AAH03182.1
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
83,786 Da
NCBI Official Full Name
GYS1 protein
NCBI Official Synonym Full Names
glycogen synthase 1 (muscle)
NCBI Official Synonym Symbols
NCBI Protein Information
glycogen [starch] synthase, muscle; glycogen [starch] synthase, muscle
UniProt Protein Name
Glycogen [starch] synthase, muscle
UniProt Synonym Gene Names
UniProt Entry Name
GYS1_HUMAN
NCBI Summary for GYS/GYS1
The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1,4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]
UniProt Comments for GYS/GYS1
GYS1: muscle glycogen synthase 1. Transfers glucosyl residue from UDP-glucose to glycogen. Regulated allosterically by glucose-6-phosphate, and by PKA-mediated phosphorylation.
Protein type: EC 2.4.1.11; Carbohydrate Metabolism - starch and sucrose; Transferase
Chromosomal Location of Human Ortholog: 19q13.3
Cellular Component: membrane; cytoplasm; inclusion body; cytosol
Molecular Function: protein binding; glycogen (starch) synthase activity; protein kinase binding; glucose binding
Biological Process: glycogen biosynthetic process; heart development; carbohydrate metabolic process; glucose metabolic process; pathogenesis
Disease: Glycogen Storage Disease 0, Muscle
Research Articles on GYS/GYS1
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Products associated with GYS/GYS1 elisa kit
Pathways associated with GYS/GYS1 elisa kit
Diseases associated with GYS/GYS1 elisa kit
Organs/Tissues associated with GYS/GYS1 elisa kit
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