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. 2016 Jan 6;6(1):8. doi: 10.3390/biom6010008

Table 1.

Potentially O-glycosylated proteins which were highly modified with GlcA after overexpression of dGlcAT-P in S2-cells. Proteins within a mass range of 60–70 kDa were intensively stained by mAb 114-2G11-A and therefore excised from an SDS-gel and identified by LC-ESI-MS/MS (experiment “gel”) The same lysates was immunoprecipitated with mAb 114-2G11-A and identified likewise (experiment “IP”). (ER: endoplasmatic reticulum, EC: extracellular, N: nucleus, CP: cytoplasm, MI: mitochondrium, MT: microtubule, M: membrane).

Protein Identified in Experiment IP (+/−) Reported Localization Accession No. (NCBI)
calnexin + M, ER gi|2213427
CD98 heavy chain + M gi|17945866
CG2918, HSP70 family +/− EC, M gi|20128923
ERp60 +/− ER gi|45551086
glycoprotein 93 +/− EC gi|21357739
heat shock protein 60 +/− MI gi|33636453
heat shock protein 83 +/− CP gi|17647529
heat shock protein cognate 1 MT gi|17647515
heat shock protein cognate 4 +/− N, CP, EC gi|17737967
heat shock protein cognate 71 +/− ER gi|157667
heat shock protein cognate 72 +/− ER, EC gi|157658
Hexosaminidase 2 + M, EC gi|17933586
Inos +/− CP gi|17137626
oligosaccharide transferase + M gi|19922486
peptidase S28 + EC, M gi|20129649
protein disulfide isomerase +/− ER, EC gi|17647799
Scavenger receptor class C + M gi|984515
Ugt58Fa glycosyltransferase + M gi|22024248
Ugt86Da glycosyltransferase + M gi|21357701
vacuolar H[+]-ATPase + M, CP gi|17136796

Proteins were identified prior to IP (−), after IP (+) or in both experimental settings (+/−).