SrasV1, PascalFrancis, Curation, bibRecord, 000986

Accessory proteins of SARS-CoV and other coronaviruses

Identifieur interne : 000986 ( PascalFrancis/Curation ); précédent : 000985; suivant : 000987

Accessory proteins of SARS-CoV and other coronaviruses

Auteurs : DING XIANG LIU [Singapour] ; TO SING FUNG [Singapour] ; Kelvin Kian-Long Chong [Singapour] ; Aditi Shukla [Allemagne] ; Rolf Hilgenfeld [Allemagne]

Source :

Antiviral research [ 0166-3542 ] ; 2014.

RBID : Pascal:14-0232439

Descripteurs français

Pascal (Inist)
- Protéine, Virus syndrome respiratoire aigu sévère, Structure.

English descriptors

KwdEn :
- Protein, Severe acute respiratory syndrome virus, Structure.

Abstract

The huge RNA genome of SARS coronavirus comprises a number of open reading frames that code for a total of eight accessory proteins. Although none of these are essential for virus replication, some appear to have a role in virus pathogenesis. Notably, some SARS-CoV accessory proteins have been shown to modulate the interferon signaling pathways and the production of pro-inflammatory cytokines. The structural information on these proteins is also limited, with only two (p7a and p9b) having their structures determined by X-ray crystallography. This review makes an attempt to summarize the published knowledge on SARS-CoV accessory proteins, with an emphasis on their involvement in virus-host interaction. The accessory proteins of other coronaviruses are also briefly discussed. This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10 years of research on highly pathogenic human coronaviruses" (see Introduction by Hilgenfeld and Peiris (2013)).

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A11	`03`	`1`		`@1 CHONG (Kelvin Kian-Long)`
A11	`04`	`1`		`@1 SHUKLA (Aditi)`
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A14	`01`			`@1 School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive @2 Singapore 637551 @3 SGP @Z 1 aut. @Z 2 aut. @Z 3 aut.`
A14	`02`			`@1 Institute of Biochemistry, Center for Structural and Cell Biology in Medicine, University of Lübeck, Ratzeburger Allee 160 @2 23538 Lübeck @3 DEU @Z 4 aut. @Z 5 aut.`
A14	`03`			`@1 German Center for Infection Research (DZIF), University of Lübeck @3 DEU @Z 4 aut. @Z 5 aut.`
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A66	`01`			`@0 GBR`
C01	`01`		`ENG`	@0 The huge RNA genome of SARS coronavirus comprises a number of open reading frames that code for a total of eight accessory proteins. Although none of these are essential for virus replication, some appear to have a role in virus pathogenesis. Notably, some SARS-CoV accessory proteins have been shown to modulate the interferon signaling pathways and the production of pro-inflammatory cytokines. The structural information on these proteins is also limited, with only two (p7a and p9b) having their structures determined by X-ray crystallography. This review makes an attempt to summarize the published knowledge on SARS-CoV accessory proteins, with an emphasis on their involvement in virus-host interaction. The accessory proteins of other coronaviruses are also briefly discussed. This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10 years of research on highly pathogenic human coronaviruses" (see Introduction by Hilgenfeld and Peiris (2013)).
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C03	`01`	`X`	`FRE`	`@0 Protéine @5 01`
C03	`01`	`X`	`ENG`	`@0 Protein @5 01`
C03	`01`	`X`	`SPA`	`@0 Proteína @5 01`
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C03	`02`	`X`	`SPA`	`@0 Severe acute respiratory syndrome virus @2 NW @5 02`
C03	`03`	`X`	`FRE`	`@0 Structure @5 03`
C03	`03`	`X`	`ENG`	`@0 Structure @5 03`
C03	`03`	`X`	`SPA`	`@0 Estructura @5 03`
C07	`01`	`X`	`FRE`	`@0 Coronavirus @2 NW`
C07	`01`	`X`	`ENG`	`@0 Coronavirus @2 NW`
C07	`01`	`X`	`SPA`	`@0 Coronavirus @2 NW`
C07	`02`	`X`	`FRE`	`@0 Coronaviridae @2 NW`
C07	`02`	`X`	`ENG`	`@0 Coronaviridae @2 NW`
C07	`02`	`X`	`SPA`	`@0 Coronaviridae @2 NW`
C07	`03`	`X`	`FRE`	`@0 Nidovirales @2 NW`
C07	`03`	`X`	`ENG`	`@0 Nidovirales @2 NW`
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C07	`04`	`X`	`FRE`	`@0 Virus @2 NW`
C07	`04`	`X`	`ENG`	`@0 Virus @2 NW`
C07	`04`	`X`	`SPA`	`@0 Virus @2 NW`
N21				`@1 279`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

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Pascal:14-0232439

Le document en format XML

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<author><name sortKey="Ding Xiang Liu" sort="Ding Xiang Liu" uniqKey="Ding Xiang Liu" last="Ding Xiang Liu">DING XIANG LIU</name>
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<s2>Singapore 637551</s2>
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<country>Singapour</country>
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<front><div type="abstract" xml:lang="en">The huge RNA genome of SARS coronavirus comprises a number of open reading frames that code for a total of eight accessory proteins. Although none of these are essential for virus replication, some appear to have a role in virus pathogenesis. Notably, some SARS-CoV accessory proteins have been shown to modulate the interferon signaling pathways and the production of pro-inflammatory cytokines. The structural information on these proteins is also limited, with only two (p7a and p9b) having their structures determined by X-ray crystallography. This review makes an attempt to summarize the published knowledge on SARS-CoV accessory proteins, with an emphasis on their involvement in virus-host interaction. The accessory proteins of other coronaviruses are also briefly discussed. This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10 years of research on highly pathogenic human coronaviruses" (see Introduction by Hilgenfeld and Peiris (2013)).</div>
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Accessory proteins of SARS-CoV and other coronaviruses

Accessory proteins of SARS-CoV and other coronaviruses

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Descripteurs français

English descriptors

Abstract

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

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

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