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PMID: 6309560 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The interaction of fructose 2,6-bisphosphate with an allosteric site of rat liver fructose 1,6-bisphosphatase.

FEBS letters ·Vol. 160 ·No. 1-2 ·1983-08-22 ·Pages 105-9

Meek DW, Nimmo HG

Abstract

Rat liver fructose 1,6-bisphosphatase can be protected against partial inactivation by N-ethylmaleimide by low concentrations of fructose 2,6-bisphosphate or high concentrations of fructose 1,6-bisphosphate. The partially inactivated enzyme has a much reduced sensitivity to high substrate inhibition and has lost the sigmoid component of the inhibition by fructose 2,6-bisphosphate; this compound is a simple linear competitive inhibitor of the modified enzyme. The results suggest that fructose 2,6-bisphosphate can bind to the enzyme at two distinct sites, the catalytic site and an allosteric site. High levels of fructose 1,6-bisphosphate probably inhibit by binding to the allosteric site.

MeSH Terms
Allosteric Regulation Allosteric Site Animals Ethylmaleimide/pharmacology Fructose-Bisphosphatase/metabolism Fructosediphosphates/metabolism Hexosediphosphates/metabolism Kinetics Liver/enzymology Rats
Chemicals
Fructosediphosphates Hexosediphosphates fructose 2,6-diphosphate Fructose-Bisphosphatase Ethylmaleimide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Meek D W
Nimmo H G
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1983-08-22
Pages
105-9
Language
English
Region
England
NLM ID
0155157
Subset
IM
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