5vg7 | pdb_00005vg7
From Proteopedia
Crystal Structure of the R503Q missense variant of human PGM1
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Structural highlights
Disease[PGM1_HUMAN] PGM-CDG;Glycogen storage disease due to phosphoglucomutase deficiency. The disease is caused by mutations affecting the gene represented in this entry. Function[PGM1_HUMAN] This enzyme participates in both the breakdown and synthesis of glucose. Contents | ||||||||||||||||||||||||
This page was last modified 05:39, 20 June 2018.