat liver low M(r) phosphotyrosine protein phosphatases. The activation mechanism of the isoenzyme AcP2 by cGMP

Biochim Biophys Acta. 1995 Jan 18;1243(1):129-35. doi: 10.1016/0304-4165(94)00055-3.

Abstract

The reaction mechanisms of p-nitrophenyl phosphate hydrolysis catalyzed by two rat liver isoenzymes of the low M(r) phosphotyrosine protein phosphatase (AcP1 and AcP2) were compared. Furthermore, the effect of some heterocyclic compounds on their activities were tested. Cyclic GMP and guanosine causes a particularly high activation of the isoenzyme AcP2, whereas its effect on AcP1 is very poor. A study on the mechanism of cyclic GMP activation was carried out. The results suggest that cyclic GMP activates the AcP2 isoenzyme by increasing the rate of the step that leads to the hydrolysis of the covalent enzyme-substrate phosphorylated complex formed during the catalytic process. The physiological significance of cyclic GMP activation of only one of the two isoenzymes (AcP2) remains uncertain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acid Phosphatase
  • Amino Acid Sequence
  • Animals
  • Cyclic GMP / pharmacology*
  • Enzyme Activation / drug effects
  • Glycerol / metabolism
  • Isoenzymes / drug effects
  • Isoenzymes / metabolism*
  • Kinetics
  • Liver / enzymology
  • Methanol / metabolism
  • Models, Chemical
  • Molecular Sequence Data
  • Nitrophenols / metabolism
  • Organophosphorus Compounds / metabolism
  • Protein Tyrosine Phosphatases / drug effects
  • Protein Tyrosine Phosphatases / metabolism*
  • Proto-Oncogene Proteins*
  • Rats
  • Sequence Homology, Amino Acid

Substances

  • Isoenzymes
  • Nitrophenols
  • Organophosphorus Compounds
  • Proto-Oncogene Proteins
  • nitrophenylphosphate
  • Acid Phosphatase
  • Acp2 protein, rat
  • Acp1 protein, rat
  • Protein Tyrosine Phosphatases
  • Cyclic GMP
  • Glycerol
  • Methanol