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Biochem J ; 317 ( Pt 3): 797-801, 1996 Aug 01.
Article in English | MEDLINE | ID: mdl-8760365

ABSTRACT

Cytosolic 5'-nucleotidase preferentially catalysing the hydrolysis of IMP, GMP and their deoxy derivatives, and endowed with phosphotransferase activity, was purified from calf thymus and its reaction mechanism was studied. In the presence of [32P]IMP, ATP and MgCl2, a covalent enzyme-phosphate intermediate was trapped by mixing with an SDS solution. Heart or acid treatment of the enzyme before incubation with radiolabelled substrate prevented formation of the intermediate. Furthermore, on the basis of studies on the kinetic parameters of the enzyme as function of pH, and of experiments on thiol oxidation and photo-oxidation, we suggest the involvement of cysteine and histidine residue(s) in the reaction mechanism.


Subject(s)
5'-Nucleotidase/metabolism , Cytosol/enzymology , Phosphotransferases/metabolism , 5'-Nucleotidase/antagonists & inhibitors , Animals , Catalysis , Cattle , Hydrogen-Ion Concentration , Kinetics , Light , Phosphorus Radioisotopes , Phosphorylation , Phosphotransferases/antagonists & inhibitors , Sulfhydryl Compounds/pharmacology
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