PubMed:15470230
Annnotations
Glycan-Motif
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 95-100 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
T2 | 135-140 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
T3 | 250-255 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
T4 | 349-354 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
T5 | 686-699 | https://glytoucan.org/Structures/Glycans/G40585SO | denotes | paragloboside |
T6 | 686-699 | https://glytoucan.org/Structures/Glycans/G48059CD | denotes | paragloboside |
T7 | 686-699 | https://glytoucan.org/Structures/Glycans/G58896AZ | denotes | paragloboside |
T8 | 880-893 | https://glytoucan.org/Structures/Glycans/G40585SO | denotes | paragloboside |
T9 | 880-893 | https://glytoucan.org/Structures/Glycans/G48059CD | denotes | paragloboside |
T10 | 880-893 | https://glytoucan.org/Structures/Glycans/G58896AZ | denotes | paragloboside |
T11 | 1075-1088 | https://glytoucan.org/Structures/Glycans/G40585SO | denotes | paragloboside |
T12 | 1075-1088 | https://glytoucan.org/Structures/Glycans/G48059CD | denotes | paragloboside |
T13 | 1075-1088 | https://glytoucan.org/Structures/Glycans/G58896AZ | denotes | paragloboside |
T14 | 1213-1232 | https://glytoucan.org/Structures/Glycans/G00055MO | denotes | N-acetyllactosamine |
T15 | 1810-1815 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
ggdb-test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 250-258 | https://acgg.asia/db/ggdb/info/gg035 | denotes | HNK-1 ST |
GlyCosmos6-Glycan-Motif-Image
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 95-100 | Glycan_Motif | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G54406UD |
T2 | 135-140 | Glycan_Motif | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G54406UD |
T3 | 250-255 | Glycan_Motif | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G54406UD |
T4 | 349-354 | Glycan_Motif | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G54406UD |
T5 | 686-699 | Glycan_Motif | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G58896AZ|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G48059CD|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G40585SO |
T8 | 880-893 | Glycan_Motif | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G58896AZ|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G48059CD|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G40585SO |
T11 | 1075-1088 | Glycan_Motif | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G58896AZ|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G48059CD|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G40585SO |
T14 | 1213-1232 | Glycan_Motif | denotes | N-acetyllactosamine | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00055MO |
T15 | 1810-1815 | Glycan_Motif | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G54406UD |
GGDB-2020
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 250-258 | https://acgg.asia/db/ggdb/info/gg035 | denotes | HNK-1 ST |
GlyCosmos6-Glycan-Motif-Structure
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 95-100 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
T2 | 135-140 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
T3 | 250-255 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
T4 | 349-354 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
T5 | 686-699 | https://glytoucan.org/Structures/Glycans/G40585SO | denotes | paragloboside |
T6 | 686-699 | https://glytoucan.org/Structures/Glycans/G48059CD | denotes | paragloboside |
T7 | 686-699 | https://glytoucan.org/Structures/Glycans/G58896AZ | denotes | paragloboside |
T8 | 880-893 | https://glytoucan.org/Structures/Glycans/G40585SO | denotes | paragloboside |
T9 | 880-893 | https://glytoucan.org/Structures/Glycans/G48059CD | denotes | paragloboside |
T10 | 880-893 | https://glytoucan.org/Structures/Glycans/G58896AZ | denotes | paragloboside |
T11 | 1075-1088 | https://glytoucan.org/Structures/Glycans/G40585SO | denotes | paragloboside |
T12 | 1075-1088 | https://glytoucan.org/Structures/Glycans/G48059CD | denotes | paragloboside |
T13 | 1075-1088 | https://glytoucan.org/Structures/Glycans/G58896AZ | denotes | paragloboside |
T14 | 1213-1232 | https://glytoucan.org/Structures/Glycans/G00055MO | denotes | N-acetyllactosamine |
T15 | 1810-1815 | https://glytoucan.org/Structures/Glycans/G54406UD | denotes | HNK-1 |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-114 | Sentence | denotes | Different acceptor specificities of two glucuronyltransferases involved in the biosynthesis of HNK-1 carbohydrate. |
TextSentencer_T2 | 115-260 | Sentence | denotes | The biosynthesis of HNK-1 carbohydrate is mainly regulated by two glucuronyltransferases (GlcAT-P and GlcAT-S) and a sulfotransferase (HNK-1 ST). |
TextSentencer_T3 | 261-527 | Sentence | denotes | To determine how the two glucuronyltransferases are involved in the biosynthesis of the HNK-1 carbohydrate, we prepared soluble forms of GlcAT-P and GlcAT-S fused with the IgG-binding domain of protein A and then compared the enzymatic properties of the two enzymes. |
TextSentencer_T4 | 528-700 | Sentence | denotes | Both GlcAT-P and GlcAT-S transferred glucuronic acid (GlcA) not only to a glycoprotein acceptor, asialoorosomucoid (ASOR), but also to a glycolipid acceptor, paragloboside. |
TextSentencer_T5 | 701-838 | Sentence | denotes | The activity of GlcAT-P toward ASOR was enhanced fivefold in the presence of sphingomyelin, but there were no effects on that of GlcAT-S. |
TextSentencer_T6 | 839-975 | Sentence | denotes | The activities of the two enzymes toward paragloboside were only detected in the presence of phospholipids such as phosphatidylinositol. |
TextSentencer_T7 | 976-1089 | Sentence | denotes | Kinetic analysis revealed that the K(m) value of GlcAT-P for ASOR was 10 times lower than that for paragloboside. |
TextSentencer_T8 | 1090-1304 | Sentence | denotes | Furthermore, acceptor specificity analysis involving various oligosaccarides revealed that GlcAT-P specifically recognized N-acetyllactosamine (Galbeta1-4GlcNAc) at the nonreducing terminals of acceptor substrates. |
TextSentencer_T9 | 1305-1504 | Sentence | denotes | In contrast, GlcAT-S recognized not only the terminal Galbeta1-4GlcNAc structure but also the Galbeta1-3GlcNAc structure and showed the highest activity toward triantennary N-linked oligosaccharides. |
TextSentencer_T10 | 1505-1624 | Sentence | denotes | GlcAT-P transferred GlcA to NCAM about twice as much as to ASOR, whereas GlcAT-S did not show any activity toward NCAM. |
TextSentencer_T11 | 1625-1852 | Sentence | denotes | These lines of evidence indicate that these two enzymes have significantly different acceptor specificities, suggesting that they may synthesize functionally and structurally different HNK-1 carbohydrates in the nervous system. |
T1 | 0-114 | Sentence | denotes | Different acceptor specificities of two glucuronyltransferases involved in the biosynthesis of HNK-1 carbohydrate. |
T2 | 115-260 | Sentence | denotes | The biosynthesis of HNK-1 carbohydrate is mainly regulated by two glucuronyltransferases (GlcAT-P and GlcAT-S) and a sulfotransferase (HNK-1 ST). |
T3 | 261-527 | Sentence | denotes | To determine how the two glucuronyltransferases are involved in the biosynthesis of the HNK-1 carbohydrate, we prepared soluble forms of GlcAT-P and GlcAT-S fused with the IgG-binding domain of protein A and then compared the enzymatic properties of the two enzymes. |
T4 | 528-700 | Sentence | denotes | Both GlcAT-P and GlcAT-S transferred glucuronic acid (GlcA) not only to a glycoprotein acceptor, asialoorosomucoid (ASOR), but also to a glycolipid acceptor, paragloboside. |
T5 | 701-975 | Sentence | denotes | The activity of GlcAT-P toward ASOR was enhanced fivefold in the presence of sphingomyelin, but there were no effects on that of GlcAT-S. The activities of the two enzymes toward paragloboside were only detected in the presence of phospholipids such as phosphatidylinositol. |
T6 | 976-1089 | Sentence | denotes | Kinetic analysis revealed that the K(m) value of GlcAT-P for ASOR was 10 times lower than that for paragloboside. |
T7 | 1090-1304 | Sentence | denotes | Furthermore, acceptor specificity analysis involving various oligosaccarides revealed that GlcAT-P specifically recognized N-acetyllactosamine (Galbeta1-4GlcNAc) at the nonreducing terminals of acceptor substrates. |
T8 | 1305-1504 | Sentence | denotes | In contrast, GlcAT-S recognized not only the terminal Galbeta1-4GlcNAc structure but also the Galbeta1-3GlcNAc structure and showed the highest activity toward triantennary N-linked oligosaccharides. |
T9 | 1505-1624 | Sentence | denotes | GlcAT-P transferred GlcA to NCAM about twice as much as to ASOR, whereas GlcAT-S did not show any activity toward NCAM. |
T10 | 1625-1852 | Sentence | denotes | These lines of evidence indicate that these two enzymes have significantly different acceptor specificities, suggesting that they may synthesize functionally and structurally different HNK-1 carbohydrates in the nervous system. |
T1 | 0-114 | Sentence | denotes | Different acceptor specificities of two glucuronyltransferases involved in the biosynthesis of HNK-1 carbohydrate. |
T2 | 115-260 | Sentence | denotes | The biosynthesis of HNK-1 carbohydrate is mainly regulated by two glucuronyltransferases (GlcAT-P and GlcAT-S) and a sulfotransferase (HNK-1 ST). |
T3 | 261-527 | Sentence | denotes | To determine how the two glucuronyltransferases are involved in the biosynthesis of the HNK-1 carbohydrate, we prepared soluble forms of GlcAT-P and GlcAT-S fused with the IgG-binding domain of protein A and then compared the enzymatic properties of the two enzymes. |
T4 | 528-700 | Sentence | denotes | Both GlcAT-P and GlcAT-S transferred glucuronic acid (GlcA) not only to a glycoprotein acceptor, asialoorosomucoid (ASOR), but also to a glycolipid acceptor, paragloboside. |
T5 | 701-838 | Sentence | denotes | The activity of GlcAT-P toward ASOR was enhanced fivefold in the presence of sphingomyelin, but there were no effects on that of GlcAT-S. |
T6 | 839-975 | Sentence | denotes | The activities of the two enzymes toward paragloboside were only detected in the presence of phospholipids such as phosphatidylinositol. |
T7 | 976-1089 | Sentence | denotes | Kinetic analysis revealed that the K(m) value of GlcAT-P for ASOR was 10 times lower than that for paragloboside. |
T8 | 1090-1304 | Sentence | denotes | Furthermore, acceptor specificity analysis involving various oligosaccarides revealed that GlcAT-P specifically recognized N-acetyllactosamine (Galbeta1-4GlcNAc) at the nonreducing terminals of acceptor substrates. |
T9 | 1305-1504 | Sentence | denotes | In contrast, GlcAT-S recognized not only the terminal Galbeta1-4GlcNAc structure but also the Galbeta1-3GlcNAc structure and showed the highest activity toward triantennary N-linked oligosaccharides. |
T10 | 1505-1624 | Sentence | denotes | GlcAT-P transferred GlcA to NCAM about twice as much as to ASOR, whereas GlcAT-S did not show any activity toward NCAM. |
T11 | 1625-1852 | Sentence | denotes | These lines of evidence indicate that these two enzymes have significantly different acceptor specificities, suggesting that they may synthesize functionally and structurally different HNK-1 carbohydrates in the nervous system. |
Glycosmos6-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 95-100 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
T2 | 135-140 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
T3 | 250-255 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
T4 | 349-354 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
T5 | 686-699 | http://www.glycoepitope.jp/epitopes/EP0075 | denotes | paragloboside |
T6 | 880-893 | http://www.glycoepitope.jp/epitopes/EP0075 | denotes | paragloboside |
T7 | 1075-1088 | http://www.glycoepitope.jp/epitopes/EP0075 | denotes | paragloboside |
T8 | 1810-1815 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
Glycosmos6-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1837-1851 | http://purl.obolibrary.org/obo/MAT_0000026 | denotes | nervous system |
ICD10
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1837-1844 | http://purl.bioontology.org/ontology/ICD10/R45.0 | denotes | nervous |
uniprot-human
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 211-222 | http://www.uniprot.org/uniprot/Q9P2W7 | denotes | P and GlcAT |
T2 | 404-415 | http://www.uniprot.org/uniprot/Q9P2W7 | denotes | P and GlcAT |
T3 | 539-550 | http://www.uniprot.org/uniprot/Q9P2W7 | denotes | P and GlcAT |
T4 | 217-224 | http://www.uniprot.org/uniprot/Q9NPZ5 | denotes | GlcAT-S |
T5 | 410-417 | http://www.uniprot.org/uniprot/Q9NPZ5 | denotes | GlcAT-S |
T6 | 545-552 | http://www.uniprot.org/uniprot/Q9NPZ5 | denotes | GlcAT-S |
T7 | 830-837 | http://www.uniprot.org/uniprot/Q9NPZ5 | denotes | GlcAT-S |
T8 | 1318-1325 | http://www.uniprot.org/uniprot/Q9NPZ5 | denotes | GlcAT-S |
T9 | 1578-1585 | http://www.uniprot.org/uniprot/Q9NPZ5 | denotes | GlcAT-S |
T10 | 232-255 | http://www.uniprot.org/uniprot/O43529 | denotes | sulfotransferase (HNK-1 |
T11 | 1533-1537 | http://www.uniprot.org/uniprot/Q59FL7 | denotes | NCAM |
T12 | 1619-1623 | http://www.uniprot.org/uniprot/Q59FL7 | denotes | NCAM |
uniprot-mouse
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 211-222 | http://www.uniprot.org/uniprot/Q9CW73 | denotes | P and GlcAT |
T2 | 404-415 | http://www.uniprot.org/uniprot/Q9CW73 | denotes | P and GlcAT |
T3 | 539-550 | http://www.uniprot.org/uniprot/Q9CW73 | denotes | P and GlcAT |
T4 | 217-224 | http://www.uniprot.org/uniprot/P59270 | denotes | GlcAT-S |
T5 | 410-417 | http://www.uniprot.org/uniprot/P59270 | denotes | GlcAT-S |
T6 | 545-552 | http://www.uniprot.org/uniprot/P59270 | denotes | GlcAT-S |
T7 | 830-837 | http://www.uniprot.org/uniprot/P59270 | denotes | GlcAT-S |
T8 | 1318-1325 | http://www.uniprot.org/uniprot/P59270 | denotes | GlcAT-S |
T9 | 1578-1585 | http://www.uniprot.org/uniprot/P59270 | denotes | GlcAT-S |
T10 | 232-255 | http://www.uniprot.org/uniprot/Q6PGK7 | denotes | sulfotransferase (HNK-1 |
T11 | 256-258 | http://www.uniprot.org/uniprot/P50236 | denotes | ST |
T12 | 256-258 | http://www.uniprot.org/uniprot/P52843 | denotes | ST |
T13 | 418-423 | http://www.uniprot.org/uniprot/O35625 | denotes | fused |
GO-BP
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 79-91 | http://purl.obolibrary.org/obo/GO_0009058 | denotes | biosynthesis |
T2 | 119-131 | http://purl.obolibrary.org/obo/GO_0009058 | denotes | biosynthesis |
T3 | 329-341 | http://purl.obolibrary.org/obo/GO_0009058 | denotes | biosynthesis |
T4 | 101-131 | http://purl.obolibrary.org/obo/GO_0016051 | denotes | carbohydrate. The biosynthesis |
T5 | 164-173 | http://purl.obolibrary.org/obo/GO_0065007 | denotes | regulated |
T6 | 582-586 | http://purl.obolibrary.org/obo/GO_0043879 | denotes | GlcA |
T7 | 1525-1529 | http://purl.obolibrary.org/obo/GO_0043879 | denotes | GlcA |
GO-MF
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 433-444 | http://purl.obolibrary.org/obo/GO_0019864 | denotes | IgG-binding |
T2 | 437-444 | http://purl.obolibrary.org/obo/GO_0070026 | denotes | binding |
T3 | 437-444 | http://purl.obolibrary.org/obo/GO_0003680 | denotes | binding |
T4 | 437-444 | http://purl.obolibrary.org/obo/GO_0017091 | denotes | binding |
T5 | 437-444 | http://purl.obolibrary.org/obo/GO_0005488 | denotes | binding |
T6 | 437-462 | http://purl.obolibrary.org/obo/GO_0019904 | denotes | binding domain of protein |
T7 | 437-462 | http://purl.obolibrary.org/obo/GO_0089719 | denotes | binding domain of protein |
UBERON-AE
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1837-1851 | http://purl.obolibrary.org/obo/UBERON_0001016 | denotes | nervous system |
glycogenes
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-GlycoGenes20190927-B_T1 | 205-212 | https://acgg.asia/db/ggdb/info/gg157 | denotes | GlcAT-P |
PD-GlycoGenes20190927-B_T2 | 217-222 | https://acgg.asia/db/ggdb/info/gg156 | denotes | GlcAT |
PD-GlycoGenes20190927-B_T3 | 250-258 | https://acgg.asia/db/ggdb/info/gg035 | denotes | HNK-1 ST |
PD-GlycoGenes20190927-B_T4 | 398-405 | https://acgg.asia/db/ggdb/info/gg157 | denotes | GlcAT-P |
PD-GlycoGenes20190927-B_T5 | 410-415 | https://acgg.asia/db/ggdb/info/gg156 | denotes | GlcAT |
PD-GlycoGenes20190927-B_T6 | 533-540 | https://acgg.asia/db/ggdb/info/gg157 | denotes | GlcAT-P |
PD-GlycoGenes20190927-B_T7 | 545-550 | https://acgg.asia/db/ggdb/info/gg156 | denotes | GlcAT |
PD-GlycoGenes20190927-B_T8 | 717-724 | https://acgg.asia/db/ggdb/info/gg157 | denotes | GlcAT-P |
PD-GlycoGenes20190927-B_T9 | 830-835 | https://acgg.asia/db/ggdb/info/gg156 | denotes | GlcAT |
PD-GlycoGenes20190927-B_T10 | 1025-1032 | https://acgg.asia/db/ggdb/info/gg157 | denotes | GlcAT-P |
PD-GlycoGenes20190927-B_T11 | 1181-1188 | https://acgg.asia/db/ggdb/info/gg157 | denotes | GlcAT-P |
PD-GlycoGenes20190927-B_T12 | 1318-1323 | https://acgg.asia/db/ggdb/info/gg156 | denotes | GlcAT |
PD-GlycoGenes20190927-B_T13 | 1505-1512 | https://acgg.asia/db/ggdb/info/gg157 | denotes | GlcAT-P |
PD-GlycoGenes20190927-B_T14 | 1578-1583 | https://acgg.asia/db/ggdb/info/gg156 | denotes | GlcAT |
GlycoBiology-MAT
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1837-1851 | http://purl.obolibrary.org/obo/MAT_0000026 | denotes | nervous system |
GlycoBiology-Epitope
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-GlycoEpitope-B_T1 | 95-100 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
PD-GlycoEpitope-B_T2 | 135-140 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
PD-GlycoEpitope-B_T3 | 250-255 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
PD-GlycoEpitope-B_T4 | 349-354 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
PD-GlycoEpitope-B_T5 | 1810-1815 | http://www.glycoepitope.jp/epitopes/EP0001 | denotes | HNK-1 |
PD-GlycoEpitope-B_T6 | 686-699 | http://www.glycoepitope.jp/epitopes/EP0075 | denotes | paragloboside |
PD-GlycoEpitope-B_T7 | 880-893 | http://www.glycoepitope.jp/epitopes/EP0075 | denotes | paragloboside |
PD-GlycoEpitope-B_T8 | 1075-1088 | http://www.glycoepitope.jp/epitopes/EP0075 | denotes | paragloboside |
GlyTouCan-IUPAC
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
GlycanIUPAC_T1 | 582-586 | "http://rdf.glycoinfo.org/glycan/G91489RT" | denotes | GlcA |
GlycanIUPAC_T2 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G91489RT" | denotes | GlcA |
GlycanIUPAC_T3 | 582-586 | "http://rdf.glycoinfo.org/glycan/G54004DL" | denotes | GlcA |
GlycanIUPAC_T4 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G54004DL" | denotes | GlcA |
GlycanIUPAC_T5 | 582-586 | "http://rdf.glycoinfo.org/glycan/G90208ZS" | denotes | GlcA |
GlycanIUPAC_T6 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G90208ZS" | denotes | GlcA |
GlycanIUPAC_T7 | 582-586 | "http://rdf.glycoinfo.org/glycan/G47973RQ" | denotes | GlcA |
GlycanIUPAC_T8 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G47973RQ" | denotes | GlcA |
GlycanIUPAC_T9 | 582-586 | "http://rdf.glycoinfo.org/glycan/G35471RR" | denotes | GlcA |
GlycanIUPAC_T10 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G35471RR" | denotes | GlcA |
GlycanIUPAC_T11 | 582-586 | "http://rdf.glycoinfo.org/glycan/G45399NV" | denotes | GlcA |
GlycanIUPAC_T12 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G45399NV" | denotes | GlcA |
GlycanIUPAC_T13 | 582-586 | "http://rdf.glycoinfo.org/glycan/G52061FU" | denotes | GlcA |
GlycanIUPAC_T14 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G52061FU" | denotes | GlcA |
GlycanIUPAC_T15 | 582-586 | "http://rdf.glycoinfo.org/glycan/G10736YH" | denotes | GlcA |
GlycanIUPAC_T16 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G10736YH" | denotes | GlcA |
GlycanIUPAC_T17 | 582-586 | "http://rdf.glycoinfo.org/glycan/G30254CI" | denotes | GlcA |
GlycanIUPAC_T18 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G30254CI" | denotes | GlcA |
GlycanIUPAC_T19 | 582-586 | "http://rdf.glycoinfo.org/glycan/G57856MN" | denotes | GlcA |
GlycanIUPAC_T20 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G57856MN" | denotes | GlcA |
GlycanIUPAC_T21 | 582-586 | "http://rdf.glycoinfo.org/glycan/G95754KF" | denotes | GlcA |
GlycanIUPAC_T22 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G95754KF" | denotes | GlcA |
GlycanIUPAC_T23 | 582-586 | "http://rdf.glycoinfo.org/glycan/G90067UQ" | denotes | GlcA |
GlycanIUPAC_T24 | 1525-1529 | "http://rdf.glycoinfo.org/glycan/G90067UQ" | denotes | GlcA |
performance-test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-UBERON-AE-B_T1 | 1837-1851 | http://purl.obolibrary.org/obo/UBERON_0001016 | denotes | nervous system |
Anatomy-MAT
Id | Subject | Object | Predicate | Lexical cue | mat_id |
---|---|---|---|---|---|
T1 | 1837-1851 | Body_part | denotes | nervous system | http://purl.obolibrary.org/obo/MAT_0000026 |
Glycan-GlyCosmos
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 95-100 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
T2 | 135-140 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
T3 | 250-255 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
T4 | 349-354 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
T5 | 686-699 | Glycan | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/latest/png/binary/G58896AZ |
T6 | 880-893 | Glycan | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/latest/png/binary/G58896AZ |
T7 | 1075-1088 | Glycan | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/latest/png/binary/G58896AZ |
T8 | 1810-1815 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
GlyCosmos15-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 1837-1851 | Body_part | denotes | nervous system | http://purl.obolibrary.org/obo/UBERON_0001016 |
GlyCosmos15-MAT
Id | Subject | Object | Predicate | Lexical cue | mat_id |
---|---|---|---|---|---|
T1 | 1837-1851 | Body_part | denotes | nervous system | http://purl.obolibrary.org/obo/MAT_0000026 |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-114 | Sentence | denotes | Different acceptor specificities of two glucuronyltransferases involved in the biosynthesis of HNK-1 carbohydrate. |
TextSentencer_T2 | 115-260 | Sentence | denotes | The biosynthesis of HNK-1 carbohydrate is mainly regulated by two glucuronyltransferases (GlcAT-P and GlcAT-S) and a sulfotransferase (HNK-1 ST). |
TextSentencer_T3 | 261-527 | Sentence | denotes | To determine how the two glucuronyltransferases are involved in the biosynthesis of the HNK-1 carbohydrate, we prepared soluble forms of GlcAT-P and GlcAT-S fused with the IgG-binding domain of protein A and then compared the enzymatic properties of the two enzymes. |
TextSentencer_T4 | 528-700 | Sentence | denotes | Both GlcAT-P and GlcAT-S transferred glucuronic acid (GlcA) not only to a glycoprotein acceptor, asialoorosomucoid (ASOR), but also to a glycolipid acceptor, paragloboside. |
TextSentencer_T5 | 701-838 | Sentence | denotes | The activity of GlcAT-P toward ASOR was enhanced fivefold in the presence of sphingomyelin, but there were no effects on that of GlcAT-S. |
TextSentencer_T6 | 839-975 | Sentence | denotes | The activities of the two enzymes toward paragloboside were only detected in the presence of phospholipids such as phosphatidylinositol. |
TextSentencer_T7 | 976-1089 | Sentence | denotes | Kinetic analysis revealed that the K(m) value of GlcAT-P for ASOR was 10 times lower than that for paragloboside. |
TextSentencer_T8 | 1090-1304 | Sentence | denotes | Furthermore, acceptor specificity analysis involving various oligosaccarides revealed that GlcAT-P specifically recognized N-acetyllactosamine (Galbeta1-4GlcNAc) at the nonreducing terminals of acceptor substrates. |
TextSentencer_T9 | 1305-1504 | Sentence | denotes | In contrast, GlcAT-S recognized not only the terminal Galbeta1-4GlcNAc structure but also the Galbeta1-3GlcNAc structure and showed the highest activity toward triantennary N-linked oligosaccharides. |
TextSentencer_T10 | 1505-1624 | Sentence | denotes | GlcAT-P transferred GlcA to NCAM about twice as much as to ASOR, whereas GlcAT-S did not show any activity toward NCAM. |
TextSentencer_T11 | 1625-1852 | Sentence | denotes | These lines of evidence indicate that these two enzymes have significantly different acceptor specificities, suggesting that they may synthesize functionally and structurally different HNK-1 carbohydrates in the nervous system. |
T1 | 0-114 | Sentence | denotes | Different acceptor specificities of two glucuronyltransferases involved in the biosynthesis of HNK-1 carbohydrate. |
T2 | 115-260 | Sentence | denotes | The biosynthesis of HNK-1 carbohydrate is mainly regulated by two glucuronyltransferases (GlcAT-P and GlcAT-S) and a sulfotransferase (HNK-1 ST). |
T3 | 261-527 | Sentence | denotes | To determine how the two glucuronyltransferases are involved in the biosynthesis of the HNK-1 carbohydrate, we prepared soluble forms of GlcAT-P and GlcAT-S fused with the IgG-binding domain of protein A and then compared the enzymatic properties of the two enzymes. |
T4 | 528-700 | Sentence | denotes | Both GlcAT-P and GlcAT-S transferred glucuronic acid (GlcA) not only to a glycoprotein acceptor, asialoorosomucoid (ASOR), but also to a glycolipid acceptor, paragloboside. |
T5 | 701-975 | Sentence | denotes | The activity of GlcAT-P toward ASOR was enhanced fivefold in the presence of sphingomyelin, but there were no effects on that of GlcAT-S. The activities of the two enzymes toward paragloboside were only detected in the presence of phospholipids such as phosphatidylinositol. |
T6 | 976-1089 | Sentence | denotes | Kinetic analysis revealed that the K(m) value of GlcAT-P for ASOR was 10 times lower than that for paragloboside. |
T7 | 1090-1304 | Sentence | denotes | Furthermore, acceptor specificity analysis involving various oligosaccarides revealed that GlcAT-P specifically recognized N-acetyllactosamine (Galbeta1-4GlcNAc) at the nonreducing terminals of acceptor substrates. |
T8 | 1305-1504 | Sentence | denotes | In contrast, GlcAT-S recognized not only the terminal Galbeta1-4GlcNAc structure but also the Galbeta1-3GlcNAc structure and showed the highest activity toward triantennary N-linked oligosaccharides. |
T9 | 1505-1624 | Sentence | denotes | GlcAT-P transferred GlcA to NCAM about twice as much as to ASOR, whereas GlcAT-S did not show any activity toward NCAM. |
T10 | 1625-1852 | Sentence | denotes | These lines of evidence indicate that these two enzymes have significantly different acceptor specificities, suggesting that they may synthesize functionally and structurally different HNK-1 carbohydrates in the nervous system. |
T1 | 0-114 | Sentence | denotes | Different acceptor specificities of two glucuronyltransferases involved in the biosynthesis of HNK-1 carbohydrate. |
T2 | 115-260 | Sentence | denotes | The biosynthesis of HNK-1 carbohydrate is mainly regulated by two glucuronyltransferases (GlcAT-P and GlcAT-S) and a sulfotransferase (HNK-1 ST). |
T3 | 261-527 | Sentence | denotes | To determine how the two glucuronyltransferases are involved in the biosynthesis of the HNK-1 carbohydrate, we prepared soluble forms of GlcAT-P and GlcAT-S fused with the IgG-binding domain of protein A and then compared the enzymatic properties of the two enzymes. |
T4 | 528-700 | Sentence | denotes | Both GlcAT-P and GlcAT-S transferred glucuronic acid (GlcA) not only to a glycoprotein acceptor, asialoorosomucoid (ASOR), but also to a glycolipid acceptor, paragloboside. |
T5 | 701-838 | Sentence | denotes | The activity of GlcAT-P toward ASOR was enhanced fivefold in the presence of sphingomyelin, but there were no effects on that of GlcAT-S. |
T6 | 839-975 | Sentence | denotes | The activities of the two enzymes toward paragloboside were only detected in the presence of phospholipids such as phosphatidylinositol. |
T7 | 976-1089 | Sentence | denotes | Kinetic analysis revealed that the K(m) value of GlcAT-P for ASOR was 10 times lower than that for paragloboside. |
T8 | 1090-1304 | Sentence | denotes | Furthermore, acceptor specificity analysis involving various oligosaccarides revealed that GlcAT-P specifically recognized N-acetyllactosamine (Galbeta1-4GlcNAc) at the nonreducing terminals of acceptor substrates. |
T9 | 1305-1504 | Sentence | denotes | In contrast, GlcAT-S recognized not only the terminal Galbeta1-4GlcNAc structure but also the Galbeta1-3GlcNAc structure and showed the highest activity toward triantennary N-linked oligosaccharides. |
T10 | 1505-1624 | Sentence | denotes | GlcAT-P transferred GlcA to NCAM about twice as much as to ASOR, whereas GlcAT-S did not show any activity toward NCAM. |
T11 | 1625-1852 | Sentence | denotes | These lines of evidence indicate that these two enzymes have significantly different acceptor specificities, suggesting that they may synthesize functionally and structurally different HNK-1 carbohydrates in the nervous system. |
GlyCosmos15-Sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-114 | Sentence | denotes | Different acceptor specificities of two glucuronyltransferases involved in the biosynthesis of HNK-1 carbohydrate. |
T2 | 115-260 | Sentence | denotes | The biosynthesis of HNK-1 carbohydrate is mainly regulated by two glucuronyltransferases (GlcAT-P and GlcAT-S) and a sulfotransferase (HNK-1 ST). |
T3 | 261-527 | Sentence | denotes | To determine how the two glucuronyltransferases are involved in the biosynthesis of the HNK-1 carbohydrate, we prepared soluble forms of GlcAT-P and GlcAT-S fused with the IgG-binding domain of protein A and then compared the enzymatic properties of the two enzymes. |
T4 | 528-700 | Sentence | denotes | Both GlcAT-P and GlcAT-S transferred glucuronic acid (GlcA) not only to a glycoprotein acceptor, asialoorosomucoid (ASOR), but also to a glycolipid acceptor, paragloboside. |
T5 | 701-975 | Sentence | denotes | The activity of GlcAT-P toward ASOR was enhanced fivefold in the presence of sphingomyelin, but there were no effects on that of GlcAT-S. The activities of the two enzymes toward paragloboside were only detected in the presence of phospholipids such as phosphatidylinositol. |
T6 | 976-1089 | Sentence | denotes | Kinetic analysis revealed that the K(m) value of GlcAT-P for ASOR was 10 times lower than that for paragloboside. |
T7 | 1090-1304 | Sentence | denotes | Furthermore, acceptor specificity analysis involving various oligosaccarides revealed that GlcAT-P specifically recognized N-acetyllactosamine (Galbeta1-4GlcNAc) at the nonreducing terminals of acceptor substrates. |
T8 | 1305-1504 | Sentence | denotes | In contrast, GlcAT-S recognized not only the terminal Galbeta1-4GlcNAc structure but also the Galbeta1-3GlcNAc structure and showed the highest activity toward triantennary N-linked oligosaccharides. |
T9 | 1505-1624 | Sentence | denotes | GlcAT-P transferred GlcA to NCAM about twice as much as to ASOR, whereas GlcAT-S did not show any activity toward NCAM. |
T10 | 1625-1852 | Sentence | denotes | These lines of evidence indicate that these two enzymes have significantly different acceptor specificities, suggesting that they may synthesize functionally and structurally different HNK-1 carbohydrates in the nervous system. |
GlyCosmos15-Glycan
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 95-100 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
T2 | 135-140 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
T3 | 250-255 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
T4 | 349-354 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
T5 | 686-699 | Glycan | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/latest/png/binary/G58896AZ |
T6 | 880-893 | Glycan | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/latest/png/binary/G58896AZ |
T7 | 1075-1088 | Glycan | denotes | paragloboside | https://api.glycosmos.org/wurcs2image/latest/png/binary/G58896AZ |
T8 | 1810-1815 | Glycan | denotes | HNK-1 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G54406UD |
GlyCosmos15-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue | glycoepitope_id |
---|---|---|---|---|---|
T1 | 95-100 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
T2 | 135-140 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
T3 | 250-255 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
T4 | 349-354 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
T5 | 686-699 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | paragloboside | http://www.glycoepitope.jp/epitopes/EP0075 |
T6 | 880-893 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | paragloboside | http://www.glycoepitope.jp/epitopes/EP0075 |
T7 | 1075-1088 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | paragloboside | http://www.glycoepitope.jp/epitopes/EP0075 |
T8 | 1810-1815 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
GlyCosmos-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue | glycoepitope_id |
---|---|---|---|---|---|
T1 | 95-100 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
T2 | 135-140 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
T3 | 250-255 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
T4 | 349-354 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
T5 | 686-699 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | paragloboside | http://www.glycoepitope.jp/epitopes/EP0075 |
T6 | 880-893 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | paragloboside | http://www.glycoepitope.jp/epitopes/EP0075 |
T7 | 1075-1088 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | paragloboside | http://www.glycoepitope.jp/epitopes/EP0075 |
T8 | 1810-1815 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | HNK-1 | http://www.glycoepitope.jp/epitopes/EP0001 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 1837-1851 | Body_part | denotes | nervous system | http://purl.obolibrary.org/obo/UBERON_0001016 |