Sequence analysis and structural prediction of the severe acute respiratory syndrome coronavirus nsp5.
Identifieur interne : 002657 ( PubMed/Curation ); précédent : 002656; suivant : 002658Sequence analysis and structural prediction of the severe acute respiratory syndrome coronavirus nsp5.
Auteurs : Jia-Hai Lu [République populaire de Chine] ; Ding-Mei Zhang ; Guo-Ling Wang ; Zhong-Min Guo ; Juan Li ; Bing-Yan Tan ; Li-Ping Ou-Yang ; Wen-Hua Ling ; Xin-Bing Yu ; Nan-Shan ZhongSource :
- Acta biochimica et biophysica Sinica [ 1672-9145 ] ; 2005.
Descripteurs français
- KwdFr :
- MESH :
- biosynthèse : Protéines virales non structurales.
- génétique : Plasmides, Virus du SRAS.
- virologie : Syndrome respiratoire aigu sévère.
- Adulte d'âge moyen, Animaux, Cellules COS, Femelle, Humains, Protéines virales non structurales, RT-PCR, Séquence d'acides aminés.
English descriptors
- KwdEn :
- Amino Acid Sequence, Animals, COS Cells, Chlorocebus aethiops, Female, Humans, Middle Aged, Plasmids (genetics), Reverse Transcriptase Polymerase Chain Reaction, SARS Virus (genetics), Severe Acute Respiratory Syndrome (virology), Viral Nonstructural Proteins (biosynthesis), Viral Nonstructural Proteins (chemistry).
- MESH :
- chemical , biosynthesis : Viral Nonstructural Proteins.
- chemical , chemistry : Viral Nonstructural Proteins.
- genetics : Plasmids, SARS Virus.
- virology : Severe Acute Respiratory Syndrome.
- Amino Acid Sequence, Animals, COS Cells, Chlorocebus aethiops, Female, Humans, Middle Aged, Reverse Transcriptase Polymerase Chain Reaction.
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.
DOI: 10.1111/j.1745-7270.2005.00066.x
PubMed: 15999208
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pubmed:15999208Le document en format XML
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<front><div type="abstract" xml:lang="en">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.</div>
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<Abstract><AbstractText>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.</AbstractText>
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