Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions.
about
Translation enhancing ACA motifs and their silencing by a bacterial small regulatory RNAGTP-independent tRNA delivery to the ribosomal P-site by a novel eukaryotic translation factorThe role of mRNA structure in bacterial translational regulationA key role for the mRNA leader structure in translational control of ribosomal protein S1 synthesis in gamma-proteobacteriaRecombinational repair of DNA damage in Escherichia coli and bacteriophage lambdaTranslation initiation region sequence preferences in Escherichia coli.How Changes in Anti-SD Sequences Would Affect SD Sequences in Escherichia coli and Bacillus subtilis.The expression of recombinant genes in Escherichia coli can be strongly stimulated at the transcript production level by mutating the DNA-region corresponding to the 5'-untranslated part of mRNA.The last RNA-binding repeat of the Escherichia coli ribosomal protein S1 is specifically involved in autogenous controlVisualization of protein S1 within the 30S ribosomal subunit and its interaction with messenger RNA.The roles of individual eukaryotic translation initiation factors in ribosomal scanning and initiation codon selection.Non-canonical mechanism for translational control in bacteria: synthesis of ribosomal protein S1.Emerging views on tmRNA-mediated protein tagging and ribosome rescue.MSMEG_2731, an uncharacterized nucleic acid binding protein from Mycobacterium smegmatis, physically interacts with RPS1.Initiation of protein synthesis in bacteria.Influences on gene expression in vivo by a Shine-Dalgarno sequence.Ribosomal protein S1 promotes transcriptional cyclingEscherichia coli ribosomal protein S1 unfolds structured mRNAs onto the ribosome for active translation initiation.The highly efficient translation initiation region from the Escherichia coli rpsA gene lacks a shine-dalgarno element.Enhancement of translation by the epsilon element is independent of the sequence of the 460 region of 16S rRNA.Regulation of the rplY gene encoding 5S rRNA binding protein L25 in Escherichia coli and related bacteriaA whole-cell assay for specific inhibitors of translation initiation in bacteria.Enhancement of translation by the downstream box does not involve base pairing of mRNA with the penultimate stem sequence of 16S rRNA.Naturally occurring adenines within mRNA coding sequences affect ribosome binding and expression in Escherichia coli.In vitro trans-translation of Thermus thermophilus: ribosomal protein S1 is not required for the early stage of trans-translation.Expression of tobacco mosaic virus coat protein and assembly of pseudovirus particles in Escherichia coli.Transcription antitermination by translation initiation factor IF1.The deleterious effect of an insertion sequence removing the last twenty percent of the essential Escherichia coli rpsA gene is due to mRNA destabilization, not protein truncationAbundant Intergenic TAACTGA Direct Repeats and Putative Alternate RNA Polymerase β' Subunits in Marine Beggiatoaceae Genomes: Possible Regulatory Roles and Origins.Dynamics of ribosomal protein S1 on a bacterial ribosome with cross-linking and mass spectrometry.Inhibition of Mitogen-activated Protein Kinase (MAPK)-interacting Kinase (MNK) Preferentially Affects Translation of mRNAs Containing Both a 5'-Terminal Cap and Hairpin.Strategies for achieving high-level expression of genes in Escherichia coli.Biochemical and structural insights into RNA binding by Ssh10b, a member of the highly conserved Sac10b protein family in Archaea.Positive and negative effects of the major mammalian messenger ribonucleoprotein p50 on binding of 40 S ribosomal subunits to the initiation codon of beta-globin mRNA.Discrimination of 5'-terminal start codons by translation initiation factor 3 is mediated by ribosomal protein S1.The translational termination signal database (TransTerm) now also includes initiation contexts.AU-rich sequences within 5' untranslated leaders enhance translation and stabilize mRNA in Escherichia coli.Downstream box-anti-downstream box interactions are dispensable for translation initiation of leaderless mRNAs.Activation of RegB endoribonuclease by S1 ribosomal protein requires an 11 nt conserved sequence.Comparison of mRNA features affecting translation initiation and reinitiation.
P2860
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P2860
Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
1994年學術文章
@zh
1994年學術文章
@zh-hant
name
Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions.
@en
Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions.
@nl
type
label
Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions.
@en
Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions.
@nl
prefLabel
Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions.
@en
Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions.
@nl
P2860
P1433
P1476
Ribosome-messenger recognition in the absence of the Shine-Dalgarno interactions
@en
P2093
N V Tzareva
V I Makhno
P2860
P304
P356
10.1016/0014-5793(94)80271-8
P407
P50
P577
1994-01-01T00:00:00Z