PubMed:26206502
Annnotations
CL-cell
| Id | Subject | Object | Predicate | Lexical cue | cl_id |
|---|---|---|---|---|---|
| T1 | 187-203 | Cell | denotes | eukaryotic cells | http://purl.obolibrary.org/obo/CL:0000255 |
| T2 | 869-890 | Cell | denotes | embryonic fibroblasts | http://purl.obolibrary.org/obo/CL:2000042 |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-134 | Sentence | denotes | Cytosolic-free oligosaccharides are predominantly generated by the degradation of dolichol-linked oligosaccharides in mammalian cells. |
| TextSentencer_T2 | 135-281 | Sentence | denotes | During asparagine (N)-linked protein glycosylation, eukaryotic cells generate considerable amounts of free oligosaccharides (fOSs) in the cytosol. |
| TextSentencer_T3 | 282-580 | Sentence | denotes | It is generally assumed that such fOSs are produced by the deglycosylation of misfolded N-glycoproteins that are destined for proteasomal degradation or as the result of the degradation of dolichol-linked oligosaccharides (DLOs), which serve as glycan donor substrates in N-glycosylation reactions. |
| TextSentencer_T4 | 581-785 | Sentence | denotes | The findings reported herein show that the majority of cytosolic fOSs are generated by a peptide:N-glycanase (PNGase) and an endo-β-N-acetylglucosaminidase (ENGase)-independent pathway in mammalian cells. |
| TextSentencer_T5 | 786-951 | Sentence | denotes | The ablation of the cytosolic deglycosylating enzymes, PNGase and ENGase, in mouse embryonic fibroblasts had little effect on the amount of cytosolic fOSs generated. |
| TextSentencer_T6 | 952-1179 | Sentence | denotes | Quantitative analyses of fOSs using digitonin-permeabilized cells revealed that they are generated by the degradation of fully assembled Glc3Man9GlcNAc2-pyrophosphate-dolichol (PP-Dol) in the lumen of the endoplasmic reticulum. |
| TextSentencer_T7 | 1180-1502 | Sentence | denotes | Because the degradation of Glc3Man9GlcNAc2-PP-Dol is greatly inhibited in the presence of an N-glycosylation acceptor peptide that is recognized by the oligosaccharyltransferase (OST), the OST-mediated hydrolysis of DLO is the most likely mechanism responsible for the production of a large fraction of the cytosolic fOSs. |
| T1 | 0-134 | Sentence | denotes | Cytosolic-free oligosaccharides are predominantly generated by the degradation of dolichol-linked oligosaccharides in mammalian cells. |
| T2 | 135-281 | Sentence | denotes | During asparagine (N)-linked protein glycosylation, eukaryotic cells generate considerable amounts of free oligosaccharides (fOSs) in the cytosol. |
| T3 | 282-580 | Sentence | denotes | It is generally assumed that such fOSs are produced by the deglycosylation of misfolded N-glycoproteins that are destined for proteasomal degradation or as the result of the degradation of dolichol-linked oligosaccharides (DLOs), which serve as glycan donor substrates in N-glycosylation reactions. |
| T4 | 581-785 | Sentence | denotes | The findings reported herein show that the majority of cytosolic fOSs are generated by a peptide:N-glycanase (PNGase) and an endo-β-N-acetylglucosaminidase (ENGase)-independent pathway in mammalian cells. |
| T5 | 786-951 | Sentence | denotes | The ablation of the cytosolic deglycosylating enzymes, PNGase and ENGase, in mouse embryonic fibroblasts had little effect on the amount of cytosolic fOSs generated. |
| T6 | 952-1179 | Sentence | denotes | Quantitative analyses of fOSs using digitonin-permeabilized cells revealed that they are generated by the degradation of fully assembled Glc3Man9GlcNAc2-pyrophosphate-dolichol (PP-Dol) in the lumen of the endoplasmic reticulum. |
| T7 | 1180-1502 | Sentence | denotes | Because the degradation of Glc3Man9GlcNAc2-PP-Dol is greatly inhibited in the presence of an N-glycosylation acceptor peptide that is recognized by the oligosaccharyltransferase (OST), the OST-mediated hydrolysis of DLO is the most likely mechanism responsible for the production of a large fraction of the cytosolic fOSs. |
| T1 | 0-134 | Sentence | denotes | Cytosolic-free oligosaccharides are predominantly generated by the degradation of dolichol-linked oligosaccharides in mammalian cells. |
| T2 | 135-281 | Sentence | denotes | During asparagine (N)-linked protein glycosylation, eukaryotic cells generate considerable amounts of free oligosaccharides (fOSs) in the cytosol. |
| T3 | 282-580 | Sentence | denotes | It is generally assumed that such fOSs are produced by the deglycosylation of misfolded N-glycoproteins that are destined for proteasomal degradation or as the result of the degradation of dolichol-linked oligosaccharides (DLOs), which serve as glycan donor substrates in N-glycosylation reactions. |
| T4 | 581-785 | Sentence | denotes | The findings reported herein show that the majority of cytosolic fOSs are generated by a peptide:N-glycanase (PNGase) and an endo-β-N-acetylglucosaminidase (ENGase)-independent pathway in mammalian cells. |
| T5 | 786-951 | Sentence | denotes | The ablation of the cytosolic deglycosylating enzymes, PNGase and ENGase, in mouse embryonic fibroblasts had little effect on the amount of cytosolic fOSs generated. |
| T6 | 952-1179 | Sentence | denotes | Quantitative analyses of fOSs using digitonin-permeabilized cells revealed that they are generated by the degradation of fully assembled Glc3Man9GlcNAc2-pyrophosphate-dolichol (PP-Dol) in the lumen of the endoplasmic reticulum. |
| T7 | 1180-1502 | Sentence | denotes | Because the degradation of Glc3Man9GlcNAc2-PP-Dol is greatly inhibited in the presence of an N-glycosylation acceptor peptide that is recognized by the oligosaccharyltransferase (OST), the OST-mediated hydrolysis of DLO is the most likely mechanism responsible for the production of a large fraction of the cytosolic fOSs. |
GlycoBiology-FMA
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T1 | 15-31 | FMAID:196731 | denotes | oligosaccharides |
| _T2 | 15-31 | FMAID:82742 | denotes | oligosaccharides |
| _T3 | 98-114 | FMAID:196731 | denotes | oligosaccharides |
| _T4 | 98-114 | FMAID:82742 | denotes | oligosaccharides |
| _T5 | 128-133 | FMAID:169002 | denotes | cells |
| _T6 | 128-133 | FMAID:68646 | denotes | cells |
| _T7 | 142-152 | FMAID:196739 | denotes | asparagine |
| _T8 | 142-152 | FMAID:82750 | denotes | asparagine |
| _T9 | 164-171 | FMAID:67257 | denotes | protein |
| _T10 | 164-171 | FMAID:165447 | denotes | protein |
| _T11 | 198-203 | FMAID:68646 | denotes | cells |
| _T12 | 198-203 | FMAID:169002 | denotes | cells |
| _T13 | 242-258 | FMAID:196731 | denotes | oligosaccharides |
| _T14 | 242-258 | FMAID:82742 | denotes | oligosaccharides |
| _T15 | 273-280 | FMAID:256055 | denotes | cytosol |
| _T16 | 372-385 | FMAID:167256 | denotes | glycoproteins |
| _T17 | 372-385 | FMAID:62925 | denotes | glycoproteins |
| _T18 | 487-503 | FMAID:196731 | denotes | oligosaccharides |
| _T19 | 487-503 | FMAID:82742 | denotes | oligosaccharides |
| _T20 | 713-736 | FMAID:82787 | denotes | N-acetylglucosaminidase |
| _T21 | 713-736 | FMAID:196781 | denotes | N-acetylglucosaminidase |
| _T22 | 779-784 | FMAID:169002 | denotes | cells |
| _T23 | 779-784 | FMAID:68646 | denotes | cells |
| _T24 | 879-890 | FMAID:63877 | denotes | fibroblasts |
| _T25 | 879-890 | FMAID:162340 | denotes | fibroblasts |
| _T26 | 1012-1017 | FMAID:169002 | denotes | cells |
| _T27 | 1012-1017 | FMAID:68646 | denotes | cells |
| _T28 | 1144-1178 | FMAID:199160 | denotes | lumen of the endoplasmic reticulum |
| _T29 | 1144-1178 | FMAID:67672 | denotes | lumen of the endoplasmic reticulum |
| _T30 | 1144-1178 | FMAID:165580 | denotes | lumen of the endoplasmic reticulum |
| _T31 | 1144-1178 | FMAID:199094 | denotes | lumen of the endoplasmic reticulum |
| _T32 | 1144-1178 | FMAID:165060 | denotes | lumen of the endoplasmic reticulum |
| _T33 | 1144-1178 | FMAID:199158 | denotes | lumen of the endoplasmic reticulum |
| _T34 | 1157-1168 | FMAID:66856 | denotes | endoplasmic |
| _T35 | 1157-1168 | FMAID:165003 | denotes | endoplasmic |
| _T36 | 1157-1178 | FMAID:165250 | denotes | endoplasmic reticulum |
| _T37 | 1157-1178 | FMAID:165144 | denotes | endoplasmic reticulum |
| _T38 | 1157-1178 | FMAID:210694 | denotes | endoplasmic reticulum |
| _T39 | 1157-1178 | FMAID:211269 | denotes | endoplasmic reticulum |
| _T40 | 1157-1178 | FMAID:199093 | denotes | endoplasmic reticulum |
| _T41 | 1157-1178 | FMAID:67429 | denotes | endoplasmic reticulum |
| _T42 | 1157-1178 | FMAID:165142 | denotes | endoplasmic reticulum |
| _T43 | 1157-1178 | FMAID:212510 | denotes | endoplasmic reticulum |
| _T44 | 1157-1178 | FMAID:63842 | denotes | endoplasmic reticulum |
| _T45 | 1157-1178 | FMAID:162308 | denotes | endoplasmic reticulum |
| _T46 | 1157-1178 | FMAID:67434 | denotes | endoplasmic reticulum |
| _T47 | 1157-1178 | FMAID:165026 | denotes | endoplasmic reticulum |
| _T48 | 1157-1178 | FMAID:67438 | denotes | endoplasmic reticulum |
| _T49 | 1157-1178 | FMAID:210679 | denotes | endoplasmic reticulum |
| _T50 | 1157-1178 | FMAID:80351 | denotes | endoplasmic reticulum |
| _T51 | 1157-1178 | FMAID:188464 | denotes | endoplasmic reticulum |
| _T52 | 1157-1178 | FMAID:165027 | denotes | endoplasmic reticulum |
| _T53 | 1157-1178 | FMAID:66898 | denotes | endoplasmic reticulum |
| _T54 | 1157-1178 | FMAID:66897 | denotes | endoplasmic reticulum |
| _T55 | 1157-1178 | FMAID:165141 | denotes | endoplasmic reticulum |
| _T56 | 1169-1178 | FMAID:7646 | denotes | reticulum |
| _T57 | 1169-1178 | FMAID:94520 | denotes | reticulum |
uniprot-human
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 670-689 | http://www.uniprot.org/uniprot/Q96IV0 | denotes | peptide:N-glycanase |
| T2 | 691-697 | http://www.uniprot.org/uniprot/Q96IV0 | denotes | PNGase |
| T3 | 841-847 | http://www.uniprot.org/uniprot/Q96IV0 | denotes | PNGase |
| T4 | 711-736 | http://www.uniprot.org/uniprot/Q9HAR0 | denotes | β-N-acetylglucosaminidase |
| T5 | 738-744 | http://www.uniprot.org/uniprot/Q8NFI3 | denotes | ENGase |
| T6 | 852-858 | http://www.uniprot.org/uniprot/Q8NFI3 | denotes | ENGase |
| T7 | 1129-1131 | http://www.uniprot.org/uniprot/Q15181 | denotes | PP |
| T8 | 1223-1225 | http://www.uniprot.org/uniprot/Q15181 | denotes | PP |
| T9 | 1129-1131 | http://www.uniprot.org/uniprot/P01298 | denotes | PP |
| T10 | 1223-1225 | http://www.uniprot.org/uniprot/P01298 | denotes | PP |
uniprot-mouse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 670-689 | http://www.uniprot.org/uniprot/Q9JI78 | denotes | peptide:N-glycanase |
| T2 | 691-697 | http://www.uniprot.org/uniprot/Q9JI78 | denotes | PNGase |
| T3 | 841-847 | http://www.uniprot.org/uniprot/Q9JI78 | denotes | PNGase |
| T4 | 738-744 | http://www.uniprot.org/uniprot/Q8BX80 | denotes | ENGase |
| T5 | 852-858 | http://www.uniprot.org/uniprot/Q8BX80 | denotes | ENGase |
| T6 | 1129-1131 | http://www.uniprot.org/uniprot/P10601 | denotes | PP |
| T7 | 1223-1225 | http://www.uniprot.org/uniprot/P10601 | denotes | PP |
GlycoBiology-NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 128-133 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
| T2 | 187-197 | http://purl.bioontology.org/ontology/NCBITAXON/2759 | denotes | eukaryotic |
| T3 | 198-203 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
| T4 | 585-593 | http://purl.bioontology.org/ontology/STY/T033 | denotes | findings |
| T5 | 779-784 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
| T6 | 1012-1017 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
| T7 | 1419-1428 | http://purl.bioontology.org/ontology/NCBITAXON/127244 | denotes | mechanism |
GO-BP
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 67-78 | http://purl.obolibrary.org/obo/GO_0009056 | denotes | degradation |
| T2 | 420-431 | http://purl.obolibrary.org/obo/GO_0009056 | denotes | degradation |
| T3 | 456-467 | http://purl.obolibrary.org/obo/GO_0009056 | denotes | degradation |
| T4 | 1058-1069 | http://purl.obolibrary.org/obo/GO_0009056 | denotes | degradation |
| T5 | 1192-1203 | http://purl.obolibrary.org/obo/GO_0009056 | denotes | degradation |
| T6 | 164-185 | http://purl.obolibrary.org/obo/GO_0006486 | denotes | protein glycosylation |
| T7 | 172-185 | http://purl.obolibrary.org/obo/GO_0070085 | denotes | glycosylation |
| T8 | 556-569 | http://purl.obolibrary.org/obo/GO_0070085 | denotes | glycosylation |
| T9 | 1275-1288 | http://purl.obolibrary.org/obo/GO_0070085 | denotes | glycosylation |
| T10 | 408-431 | http://purl.obolibrary.org/obo/GO_1903009 | denotes | proteasomal degradation |
| T11 | 670-689 | http://purl.obolibrary.org/obo/GO_0000224 | denotes | peptide:N-glycanase |
| T12 | 691-697 | http://purl.obolibrary.org/obo/GO_0000224 | denotes | PNGase |
| T13 | 841-847 | http://purl.obolibrary.org/obo/GO_0000224 | denotes | PNGase |
GO-CC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-9 | http://purl.obolibrary.org/obo/GO_0005829 | denotes | Cytosolic |
| T2 | 273-280 | http://purl.obolibrary.org/obo/GO_0005829 | denotes | cytosol |
| T3 | 636-645 | http://purl.obolibrary.org/obo/GO_0005829 | denotes | cytosolic |
| T4 | 806-815 | http://purl.obolibrary.org/obo/GO_0005829 | denotes | cytosolic |
| T5 | 926-935 | http://purl.obolibrary.org/obo/GO_0005829 | denotes | cytosolic |
| T6 | 1487-1496 | http://purl.obolibrary.org/obo/GO_0005829 | denotes | cytosolic |
| T7 | 128-133 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
| T8 | 198-203 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
| T9 | 779-784 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
| T10 | 1012-1017 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
| T11 | 408-419 | http://purl.obolibrary.org/obo/GO_0000502 | denotes | proteasomal |
| T12 | 1144-1178 | http://purl.obolibrary.org/obo/GO_0048238 | denotes | lumen of the endoplasmic reticulum |
| T13 | 1144-1178 | http://purl.obolibrary.org/obo/GO_0044166 | denotes | lumen of the endoplasmic reticulum |
| T14 | 1144-1178 | http://purl.obolibrary.org/obo/GO_0005788 | denotes | lumen of the endoplasmic reticulum |
| T15 | 1144-1178 | http://purl.obolibrary.org/obo/GO_0048237 | denotes | lumen of the endoplasmic reticulum |
| T16 | 1157-1178 | http://purl.obolibrary.org/obo/GO_0005783 | denotes | endoplasmic reticulum |
NGLY1-deficiency
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-NGLY1-deficiency-B_T1 | 691-697 | hgnc:17646 | denotes | PNGase |
| PD-NGLY1-deficiency-B_T2 | 841-847 | hgnc:17646 | denotes | PNGase |
| PD-NGLY1-deficiency-B_T3 | 738-744 | hgnc:24622 | denotes | ENGase |
| PD-NGLY1-deficiency-B_T4 | 852-858 | hgnc:24622 | denotes | ENGase |
GlycoGenes
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-GlycoGenes-B_T1 | 1465-1470 | GGDB:LARGE | denotes | large |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 863-868 | OrganismTaxon | denotes | mouse | 10088|10090 |
Anatomy-UBERON
| Id | Subject | Object | Predicate | Lexical cue | uberon_id |
|---|---|---|---|---|---|
| T1 | 187-203 | Body_part | denotes | eukaryotic cells | http://purl.obolibrary.org/obo/CL_0000255 |
| T2 | 273-280 | Body_part | denotes | cytosol | http://purl.obolibrary.org/obo/GO_0005829 |
| T3 | 869-890 | Body_part | denotes | embryonic fibroblasts | http://purl.obolibrary.org/obo/CL_2000042 |
| T4 | 1144-1149 | Body_part | denotes | lumen | http://purl.obolibrary.org/obo/UBERON_0000464 |
| T5 | 1169-1178 | Body_part | denotes | reticulum | http://purl.obolibrary.org/obo/UBERON_0007361 |