Literature DB >> 2345367

Nucleotide sequence of the gene encoding the spike glycoprotein of human coronavirus HCV 229E.

T Raabe1, B Schelle-Prinz, S G Siddell.   

Abstract

The gene encoding the spike glycoprotein of the human coronavirus HCV 229E has been cloned and sequenced. This analysis predicts an S polypeptide of 1173 amino acids with an Mr of 128,600. The polypeptide has 30 potential N-glycosylation sites. A number of structural features typical of coronavirus S proteins can be recognized, including a signal sequence, a membrane anchor, heptad repeat structures and a carboxy-terminal cysteine cluster. A detailed, computer-aided comparison with the S proteins of infectious bronchitis virus, feline infectious peritonitis virus, transmissible gastroenteritis virus and murine hepatitis virus, strain JHM is presented. We have also done a Northern blot analysis of viral RNAs in HCV 229E-infected cells using synthetic oligonucleotides. On the basis of this analysis, and by analogy to the replication strategy of other coronaviruses, we are able to propose a model for the organization and expression of the HCV 229E genome.

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Year:  1990        PMID: 2345367     DOI: 10.1099/0022-1317-71-5-1065

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  22 in total

1.  ADP-ribose-1"-monophosphatase: a conserved coronavirus enzyme that is dispensable for viral replication in tissue culture.

Authors:  Akos Putics; Witold Filipowicz; Jonathan Hall; Alexander E Gorbalenya; John Ziebuhr
Journal:  J Virol       Date:  2005-10       Impact factor: 5.103

2.  Human coronavirus 229E infects polarized airway epithelia from the apical surface.

Authors:  G Wang; C Deering; M Macke; J Shao; R Burns; D M Blau; K V Holmes; B L Davidson; S Perlman; P B McCray
Journal:  J Virol       Date:  2000-10       Impact factor: 5.103

3.  Coronavirus-induced membrane fusion requires the cysteine-rich domain in the spike protein.

Authors:  K W Chang; Y Sheng; J L Gombold
Journal:  Virology       Date:  2000-03-30       Impact factor: 3.616

4.  Proteolytic processing at the amino terminus of human coronavirus 229E gene 1-encoded polyproteins: identification of a papain-like proteinase and its substrate.

Authors:  J Herold; A E Gorbalenya; V Thiel; B Schelle; S G Siddell
Journal:  J Virol       Date:  1998-02       Impact factor: 5.103

5.  Persistent infection of human oligodendrocytic and neuroglial cell lines by human coronavirus 229E.

Authors:  N Arbour; S Ekandé; G Côté; C Lachance; F Chagnon; M Tardieu; N R Cashman; P J Talbot
Journal:  J Virol       Date:  1999-04       Impact factor: 5.103

6.  Identification of a receptor-binding domain of the spike glycoprotein of human coronavirus HCoV-229E.

Authors:  Aurelio Bonavia; Bruce D Zelus; David E Wentworth; Pierre J Talbot; Kathryn V Holmes
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

7.  Characterization of a human coronavirus (strain 229E) 3C-like proteinase activity.

Authors:  J Ziebuhr; J Herold; S G Siddell
Journal:  J Virol       Date:  1995-07       Impact factor: 5.103

8.  Human coronavirus 229E nonstructural protein 13: characterization of duplex-unwinding, nucleoside triphosphatase, and RNA 5'-triphosphatase activities.

Authors:  Konstantin A Ivanov; John Ziebuhr
Journal:  J Virol       Date:  2004-07       Impact factor: 5.103

9.  Involvement of aminopeptidase N (CD13) in infection of human neural cells by human coronavirus 229E.

Authors:  C Lachance; N Arbour; N R Cashman; P J Talbot
Journal:  J Virol       Date:  1998-08       Impact factor: 5.103

10.  Direct RNA nanopore sequencing of full-length coronavirus genomes provides novel insights into structural variants and enables modification analysis.

Authors:  Adrian Viehweger; Sebastian Krautwurst; Kevin Lamkiewicz; Ramakanth Madhugiri; John Ziebuhr; Martin Hölzer; Manja Marz
Journal:  Genome Res       Date:  2019-08-22       Impact factor: 9.043

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