The complete nucleotide sequence of cloned cDNAs containing the E2 glycoprotein-encoding region of the genome of transmissible gastroenteritis virus (TGEV) has been determined. A single large translatable frame of 4.3 kb starting at 8.2 kb from the 3' end of the genome was identified. Its deduced amino acid sequence contains the characteristic features of a coronavirus peplomer protein: the precursor polypeptide of TGEV E2 is 1447 residues long (i.e. 285 longer than the avian infectious bronchitis coronavirus spike protein); partial N-terminal sequencing demonstrated that a putative secretory signal sequence of 16 amino acids is absent in the virion-associated protein; the predicted mol. wt. of the apoprotein is 158K; most of the 32 potential N-glycosylation sites available in the sequence are presumed to be functional to account for the difference between this and the experimentally determined value (200K to 220K); a typical hydrophobic sequence near the C terminus is likely to be responsible for anchoring the peplomer to the virion envelope.
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http://purl.uniprot.org/cit... | rdf:type | uniprot:Journal_Citation | lld:uniprot |
http://purl.uniprot.org/cit... | rdfs:comment | The complete nucleotide sequence of cloned cDNAs containing the E2 glycoprotein-encoding region of the genome of transmissible gastroenteritis virus (TGEV) has been determined. A single large translatable frame of 4.3 kb starting at 8.2 kb from the 3' end of the genome was identified. Its deduced amino acid sequence contains the characteristic features of a coronavirus peplomer protein: the precursor polypeptide of TGEV E2 is 1447 residues long (i.e. 285 longer than the avian infectious bronchitis coronavirus spike protein); partial N-terminal sequencing demonstrated that a putative secretory signal sequence of 16 amino acids is absent in the virion-associated protein; the predicted mol. wt. of the apoprotein is 158K; most of the 32 potential N-glycosylation sites available in the sequence are presumed to be functional to account for the difference between this and the experimentally determined value (200K to 220K); a typical hydrophobic sequence near the C terminus is likely to be responsible for anchoring the peplomer to the virion envelope. | lld:uniprot |
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http://purl.uniprot.org/cit... | skos:exactMatch | http://purl.uniprot.org/pub... | lld:uniprot |
http://purl.uniprot.org/cit... | uniprot:name | J. Gen. Virol. | lld:uniprot |
http://purl.uniprot.org/cit... | uniprot:author | Laude H. | lld:uniprot |
http://purl.uniprot.org/cit... | uniprot:author | Rasschaert D. | lld:uniprot |
http://purl.uniprot.org/cit... | uniprot:date | 1987 | lld:uniprot |
http://purl.uniprot.org/cit... | uniprot:pages | 1883-1890 | lld:uniprot |
http://purl.uniprot.org/cit... | uniprot:title | The predicted primary structure of the peplomer protein E2 of the porcine coronavirus transmissible gastroenteritis virus. | lld:uniprot |
http://purl.uniprot.org/cit... | uniprot:volume | 68 | lld:uniprot |
uniprot-protein:P07946 | uniprot:citation | http://purl.uniprot.org/cit... | lld:uniprot |
http://purl.uniprot.org/emb... | uniprot:citation | http://purl.uniprot.org/cit... | lld:uniprot |
uniprot-protein:Q66203 | uniprot:citation | http://purl.uniprot.org/cit... | lld:uniprot |
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http://linkedlifedata.com/r... | rdf:object | http://purl.uniprot.org/cit... | lld:uniprot |