2y7j | pdb_00002y7j
From Proteopedia
Structure of human phosphorylase kinase, gamma 2
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Structural highlights
Disease[PHKG2_HUMAN] Glycogen storage disease due to liver phosphorylase kinase deficiency. The disease is caused by mutations affecting the gene represented in this entry. Function[PHKG2_HUMAN] Catalytic subunit of the phosphorylase b kinase (PHK), which mediates the neural and hormonal regulation of glycogen breakdown (glycogenolysis) by phosphorylating and thereby activating glycogen phosphorylase. May regulate glycogeneolysis in the testis. In vitro, phosphorylates PYGM (By similarity).[1] References | ||||||||||||||||||||
This page was last modified 14:05, 25 December 2019.