SrasV1, PubMed, Curation, bibRecord, 002294

Tertiary structure prediction of SARS coronavirus helicase.

Identifieur interne : 002294 ( PubMed/Curation ); précédent : 002293; suivant : 002295

Tertiary structure prediction of SARS coronavirus helicase.

Auteurs : Andrea Bernini [Italie] ; Ottavia Spiga ; Vincenzo Venditti ; Filippo Prischi ; Luisa Bracci ; Jiandong Huang ; Julian A. Tanner ; Neri Niccolai

Source :

Biochemical and biophysical research communications [ 0006-291X ] ; 2006.

RBID : pubmed:16579970

Descripteurs français

KwdFr :
- Analyse de séquence de protéine, Helicase (), Modèles moléculaires, Protéines virales (), Simulation numérique, Sites de fixation, Structure tertiaire des protéines, Virus du SRAS (enzymologie).
MESH :
- enzymologie : Virus du SRAS.
- Analyse de séquence de protéine, Helicase, Modèles moléculaires, Protéines virales, Simulation numérique, Sites de fixation, Structure tertiaire des protéines.

English descriptors

KwdEn :
- Binding Sites, Computer Simulation, DNA Helicases (chemistry), Models, Molecular, Protein Structure, Tertiary, SARS Virus (enzymology), Sequence Analysis, Protein, Viral Proteins (chemistry).
MESH :
- chemical , chemistry : DNA Helicases, Viral Proteins.
- enzymology : SARS Virus.
- Binding Sites, Computer Simulation, Models, Molecular, Protein Structure, Tertiary, Sequence Analysis, Protein.

Abstract

SARS coronavirus, SCV, has been recently responsible of a sudden and widespread infection which caused almost 800 victims. The limited amount of SCV protein structural information is partially responsible of the lack of specific drugs against the virus. Coronavirus helicases are very conserved and peculiar proteins which have been proposed as suitable targets for antiviral drugs, such as bananins, which have been recently shown to inhibit the SCV helicase in vitro. Here, the quaternary structure of SCV helicase has been predicted, which will provide a solid foundation for the rational design of other antiviral helicase inhibitors.

DOI: 10.1016/j.bbrc.2006.03.069
PubMed: 16579970

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Le document en format XML

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<author><name sortKey="Bernini, Andrea" sort="Bernini, Andrea" uniqKey="Bernini A" first="Andrea" last="Bernini">Andrea Bernini</name>
<affiliation wicri:level="1"><nlm:affiliation>Biomolecular Structure Research Center, Department of Molecular Biology, University of Siena, I-53100 Siena, Italy.</nlm:affiliation>
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<author><name sortKey="Spiga, Ottavia" sort="Spiga, Ottavia" uniqKey="Spiga O" first="Ottavia" last="Spiga">Ottavia Spiga</name>
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<author><name sortKey="Prischi, Filippo" sort="Prischi, Filippo" uniqKey="Prischi F" first="Filippo" last="Prischi">Filippo Prischi</name>
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<author><name sortKey="Bracci, Luisa" sort="Bracci, Luisa" uniqKey="Bracci L" first="Luisa" last="Bracci">Luisa Bracci</name>
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<author><name sortKey="Huang, Jiandong" sort="Huang, Jiandong" uniqKey="Huang J" first="Jiandong" last="Huang">Jiandong Huang</name>
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<author><name sortKey="Tanner, Julian A" sort="Tanner, Julian A" uniqKey="Tanner J" first="Julian A" last="Tanner">Julian A. Tanner</name>
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<author><name sortKey="Niccolai, Neri" sort="Niccolai, Neri" uniqKey="Niccolai N" first="Neri" last="Niccolai">Neri Niccolai</name>
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<term>Computer Simulation</term>
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<term>Models, Molecular</term>
<term>Protein Structure, Tertiary</term>
<term>SARS Virus (enzymology)</term>
<term>Sequence Analysis, Protein</term>
<term>Viral Proteins (chemistry)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Analyse de séquence de protéine</term>
<term>Helicase ()</term>
<term>Modèles moléculaires</term>
<term>Protéines virales ()</term>
<term>Simulation numérique</term>
<term>Sites de fixation</term>
<term>Structure tertiaire des protéines</term>
<term>Virus du SRAS (enzymologie)</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>DNA Helicases</term>
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<term>Modèles moléculaires</term>
<term>Protéines virales</term>
<term>Simulation numérique</term>
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<front><div type="abstract" xml:lang="en">SARS coronavirus, SCV, has been recently responsible of a sudden and widespread infection which caused almost 800 victims. The limited amount of SCV protein structural information is partially responsible of the lack of specific drugs against the virus. Coronavirus helicases are very conserved and peculiar proteins which have been proposed as suitable targets for antiviral drugs, such as bananins, which have been recently shown to inhibit the SCV helicase in vitro. Here, the quaternary structure of SCV helicase has been predicted, which will provide a solid foundation for the rational design of other antiviral helicase inhibitors.</div>
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Tertiary structure prediction of SARS coronavirus helicase.

Tertiary structure prediction of SARS coronavirus helicase.

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

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Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

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Pour générer des pages wiki