Glycogen synthase

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glycogen synthase 1 (muscle)
Identifiers
Symbol GYS1
Alt. Symbols GYS
Entrez 2997
HUGO 4706
OMIM 138570
RefSeq NM_002103
UniProt P13807
Other data
EC number 2.4.1.11
Locus Chr. 19 q13.3
glycogen synthase 2 (liver)
Identifiers
Symbol GYS2
Entrez 2998
HUGO 4707
OMIM 138571
RefSeq NM_021957
UniProt P54840
Other data
EC number 2.4.1.11
Locus Chr. 12 p12.2-11.2

Glycogen synthase (UDP-glucose-glycogen glucosyltransferase') is a glycosyltransferase enzyme (EC number 2.4.1) that catalyses the reaction of UDP-glucose and (1,4-α-D-glucosyl)n to yield UDP and (1,4-α-D-glucosyl)n+1.

In other words, this enzyme converts excess glucose residues one by one into a polymeric chain for storage as glycogen.

Regulation

The reaction is highly regulated by allosteric effectors such as glucose-6-phosphate, by phosphorylation reactions, and indirectly triggered by the hormone insulin, which is secreted by the pancreas. Phosphorylation of glycogen synthase decreases its activity.

Pathology

A deficiency is associated with glycogen storage disease type 0.

References

de:Glykogen-Synthase


Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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