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Literature summary extracted from

  • Wan, L.; Lee, C.C.; Hsu, C.M.; Hwu, W.L.; Yang, C.C.; Tsai, C.H.; Tsai, F.J.
    Identification of eight novel mutations of the acid alpha-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II (2008), J. Neurol., 255, 831-838.
    View publication on PubMed

Protein Variants

EC Number Protein Variants Comment Organism
3.2.1.20 additional information identification of eight novel mutations of the acid alpha-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II Homo sapiens

Organism

EC Number Organism UniProt Comment Textmining
3.2.1.20 Homo sapiens
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.2.1.20 glycogen + H2O
-
Homo sapiens alpha-D-glucose
-
?

Synonyms

EC Number Synonyms Comment Organism
3.2.1.20 acid alpha-glucosidase
-
Homo sapiens
3.2.1.20 acid GAA
-
Homo sapiens
3.2.1.20 acid maltase
-
Homo sapiens