| Descriptor English: | Glycogen Phosphorylase, Muscle Form | ||||||
| Descriptor Spanish: |
Glucógeno Fosforilasa de Forma Muscular
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| Descriptor Portuguese: | Glicogênio Fosforilase Muscular | ||||||
| Descriptor French: | Myophosphorylase | ||||||
| Entry term(s): |
Glycogen Phosphorylase a, Muscle Form Glycogen Phosphorylase b, Muscle Form Myophosphorylase Myophosphorylase a and b |
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| Tree number(s): |
D08.811.913.400.450.460.400.186.312 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D024982 | ||||||
| Scope note: | 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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| Allowable Qualifiers: |
AD administration & dosage AE adverse effects AI antagonists & inhibitors AN analysis BI biosynthesis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis DE drug effects DF deficiency EC economics GE genetics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PH physiology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UL ultrastructure UR urine |
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| Registry Number: | EC 2.4.1.- | ||||||
| Previous Indexing: |
Glucosyltransferases (1967-1978) Phosphorylases (1979-2001) |
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| Public MeSH Note: | 2002 |
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| History Note: | 2002 |
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| Related: |
Glycogen Storage Disease Type V
MeSH | ||||||
| DeCS ID: | 36107 | ||||||
| Unique ID: | D024982 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2002/01/01 | ||||||
| Date of Entry: | 2001/07/25 | ||||||
| Revision Date: | 2003/07/09 |
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CHEMICALS AND DRUGS
Enzymes and Coenzymes [D08]Enzymes and Coenzymes
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Glycogen Phosphorylase, Muscle Form
- Preferred
Glycogen Phosphorylase b, Muscle Form
- Narrower
Glycogen Phosphorylase a, Muscle Form
- Narrower
| Concept UI |
M0332561 |
| Scope note | 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). |
| Preferred term | Glycogen Phosphorylase, Muscle Form |
| Entry term(s) |
Myophosphorylase Myophosphorylase a and b |
| Concept UI |
M0378532 |
| Preferred term | Glycogen Phosphorylase b, Muscle Form |
| Concept UI |
M0378531 |
| Preferred term | Glycogen Phosphorylase a, Muscle Form |
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