PubMed:1665373
Annnotations
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-164 | Sentence | denotes | Conditional intercellular cohesion in a Dictyostelium discoideum mutant which is temperature sensitive for correct processing of asparagine-linked oligosaccharides. |
TextSentencer_T2 | 165-340 | Sentence | denotes | Mutants of Dictyostelium discoideum have been isolated by a selection for cells with temperature-sensitive defects in the maturation of glycoprotein N-linked oligosaccharides. |
TextSentencer_T3 | 341-511 | Sentence | denotes | Here we describe a mutant, HT7, which is unable to aggregate at the restrictive temperature, but which aggregates and makes fruiting bodies at the permissive temperature. |
TextSentencer_T4 | 512-713 | Sentence | denotes | HT7 shows normal early developmental intercellular cohesion, but is temperature sensitive for expression of the ethylenediamine-tetraacetic acid (EDTA)-resistant cohesion characteristic of aggregation. |
TextSentencer_T5 | 714-802 | Sentence | denotes | The mutant initiates aggregation, but forms only loose cell mounds which later disperse. |
TextSentencer_T6 | 803-1007 | Sentence | denotes | Metabolic labelling studies indicate that the thermolabile defect is not in protein synthesis, assembly of the lipid-linked precursor of N-linked oligosaccharides or transfer of the precursor to proteins. |
TextSentencer_T7 | 1008-1095 | Sentence | denotes | However, the defect does prevent assembly of fully processed N-linked oligosaccharides. |
TextSentencer_T8 | 1096-1277 | Sentence | denotes | Further, two glycopeptides, obtained from exhaustive Pronase digests of wild-type plasma membrane glycoproteins, inhibit intercellular cohesion of aggregation-stage wild-type cells. |
TextSentencer_T9 | 1278-1460 | Sentence | denotes | HT7 produces only approximately 50% of the wild-type level of these glycopeptides at the restrictive temperature and one of the glycopeptides has reduced cohesion inhibition ability. |
TextSentencer_T10 | 1461-1674 | Sentence | denotes | A revertant of HT7 was found to aggregate normally, to have restored EDTA-resistant cohesion, to have normal profiles of N-linked oligosaccharides and to express the two cohesion-inhibiting glycopeptides normally. |
TextSentencer_T11 | 1675-1852 | Sentence | denotes | These data strongly support a model in which cohesion during late aggregation is at least in part due to recognition between surface glycans and receptors on neighbouring cells. |
T1 | 0-164 | Sentence | denotes | Conditional intercellular cohesion in a Dictyostelium discoideum mutant which is temperature sensitive for correct processing of asparagine-linked oligosaccharides. |
T2 | 165-340 | Sentence | denotes | Mutants of Dictyostelium discoideum have been isolated by a selection for cells with temperature-sensitive defects in the maturation of glycoprotein N-linked oligosaccharides. |
T3 | 341-511 | Sentence | denotes | Here we describe a mutant, HT7, which is unable to aggregate at the restrictive temperature, but which aggregates and makes fruiting bodies at the permissive temperature. |
T4 | 512-713 | Sentence | denotes | HT7 shows normal early developmental intercellular cohesion, but is temperature sensitive for expression of the ethylenediamine-tetraacetic acid (EDTA)-resistant cohesion characteristic of aggregation. |
T5 | 714-802 | Sentence | denotes | The mutant initiates aggregation, but forms only loose cell mounds which later disperse. |
T6 | 803-1007 | Sentence | denotes | Metabolic labelling studies indicate that the thermolabile defect is not in protein synthesis, assembly of the lipid-linked precursor of N-linked oligosaccharides or transfer of the precursor to proteins. |
T7 | 1008-1095 | Sentence | denotes | However, the defect does prevent assembly of fully processed N-linked oligosaccharides. |
T8 | 1096-1277 | Sentence | denotes | Further, two glycopeptides, obtained from exhaustive Pronase digests of wild-type plasma membrane glycoproteins, inhibit intercellular cohesion of aggregation-stage wild-type cells. |
T9 | 1278-1460 | Sentence | denotes | HT7 produces only approximately 50% of the wild-type level of these glycopeptides at the restrictive temperature and one of the glycopeptides has reduced cohesion inhibition ability. |
T10 | 1461-1674 | Sentence | denotes | A revertant of HT7 was found to aggregate normally, to have restored EDTA-resistant cohesion, to have normal profiles of N-linked oligosaccharides and to express the two cohesion-inhibiting glycopeptides normally. |
T11 | 1675-1852 | Sentence | denotes | These data strongly support a model in which cohesion during late aggregation is at least in part due to recognition between surface glycans and receptors on neighbouring cells. |
T1 | 0-164 | Sentence | denotes | Conditional intercellular cohesion in a Dictyostelium discoideum mutant which is temperature sensitive for correct processing of asparagine-linked oligosaccharides. |
T2 | 165-340 | Sentence | denotes | Mutants of Dictyostelium discoideum have been isolated by a selection for cells with temperature-sensitive defects in the maturation of glycoprotein N-linked oligosaccharides. |
T3 | 341-511 | Sentence | denotes | Here we describe a mutant, HT7, which is unable to aggregate at the restrictive temperature, but which aggregates and makes fruiting bodies at the permissive temperature. |
T4 | 512-713 | Sentence | denotes | HT7 shows normal early developmental intercellular cohesion, but is temperature sensitive for expression of the ethylenediamine-tetraacetic acid (EDTA)-resistant cohesion characteristic of aggregation. |
T5 | 714-802 | Sentence | denotes | The mutant initiates aggregation, but forms only loose cell mounds which later disperse. |
T6 | 803-1007 | Sentence | denotes | Metabolic labelling studies indicate that the thermolabile defect is not in protein synthesis, assembly of the lipid-linked precursor of N-linked oligosaccharides or transfer of the precursor to proteins. |
T7 | 1008-1095 | Sentence | denotes | However, the defect does prevent assembly of fully processed N-linked oligosaccharides. |
T8 | 1096-1277 | Sentence | denotes | Further, two glycopeptides, obtained from exhaustive Pronase digests of wild-type plasma membrane glycoproteins, inhibit intercellular cohesion of aggregation-stage wild-type cells. |
T9 | 1278-1460 | Sentence | denotes | HT7 produces only approximately 50% of the wild-type level of these glycopeptides at the restrictive temperature and one of the glycopeptides has reduced cohesion inhibition ability. |
T10 | 1461-1674 | Sentence | denotes | A revertant of HT7 was found to aggregate normally, to have restored EDTA-resistant cohesion, to have normal profiles of N-linked oligosaccharides and to express the two cohesion-inhibiting glycopeptides normally. |
T11 | 1675-1852 | Sentence | denotes | These data strongly support a model in which cohesion during late aggregation is at least in part due to recognition between surface glycans and receptors on neighbouring cells. |
Glycosmos6-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 787-792 | http://purl.obolibrary.org/obo/MAT_0000488 | denotes | later |
GlycoBiology-FMA
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
_T1 | 129-139 | FMAID:82750 | denotes | asparagine |
_T2 | 129-139 | FMAID:196739 | denotes | asparagine |
_T3 | 147-163 | FMAID:196731 | denotes | oligosaccharides |
_T4 | 147-163 | FMAID:82742 | denotes | oligosaccharides |
_T5 | 239-244 | FMAID:68646 | denotes | cells |
_T6 | 239-244 | FMAID:169002 | denotes | cells |
_T7 | 301-313 | FMAID:62925 | denotes | glycoprotein |
_T8 | 301-313 | FMAID:167256 | denotes | glycoprotein |
_T9 | 323-339 | FMAID:82742 | denotes | oligosaccharides |
_T10 | 323-339 | FMAID:196731 | denotes | oligosaccharides |
_T11 | 474-480 | FMAID:256135 | denotes | bodies |
_T12 | 474-480 | FMAID:256134 | denotes | bodies |
_T13 | 787-792 | FMAID:171168 | denotes | later |
_T14 | 787-792 | FMAID:30332 | denotes | later |
_T15 | 879-886 | FMAID:67257 | denotes | protein |
_T16 | 879-886 | FMAID:165447 | denotes | protein |
_T17 | 914-919 | FMAID:165448 | denotes | lipid |
_T18 | 914-919 | FMAID:67264 | denotes | lipid |
_T19 | 949-965 | FMAID:196731 | denotes | oligosaccharides |
_T20 | 949-965 | FMAID:82742 | denotes | oligosaccharides |
_T21 | 998-1006 | FMAID:67257 | denotes | proteins |
_T22 | 998-1006 | FMAID:165447 | denotes | proteins |
_T23 | 1078-1094 | FMAID:196731 | denotes | oligosaccharides |
_T24 | 1078-1094 | FMAID:82742 | denotes | oligosaccharides |
_T25 | 1109-1122 | FMAID:82784 | denotes | glycopeptides |
_T26 | 1109-1122 | FMAID:196778 | denotes | glycopeptides |
_T27 | 1178-1184 | FMAID:162307 | denotes | plasma |
_T28 | 1178-1193 | FMAID:63841 | denotes | plasma membrane |
_T29 | 1178-1193 | FMAID:210691 | denotes | plasma membrane |
_T30 | 1178-1193 | FMAID:166047 | denotes | plasma membrane |
_T31 | 1178-1193 | FMAID:162306 | denotes | plasma membrane |
_T32 | 1178-1207 | FMAID:164993 | denotes | plasma membrane glycoproteins |
_T33 | 1178-1207 | FMAID:66843 | denotes | plasma membrane glycoproteins |
_T34 | 1194-1207 | FMAID:167256 | denotes | glycoproteins |
_T35 | 1194-1207 | FMAID:62925 | denotes | glycoproteins |
_T36 | 1271-1276 | FMAID:169002 | denotes | cells |
_T37 | 1271-1276 | FMAID:68646 | denotes | cells |
_T38 | 1346-1359 | FMAID:82784 | denotes | glycopeptides |
_T39 | 1346-1359 | FMAID:196778 | denotes | glycopeptides |
_T40 | 1406-1419 | FMAID:82784 | denotes | glycopeptides |
_T41 | 1406-1419 | FMAID:196778 | denotes | glycopeptides |
_T42 | 1591-1607 | FMAID:82742 | denotes | oligosaccharides |
_T43 | 1591-1607 | FMAID:196731 | denotes | oligosaccharides |
_T44 | 1651-1664 | FMAID:82784 | denotes | glycopeptides |
_T45 | 1651-1664 | FMAID:196778 | denotes | glycopeptides |
_T46 | 1800-1807 | FMAID:50594 | denotes | surface |
_T47 | 1800-1807 | FMAID:146300 | denotes | surface |
_T48 | 1846-1851 | FMAID:169002 | denotes | cells |
_T49 | 1846-1851 | FMAID:68646 | denotes | cells |
GlycoBiology-NCBITAXON
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/306026 | denotes | Dictyostelium |
T2 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/361082 | denotes | Dictyostelium |
T3 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/1037912 | denotes | Dictyostelium |
T4 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/5782 | denotes | Dictyostelium |
T5 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/741935 | denotes | Dictyostelium |
T6 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/1037943 | denotes | Dictyostelium |
T7 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/1037920 | denotes | Dictyostelium |
T8 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/361067 | denotes | Dictyostelium |
T9 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/1037580 | denotes | Dictyostelium |
T10 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/361070 | denotes | Dictyostelium |
T11 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/217135 | denotes | Dictyostelium |
T12 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/882401 | denotes | Dictyostelium |
T13 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/1037946 | denotes | Dictyostelium |
T14 | 40-53 | http://purl.bioontology.org/ontology/NCBITAXON/361072 | denotes | Dictyostelium |
T15 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/361072 | denotes | Dictyostelium |
T16 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/882401 | denotes | Dictyostelium |
T17 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/306026 | denotes | Dictyostelium |
T18 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/361070 | denotes | Dictyostelium |
T19 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/217135 | denotes | Dictyostelium |
T20 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/361067 | denotes | Dictyostelium |
T21 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/1037580 | denotes | Dictyostelium |
T22 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/1037943 | denotes | Dictyostelium |
T23 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/1037920 | denotes | Dictyostelium |
T24 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/5782 | denotes | Dictyostelium |
T25 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/741935 | denotes | Dictyostelium |
T26 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/1037912 | denotes | Dictyostelium |
T27 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/361082 | denotes | Dictyostelium |
T28 | 176-189 | http://purl.bioontology.org/ontology/NCBITAXON/1037946 | denotes | Dictyostelium |
T29 | 239-244 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T30 | 1271-1276 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T31 | 1736-1740 | http://purl.bioontology.org/ontology/NCBITAXON/8186 | denotes | late |
T32 | 1820-1829 | http://purl.bioontology.org/ontology/STY/T192 | denotes | receptors |
T33 | 1846-1851 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
GO-BP
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 93-102 | http://purl.obolibrary.org/obo/GO_0046960 | denotes | sensitive |
T2 | 262-271 | http://purl.obolibrary.org/obo/GO_0046960 | denotes | sensitive |
T3 | 592-601 | http://purl.obolibrary.org/obo/GO_0046960 | denotes | sensitive |
T4 | 803-812 | http://purl.obolibrary.org/obo/GO_0008152 | denotes | Metabolic |
T5 | 879-896 | http://purl.obolibrary.org/obo/GO_0006412 | denotes | protein synthesis |
T6 | 887-896 | http://purl.obolibrary.org/obo/GO_0009058 | denotes | synthesis |
T7 | 1157-1164 | http://purl.obolibrary.org/obo/GO_0007586 | denotes | digests |
GO-CC
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 239-244 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T2 | 1271-1276 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T3 | 769-773 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
T4 | 1178-1193 | http://purl.obolibrary.org/obo/GO_0005886 | denotes | plasma membrane |
T5 | 1185-1193 | http://purl.obolibrary.org/obo/GO_0016020 | denotes | membrane |
EDAM-topics
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 803-812 | http://edamontology.org/topic_3407 | denotes | Metabolic |
T2 | 823-830 | http://edamontology.org/topic_3678 | denotes | studies |
T3 | 879-886 | http://edamontology.org/topic_0078 | denotes | protein |
T4 | 898-906 | http://edamontology.org/topic_0196 | denotes | assembly |
T5 | 914-919 | http://edamontology.org/topic_0153 | denotes | lipid |
T6 | 998-1006 | http://edamontology.org/topic_0078 | denotes | proteins |
T7 | 1041-1049 | http://edamontology.org/topic_0196 | denotes | assembly |
T8 | 1185-1207 | http://edamontology.org/topic_0820 | denotes | membrane glycoproteins |
EDAM-DFO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 81-92 | http://edamontology.org/data_3724 | denotes | temperature |
T2 | 115-125 | http://edamontology.org/operation_0004 | denotes | processing |
T3 | 115-125 | http://edamontology.org/operation_2409 | denotes | processing |
T4 | 250-261 | http://edamontology.org/data_3724 | denotes | temperature |
T5 | 392-404 | http://edamontology.org/operation_3436 | denotes | aggregate at |
T6 | 421-432 | http://edamontology.org/data_3724 | denotes | temperature |
T7 | 499-510 | http://edamontology.org/data_3724 | denotes | temperature |
T8 | 522-528 | http://edamontology.org/operation_3435 | denotes | normal |
T9 | 580-591 | http://edamontology.org/data_3724 | denotes | temperature |
T10 | 803-822 | http://edamontology.org/operation_3715 | denotes | Metabolic labelling |
T11 | 879-886 | http://edamontology.org/data_1467 | denotes | protein |
T12 | 879-886 | http://edamontology.org/format_1208 | denotes | protein |
T13 | 898-906 | http://edamontology.org/operation_3433 | denotes | assembly |
T14 | 998-1006 | http://edamontology.org/format_1208 | denotes | proteins |
T15 | 998-1006 | http://edamontology.org/data_1467 | denotes | proteins |
T16 | 1041-1049 | http://edamontology.org/operation_3433 | denotes | assembly |
T17 | 1059-1068 | http://edamontology.org/operation_2409 | denotes | processed |
T18 | 1059-1068 | http://edamontology.org/operation_0004 | denotes | processed |
T19 | 1379-1390 | http://edamontology.org/data_3724 | denotes | temperature |
T20 | 1503-1511 | http://edamontology.org/operation_3435 | denotes | normally |
T21 | 1563-1569 | http://edamontology.org/operation_3435 | denotes | normal |
T22 | 1665-1673 | http://edamontology.org/operation_3435 | denotes | normally |
T23 | 1681-1685 | http://edamontology.org/data_0006 | denotes | data |
T24 | 1780-1791 | http://edamontology.org/operation_2423 | denotes | recognition |
GlycoBiology-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 787-792 | http://purl.obolibrary.org/obo/MAT_0000488 | denotes | later |
Anatomy-MAT
Id | Subject | Object | Predicate | Lexical cue | mat_id |
---|---|---|---|---|---|
T1 | 787-792 | Body_part | denotes | later | http://purl.obolibrary.org/obo/MAT_0000488 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 40-64 | OrganismTaxon | denotes | Dictyostelium discoideum | 44689 |
T2 | 176-200 | OrganismTaxon | denotes | Dictyostelium discoideum | 44689 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 1178-1193 | Body_part | denotes | plasma membrane | http://purl.obolibrary.org/obo/GO_0005886 |