PubMed:1822240
Annnotations
Glycan-Motif
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 1551-1559 | https://glytoucan.org/Structures/Glycans/G70323CJ | denotes | mannoses |
| T2 | 1674-1681 | https://glytoucan.org/Structures/Glycans/G70323CJ | denotes | mannose |
| T3 | 2448-2455 | https://glytoucan.org/Structures/Glycans/G70323CJ | denotes | mannose |
GlyCosmos6-Glycan-Motif-Image
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 1551-1559 | Glycan_Motif | denotes | mannoses | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G70323CJ |
| T2 | 1674-1681 | Glycan_Motif | denotes | mannose | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G70323CJ |
| T3 | 2448-2455 | Glycan_Motif | denotes | mannose | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G70323CJ |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-133 | Sentence | denotes | Glycoprotein biosynthesis in yeast: purification and characterization of the endoplasmic reticulum Man9 processing alpha-mannosidase. |
| TextSentencer_T2 | 134-419 | Sentence | denotes | Saccharomyces cerevisiae Man9-alpha-mannosidase, responsible for trimming Man9GlcNAc2 in the endoplasmic reticulum to Man8GlcNAc2, the substrate for oligosaccharide elongation, has been purified to homogeneity from stabilized microsomal membranes without employing autolytic digestion. |
| TextSentencer_T3 | 420-599 | Sentence | denotes | The activity was solubilized by the zwitterionic detergent, 3-[(3-cholamidopropyl)dimethyl ammonio]-1-propanesulphonate (CHAPS), whose presence was necessary for maximal activity. |
| TextSentencer_T4 | 600-739 | Sentence | denotes | Purification included Q-Sepharose ion-exchange chromatography, preparative isoelectric focusing and HPLC gel filtration on TSK 3000 matrix. |
| TextSentencer_T5 | 740-857 | Sentence | denotes | Overall purification from post-nuclear supernatants was estimated to be 110,000-fold with a 50% recovery of activity. |
| TextSentencer_T6 | 858-1047 | Sentence | denotes | The purified enzyme hydrolysed Man9GlcNAc1,2 from thyroglobulin or oligosaccharide-lipid, but not invertase Man9GlcNAc, Man1 alpha 2Man1 alpha OCH3 or p-nitrophenyl-alpha-D-mannopyranoside. |
| TextSentencer_T7 | 1048-1215 | Sentence | denotes | Conversion of thyroglobulin Man9GlcNAc to Man8GlcNAc was linear with time and enzyme concentration, with an apparent Km of 0.2 mM and a specific activity of 220 IU/mg. |
| TextSentencer_T8 | 1216-1378 | Sentence | denotes | Glc3Man9GlcNAc2 from oligosaccharide-lipid was as good a substrate as Man9GlcNAc, but the lipid-linked Man7GlcNAc2 isomer was hydrolysed at only 10% of this rate. |
| TextSentencer_T9 | 1379-1627 | Sentence | denotes | Hydrolysis of defined isomers of IgM and bovine thyroglobulin Man6,7,8GlcNAc indicated that, for maximal alpha 1,2-mannosidase activity, only the alpha 1,2-linked terminal mannoses on the alpha 3 branch of the Man9GlcNAc precursor were dispensable. |
| TextSentencer_T10 | 1628-1766 | Sentence | denotes | Isomers lacking the terminal alpha 1,2-linked mannose on the alpha 6 branch were hydrolysed at only approximately 10% of the maximal rate. |
| TextSentencer_T11 | 1767-1824 | Sentence | denotes | The enzyme exhibited a pI of 5.3 and a pH optimum at 6.5. |
| TextSentencer_T12 | 1825-2082 | Sentence | denotes | Sodium dodecyl sulphate-polyacrylamide gel electrophoresis in the absence of reducing agents gave a single sharp band at 66 kDa, while in the presence of beta-mercaptoethanol equimolar amounts of two peptides, one of 44 kDa and one of 23 kDa, were obtained. |
| TextSentencer_T13 | 2083-2320 | Sentence | denotes | Sizing on Sephacryl SF300, Superose 12 and TSK 3000 provided a holoenzyme mol. wt of 60-68 kDa, indicating that the isolated active form of the Man9-alpha-mannosidase was composed of one each of the sulphydryl-bonded dissimilar peptides. |
| TextSentencer_T14 | 2321-2473 | Sentence | denotes | The enzyme bound to concanavalin A (ConA)-Sepharose and was eluted with alpha-methylmannoside, indicating the presence of high-mannose oligosaccharides. |
| TextSentencer_T15 | 2474-2561 | Sentence | denotes | The Man9-alpha-mannosidase required low levels of Ca2+, which could be removed by EGTA. |
| TextSentencer_T16 | 2562-2625 | Sentence | denotes | Activity was restored by Ca2+ or Zn2+, but not by Mg2+ or Mn2+. |
| T1 | 0-133 | Sentence | denotes | Glycoprotein biosynthesis in yeast: purification and characterization of the endoplasmic reticulum Man9 processing alpha-mannosidase. |
| T2 | 134-419 | Sentence | denotes | Saccharomyces cerevisiae Man9-alpha-mannosidase, responsible for trimming Man9GlcNAc2 in the endoplasmic reticulum to Man8GlcNAc2, the substrate for oligosaccharide elongation, has been purified to homogeneity from stabilized microsomal membranes without employing autolytic digestion. |
| T3 | 420-599 | Sentence | denotes | The activity was solubilized by the zwitterionic detergent, 3-[(3-cholamidopropyl)dimethyl ammonio]-1-propanesulphonate (CHAPS), whose presence was necessary for maximal activity. |
| T4 | 600-739 | Sentence | denotes | Purification included Q-Sepharose ion-exchange chromatography, preparative isoelectric focusing and HPLC gel filtration on TSK 3000 matrix. |
| T5 | 740-857 | Sentence | denotes | Overall purification from post-nuclear supernatants was estimated to be 110,000-fold with a 50% recovery of activity. |
| T6 | 858-1047 | Sentence | denotes | The purified enzyme hydrolysed Man9GlcNAc1,2 from thyroglobulin or oligosaccharide-lipid, but not invertase Man9GlcNAc, Man1 alpha 2Man1 alpha OCH3 or p-nitrophenyl-alpha-D-mannopyranoside. |
| T7 | 1048-1215 | Sentence | denotes | Conversion of thyroglobulin Man9GlcNAc to Man8GlcNAc was linear with time and enzyme concentration, with an apparent Km of 0.2 mM and a specific activity of 220 IU/mg. |
| T8 | 1216-1378 | Sentence | denotes | Glc3Man9GlcNAc2 from oligosaccharide-lipid was as good a substrate as Man9GlcNAc, but the lipid-linked Man7GlcNAc2 isomer was hydrolysed at only 10% of this rate. |
| T9 | 1379-1627 | Sentence | denotes | Hydrolysis of defined isomers of IgM and bovine thyroglobulin Man6,7,8GlcNAc indicated that, for maximal alpha 1,2-mannosidase activity, only the alpha 1,2-linked terminal mannoses on the alpha 3 branch of the Man9GlcNAc precursor were dispensable. |
| T10 | 1628-1766 | Sentence | denotes | Isomers lacking the terminal alpha 1,2-linked mannose on the alpha 6 branch were hydrolysed at only approximately 10% of the maximal rate. |
| T11 | 1767-1824 | Sentence | denotes | The enzyme exhibited a pI of 5.3 and a pH optimum at 6.5. |
| T12 | 1825-2082 | Sentence | denotes | Sodium dodecyl sulphate-polyacrylamide gel electrophoresis in the absence of reducing agents gave a single sharp band at 66 kDa, while in the presence of beta-mercaptoethanol equimolar amounts of two peptides, one of 44 kDa and one of 23 kDa, were obtained. |
| T13 | 2083-2320 | Sentence | denotes | Sizing on Sephacryl SF300, Superose 12 and TSK 3000 provided a holoenzyme mol. wt of 60-68 kDa, indicating that the isolated active form of the Man9-alpha-mannosidase was composed of one each of the sulphydryl-bonded dissimilar peptides. |
| T14 | 2321-2473 | Sentence | denotes | The enzyme bound to concanavalin A (ConA)-Sepharose and was eluted with alpha-methylmannoside, indicating the presence of high-mannose oligosaccharides. |
| T15 | 2474-2561 | Sentence | denotes | The Man9-alpha-mannosidase required low levels of Ca2+, which could be removed by EGTA. |
| T16 | 2562-2625 | Sentence | denotes | Activity was restored by Ca2+ or Zn2+, but not by Mg2+ or Mn2+. |
| T1 | 0-133 | Sentence | denotes | Glycoprotein biosynthesis in yeast: purification and characterization of the endoplasmic reticulum Man9 processing alpha-mannosidase. |
| T2 | 134-419 | Sentence | denotes | Saccharomyces cerevisiae Man9-alpha-mannosidase, responsible for trimming Man9GlcNAc2 in the endoplasmic reticulum to Man8GlcNAc2, the substrate for oligosaccharide elongation, has been purified to homogeneity from stabilized microsomal membranes without employing autolytic digestion. |
| T3 | 420-599 | Sentence | denotes | The activity was solubilized by the zwitterionic detergent, 3-[(3-cholamidopropyl)dimethyl ammonio]-1-propanesulphonate (CHAPS), whose presence was necessary for maximal activity. |
| T4 | 600-739 | Sentence | denotes | Purification included Q-Sepharose ion-exchange chromatography, preparative isoelectric focusing and HPLC gel filtration on TSK 3000 matrix. |
| T5 | 740-857 | Sentence | denotes | Overall purification from post-nuclear supernatants was estimated to be 110,000-fold with a 50% recovery of activity. |
| T6 | 858-1047 | Sentence | denotes | The purified enzyme hydrolysed Man9GlcNAc1,2 from thyroglobulin or oligosaccharide-lipid, but not invertase Man9GlcNAc, Man1 alpha 2Man1 alpha OCH3 or p-nitrophenyl-alpha-D-mannopyranoside. |
| T7 | 1048-1215 | Sentence | denotes | Conversion of thyroglobulin Man9GlcNAc to Man8GlcNAc was linear with time and enzyme concentration, with an apparent Km of 0.2 mM and a specific activity of 220 IU/mg. |
| T8 | 1216-1378 | Sentence | denotes | Glc3Man9GlcNAc2 from oligosaccharide-lipid was as good a substrate as Man9GlcNAc, but the lipid-linked Man7GlcNAc2 isomer was hydrolysed at only 10% of this rate. |
| T9 | 1379-1627 | Sentence | denotes | Hydrolysis of defined isomers of IgM and bovine thyroglobulin Man6,7,8GlcNAc indicated that, for maximal alpha 1,2-mannosidase activity, only the alpha 1,2-linked terminal mannoses on the alpha 3 branch of the Man9GlcNAc precursor were dispensable. |
| T10 | 1628-1766 | Sentence | denotes | Isomers lacking the terminal alpha 1,2-linked mannose on the alpha 6 branch were hydrolysed at only approximately 10% of the maximal rate. |
| T11 | 1767-1824 | Sentence | denotes | The enzyme exhibited a pI of 5.3 and a pH optimum at 6.5. |
| T12 | 1825-2082 | Sentence | denotes | Sodium dodecyl sulphate-polyacrylamide gel electrophoresis in the absence of reducing agents gave a single sharp band at 66 kDa, while in the presence of beta-mercaptoethanol equimolar amounts of two peptides, one of 44 kDa and one of 23 kDa, were obtained. |
| T13 | 2083-2320 | Sentence | denotes | Sizing on Sephacryl SF300, Superose 12 and TSK 3000 provided a holoenzyme mol. wt of 60-68 kDa, indicating that the isolated active form of the Man9-alpha-mannosidase was composed of one each of the sulphydryl-bonded dissimilar peptides. |
| T14 | 2321-2473 | Sentence | denotes | The enzyme bound to concanavalin A (ConA)-Sepharose and was eluted with alpha-methylmannoside, indicating the presence of high-mannose oligosaccharides. |
| T15 | 2474-2561 | Sentence | denotes | The Man9-alpha-mannosidase required low levels of Ca2+, which could be removed by EGTA. |
| T16 | 2562-2625 | Sentence | denotes | Activity was restored by Ca2+ or Zn2+, but not by Mg2+ or Mn2+. |
GlyCosmos6-Glycan-Motif-Structure
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 1551-1559 | https://glytoucan.org/Structures/Glycans/G70323CJ | denotes | mannoses |
| T2 | 1674-1681 | https://glytoucan.org/Structures/Glycans/G70323CJ | denotes | mannose |
| T3 | 2448-2455 | https://glytoucan.org/Structures/Glycans/G70323CJ | denotes | mannose |
GlycoBiology-GDGDB
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T1 | 115-132 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00008 | denotes | alpha-mannosidase |
| _T2 | 164-181 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00008 | denotes | alpha-mannosidase |
| _T3 | 2232-2249 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00008 | denotes | alpha-mannosidase |
| _T4 | 2483-2500 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00008 | denotes | alpha-mannosidase |
GlycoBiology-PACDB
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T1 | 134-158 | http://acgg.asia/db/diseases/pacdb/lec?ids=LEC297 | denotes | Saccharomyces cerevisiae |
GlycoBiology-FMA
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T1 | 0-12 | FMAID:62925 | denotes | Glycoprotein |
| _T2 | 0-12 | FMAID:167256 | denotes | Glycoprotein |
| _T3 | 77-88 | FMAID:165003 | denotes | endoplasmic |
| _T4 | 77-88 | FMAID:66856 | denotes | endoplasmic |
| _T5 | 77-98 | FMAID:66898 | denotes | endoplasmic reticulum |
| _T6 | 77-98 | FMAID:165027 | denotes | endoplasmic reticulum |
| _T7 | 77-98 | FMAID:165026 | denotes | endoplasmic reticulum |
| _T8 | 77-98 | FMAID:66897 | denotes | endoplasmic reticulum |
| _T9 | 77-98 | FMAID:80351 | denotes | endoplasmic reticulum |
| _T10 | 77-98 | FMAID:188464 | denotes | endoplasmic reticulum |
| _T11 | 77-98 | FMAID:210694 | denotes | endoplasmic reticulum |
| _T12 | 77-98 | FMAID:165144 | denotes | endoplasmic reticulum |
| _T13 | 77-98 | FMAID:199093 | denotes | endoplasmic reticulum |
| _T14 | 77-98 | FMAID:67434 | denotes | endoplasmic reticulum |
| _T15 | 77-98 | FMAID:165141 | denotes | endoplasmic reticulum |
| _T16 | 77-98 | FMAID:63842 | denotes | endoplasmic reticulum |
| _T17 | 77-98 | FMAID:210679 | denotes | endoplasmic reticulum |
| _T18 | 77-98 | FMAID:67438 | denotes | endoplasmic reticulum |
| _T19 | 77-98 | FMAID:212510 | denotes | endoplasmic reticulum |
| _T20 | 77-98 | FMAID:165142 | denotes | endoplasmic reticulum |
| _T21 | 77-98 | FMAID:165250 | denotes | endoplasmic reticulum |
| _T22 | 77-98 | FMAID:67429 | denotes | endoplasmic reticulum |
| _T23 | 77-98 | FMAID:162308 | denotes | endoplasmic reticulum |
| _T24 | 77-103 | FMAID:211269 | denotes | endoplasmic reticulum Man9 |
| _T25 | 89-98 | FMAID:7646 | denotes | reticulum |
| _T26 | 89-98 | FMAID:94520 | denotes | reticulum |
| _T27 | 227-238 | FMAID:66856 | denotes | endoplasmic |
| _T28 | 227-238 | FMAID:165003 | denotes | endoplasmic |
| _T29 | 227-248 | FMAID:80351 | denotes | endoplasmic reticulum |
| _T30 | 227-248 | FMAID:210694 | denotes | endoplasmic reticulum |
| _T31 | 227-248 | FMAID:199093 | denotes | endoplasmic reticulum |
| _T32 | 227-248 | FMAID:165144 | denotes | endoplasmic reticulum |
| _T33 | 227-248 | FMAID:165250 | denotes | endoplasmic reticulum |
| _T34 | 227-248 | FMAID:67429 | denotes | endoplasmic reticulum |
| _T35 | 227-248 | FMAID:188464 | denotes | endoplasmic reticulum |
| _T36 | 227-248 | FMAID:165026 | denotes | endoplasmic reticulum |
| _T37 | 227-248 | FMAID:66897 | denotes | endoplasmic reticulum |
| _T38 | 227-248 | FMAID:212510 | denotes | endoplasmic reticulum |
| _T39 | 227-248 | FMAID:63842 | denotes | endoplasmic reticulum |
| _T40 | 227-248 | FMAID:67438 | denotes | endoplasmic reticulum |
| _T41 | 227-248 | FMAID:165142 | denotes | endoplasmic reticulum |
| _T42 | 227-248 | FMAID:162308 | denotes | endoplasmic reticulum |
| _T43 | 227-248 | FMAID:210679 | denotes | endoplasmic reticulum |
| _T44 | 227-248 | FMAID:66898 | denotes | endoplasmic reticulum |
| _T45 | 227-248 | FMAID:165027 | denotes | endoplasmic reticulum |
| _T46 | 227-248 | FMAID:211269 | denotes | endoplasmic reticulum |
| _T47 | 227-251 | FMAID:165141 | denotes | endoplasmic reticulum to |
| _T48 | 227-251 | FMAID:210706 | denotes | endoplasmic reticulum to |
| _T49 | 227-251 | FMAID:67434 | denotes | endoplasmic reticulum to |
| _T50 | 239-248 | FMAID:94520 | denotes | reticulum |
| _T51 | 239-248 | FMAID:7646 | denotes | reticulum |
| _T52 | 283-298 | FMAID:82742 | denotes | oligosaccharide |
| _T53 | 283-298 | FMAID:196731 | denotes | oligosaccharide |
| _T54 | 360-370 | FMAID:165145 | denotes | microsomal |
| _T55 | 371-380 | FMAID:7145 | denotes | membranes |
| _T56 | 371-380 | FMAID:93573 | denotes | membranes |
| _T57 | 371-380 | FMAID:30322 | denotes | membranes |
| _T58 | 371-380 | FMAID:167608 | denotes | membranes |
| _T59 | 908-921 | FMAID:169236 | denotes | thyroglobulin |
| _T60 | 908-921 | FMAID:68833 | denotes | thyroglobulin |
| _T61 | 925-940 | FMAID:82742 | denotes | oligosaccharide |
| _T62 | 925-940 | FMAID:196731 | denotes | oligosaccharide |
| _T63 | 941-946 | FMAID:67264 | denotes | lipid |
| _T64 | 941-946 | FMAID:165448 | denotes | lipid |
| _T65 | 1062-1075 | FMAID:68833 | denotes | thyroglobulin |
| _T66 | 1062-1075 | FMAID:169236 | denotes | thyroglobulin |
| _T67 | 1237-1252 | FMAID:82742 | denotes | oligosaccharide |
| _T68 | 1237-1252 | FMAID:196731 | denotes | oligosaccharide |
| _T69 | 1253-1258 | FMAID:165448 | denotes | lipid |
| _T70 | 1253-1258 | FMAID:67264 | denotes | lipid |
| _T71 | 1306-1311 | FMAID:165448 | denotes | lipid |
| _T72 | 1306-1311 | FMAID:67264 | denotes | lipid |
| _T73 | 1373-1377 | FMAID:217859 | denotes | rate |
| _T74 | 1412-1415 | FMAID:167182 | denotes | IgM |
| _T75 | 1427-1440 | FMAID:68833 | denotes | thyroglobulin |
| _T76 | 1427-1440 | FMAID:169236 | denotes | thyroglobulin |
| _T77 | 1551-1559 | FMAID:196796 | denotes | mannoses |
| _T78 | 1551-1559 | FMAID:82801 | denotes | mannoses |
| _T79 | 1575-1581 | FMAID:226027 | denotes | branch |
| _T80 | 1575-1581 | FMAID:226028 | denotes | branch |
| _T81 | 1674-1681 | FMAID:196796 | denotes | mannose |
| _T82 | 1674-1681 | FMAID:82801 | denotes | mannose |
| _T83 | 1697-1703 | FMAID:226028 | denotes | branch |
| _T84 | 1697-1703 | FMAID:226027 | denotes | branch |
| _T85 | 1761-1765 | FMAID:217859 | denotes | rate |
| _T86 | 1790-1792 | FMAID:214745 | denotes | pI |
| _T87 | 2448-2455 | FMAID:82801 | denotes | mannose |
| _T88 | 2448-2455 | FMAID:196796 | denotes | mannose |
| _T89 | 2456-2472 | FMAID:196731 | denotes | oligosaccharides |
| _T90 | 2456-2472 | FMAID:82742 | denotes | oligosaccharides |
| _T91 | 2524-2527 | FMAID:272430 | denotes | Ca2 |
| _T92 | 2524-2527 | FMAID:182506 | denotes | Ca2 |
| _T93 | 2524-2527 | FMAID:272658 | denotes | Ca2 |
| _T94 | 2587-2590 | FMAID:272658 | denotes | Ca2 |
| _T95 | 2587-2590 | FMAID:272430 | denotes | Ca2 |
| _T96 | 2587-2590 | FMAID:182506 | denotes | Ca2 |
uniprot-human
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 723-726 | http://www.uniprot.org/uniprot/Q8WUA8 | denotes | TSK |
| T2 | 2126-2129 | http://www.uniprot.org/uniprot/Q8WUA8 | denotes | TSK |
| T3 | 908-921 | http://www.uniprot.org/uniprot/Q9UNY3 | denotes | thyroglobulin |
| T4 | 1062-1075 | http://www.uniprot.org/uniprot/Q9UNY3 | denotes | thyroglobulin |
| T5 | 1427-1440 | http://www.uniprot.org/uniprot/Q9UNY3 | denotes | thyroglobulin |
| T6 | 1484-1505 | http://www.uniprot.org/uniprot/O60476 | denotes | alpha 1,2-mannosidase |
| T7 | 1484-1505 | http://www.uniprot.org/uniprot/Q9UKM7 | denotes | alpha 1,2-mannosidase |
| T8 | 1484-1505 | http://www.uniprot.org/uniprot/Q9BZQ6 | denotes | alpha 1,2-mannosidase |
| T9 | 1484-1505 | http://www.uniprot.org/uniprot/Q5SRI9 | denotes | alpha 1,2-mannosidase |
| T10 | 1484-1505 | http://www.uniprot.org/uniprot/Q9NR34 | denotes | alpha 1,2-mannosidase |
| T11 | 1484-1505 | http://www.uniprot.org/uniprot/P33908 | denotes | alpha 1,2-mannosidase |
uniprot-mouse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 908-921 | http://www.uniprot.org/uniprot/O08710 | denotes | thyroglobulin |
| T2 | 1062-1075 | http://www.uniprot.org/uniprot/O08710 | denotes | thyroglobulin |
| T3 | 1427-1440 | http://www.uniprot.org/uniprot/O08710 | denotes | thyroglobulin |
| T4 | 978-982 | http://www.uniprot.org/uniprot/Q9WU40 | denotes | Man1 |
| T5 | 1932-1937 | http://www.uniprot.org/uniprot/Q62504 | denotes | sharp |
| T6 | 2524-2527 | http://www.uniprot.org/uniprot/P00920 | denotes | Ca2 |
| T7 | 2587-2590 | http://www.uniprot.org/uniprot/P00920 | denotes | Ca2 |
GlycoBiology-NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 134-147 | http://purl.bioontology.org/ontology/NCBITAXON/4895 | denotes | Saccharomyces |
| T2 | 134-147 | http://purl.bioontology.org/ontology/NCBITAXON/36034 | denotes | Saccharomyces |
| T3 | 134-147 | http://purl.bioontology.org/ontology/NCBITAXON/4891 | denotes | Saccharomyces |
| T4 | 134-147 | http://purl.bioontology.org/ontology/NCBITAXON/4930 | denotes | Saccharomyces |
| T5 | 1979-1983 | http://purl.bioontology.org/ontology/NCBITAXON/158455 | denotes | beta |
| T6 | 1979-1983 | http://purl.bioontology.org/ontology/NCBITAXON/3554 | denotes | beta |
| T7 | 2562-2570 | http://purl.bioontology.org/ontology/STY/T052 | denotes | Activity |
| T8 | 2562-2570 | http://purl.bioontology.org/ontology/NCBITAXON/190658 | denotes | Activity |
GO-BP
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-25 | http://purl.obolibrary.org/obo/GO_0009101 | denotes | Glycoprotein biosynthesis |
| T2 | 13-25 | http://purl.obolibrary.org/obo/GO_0009058 | denotes | biosynthesis |
| T3 | 409-418 | http://purl.obolibrary.org/obo/GO_0007586 | denotes | digestion |
| T4 | 638-646 | http://purl.obolibrary.org/obo/GO_0015297 | denotes | exchange |
| T5 | 1484-1505 | http://purl.obolibrary.org/obo/GO_0004559 | denotes | alpha 1,2-mannosidase |
| T6 | 1484-1505 | http://purl.obolibrary.org/obo/GO_0004571 | denotes | alpha 1,2-mannosidase |
| T7 | 1484-1514 | http://purl.obolibrary.org/obo/GO_0004559 | denotes | alpha 1,2-mannosidase activity |
| T8 | 1494-1514 | http://purl.obolibrary.org/obo/GO_0015923 | denotes | mannosidase activity |
| T9 | 1840-1848 | http://purl.obolibrary.org/obo/GO_0051923 | denotes | sulphate |
GO-CC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 77-98 | http://purl.obolibrary.org/obo/GO_0005783 | denotes | endoplasmic reticulum |
| T2 | 227-248 | http://purl.obolibrary.org/obo/GO_0005783 | denotes | endoplasmic reticulum |
| T3 | 371-380 | http://purl.obolibrary.org/obo/GO_0016020 | denotes | membranes |
EDAM-topics
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 29-34 | http://edamontology.org/topic_2817 | denotes | yeast |
| T2 | 29-34 | http://edamontology.org/topic_0782 | denotes | yeast |
| T3 | 77-98 | http://edamontology.org/topic_0616 | denotes | endoplasmic reticulum |
| T4 | 227-248 | http://edamontology.org/topic_0616 | denotes | endoplasmic reticulum |
| T5 | 941-946 | http://edamontology.org/topic_0153 | denotes | lipid |
| T6 | 1253-1258 | http://edamontology.org/topic_0153 | denotes | lipid |
| T7 | 1306-1311 | http://edamontology.org/topic_0153 | denotes | lipid |
| T8 | 1542-1550 | http://edamontology.org/topic_0749 | denotes | terminal |
| T9 | 1648-1656 | http://edamontology.org/topic_0749 | denotes | terminal |
| T10 | 2025-2033 | http://edamontology.org/topic_0154 | denotes | peptides |
| T11 | 2311-2319 | http://edamontology.org/topic_0154 | denotes | peptides |
EDAM-DFO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 104-114 | http://edamontology.org/operation_0004 | denotes | processing |
| T2 | 104-114 | http://edamontology.org/operation_2409 | denotes | processing |
| T3 | 199-207 | http://edamontology.org/operation_3192 | denotes | trimming |
| T4 | 502-510 | http://edamontology.org/operation_3642 | denotes | dimethyl |
| T5 | 732-738 | http://edamontology.org/data_2082 | denotes | matrix |
| T6 | 1048-1058 | http://edamontology.org/operation_3434 | denotes | Conversion |
| T7 | 1133-1146 | http://edamontology.org/data_2140 | denotes | concentration |
| T8 | 1165-1167 | http://edamontology.org/data_0910 | denotes | Km |
| T9 | 1806-1808 | http://edamontology.org/format_1997 | denotes | pH |
| T10 | 2025-2033 | http://edamontology.org/data_2906 | denotes | peptides |
| T11 | 2311-2319 | http://edamontology.org/data_2906 | denotes | peptides |
GlycoBiology-Motifs
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 2443-2455 | http://rdf.glycoinfo.org/glycan/G00028MO | denotes | high-mannose |
Lectin
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| Lectin_T1 | 2357-2361 | https://acgg.asia/db/lfdb/LfDB0170 | denotes | ConA |
GlyTouCan-IUPAC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| GlycanIUPAC_T1 | 978-982 | "http://rdf.glycoinfo.org/glycan/G48232PN" | denotes | Man1 |
| GlycanIUPAC_T2 | 978-982 | "http://rdf.glycoinfo.org/glycan/G63049JM" | denotes | Man1 |
| GlycanIUPAC_T3 | 978-982 | "http://rdf.glycoinfo.org/glycan/G43927EM" | denotes | Man1 |
| GlycanIUPAC_T4 | 978-982 | "http://rdf.glycoinfo.org/glycan/G56756HZ" | denotes | Man1 |
| GlycanIUPAC_T5 | 978-982 | "http://rdf.glycoinfo.org/glycan/G33141UW" | denotes | Man1 |
| GlycanIUPAC_T6 | 978-982 | "http://rdf.glycoinfo.org/glycan/G70323CJ" | denotes | Man1 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 134-158 | OrganismTaxon | denotes | Saccharomyces cerevisiae | 4932 |
| T2 | 1420-1426 | OrganismTaxon | denotes | bovine | 9913 |
Anatomy-UBERON
| Id | Subject | Object | Predicate | Lexical cue | uberon_id |
|---|---|---|---|---|---|
| T1 | 89-98 | Body_part | denotes | reticulum | http://purl.obolibrary.org/obo/UBERON_0007361 |
| T2 | 239-248 | Body_part | denotes | reticulum | http://purl.obolibrary.org/obo/UBERON_0007361 |
| T3 | 371-380 | Body_part | denotes | membranes | http://purl.obolibrary.org/obo/GO_0016020|http://purl.obolibrary.org/obo/UBERON_0000094|http://purl.obolibrary.org/obo/UBERON_0000158 |
CL-cell
| Id | Subject | Object | Predicate | Lexical cue | cl_id |
|---|---|---|---|---|---|
| T1 | 1938-1942 | Cell | denotes | band | http://purl.obolibrary.org/obo/CL:0000560 |