Murine Hepatitis Virus Nonstructural Protein 4 Regulates Virus-Induced Membrane Modifications and Replication Complex Function - sprookjes - yvandenbroek - TriplyDB

Murine Hepatitis Virus Nonstructural Protein 4 Regulates Virus-Induced Membrane Modifications and Replication Complex Function

Murine Hepatitis Virus Nonstructural Protein 4 Regulates Virus-Induced Membrane Modifications and Replication Complex Function

http://www.wikidata.org/entity/Q27490532

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Targeting membrane-bound viral RNA synthesis reveals potent inhibition of diverse coronaviruses including the middle East respiratory syndrome virus Architecture and biogenesis of plus-strand RNA virus replication factories Membranous replication factories induced by plus-strand RNA viruses Mobility and interactions of coronavirus nonstructural protein 4.Coronaviruses: an overview of their replication and pathogenesis.Aminoterminal amphipathic α-helix AH1 of hepatitis C virus nonstructural protein 4B possesses a dual role in RNA replication and virus production.NS4B self-interaction through conserved C-terminal elements is required for the establishment of functional hepatitis C virus replication complexes.Mutations across murine hepatitis virus nsp4 alter virus fitness and membrane modifications.RNA-RNA and RNA-protein interactions in coronavirus replication and transcription Temperature-sensitive mutants and revertants in the coronavirus nonstructural protein 5 protease (3CLpro) define residues involved in long-distance communication and regulation of protease activity Severe acute respiratory syndrome coronavirus nonstructural proteins 3, 4, and 6 induce double-membrane vesicles Murine hepatitis virus nsp4 N258T mutants are not temperature-sensitive.Untangling membrane rearrangement in the nidovirales.Competitive fitness in coronaviruses is not correlated with size or number of double-membrane vesicles under reduced-temperature growth conditions.Biogenesis and dynamics of the coronavirus replicative structures.Involvement of autophagy in coronavirus replication.Continuous and Discontinuous RNA Synthesis in Coronaviruses.Extensive coronavirus-induced membrane rearrangements are not a determinant of pathogenicity.Ultrastructural characterization of membranous torovirus replication factories.Expression and Cleavage of Middle East Respiratory Syndrome Coronavirus nsp3-4 Polyprotein Induce the Formation of Double-Membrane Vesicles That Mimic Those Associated with Coronaviral RNA Replication.Infectious Bronchitis Virus Nonstructural Protein 4 Alone Induces Membrane Pairing

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P2860

Murine Hepatitis Virus Nonstructural Protein 4 Regulates Virus-Induced Membrane Modifications and Replication Complex Function

http://www.wikidata.org/entity/Q27490532

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Murine Hepatitis Virus Nonstru ...... d Replication Complex Function

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Christopher C Stobart

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Dia C Beachboard

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Jennifer S Sparks

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Joshua D Doyle

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Mark J Gadlage

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Reagan G Cox

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P2860

SARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulum

Open reading frame 1a-encoded subunits of the arterivirus replicase induce endoplasmic reticulum-derived double-membrane vesicles which carry the viral replication complex

Genetic interaction of flavivirus nonstructural proteins NS1 and NS4A as a determinant of replicase function.

Brome mosaic virus helicase- and polymerase-like proteins colocalize on the endoplasmic reticulum at sites of viral RNA synthesis

Localization and Membrane Topology of Coronavirus Nonstructural Protein 4: Involvement of the Early Secretory Pathway in Replication

Formation of the Arterivirus Replication/Transcription Complex: a Key Role for Nonstructural Protein 3 in the Remodeling of Intracellular Membranes

Seeking Membranes: Positive-Strand RNA Virus Replication Complexes

Intracellular functions of N-linked glycans

Virus factories: associations of cell organelles for viral replication and morphogenesis

Remodeling the endoplasmic reticulum by poliovirus infection and by individual viral proteins: an autophagy-like origin for virus-induced vesicles.

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280-90

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1043051

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10.1128/JVI.01772-09

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1

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84

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Mark R. Denison

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2010-01-01T00:00:00Z

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38027406

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19846526

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2798404

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