• Call +1.858.633.0165 or Fax +1.858.633.0166 or Contact Us

Alpha-galactosidase

CATALYTIC ACTIVITY: Hydrolysis of terminal, non-reducing alpha-D-galactose residues in alpha-D-galactosides, including galactose oligosaccharides, galactomannans and galactolipids.

Below are the list of possible Alpha-galactosidase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the reer's specifications.

Alpha-galactosidase 2

Also known as Alpha-galactosidase 2 (Alpha-D-galactoside galactohydrolase 2) (Melibiase 2).
Alpha-galactosidase involved in the degradation of simple oligosaccharides like melibiose, raffinose and stachyose, and of polymeric galacto(gluco)mannans.

Alpha-galactosidase 3

Also known as Alpha-galactosidase 3 (Alpha-D-galactoside galactohydrolase 3) (Melibiase 3).
Alpha-galactosidase involved in the degradation of simple oligosaccharides like melibiose, raffinose and stachyose, and of polymeric galacto(gluco)mannans.

Alpha-galactosidase A

Also known as Alpha-galactosidase A (Alpha-D-galactosidase A) (Alpha-D-galactoside galactohydrolase) (Melibiase).
GLA: Defects in GLA are the cause of Fabry disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. The disease consists of an inborn error of glycosphingolipid catabolism. FD patients show systemic accumulation of globotriaoslyceramide (Gb3) and related glycosphingolipids in the plasma and cellular lysosomes throughout the body. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities. Belongs to the glycosyl hydrolase 27 family.

Protein type: Carbohydrate Metabolism - galactose; EC 3.2.1.22; Glycan Metabolism - glycosphingolipid biosynthesis - globo series; Hydrolase; Lipid Metabolism - glycerolipid; Lipid Metabolism - sphingolipid

Cellular Component: cytoplasm; extracellular region; extracellular space; Golgi apparatus; lysosome

Molecular Function: alpha-galactosidase activity; catalytic activity; galactoside binding; hydrolase activity; protein homodimerization activity; receptor binding

Biological Process: bone mineralization; glycosylceramide catabolic process; negative regulation of nitric oxide biosynthetic process; negative regulation of nitric-oxide synthase activity; oligosaccharide metabolic process

Alpha-galactosidase C

Also known as Alpha-galactosidase C (Melibiase C).
Hydrolyzes a variety of simple alpha-D-galactoside as well as more complex molecules such as oligosaccharides and polysaccharides. Active on paranitrophenyl-alpha-galactoside, raffinose, locust bean gum and gum guar.

Alpha-galactosidase D

Also known as Alpha-galactosidase D (Melibiase D).
Hydrolyzes a variety of simple alpha-D-galactoside as well as more complex molecules such as oligosaccharides and polysaccharides. Active on paranitrophenyl-alpha-galactoside but not on raffinose, locust bean gum and gum guar.

Alpha-galactosidase mel1

Also known as Alpha-galactosidase mel1 (Alpha-D-galactoside galactohydrolase) (Melibiase).
Secreted alpha-galactosidase required for catabolic conversion of melibiose to glucose and galactose.

Go back to Proteins Root Name Listing
Request a Quote

Please fill out the form below and our representative will get back to you shortly.

MBS000000
Contact Us

Please fill out the form below and our representative will get back to you shortly.

MBS000000