-
Mannosidase is an
enzyme which hydrolyses mannose.
There are two types: alpha-
Mannosidase beta-
Mannosidase A
deficiency is ****ociated with mannosidosis...
- β-
Mannosidase (EC 3.2.1.25}, mannanase, mannase, β-D-
mannosidase, β-mannoside mannohydrolase, exo-β-D-mannanase,
lysosomal β A
mannosidase) is an enzyme...
- α-
Mannosidase (EC 3.2.1.24, α-D-
mannosidase, p-nitrophenyl-α-
mannosidase, α-D-mannopyranosidase, 1,2-α-
mannosidase, 1,2-α-D-
mannosidase, exo-α-mannosidase)...
- 1,2-alpha-
mannosidase may
refer to: alpha-
Mannosidase, an
enzyme Mannosyl-oligosaccharide 1,2-alpha-
mannosidase, an
enzyme This set
index page
lists enzyme...
-
lysosomal beta-
mannosidase deficiency, is a
disorder of
oligosaccharide metabolism caused by
decreased activity of the
enzyme beta-
mannosidase. This enzyme...
-
located on
chromosome 19,
affecting the
production of the
enzyme alpha-D-
mannosidase,
resulting in its deficiency. Consequently, if both
parents are carriers...
- 1,2-α-
mannosidase (EC 3.2.1.113,
mannosidase 1A,
mannosidase 1B, 1,2-α-
mannosidase, exo-α-1,2-mannanase, mannose-9
processing α-
mannosidase, glycoprotein...
- compound.[citation needed]
Kifunensine is a
potent inhibitor of the
mannosidase I
enzyme and is
primarily used in cell
culture to make high
mannose glycoproteins...
-
protein and the
mannose moieties are
hydrolyzed by ER and Golgi-resident
mannosidases. Typically,
mature human glycoproteins only
contain three mannose residues...
- Mannosyl-oligosaccharide 1,3-1,6-α-
mannosidase, also
known as
Golgi α-
mannosidase II, is an
enzyme with
systematic name (1→3)-(1→6)-mannosyl-oligosaccharide...
