Bioinformatic and biochemical studies point to AAGR-1 as the ortholog of human acid α-glucosidase in Caenorhabditis elegans

Author:

Sikora Jakub,Uřinovská Jana,Majer Filip,Poupětová Helena,Hlavatá Jitka,Kostrouchová Marta,Ledvinová Jana,Hřebíček Martin

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,General Medicine

Reference56 articles.

1. Hirschhorn R, Reuser AJJ (2001) Glycogen storage disease type II: acid α-glucosidase (acid maltase) deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B (eds) The metabolic & molecular bases of inherited disease, 8th edn. The McGraw-Hill Companies, Inc., New York, pp 3389–3420

2. Carbohydrate-Active Enzymes Server, http://www.cazy.org

3. Protein Families Database of Alignments and HMMs, http://www.sanger.ac.uk/cgi-bin/Pfam/

4. Henrissat B (1991) A classification of glycosyl hydrolases based on amino acid sequence similarities. Biochem J 280(Pt 2):309–316

5. Janecek S, Svensson B, MacGregor EA (2007) A remote but significant sequence homology between glycoside hydrolase clan GH-H and family GH31. FEBS Lett 581:1261–1268. doi: 10.1016/j.febslet.2007.02.036

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