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. 1976 Feb 2;62(1):125-30.
doi: 10.1111/j.1432-1033.1976.tb10105.x.

Pyruvate carboxylase: affinity labelling of the magnesium adenosine triphosphate binding site

Free article

Pyruvate carboxylase: affinity labelling of the magnesium adenosine triphosphate binding site

S B Easterbrook-Smith et al. Eur J Biochem. .
Free article

Abstract

The 2' , 3'-dialdehyde derivative of ATP (oATP) was prepared by periodate oxidation and on the following criteria was considered to be an effective affinity label. The magnesium complex of this derivative (Mg-oATP2) was shown to ba linear competitive inhibitor with respect to MgATP2-in both the acetyl-CoA-dependent and -independent activities of the enzyme but was a non-competitive inhibitor with respect to bicarbonate, and an uncompetitive inhibitor with respect to pyruvate. Mg-oATP was covalently bound to pyruvate carboxylase by reduction using sodium borohydride with concurrent irreversible inactivation of the enzyme...

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