PubMed:28616799
Annnotations
GlyCosmos6-Glycan-Motif-Image
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 19-26 | Glycan_Motif | denotes | mannose | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G70323CJ |
| T2 | 636-643 | Glycan_Motif | denotes | mannose | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G70323CJ |
| T3 | 1003-1006 | Glycan_Motif | denotes | GT2 | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G36476BA|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G35228ZS |
GlyCosmos6-Glycan-Motif-Structure
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 19-26 | https://glytoucan.org/Structures/Glycans/G70323CJ | denotes | mannose |
| T2 | 636-643 | https://glytoucan.org/Structures/Glycans/G70323CJ | denotes | mannose |
| T3 | 1003-1006 | https://glytoucan.org/Structures/Glycans/G35228ZS | denotes | GT2 |
| T4 | 1003-1006 | https://glytoucan.org/Structures/Glycans/G36476BA | denotes | GT2 |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-95 | Sentence | denotes | Dolichol phosphate mannose synthase: a Glycosyltransferase with Unity in molecular diversities. |
| TextSentencer_T2 | 96-217 | Sentence | denotes | N-glycans provide structural and functional stability to asparagine-linked (N-linked) glycoproteins, and add flexibility. |
| TextSentencer_T3 | 218-313 | Sentence | denotes | Glycan biosynthesis is elaborative, multi-compartmental and involves many glycosyltransferases. |
| TextSentencer_T4 | 314-460 | Sentence | denotes | Failure to assemble N-glycans leads to phenotypic changes developing infection, cancer, congenital disorders of glycosylation (CDGs) among others. |
| TextSentencer_T5 | 461-681 | Sentence | denotes | Biosynthesis of N-glycans begins at the endoplasmic reticulum (ER) with the assembly of dolichol-linked tetra-decasaccharide (Glc3Man9GlcNAc2-PP-Dol) where dolichol phosphate mannose synthase (DPMS) plays a central role. |
| TextSentencer_T6 | 682-815 | Sentence | denotes | DPMS is also essential for GPI anchor biosynthesis as well as for O- and C-mannosylation of proteins in yeast and in mammalian cells. |
| TextSentencer_T7 | 816-946 | Sentence | denotes | DPMS has been purified from several sources and its gene has been cloned from 39 species (e.g., from protozoan parasite to human). |
| TextSentencer_T8 | 947-1066 | Sentence | denotes | It is an inverting GT-A folded enzyme and classified as GT2 by CAZy (carbohydrate active enZyme; http://www.cazy.org ). |
| TextSentencer_T9 | 1067-1258 | Sentence | denotes | The sequence alignment detects the presence of a metal binding DAD signature in DPMS from all 39 species but finds cAMP-dependent protein phosphorylation motif (PKA motif) in only 38 species. |
| TextSentencer_T10 | 1259-1295 | Sentence | denotes | DPMS also has hydrophobic region(s). |
| TextSentencer_T11 | 1296-1452 | Sentence | denotes | Hydropathy analysis of amino acid sequences from bovine, human, S. crevisiae and A. thaliana DPMS show PKA motif is present between the hydrophobic domains. |
| TextSentencer_T12 | 1453-1566 | Sentence | denotes | The location of PKA motif as well as the hydrophobic domain(s) in the DPMS sequence vary from species to species. |
| TextSentencer_T13 | 1567-1656 | Sentence | denotes | For example, the domain(s) could be located at the center or more towards the C-terminus. |
| TextSentencer_T14 | 1657-1878 | Sentence | denotes | Irrespective of their catalytic similarity, the DNA sequence, the amino acid identity, and the lack of a stretch of hydrophobic amino acid residues at the C-terminus, DPMS is still classified as Type I and Type II enzyme. |
| TextSentencer_T15 | 1879-2001 | Sentence | denotes | Because of an apparent bio-sensing ability, extracellular signaling and microenvironment regulate DPMS catalytic activity. |
| TextSentencer_T16 | 2002-2093 | Sentence | denotes | In this review, we highlight some important features and the molecular diversities of DPMS. |
| T1 | 0-95 | Sentence | denotes | Dolichol phosphate mannose synthase: a Glycosyltransferase with Unity in molecular diversities. |
| T2 | 96-217 | Sentence | denotes | N-glycans provide structural and functional stability to asparagine-linked (N-linked) glycoproteins, and add flexibility. |
| T3 | 218-313 | Sentence | denotes | Glycan biosynthesis is elaborative, multi-compartmental and involves many glycosyltransferases. |
| T4 | 314-460 | Sentence | denotes | Failure to assemble N-glycans leads to phenotypic changes developing infection, cancer, congenital disorders of glycosylation (CDGs) among others. |
| T5 | 461-681 | Sentence | denotes | Biosynthesis of N-glycans begins at the endoplasmic reticulum (ER) with the assembly of dolichol-linked tetra-decasaccharide (Glc3Man9GlcNAc2-PP-Dol) where dolichol phosphate mannose synthase (DPMS) plays a central role. |
| T6 | 682-815 | Sentence | denotes | DPMS is also essential for GPI anchor biosynthesis as well as for O- and C-mannosylation of proteins in yeast and in mammalian cells. |
| T7 | 816-946 | Sentence | denotes | DPMS has been purified from several sources and its gene has been cloned from 39 species (e.g., from protozoan parasite to human). |
| T8 | 947-1066 | Sentence | denotes | It is an inverting GT-A folded enzyme and classified as GT2 by CAZy (carbohydrate active enZyme; http://www.cazy.org ). |
| T9 | 1067-1258 | Sentence | denotes | The sequence alignment detects the presence of a metal binding DAD signature in DPMS from all 39 species but finds cAMP-dependent protein phosphorylation motif (PKA motif) in only 38 species. |
| T10 | 1259-1295 | Sentence | denotes | DPMS also has hydrophobic region(s). |
| T11 | 1296-1452 | Sentence | denotes | Hydropathy analysis of amino acid sequences from bovine, human, S. crevisiae and A. thaliana DPMS show PKA motif is present between the hydrophobic domains. |
| T12 | 1453-1566 | Sentence | denotes | The location of PKA motif as well as the hydrophobic domain(s) in the DPMS sequence vary from species to species. |
| T13 | 1567-1656 | Sentence | denotes | For example, the domain(s) could be located at the center or more towards the C-terminus. |
| T14 | 1657-1878 | Sentence | denotes | Irrespective of their catalytic similarity, the DNA sequence, the amino acid identity, and the lack of a stretch of hydrophobic amino acid residues at the C-terminus, DPMS is still classified as Type I and Type II enzyme. |
| T15 | 1879-2001 | Sentence | denotes | Because of an apparent bio-sensing ability, extracellular signaling and microenvironment regulate DPMS catalytic activity. |
| T16 | 2002-2093 | Sentence | denotes | In this review, we highlight some important features and the molecular diversities of DPMS. |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 383-392 | Disease | denotes | infection | http://purl.obolibrary.org/obo/MONDO_0005550 |
| T2 | 394-400 | Disease | denotes | cancer | http://purl.obolibrary.org/obo/MONDO_0004992 |
| T3 | 402-439 | Disease | denotes | congenital disorders of glycosylation | http://purl.obolibrary.org/obo/MONDO_0015286 |
| T4 | 441-445 | Disease | denotes | CDGs | http://purl.obolibrary.org/obo/MONDO_0015286 |
Glycan-GlyCosmos
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 1003-1006 | Glycan | denotes | GT2 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G36476BA |
GlyCosmos15-HP
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 394-400 | Phenotype | denotes | cancer | HP:0002664 |
GlyCosmos15-Glycan
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 1003-1006 | Glycan | denotes | GT2 | https://api.glycosmos.org/wurcs2image/latest/png/binary/G36476BA |
GlyCosmos15-CL
| Id | Subject | Object | Predicate | Lexical cue | cl_id |
|---|---|---|---|---|---|
| T1 | 1852-1858 | Cell | denotes | Type I | http://purl.obolibrary.org/obo/CL:0004120|http://purl.obolibrary.org/obo/CL:0004138 |
GlyCosmos15-UBERON
| Id | Subject | Object | Predicate | Lexical cue | uberon_id |
|---|---|---|---|---|---|
| T1 | 513-522 | Body_part | denotes | reticulum | http://purl.obolibrary.org/obo/UBERON_0007361 |
| T2 | 1923-1936 | Body_part | denotes | extracellular | http://purl.obolibrary.org/obo/GO_0005576 |
GlyCosmos15-MONDO
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 383-392 | Disease | denotes | infection | MONDO:0005550 |
| T2 | 394-400 | Disease | denotes | cancer | MONDO:0004992 |
| T3 | 402-439 | Disease | denotes | congenital disorders of glycosylation | MONDO:0015286 |
| T4 | 441-445 | Disease | denotes | CDGs | MONDO:0015286 |
GlyCosmos15-Taxon
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 799-808 | Organism | denotes | mammalian | 40674 |
| T2 | 939-944 | Organism | denotes | human | 9606 |
| T3 | 1345-1351 | Organism | denotes | bovine | 9913 |
| T4 | 1353-1358 | Organism | denotes | human | 9606 |
GlyCosmos15-Sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-95 | Sentence | denotes | Dolichol phosphate mannose synthase: a Glycosyltransferase with Unity in molecular diversities. |
| T2 | 96-217 | Sentence | denotes | N-glycans provide structural and functional stability to asparagine-linked (N-linked) glycoproteins, and add flexibility. |
| T3 | 218-313 | Sentence | denotes | Glycan biosynthesis is elaborative, multi-compartmental and involves many glycosyltransferases. |
| T4 | 314-460 | Sentence | denotes | Failure to assemble N-glycans leads to phenotypic changes developing infection, cancer, congenital disorders of glycosylation (CDGs) among others. |
| T5 | 461-681 | Sentence | denotes | Biosynthesis of N-glycans begins at the endoplasmic reticulum (ER) with the assembly of dolichol-linked tetra-decasaccharide (Glc3Man9GlcNAc2-PP-Dol) where dolichol phosphate mannose synthase (DPMS) plays a central role. |
| T6 | 682-815 | Sentence | denotes | DPMS is also essential for GPI anchor biosynthesis as well as for O- and C-mannosylation of proteins in yeast and in mammalian cells. |
| T7 | 816-946 | Sentence | denotes | DPMS has been purified from several sources and its gene has been cloned from 39 species (e.g., from protozoan parasite to human). |
| T8 | 947-1066 | Sentence | denotes | It is an inverting GT-A folded enzyme and classified as GT2 by CAZy (carbohydrate active enZyme; http://www.cazy.org ). |
| T9 | 1067-1258 | Sentence | denotes | The sequence alignment detects the presence of a metal binding DAD signature in DPMS from all 39 species but finds cAMP-dependent protein phosphorylation motif (PKA motif) in only 38 species. |
| T10 | 1259-1295 | Sentence | denotes | DPMS also has hydrophobic region(s). |
| T11 | 1296-1452 | Sentence | denotes | Hydropathy analysis of amino acid sequences from bovine, human, S. crevisiae and A. thaliana DPMS show PKA motif is present between the hydrophobic domains. |
| T12 | 1453-1566 | Sentence | denotes | The location of PKA motif as well as the hydrophobic domain(s) in the DPMS sequence vary from species to species. |
| T13 | 1567-1656 | Sentence | denotes | For example, the domain(s) could be located at the center or more towards the C-terminus. |
| T14 | 1657-1878 | Sentence | denotes | Irrespective of their catalytic similarity, the DNA sequence, the amino acid identity, and the lack of a stretch of hydrophobic amino acid residues at the C-terminus, DPMS is still classified as Type I and Type II enzyme. |
| T15 | 1879-2001 | Sentence | denotes | Because of an apparent bio-sensing ability, extracellular signaling and microenvironment regulate DPMS catalytic activity. |
| T16 | 2002-2093 | Sentence | denotes | In this review, we highlight some important features and the molecular diversities of DPMS. |
GlyCosmos15-FMA
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 501-522 | Body_part | denotes | endoplasmic reticulum | FMA:63842 |
| T2 | 524-526 | Body_part | denotes | ER | FMA:63842 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 939-944 | OrganismTaxon | denotes | human | 9606 |
| T2 | 1345-1351 | OrganismTaxon | denotes | bovine | 9913 |
| T3 | 1353-1358 | OrganismTaxon | denotes | human | 9606 |
Anatomy-UBERON
| Id | Subject | Object | Predicate | Lexical cue | uberon_id |
|---|---|---|---|---|---|
| T1 | 513-522 | Body_part | denotes | reticulum | http://purl.obolibrary.org/obo/UBERON_0007361 |
| T2 | 1923-1936 | Body_part | denotes | extracellular | http://purl.obolibrary.org/obo/GO_0005576 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 394-400 | Phenotype | denotes | cancer | HP:0002664 |
CL-cell
| Id | Subject | Object | Predicate | Lexical cue | cl_id |
|---|---|---|---|---|---|
| T1 | 1852-1858 | Cell | denotes | Type I | http://purl.obolibrary.org/obo/CL:0004120|http://purl.obolibrary.org/obo/CL:0004138 |