Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex.

Lysosomal alpha-glucosidase (acid maltase) is essential for degradation of glycogen in lysosomes. Enzyme deficiency results in glycogenosis type II. The amino acid sequence of the entire enzyme was derived from the nucleotide sequence of cloned cDNA. The cDNA comprises 3636 nt, and hybridizes with a...

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Detaylı Bibliyografya
Asıl Yazarlar: Hoefsloot, L H, Hoogeveen-Westerveld, M, Kroos, M A, van Beeumen, J, Reuser, A J, Oostra, B A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1988
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC457155/
https://ncbi.nlm.nih.gov/pubmed/3049072
Etiketler: Etiketle
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