EC Number   |
Posttranslational Modification |
Reference |
|---|
   3.1.4.38 | glycoprotein |
truncated high mannose and bisected hybrid type glycans are linked to N118 and N341 of the soluble isozyme sGPC-Cpde, a hallmark of glycans in lysosomal glycoproteins, subjected to GlcNAc-1-phosphorylation en route through the Golgi apparatus. All the four N-glycosylation sites N100KS, N118GS, N341ST and N406GS in the soluble isozyme sGPC-Cpde are occupied, mainly with endo H-sensitive glycans, QTOF-MS-MS analysis |
-, 730472 |
| 3.1.4.38 | phosphoprotein |
truncated high mannose and bisected hybrid type glycans are linked to N118 and N341 of the soluble isozyme sGPC-Cpde, a hallmark of glycans in lysosomal glycoproteins, subjected to GlcNAc-1-phosphorylation en route through the Golgi apparatus |
-, 730472 |
| 3.1.4.38 | proteolytic modification |
two forms of brain GPC-Cpde, a membrane-linked, mGPC-Cpde, and a soluble, sGPC-Cpde. The enzyme is solubilised by C-terminal proteolysis, releasing the GPI-anchor, the resulting soluble isozyme sGPCCpde exists as two conformations, a homodimer joined by a disulfide bridge linking C414 from each monomer, and a monomer resulting from proteolysis N-terminally to this disulfide bond |
-, 730472 |
