Glycogen breakdown (glycogenolysis)

Summary
Organism
Homo sapiens (human)
Reactome
R-HSA-70221
PubChem
R-HSA-70221
Description
  • Cytosolic glycogen breakdown occurs via the same chemical steps in all tissues but is separately regulated via tissue specific isozymes and signaling pathways that enable distinct physiological fates for liver glycogen and that in other tissues. Glycogen phosphorylase, which can be activated by phosphorylase kinase, catalyzes the removal of glucose residues as glucose 1-phosphate from the ends of glycogen branches. The final four residues of each branch are removed in two steps catalyzed by debranching enzyme, and further glycogen phosphorylase activity completes the process of glycogen breakdown. The figure shows the actions of phosphorylase and debranching enzyme. The first glucose residue in each branch is released as free glucose; all other residues are released as glucose 1-phosphate. The latter molecule can be converted to glucose 6-phosphate in a step shared with other pathways (Villar-Palasi and Larner 1970; Hers 1976).

    Glycogen can also be taken up into lysosomes, where it is normally broken done by the action of a single enzyme, lysosomal alpha-glucosidase (GAA).

    Enzymes in liver generate 1,5-anhydro-D-fructose from glycogen, which in turn can be reduced to 1,5-anhydro-D-glucitol, a sequence of events that may represent a novel minor pathway for glycogen breakdown (Kametani et al. 1996).

Click on a node on the pathway to see its details. Glycoproteins are marked with a glycoprotein icon in their name.
Displaying all 3 entries
GlyCosmos Lectin UniProt ID Lectin Name Pathway Viewer
GL_001691 P10253 Lysosomal alpha-glucosidase view
GL_002529 P06737 Glycogen phosphorylase, liver form view
GL_002763 P35573 Glycogen debranching enzyme view
Displaying 1 entry
GlyTouCan ID KEGG GLYCAN ChEBI Pathway Viewer
G15021LG
view

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026