EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.4.1.267 | Cricetulus griseus | G3GZD6 | - |
- |
2.4.1.267 | Homo sapiens | Q9Y672 | - |
- |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
2.4.1.267 | fibroblast | - |
Homo sapiens | - |
2.4.1.267 | MI8-5 CHO cell | CHO cell line | Cricetulus griseus | - |
EC Number | General Information | Comment | Organism |
---|---|---|---|
2.4.1.267 | physiological function | ALG6 deficient MI8-5 cells express 2fold lower levels of oligosaccharyltransferase STT3B than the parental Chinese hamster ovary cells. The combination of reduced expression of STT3B and the lack of the optimal Dol-PP-GlcNAc2Man9Glc3 donor synergize to cause very severe hypoglycosylation of proteins in MI8-5 cells | Cricetulus griseus |
2.4.1.267 | physiological function | fibroblasts from an ALG6-congenital disorders of glycosylation patient that carries the A333V mutation on the maternal ALG6 allele and the S308R and Y131H mutations on the paternal ALG6 allele assemble Dol-PP-GlcNAc2Man9 as the largest oligosaccharide donor. 3040% of oligosaccharyltransferase STT3A-dependent glycosylation sites and 20% of oligosaccharyltransferase STT3B-dependent sites are skipped in ALG6-congenital disorders of glycosylation fibroblasts | Homo sapiens |