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2. α-Galactosidase - Wikipedia

   en.wikipedia.org/wiki/Α-Galactosidase

   α-Galactosidase ( EC 3.2.1.22, α-GAL, α-GAL A; systematic name α-D-galactoside galactohydrolase) is a glycoside hydrolase enzyme that catalyses the following reaction: [1] Hydrolysis of terminal, non-reducing α- D -galactose residues in α- D -galactosides, including galactose oligosaccharides, galactomannans and galactolipids

3. GLA (gene) - Wikipedia

   en.wikipedia.org/wiki/GLA_(gene)

   2717 11605 Ensembl ENSG00000102393 ENSMUSG00000031266 UniProt P06280 P51569 RefSeq (mRNA) NM_000169 NM_013463 RefSeq (protein) NP_000160 NP_038491 Location (UCSC) Chr X: 101.39 – 101.41 Mb Chr X: 133.49 – 133.5 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Galactosidase alpha is an enzyme that in humans is encoded by the GLA gene. Two recombinant forms of human α-galactosidase ...

4. Galactosidases - Wikipedia

   en.wikipedia.org/wiki/Galactosidases

   Galactosidases are enzymes (glycoside hydrolases) that catalyze the hydrolysis of galactosides into monosaccharides.. Galactosides can be classified as either alpha or beta. If the galactoside is classified as an alpha-galactoside, the enzyme is called alpha-galactosidase, and is responsible for catalyzing the hydrolysis of substrates that contain α-galactosidic residues, such as ...

5. Beano (dietary supplement) - Wikipedia

   en.wikipedia.org/wiki/Beano_(dietary_supplement)

   The estimated expiration date of the patent is December 5, 2014. As of early 2013, more than four dozen competing products were on the market. In April 2014, the brand introduced Beano +Dairy Defense, a product combining α-GAL with lactase. [11] In India, alpha galactosidase tablets are available as Bloateez marketed by Geminova Life.

6. Pegunigalsidase alfa - Wikipedia

   en.wikipedia.org/wiki/Pegunigalsidase_alfa

   Pegunigalsidase alfa, sold under the brand name Elfabrio, is an enzyme replacement therapy for the treatment of Fabry disease. [2] [4] It is a recombinant human α-galactosidase-A. [4] It is a hydrolytic lysosomal neutral glycosphingolipid-specific enzyme. [2] The most common side effects are infusion-related reactions, hypersensitivity and ...

7. Glycoside hydrolase family 27 - Wikipedia

   en.wikipedia.org/wiki/Glycoside_hydrolase_family_27

   Alpha-galactosidase (EC 3.2.1.22) (melibiase) [8] catalyzes the hydrolysis of melibiose into galactose and glucose. In man, the deficiency of this enzyme is the cause of Fabry's disease (X-linked sphingolipidosis). Alpha-galactosidase is present in a variety of organisms.