glycogen phosphorylase, liver form

Preferred Label : glycogen phosphorylase, liver form;

MeSH definition : An isoenzyme of GLYCOGEN PHOSPHORYLASE that catalyzes the degradation of GLYCOGEN in liver tissue. Mutation of the gene coding this enzyme on chromosome 14 is the cause of GLYCOGEN STORAGE DISEASE TYPE VI.;

MeSH hyponym : glycogen phosphorylase a, liver form; glycogen phosphorylase b, liver form;

MeSH Related Number : glycogen phosphorylase b, liver form; glycogen phosphorylase a, liver form;

Registry Number MeSH : EC 2.4.1.-;

Related CAS MeSH : EC 2.4.1.- (Glycogen phosphorylase b, liver form); EC 2.4.1.- (Glycogen phosphorylase a, liver form);

Is substance : O;

Détails

Origin ID

D025001;

UMLS CUI

C0969684;

Allowable qualifiers
- administration and dosage [MeSH Qualifier]
- adverse effects [MeSH Qualifier]
- analysis [MeSH Qualifier]
- antagonists and inhibitors [MeSH Qualifier]
- biosynthesis [MeSH Qualifier]
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemical synthesis [MeSH Qualifier]
- chemistry [MeSH Qualifier]
- classification [MeSH Qualifier]
- contraindications [MeSH Qualifier]
- deficiency [MeSH Qualifier]
- drug effects [MeSH Qualifier]
- economics [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- isolation and purification [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- pharmacokinetics [MeSH Qualifier]
- pharmacology [MeSH Qualifier]
- physiology [MeSH Qualifier]
- poisoning [MeSH Qualifier]
- radiation effects [MeSH Qualifier]
- standards [MeSH Qualifier]
- supply and distribution [MeSH Qualifier]
- therapeutic use [MeSH Qualifier]
- toxicity [MeSH Qualifier]
- ultrastructure [MeSH Qualifier]
- urine [MeSH Qualifier]
Indexing information
- N-(1-benzyl-3-(3,4-dihydroxypyrrolidin-1-yl)-2-hydroxy-3-oxopropyl)-5-chloro-1H-indole-2-carboxamide [MeSH Supplementary Concept]
Metaterm(s)
- hepatology [CISMeF Metaterm]
Record concept(s)
- glycogen phosphorylase a, liver form [MeSH concept]
- glycogen phosphorylase b, liver form [MeSH concept]
- glycogen phosphorylase, liver form [MeSH concept]
Related MeSH Supplementary Concept(s)
- PYGL protein, human [MeSH Supplementary Concept]
See also
- glycogen storage disease type vi [MeSH Descriptor]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

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