PubMed:28334971
Annnotations
GlyCosmos6-Glycan-Motif-Image
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 750-757 | Glycan_Motif | denotes | glucose | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G15021LG |
T2 | 759-762 | Glycan_Motif | denotes | Glc | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G15021LG |
T3 | 867-877 | Glycan_Motif | denotes | hyaluronan | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00017MO |
T4 | 879-881 | Glycan_Motif | denotes | HA | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00017MO |
T5 | 897-899 | Glycan_Motif | denotes | HA | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00017MO |
T6 | 1150-1153 | Glycan_Motif | denotes | Glc | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G15021LG |
T7 | 1256-1259 | Glycan_Motif | denotes | Glc | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G15021LG |
T8 | 1331-1333 | Glycan_Motif | denotes | HA | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00017MO |
T9 | 1386-1405 | Glycan_Motif | denotes | N-acetylglucosamine | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G64581RP |
GlyCosmos6-Glycan-Motif-Structure
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 750-757 | https://glytoucan.org/Structures/Glycans/G15021LG | denotes | glucose |
T2 | 867-877 | https://glytoucan.org/Structures/Glycans/G00017MO | denotes | hyaluronan |
T3 | 1386-1405 | https://glytoucan.org/Structures/Glycans/G64581RP | denotes | N-acetylglucosamine |
Inflammaging
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-125 | Sentence | denotes | Expanding glycosaminoglycan chemical space: towards the creation of sulfated analogs, novel polymers and chimeric constructs. |
T2 | 126-251 | Sentence | denotes | Glycosaminoglycans (GAGs) have therapeutic potential in areas ranging from angiogenesis, inflammation, hemostasis and cancer. |
T3 | 252-391 | Sentence | denotes | GAG bioactivity is conferred by intrinsic structural features, such as disaccharide composition, glycosidic linkages and sulfation pattern. |
T4 | 392-550 | Sentence | denotes | Unfortunately, the in vitro enzymatic synthesis of defined GAGs is quite restricted by a limited understanding of current GAG synthases and modifying enzymes. |
T5 | 551-696 | Sentence | denotes | Our work provides insights into GAG-active enzymes through the creation of sulfated oligosaccharides, a new polysaccharide and chimeric polymers. |
T6 | 697-948 | Sentence | denotes | We show that a C6-sulfonated uridine diphospho (UDP)-glucose (Glc) derivative, sulfoquinovose, can be used as an uronic acid donor, but not as a hexosamine donor, to cap hyaluronan (HA) chains by the HA synthase from the microbe Pasteurella multocida. |
T7 | 949-1097 | Sentence | denotes | However, the two heparosan (HEP) synthases from the same species, PmHS1 and PmHS2, could not employ the UDP-sulfoquinovose under similar conditions. |
T8 | 1098-1265 | Sentence | denotes | Serendipitously, we found that PmHS2 co-polymerized Glc with glucuronic acid (GlcA), creating a novel HEP-like polymer we named hepbiuronic acid [-4-GlcAβ1-4-Glcα1-]n. |
T9 | 1266-1592 | Sentence | denotes | In addition, we created chimeric block polymers composed of both HA and HEP segments; in these reactions GlcA-, but not N-acetylglucosamine-(GlcNAc), terminated GAG acceptors were recognized by their noncognate synthase for further extension, likely due to the common β-linkage connecting GlcA to GlcNAc in both of these GAGs. |
T10 | 1593-1718 | Sentence | denotes | Overall, these GAG constructs provide new tools for studying biology and offer potential for future sugar-based therapeutics. |
T1 | 0-125 | Sentence | denotes | Expanding glycosaminoglycan chemical space: towards the creation of sulfated analogs, novel polymers and chimeric constructs. |
T2 | 126-251 | Sentence | denotes | Glycosaminoglycans (GAGs) have therapeutic potential in areas ranging from angiogenesis, inflammation, hemostasis and cancer. |
T3 | 252-391 | Sentence | denotes | GAG bioactivity is conferred by intrinsic structural features, such as disaccharide composition, glycosidic linkages and sulfation pattern. |
T4 | 392-550 | Sentence | denotes | Unfortunately, the in vitro enzymatic synthesis of defined GAGs is quite restricted by a limited understanding of current GAG synthases and modifying enzymes. |
T5 | 551-696 | Sentence | denotes | Our work provides insights into GAG-active enzymes through the creation of sulfated oligosaccharides, a new polysaccharide and chimeric polymers. |
T6 | 697-948 | Sentence | denotes | We show that a C6-sulfonated uridine diphospho (UDP)-glucose (Glc) derivative, sulfoquinovose, can be used as an uronic acid donor, but not as a hexosamine donor, to cap hyaluronan (HA) chains by the HA synthase from the microbe Pasteurella multocida. |
T7 | 949-1097 | Sentence | denotes | However, the two heparosan (HEP) synthases from the same species, PmHS1 and PmHS2, could not employ the UDP-sulfoquinovose under similar conditions. |
T8 | 1098-1265 | Sentence | denotes | Serendipitously, we found that PmHS2 co-polymerized Glc with glucuronic acid (GlcA), creating a novel HEP-like polymer we named hepbiuronic acid [-4-GlcAβ1-4-Glcα1-]n. |
T9 | 1266-1592 | Sentence | denotes | In addition, we created chimeric block polymers composed of both HA and HEP segments; in these reactions GlcA-, but not N-acetylglucosamine-(GlcNAc), terminated GAG acceptors were recognized by their noncognate synthase for further extension, likely due to the common β-linkage connecting GlcA to GlcNAc in both of these GAGs. |
T10 | 1593-1718 | Sentence | denotes | Overall, these GAG constructs provide new tools for studying biology and offer potential for future sugar-based therapeutics. |
NGLY1-deficiency
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-NGLY1-deficiency-B_T1 | 1386-1405 | chem:24139 | denotes | N-acetylglucosamine |
PD-NGLY1-deficiency-B_T2 | 1407-1413 | chem:24139 | denotes | GlcNAc |
PD-NGLY1-deficiency-B_T3 | 1563-1569 | chem:24139 | denotes | GlcNAc |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-125 | Sentence | denotes | Expanding glycosaminoglycan chemical space: towards the creation of sulfated analogs, novel polymers and chimeric constructs. |
TextSentencer_T2 | 126-251 | Sentence | denotes | Glycosaminoglycans (GAGs) have therapeutic potential in areas ranging from angiogenesis, inflammation, hemostasis and cancer. |
TextSentencer_T3 | 252-391 | Sentence | denotes | GAG bioactivity is conferred by intrinsic structural features, such as disaccharide composition, glycosidic linkages and sulfation pattern. |
TextSentencer_T4 | 392-550 | Sentence | denotes | Unfortunately, the in vitro enzymatic synthesis of defined GAGs is quite restricted by a limited understanding of current GAG synthases and modifying enzymes. |
TextSentencer_T5 | 551-696 | Sentence | denotes | Our work provides insights into GAG-active enzymes through the creation of sulfated oligosaccharides, a new polysaccharide and chimeric polymers. |
TextSentencer_T6 | 697-948 | Sentence | denotes | We show that a C6-sulfonated uridine diphospho (UDP)-glucose (Glc) derivative, sulfoquinovose, can be used as an uronic acid donor, but not as a hexosamine donor, to cap hyaluronan (HA) chains by the HA synthase from the microbe Pasteurella multocida. |
TextSentencer_T7 | 949-1097 | Sentence | denotes | However, the two heparosan (HEP) synthases from the same species, PmHS1 and PmHS2, could not employ the UDP-sulfoquinovose under similar conditions. |
TextSentencer_T8 | 1098-1265 | Sentence | denotes | Serendipitously, we found that PmHS2 co-polymerized Glc with glucuronic acid (GlcA), creating a novel HEP-like polymer we named hepbiuronic acid [-4-GlcAβ1-4-Glcα1-]n. |
TextSentencer_T9 | 1266-1592 | Sentence | denotes | In addition, we created chimeric block polymers composed of both HA and HEP segments; in these reactions GlcA-, but not N-acetylglucosamine-(GlcNAc), terminated GAG acceptors were recognized by their noncognate synthase for further extension, likely due to the common β-linkage connecting GlcA to GlcNAc in both of these GAGs. |
TextSentencer_T10 | 1593-1718 | Sentence | denotes | Overall, these GAG constructs provide new tools for studying biology and offer potential for future sugar-based therapeutics. |
T1 | 0-125 | Sentence | denotes | Expanding glycosaminoglycan chemical space: towards the creation of sulfated analogs, novel polymers and chimeric constructs. |
T2 | 126-251 | Sentence | denotes | Glycosaminoglycans (GAGs) have therapeutic potential in areas ranging from angiogenesis, inflammation, hemostasis and cancer. |
T3 | 252-391 | Sentence | denotes | GAG bioactivity is conferred by intrinsic structural features, such as disaccharide composition, glycosidic linkages and sulfation pattern. |
T4 | 392-550 | Sentence | denotes | Unfortunately, the in vitro enzymatic synthesis of defined GAGs is quite restricted by a limited understanding of current GAG synthases and modifying enzymes. |
T5 | 551-696 | Sentence | denotes | Our work provides insights into GAG-active enzymes through the creation of sulfated oligosaccharides, a new polysaccharide and chimeric polymers. |
T6 | 697-948 | Sentence | denotes | We show that a C6-sulfonated uridine diphospho (UDP)-glucose (Glc) derivative, sulfoquinovose, can be used as an uronic acid donor, but not as a hexosamine donor, to cap hyaluronan (HA) chains by the HA synthase from the microbe Pasteurella multocida. |
T7 | 949-1097 | Sentence | denotes | However, the two heparosan (HEP) synthases from the same species, PmHS1 and PmHS2, could not employ the UDP-sulfoquinovose under similar conditions. |
T8 | 1098-1265 | Sentence | denotes | Serendipitously, we found that PmHS2 co-polymerized Glc with glucuronic acid (GlcA), creating a novel HEP-like polymer we named hepbiuronic acid [-4-GlcAβ1-4-Glcα1-]n. |
T9 | 1266-1592 | Sentence | denotes | In addition, we created chimeric block polymers composed of both HA and HEP segments; in these reactions GlcA-, but not N-acetylglucosamine-(GlcNAc), terminated GAG acceptors were recognized by their noncognate synthase for further extension, likely due to the common β-linkage connecting GlcA to GlcNAc in both of these GAGs. |
T10 | 1593-1718 | Sentence | denotes | Overall, these GAG constructs provide new tools for studying biology and offer potential for future sugar-based therapeutics. |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 215-227 | Disease | denotes | inflammation | http://purl.obolibrary.org/obo/MONDO_0021166 |
T2 | 244-250 | Disease | denotes | cancer | http://purl.obolibrary.org/obo/MONDO_0004992 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 926-947 | OrganismTaxon | denotes | Pasteurella multocida | 747 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 37-42 | Body_part | denotes | space | http://purl.obolibrary.org/obo/UBERON_0000464 |
T2 | 1342-1350 | Body_part | denotes | segments | http://purl.obolibrary.org/obo/UBERON_0000914 |
T3 | 1498-1507 | Body_part | denotes | extension | http://purl.obolibrary.org/obo/UBERON_2000106 |
HP-phenotype
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T1 | 244-250 | Phenotype | denotes | cancer | HP:0002664 |