Structured Summary
Abstract
An isoenzyme of GLYCOGEN PHOSPHORYLASE that catalyzes the degradation of GLYCOGEN in muscle. Mutation of the gene coding this enzyme is the cause of McArdle disease (GLYCOGEN STORAGE DISEASE TYPE V).
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Synonyms
5 entry terms
- Glycogen Phosphorylase, Muscle Form
- Myophosphorylase
- Myophosphorylase a and b
- Glycogen Phosphorylase a, Muscle Form
- Glycogen Phosphorylase b, Muscle Form
MeSH Record
Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2002
MeSH Record
Previous Indexing
- Glucosyltransferases (1967-1978)
- Phosphorylases (1979-2001)
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AMA Style
References
- National Library of Medicine. Muscle Form Glycogen Phosphorylase. Medical Subject Headings (MeSH). 2026. Unique ID D024982. http://id.nlm.nih.gov/mesh/2026/D024982
- Muscle Form Glycogen Phosphorylase. In: Wikipedia. https://en.wikipedia.org/wiki/Myophosphorylase
- Muscle Form Glycogen Phosphorylase. In: Wikidata. https://www.wikidata.org/wiki/Q21115156