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Short‐term control of glucokinase activity: role of a regulatory protein

Van Schaftingen, Emile, Detheux, Michel, Da Cunha, Maria Veiga·1994·The FASEB Journal

Abstract

Glucokinase is one of the four hexokinases present in mammalian tissues. It is expressed in two cell types that have to respond to changes in the blood glucose concentration, the liver parenchymal cell and the β‐cells of pancreatic islets. The former are responsible for the metabolism and storage of an important part of the ingested glucose, whereas the latter secrete insulin in response to an increase in the blood glucose level. One major characteristic of glucokinase is that it has a relatively low affinity for glucose and displays positive cooperativity for this substrate, despite the fact that it is a monometic enzyme. Furthermore, unlike other hexokinases, it is not inhibited by micromolar (physiological) concentrations of glucose 6‐phosphate but by a regulatory protein that transduces the effect of fructose 6‐phosphate and of fructose 1‐phosphate. The purpose of this review is to describe these aspects of the regulation of glucokinase.— Van Schaftingen, E., Detheux, M., Veiga da Cunha, M. Short‐term control of glucokinase activity; role of a regulatory protein. FASEB J. 8: 414‐419; 1994.

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Metadata

Authors
Van Schaftingen, E., Detheux, M., & Da Cunha, M. V.
Venue
The FASEB Journal
Publisher
Wiley
Published
1994-04
Volume
8
Issue
6
Pages
414-419
ISSN
  • 0892-6638 (ISSN-L)
  • 1530-6860
OpenAlex
W2103845188
Cited by
232
References
0
FWCI
8.23
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Short‐term control of glucokinase activity: role of a regulatory protein. https://app.cochat.ai/papers/10.1096/fasebj.8.6.8168691
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Van Schaftingen, E., Detheux, M., & Da Cunha, M. V. (1994). Short‐term control of glucokinase activity: role of a regulatory protein. The FASEB Journal. https://doi.org/10.1096/fasebj.8.6.8168691

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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