Accurate translation of the genetic code depends on tRNA modified nucleosides.
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A functional proteomics approach links the ubiquitin-related modifier Urm1 to a tRNA modification pathwayPurine bases at position 37 of tRNA stabilize codon-anticodon interaction in the ribosomal A site by stacking and Mg2+-dependent interactions.Mutations in MTO2 related to tRNA modification impair mitochondrial gene expression and protein synthesis in the presence of a paromomycin resistance mutation in mitochondrial 15 S rRNAMutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutationsNucleoside modifications in the regulation of gene expression: focus on tRNAFrom Prebiotics to Probiotics: The Evolution and Functions of tRNA ModificationsExploiting tRNAs to Boost VirulenceCodon-biased translation can be regulated by wobble-base tRNA modification systems during cellular stress responsesDiversity of the biosynthesis pathway for threonylcarbamoyladenosine (t(6)A), a universal modification of tRNAKissing G domains of MnmE monitored by X-ray crystallography and pulse electron paramagnetic resonance spectroscopySnapshots of Dynamics in Synthesizing N 6 -Isopentenyladenosine at the tRNA AnticodonHuman tRNALys3UUU Is Pre-Structured by Natural Modifications for Cognate and Wobble Codon Binding through Keto–Enol TautomerismThe universal YrdC/Sua5 family is required for the formation of threonylcarbamoyladenosine in tRNA.Novel methyltransferase for modified uridine residues at the wobble position of tRNA.The highly conserved KEOPS/EKC complex is essential for a universal tRNA modification, t6A.Reprogramming of tRNA modifications controls the oxidative stress response by codon-biased translation of proteinsMitochondria-specific RNA-modifying enzymes responsible for the biosynthesis of the wobble base in mitochondrial tRNAs. Implications for the molecular pathogenesis of human mitochondrial diseases.Controlling translation via modulation of tRNA levelsA human tRNA methyltransferase 9-like protein prevents tumour growth by regulating LIN9 and HIF1-αDiscovery of the β-barrel-type RNA methyltransferase responsible for N6-methylation of N6-threonylcarbamoyladenosine in tRNAsA quantitative systems approach reveals dynamic control of tRNA modifications during cellular stressFurther insights into the tRNA modification process controlled by proteins MnmE and GidA of Escherichia coliAn insight into the transcriptome of the digestive tract of the bloodsucking bug, Rhodnius prolixusQuantitative analysis of ribonucleoside modifications in tRNA by HPLC-coupled mass spectrometryThe crystal structure and small-angle X-ray analysis of CsdL/TcdA reveal a new tRNA binding motif in the MoeB/E1 superfamilyPhytohormone Involvement in the Ustilago maydis- Zea mays Pathosystem: Relationships between Abscisic Acid and Cytokinin Levels and Strain Virulence in Infected Cob TissueTrm9-Catalyzed tRNA Modifications Regulate Global Protein Expression by Codon-Biased TranslationTaurine as a constituent of mitochondrial tRNAs: new insights into the functions of taurine and human mitochondrial diseasesDiscovery and biological characterization of geranylated RNA in bacteriaCrystal structure of the two-subunit tRNA m(1)A58 methyltransferase TRM6-TRM61 from Saccharomyces cerevisiae.tRNAGlu wobble uridine methylation by Trm9 identifies Elongator's key role for zymocin-induced cell death in yeast.NMR-based Structural Analysis of Threonylcarbamoyl-AMP Synthase and Its Substrate Interactions.Single-cell time-lapse analysis of depletion of the universally conserved essential protein YgjDA hydantoin isoform of cyclic N6-threonylcarbamoyladenosine (ct6A) is present in tRNAsThe cytosolic thiouridylase CTU2 of Arabidopsis thaliana is essential for posttranscriptional thiolation of tRNAs and influences root developmentMTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeast.Functional recognition of the modified human tRNALys3(UUU) anticodon domain by HIV's nucleocapsid protein and a peptide mimic.Decoding the genome: a modified view.3-(3-amino-3-carboxypropyl)-5,6-dihydrouridine is one of two novel post-transcriptional modifications in tRNALys(UUU) from Trypanosoma brucei.eIF5 and eIF5B together stimulate 48S initiation complex formation during ribosomal scanning.
P2860
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P2860
Accurate translation of the genetic code depends on tRNA modified nucleosides.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Accurate translation of the genetic code depends on tRNA modified nucleosides.
@en
Accurate translation of the genetic code depends on tRNA modified nucleosides.
@nl
type
label
Accurate translation of the genetic code depends on tRNA modified nucleosides.
@en
Accurate translation of the genetic code depends on tRNA modified nucleosides.
@nl
prefLabel
Accurate translation of the genetic code depends on tRNA modified nucleosides.
@en
Accurate translation of the genetic code depends on tRNA modified nucleosides.
@nl
P2093
P356
P1476
Accurate translation of the genetic code depends on tRNA modified nucleosides
@en
P2093
Agnieszka Miskiewicz
Andrzej J Malkiewicz
Connie Yarian
Hannah Townsend
Paul F Agris
Richard Guenther
Wojciech Czestkowski
P304
16391-16395
P356
10.1074/JBC.M200253200
P407
P50
P577
2002-02-22T00:00:00Z