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Vocabulary flashcards covering the structural features, enzymatic machinery, and reciprocal hormonal and allosteric regulation of glycogen breakdown and synthesis.
Glycogen
A highly branched homopolymer of glucose found in all tissues, primarily stored in the liver and skeletal muscle.

Glycogen Storage Particle
A cellular storage complex containing a central glycogenin protein surrounded by α-1,4-linked glucose chains, with α-1,6 branches occurring every 10 residues and nonreducing ends exposed on the surface.

α-1,4-Glycosidic Bond
The primary covalent linkage connecting linear glucose residues in glycogen, cleaved by glycogen phosphorylase during breakdown and formed by glycogen synthase during synthesis.
α-1,6-Glycosidic Bond
The covalent linkage responsible for forming branch points in glycogen, occurring approximately every 10 residues.
Liver Glycogen
A glycogen reserve broken down to release free glucose into the bloodstream, maintaining blood glucose levels to nourish tissues such as the brain and red blood cells.
Muscle Glycogen
A glycogen store mobilized internally to generate glucose 6-phosphate for glycolysis, supplying ATP directly for muscle contraction.
Glycogen Phosphorylase
The key regulatory enzyme of glycogenolysis that catalyzes phosphorolysis of α-1,4-glycosidic bonds from the nonreducing ends to produce glucose 1-phosphate.
Phosphorolysis
The cleavage of a covalent bond by the addition of inorganic orthophosphate (HPO42−), yielding a phosphorylated product (glucose 1-phosphate) while conserving energy without expending ATP.
Glucosyltransferase
A remodeling enzyme that shifts a small oligosaccharide near a branch point to a nearby chain, exposing the remaining α-1,6-linked residue to debranching enzyme.
α-1,6-Glucosidase
A debranching enzyme that hydrolytically cleaves the α-1,6 bond at a branch point, releasing one molecule of free glucose.

Glucose 1,6-Bisphosphate
The intermediate formed during the phosphoglucomutase reaction when a catalytic phosphoserine transfers its phosphoryl group to glucose 1-phosphate.
Phosphoglucomutase
A phosphoserine-dependent mutase that interconverts glucose 1-phosphate and glucose 6-phosphate via a glucose 1,6-bisphosphate intermediate.

Glucose 6-Phosphatase
A liver endoplasmic reticulum enzyme that hydrolyzes glucose 6-phosphate into free glucose and inorganic phosphate for release into the bloodstream.
Phosphorylase a
The phosphorylated, catalytically active form of glycogen phosphorylase.
Phosphorylase b
The unphosphorylated, generally less active form of glycogen phosphorylase.
Liver Glycogen Phosphorylase Isoform
An isozyme whose default state is phosphorylase a in the active R state (usually ON), which is allosterically inhibited by glucose shifting it to the T state.
Muscle Glycogen Phosphorylase Isoform
An isozyme whose default state is phosphorylase b in the inactive T state (usually OFF), which is allosterically activated by high concentrations of AMP and inhibited by ATP and glucose 6-phosphate.
Phosphorylase Kinase
An enzyme activated by Protein Kinase A that phosphorylates phosphorylase b, converting it into the more active phosphorylase a.
Protein Phosphatase 1 (PP1)
An insulin-stimulated phosphatase that removes phosphoryl groups from phosphorylase kinase and glycogen phosphorylase to inactivate breakdown, while activating glycogen synthase.
UDP-Glucose (Uridine Diphosphate Glucose)
The activated glucosyl donor substrate required by glycogen synthase for glycogen polymer elongation.
UDP-Glucose Pyrophosphorylase
The enzyme that synthesizes UDP-glucose and pyrophosphate (PPi) from glucose 1-phosphate and UTP.
Pyrophosphate Hydrolysis
The exergonic breakdown of pyrophosphate (PPi+H2O→2Pi) that drives the net synthesis of UDP-glucose toward completion.
Glycogen Synthase
The key regulatory enzyme of glycogen synthesis that transfers a glucosyl unit from UDP-glucose to the C-4 terminal hydroxyl group of an existing glycogen chain, creating an α-1,4-glycosidic bond.
Glycogenin
A dimeric protein that initiates glycogen synthesis by autocatalytically synthesizing an oligosaccharide primer of 10–20 glucose units per subunit.
Branching Enzyme
An enzyme that forms α-1,6 branches by cleaving an α-1,4 bond, transferring an oligosaccharide block of approximately 7 glucose residues, and attaching it via an α-1,6 linkage.
Glycogen Synthase a
The unphosphorylated, catalytically active state of glycogen synthase.
Glycogen Synthase b
The phosphorylated, inactive or less active state of glycogen synthase, which can be allosterically activated by glucose 6-phosphate.
Reciprocal Regulation
A regulatory mechanism where signaling events (such as phosphorylation triggered by glucagon or epinephrine) activate glycogen breakdown while simultaneously inactivating glycogen synthesis, preventing futile cycles.