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  2. β-Galactosidase - Wikipedia

    en.wikipedia.org/wiki/Β-Galactosidase

    β-Galactosidase (EC 3.2.1.23, beta-gal or β-gal; systematic name β-D-galactoside galactohydrolase) is a glycoside hydrolase enzyme that catalyzes hydrolysis of terminal non-reducing β-D-galactose residues in β-D-galactosides. (This enzyme digests many β-Galactosides, not just lactose.

  3. Galactosidases - Wikipedia

    en.wikipedia.org/wiki/Galactosidases

    The galactosidases are categorized as either alpha or beta, according to the category of glycoside they hydrolyze. The enzyme corresponding to an alpha-galactoside is called alpha-galactosidase; it catalyzes the hydrolysis of substrates that contain α-galactosidic residues, such as glycosphingolipids or glycoproteins. [1]

  4. Senescence-associated beta-galactosidase - Wikipedia

    en.wikipedia.org/wiki/Senescence-associated_beta...

    Senescence-associated beta-galactosidase (SA-β-gal or SABG) is a hypothetical hydrolase enzyme that catalyzes the hydrolysis of β-galactosides into monosaccharides.Senescence-associated beta-galactosidase, along with p16 Ink4A, is regarded to be a biomarker of cellular senescence.

  5. GLB1 - Wikipedia

    en.wikipedia.org/wiki/GLB1

    The RNA transcript of the GLB1 gene is alternatively spliced and produces 2 mRNAs. The 2.5-kilobase transcript encodes the beta-galactosidase enzyme of 677 amino acids.The alternative 2.0-kb mRNA encodes a beta-galactosidase-related protein (S-Gal) that is only 546 amino acids long and that has no enzymatic activity.

  6. Galactosialidosis - Wikipedia

    en.wikipedia.org/wiki/Galactosialidosis

    Galactosialidosis, also known as neuraminidase deficiency with beta-galactosidase deficiency, is a genetic lysosomal storage disease. [2] It is caused by a mutation in the CTSA gene which leads to a deficiency of enzymes β-galactosidase and neuraminidase.

  7. Glycoside hydrolase family 42 - Wikipedia

    en.wikipedia.org/wiki/Glycoside_hydrolase_family_42

    The glycosyl hydrolase 42 family CAZY GH_42 comprises beta-galactosidase enzymes (EC 3.2.1.23). These enzyme catalyse the hydrolysis of terminal, non-reducing terminal beta-D-galactoside residues. The middle domain of these three-domain enzymes is involved in trimerisation. [8]

  8. 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

  9. Glycoside hydrolase family 2 - Wikipedia

    en.wikipedia.org/wiki/Glycoside_hydrolase_family_2

    Glycoside hydrolase family 2 [8] comprises enzymes with several known activities: beta-galactosidase (EC 3.2.1.23); beta-mannosidase (EC 3.2.1.25); beta-glucuronidase (EC 3.2.1.31). These enzymes contain a conserved glutamic acid residue which has been shown, [ 9 ] in Escherichia coli lacZ ( P00722 ), to be the general acid/base catalyst in the ...

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