PubMed:11479274
Annnotations
Glycosmos6-MAT
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 568-574 | http://purl.obolibrary.org/obo/MAT_0000490 | denotes | medial |
GlycoBiology-FMA
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T1 | 28-43 | FMAID:162311 | denotes | Golgi apparatus |
| _T2 | 229-231 | FMAID:169149 | denotes | A1 |
| _T3 | 261-266 | FMAID:68646 | denotes | cells |
| _T4 | 261-266 | FMAID:169002 | denotes | cells |
| _T5 | 551-562 | FMAID:67103 | denotes | Golgi stack |
| _T6 | 551-562 | FMAID:165050 | denotes | Golgi stack |
| _T7 | 568-574 | FMAID:171165 | denotes | medial |
| _T8 | 568-574 | FMAID:49444 | denotes | medial |
| _T9 | 847-856 | FMAID:165070 | denotes | endosomal |
| _T10 | 847-856 | FMAID:67180 | denotes | endosomal |
| _T11 | 883-885 | FMAID:169149 | denotes | A1 |
| _T12 | 898-910 | FMAID:200942 | denotes | cell surface |
| _T13 | 898-910 | FMAID:212684 | denotes | cell surface |
| _T14 | 903-910 | FMAID:146300 | denotes | surface |
| _T15 | 903-910 | FMAID:50594 | denotes | surface |
| _T16 | 951-962 | FMAID:66856 | denotes | endoplasmic |
| _T17 | 951-962 | FMAID:165003 | denotes | endoplasmic |
| _T18 | 951-972 | FMAID:210679 | denotes | endoplasmic reticulum |
| _T19 | 951-972 | FMAID:165144 | denotes | endoplasmic reticulum |
| _T20 | 951-972 | FMAID:165141 | denotes | endoplasmic reticulum |
| _T21 | 951-972 | FMAID:67434 | denotes | endoplasmic reticulum |
| _T22 | 951-972 | FMAID:67438 | denotes | endoplasmic reticulum |
| _T23 | 951-972 | FMAID:165142 | denotes | endoplasmic reticulum |
| _T24 | 951-972 | FMAID:210694 | denotes | endoplasmic reticulum |
| _T25 | 951-972 | FMAID:211269 | denotes | endoplasmic reticulum |
| _T26 | 951-972 | FMAID:199093 | denotes | endoplasmic reticulum |
| _T27 | 951-972 | FMAID:80351 | denotes | endoplasmic reticulum |
| _T28 | 951-972 | FMAID:67429 | denotes | endoplasmic reticulum |
| _T29 | 951-972 | FMAID:188464 | denotes | endoplasmic reticulum |
| _T30 | 951-972 | FMAID:165026 | denotes | endoplasmic reticulum |
| _T31 | 951-972 | FMAID:165250 | denotes | endoplasmic reticulum |
| _T32 | 951-972 | FMAID:212510 | denotes | endoplasmic reticulum |
| _T33 | 951-972 | FMAID:165027 | denotes | endoplasmic reticulum |
| _T34 | 951-972 | FMAID:63842 | denotes | endoplasmic reticulum |
| _T35 | 951-972 | FMAID:66897 | denotes | endoplasmic reticulum |
| _T36 | 951-972 | FMAID:66898 | denotes | endoplasmic reticulum |
| _T37 | 951-972 | FMAID:162308 | denotes | endoplasmic reticulum |
| _T38 | 963-972 | FMAID:94520 | denotes | reticulum |
| _T39 | 963-972 | FMAID:7646 | denotes | reticulum |
| _T40 | 977-992 | FMAID:162311 | denotes | Golgi apparatus |
| _T41 | 1166-1171 | FMAID:68646 | denotes | cells |
| _T42 | 1166-1171 | FMAID:169002 | denotes | cells |
| _T43 | 1189-1192 | FMAID:85816 | denotes | gas |
| _T44 | 1368-1383 | FMAID:82742 | denotes | oligosaccharide |
| _T45 | 1368-1383 | FMAID:196731 | denotes | oligosaccharide |
| _T46 | 1539-1554 | FMAID:162311 | denotes | Golgi apparatus |
uniprot-human
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 195-206 | http://www.uniprot.org/uniprot/P20648 | denotes | proton pump |
| T2 | 195-206 | http://www.uniprot.org/uniprot/P54707 | denotes | proton pump |
| T3 | 408-443 | http://www.uniprot.org/uniprot/Q10471 | denotes | N-acetylgalactosaminyltransferase 2 |
| T4 | 408-443 | http://www.uniprot.org/uniprot/Q8IZ52 | denotes | N-acetylgalactosaminyltransferase 2 |
| T5 | 453-484 | http://www.uniprot.org/uniprot/Q06430 | denotes | N-acetylglucosaminyltransferase |
| T6 | 453-484 | http://www.uniprot.org/uniprot/Q8N0V5 | denotes | N-acetylglucosaminyltransferase |
| T7 | 453-484 | http://www.uniprot.org/uniprot/Q8NFS9 | denotes | N-acetylglucosaminyltransferase |
uniprot-mouse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 195-206 | http://www.uniprot.org/uniprot/Q64436 | denotes | proton pump |
| T2 | 195-206 | http://www.uniprot.org/uniprot/Q9Z1W8 | denotes | proton pump |
| T3 | 229-231 | http://www.uniprot.org/uniprot/Q07440 | denotes | A1 |
| T4 | 883-885 | http://www.uniprot.org/uniprot/Q07440 | denotes | A1 |
| T5 | 408-443 | http://www.uniprot.org/uniprot/Q6IQX7 | denotes | N-acetylgalactosaminyltransferase 2 |
| T6 | 453-484 | http://www.uniprot.org/uniprot/P97402 | denotes | N-acetylglucosaminyltransferase |
| T7 | 500-521 | http://www.uniprot.org/uniprot/P23336 | denotes | galactosyltransferase |
GlycoBiology-NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 195-201 | http://purl.bioontology.org/ontology/NCBITAXON/429025 | denotes | proton |
| T2 | 261-266 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
| T3 | 1044-1052 | http://purl.bioontology.org/ontology/NCBITAXON/68518 | denotes | electron |
| T4 | 1166-1171 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
| T5 | 1292-1296 | http://purl.bioontology.org/ontology/NCBITAXON/82391 | denotes | days |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-135 | Sentence | denotes | Neutralization of pH in the Golgi apparatus causes redistribution of glycosyltransferases and changes in the O-glycosylation of mucins. |
| TextSentencer_T2 | 136-332 | Sentence | denotes | Addition of the weak base ammonium chloride (NH4Cl) or the proton pump inhibitor bafilomycin A1 to cultured HeLa and LS 174T cells effectively neutralized the pH gradient of the secretory pathway. |
| TextSentencer_T3 | 333-625 | Sentence | denotes | This resulted in relocalization of the three studied glycosyltransferases, N-acetylgalactosaminyltransferase 2, beta1,2 N-acetylglucosaminyltransferase I, and beta1,4 galactosyltransferase 1, normally localized to the Golgi stack, the medial/trans-Golgi and the trans-Golgi/TGN, respectively. |
| TextSentencer_T4 | 626-920 | Sentence | denotes | Indirect immunofluorescence microscopy, immunoelectron microscopy, and subcellular fractionation of the tagged or native glycosyltransferases showed that NH4Cl caused a relocalization of the enzymes mainly to vesicles of endosomal type, whereas bafilomycin A1 gave mainly cell surface staining. |
| TextSentencer_T5 | 921-1072 | Sentence | denotes | The general morphology of the endoplasmic reticulum and Golgi apparatus was retained as judged from immunofluorescence and electron microscopy studies. |
| TextSentencer_T6 | 1073-1329 | Sentence | denotes | When the O-glycans on the guanidinium chloride insoluble gel-forming mucins from the LS 174T cells were analyzed by gas chromatography-mass spectrometry after neutralization of the secretory pathway pH by NH4Cl over 10 days shorter O-glycans were observed. |
| TextSentencer_T7 | 1330-1405 | Sentence | denotes | However, no decrease in the number of oligosaccharide chains was indicated. |
| TextSentencer_T8 | 1406-1671 | Sentence | denotes | Together, the results suggest that pH is a contributing factor for proper steady-state distribution of glycosyltransferases over the Golgi apparatus and that altered pH may cause alterations in glycosylation possibly due to a relocalization of glycosyltransferases. |
| T1 | 0-135 | Sentence | denotes | Neutralization of pH in the Golgi apparatus causes redistribution of glycosyltransferases and changes in the O-glycosylation of mucins. |
| T2 | 136-332 | Sentence | denotes | Addition of the weak base ammonium chloride (NH4Cl) or the proton pump inhibitor bafilomycin A1 to cultured HeLa and LS 174T cells effectively neutralized the pH gradient of the secretory pathway. |
| T3 | 333-625 | Sentence | denotes | This resulted in relocalization of the three studied glycosyltransferases, N-acetylgalactosaminyltransferase 2, beta1,2 N-acetylglucosaminyltransferase I, and beta1,4 galactosyltransferase 1, normally localized to the Golgi stack, the medial/trans-Golgi and the trans-Golgi/TGN, respectively. |
| T4 | 626-920 | Sentence | denotes | Indirect immunofluorescence microscopy, immunoelectron microscopy, and subcellular fractionation of the tagged or native glycosyltransferases showed that NH4Cl caused a relocalization of the enzymes mainly to vesicles of endosomal type, whereas bafilomycin A1 gave mainly cell surface staining. |
| T5 | 921-1072 | Sentence | denotes | The general morphology of the endoplasmic reticulum and Golgi apparatus was retained as judged from immunofluorescence and electron microscopy studies. |
| T6 | 1073-1329 | Sentence | denotes | When the O-glycans on the guanidinium chloride insoluble gel-forming mucins from the LS 174T cells were analyzed by gas chromatography-mass spectrometry after neutralization of the secretory pathway pH by NH4Cl over 10 days shorter O-glycans were observed. |
| T7 | 1330-1405 | Sentence | denotes | However, no decrease in the number of oligosaccharide chains was indicated. |
| T8 | 1406-1671 | Sentence | denotes | Together, the results suggest that pH is a contributing factor for proper steady-state distribution of glycosyltransferases over the Golgi apparatus and that altered pH may cause alterations in glycosylation possibly due to a relocalization of glycosyltransferases. |
| T1 | 0-135 | Sentence | denotes | Neutralization of pH in the Golgi apparatus causes redistribution of glycosyltransferases and changes in the O-glycosylation of mucins. |
| T2 | 136-332 | Sentence | denotes | Addition of the weak base ammonium chloride (NH4Cl) or the proton pump inhibitor bafilomycin A1 to cultured HeLa and LS 174T cells effectively neutralized the pH gradient of the secretory pathway. |
| T3 | 333-625 | Sentence | denotes | This resulted in relocalization of the three studied glycosyltransferases, N-acetylgalactosaminyltransferase 2, beta1,2 N-acetylglucosaminyltransferase I, and beta1,4 galactosyltransferase 1, normally localized to the Golgi stack, the medial/trans-Golgi and the trans-Golgi/TGN, respectively. |
| T4 | 626-920 | Sentence | denotes | Indirect immunofluorescence microscopy, immunoelectron microscopy, and subcellular fractionation of the tagged or native glycosyltransferases showed that NH4Cl caused a relocalization of the enzymes mainly to vesicles of endosomal type, whereas bafilomycin A1 gave mainly cell surface staining. |
| T5 | 921-1072 | Sentence | denotes | The general morphology of the endoplasmic reticulum and Golgi apparatus was retained as judged from immunofluorescence and electron microscopy studies. |
| T6 | 1073-1329 | Sentence | denotes | When the O-glycans on the guanidinium chloride insoluble gel-forming mucins from the LS 174T cells were analyzed by gas chromatography-mass spectrometry after neutralization of the secretory pathway pH by NH4Cl over 10 days shorter O-glycans were observed. |
| T7 | 1330-1405 | Sentence | denotes | However, no decrease in the number of oligosaccharide chains was indicated. |
| T8 | 1406-1671 | Sentence | denotes | Together, the results suggest that pH is a contributing factor for proper steady-state distribution of glycosyltransferases over the Golgi apparatus and that altered pH may cause alterations in glycosylation possibly due to a relocalization of glycosyltransferases. |
GO-BP
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 111-124 | http://purl.obolibrary.org/obo/GO_0070085 | denotes | glycosylation |
| T2 | 1600-1613 | http://purl.obolibrary.org/obo/GO_0070085 | denotes | glycosylation |
| T3 | 253-255 | http://purl.obolibrary.org/obo/GO_0016992 | denotes | LS |
| T4 | 1158-1160 | http://purl.obolibrary.org/obo/GO_0016992 | denotes | LS |
| T5 | 453-486 | http://purl.obolibrary.org/obo/GO_0003827 | denotes | N-acetylglucosaminyltransferase I |
| T6 | 534-543 | http://purl.obolibrary.org/obo/GO_0051179 | denotes | localized |
| T7 | 534-556 | http://purl.obolibrary.org/obo/GO_0051645 | denotes | localized to the Golgi |
| T8 | 933-972 | http://purl.obolibrary.org/obo/GO_0007029 | denotes | morphology of the endoplasmic reticulum |
| T9 | 951-982 | http://purl.obolibrary.org/obo/GO_0006888 | denotes | endoplasmic reticulum and Golgi |
| T10 | 1189-1192 | http://purl.obolibrary.org/obo/GO_0034005 | denotes | gas |
GO-CC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 28-33 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi |
| T2 | 551-556 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi |
| T3 | 581-586 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi |
| T4 | 601-606 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi |
| T5 | 977-982 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi |
| T6 | 1539-1544 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi |
| T7 | 28-43 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi apparatus |
| T8 | 977-992 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi apparatus |
| T9 | 1539-1554 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi apparatus |
| T10 | 195-206 | http://purl.obolibrary.org/obo/GO_0005889 | denotes | proton pump |
| T11 | 261-266 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
| T12 | 898-902 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
| T13 | 551-562 | http://purl.obolibrary.org/obo/GO_0005795 | denotes | Golgi stack |
| T14 | 607-610 | http://purl.obolibrary.org/obo/GO_0005802 | denotes | TGN |
| T15 | 835-843 | http://purl.obolibrary.org/obo/GO_0031982 | denotes | vesicles |
| T16 | 847-856 | http://purl.obolibrary.org/obo/GO_0005768 | denotes | endosomal |
| T17 | 898-910 | http://purl.obolibrary.org/obo/GO_0009986 | denotes | cell surface |
| T18 | 951-972 | http://purl.obolibrary.org/obo/GO_0005783 | denotes | endoplasmic reticulum |
UBERON-AE
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 568-574 | http://purl.obolibrary.org/obo/UBERON_3010194 | denotes | medial |
EDAM-topics
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 28-43 | http://edamontology.org/topic_0616 | denotes | Golgi apparatus |
| T2 | 324-331 | http://edamontology.org/topic_0602 | denotes | pathway |
| T3 | 378-385 | http://edamontology.org/topic_3678 | denotes | studied |
| T4 | 654-664 | http://edamontology.org/topic_3382 | denotes | microscopy |
| T5 | 654-691 | http://edamontology.org/topic_0611 | denotes | microscopy, immunoelectron microscopy |
| T6 | 666-691 | http://edamontology.org/topic_0611 | denotes | immunoelectron microscopy |
| T7 | 681-691 | http://edamontology.org/topic_3382 | denotes | microscopy |
| T8 | 951-972 | http://edamontology.org/topic_0616 | denotes | endoplasmic reticulum |
| T9 | 977-992 | http://edamontology.org/topic_0616 | denotes | Golgi apparatus |
| T10 | 1044-1063 | http://edamontology.org/topic_0611 | denotes | electron microscopy |
| T11 | 1053-1063 | http://edamontology.org/topic_3382 | denotes | microscopy |
| T12 | 1064-1071 | http://edamontology.org/topic_3678 | denotes | studies |
| T13 | 1208-1225 | http://edamontology.org/topic_3520 | denotes | mass spectrometry |
| T14 | 1208-1225 | http://edamontology.org/topic_0134 | denotes | mass spectrometry |
| T15 | 1264-1271 | http://edamontology.org/topic_0602 | denotes | pathway |
| T16 | 1539-1554 | http://edamontology.org/topic_0616 | denotes | Golgi apparatus |
EDAM-DFO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 18-20 | http://edamontology.org/format_1997 | denotes | pH |
| T2 | 295-297 | http://edamontology.org/format_1997 | denotes | pH |
| T3 | 324-331 | http://edamontology.org/data_2600 | denotes | pathway |
| T4 | 525-533 | http://edamontology.org/operation_3435 | denotes | normally |
| T5 | 654-691 | http://edamontology.org/data_0941 | denotes | microscopy, immunoelectron microscopy |
| T6 | 925-932 | http://edamontology.org/operation_3429 | denotes | general |
| T7 | 1044-1063 | http://edamontology.org/data_0941 | denotes | electron microscopy |
| T8 | 1208-1225 | http://edamontology.org/data_2536 | denotes | mass spectrometry |
| T9 | 1208-1225 | http://edamontology.org/data_3147 | denotes | mass spectrometry |
| T10 | 1264-1271 | http://edamontology.org/data_2600 | denotes | pathway |
| T11 | 1272-1274 | http://edamontology.org/format_1997 | denotes | pH |
| T12 | 1441-1443 | http://edamontology.org/format_1997 | denotes | pH |
| T13 | 1572-1574 | http://edamontology.org/format_1997 | denotes | pH |
GlycoBiology-MAT
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 568-574 | http://purl.obolibrary.org/obo/MAT_0000490 | denotes | medial |
performance-test
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-UBERON-AE-B_T1 | 568-574 | http://purl.obolibrary.org/obo/UBERON_3010194 | denotes | medial |
Anatomy-MAT
| Id | Subject | Object | Predicate | Lexical cue | mat_id |
|---|---|---|---|---|---|
| T1 | 568-574 | Body_part | denotes | medial | http://purl.obolibrary.org/obo/MAT_0000490 |
Anatomy-UBERON
| Id | Subject | Object | Predicate | Lexical cue | uberon_id |
|---|---|---|---|---|---|
| T1 | 28-43 | Body_part | denotes | Golgi apparatus | http://purl.obolibrary.org/obo/GO_0005794 |
| T2 | 551-556 | Body_part | denotes | Golgi | http://purl.obolibrary.org/obo/GO_0005794 |
| T3 | 581-586 | Body_part | denotes | Golgi | http://purl.obolibrary.org/obo/GO_0005794 |
| T4 | 601-606 | Body_part | denotes | Golgi | http://purl.obolibrary.org/obo/GO_0005794 |
| T5 | 963-972 | Body_part | denotes | reticulum | http://purl.obolibrary.org/obo/UBERON_0007361 |
| T6 | 977-992 | Body_part | denotes | Golgi apparatus | http://purl.obolibrary.org/obo/GO_0005794 |
| T7 | 1539-1554 | Body_part | denotes | Golgi apparatus | http://purl.obolibrary.org/obo/GO_0005794 |