PMC:7352545 / 22147-23214 JSONTXT

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    LitCovid_Glycan-Motif-Structure

    {"project":"LitCovid_Glycan-Motif-Structure","denotations":[{"id":"T66","span":{"begin":55,"end":61},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T67","span":{"begin":63,"end":65},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T68","span":{"begin":103,"end":105},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T69","span":{"begin":135,"end":141},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T70","span":{"begin":344,"end":350},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T71","span":{"begin":415,"end":418},"obj":"https://glytoucan.org/Structures/Glycans/G56516VH"},{"id":"T72","span":{"begin":415,"end":418},"obj":"https://glytoucan.org/Structures/Glycans/G91237TK"},{"id":"T73","span":{"begin":482,"end":488},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T74","span":{"begin":730,"end":736},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T75","span":{"begin":868,"end":874},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T76","span":{"begin":929,"end":931},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T77","span":{"begin":993,"end":999},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"},{"id":"T78","span":{"begin":1016,"end":1018},"obj":"https://glytoucan.org/Structures/Glycans/G81533KY"}],"text":"For example, in the horse, C4-O-acetyl modification of Neu5Ac (SA) occupies more than 50% of the total SA content. The C4-O-acetylated Neu5Ac, Neu4,5Ac2, inhibits the influenza A2 virus HA. De-acetylation reagents such as NaOH or NaIO4 treatment completely hemagglutinate Neu4,5Ac2 by elimination of the C4-O-acetyl group [33]. The C4-O-acetyl Neu5Ac species are found in various sources such as equine erythrocyte GM3, starfish A. rubens and fish [34,35,36,37,38]. C4-O-acetylated Neu5Ac facilitates the initial attachment of viruses to target cells. Like the influenza C virus, infectious salmon anemia virus (ISAV), a member of the Orthomyxoviridae family, contains HE and HEF proteins to mediate virus entry and exit. C4-O-Ac Neu5Ac is the major receptor determinant of ISAV in receptor binding and destruction [38], while the influenza C virus recognizes C9-O-Ac Neu5Ac. The acetylesterase RDE of ISAV cleaves C4-O-Ac via 4-SA-O-acetylesterase with a short turnover time, whereas C9-O-Ac Neu5Ac is cleaved by 9-SA-O-acetylesterase with a long turnover time [34]."}

    LitCovid-PD-FMA-UBERON

    {"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T211","span":{"begin":177,"end":179},"obj":"Body_part"},{"id":"T212","span":{"begin":403,"end":414},"obj":"Body_part"},{"id":"T213","span":{"begin":545,"end":550},"obj":"Body_part"},{"id":"T214","span":{"begin":680,"end":688},"obj":"Body_part"}],"attributes":[{"id":"A211","pred":"fma_id","subj":"T211","obj":"http://purl.org/sig/ont/fma/fma66595"},{"id":"A212","pred":"fma_id","subj":"T212","obj":"http://purl.org/sig/ont/fma/fma62845"},{"id":"A213","pred":"fma_id","subj":"T213","obj":"http://purl.org/sig/ont/fma/fma68646"},{"id":"A214","pred":"fma_id","subj":"T214","obj":"http://purl.org/sig/ont/fma/fma67257"}],"text":"For example, in the horse, C4-O-acetyl modification of Neu5Ac (SA) occupies more than 50% of the total SA content. The C4-O-acetylated Neu5Ac, Neu4,5Ac2, inhibits the influenza A2 virus HA. De-acetylation reagents such as NaOH or NaIO4 treatment completely hemagglutinate Neu4,5Ac2 by elimination of the C4-O-acetyl group [33]. The C4-O-acetyl Neu5Ac species are found in various sources such as equine erythrocyte GM3, starfish A. rubens and fish [34,35,36,37,38]. C4-O-acetylated Neu5Ac facilitates the initial attachment of viruses to target cells. Like the influenza C virus, infectious salmon anemia virus (ISAV), a member of the Orthomyxoviridae family, contains HE and HEF proteins to mediate virus entry and exit. C4-O-Ac Neu5Ac is the major receptor determinant of ISAV in receptor binding and destruction [38], while the influenza C virus recognizes C9-O-Ac Neu5Ac. The acetylesterase RDE of ISAV cleaves C4-O-Ac via 4-SA-O-acetylesterase with a short turnover time, whereas C9-O-Ac Neu5Ac is cleaved by 9-SA-O-acetylesterase with a long turnover time [34]."}

    LitCovid-PD-MONDO

    {"project":"LitCovid-PD-MONDO","denotations":[{"id":"T84","span":{"begin":167,"end":176},"obj":"Disease"},{"id":"T85","span":{"begin":561,"end":570},"obj":"Disease"},{"id":"T86","span":{"begin":580,"end":590},"obj":"Disease"},{"id":"T87","span":{"begin":598,"end":604},"obj":"Disease"},{"id":"T88","span":{"begin":831,"end":840},"obj":"Disease"}],"attributes":[{"id":"A84","pred":"mondo_id","subj":"T84","obj":"http://purl.obolibrary.org/obo/MONDO_0005812"},{"id":"A85","pred":"mondo_id","subj":"T85","obj":"http://purl.obolibrary.org/obo/MONDO_0005812"},{"id":"A86","pred":"mondo_id","subj":"T86","obj":"http://purl.obolibrary.org/obo/MONDO_0005550"},{"id":"A87","pred":"mondo_id","subj":"T87","obj":"http://purl.obolibrary.org/obo/MONDO_0002280"},{"id":"A88","pred":"mondo_id","subj":"T88","obj":"http://purl.obolibrary.org/obo/MONDO_0005812"}],"text":"For example, in the horse, C4-O-acetyl modification of Neu5Ac (SA) occupies more than 50% of the total SA content. The C4-O-acetylated Neu5Ac, Neu4,5Ac2, inhibits the influenza A2 virus HA. De-acetylation reagents such as NaOH or NaIO4 treatment completely hemagglutinate Neu4,5Ac2 by elimination of the C4-O-acetyl group [33]. The C4-O-acetyl Neu5Ac species are found in various sources such as equine erythrocyte GM3, starfish A. rubens and fish [34,35,36,37,38]. C4-O-acetylated Neu5Ac facilitates the initial attachment of viruses to target cells. Like the influenza C virus, infectious salmon anemia virus (ISAV), a member of the Orthomyxoviridae family, contains HE and HEF proteins to mediate virus entry and exit. C4-O-Ac Neu5Ac is the major receptor determinant of ISAV in receptor binding and destruction [38], while the influenza C virus recognizes C9-O-Ac Neu5Ac. The acetylesterase RDE of ISAV cleaves C4-O-Ac via 4-SA-O-acetylesterase with a short turnover time, whereas C9-O-Ac Neu5Ac is cleaved by 9-SA-O-acetylesterase with a long turnover time [34]."}

    LitCovid-PD-CLO

    {"project":"LitCovid-PD-CLO","denotations":[{"id":"T261","span":{"begin":20,"end":25},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_9796"},{"id":"T262","span":{"begin":27,"end":29},"obj":"http://purl.obolibrary.org/obo/CLO_0037284"},{"id":"T263","span":{"begin":119,"end":121},"obj":"http://purl.obolibrary.org/obo/CLO_0037284"},{"id":"T264","span":{"begin":177,"end":179},"obj":"http://purl.obolibrary.org/obo/CLO_0001562"},{"id":"T265","span":{"begin":180,"end":185},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_10239"},{"id":"T266","span":{"begin":304,"end":306},"obj":"http://purl.obolibrary.org/obo/CLO_0037284"},{"id":"T267","span":{"begin":332,"end":334},"obj":"http://purl.obolibrary.org/obo/CLO_0037284"},{"id":"T268","span":{"begin":396,"end":402},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_9796"},{"id":"T269","span":{"begin":403,"end":414},"obj":"http://purl.obolibrary.org/obo/CL_0000232"},{"id":"T270","span":{"begin":429,"end":430},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T271","span":{"begin":443,"end":447},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_117565"},{"id":"T272","span":{"begin":466,"end":468},"obj":"http://purl.obolibrary.org/obo/CLO_0037284"},{"id":"T273","span":{"begin":527,"end":534},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_10239"},{"id":"T274","span":{"begin":545,"end":550},"obj":"http://purl.obolibrary.org/obo/GO_0005623"},{"id":"T275","span":{"begin":573,"end":578},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_10239"},{"id":"T276","span":{"begin":605,"end":610},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_10239"},{"id":"T277","span":{"begin":619,"end":620},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T278","span":{"begin":700,"end":705},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_10239"},{"id":"T279","span":{"begin":722,"end":724},"obj":"http://purl.obolibrary.org/obo/CLO_0037284"},{"id":"T280","span":{"begin":843,"end":848},"obj":"http://purl.obolibrary.org/obo/NCBITaxon_10239"},{"id":"T281","span":{"begin":915,"end":917},"obj":"http://purl.obolibrary.org/obo/CLO_0037284"},{"id":"T282","span":{"begin":954,"end":955},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T283","span":{"begin":1041,"end":1042},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T284","span":{"begin":1063,"end":1065},"obj":"http://purl.obolibrary.org/obo/CLO_0001302"}],"text":"For example, in the horse, C4-O-acetyl modification of Neu5Ac (SA) occupies more than 50% of the total SA content. The C4-O-acetylated Neu5Ac, Neu4,5Ac2, inhibits the influenza A2 virus HA. De-acetylation reagents such as NaOH or NaIO4 treatment completely hemagglutinate Neu4,5Ac2 by elimination of the C4-O-acetyl group [33]. The C4-O-acetyl Neu5Ac species are found in various sources such as equine erythrocyte GM3, starfish A. rubens and fish [34,35,36,37,38]. C4-O-acetylated Neu5Ac facilitates the initial attachment of viruses to target cells. Like the influenza C virus, infectious salmon anemia virus (ISAV), a member of the Orthomyxoviridae family, contains HE and HEF proteins to mediate virus entry and exit. C4-O-Ac Neu5Ac is the major receptor determinant of ISAV in receptor binding and destruction [38], while the influenza C virus recognizes C9-O-Ac Neu5Ac. The acetylesterase RDE of ISAV cleaves C4-O-Ac via 4-SA-O-acetylesterase with a short turnover time, whereas C9-O-Ac Neu5Ac is cleaved by 9-SA-O-acetylesterase with a long turnover time [34]."}

    LitCovid-PD-CHEBI

    {"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T535","span":{"begin":32,"end":38},"obj":"Chemical"},{"id":"T537","span":{"begin":55,"end":61},"obj":"Chemical"},{"id":"T539","span":{"begin":63,"end":65},"obj":"Chemical"},{"id":"T544","span":{"begin":103,"end":105},"obj":"Chemical"},{"id":"T549","span":{"begin":135,"end":141},"obj":"Chemical"},{"id":"T551","span":{"begin":186,"end":188},"obj":"Chemical"},{"id":"T552","span":{"begin":205,"end":213},"obj":"Chemical"},{"id":"T553","span":{"begin":222,"end":226},"obj":"Chemical"},{"id":"T554","span":{"begin":230,"end":235},"obj":"Chemical"},{"id":"T555","span":{"begin":309,"end":321},"obj":"Chemical"},{"id":"T556","span":{"begin":309,"end":315},"obj":"Chemical"},{"id":"T557","span":{"begin":316,"end":321},"obj":"Chemical"},{"id":"T558","span":{"begin":337,"end":343},"obj":"Chemical"},{"id":"T560","span":{"begin":344,"end":350},"obj":"Chemical"},{"id":"T562","span":{"begin":415,"end":418},"obj":"Chemical"},{"id":"T564","span":{"begin":482,"end":488},"obj":"Chemical"},{"id":"T566","span":{"begin":680,"end":688},"obj":"Chemical"},{"id":"T567","span":{"begin":727,"end":729},"obj":"Chemical"},{"id":"T569","span":{"begin":730,"end":736},"obj":"Chemical"},{"id":"T571","span":{"begin":865,"end":867},"obj":"Chemical"},{"id":"T573","span":{"begin":868,"end":874},"obj":"Chemical"},{"id":"T575","span":{"begin":920,"end":922},"obj":"Chemical"},{"id":"T577","span":{"begin":929,"end":931},"obj":"Chemical"},{"id":"T582","span":{"begin":990,"end":992},"obj":"Chemical"},{"id":"T584","span":{"begin":993,"end":999},"obj":"Chemical"},{"id":"T586","span":{"begin":1016,"end":1018},"obj":"Chemical"}],"attributes":[{"id":"A535","pred":"chebi_id","subj":"T535","obj":"http://purl.obolibrary.org/obo/CHEBI_40574"},{"id":"A536","pred":"chebi_id","subj":"T535","obj":"http://purl.obolibrary.org/obo/CHEBI_46887"},{"id":"A537","pred":"chebi_id","subj":"T537","obj":"http://purl.obolibrary.org/obo/CHEBI_17012"},{"id":"A538","pred":"chebi_id","subj":"T537","obj":"http://purl.obolibrary.org/obo/CHEBI_75133"},{"id":"A539","pred":"chebi_id","subj":"T539","obj":"http://purl.obolibrary.org/obo/CHEBI_35962"},{"id":"A540","pred":"chebi_id","subj":"T539","obj":"http://purl.obolibrary.org/obo/CHEBI_38358"},{"id":"A541","pred":"chebi_id","subj":"T539","obj":"http://purl.obolibrary.org/obo/CHEBI_45373"},{"id":"A542","pred":"chebi_id","subj":"T539","obj":"http://purl.obolibrary.org/obo/CHEBI_74801"},{"id":"A543","pred":"chebi_id","subj":"T539","obj":"http://purl.obolibrary.org/obo/CHEBI_26667"},{"id":"A544","pred":"chebi_id","subj":"T544","obj":"http://purl.obolibrary.org/obo/CHEBI_35962"},{"id":"A545","pred":"chebi_id","subj":"T544","obj":"http://purl.obolibrary.org/obo/CHEBI_38358"},{"id":"A546","pred":"chebi_id","subj":"T544","obj":"http://purl.obolibrary.org/obo/CHEBI_45373"},{"id":"A547","pred":"chebi_id","subj":"T544","obj":"http://purl.obolibrary.org/obo/CHEBI_74801"},{"id":"A548","pred":"chebi_id","subj":"T544","obj":"http://purl.obolibrary.org/obo/CHEBI_26667"},{"id":"A549","pred":"chebi_id","subj":"T549","obj":"http://purl.obolibrary.org/obo/CHEBI_17012"},{"id":"A550","pred":"chebi_id","subj":"T549","obj":"http://purl.obolibrary.org/obo/CHEBI_75133"},{"id":"A551","pred":"chebi_id","subj":"T551","obj":"http://purl.obolibrary.org/obo/CHEBI_73924"},{"id":"A552","pred":"chebi_id","subj":"T552","obj":"http://purl.obolibrary.org/obo/CHEBI_33893"},{"id":"A553","pred":"chebi_id","subj":"T553","obj":"http://purl.obolibrary.org/obo/CHEBI_32145"},{"id":"A554","pred":"chebi_id","subj":"T554","obj":"http://purl.obolibrary.org/obo/CHEBI_75226"},{"id":"A555","pred":"chebi_id","subj":"T555","obj":"http://purl.obolibrary.org/obo/CHEBI_40574"},{"id":"A556","pred":"chebi_id","subj":"T556","obj":"http://purl.obolibrary.org/obo/CHEBI_46887"},{"id":"A557","pred":"chebi_id","subj":"T557","obj":"http://purl.obolibrary.org/obo/CHEBI_24433"},{"id":"A558","pred":"chebi_id","subj":"T558","obj":"http://purl.obolibrary.org/obo/CHEBI_40574"},{"id":"A559","pred":"chebi_id","subj":"T558","obj":"http://purl.obolibrary.org/obo/CHEBI_46887"},{"id":"A560","pred":"chebi_id","subj":"T560","obj":"http://purl.obolibrary.org/obo/CHEBI_17012"},{"id":"A561","pred":"chebi_id","subj":"T560","obj":"http://purl.obolibrary.org/obo/CHEBI_75133"},{"id":"A562","pred":"chebi_id","subj":"T562","obj":"http://purl.obolibrary.org/obo/CHEBI_15681"},{"id":"A563","pred":"chebi_id","subj":"T562","obj":"http://purl.obolibrary.org/obo/CHEBI_84118"},{"id":"A564","pred":"chebi_id","subj":"T564","obj":"http://purl.obolibrary.org/obo/CHEBI_17012"},{"id":"A565","pred":"chebi_id","subj":"T564","obj":"http://purl.obolibrary.org/obo/CHEBI_75133"},{"id":"A566","pred":"chebi_id","subj":"T566","obj":"http://purl.obolibrary.org/obo/CHEBI_36080"},{"id":"A567","pred":"chebi_id","subj":"T567","obj":"http://purl.obolibrary.org/obo/CHEBI_33337"},{"id":"A568","pred":"chebi_id","subj":"T567","obj":"http://purl.obolibrary.org/obo/CHEBI_40574"},{"id":"A569","pred":"chebi_id","subj":"T569","obj":"http://purl.obolibrary.org/obo/CHEBI_17012"},{"id":"A570","pred":"chebi_id","subj":"T569","obj":"http://purl.obolibrary.org/obo/CHEBI_75133"},{"id":"A571","pred":"chebi_id","subj":"T571","obj":"http://purl.obolibrary.org/obo/CHEBI_33337"},{"id":"A572","pred":"chebi_id","subj":"T571","obj":"http://purl.obolibrary.org/obo/CHEBI_40574"},{"id":"A573","pred":"chebi_id","subj":"T573","obj":"http://purl.obolibrary.org/obo/CHEBI_17012"},{"id":"A574","pred":"chebi_id","subj":"T573","obj":"http://purl.obolibrary.org/obo/CHEBI_75133"},{"id":"A575","pred":"chebi_id","subj":"T575","obj":"http://purl.obolibrary.org/obo/CHEBI_33337"},{"id":"A576","pred":"chebi_id","subj":"T575","obj":"http://purl.obolibrary.org/obo/CHEBI_40574"},{"id":"A577","pred":"chebi_id","subj":"T577","obj":"http://purl.obolibrary.org/obo/CHEBI_35962"},{"id":"A578","pred":"chebi_id","subj":"T577","obj":"http://purl.obolibrary.org/obo/CHEBI_38358"},{"id":"A579","pred":"chebi_id","subj":"T577","obj":"http://purl.obolibrary.org/obo/CHEBI_45373"},{"id":"A580","pred":"chebi_id","subj":"T577","obj":"http://purl.obolibrary.org/obo/CHEBI_74801"},{"id":"A581","pred":"chebi_id","subj":"T577","obj":"http://purl.obolibrary.org/obo/CHEBI_26667"},{"id":"A582","pred":"chebi_id","subj":"T582","obj":"http://purl.obolibrary.org/obo/CHEBI_33337"},{"id":"A583","pred":"chebi_id","subj":"T582","obj":"http://purl.obolibrary.org/obo/CHEBI_40574"},{"id":"A584","pred":"chebi_id","subj":"T584","obj":"http://purl.obolibrary.org/obo/CHEBI_17012"},{"id":"A585","pred":"chebi_id","subj":"T584","obj":"http://purl.obolibrary.org/obo/CHEBI_75133"},{"id":"A586","pred":"chebi_id","subj":"T586","obj":"http://purl.obolibrary.org/obo/CHEBI_35962"},{"id":"A587","pred":"chebi_id","subj":"T586","obj":"http://purl.obolibrary.org/obo/CHEBI_38358"},{"id":"A588","pred":"chebi_id","subj":"T586","obj":"http://purl.obolibrary.org/obo/CHEBI_45373"},{"id":"A589","pred":"chebi_id","subj":"T586","obj":"http://purl.obolibrary.org/obo/CHEBI_74801"},{"id":"A590","pred":"chebi_id","subj":"T586","obj":"http://purl.obolibrary.org/obo/CHEBI_26667"}],"text":"For example, in the horse, C4-O-acetyl modification of Neu5Ac (SA) occupies more than 50% of the total SA content. The C4-O-acetylated Neu5Ac, Neu4,5Ac2, inhibits the influenza A2 virus HA. De-acetylation reagents such as NaOH or NaIO4 treatment completely hemagglutinate Neu4,5Ac2 by elimination of the C4-O-acetyl group [33]. The C4-O-acetyl Neu5Ac species are found in various sources such as equine erythrocyte GM3, starfish A. rubens and fish [34,35,36,37,38]. C4-O-acetylated Neu5Ac facilitates the initial attachment of viruses to target cells. Like the influenza C virus, infectious salmon anemia virus (ISAV), a member of the Orthomyxoviridae family, contains HE and HEF proteins to mediate virus entry and exit. C4-O-Ac Neu5Ac is the major receptor determinant of ISAV in receptor binding and destruction [38], while the influenza C virus recognizes C9-O-Ac Neu5Ac. The acetylesterase RDE of ISAV cleaves C4-O-Ac via 4-SA-O-acetylesterase with a short turnover time, whereas C9-O-Ac Neu5Ac is cleaved by 9-SA-O-acetylesterase with a long turnover time [34]."}

    LitCovid-sentences

    {"project":"LitCovid-sentences","denotations":[{"id":"T213","span":{"begin":0,"end":114},"obj":"Sentence"},{"id":"T214","span":{"begin":115,"end":189},"obj":"Sentence"},{"id":"T215","span":{"begin":190,"end":327},"obj":"Sentence"},{"id":"T216","span":{"begin":328,"end":465},"obj":"Sentence"},{"id":"T217","span":{"begin":466,"end":551},"obj":"Sentence"},{"id":"T218","span":{"begin":552,"end":721},"obj":"Sentence"},{"id":"T219","span":{"begin":722,"end":875},"obj":"Sentence"},{"id":"T220","span":{"begin":876,"end":1067},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"For example, in the horse, C4-O-acetyl modification of Neu5Ac (SA) occupies more than 50% of the total SA content. The C4-O-acetylated Neu5Ac, Neu4,5Ac2, inhibits the influenza A2 virus HA. De-acetylation reagents such as NaOH or NaIO4 treatment completely hemagglutinate Neu4,5Ac2 by elimination of the C4-O-acetyl group [33]. The C4-O-acetyl Neu5Ac species are found in various sources such as equine erythrocyte GM3, starfish A. rubens and fish [34,35,36,37,38]. C4-O-acetylated Neu5Ac facilitates the initial attachment of viruses to target cells. Like the influenza C virus, infectious salmon anemia virus (ISAV), a member of the Orthomyxoviridae family, contains HE and HEF proteins to mediate virus entry and exit. C4-O-Ac Neu5Ac is the major receptor determinant of ISAV in receptor binding and destruction [38], while the influenza C virus recognizes C9-O-Ac Neu5Ac. The acetylesterase RDE of ISAV cleaves C4-O-Ac via 4-SA-O-acetylesterase with a short turnover time, whereas C9-O-Ac Neu5Ac is cleaved by 9-SA-O-acetylesterase with a long turnover time [34]."}

    2_test

    {"project":"2_test","denotations":[{"id":"32604730-21618128-51943973","span":{"begin":323,"end":325},"obj":"21618128"},{"id":"32604730-31683930-51943974","span":{"begin":449,"end":451},"obj":"31683930"},{"id":"32604730-9090814-51943975","span":{"begin":452,"end":454},"obj":"9090814"},{"id":"32604730-16181722-51943976","span":{"begin":455,"end":457},"obj":"16181722"},{"id":"32604730-24833039-51943977","span":{"begin":458,"end":460},"obj":"24833039"},{"id":"32604730-14990724-51943978","span":{"begin":461,"end":463},"obj":"14990724"},{"id":"32604730-14990724-51943979","span":{"begin":816,"end":818},"obj":"14990724"},{"id":"32604730-31683930-51943980","span":{"begin":1063,"end":1065},"obj":"31683930"},{"id":"T78050","span":{"begin":323,"end":325},"obj":"21618128"},{"id":"T53753","span":{"begin":449,"end":451},"obj":"31683930"},{"id":"T38465","span":{"begin":452,"end":454},"obj":"9090814"},{"id":"T72587","span":{"begin":455,"end":457},"obj":"16181722"},{"id":"T75131","span":{"begin":458,"end":460},"obj":"24833039"},{"id":"T15211","span":{"begin":461,"end":463},"obj":"14990724"},{"id":"T68693","span":{"begin":816,"end":818},"obj":"14990724"},{"id":"T49725","span":{"begin":1063,"end":1065},"obj":"31683930"}],"text":"For example, in the horse, C4-O-acetyl modification of Neu5Ac (SA) occupies more than 50% of the total SA content. The C4-O-acetylated Neu5Ac, Neu4,5Ac2, inhibits the influenza A2 virus HA. De-acetylation reagents such as NaOH or NaIO4 treatment completely hemagglutinate Neu4,5Ac2 by elimination of the C4-O-acetyl group [33]. The C4-O-acetyl Neu5Ac species are found in various sources such as equine erythrocyte GM3, starfish A. rubens and fish [34,35,36,37,38]. C4-O-acetylated Neu5Ac facilitates the initial attachment of viruses to target cells. Like the influenza C virus, infectious salmon anemia virus (ISAV), a member of the Orthomyxoviridae family, contains HE and HEF proteins to mediate virus entry and exit. C4-O-Ac Neu5Ac is the major receptor determinant of ISAV in receptor binding and destruction [38], while the influenza C virus recognizes C9-O-Ac Neu5Ac. The acetylesterase RDE of ISAV cleaves C4-O-Ac via 4-SA-O-acetylesterase with a short turnover time, whereas C9-O-Ac Neu5Ac is cleaved by 9-SA-O-acetylesterase with a long turnover time [34]."}

    LitCovid-PD-HP

    {"project":"LitCovid-PD-HP","denotations":[{"id":"T7","span":{"begin":598,"end":604},"obj":"Phenotype"}],"attributes":[{"id":"A7","pred":"hp_id","subj":"T7","obj":"http://purl.obolibrary.org/obo/HP_0001903"}],"text":"For example, in the horse, C4-O-acetyl modification of Neu5Ac (SA) occupies more than 50% of the total SA content. The C4-O-acetylated Neu5Ac, Neu4,5Ac2, inhibits the influenza A2 virus HA. De-acetylation reagents such as NaOH or NaIO4 treatment completely hemagglutinate Neu4,5Ac2 by elimination of the C4-O-acetyl group [33]. The C4-O-acetyl Neu5Ac species are found in various sources such as equine erythrocyte GM3, starfish A. rubens and fish [34,35,36,37,38]. C4-O-acetylated Neu5Ac facilitates the initial attachment of viruses to target cells. Like the influenza C virus, infectious salmon anemia virus (ISAV), a member of the Orthomyxoviridae family, contains HE and HEF proteins to mediate virus entry and exit. C4-O-Ac Neu5Ac is the major receptor determinant of ISAV in receptor binding and destruction [38], while the influenza C virus recognizes C9-O-Ac Neu5Ac. The acetylesterase RDE of ISAV cleaves C4-O-Ac via 4-SA-O-acetylesterase with a short turnover time, whereas C9-O-Ac Neu5Ac is cleaved by 9-SA-O-acetylesterase with a long turnover time [34]."}