Glycogen Phosphorylase, Muscle Form

MeSH 搜索器

Glycogen Phosphorylase, Muscle Form

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).

推出的年份: 2002

树号: D08.811.913.400.450.460.400.186.312

MeSH 单一 ID: D024982

进入的组:

Myophosphorylase
Myophosphorylase a and b
Glycogen Phosphorylase b, Muscle Form
Glycogen Phosphorylase a, Muscle Form

早前的内容:

Glucosyltransferases (1967-1978)
Phosphorylases (1979-2001)

All MeSH Categories
- Chemicals and Drugs Category
  - Enzymes and Coenzymes [D08]
    - Enzymes [D08.811]
      - Transferases [D08.811.913]
        
        Glycosyltransferases [D08.811.913.400]
        
        Hexosyltransferases [D08.811.913.400.450]
        
        Glucosyltransferases [D08.811.913.400.450.460]
        
        Phosphorylases [D08.811.913.400.450.460.400]
        
        Glycogen Phosphorylase [D08.811.913.400.450.460.400.186]
        
        Glycogen Phosphorylase, Brain Form [D08.811.913.400.450.460.400.186.061]
        
        Glycogen Phosphorylase, Liver Form [D08.811.913.400.450.460.400.186.124]
        
        Glycogen Phosphorylase, Muscle Form [D08.811.913.400.450.460.400.186.312]

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MeSH 搜索器

Glycogen Phosphorylase, Muscle Form

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