8cvx
From Proteopedia
(Difference between revisions)
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</table> | </table> | ||
== Disease == | == Disease == | ||
| - | + | [https://www.uniprot.org/uniprot/GYS1_HUMAN GYS1_HUMAN] Glycogen storage disease due to muscle and heart glycogen synthase deficiency. The disease is caused by variants affecting the gene represented in this entry. | |
== Function == | == Function == | ||
| - | + | [https://www.uniprot.org/uniprot/GYS1_HUMAN GYS1_HUMAN] Transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan.[UniProtKB:P13834] | |
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
Revision as of 10:23, 14 December 2022
Human glycogenin-1 and glycogen synthase-1 complex in the presence of glucose-6-phosphate
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