EC Number | Application | Comment | Organism |
---|---|---|---|
2.4.1.83 | medicine | D-P-M enzyme activity represents a potentially useful approach to address the problem of porcine endogenous retrovirus infections in clinical xenotransplantations | Sus scrofa |
EC Number | Cloned (Comment) | Organism |
---|---|---|
2.4.1.83 | cDNA fragments containing the start and stop codons amplified and subcloned into the EcoRV site of the pBluescript II SK(-) cloning vector | Sus scrofa |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.4.1.83 | Sus scrofa | - |
- |
- |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
2.4.1.83 | liver | - |
Sus scrofa | - |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
2.4.1.83 | D-P-M | - |
Sus scrofa |
2.4.1.83 | dolichyl-phosphate mannosyltransferase | - |
Sus scrofa |
EC Number | Organism | Comment | Expression |
---|---|---|---|
2.4.1.83 | Sus scrofa | compared with the mock line, the temporary PEC(Z)/PB lines show a decreased mRNA expression for D-P-M and a clear destruction of porcine endogenous retrovirus infectivity to human cells in the Lac Z pseudotype assay. Compared with parental and mock cells, all PEC(Z)/PB cells transfected with siRNA show a decreased mRNA expression for the D-P-M by one-fifth | down |