8cvz
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Human glycogenin-1 and glycogen synthase-1 complex in the apo ordered state
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Structural highlights
DiseaseGLYG_HUMAN Glycogen storage disease due to glycogenin deficiency. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. FunctionGLYG_HUMAN Self-glucosylates, via an inter-subunit mechanism, to form an oligosaccharide primer that serves as substrate for glycogen synthase. See Also | ||||||||||||||||||
This page was last modified 09:40, 14 February 2024.