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Literature summary extracted from

  • Faid, V.; Evjen, G.; Tollersrud, O.K.; Michalski, J.C.; Morelle, W.
    Site-specific glycosylation analysis of the bovine lysosomal alpha-mannosidase (2006), Glycobiology, 16, 440-461.
    View publication on PubMed

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
3.2.1.24 lysosome
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 Bos taurus 5764
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Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
3.2.1.24 additional information Bos taurus the enzyme is involved in ordered degradation of glycoproteins, inborn enzyme-deficiency results in lysosomal storage disorder alpha-mannosidosis ?
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 ?

Organism

EC Number Organism UniProt Comment Textmining
3.2.1.24 Bos taurus
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-
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Posttranslational Modification

EC Number Posttranslational Modification Comment Organism
3.2.1.24 glycoprotein the enzyme contains 8 N-glycosylation sites, e.g. at residues 133, 367, 497, 692, 766, and 930, site-specific glycosylation analysis, high mannose and complex type N-glycans, overview, the N497 glycosylation is very important for maintenance of lysosomal stability of the enzyme Bos taurus

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.2.1.24 additional information the enzyme is involved in ordered degradation of glycoproteins, inborn enzyme-deficiency results in lysosomal storage disorder alpha-mannosidosis Bos taurus ?
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 ?
3.2.1.24 additional information broad substrate specific exoglycosidase Bos taurus ?
-
 ?