Mannosidase

Mannosidase is an enzyme which hydrolyses mannose.[1]

There are two types:

A deficiency is associated with mannosidosis.

A family of mannosidases are also responsible for processing newly formed glycoproteins in the endoplasmic reticulum into mature glycoproteins containing highly heterogeneous complex-type glycans.

References

Mannosidases at the US National Library of Medicine Medical Subject Headings (MeSH)

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[1] Mannosidases at the US National Library of Medicine Medical Subject Headings (MeSH)

Metabolism: carbohydrate metabolism · glycoprotein enzymes
Anabolism	Dolichol kinase GCS1 Oligosaccharyltransferase
Catabolism	Neuraminidase Beta-galactosidase Hexosaminidase mannosidase alpha-Mannosidase beta-mannosidase Aspartylglucosaminidase Fucosidase NAGA
Transport	SLC17A5
M6P tagging	N-acetylglucosamine-1-phosphate transferase

Enzymes
Activity	Active site Binding site Catalytic triad Oxyanion hole Enzyme promiscuity Catalytically perfect enzyme Coenzyme Cofactor Enzyme catalysis
Regulation	Allosteric regulation Cooperativity Enzyme inhibitor Enzyme activator
Classification	EC number Enzyme superfamily Enzyme family List of enzymes
Kinetics	Enzyme kinetics Eadie–Hofstee diagram Hanes–Woolf plot Lineweaver–Burk plot Michaelis–Menten kinetics
Types	EC1 Oxidoreductases (list) EC2 Transferases (list) EC3 Hydrolases (list) EC4 Lyases (list) EC5 Isomerases (list) EC6 Ligases (list) EC7 Translocases (list)