• Thumbnail for Glucosidases
    Glucosidases are the glycoside hydrolase enzymes categorized under the EC number 3.2.1. Alpha-glucosidases are enzymes involved in breaking down complex...
    3 KB (160 words) - 10:12, 12 August 2024
  • Thumbnail for Α-Glucosidase
    α-Glucosidase (EC 3.2.1.20, (systematic name α-D-glucoside glucohydrolase) is a glucosidase located in the brush border of the small intestine that acts...
    15 KB (1,751 words) - 14:31, 1 July 2024
  • Thumbnail for Β-Glucosidase
    β-Glucosidase (EC 3.2.1.21; systematic name β-D-glucoside glucohydrolase) is an enzyme that catalyses the following reaction: Hydrolysis of terminal,...
    12 KB (1,299 words) - 05:02, 11 June 2024
  • Alpha-glucosidase inhibitors (AGIs) are oral anti-diabetic drugs used for diabetes mellitus type 2 that work by preventing the digestion of carbohydrates...
    12 KB (1,431 words) - 06:10, 6 May 2024
  • Thumbnail for Maltase
    Maltase (redirect from A-glucosidase)
    are luminal endo-glucosidases named alpha-amylases. The other four enzymes have been identified as different maltases, exo-glucosidases bound to the luminal...
    11 KB (1,198 words) - 07:01, 30 June 2024
  • Thumbnail for Gaucher's disease
    housekeeping gene for lysosomal glucocerebrosidase (also known as beta-glucosidase, EC 3.2.1.45, PDB: 1OGS​) on the first chromosome (1q22). The enzyme...
    30 KB (3,311 words) - 23:17, 13 August 2024
  • fructosidase, whereas sucrase is a glucosidase. EC 3.2.1.10 is sucrase-isomaltase EC 3.2.1.48 is sucrose alpha-glucosidase Sucrose intolerance (also known...
    3 KB (385 words) - 17:00, 18 January 2024
  • The enzyme amygdalin β-glucosidase (EC 3.2.1.117) catalyzes the following chemical reaction: (R)-amygdalin + H2O ⇌ {\displaystyle \rightleftharpoons }...
    2 KB (181 words) - 13:09, 26 August 2023
  • Amylo-α-1,6-glucosidase (EC 3.2.1.33, amylo-1,6-glucosidase, dextrin 6-α-D-glucosidase, amylopectin 1,6-glucosidase, dextrin-1,6-glucosidase, glycogen phosphorylase-limit...
    2 KB (178 words) - 21:38, 21 June 2024
  • Thumbnail for Glycogen storage disease type II
    glycogen in the lysosome due to deficiency of the lysosomal acid alpha-glucosidase enzyme (GAA). The inability to breakdown glycogen within the lysosomes...
    36 KB (4,291 words) - 10:01, 3 August 2024