Enzymes of glycogen synthesis in glycogen-deposition disease.
1959
R HAUK, and
B ILLINGWORTH, and
D H BROWN, and
C F CORI
UI
MeSH Term
Description
Entries
D004798
Enzymes
Biological molecules that possess catalytic activity. They may occur naturally or be synthetically created. Enzymes are usually proteins, however CATALYTIC RNA and CATALYTIC DNA molecules have also been identified.
Biocatalyst,Enzyme,Biocatalysts
D006003
Glycogen
D006008
Glycogen Storage Disease
A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014166
Transferases
Transferases are enzymes transferring a group, for example, the methyl group or a glycosyl group, from one compound (generally regarded as donor) to another compound (generally regarded as acceptor). The classification is based on the scheme "donor:acceptor group transferase". (Enzyme Nomenclature, 1992) EC 2.
Transferase
D050260
Carbohydrate Metabolism
Cellular processes in biosynthesis (anabolism) and degradation (catabolism) of CARBOHYDRATES.
Metabolism, Carbohydrate
D050261
Glycogenolysis
The release of GLUCOSE from GLYCOGEN by GLYCOGEN PHOSPHORYLASE (phosphorolysis). The released glucose-1-phosphate is then converted to GLUCOSE-6-PHOSPHATE by PHOSPHOGLUCOMUTASE before entering GLYCOLYSIS. Glycogenolysis is stimulated by GLUCAGON or EPINEPHRINE via the activation of PHOSPHORYLASE KINASE.
Glycogenolyses
Related Publications
R HAUK, and
B ILLINGWORTH, and
D H BROWN, and
C F CORI