GLYCOGEN DEBRANCHING ENZYME SYSTEM
\ɡlˈa͡ɪkəd͡ʒən dˈɛbɹant͡ʃɪŋ ˈɛnza͡ɪm sˈɪstəm], \ɡlˈaɪkədʒən dˈɛbɹantʃɪŋ ˈɛnzaɪm sˈɪstəm], \ɡ_l_ˈaɪ_k_ə_dʒ_ə_n d_ˈɛ_b_ɹ_a_n_tʃ_ɪ_ŋ ˈɛ_n_z_aɪ_m s_ˈɪ_s_t_ə_m]\
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1,4-alpha-D-Glucan-1,4-alpha-D-glucan 4-alpha-D-glucosyltransferase/dextrin 6 alpha-D-glucanohydrolase. An enzyme system having both 4-alpha-glucanotransferase (EC 2.4.1.25) and amylo-1,6-glucosidase (EC 3.2.1.33) activities. As a transferase it transfers a segment of a 1,4-alpha-D-glucan to a new 4-position in an acceptor, which may be glucose or another 1,4-alpha-D-glucan. As a glucosidase it catalyzes the endohydrolysis of 1,6-alpha-D-glucoside linkages at points of branching in chains of 1,4-linked alpha-D-glucose residues. Amylo-1,6-glucosidase activity is deficient in glycogen storage disease type III.
By DataStellar Co., Ltd
Word of the day
Diabetic Ketosis
- Complication diabetes from severe insulin deficiency coupled with an absolute or relative increase in concentration. metabolic acidosis is caused by breakdown of adipose stores and resulting increased levels free fatty acids. Glucagon accelerates the oxidation acids producing excess ketone bodies (ketosis).
Nearby Words
- glycogen
- glycogen (starch) synthase
- glycogen branching enzyme
- glycogen debranching enzyme
- glycogen debranching enzyme deficiency
- Glycogen Debranching Enzyme System
- glycogen dextrin
- glycogen phosphorylase
- glycogen phosphorylase a, brain form
- glycogen phosphorylase a, liver form
- glycogen phosphorylase a, muscle form