Interaction in vitro between the proteinase of Tomato ringspot virus (genus Nepovirus) and the eukaryotic translation initiation factor iso4E from Arabidopsis thaliana.
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[1] D. Gallie. Cap-Independent Translation Conferred by the 5′ Leader of Tobacco Etch Virus Is Eukaryotic Initiation Factor 4G Dependent , 2001, Journal of Virology.
[2] R. Olsthoorn,et al. Translation of a nonpolyadenylated viral RNA is enhanced by binding of viral coat protein or polyadenylation of the RNA , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[3] H. Sanfaçon,et al. Expression and partial purification of recombinant tomato ringspot nepovirus 3C-like proteinase: comparison of the activity of the mature proteinase and the VPg-proteinase precursor , 2001, Virus Research.
[4] R. Jackson,et al. Activity of the Hepatitis A Virus IRES Requires Association between the Cap-Binding Translation Initiation Factor (eIF4E) and eIF4G , 2001, Journal of Virology.
[5] Esther M. Lafuente,et al. IRES interaction with translation initiation factors: functional characterization of novel RNA contacts with eIF3, eIF4B, and eIF4GII. , 2001, RNA.
[6] K. Kean,et al. Detailed Analysis of the Requirements of Hepatitis A Virus Internal Ribosome Entry Segment for the Eukaryotic Initiation Factor Complex eIF4F , 2001, Journal of Virology.
[7] S. Paulous,et al. Eukaryotic Initiation Factor 4G-Poly(A) Binding Protein Interaction Is Required for Poly(A) Tail-Mediated Stimulation of Picornavirus Internal Ribosome Entry Segment-Driven Translation but Not for X-Mediated Stimulation of Hepatitis C Virus Translation , 2001, Molecular and Cellular Biology.
[8] Esther M. Lafuente,et al. Functional interactions in internal translation initiation directed by viral and cellular IRES elements. , 2001, The Journal of general virology.
[9] R. Andino,et al. Poliovirus RNA Replication Requires Genome Circularization through a Protein–Protein Bridge , 2001, Molecular Cell.
[10] A. Wang,et al. Proteolytic processing at a novel cleavage site in the N-terminal region of the tomato ringspot nepovirus RNA-1-encoded polyprotein in vitro. , 2000, The Journal of general virology.
[11] J. Laliberté,et al. Complex Formation between Potyvirus VPg and Translation Eukaryotic Initiation Factor 4E Correlates with Virus Infectivity , 2000, Journal of Virology.
[12] P. Sarnow,et al. Regulation of host cell translation by viruses and effects on cell function. , 2000, Current opinion in microbiology.
[13] J. Carrington,et al. Strain-specific interaction of the tobacco etch virus NIa protein with the translation initiation factor eIF4E in the yeast two-hybrid system. , 2000, Virology.
[14] P. Vende,et al. Efficient Translation of Rotavirus mRNA Requires Simultaneous Interaction of NSP3 with the Eukaryotic Translation Initiation Factor eIF4G and the mRNA 3′ End , 2000, Journal of Virology.
[15] M. Katze,et al. Translational Control of Viral Gene Expression in Eukaryotes , 2000, Microbiology and Molecular Biology Reviews.
[16] R. Andino,et al. Interactions of Viral Protein 3CD and Poly(rC) Binding Protein with the 5′ Untranslated Region of the Poliovirus Genome , 2000, Journal of Virology.
[17] J. Grosclaude,et al. Identification of the RNA-Binding, Dimerization, and eIF4GI-Binding Domains of Rotavirus Nonstructural Protein NSP3 , 1999, Journal of Virology.
[18] H. Sanfaçon,et al. Proteolytic processing of tomato ringspot nepovirus 3C-like protease precursors: definition of the domains for the VPg, protease and putative RNA-dependent RNA polymerase. , 1999, The Journal of general virology.
[19] Jean Cohen,et al. Rotavirus RNA‐binding protein NSP3 interacts with eIF4GI and evicts the poly(A) binding protein from eIF4F , 1998, The EMBO journal.
[20] A. Gingras,et al. The mRNA 5' cap-binding protein eIF4E and control of cell growth. , 1998, Current opinion in cell biology.
[21] B. Cullen,et al. Utilization of a mammalian cell-based RNA binding assay to characterize the RNA binding properties of picornavirus 3C proteinases. , 1998, RNA.
[22] C. Camilleri,et al. The Arabidopsis thaliana cDNAs coding for eIF4E and eIF(iso)4E are not functionally equivalent for yeast complementation and are differentially expressed during plant development. , 1998, The Plant journal : for cell and molecular biology.
[23] J. Carrington,et al. RNA binding activity of NIa proteinase of tobacco etch potyvirus. , 1997, Virology.
[24] Y. Kusov,et al. Interaction of hepatitis A virus (HAV) precursor proteins 3AB and 3ABC with the 5' and 3' termini of the HAV RNA. , 1997, Virus research.
[25] J. Laliberté,et al. Interaction of the viral protein genome linked of turnip mosaic potyvirus with the translational eukaryotic initiation factor (iso) 4E of Arabidopsis thaliana using the yeast two-hybrid system. , 1997, Virology.
[26] Y. Kusov,et al. In vitro RNA binding of the hepatitis A virus proteinase 3C (HAV 3Cpro) to secondary structure elements within the 5' terminus of the HAV genome. , 1997, RNA.
[27] A. Porter,et al. Sequence and Structural Determinants of the Interaction between the 5′-Noncoding Region of Picornavirus RNA and Rhinovirus Protease 3C (*) , 1995, The Journal of Biological Chemistry.
[28] H. Sanfaçon,et al. Tomato ringspot nepovirus protease: characterization and cleavage site specificity. , 1995, The Journal of general virology.
[29] C. Fritsch,et al. A possible consensus sequence for VPg of viruses in the family Comoviridae , 1994, FEBS letters.
[30] E. Wimmer,et al. Interaction of poliovirus polypeptide 3CDpro with the 5' and 3' termini of the poliovirus genome. Identification of viral and cellular cofactors needed for efficient binding. , 1994, The Journal of biological chemistry.
[31] P. Ahlquist,et al. Brome mosaic virus RNA replication proteins 1a and 2a from a complex in vitro , 1992, Journal of virology.
[32] D. Rochon,et al. Nucleotide sequence of tomato ringspot virus RNA1. , 1991, The Journal of general virology.
[33] A. Sachs. 10 Physical and Functional Interactions between the mRNA Cap Structure and the Poly(A) Tail , 2000 .
[34] J. Riechmann,et al. Highlights and prospects of potyvirus molecular biology. , 1992, The Journal of general virology.