Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction - Wikidata - awgldk - TriplyDB

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

http://www.wikidata.org/entity/Q27472964

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Roles of the negatively charged N-terminal extension of Saccharomyces cerevisiae ribosomal protein S5 revealed by characterization of a yeast strain containing human ribosomal protein S5 Proteins surrounding hairpin IIIe of the hepatitis C virus internal ribosome entry site on the human 40S ribosomal subunit Initiation factor-independent translation mediated by the hepatitis C virus internal ribosome entry site Viral Internal Ribosome Entry Site Elements: Novel Ribosome-RNA Complexes and Roles in Viral Pathogenesis Discovery of significant variants containing large deletions in the 5'UTR of human hepatitis C virus (HCV)HCV and CSFV IRES domain II mediate eIF2 release during 80S ribosome assembly Studying Hepatitis C Virus: Making the Best of a Bad Virus Positioning of subdomain IIId and apical loop of domain II of the hepatitis C IRES on the human 40S ribosome Structure and function of HCV IRES domains Conserved functional domains and a novel tertiary interaction near the pseudoknot drive translational activity of hepatitis C virus and hepatitis C virus-like internal ribosome entry sites Insights into the Biology of IRES Elements through Riboproteomic Approaches A ribosome-specialized translation initiation pathway is required for cap-dependent translation of vesicular stomatitis virus mRNAs HCV IRES interacts with the 18S rRNA to activate the 40S ribosome for subsequent steps of translation initiation Viral IRES RNA structures and ribosome interactions MAID : an effect size based model for microarray data integration across laboratories and platforms.Re-analysis of cryoEM data on HCV IRES bound to 40S subunit of human ribosome integrated with recent structural information suggests new contact regions between ribosomal proteins and HCV RNA Toward a structural understanding of IRES RNA function IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES).The ribosome filter redux.The internal ribosome entry site (IRES) contained within the RNA-binding motif protein 3 (Rbm3) mRNA is composed of functionally distinct elements.Accessibility of 18S rRNA in human 40S subunits and 80S ribosomes at physiological magnesium ion concentrations--implications for the study of ribosome dynamics.Base pairing between hepatitis C virus RNA and 18S rRNA is required for IRES-dependent translation initiation in vivo.Structural and mechanistic insights into hepatitis C viral translation initiation.HCV IRES domain IIb affects the configuration of coding RNA in the 40S subunit's decoding groove.Eukaryotic ribosomal protein RPS25 interacts with the conserved loop region in a dicistroviral intergenic internal ribosome entry site.Alphavirus replicon approach to promoterless analysis of IRES elements.Conservation and diversity among the three-dimensional folds of the Dicistroviridae intergenic region IRESes Ribosome profiling reveals an important role for translational control in circadian gene expression Eukaryotic ribosomal proteins lacking a eubacterial counterpart: important players in ribosomal function.Biochemical and functional analysis of a 9-nt RNA sequence that affects translation efficiency in eukaryotic cells.Inhibitor RNA blocks the protein translation mediated by hepatitis C virus internal ribosome entry site in vivo Hepatitis C virus 3'UTR regulates viral translation through direct interactions with the host translation machinery.Translation regulation by ribosomes: Increased complexity and expanded scope.The DNA virus white spot syndrome virus uses an internal ribosome entry site for translation of the highly expressed nonstructural protein ICP35.Translation initiation by the hepatitis C virus IRES requires eIF1A and ribosomal complex remodeling.The beta hairpin structure within ribosomal protein S5 mediates interplay between domains II and IV and regulates HCV IRES function.A researcher's guide to the galaxy of IRESs.Dynamics of IRES-mediated translation.Molecular architecture of the ribosome-bound Hepatitis C Virus internal ribosomal entry site RNA.A small yeast RNA inhibits HCV IRES mediated translation and inhibits replication of poliovirus in vivo.

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Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

http://www.wikidata.org/entity/Q27472964

description

2002 nî lūn-bûn

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2002 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2002 թվականի հուլիսին հրատարակված գիտական հոդված

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2002年の論文

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2002年学术文章

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2002年学术文章

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2002年学术文章

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name

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

@ast

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

@en

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

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type

label

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

@ast

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

@en

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

@nl

prefLabel

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

@ast

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

@en

Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

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Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction

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Alissa M Lancaster

http://www.w3.org/2001/XMLSchema#string

Geoff A Otto

http://www.w3.org/2001/XMLSchema#string

Joseph D Puglisi

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Peter J Lukavsky

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Peter Sarnow

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P2860

A phylogenetically conserved stem-loop structure at the 5' border of the internal ribosome entry site of hepatitis C virus is required for cap-independent viral translation.

Specific interaction of eukaryotic translation initiation factor 3 with the 5' nontranslated regions of hepatitis C virus and classical swine fever virus RNAs.

Hepatitis C virus internal ribosome entry site (IRES) stem loop IIId contains a phylogenetically conserved GGG triplet essential for translation and IRES folding.

An enzymatic footprinting analysis of the interaction of 40S ribosomal subunits with the internal ribosomal entry site of hepatitis C virus

Genetic analysis of a poliovirus/hepatitis C virus chimera: new structure for domain II of the internal ribosomal entry site of hepatitis C virus

Stability of a stem-loop involving the initiator AUG controls the efficiency of internal initiation of translation on hepatitis C virus RNA.

A potential RNA drug target in the hepatitis C virus internal ribosomal entry site.

Mechanism of ribosome recruitment by hepatitis C IRES RNA

Translation of human hepatitis C virus RNA in cultured cells is mediated by an internal ribosome-binding mechanism

Internal ribosome entry site within hepatitis C virus RNA

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10.1017/S1355838202022057

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Hepatitis C virus

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1370308

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