PubMed:10536041
Annnotations
CL-cell
| Id | Subject | Object | Predicate | Lexical cue | cl_id |
|---|---|---|---|---|---|
| T1 | 501-505 | Cell | denotes | poly | http://purl.obolibrary.org/obo/CL:0000096|http://purl.obolibrary.org/obo/CL:0000775 |
GlycoBiology-FMA
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T1 | 118-123 | FMAID:214748 | denotes | plant |
| _T2 | 143-158 | FMAID:167185 | denotes | immunoglobulins |
| _T3 | 143-158 | FMAID:167181 | denotes | immunoglobulins |
| _T4 | 143-158 | FMAID:167177 | denotes | immunoglobulins |
| _T5 | 143-158 | FMAID:167178 | denotes | immunoglobulins |
| _T6 | 143-158 | FMAID:62871 | denotes | immunoglobulins |
| _T7 | 143-158 | FMAID:62872 | denotes | immunoglobulins |
| _T8 | 143-158 | FMAID:62875 | denotes | immunoglobulins |
| _T9 | 143-158 | FMAID:62873 | denotes | immunoglobulins |
| _T10 | 143-158 | FMAID:62874 | denotes | immunoglobulins |
| _T11 | 143-158 | FMAID:62876 | denotes | immunoglobulins |
| _T12 | 143-158 | FMAID:167183 | denotes | immunoglobulins |
| _T13 | 143-158 | FMAID:167187 | denotes | immunoglobulins |
| _T14 | 287-292 | FMAID:196724 | denotes | sugar |
| _T15 | 376-381 | FMAID:196724 | denotes | sugar |
| _T16 | 449-463 | FMAID:196730 | denotes | monosaccharide |
| _T17 | 449-463 | FMAID:82741 | denotes | monosaccharide |
| _T18 | 701-709 | FMAID:67257 | denotes | proteins |
| _T19 | 701-709 | FMAID:165447 | denotes | proteins |
| _T20 | 799-813 | FMAID:167177 | denotes | immunoglobulin |
| _T21 | 799-813 | FMAID:62871 | denotes | immunoglobulin |
| _T22 | 799-815 | FMAID:167181 | denotes | immunoglobulin G |
| _T23 | 799-815 | FMAID:167178 | denotes | immunoglobulin G |
| _T24 | 799-815 | FMAID:167185 | denotes | immunoglobulin G |
| _T25 | 799-815 | FMAID:62872 | denotes | immunoglobulin G |
| _T26 | 799-815 | FMAID:62873 | denotes | immunoglobulin G |
| _T27 | 799-815 | FMAID:62875 | denotes | immunoglobulin G |
| _T28 | 799-815 | FMAID:62876 | denotes | immunoglobulin G |
| _T29 | 799-815 | FMAID:167183 | denotes | immunoglobulin G |
| _T30 | 799-815 | FMAID:62874 | denotes | immunoglobulin G |
| _T31 | 799-815 | FMAID:167187 | denotes | immunoglobulin G |
| _T32 | 931-938 | FMAID:67257 | denotes | protein |
| _T33 | 931-938 | FMAID:165447 | denotes | protein |
| _T34 | 972-977 | FMAID:85813 | denotes | solid |
| _T35 | 996-1003 | FMAID:146300 | denotes | surface |
| _T36 | 996-1003 | FMAID:50594 | denotes | surface |
| _T37 | 1094-1103 | FMAID:226027 | denotes | branching |
| _T38 | 1094-1103 | FMAID:226028 | denotes | branching |
| _T39 | 1112-1117 | FMAID:214748 | denotes | plant |
| _T40 | 1157-1165 | FMAID:167180 | denotes | antibody |
| _T41 | 1293-1299 | FMAID:50596 | denotes | points |
| _T42 | 1293-1299 | FMAID:146304 | denotes | points |
| _T43 | 1303-1328 | FMAID:62290 | denotes | favorable protein-protein |
| _T44 | 1303-1328 | FMAID:90067 | denotes | favorable protein-protein |
| _T45 | 1313-1320 | FMAID:67257 | denotes | protein |
| _T46 | 1313-1320 | FMAID:165447 | denotes | protein |
| _T47 | 1313-1328 | FMAID:67119 | denotes | protein-protein |
| _T48 | 1313-1328 | FMAID:167415 | denotes | protein-protein |
| _T49 | 1313-1328 | FMAID:198030 | denotes | protein-protein |
| _T50 | 1313-1328 | FMAID:165914 | denotes | protein-protein |
| _T51 | 1313-1328 | FMAID:62378 | denotes | protein-protein |
| _T52 | 1313-1328 | FMAID:165430 | denotes | protein-protein |
| _T53 | 1313-1328 | FMAID:231303 | denotes | protein-protein |
| _T54 | 1313-1328 | FMAID:231312 | denotes | protein-protein |
| _T55 | 1313-1328 | FMAID:231313 | denotes | protein-protein |
| _T56 | 1313-1328 | FMAID:165476 | denotes | protein-protein |
| _T57 | 1313-1328 | FMAID:165470 | denotes | protein-protein |
| _T58 | 1313-1328 | FMAID:165475 | denotes | protein-protein |
| _T59 | 1313-1328 | FMAID:62925 | denotes | protein-protein |
| _T60 | 1313-1328 | FMAID:167256 | denotes | protein-protein |
| _T61 | 1313-1328 | FMAID:231302 | denotes | protein-protein |
| _T62 | 1313-1328 | FMAID:166112 | denotes | protein-protein |
| _T63 | 1313-1328 | FMAID:199792 | denotes | protein-protein |
| _T64 | 1313-1328 | FMAID:85438 | denotes | protein-protein |
| _T65 | 1313-1328 | FMAID:63169 | denotes | protein-protein |
| _T66 | 1313-1328 | FMAID:165434 | denotes | protein-protein |
| _T67 | 1313-1328 | FMAID:231305 | denotes | protein-protein |
| _T68 | 1313-1328 | FMAID:67906 | denotes | protein-protein |
| _T69 | 1313-1328 | FMAID:174224 | denotes | protein-protein |
| _T70 | 1313-1328 | FMAID:72158 | denotes | protein-protein |
| _T71 | 1313-1328 | FMAID:165438 | denotes | protein-protein |
| _T72 | 1313-1328 | FMAID:165866 | denotes | protein-protein |
| _T73 | 1313-1328 | FMAID:231304 | denotes | protein-protein |
| _T74 | 1321-1328 | FMAID:67257 | denotes | protein |
| _T75 | 1321-1328 | FMAID:165447 | denotes | protein |
| _T76 | 1556-1571 | FMAID:62925 | denotes | neoglycoprotein |
| _T77 | 1556-1571 | FMAID:167256 | denotes | neoglycoprotein |
| _T78 | 1652-1661 | FMAID:117680 | denotes | second to |
| _T79 | 1652-1661 | FMAID:25048 | denotes | second to |
| _T80 | 1689-1694 | FMAID:214748 | denotes | plant |
| _T81 | 1848-1853 | FMAID:196724 | denotes | sugar |
| _T82 | 1876-1891 | FMAID:167256 | denotes | neoglycoprotein |
| _T83 | 1876-1891 | FMAID:62925 | denotes | neoglycoprotein |
| _T84 | 1920-1928 | FMAID:274208 | denotes | superior |
| _T85 | 1920-1928 | FMAID:174814 | denotes | superior |
| _T86 | 1920-1928 | FMAID:30337 | denotes | superior |
| _T87 | 1948-1956 | FMAID:167180 | denotes | antibody |
uniprot-human
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 681-709 | http://www.uniprot.org/uniprot/P17931 | denotes | galactoside-binding proteins |
| T2 | 953-963 | http://www.uniprot.org/uniprot/P17931 | denotes | galectin-3 |
| T3 | 1209-1219 | http://www.uniprot.org/uniprot/P17931 | denotes | galectin-3 |
| T4 | 1989-1999 | http://www.uniprot.org/uniprot/P17931 | denotes | galectin-3 |
| T5 | 842-852 | http://www.uniprot.org/uniprot/P09382 | denotes | galectin-1 |
| T6 | 1170-1180 | http://www.uniprot.org/uniprot/P09382 | denotes | galectin-1 |
| T7 | 1752-1762 | http://www.uniprot.org/uniprot/P09382 | denotes | galectin-1 |
| T8 | 1198-1219 | http://www.uniprot.org/uniprot/Q08380 | denotes | binding of galectin-3 |
uniprot-mouse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 842-852 | http://www.uniprot.org/uniprot/P16045 | denotes | galectin-1 |
| T2 | 1170-1180 | http://www.uniprot.org/uniprot/P16045 | denotes | galectin-1 |
| T3 | 1752-1762 | http://www.uniprot.org/uniprot/P16045 | denotes | galectin-1 |
| T4 | 953-963 | http://www.uniprot.org/uniprot/P16110 | denotes | galectin-3 |
| T5 | 1209-1219 | http://www.uniprot.org/uniprot/P16110 | denotes | galectin-3 |
| T6 | 1989-1999 | http://www.uniprot.org/uniprot/P16110 | denotes | galectin-3 |
GlycoBiology-NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 107-116 | http://purl.bioontology.org/ontology/STY/T192 | denotes | receptors |
| T2 | 293-302 | http://purl.bioontology.org/ontology/STY/T192 | denotes | receptors |
| T3 | 323-328 | http://purl.bioontology.org/ontology/NCBITAXON/293505 | denotes | areas |
| T4 | 359-367 | http://purl.bioontology.org/ontology/STY/T053 | denotes | behavior |
| T5 | 382-391 | http://purl.bioontology.org/ontology/STY/T192 | denotes | receptors |
| T6 | 623-627 | http://purl.bioontology.org/ontology/NCBITAXON/158455 | denotes | beta |
| T7 | 623-627 | http://purl.bioontology.org/ontology/NCBITAXON/3554 | denotes | beta |
| T8 | 650-655 | http://purl.bioontology.org/ontology/STY/T096 | denotes | group |
| T9 | 1313-1328 | http://purl.bioontology.org/ontology/NCBITAXON/66543 | denotes | protein-protein |
| T10 | 1313-1328 | http://purl.bioontology.org/ontology/NCBITAXON/415014 | denotes | protein-protein |
| T11 | 1313-1328 | http://purl.bioontology.org/ontology/NCBITAXON/66322 | denotes | protein-protein |
| T12 | 1401-1407 | http://purl.bioontology.org/ontology/STY/T096 | denotes | groups |
| T13 | 1784-1797 | http://purl.bioontology.org/ontology/NCBITAXON/691256 | denotes | heterogeneous |
| T14 | 1784-1797 | http://purl.bioontology.org/ontology/NCBITAXON/1113441 | denotes | heterogeneous |
| T15 | 1910-1915 | http://purl.bioontology.org/ontology/STY/T096 | denotes | group |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-182 | Sentence | denotes | Lactose-containing starburst dendrimers: influence of dendrimer generation and binding-site orientation of receptors (plant/animal lectins and immunoglobulins) on binding properties. |
| TextSentencer_T2 | 183-303 | Sentence | denotes | Starburst glycodendrimers offer the potential to serve as high-affinity ligands for clinically relevant sugar receptors. |
| TextSentencer_T3 | 304-494 | Sentence | denotes | In order to define areas of application, their binding behavior towards sugar receptors with differential binding-site orientation but identical monosaccharide specificity must be evaluated. |
| TextSentencer_T4 | 495-964 | Sentence | denotes | Using poly(amidoamine) starburst dendrimers of five generations, which contain the p-isothiocyanato derivative of p-aminophenyl-beta-D-lactoside as ligand group, four different types of galactoside-binding proteins were chosen for this purpose, i.e., the (AB)(2)-toxic agglutinin from mistletoe, a human immunoglobulin G fraction, the homodimeric galectin-1 with its two binding sites at opposite ends of the jelly-roll-motif-harboring protein and monomeric galectin-3. |
| TextSentencer_T5 | 965-1181 | Sentence | denotes | Direct solid-phase assays with surface-immobilized glycodendrimers resulted in obvious affinity enhancements by progressive core branching for the plant agglutinin and less pronounced for the antibody and galectin-1. |
| TextSentencer_T6 | 1182-1445 | Sentence | denotes | High density of binding of galectin-3 with modest affinity increases only from the level of the 32-mer onwards points to favorable protein-protein interactions of the monomeric lectin and a spherical display of the end groups without a major share of backfolding. |
| TextSentencer_T7 | 1446-1626 | Sentence | denotes | When the inhibitory potency of these probes was evaluated as competitor of receptor binding to an immobilized neoglycoprotein or to asialofetuin, a marked selectivity was detected. |
| TextSentencer_T8 | 1627-1860 | Sentence | denotes | The 32- and 64-mers were second to none as inhibitors for the plant agglutinin against both ligand-exposing matrices and for galectin-1 on the matrix with a heterogeneous array of interglycoside distances even on the per-sugar basis. |
| TextSentencer_T9 | 1861-2000 | Sentence | denotes | In contrast, a neoglycoprotein with the same end group was superior in the case of the antibody and, less pronounced, monomeric galectin-3. |
| TextSentencer_T10 | 2001-2275 | Sentence | denotes | Intimate details of topological binding-site presentation and the ligand display on different generations of core assembly are major operative factors which determine the potential of dendrimers for applications as lectin-targeting device, as attested by these observations. |
| T1 | 0-182 | Sentence | denotes | Lactose-containing starburst dendrimers: influence of dendrimer generation and binding-site orientation of receptors (plant/animal lectins and immunoglobulins) on binding properties. |
| T2 | 183-303 | Sentence | denotes | Starburst glycodendrimers offer the potential to serve as high-affinity ligands for clinically relevant sugar receptors. |
| T3 | 304-494 | Sentence | denotes | In order to define areas of application, their binding behavior towards sugar receptors with differential binding-site orientation but identical monosaccharide specificity must be evaluated. |
| T4 | 495-964 | Sentence | denotes | Using poly(amidoamine) starburst dendrimers of five generations, which contain the p-isothiocyanato derivative of p-aminophenyl-beta-D-lactoside as ligand group, four different types of galactoside-binding proteins were chosen for this purpose, i.e., the (AB)(2)-toxic agglutinin from mistletoe, a human immunoglobulin G fraction, the homodimeric galectin-1 with its two binding sites at opposite ends of the jelly-roll-motif-harboring protein and monomeric galectin-3. |
| T5 | 965-1181 | Sentence | denotes | Direct solid-phase assays with surface-immobilized glycodendrimers resulted in obvious affinity enhancements by progressive core branching for the plant agglutinin and less pronounced for the antibody and galectin-1. |
| T6 | 1182-1445 | Sentence | denotes | High density of binding of galectin-3 with modest affinity increases only from the level of the 32-mer onwards points to favorable protein-protein interactions of the monomeric lectin and a spherical display of the end groups without a major share of backfolding. |
| T7 | 1446-1626 | Sentence | denotes | When the inhibitory potency of these probes was evaluated as competitor of receptor binding to an immobilized neoglycoprotein or to asialofetuin, a marked selectivity was detected. |
| T8 | 1627-1860 | Sentence | denotes | The 32- and 64-mers were second to none as inhibitors for the plant agglutinin against both ligand-exposing matrices and for galectin-1 on the matrix with a heterogeneous array of interglycoside distances even on the per-sugar basis. |
| T9 | 1861-2000 | Sentence | denotes | In contrast, a neoglycoprotein with the same end group was superior in the case of the antibody and, less pronounced, monomeric galectin-3. |
| T10 | 2001-2275 | Sentence | denotes | Intimate details of topological binding-site presentation and the ligand display on different generations of core assembly are major operative factors which determine the potential of dendrimers for applications as lectin-targeting device, as attested by these observations. |
| T1 | 0-182 | Sentence | denotes | Lactose-containing starburst dendrimers: influence of dendrimer generation and binding-site orientation of receptors (plant/animal lectins and immunoglobulins) on binding properties. |
| T2 | 183-303 | Sentence | denotes | Starburst glycodendrimers offer the potential to serve as high-affinity ligands for clinically relevant sugar receptors. |
| T3 | 304-494 | Sentence | denotes | In order to define areas of application, their binding behavior towards sugar receptors with differential binding-site orientation but identical monosaccharide specificity must be evaluated. |
| T4 | 495-964 | Sentence | denotes | Using poly(amidoamine) starburst dendrimers of five generations, which contain the p-isothiocyanato derivative of p-aminophenyl-beta-D-lactoside as ligand group, four different types of galactoside-binding proteins were chosen for this purpose, i.e., the (AB)(2)-toxic agglutinin from mistletoe, a human immunoglobulin G fraction, the homodimeric galectin-1 with its two binding sites at opposite ends of the jelly-roll-motif-harboring protein and monomeric galectin-3. |
| T5 | 965-1181 | Sentence | denotes | Direct solid-phase assays with surface-immobilized glycodendrimers resulted in obvious affinity enhancements by progressive core branching for the plant agglutinin and less pronounced for the antibody and galectin-1. |
| T6 | 1182-1445 | Sentence | denotes | High density of binding of galectin-3 with modest affinity increases only from the level of the 32-mer onwards points to favorable protein-protein interactions of the monomeric lectin and a spherical display of the end groups without a major share of backfolding. |
| T7 | 1446-1626 | Sentence | denotes | When the inhibitory potency of these probes was evaluated as competitor of receptor binding to an immobilized neoglycoprotein or to asialofetuin, a marked selectivity was detected. |
| T8 | 1627-1860 | Sentence | denotes | The 32- and 64-mers were second to none as inhibitors for the plant agglutinin against both ligand-exposing matrices and for galectin-1 on the matrix with a heterogeneous array of interglycoside distances even on the per-sugar basis. |
| T9 | 1861-2000 | Sentence | denotes | In contrast, a neoglycoprotein with the same end group was superior in the case of the antibody and, less pronounced, monomeric galectin-3. |
| T10 | 2001-2275 | Sentence | denotes | Intimate details of topological binding-site presentation and the ligand display on different generations of core assembly are major operative factors which determine the potential of dendrimers for applications as lectin-targeting device, as attested by these observations. |
GO-BP
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 359-367 | http://purl.obolibrary.org/obo/GO_0007610 | denotes | behavior |
| T2 | 1281-1284 | http://purl.obolibrary.org/obo/GO_0016152 | denotes | mer |
| T3 | 1642-1646 | http://purl.obolibrary.org/obo/GO_0016152 | denotes | mers |
GO-MF
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 79-86 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T2 | 163-170 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T3 | 351-358 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T4 | 410-417 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T5 | 693-700 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T6 | 866-873 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T7 | 1198-1205 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T8 | 1530-1537 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T9 | 2033-2040 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
| T10 | 79-86 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T11 | 163-170 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T12 | 351-358 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T13 | 410-417 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T14 | 693-700 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T15 | 866-873 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T16 | 1198-1205 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T17 | 1530-1537 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T18 | 2033-2040 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
| T19 | 79-86 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T20 | 163-170 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T21 | 351-358 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T22 | 410-417 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T23 | 693-700 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T24 | 866-873 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T25 | 1198-1205 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T26 | 1530-1537 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T27 | 2033-2040 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
| T28 | 79-86 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T29 | 163-170 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T30 | 351-358 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T31 | 410-417 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T32 | 693-700 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T33 | 866-873 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T34 | 1198-1205 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T35 | 1530-1537 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T36 | 2033-2040 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
| T37 | 143-158 | http://purl.obolibrary.org/obo/GO_0003823 | denotes | immunoglobulins |
| T38 | 799-813 | http://purl.obolibrary.org/obo/GO_0003823 | denotes | immunoglobulin |
| T39 | 143-170 | http://purl.obolibrary.org/obo/GO_0019865 | denotes | immunoglobulins) on binding |
| T40 | 255-262 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | ligands |
| T41 | 643-649 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | ligand |
| T42 | 1719-1725 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | ligand |
| T43 | 2067-2073 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | ligand |
| T44 | 681-700 | http://purl.obolibrary.org/obo/GO_0016936 | denotes | galactoside-binding |
| T45 | 693-709 | http://purl.obolibrary.org/obo/GO_0005515 | denotes | binding proteins |
| T46 | 1157-1165 | http://purl.obolibrary.org/obo/GO_0003823 | denotes | antibody |
| T47 | 1948-1956 | http://purl.obolibrary.org/obo/GO_0003823 | denotes | antibody |
| T48 | 1521-1537 | http://purl.obolibrary.org/obo/GO_0005102 | denotes | receptor binding |
GO-CC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 1089-1093 | http://purl.obolibrary.org/obo/GO_0019013 | denotes | core |
| T2 | 2110-2114 | http://purl.obolibrary.org/obo/GO_0019013 | denotes | core |
EDAM-topics
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 118-123 | http://edamontology.org/topic_0780 | denotes | plant |
| T2 | 701-709 | http://edamontology.org/topic_0078 | denotes | proteins |
| T3 | 793-798 | http://edamontology.org/topic_2815 | denotes | human |
| T4 | 915-920 | http://edamontology.org/topic_0158 | denotes | motif |
| T5 | 931-938 | http://edamontology.org/topic_0078 | denotes | protein |
| T6 | 1112-1117 | http://edamontology.org/topic_0780 | denotes | plant |
| T7 | 1313-1320 | http://edamontology.org/topic_0078 | denotes | protein |
| T8 | 1313-1341 | http://edamontology.org/topic_0147 | denotes | protein-protein interactions |
| T9 | 1313-1341 | http://edamontology.org/topic_3526 | denotes | protein-protein interactions |
| T10 | 1313-1341 | http://edamontology.org/topic_0128 | denotes | protein-protein interactions |
| T11 | 1313-1341 | http://edamontology.org/topic_3525 | denotes | protein-protein interactions |
| T12 | 1313-1341 | http://edamontology.org/topic_0149 | denotes | protein-protein interactions |
| T13 | 1313-1341 | http://edamontology.org/topic_0078 | denotes | protein-protein interactions |
| T14 | 1313-1344 | http://edamontology.org/topic_3557 | denotes | protein-protein interactions of |
| T15 | 1313-1344 | http://edamontology.org/topic_3044 | denotes | protein-protein interactions of |
| T16 | 1313-1344 | http://edamontology.org/topic_0128 | denotes | protein-protein interactions of |
| T17 | 1313-1344 | http://edamontology.org/topic_0147 | denotes | protein-protein interactions of |
| T18 | 1321-1328 | http://edamontology.org/topic_0078 | denotes | protein |
| T19 | 1321-1341 | http://edamontology.org/topic_0130 | denotes | protein interactions |
| T20 | 1321-1341 | http://edamontology.org/topic_0128 | denotes | protein interactions |
| T21 | 1321-1341 | http://edamontology.org/topic_3514 | denotes | protein interactions |
| T22 | 1321-1341 | http://edamontology.org/topic_0148 | denotes | protein interactions |
| T23 | 1321-1341 | http://edamontology.org/topic_3515 | denotes | protein interactions |
| T24 | 1321-1341 | http://edamontology.org/topic_0144 | denotes | protein interactions |
| T25 | 1329-1341 | http://edamontology.org/topic_0602 | denotes | interactions |
| T26 | 1483-1489 | http://edamontology.org/topic_0632 | denotes | probes |
| T27 | 1689-1694 | http://edamontology.org/topic_0780 | denotes | plant |
| T28 | 2115-2123 | http://edamontology.org/topic_0196 | denotes | assembly |
| T29 | 2223-2232 | http://edamontology.org/topic_0154 | denotes | targeting |
EDAM-DFO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 64-74 | http://edamontology.org/operation_3429 | denotes | generation |
| T2 | 449-463 | http://edamontology.org/data_2746 | denotes | monosaccharide |
| T3 | 547-558 | http://edamontology.org/operation_3429 | denotes | generations |
| T4 | 672-677 | http://edamontology.org/data_2100 | denotes | types |
| T5 | 701-709 | http://edamontology.org/format_1208 | denotes | proteins |
| T6 | 701-709 | http://edamontology.org/data_1467 | denotes | proteins |
| T7 | 931-938 | http://edamontology.org/format_1208 | denotes | protein |
| T8 | 931-938 | http://edamontology.org/data_1467 | denotes | protein |
| T9 | 978-983 | http://edamontology.org/operation_3454 | denotes | phase |
| T10 | 978-983 | http://edamontology.org/data_2336 | denotes | phase |
| T11 | 1313-1320 | http://edamontology.org/format_1208 | denotes | protein |
| T12 | 1313-1320 | http://edamontology.org/data_1467 | denotes | protein |
| T13 | 1313-1341 | http://edamontology.org/data_1565 | denotes | protein-protein interactions |
| T14 | 1313-1341 | http://edamontology.org/data_1566 | denotes | protein-protein interactions |
| T15 | 1313-1341 | http://edamontology.org/operation_2464 | denotes | protein-protein interactions |
| T16 | 1313-1341 | http://edamontology.org/data_2402 | denotes | protein-protein interactions |
| T17 | 1313-1341 | http://edamontology.org/operation_3094 | denotes | protein-protein interactions |
| T18 | 1313-1341 | http://edamontology.org/data_1550 | denotes | protein-protein interactions |
| T19 | 1313-1341 | http://edamontology.org/data_0906 | denotes | protein-protein interactions |
| T20 | 1313-1344 | http://edamontology.org/operation_2445 | denotes | protein-protein interactions of |
| T21 | 1313-1344 | http://edamontology.org/operation_2405 | denotes | protein-protein interactions of |
| T22 | 1313-1344 | http://edamontology.org/data_1663 | denotes | protein-protein interactions of |
| T23 | 1313-1344 | http://edamontology.org/data_0905 | denotes | protein-protein interactions of |
| T24 | 1313-1344 | http://edamontology.org/operation_2949 | denotes | protein-protein interactions of |
| T25 | 1313-1344 | http://edamontology.org/data_0906 | denotes | protein-protein interactions of |
| T26 | 1321-1328 | http://edamontology.org/format_1208 | denotes | protein |
| T27 | 1321-1328 | http://edamontology.org/data_1467 | denotes | protein |
| T28 | 1321-1341 | http://edamontology.org/data_0906 | denotes | protein interactions |
| T29 | 1321-1341 | http://edamontology.org/format_2054 | denotes | protein interactions |
| T30 | 1321-1341 | http://edamontology.org/data_1074 | denotes | protein interactions |
| T31 | 1321-1341 | http://edamontology.org/data_1550 | denotes | protein interactions |
| T32 | 1321-1341 | http://edamontology.org/data_2378 | denotes | protein interactions |
| T33 | 1321-1341 | http://edamontology.org/operation_2492 | denotes | protein interactions |
| T34 | 1617-1625 | http://edamontology.org/operation_2423 | denotes | detected |
| T35 | 1770-1776 | http://edamontology.org/data_2082 | denotes | matrix |
| T36 | 1798-1803 | http://edamontology.org/data_2082 | denotes | array |
| T37 | 2095-2106 | http://edamontology.org/operation_3429 | denotes | generations |
| T38 | 2115-2123 | http://edamontology.org/operation_3433 | denotes | assembly |
Lectin
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| Lectin_T1 | 842-852 | https://acgg.asia/db/lfdb/LfDB0270 | denotes | galectin-1 |
| Lectin_T2 | 1170-1180 | https://acgg.asia/db/lfdb/LfDB0270 | denotes | galectin-1 |
| Lectin_T3 | 1752-1762 | https://acgg.asia/db/lfdb/LfDB0270 | denotes | galectin-1 |
| Lectin_T4 | 842-852 | https://acgg.asia/db/lfdb/LfDB0057 | denotes | galectin-1 |
| Lectin_T5 | 1170-1180 | https://acgg.asia/db/lfdb/LfDB0057 | denotes | galectin-1 |
| Lectin_T6 | 1752-1762 | https://acgg.asia/db/lfdb/LfDB0057 | denotes | galectin-1 |
GlyTouCan-IUPAC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| GlycanIUPAC_T1 | 287-292 | "http://rdf.glycoinfo.org/glycan/G59665TO" | denotes | sugar |
| GlycanIUPAC_T2 | 376-381 | "http://rdf.glycoinfo.org/glycan/G59665TO" | denotes | sugar |
| GlycanIUPAC_T3 | 1848-1853 | "http://rdf.glycoinfo.org/glycan/G59665TO" | denotes | sugar |
| GlycanIUPAC_T4 | 287-292 | "http://rdf.glycoinfo.org/glycan/G32915EI" | denotes | sugar |
| GlycanIUPAC_T5 | 376-381 | "http://rdf.glycoinfo.org/glycan/G32915EI" | denotes | sugar |
| GlycanIUPAC_T6 | 1848-1853 | "http://rdf.glycoinfo.org/glycan/G32915EI" | denotes | sugar |
| GlycanIUPAC_T7 | 287-292 | "http://rdf.glycoinfo.org/glycan/G60625TS" | denotes | sugar |
| GlycanIUPAC_T8 | 376-381 | "http://rdf.glycoinfo.org/glycan/G60625TS" | denotes | sugar |
| GlycanIUPAC_T9 | 1848-1853 | "http://rdf.glycoinfo.org/glycan/G60625TS" | denotes | sugar |
GlyCosmos15-Glycan
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 0-7 | Glycan | denotes | Lactose | https://api.glycosmos.org/wurcs2image/latest/png/binary/G15541SE |
Glycan-GlyCosmos
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 0-7 | Glycan | denotes | Lactose | https://api.glycosmos.org/wurcs2image/latest/png/binary/G15541SE |
GlyCosmos15-CL
| Id | Subject | Object | Predicate | Lexical cue | cl_id |
|---|---|---|---|---|---|
| T1 | 501-505 | Cell | denotes | poly | http://purl.obolibrary.org/obo/CL:0000096|http://purl.obolibrary.org/obo/CL:0000775 |
GlyCosmos15-Taxon
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 793-798 | Organism | denotes | human | 9606 |
GlyCosmos15-Sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-182 | Sentence | denotes | Lactose-containing starburst dendrimers: influence of dendrimer generation and binding-site orientation of receptors (plant/animal lectins and immunoglobulins) on binding properties. |
| T2 | 183-303 | Sentence | denotes | Starburst glycodendrimers offer the potential to serve as high-affinity ligands for clinically relevant sugar receptors. |
| T3 | 304-494 | Sentence | denotes | In order to define areas of application, their binding behavior towards sugar receptors with differential binding-site orientation but identical monosaccharide specificity must be evaluated. |
| T4 | 495-964 | Sentence | denotes | Using poly(amidoamine) starburst dendrimers of five generations, which contain the p-isothiocyanato derivative of p-aminophenyl-beta-D-lactoside as ligand group, four different types of galactoside-binding proteins were chosen for this purpose, i.e., the (AB)(2)-toxic agglutinin from mistletoe, a human immunoglobulin G fraction, the homodimeric galectin-1 with its two binding sites at opposite ends of the jelly-roll-motif-harboring protein and monomeric galectin-3. |
| T5 | 965-1181 | Sentence | denotes | Direct solid-phase assays with surface-immobilized glycodendrimers resulted in obvious affinity enhancements by progressive core branching for the plant agglutinin and less pronounced for the antibody and galectin-1. |
| T6 | 1182-1445 | Sentence | denotes | High density of binding of galectin-3 with modest affinity increases only from the level of the 32-mer onwards points to favorable protein-protein interactions of the monomeric lectin and a spherical display of the end groups without a major share of backfolding. |
| T7 | 1446-1626 | Sentence | denotes | When the inhibitory potency of these probes was evaluated as competitor of receptor binding to an immobilized neoglycoprotein or to asialofetuin, a marked selectivity was detected. |
| T8 | 1627-1860 | Sentence | denotes | The 32- and 64-mers were second to none as inhibitors for the plant agglutinin against both ligand-exposing matrices and for galectin-1 on the matrix with a heterogeneous array of interglycoside distances even on the per-sugar basis. |
| T9 | 1861-2000 | Sentence | denotes | In contrast, a neoglycoprotein with the same end group was superior in the case of the antibody and, less pronounced, monomeric galectin-3. |
| T10 | 2001-2275 | Sentence | denotes | Intimate details of topological binding-site presentation and the ligand display on different generations of core assembly are major operative factors which determine the potential of dendrimers for applications as lectin-targeting device, as attested by these observations. |
Lectin-Jamboree
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 131-138 | lectin | denotes | lectins |
| T2 | 1359-1365 | lectin | denotes | lectin |
| T3 | 2216-2222 | lectin | denotes | lectin |
Lectin-Jamboree-Sentence
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-182 | Sentence | denotes | Lactose-containing starburst dendrimers: influence of dendrimer generation and binding-site orientation of receptors (plant/animal lectins and immunoglobulins) on binding properties. |
| T2 | 183-303 | Sentence | denotes | Starburst glycodendrimers offer the potential to serve as high-affinity ligands for clinically relevant sugar receptors. |
| T3 | 304-494 | Sentence | denotes | In order to define areas of application, their binding behavior towards sugar receptors with differential binding-site orientation but identical monosaccharide specificity must be evaluated. |
| T4 | 495-964 | Sentence | denotes | Using poly(amidoamine) starburst dendrimers of five generations, which contain the p-isothiocyanato derivative of p-aminophenyl-beta-D-lactoside as ligand group, four different types of galactoside-binding proteins were chosen for this purpose, i.e., the (AB)(2)-toxic agglutinin from mistletoe, a human immunoglobulin G fraction, the homodimeric galectin-1 with its two binding sites at opposite ends of the jelly-roll-motif-harboring protein and monomeric galectin-3. |
| T5 | 965-1181 | Sentence | denotes | Direct solid-phase assays with surface-immobilized glycodendrimers resulted in obvious affinity enhancements by progressive core branching for the plant agglutinin and less pronounced for the antibody and galectin-1. |
| T6 | 1182-1445 | Sentence | denotes | High density of binding of galectin-3 with modest affinity increases only from the level of the 32-mer onwards points to favorable protein-protein interactions of the monomeric lectin and a spherical display of the end groups without a major share of backfolding. |
| T7 | 1446-1626 | Sentence | denotes | When the inhibitory potency of these probes was evaluated as competitor of receptor binding to an immobilized neoglycoprotein or to asialofetuin, a marked selectivity was detected. |
| T8 | 1627-1860 | Sentence | denotes | The 32- and 64-mers were second to none as inhibitors for the plant agglutinin against both ligand-exposing matrices and for galectin-1 on the matrix with a heterogeneous array of interglycoside distances even on the per-sugar basis. |
| T9 | 1861-2000 | Sentence | denotes | In contrast, a neoglycoprotein with the same end group was superior in the case of the antibody and, less pronounced, monomeric galectin-3. |
| T10 | 2001-2275 | Sentence | denotes | Intimate details of topological binding-site presentation and the ligand display on different generations of core assembly are major operative factors which determine the potential of dendrimers for applications as lectin-targeting device, as attested by these observations. |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 793-798 | OrganismTaxon | denotes | human | 9606 |