The endoribonucleolytic N-terminal half of Escherichia coli RNase E is evolutionarily conserved in Synechocystis sp. and other bacteria but not the C-terminal half, which is sufficient for degradosome assembly
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Engineered transcriptional systems for cyanobacterial biotechnologySki7p G protein interacts with the exosome and the Ski complex for 3'-to-5' mRNA decay in yeastThe catalytic domain of RNase E shows inherent 3' to 5' directionality in cleavage site selectionEmerging features of mRNA decay in bacteria.Characterization of the RNA degradosome of Pseudoalteromonas haloplanktis: conservation of the RNase E-RhlB interaction in the gammaproteobacteriaRNase Y in Bacillus subtilis: a Natively disordered protein that is the functional equivalent of RNase E from Escherichia coliSubstrate binding and active site residues in RNases E and G: role of the 5'-sensorOrigin and evolution of the ribosomeMembrane binding of Escherichia coli RNase E catalytic domain stabilizes protein structure and increases RNA substrate affinity.Chloroplast PNPase exists as a homo-multimer enzyme complex that is distinct from the Escherichia coli degradosomeFunction, mechanism and regulation of bacterial ribonucleases.Enzymatic activity necessary to restore the lethality due to Escherichia coli RNase E deficiency is distributed among bacteria lacking RNase E homologuesEvidence in vivo that the DEAD-box RNA helicase RhlB facilitates the degradation of ribosome-free mRNA by RNase ERegions of RNase E important for 5'-end-dependent RNA cleavage and autoregulated synthesis.Mapping the bacterial cell architecture into the chromosomeGenome-wide mutant fitness profiling identifies nutritional requirements for optimal growth of Yersinia pestis in deep tissue.RhlB helicase rather than enolase is the beta-subunit of the Escherichia coli polynucleotide phosphorylase (PNPase)-exoribonucleolytic complex.mRNA decay in Escherichia coli comes of age.RNA degradosomes exist in vivo in Escherichia coli as multicomponent complexes associated with the cytoplasmic membrane via the N-terminal region of ribonuclease E.The Escherichia coli major exoribonuclease RNase II is a component of the RNA degradosome.Composition and conservation of the mRNA-degrading machinery in bacteria.RNase E in the γ-Proteobacteria: conservation of intrinsically disordered noncatalytic region and molecular evolution of microdomains.RNase E is required for the maturation of ssrA RNA and normal ssrA RNA peptide-tagging activity.The RNase E/G-type endoribonuclease of higher plants is located in the chloroplast and cleaves RNA similarly to the E. coli enzyme.A minimal bacterial RNase J-based degradosome is associated with translating ribosomes.Global analysis of Escherichia coli RNA degradosome function using DNA microarrays.Intragenic suppressors of temperature-sensitive rne mutations lead to the dissociation of RNase E activity on mRNA and tRNA substrates in Escherichia coli.Regulation of ribonuclease E activity by the L4 ribosomal protein of Escherichia coli.A Novel Strategy for Exploitation of Host RNase E Activity by a Marine CyanophageSmall Antisense RNA RblR Positively Regulates RuBisCo in Synechocystis sp. PCC 6803RNase E forms a complex with polynucleotide phosphorylase in cyanobacteria via a cyanobacterial-specific nonapeptide in the noncatalytic region.The critical role of RNA processing and degradation in the control of gene expression.Current perspectives of the Escherichia coli RNA degradosome.Determination of the catalytic parameters of the N-terminal half of Escherichia coli ribonuclease E and the identification of critical functional groups in RNA substrates.Probing the substrate specificity of Escherichia coli RNase E using a novel oligonucleotide-based assay.RNA degradosomes in bacteria and chloroplasts: classification, distribution and evolution of RNase E homologs.RNase E affects the expression of the acyl-homoserine lactone synthase gene sinI in Sinorhizobium meliloti.An mRNA degrading complex in Rhodobacter capsulatus.Different processing of an mRNA species in Bacillus subtilis and Escherichia coli.The phylogenetic distribution of bacterial ribonucleases.
P2860
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P2860
The endoribonucleolytic N-terminal half of Escherichia coli RNase E is evolutionarily conserved in Synechocystis sp. and other bacteria but not the C-terminal half, which is sufficient for degradosome assembly
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
The endoribonucleolytic N-term ...... cient for degradosome assembly
@ast
The endoribonucleolytic N-term ...... cient for degradosome assembly
@en
type
label
The endoribonucleolytic N-term ...... cient for degradosome assembly
@ast
The endoribonucleolytic N-term ...... cient for degradosome assembly
@en
prefLabel
The endoribonucleolytic N-term ...... cient for degradosome assembly
@ast
The endoribonucleolytic N-term ...... cient for degradosome assembly
@en
P2093
P2860
P356
P1476
The endoribonucleolytic N-term ...... cient for degradosome assembly
@en
P2093
A von Gabain
J S Jakobsen
K J McDowall
S Lin-Chao
V R Kaberdin
P2860
P304
11637-11642
P356
10.1073/PNAS.95.20.11637
P407
P577
1998-09-01T00:00:00Z