Isolation of 3-phosphohistidine from phosphorylated pyruvate, phosphate dikinase.

نویسندگان

  • A M Spronk
  • H Yoshida
  • H G Wood
چکیده

Pyruvate, phosphate dikinase (EC 2-7-9-1) catalyzes formation of phosphoenolpyruvate, AMP, and inorganic pyrophosphate from pyruvate, ATP, and orthophosphate. A pyrophosphoryl and phosphoryl form of the enzyme is involved in this transfer. The [32P]phosphoryl form of pyruvate, phosphate dikinase was prepared with enzyme isolated from Bacteroides symbiosus. The [32P]phosphoryl enzyme was found to have properties corresponding to a phosphoramidate linkage and this was confirmed by isolation of 3-[32P]phosphohistidine from alkaline hydrolysates of the enzyme. The histidyl residue is considered to be the pyrophosphoryl- and phosphoryl-carrier between the three substrate sites of this enzyme.

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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 73 12  شماره 

صفحات  -

تاریخ انتشار 1976