PYGL Proteine (PYGL)

Bezeichnung:
phosphorylase, Glycogen, Liver Proteine (PYGL)
Auf www.antikoerper-online.de finden Sie aktuell 17 phosphorylase, Glycogen, Liver (PYGL) Proteine von 5 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen PYGL Antikörper (90) und PYGL Kits (34) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 145 PYGL Produkte verfügbar.
Synonyme:
GSD6, zgc:66314
alle Proteine anzeigen Gen GeneID UniProt
PYGL 110095 Q9ET01
PYGL 5836 P06737
PYGL 64035 P09811

Weitere Synonyme anzeigen

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Weitere Proteine zu PYGL Interaktionspartnern

Mouse (Murine) phosphorylase, Glycogen, Liver (PYGL) Interaktionspartner

  1. The in vivo consequences of disrupting the G(L)-phosphorylase a interaction, using a mouse model containing a Tyr284Phe substitution in the phosphorylase a-binding region of the hepatic glycogen (zeige GYS1 Proteine)-associated protein phosphatase-1 (zeige PPP1CB Proteine) protein, is reported.

Human phosphorylase, Glycogen, Liver (PYGL) Interaktionspartner

  1. Susceptibility to excessive liver glycogen (zeige GYS1 Proteine) storage in patients with type 1 diabetes.

  2. Deficiency of liver glycogen phosphorylase is predominantly the result of missense mutations affecting enzyme activity. There are no common mutations and the severity of clinical symptoms varies significantly.

Pig (Porcine) phosphorylase, Glycogen, Liver (PYGL) Interaktionspartner

  1. 4-alpha-glucanotransferase action of porcine liver GDE (zeige AGL Proteine) on four 6(4)-O-alpha-maltooligosyl-pyridylamino(PA)-maltooctaoses, in the presence or absence of an acceptor, maltohexaose, was examined.

PYGL Protein Überblick

Protein Überblick

This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.

Alternative names and synonyms associated with PYGL

  • phosphorylase, glycogen, liver (PYGL)
  • phosphorylase, glycogen; liver (Hers disease, glycogen storage disease type VI) (pygl)
  • phosphorylase, glycogen, liver (pygl)
  • liver glycogen phosphorylase (Pygl)
  • phosphorylase, glycogen, liver (Pygl)
  • GSD6 Protein
  • zgc:66314 Protein

Bezeichner auf Proteinebene für PYGL

glycogen phosphorylase, liver form , liver glycogen phosphorylase , phosphorylase, glycogen; liver (Hers disease, glycogen storage disease type VI) , glycogen storage disease type VI-related protein , phosphorylase, glycogen; liver

GENE ID SPEZIES
100066726 Equus caballus
378909 Gallus gallus
493916 Danio rerio
494832 Xenopus laevis
706853 Macaca mulatta
742309 Pan troglodytes
110095 Mus musculus
5836 Homo sapiens
403738 Canis lupus familiaris
100141306 Sus scrofa
505472 Bos taurus
64035 Rattus norvegicus
554320 Ovis aries
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