Glycogen Synthase 1 Proteine (GYS1)

Bezeichnung:
Glycogen Synthase 1 (Muscle) Proteine (GYS1)
Auf www.antikoerper-online.de finden Sie aktuell 5 Glycogen Synthase 1 (Muscle) (GYS1) Proteine von 3 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen Glycogen Synthase 1 Antikörper (39) und Glycogen Synthase 1 Kits (3) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 54 Glycogen Synthase 1 Produkte verfügbar.
Synonyme:
GSY, GYS, GYS1, GYS2, Gys3, MGS, zgc:63701
alle Proteine anzeigen Gen GeneID UniProt
GYS1 2997 P13807
GYS1 14936 Q9Z1E4
GYS1 690987 A2RRU1

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Pig (Porcine) Glycogen Synthase 1 (Muscle) (GYS1) Interaktionspartner

  1. Expression analysis revealed that porcine GYS1 was highly expressed in the skeletal muscle and heart

Horse (Equine) Glycogen Synthase 1 (Muscle) (GYS1) Interaktionspartner

  1. the occurrence of the mutated GYS1 allele is influenced by coat colour

  2. The GYS1 mutation was detected in 11 breeds; with prevalence of genetic susceptibility to Type 1 Polysaccharide Storage Myopathy varied from 0.5% to 62.4%.

  3. observed that the two miRNAs, namely, eca-miR-33a and miR-17, inhibited LDHA and GYS1 expression via binding to the 3' UTR sequences of each gene

  4. The tissue expression profiles of eGYS1, equine type II hexokinase (eHKII) and muscle-type phosphofructokinase (ePFKM) were determined by real-time PCR and western blot analysis.

  5. Study identified GYS1, encoding skeletal muscle glycogen synthase (GS), as a candidate gene for Polysaccharide storage myopathy; DNA sequence analysis revealed a mutation resulting in an Arg-to-his substitution in a highly conserved region of GS.

  6. The prevalence of a missense mutation of GYS1 in horses with polysaccharide storage myopathy and the prevalence of the mutation based on disease classification are reported.

  7. This GYS1 point mutation appears to cause a gain-of-function of the enzyme and to result in the accumulation of a glycogen-like, less-branched polysaccharide in skeletal muscle.

  8. The GYS1 mutation is an important cause of exertional rhabdomyolysis in UNited Kingdom horse breeds but does not account for all forms of polysaccharide storage myopathy.

Human Glycogen Synthase 1 (Muscle) (GYS1) Interaktionspartner

  1. Overexpression of GYS1, MIF (zeige AMH Proteine), and MYC (zeige MYC Proteine) is associated with adverse outcome and poor response to azacitidine in myelodysplastic syndromes and acute myeloid leukemia (zeige BCL11A Proteine)

  2. over-expression of muscle glycogen synthase (MGS)was detected in diabetic human kidney

  3. High glycogen synthase 1 expression is associated with myeloid leukemia (zeige BCL11A Proteine).

  4. Data suggest that although COOH-terminal dephosphorylation is likely necessary for GS activation, protein kinase Akt-2- (Akt2 (zeige AKT2 Proteine))-dependent NH2-terminal dephosphorylation is site for "fine-tuning" insulin (zeige INS Proteine)-mediated GS activation in skeletal muscle.

  5. Allosteric regulation and the relationship between phosphorylation and the kinetics of glycogen synthase. [Review]

  6. The present findings demonstrate that physical inactivity-induced insulin (zeige INS Proteine) resistance in muscle is associated with lower content/activity of key proteins in glucose transport/phosphorylation and storage.

  7. GYS1 regulation by HIF plays a central role in the hypoxic accumulation of glycogen, and hypoxia also upregulates the expression of UTP:glucose-1-phosphate urydylyltransferase (UGP2 (zeige UGP2 Proteine)) and 1,4-alpha glucan branching enzyme (GBE1 (zeige GBE1 Proteine))

  8. Exercise unmaskd the effect associated with the GYS1 polymorphism, rendering carriers of this allele less susceptible to the protective effect of exercise on the risk of cardiovascular mortality.

  9. the M416V polymorphism of glycogen synthase 1 gene is not associated with insulin (zeige INS Proteine) resistance in type 2 diabetes

  10. Data show that myotubes defective in glycogen synthase (GS) activity express insulin (zeige INS Proteine)-responsive glycogen synthase kinase-3alpha, suggesting that failure of insulin (zeige INS Proteine) to decrease GS phosphorylation involves abnormal activity of another kinase or phosphatase.

Mouse (Murine) Glycogen Synthase 1 (Muscle) (GYS1) Interaktionspartner

  1. These results demonstrate that pharmacological agents that activate GYS1, the main GS subtype found in skeletal muscle, have potential for use as novel treatments for diabetes that improve glucose metabolism in skeletal muscle.

  2. We show that the absence of Epm2aip1 (zeige EPM2AIP1 Proteine) in mice impairs allosteric activation of GS by glucose 6-phosphate, decreases hepatic glycogen synthesis, increases liver fat, causes hepatic insulin (zeige INS Proteine) resistance, and protects against age-related obesity

  3. Muscle glycogen synthase isoform is responsible for testicular glycogen synthesis: glycogen overproduction induces apoptosis in male germ cells.

  4. Long-term potentiation (LTP (zeige SCP2 Proteine)) evoked in the hippocampal CA3 (zeige CA3 Proteine)-CA1 (zeige CA1 Proteine) synapse was also decreased in behaving GYS1(Nestin (zeige NES Proteine)-KO) mice.

  5. Neurodegeneration and functional impairments are associated with glycogen synthase accumulation in the mouse model of Lafora disease.

  6. GYS1 regulation by HIF plays a central role in the hypoxic accumulation of glycogen, and hypoxia also upregulates the expression of UTP:glucose-1-phosphate urydylyltransferase (UGP2 (zeige UGP2 Proteine)) and 1,4-alpha glucan branching enzyme (GBE1 (zeige GBE1 Proteine))

  7. Overexpression of glycogen synthase in skeletal muscle results in less branched glycogen.

  8. The endogenous glycogen synthase in extracts from mouse brain bound specifically to SAPK2b/p38b (zeige MAPK11 Proteine) & was phosphorylated at residues Ser644, Ser652, Thr718 and Ser724.

  9. JNK signaling regulates the phosphorylation state of several kinases in skeletal muscle. JNK activation is unlikely to be the major mechanism by which contractile activity increases glycogen synthase activity in skeletal muscle.

  10. the GYS1 gene is not essential for strenuous exercise and has relatively little effect on endurance in mice

Glycogen Synthase 1 (GYS1) Protein Überblick

Protein Überblick

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.

Alternative names and synonyms associated with Glycogen Synthase 1 (GYS1)

  • glycogen synthase 1 (muscle) (GYS1)
  • glycogen synthase 1 (muscle) (gys1)
  • glycogen synthase 1, muscle (Gys1)
  • GSY Protein
  • GYS Protein
  • GYS1 Protein
  • GYS2 Protein
  • Gys3 Protein
  • MGS Protein
  • zgc:63701 Protein

Bezeichner auf Proteinebene für GYS1

glycogen [starch] synthase, muscle , glycogen synthase 1 (muscle) , glycogen synthase 3, brain

GENE ID SPEZIES
574064 Sus scrofa
456196 Pan troglodytes
394155 Danio rerio
378934 Gallus gallus
100054723 Equus caballus
100172871 Pongo abelii
511047 Bos taurus
611993 Canis lupus familiaris
2997 Homo sapiens
786335 Bos taurus
100008660 Oryctolagus cuniculus
574233 Macaca mulatta
14936 Mus musculus
690987 Rattus norvegicus
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