6bw6 | pdb_00006bw6
From Proteopedia
Human GPT (DPAGT1) H129 variant in complex with tunicamycin
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Structural highlights
Disease[GPT_HUMAN] DPAGT1-CDG;Congenital myasthenic syndromes with glycosylation defect. 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. Function[GPT_HUMAN] Catalyzes the initial step in the synthesis of dolichol-P-P-oligosaccharides. Contents | ||||||||||||||||||||
This page was last modified 07:28, 22 February 2018.