Glycogen synthase
From Wikipedia, the free encyclopedia
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. Its presence in the bloodstream is highest in the 30 to 60 minutes following intense exercise. It is a key enzyme in glycogenesis.
[edit] 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.
[edit] Pathology
A deficiency is associated with glycogen storage disease type 0.
[edit] References
- Newcastle University Centre for Cancer Education (October 9, 1997). Glycogen synthetase. Retrieved on 2007-11-05.
|
|