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GT-C O-Mannosyltransferase TMEM260 incubated with Far-P-Man
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Structural highlights
DiseaseTM260_HUMAN Structural heart defects-renal anomalies syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionTM260_HUMAN O-mannosyl-transferase that transfers mannosyl residues to the hydroxyl group of serine or threonine residues of proteins (PubMed:37186866). Specifically glycosylates the IPT/TIG domain of target proteins, such as MET and MST1R/RON (PubMed:37186866). TMEM260-mediated O-mannosylated residues are composed of single mannose glycans that are not elongated or modified (PubMed:37186866).[1] References
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This page was last modified 07:24, 8 July 2026.