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PMID: 1248474 Published · ppublish English Journal Article

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

European journal of biochemistry ·Vol. 62 ·No. 1 ·1976-02-02 ·Pages 125-30

Easterbrook-Smith SB, Wallace JC, Keech DB

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...

MeSH Terms
Acetyl Coenzyme A/pharmacology Adenosine Triphosphate/pharmacology Affinity Labels Animals Binding Sites Kinetics Lysine/analysis Magnesium/pharmacology Mitochondria, Liver/enzymology Protein Binding Pyruvate Carboxylase/metabolism Sheep
Chemicals
Affinity Labels Acetyl Coenzyme A Adenosine Triphosphate Pyruvate Carboxylase Magnesium Lysine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Easterbrook-Smith S B
Wallace J C
Keech D B
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1976-02-02
Pages
125-30
Language
English
Region
England
NLM ID
0107600
Subset
IM
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