PubMed:12626407
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-128 | Sentence | denotes | Characterization by NMR and molecular modeling of the binding of polyisoprenols and polyisoprenyl recognition sequence peptides: |
| TextSentencer_T2 | 129-198 | Sentence | denotes | 3D structure of the complexes reveals sites of specific interactions. |
| TextSentencer_T3 | 199-498 | Sentence | denotes | The objective of these studies was to test the hypothesis that proteins that contain potential polyisoprenyl recognition sequences (PIRSs) in their transmembrane-spanning domain can bind to the polyisoprenyl (PI) glycosyl carrier lipids undecaprenyl phosphate (C55-P) and dolichyl phosphate (C95-P). |
| TextSentencer_T4 | 499-656 | Sentence | denotes | A number of prokaryotic and eukaryotic glycosyltransferases that utilize PI coenzymes contain a conserved PIRS postulated to be the active PI binding domain. |
| TextSentencer_T5 | 657-809 | Sentence | denotes | To study this problem, we first determined the 3D structure of a PIRS peptide, NeuE, by homonuclear 2D 1H-nuclear magnetic resonance (NMR) spectroscopy. |
| TextSentencer_T6 | 810-1043 | Sentence | denotes | Experimentally generated distance constraints derived from nuclear Overhauser enhancement and torsion angle constraints derived from coupling constants were used for restrained molecular dynamics and energy minimization calculations. |
| TextSentencer_T7 | 1044-1171 | Sentence | denotes | Molecular models of the NeuE peptide were built based on calculations of energy minimization using the DGII program NMRchitect. |
| TextSentencer_T8 | 1172-1437 | Sentence | denotes | 3D models of dolichol (C95) and C95-P were built based on our 2D 1H-NMR nuclear Overhauser enhancement spectroscopy (NOESY) results and refined by energy minimization with respect to all atoms using the AMBER (assisted modeling with energy refinements) force field. |
| TextSentencer_T9 | 1438-1619 | Sentence | denotes | Our energy minimization studies were carried out on a conformational model of dolichol that was originally derived from small-angle X-ray scattering and molecular mechanics methods. |
| TextSentencer_T10 | 1620-1781 | Sentence | denotes | These results revealed that the PIs are conformationally nearly identical tripartite molecules, with their three domains arranged in a coiled, helical structure. |
| TextSentencer_T11 | 1782-2050 | Sentence | denotes | Analyses of the intermolecular cross-peaks in the 2D NOESY spectra of PIRS peptides in the presence of PIs confirmed a highly specific interaction and identified key contact amino acids in the NeuE peptide that constituted a binding motif for interacting with the PIs. |
| TextSentencer_T12 | 2051-2176 | Sentence | denotes | These studies also showed that subtle conformational changes occurred within both the PIs and the NeuE peptide after binding. |
| TextSentencer_T13 | 2177-2288 | Sentence | denotes | 3D structures of the resulting molecular complexes revealed that each PI could bind more than one PIRS peptide. |
| TextSentencer_T14 | 2289-2504 | Sentence | denotes | These studies thus represent the first evidence for a direct physical interaction between specific contact amino acids in the PIRS peptides and the PIs and supports the hypothesis of a bifunctional role for the PIs. |
| TextSentencer_T15 | 2505-2759 | Sentence | denotes | The central idea is that these superlipids may serve as a structural scaffold to organize and stabilize in functional domains PIRS-containing proteins within multiglycosyltransferase complexes that participate in biosynthetic and translocation processes. |
| T1 | 0-128 | Sentence | denotes | Characterization by NMR and molecular modeling of the binding of polyisoprenols and polyisoprenyl recognition sequence peptides: |
| T2 | 129-198 | Sentence | denotes | 3D structure of the complexes reveals sites of specific interactions. |
| T3 | 199-498 | Sentence | denotes | The objective of these studies was to test the hypothesis that proteins that contain potential polyisoprenyl recognition sequences (PIRSs) in their transmembrane-spanning domain can bind to the polyisoprenyl (PI) glycosyl carrier lipids undecaprenyl phosphate (C55-P) and dolichyl phosphate (C95-P). |
| T4 | 499-656 | Sentence | denotes | A number of prokaryotic and eukaryotic glycosyltransferases that utilize PI coenzymes contain a conserved PIRS postulated to be the active PI binding domain. |
| T5 | 657-809 | Sentence | denotes | To study this problem, we first determined the 3D structure of a PIRS peptide, NeuE, by homonuclear 2D 1H-nuclear magnetic resonance (NMR) spectroscopy. |
| T6 | 810-1043 | Sentence | denotes | Experimentally generated distance constraints derived from nuclear Overhauser enhancement and torsion angle constraints derived from coupling constants were used for restrained molecular dynamics and energy minimization calculations. |
| T7 | 1044-1171 | Sentence | denotes | Molecular models of the NeuE peptide were built based on calculations of energy minimization using the DGII program NMRchitect. |
| T8 | 1172-1437 | Sentence | denotes | 3D models of dolichol (C95) and C95-P were built based on our 2D 1H-NMR nuclear Overhauser enhancement spectroscopy (NOESY) results and refined by energy minimization with respect to all atoms using the AMBER (assisted modeling with energy refinements) force field. |
| T9 | 1438-1619 | Sentence | denotes | Our energy minimization studies were carried out on a conformational model of dolichol that was originally derived from small-angle X-ray scattering and molecular mechanics methods. |
| T10 | 1620-1781 | Sentence | denotes | These results revealed that the PIs are conformationally nearly identical tripartite molecules, with their three domains arranged in a coiled, helical structure. |
| T11 | 1782-2050 | Sentence | denotes | Analyses of the intermolecular cross-peaks in the 2D NOESY spectra of PIRS peptides in the presence of PIs confirmed a highly specific interaction and identified key contact amino acids in the NeuE peptide that constituted a binding motif for interacting with the PIs. |
| T12 | 2051-2176 | Sentence | denotes | These studies also showed that subtle conformational changes occurred within both the PIs and the NeuE peptide after binding. |
| T13 | 2177-2288 | Sentence | denotes | 3D structures of the resulting molecular complexes revealed that each PI could bind more than one PIRS peptide. |
| T14 | 2289-2504 | Sentence | denotes | These studies thus represent the first evidence for a direct physical interaction between specific contact amino acids in the PIRS peptides and the PIs and supports the hypothesis of a bifunctional role for the PIs. |
| T15 | 2505-2759 | Sentence | denotes | The central idea is that these superlipids may serve as a structural scaffold to organize and stabilize in functional domains PIRS-containing proteins within multiglycosyltransferase complexes that participate in biosynthetic and translocation processes. |
| T1 | 0-128 | Sentence | denotes | Characterization by NMR and molecular modeling of the binding of polyisoprenols and polyisoprenyl recognition sequence peptides: |
| T2 | 129-198 | Sentence | denotes | 3D structure of the complexes reveals sites of specific interactions. |
| T3 | 199-498 | Sentence | denotes | The objective of these studies was to test the hypothesis that proteins that contain potential polyisoprenyl recognition sequences (PIRSs) in their transmembrane-spanning domain can bind to the polyisoprenyl (PI) glycosyl carrier lipids undecaprenyl phosphate (C55-P) and dolichyl phosphate (C95-P). |
| T4 | 499-656 | Sentence | denotes | A number of prokaryotic and eukaryotic glycosyltransferases that utilize PI coenzymes contain a conserved PIRS postulated to be the active PI binding domain. |
| T5 | 657-809 | Sentence | denotes | To study this problem, we first determined the 3D structure of a PIRS peptide, NeuE, by homonuclear 2D 1H-nuclear magnetic resonance (NMR) spectroscopy. |
| T6 | 810-1043 | Sentence | denotes | Experimentally generated distance constraints derived from nuclear Overhauser enhancement and torsion angle constraints derived from coupling constants were used for restrained molecular dynamics and energy minimization calculations. |
| T7 | 1044-1171 | Sentence | denotes | Molecular models of the NeuE peptide were built based on calculations of energy minimization using the DGII program NMRchitect. |
| T8 | 1172-1437 | Sentence | denotes | 3D models of dolichol (C95) and C95-P were built based on our 2D 1H-NMR nuclear Overhauser enhancement spectroscopy (NOESY) results and refined by energy minimization with respect to all atoms using the AMBER (assisted modeling with energy refinements) force field. |
| T9 | 1438-1619 | Sentence | denotes | Our energy minimization studies were carried out on a conformational model of dolichol that was originally derived from small-angle X-ray scattering and molecular mechanics methods. |
| T10 | 1620-1781 | Sentence | denotes | These results revealed that the PIs are conformationally nearly identical tripartite molecules, with their three domains arranged in a coiled, helical structure. |
| T11 | 1782-2050 | Sentence | denotes | Analyses of the intermolecular cross-peaks in the 2D NOESY spectra of PIRS peptides in the presence of PIs confirmed a highly specific interaction and identified key contact amino acids in the NeuE peptide that constituted a binding motif for interacting with the PIs. |
| T12 | 2051-2176 | Sentence | denotes | These studies also showed that subtle conformational changes occurred within both the PIs and the NeuE peptide after binding. |
| T13 | 2177-2288 | Sentence | denotes | 3D structures of the resulting molecular complexes revealed that each PI could bind more than one PIRS peptide. |
| T14 | 2289-2504 | Sentence | denotes | These studies thus represent the first evidence for a direct physical interaction between specific contact amino acids in the PIRS peptides and the PIs and supports the hypothesis of a bifunctional role for the PIs. |
| T15 | 2505-2759 | Sentence | denotes | The central idea is that these superlipids may serve as a structural scaffold to organize and stabilize in functional domains PIRS-containing proteins within multiglycosyltransferase complexes that participate in biosynthetic and translocation processes. |
Glycosmos6-MAT
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 511-522 | http://purl.obolibrary.org/obo/MAT_0000190 | denotes | prokaryotic |
GlycoBiology-FMA
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T3 | 262-270 | FMAID:67257 | denotes | proteins |
| _T1 | 237-241 | FMAID:178661 | denotes | test |
| _T2 | 262-270 | FMAID:165447 | denotes | proteins |
| _T4 | 408-410 | FMAID:214745 | denotes | PI |
| _T5 | 429-435 | FMAID:67264 | denotes | lipids |
| _T6 | 429-435 | FMAID:165448 | denotes | lipids |
| _T7 | 572-574 | FMAID:214745 | denotes | PI |
| _T8 | 638-640 | FMAID:214745 | denotes | PI |
| _T9 | 1652-1655 | FMAID:214745 | denotes | PIs |
| _T10 | 1798-1812 | FMAID:202234 | denotes | intermolecular |
| _T11 | 1798-1812 | FMAID:85706 | denotes | intermolecular |
| _T12 | 1885-1888 | FMAID:214745 | denotes | PIs |
| _T13 | 1956-1967 | FMAID:82739 | denotes | amino acids |
| _T14 | 1956-1967 | FMAID:196728 | denotes | amino acids |
| _T15 | 2046-2049 | FMAID:214745 | denotes | PIs |
| _T16 | 2137-2140 | FMAID:214745 | denotes | PIs |
| _T17 | 2247-2249 | FMAID:214745 | denotes | PI |
| _T18 | 2396-2407 | FMAID:82739 | denotes | amino acids |
| _T19 | 2396-2407 | FMAID:196728 | denotes | amino acids |
| _T20 | 2437-2440 | FMAID:214745 | denotes | PIs |
| _T21 | 2500-2503 | FMAID:214745 | denotes | PIs |
| _T22 | 2509-2516 | FMAID:242678 | denotes | central |
| _T23 | 2509-2516 | FMAID:30328 | denotes | central |
| _T24 | 2509-2516 | FMAID:174816 | denotes | central |
| _T25 | 2586-2594 | FMAID:67498 | denotes | organize |
| _T26 | 2586-2594 | FMAID:166081 | denotes | organize |
| _T27 | 2647-2655 | FMAID:67257 | denotes | proteins |
| _T28 | 2647-2655 | FMAID:165447 | denotes | proteins |
uniprot-human
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 408-410 | http://www.uniprot.org/uniprot/Q86U18 | denotes | PI |
| T2 | 572-574 | http://www.uniprot.org/uniprot/Q86U18 | denotes | PI |
| T3 | 638-640 | http://www.uniprot.org/uniprot/Q86U18 | denotes | PI |
| T4 | 2247-2249 | http://www.uniprot.org/uniprot/Q86U18 | denotes | PI |
| T5 | 408-410 | http://www.uniprot.org/uniprot/P01298 | denotes | PI |
| T6 | 572-574 | http://www.uniprot.org/uniprot/P01298 | denotes | PI |
| T7 | 638-640 | http://www.uniprot.org/uniprot/P01298 | denotes | PI |
| T8 | 2247-2249 | http://www.uniprot.org/uniprot/P01298 | denotes | PI |
uniprot-mouse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 1755-1761 | http://www.uniprot.org/uniprot/Q5SU73 | denotes | coiled |
GlycoBiology-NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 527-537 | http://purl.bioontology.org/ontology/NCBITAXON/2759 | denotes | eukaryotic |
| T2 | 1601-1610 | http://purl.bioontology.org/ontology/NCBITAXON/127244 | denotes | mechanics |
| T3 | 1763-1770 | http://purl.bioontology.org/ontology/NCBITAXON/53324 | denotes | helical |
GO-BP
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 412-420 | http://purl.obolibrary.org/obo/GO_0070085 | denotes | glycosyl |
GO-MF
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 54-61 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T2 | 641-648 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T3 | 2007-2014 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T4 | 381-385 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | bind |
| T5 | 2256-2260 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | bind |
| T6 | 54-61 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T7 | 641-648 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T8 | 2007-2014 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T9 | 381-385 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | bind |
| T10 | 2256-2260 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | bind |
| T11 | 54-61 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T12 | 641-648 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T13 | 2007-2014 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T14 | 381-385 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | bind |
| T15 | 2256-2260 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | bind |
| T16 | 54-61 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T17 | 641-648 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T18 | 2007-2014 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T19 | 381-385 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | bind |
| T20 | 2256-2260 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | bind |
GO-CC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 347-360 | http://purl.obolibrary.org/obo/GO_0016021 | denotes | transmembrane |
| T2 | 347-360 | http://purl.obolibrary.org/obo/GO_0044214 | denotes | transmembrane |
UBERON-AE
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 2509-2516 | http://purl.obolibrary.org/obo/UBERON_0012131 | denotes | central |
| T2 | 2586-2594 | http://purl.obolibrary.org/obo/UBERON_0000062 | denotes | organize |
EDAM-topics
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 20-23 | http://edamontology.org/topic_0593 | denotes | NMR |
| T2 | 28-46 | http://edamontology.org/topic_2275 | denotes | molecular modeling |
| T3 | 110-118 | http://edamontology.org/topic_3168 | denotes | sequence |
| T4 | 110-118 | http://edamontology.org/topic_0080 | denotes | sequence |
| T5 | 119-127 | http://edamontology.org/topic_0154 | denotes | peptides |
| T6 | 185-197 | http://edamontology.org/topic_0602 | denotes | interactions |
| T7 | 222-229 | http://edamontology.org/topic_3678 | denotes | studies |
| T8 | 262-270 | http://edamontology.org/topic_0078 | denotes | proteins |
| T9 | 320-329 | http://edamontology.org/topic_3168 | denotes | sequences |
| T10 | 320-329 | http://edamontology.org/topic_0080 | denotes | sequences |
| T11 | 429-435 | http://edamontology.org/topic_0153 | denotes | lipids |
| T12 | 511-537 | http://edamontology.org/topic_1811 | denotes | prokaryotic and eukaryotic |
| T13 | 527-537 | http://edamontology.org/topic_2818 | denotes | eukaryotic |
| T14 | 660-665 | http://edamontology.org/topic_3678 | denotes | study |
| T15 | 727-734 | http://edamontology.org/topic_0154 | denotes | peptide |
| T16 | 763-789 | http://edamontology.org/topic_3444 | denotes | nuclear magnetic resonance |
| T17 | 791-794 | http://edamontology.org/topic_0593 | denotes | NMR |
| T18 | 791-808 | http://edamontology.org/topic_0593 | denotes | NMR) spectroscopy |
| T19 | 796-808 | http://edamontology.org/topic_0593 | denotes | spectroscopy |
| T20 | 987-1005 | http://edamontology.org/topic_0176 | denotes | molecular dynamics |
| T21 | 1044-1060 | http://edamontology.org/topic_2275 | denotes | Molecular models |
| T22 | 1073-1080 | http://edamontology.org/topic_0154 | denotes | peptide |
| T23 | 1240-1243 | http://edamontology.org/topic_0593 | denotes | NMR |
| T24 | 1244-1287 | http://edamontology.org/topic_0593 | denotes | nuclear Overhauser enhancement spectroscopy |
| T25 | 1275-1287 | http://edamontology.org/topic_0593 | denotes | spectroscopy |
| T26 | 1289-1294 | http://edamontology.org/topic_0593 | denotes | NOESY |
| T27 | 1462-1469 | http://edamontology.org/topic_3678 | denotes | studies |
| T28 | 1705-1714 | http://edamontology.org/topic_2839 | denotes | molecules |
| T29 | 1835-1840 | http://edamontology.org/topic_0593 | denotes | NOESY |
| T30 | 1857-1865 | http://edamontology.org/topic_0154 | denotes | peptides |
| T31 | 1917-1928 | http://edamontology.org/topic_0602 | denotes | interaction |
| T32 | 1956-1967 | http://edamontology.org/topic_0154 | denotes | amino acids |
| T33 | 1980-1987 | http://edamontology.org/topic_0154 | denotes | peptide |
| T34 | 2015-2020 | http://edamontology.org/topic_0158 | denotes | motif |
| T35 | 2025-2036 | http://edamontology.org/topic_0602 | denotes | interacting |
| T36 | 2057-2064 | http://edamontology.org/topic_3678 | denotes | studies |
| T37 | 2154-2161 | http://edamontology.org/topic_0154 | denotes | peptide |
| T38 | 2280-2287 | http://edamontology.org/topic_0154 | denotes | peptide |
| T39 | 2295-2302 | http://edamontology.org/topic_3678 | denotes | studies |
| T40 | 2350-2358 | http://edamontology.org/topic_3318 | denotes | physical |
| T41 | 2359-2370 | http://edamontology.org/topic_0602 | denotes | interaction |
| T42 | 2396-2407 | http://edamontology.org/topic_0154 | denotes | amino acids |
| T43 | 2420-2428 | http://edamontology.org/topic_0154 | denotes | peptides |
| T44 | 2647-2655 | http://edamontology.org/topic_0078 | denotes | proteins |
EDAM-DFO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 28-46 | http://edamontology.org/operation_0322 | denotes | molecular modeling |
| T2 | 98-109 | http://edamontology.org/operation_2423 | denotes | recognition |
| T3 | 110-118 | http://edamontology.org/data_2044 | denotes | sequence |
| T4 | 110-118 | http://edamontology.org/operation_3218 | denotes | sequence |
| T5 | 119-127 | http://edamontology.org/data_2906 | denotes | peptides |
| T6 | 132-141 | http://edamontology.org/data_0883 | denotes | structure |
| T7 | 262-270 | http://edamontology.org/format_1208 | denotes | proteins |
| T8 | 262-270 | http://edamontology.org/data_1467 | denotes | proteins |
| T9 | 308-319 | http://edamontology.org/operation_2423 | denotes | recognition |
| T10 | 320-329 | http://edamontology.org/data_2044 | denotes | sequences |
| T11 | 320-329 | http://edamontology.org/operation_3218 | denotes | sequences |
| T12 | 707-716 | http://edamontology.org/data_0883 | denotes | structure |
| T13 | 727-734 | http://edamontology.org/data_2906 | denotes | peptide |
| T14 | 825-834 | http://edamontology.org/operation_3429 | denotes | generated |
| T15 | 987-1005 | http://edamontology.org/operation_2476 | denotes | molecular dynamics |
| T16 | 1030-1042 | http://edamontology.org/operation_3438 | denotes | calculations |
| T17 | 1044-1060 | http://edamontology.org/operation_0322 | denotes | Molecular models |
| T18 | 1073-1080 | http://edamontology.org/data_2906 | denotes | peptide |
| T19 | 1101-1113 | http://edamontology.org/operation_3438 | denotes | calculations |
| T20 | 1771-1780 | http://edamontology.org/data_0883 | denotes | structure |
| T21 | 1841-1848 | http://edamontology.org/data_3483 | denotes | spectra |
| T22 | 1857-1865 | http://edamontology.org/data_2906 | denotes | peptides |
| T23 | 1929-1943 | http://edamontology.org/data_0992 | denotes | and identified |
| T24 | 1933-1943 | http://edamontology.org/data_0842 | denotes | identified |
| T25 | 1933-1943 | http://edamontology.org/data_2611 | denotes | identified |
| T26 | 1956-1970 | http://edamontology.org/data_1501 | denotes | amino acids in |
| T27 | 1980-1987 | http://edamontology.org/data_2906 | denotes | peptide |
| T28 | 2154-2161 | http://edamontology.org/data_2906 | denotes | peptide |
| T29 | 2180-2190 | http://edamontology.org/data_0883 | denotes | structures |
| T30 | 2280-2287 | http://edamontology.org/data_2906 | denotes | peptide |
| T31 | 2396-2410 | http://edamontology.org/data_1501 | denotes | amino acids in |
| T32 | 2420-2428 | http://edamontology.org/data_2906 | denotes | peptides |
| T33 | 2563-2573 | http://edamontology.org/data_0883 | denotes | structural |
| T34 | 2574-2582 | http://edamontology.org/operation_3216 | denotes | scaffold |
| T35 | 2647-2655 | http://edamontology.org/data_1467 | denotes | proteins |
| T36 | 2647-2655 | http://edamontology.org/format_1208 | denotes | proteins |
| T37 | 2749-2758 | http://edamontology.org/operation_0004 | denotes | processes |
| T38 | 2749-2758 | http://edamontology.org/operation_2409 | denotes | processes |
GlycoBiology-MAT
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 511-522 | http://purl.obolibrary.org/obo/MAT_0000190 | denotes | prokaryotic |
GlyTouCan-IUPAC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| GlycanIUPAC_T1 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G41652MJ" | denotes | all |
| GlycanIUPAC_T2 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G20761YC" | denotes | all |
| GlycanIUPAC_T3 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G19807HM" | denotes | all |
| GlycanIUPAC_T4 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G20351TE" | denotes | all |
| GlycanIUPAC_T5 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G71957MR" | denotes | all |
| GlycanIUPAC_T6 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G59040AE" | denotes | all |
| GlycanIUPAC_T7 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G14987PW" | denotes | all |
| GlycanIUPAC_T8 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G95064PC" | denotes | all |
| GlycanIUPAC_T9 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G39143AQ" | denotes | all |
| GlycanIUPAC_T10 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G65149OO" | denotes | all |
| GlycanIUPAC_T11 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G02766SY" | denotes | all |
| GlycanIUPAC_T12 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G26019KJ" | denotes | all |
| GlycanIUPAC_T13 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G36429CZ" | denotes | all |
| GlycanIUPAC_T14 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G89633TP" | denotes | all |
| GlycanIUPAC_T15 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G28494FO" | denotes | all |
| GlycanIUPAC_T16 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G06219CP" | denotes | all |
| GlycanIUPAC_T17 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G44237SM" | denotes | all |
| GlycanIUPAC_T18 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G57948RL" | denotes | all |
| GlycanIUPAC_T19 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G64016DN" | denotes | all |
| GlycanIUPAC_T20 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G14536PC" | denotes | all |
| GlycanIUPAC_T21 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G14356FW" | denotes | all |
| GlycanIUPAC_T22 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G34565UO" | denotes | all |
| GlycanIUPAC_T23 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G67124MW" | denotes | all |
| GlycanIUPAC_T24 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G71457ZU" | denotes | all |
| GlycanIUPAC_T25 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G55228VZ" | denotes | all |
| GlycanIUPAC_T26 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G31034MJ" | denotes | all |
| GlycanIUPAC_T27 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G25776IP" | denotes | all |
| GlycanIUPAC_T28 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G64442BV" | denotes | all |
| GlycanIUPAC_T29 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G57018LE" | denotes | all |
| GlycanIUPAC_T30 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G61761GX" | denotes | all |
| GlycanIUPAC_T31 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G76318UX" | denotes | all |
| GlycanIUPAC_T32 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G61906ER" | denotes | all |
| GlycanIUPAC_T33 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G68723GR" | denotes | all |
| GlycanIUPAC_T34 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G19540LE" | denotes | all |
| GlycanIUPAC_T35 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G74944PO" | denotes | all |
| GlycanIUPAC_T36 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G89489ZJ" | denotes | all |
| GlycanIUPAC_T37 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G04434YU" | denotes | all |
| GlycanIUPAC_T38 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G21450PB" | denotes | all |
| GlycanIUPAC_T39 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G93629QY" | denotes | all |
| GlycanIUPAC_T40 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G02603TR" | denotes | all |
| GlycanIUPAC_T41 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G40280JP" | denotes | all |
| GlycanIUPAC_T42 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G95259IC" | denotes | all |
| GlycanIUPAC_T43 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G26900FE" | denotes | all |
| GlycanIUPAC_T44 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G21346KK" | denotes | all |
| GlycanIUPAC_T45 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G62509FF" | denotes | all |
| GlycanIUPAC_T46 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G83932AK" | denotes | all |
| GlycanIUPAC_T47 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G96978IB" | denotes | all |
| GlycanIUPAC_T48 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G34275DN" | denotes | all |
| GlycanIUPAC_T49 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G07071JF" | denotes | all |
| GlycanIUPAC_T50 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G80639QD" | denotes | all |
| GlycanIUPAC_T51 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G99460PJ" | denotes | all |
| GlycanIUPAC_T52 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G22024BZ" | denotes | all |
| GlycanIUPAC_T53 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G74097ZY" | denotes | all |
| GlycanIUPAC_T54 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G84439YP" | denotes | all |
| GlycanIUPAC_T55 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G52207WQ" | denotes | all |
| GlycanIUPAC_T56 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G90695MS" | denotes | all |
| GlycanIUPAC_T57 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G50398QX" | denotes | all |
| GlycanIUPAC_T58 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G12166ZT" | denotes | all |
| GlycanIUPAC_T59 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G48368BR" | denotes | all |
| GlycanIUPAC_T60 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G57407RW" | denotes | all |
| GlycanIUPAC_T61 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G00386TY" | denotes | all |
| GlycanIUPAC_T62 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G18723JK" | denotes | all |
| GlycanIUPAC_T63 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G93757OR" | denotes | all |
| GlycanIUPAC_T64 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G29006SI" | denotes | all |
| GlycanIUPAC_T65 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G03099OQ" | denotes | all |
| GlycanIUPAC_T66 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G53739OW" | denotes | all |
| GlycanIUPAC_T67 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G70440ZO" | denotes | all |
| GlycanIUPAC_T68 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G29951RR" | denotes | all |
| GlycanIUPAC_T69 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G58402TI" | denotes | all |
| GlycanIUPAC_T70 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G39875TP" | denotes | all |
| GlycanIUPAC_T71 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G83439QV" | denotes | all |
| GlycanIUPAC_T72 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G41762RC" | denotes | all |
| GlycanIUPAC_T73 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G91604UI" | denotes | all |
| GlycanIUPAC_T74 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G88447WE" | denotes | all |
| GlycanIUPAC_T75 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G93634BS" | denotes | all |
| GlycanIUPAC_T76 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G02587BH" | denotes | all |
| GlycanIUPAC_T77 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G43511MX" | denotes | all |
| GlycanIUPAC_T78 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G64958DH" | denotes | all |
| GlycanIUPAC_T79 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G30384TR" | denotes | all |
| GlycanIUPAC_T80 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G15624EX" | denotes | all |
| GlycanIUPAC_T81 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G22706ST" | denotes | all |
| GlycanIUPAC_T82 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G57408PI" | denotes | all |
| GlycanIUPAC_T83 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G86403XX" | denotes | all |
| GlycanIUPAC_T84 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G78043YB" | denotes | all |
| GlycanIUPAC_T85 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G18952JK" | denotes | all |
| GlycanIUPAC_T86 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G49020ND" | denotes | all |
| GlycanIUPAC_T87 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G63590YW" | denotes | all |
| GlycanIUPAC_T88 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G22793KS" | denotes | all |
| GlycanIUPAC_T89 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G64134SS" | denotes | all |
| GlycanIUPAC_T90 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G17338HY" | denotes | all |
| GlycanIUPAC_T91 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G99745XF" | denotes | all |
| GlycanIUPAC_T92 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G27782HN" | denotes | all |
| GlycanIUPAC_T93 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G57496DC" | denotes | all |
| GlycanIUPAC_T94 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G93169WB" | denotes | all |
| GlycanIUPAC_T95 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G05518TD" | denotes | all |
| GlycanIUPAC_T96 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G62603DN" | denotes | all |
| GlycanIUPAC_T97 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G59574FS" | denotes | all |
| GlycanIUPAC_T98 | 1355-1358 | "http://rdf.glycoinfo.org/glycan/G47567WC" | denotes | all |
performance-test
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-UBERON-AE-B_T1 | 2586-2594 | http://purl.obolibrary.org/obo/UBERON_0000062 | denotes | organize |
| PD-UBERON-AE-B_T2 | 2509-2516 | http://purl.obolibrary.org/obo/UBERON_0012131 | denotes | central |
Anatomy-MAT
| Id | Subject | Object | Predicate | Lexical cue | mat_id |
|---|---|---|---|---|---|
| T1 | 511-522 | Body_part | denotes | prokaryotic | http://purl.obolibrary.org/obo/MAT_0000190 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 2517-2521 | OrganismTaxon | denotes | idea | 76236 |
Anatomy-UBERON
| Id | Subject | Object | Predicate | Lexical cue | uberon_id |
|---|---|---|---|---|---|
| T1 | 347-360 | Body_part | denotes | transmembrane | http://purl.obolibrary.org/obo/GO_0016020 |
| T2 | 2586-2594 | Body_part | denotes | organize | http://purl.obolibrary.org/obo/UBERON_0003062|http://purl.obolibrary.org/obo/UBERON_3010449|http://purl.obolibrary.org/obo/UBERON_3010457 |