Serveur d'exploration SRAS

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Sequence Analysis and Structural Prediction of the Severe Acute Respiratory Syndrome Coronavirus nsp5

Identifieur interne : 000D51 ( Pmc/Curation ); précédent : 000D50; suivant : 000D52

Sequence Analysis and Structural Prediction of the Severe Acute Respiratory Syndrome Coronavirus nsp5

Auteurs : Jia-Hai Lu [République populaire de Chine] ; Ding-Mei Zhang [République populaire de Chine] ; Guo-Ling Wang [République populaire de Chine] ; Zhong-Min Guo [République populaire de Chine] ; Juan Li [République populaire de Chine] ; Bing-Yan Tan [République populaire de Chine] ; Li-Ping Ou-Yang [République populaire de Chine] ; Wen-Hua Ling [République populaire de Chine] ; Xin-Bing Yu [République populaire de Chine] ; Nan-Shan Zhong [République populaire de Chine]

Source :

RBID : PMC:7110076

Abstract

Abstract

The non-structural proteins (nsp or replicase proteins) of coronaviruses are relatively conserved and can be effective targets for drugs. Few studies have been conducted into the function of the severe acute respiratory syndrome coronavirus (SARS-CoV) nsp5. In this study, bioinformatics methods were employed to predict the secondary structure and construct 3-D models of the SARS-CoV GD strain nsp5. Sequencing and sequential comparison was performed to analyze the mutation trend of the polymerase nsp5 gene during the epidemic process using a nucleotide-nucleotide basic local alignment search tool (BLASTN) and a protein-protein basic local alignment search tool (BLASTP). The results indicated that the nsp5 gene was steady during the epidemic process and the protein was homologous with other coronavirus nsp5 proteins. The protein encoded by the nsp5 gene was expressed in COS-7 cells and analyzed by sodium dodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE). This study provided the foundation for further exploration of the protein's biological function, and contributed to the search for anti-SARS-CoV drugs.


Url:
DOI: 10.1111/j.1745-7270.2005.00066.x
PubMed: 15999208
PubMed Central: 7110076

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PMC:7110076

Le document en format XML

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<p>The non-structural proteins (nsp or replicase proteins) of coronaviruses are relatively conserved and can be effective targets for drugs. Few studies have been conducted into the function of the severe acute respiratory syndrome coronavirus (SARS-CoV) nsp5. In this study, bioinformatics methods were employed to predict the secondary structure and construct 3-D models of the SARS-CoV GD strain nsp5. Sequencing and sequential comparison was performed to analyze the mutation trend of the polymerase nsp5 gene during the epidemic process using a nucleotide-nucleotide basic local alignment search tool (BLASTN) and a protein-protein basic local alignment search tool (BLASTP). The results indicated that the nsp5 gene was steady during the epidemic process and the protein was homologous with other coronavirus nsp5 proteins. The protein encoded by the nsp5 gene was expressed in COS-7 cells and analyzed by sodium dodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE). This study provided the foundation for further exploration of the protein's biological function, and contributed to the search for anti-SARS-CoV drugs.</p>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Lu</surname>
<given-names>Jia-Hai</given-names>
</name>
<author-comment>
<title>#</title>
<p>These authors contributed equally to this work</p>
</author-comment>
<xref ref-type="aff" rid="au1">1</xref>
<xref ref-type="corresp" rid="cor1">*</xref>
<pmc-comment>jiahailu@yahoo.com.cn</pmc-comment>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Ding-Mei</given-names>
</name>
<author-comment>
<title>#</title>
<p>These authors contributed equally to this work</p>
</author-comment>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Guo-Ling</given-names>
</name>
<author-comment>
<title>#</title>
<p>These authors contributed equally to this work</p>
</author-comment>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Guo</surname>
<given-names>Zhong-Min</given-names>
</name>
<author-comment>
<title>#</title>
<p>These authors contributed equally to this work</p>
</author-comment>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Li</surname>
<given-names>Juan</given-names>
</name>
<author-comment>
<title>#</title>
<p>These authors contributed equally to this work</p>
</author-comment>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tan</surname>
<given-names>Bing-Yan</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ou-Yang</surname>
<given-names>Li-Ping</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ling</surname>
<given-names>Wen-Hua</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Yu</surname>
<given-names>Xin-Bing</given-names>
</name>
<xref ref-type="aff" rid="au1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhong</surname>
<given-names>Nan-Shan</given-names>
</name>
<xref ref-type="aff" rid="au2">1</xref>
</contrib>
</contrib-group>
<contrib-group>
<contrib contrib-type="editor">
<name>
<surname>Sun</surname>
<given-names>Bing</given-names>
</name>
</contrib>
</contrib-group>
<aff id="au1">
<label>1</label>
<institution>The Public Health School of Sun Yat-Sen University</institution>
<addr-line>Guangzhou 510080, China;</addr-line>
</aff>
<aff id="au2">
<label>1</label>
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<addr-line>Guangzhou 510120, China</addr-line>
</aff>
<author-notes>
<fn id="fn1">
<label>#</label>
<p>These authors contributed equally to this work</p>
</fn>
<corresp id="cor1">
<label>*</label>
Corresponding author: Tel,
<phone>86-20-87330605</phone>
; Fax,
<fax>86-20-87332438</fax>
; E-mail,
<email>jiahailu@yahoo.com.cn</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>7</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="epub" iso-8601-date="2005-07-01">
<month>7</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="pmc-release">
<month>7</month>
<year>2005</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on the . </pmc-comment>
<volume>37</volume>
<issue>7</issue>
<fpage>473</fpage>
<lpage>479</lpage>
<history>
<date date-type="received">
<day>27</day>
<month>1</month>
<year>2005</year>
</date>
<date date-type="accepted">
<day>25</day>
<month>4</month>
<year>2005</year>
</date>
</history>
<permissions>
<copyright-statement>© 2005 Institute of Biochemistry and Cell Biology, SIBS, CAS</copyright-statement>
<copyright-year>2005</copyright-year>
<license>
<license-p>This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.</license-p>
</license>
</permissions>
<self-uri xlink:href="37-7-473.pdf"></self-uri>
<abstract>
<title>Abstract</title>
<p>The non-structural proteins (nsp or replicase proteins) of coronaviruses are relatively conserved and can be effective targets for drugs. Few studies have been conducted into the function of the severe acute respiratory syndrome coronavirus (SARS-CoV) nsp5. In this study, bioinformatics methods were employed to predict the secondary structure and construct 3-D models of the SARS-CoV GD strain nsp5. Sequencing and sequential comparison was performed to analyze the mutation trend of the polymerase nsp5 gene during the epidemic process using a nucleotide-nucleotide basic local alignment search tool (BLASTN) and a protein-protein basic local alignment search tool (BLASTP). The results indicated that the nsp5 gene was steady during the epidemic process and the protein was homologous with other coronavirus nsp5 proteins. The protein encoded by the nsp5 gene was expressed in COS-7 cells and analyzed by sodium dodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE). This study provided the foundation for further exploration of the protein's biological function, and contributed to the search for anti-SARS-CoV drugs.</p>
</abstract>
<kwd-group>
<kwd>severe acute respiratory syndrome (SARS)</kwd>
<kwd>severe acute respiratory syndrome coronavirus(SARS-CoV)</kwd>
<kwd>non-structural protein (nsp)</kwd>
<kwd>replicase</kwd>
<kwd>secondary structure</kwd>
<kwd>3-D structure</kwd>
</kwd-group>
</article-meta>
</front>
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HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Curation/RBID.i   -Sk "pubmed:15999208" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Curation/biblio.hfd   \
       | NlmPubMed2Wicri -a SrasV1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Apr 28 14:49:16 2020. Site generation: Sat Mar 27 22:06:49 2021