enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Galactokinase - Wikipedia

    en.wikipedia.org/wiki/Galactokinase

    Galactokinase is an enzyme (phosphotransferase) that facilitates the phosphorylation of α-D-galactose to galactose 1-phosphate at the expense of one molecule of ATP. [1] Galactokinase catalyzes the second step of the Leloir pathway, a metabolic pathway found in most organisms for the catabolism of α-D-galactose to glucose 1-phosphate. [2]

  3. Leloir pathway - Wikipedia

    en.wikipedia.org/wiki/Leloir_pathway

    Intermediates and enzymes in the Leloir pathway of galactose metabolism [5] In the first step, galactose mutarotase facilitates the conversion of β-D-galactose to α-D-galactose since this is the active form in the pathway. Next, α-D-galactose is phosphorylated by galactokinase to galactose 1-phosphate.

  4. Beta-D-galactosyl-(1-4)-L-rhamnose phosphorylase - Wikipedia

    en.wikipedia.org/wiki/Beta-D-galactosyl-(1-4)-L...

    The enzyme from Clostridium phytofermentans is also active towards beta-D-galactosyl derivatives of L-mannose, L-lyxose, D-glucose, 2-deoxy-D-glucose, and D-galactose. References [ edit ]

  5. Galactose 1-phosphate - Wikipedia

    en.wikipedia.org/wiki/Galactose_1-phosphate

    D-Galactose-1-phosphate is an intermediate in the intraconversion of glucose and uridine diphosphate galactose. [1] It is formed from galactose by galactokinase .The improper metabolism of galactose-1-phosphate is a characteristic of galactosemia . [ 2 ]

  6. Galactose - Wikipedia

    en.wikipedia.org/wiki/Galactose

    The main pathway of galactose metabolism is the Leloir pathway; humans and other species, however, have been noted to contain several alternate pathways, such as the De Ley Doudoroff Pathway. The Leloir pathway consists of the latter stage of a two-part process that converts β-D-galactose to UDP-glucose. The initial stage is the conversion of ...

  7. Gal operon - Wikipedia

    en.wikipedia.org/wiki/Gal_operon

    GalT encodes for the protein galactosyltransferase which catalyzes the transfer of a galactose sugar to an acceptor, forming a glycosidic bond. [5] GalK encodes for a kinase that phosphorylates α-D-galactose to galactose 1-phosphate. [6] Lastly, galM catalyzes the conversion of β-D-galactose to α-D-galactose as the first step in galactose ...

  8. Galactokinase deficiency - Wikipedia

    en.wikipedia.org/wiki/Galactokinase_deficiency

    Unlike classic galactosemia, which is caused by a deficiency of galactose-1-phosphate uridyltransferase, galactokinase deficiency does not present with severe manifestations in early infancy. Its major clinical symptom is the development of cataracts during the first weeks or months of life, as a result of the accumulation, in the lens, of ...

  9. Galactose-1-phosphate uridylyltransferase deficiency - Wikipedia

    en.wikipedia.org/wiki/Galactose-1-phosphate...

    After the ingestion of lactose, most commonly from breast milk for an infant or cow milk and any milk from an animal, the enzyme lactase hydrolyzes the sugar into its monosaccharide constituents, glucose and galactose. In the first step of galactose metabolism, galactose is converted to galactose-1-phosphate (Gal-1-P) by the enzyme galactokinase.