8z5p
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human phosphorylase kinase - inactive state
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Structural highlights
DiseaseKPB1_HUMAN Glycogen storage disease due to muscle phosphorylase kinase deficiency. The disease is caused by variants affecting the gene represented in this entry. FunctionKPB1_HUMAN Phosphorylase b kinase catalyzes the phosphorylation of serine in certain substrates, including troponin I. The alpha chain may bind calmodulin. Contents | ||||||||||||||||||
This page was last modified 05:16, 23 April 2025.