ライフサイエンスコーパス: ribosomal

1 uitin ligase that ubiquitinates sites on the ribosomal 40S subunit to initiate pathways of mRNA and p

2 ection of correct aminoacyl (aa)-tRNA at the ribosomal A site is fundamental to maintaining translati

3 of noncognate ternary complexes (TCs) at the ribosomal A-site enhances the dissociation rate of such

4 ty of the anticodon/codon interaction in the ribosomal A-site.

5 Moreover, ribosomal abundance within the cell is coordinated with

6 th developing mouse PCs, we used translating ribosomal affinity purification (TRAP).

7 Examples are presented in the context of ribosomal and nonribosomal interfaces with analysis of a

8 complexes with essential roles in processing ribosomal and tRNAs.

9 Structural studies and ribosomal binding analyses have revealed both increased

10 somal binding might be due to cis-regulatory ribosomal binding and to defective ribosomal scanning of

11 Our results also reveal reproducible ribosomal binding apparently not resulting in productive

12 We suggest that this non-productive ribosomal binding might be due to cis-regulatory ribosom

13 This non-productive ribosomal binding seems to be especially prevalent among

14 ow how the specific location of each agent's ribosomal binding site affects the long-term distributio

15 have revealed both increased exposure of the ribosomal binding site and increased ribosomal binding t

16 of the ribosomal binding site and increased ribosomal binding to the ompA transcript at permissive t

17 mometer that directly result in differential ribosomal binding to the regulated transcript.

18 hase of the training period, suggesting that ribosomal biogenesis regulates the dose-response relatio

19 NO66 suppression of ribosomal biogenesis via demethylase activity is the mec

20 Possible contributions of Fe2+ as a ribosomal cofactor have been largely overlooked, despite

21 tinction allows us to quantify the extent of ribosomal collisions along the transcript and identify i

22 nscript and identify individual codons where ribosomal collisions are likely.

23 and can occur on pre- and post-translocation ribosomal complexes.

24 ur results suggest that VIG1 is an ancillary ribosomal component and plays a role in sRNA-mediated tr

25 important for recognition and degradation of ribosomal components.

26 Moreover, we reveal IFN-dependent changes in ribosomal composition that act to buffer IFN-stimulated

27 g cognate tRNA upon initial recognition, the ribosomal decoding centre dynamically monitors codon-ant

28 ot epidermal cell fate switch in response to ribosomal defects and, more generally, it demonstrates a

29 or G3BP1 family proteins increased lysosomal ribosomal degradation and perturbed ribosomal subunit st

30 eristic of the disease, which is a model for ribosomal diseases, related to a heterozygous allelic va

31 size, chromosome number, and organization of ribosomal DNA (45S and 5SrDNA) of A. digitata.

32 Prior to anaphase of budding yeast, the ribosomal DNA (RDN) condenses to a thin loop that is dis

33 In yeast, circular ribosomal DNA (rDNA) accumulates dramatically as cells a

34 activation of Hog1 is linked to a defect in ribosomal DNA (rDNA) and telomere segregation, and it ul

35 ucleolar organizer regions (NORs) comprising ribosomal DNA (rDNA) arrays.

36 Ribosomal DNA (rDNA) consists of highly repeated sequenc

37 d that CSA and CSB regulate transcription of ribosomal DNA (rDNA) genes and ribosome biogenesis.

38 binds to a specific upstream element in the ribosomal DNA (rDNA) promoter and interacts with two oth

39 In this assay, multicopy small-subunit (SSU) ribosomal DNA (rDNA) sequences were used as targets.

40 Deep sequencing of ribosomal DNA (rDNA) suggests thousands of different mic

41 Bacterial V4 16S ribosomal DNA amplicons were sequenced using Illumina Mi

42 d on the differential capacity to transcribe ribosomal DNA and synthesize proteins.

43 Here, we developed a mitochondrial 12S ribosomal DNA reference database for 67 fish species, re

44 Integrated 16S ribosomal DNA sequencing and liquid chromatography coupl

45 y, the fecal microbiome were analyzed by 16S ribosomal DNA sequencing.

46 We discover that the majority of ribosomal DNA transcription and protein synthesis in CRC

47 ed the enrichment of H3K4me3 and H3K36me3 on ribosomal DNA.

48 features of the PCBP2/SLIV complex vital for ribosomal docking, and the way in which this key functio

49 ce of defective snoRNP pseudouridylation and ribosomal dysfunction.

50 fic interaction of the Not5 subunit with the ribosomal E-site in Saccharomyces cerevisiae This intera

51 of structured RNA sequences, called Internal Ribosomal Entry Sites (IRES), in viral RNAs is a widespr

52 egulated profiles, including translation and ribosomal events in spindle, inflammation- and apical ju

53 he eye-lens protein gammaB-crystallin in the ribosomal exit tunnel.

54 Ribosomal expansion in Asgard and Eukarya has been incre

55 nic stages, with nearly 500 million putative ribosomal footprints mapped to mRNAs, and compare them t

56 e a molecular mechanism called programmed -1 ribosomal frameshift (-1 PRF) to control the relative ex

57 rved RNA elements located at the 5' end, the ribosomal frameshift segment and the 3'-untranslated reg

58 Programmed ribosomal frameshifting (PRF) is a conserved translation

59 Programmed ribosomal frameshifting (PRF) is a mechanism used by art

60 biochemical mechanisms, including programmed ribosomal frameshifting (PRF), which facilitates the pro

61 ved mechanism to influence the efficiency of ribosomal frameshifting during translation of viral RNA,

62 umps'-showed that they were characterized by ribosomal frameshifting events.

63 domic analyses demonstrated the induction of ribosomal frameshifting, and the generation and presenta

64 cribed spacer (ITS) and D1/D2 regions of the ribosomal gene for C. auris genotyping.

65 bone marrow failure syndrome associated with ribosomal gene mutations that lead to ribosomal insuffic

66 acterial PCR and/or 28S-internal transcribed ribosomal gene spacer (28S-ITS) fungal PCR.

67 we analyze RNAP number distribution data for ribosomal genes in Saccharomyces cerevisiae from three p

68 ic microsporidia, conservation of energy via ribosomal hibernation and recycling is critical.

69 t labeling, flow cytometry and Cre-dependent ribosomal immunoprecipitations, we describe P2ry12-CreER

70 d with ribosomal gene mutations that lead to ribosomal insufficiency.

71 Here, we assess ribosomal integrity following oxidative stress both in v

72 nd off the ribosome, their results show that ribosomal interactions have little impact on the folding

73 NA modification state, and structures of 40S ribosomal intermediates that form upon SrmB deletion.

74 approaches for taxonomic assertions based on ribosomal internal transcribed spacer regions (ITS1/2) a

75 7 single copy nuclear genes, and the nuclear ribosomal ITS from 29 species representing all but one t

76 he poliovirus type I IRES is able to recruit ribosomal machinery only in the presence of host factor

77 des have revealed major growth laws relating ribosomal mass fraction and cell size to the growth rate

78 the aminoglycoside-modifying enzymes and the ribosomal methyltransferases whose widespread presence s

79 Synthesis defects are rescued by various ribosomal mutations, as well as by reducing cellular rib

80 l transcribed spacer region 2 of the nuclear ribosomal operon to identify the fungal species present.

81 Loss of a tRNA gene leads to ribosomal pausing that is resolved by the translational

82 egin to fold in the constrained space of the ribosomal peptide exit tunnel.

83 nally modified peptides (RiPPs), also called ribosomal peptide natural products (RPNPs), form a growi

84 e type I, polyketide synthase type II or non-ribosomal peptide synthase genes within their genome.

85 In vitro assays reveal two single-module non-ribosomal peptide synthetases (NRPs) that incorporate th

86 The most common BGCs are non-ribosomal peptide synthetases, type 1 polyketide synthas

87 fied amygdalin as an elicitor of a novel non-ribosomal peptide, which we term cinnapeptin.

88 SVC112 preferentially impeded ribosomal processing of mRNAs critical for stress respon

89 from non-canonical translation of defective ribosomal products, relate this to the dysregulated tran

90 Ribosomal profiling has shed new light on how ribosomes

91 ing our RiboFlow pipeline that processes raw ribosomal profiling sequencing data.

92 Contrasting with in vivo ribosomal profiling, we unearth a correlation between m6

93 transcriptional interference from divergent ribosomal promoters.

94 ed a transgene that expresses an eGFP-tagged ribosomal protein (L10a) under the control of the macrop

95 Immunostaining of phosphor-S6 ribosomal protein (pS6RP) revealed high mTOR activity in

96 Reduced copy number of ribosomal protein (Rp) genes adversely affects both flie

97 wild-type cells and cells with mutations in ribosomal protein (Rp) genes in Drosophila melanogaster.

98 ls, TOR specifically promotes translation of ribosomal protein (RP) mRNAs when amino acids are availa

99 d Mrt4 that prevent premature loading of the ribosomal protein eL24, the protein-folding machinery at

100 translated proteins but also at the level of ribosomal protein expression, ribosome assembly, and rib

101 is report, we analyzed the eight-member uL18 ribosomal protein family in Arabidopsis uL18 proteins sh

102 nd suggests caution in the interpretation of ribosomal protein gene mutation data.

103 tern of enrichment around the start codon of ribosomal protein genes in all stages but male gametocyt

104 eterozygous allelic variation in 1 of the 20 ribosomal protein genes of either the small or large rib

105 ith wide nucleosome-deficient regions (e.g., ribosomal protein genes), known to harbor partially-unwr

106 firmed layer-specific increase of phospho-S6 ribosomal protein in mouse M1.

107 n in bacterial 23S rRNA is directly bound by ribosomal protein L11, and this complex is essential to

108 d identifies a G70D mutation in the RplD 50S ribosomal protein L4 as significantly associated with in

109 d protein synthesis requires isoforms of the ribosomal protein L4 encoded by the cytokinin-inducible

110 Phosphorylation of ribosomal protein of the small subunit 6 (eS6), a ubiqui

111 ould inhibit trans-translation by binding to Ribosomal protein S1 (RpsA) and competing with tmRNA, th

112 Ribosomal protein S1 plays important roles in the transl

113 raction between the translation enhancer and ribosomal protein S1 to repress translation of manY mRNA

114 atterns of three putative dual-coding genes, ribosomal protein S12 (RPS12), the 5' editing domain of

115 We further showed that the ribosomal protein S25 (eS25), which is required by funct

116 Differential expression of the RPS27L (40S ribosomal protein S27-like) gene, part of the p53/mammal

117 sis and contribute to the phosphorylation of ribosomal protein S6 and NK cell proliferation.

118 mTOR pathway, as assessed by phosphorylated ribosomal protein S6 expression.

119 ma model in which constitutive activation of ribosomal protein S6 kinase A1 drives tumor invasion.

120 Transcriptomic analysis of ribosomal protein S6 kinase A1-activated tumors identifi

121 The human kinase ribosomal protein S6 kinase beta-1 (RPS6KB1) was shown t

122 educed constitutive activation of the mTORC1/ribosomal protein S6 pathway and downregulated constitut

123 1(Thr412) , 19%; p70 S6K1(Thr389) , 58%) and ribosomal protein S6(Ser235/236) (37%), greater rested-s

124 Both EIF4EBPs and ribosomal protein S6K kinase (RP-S6K) are downstream eff

125 umber of rRNA genes, and codon usage bias in ribosomal protein sequences were all higher in the ferti

126 his drug across glioma cell lines, revealing ribosomal protein subunit RPS11, 16, and 18 as putative

127 slation-related proteins such as 50S and 30S ribosomal protein subunit variants and elongation factor

128 for higher-order purposes, as in the case of ribosomal protein synthesis.

129 ormal mRNA levels and for normal splicing of ribosomal protein transcripts.

130 e functions of two NPET-associated proteins, ribosomal protein uL4 and assembly factor Nog1, in NPET

131 In yeast, the ribosomal protein Var1, alias uS3m, is mitochondrion-enc

132 tants deficient in PSRP7, a plastid-specific ribosomal protein, OTP86, an RNA editing factor, and cpP

133 Translation of ribosomal protein-coding mRNAs (RP-mRNAs) constitutes a

134 ring ribosomal RNA synthesis and evoking the ribosomal protein-dependent activation of p53.

135 rsions of OVA model Ags displaying defective ribosomal protein-dependent and -independent Ag presenta

136 ts to silence Phytoene desaturase (PDS) or a ribosomal protein-encoding gene, RPL10 (QM), in Nicotian

137 or margin were associated with expression of ribosomal proteins (false discovery rate <0.25; NES, 1.9

138 n genome, many nuclear-encoded mitochondrial ribosomal proteins (MRPs) are required for proper functi

139 f the mitoribosome reveals an assembly of 94-ribosomal proteins and four-rRNAs with an additional pro

140 in hippocampal neurons resulted in increased ribosomal proteins and initiation factors, but decreased

141 Genes coding for ribosomal proteins and regulators of translation were en

142 environmental effects is challenging because ribosomal proteins and rRNA preclude most spectroscopic

143 f 5'TOP mRNAs, which includes mRNAs encoding ribosomal proteins and several translation factors.

144 ith significantly lower expression levels of ribosomal proteins and transcriptional and translational

145 fficiency following loss of ARF include many ribosomal proteins and translation factors.

146 In total, 48 of the 55 known E. coli ribosomal proteins are identified as 84 unique proteofor

147 In prokaryotes, only ribosomal proteins are known to be N-terminally acetylat

148 How stable proteins that rely on defective ribosomal proteins for direct presentation are captured

149 eveals that the RNA-binding capacity of uL18 ribosomal proteins has been repurposed to create factors

150 The binding of GAG to ribosomal proteins inhibited cellular translation machin

151 f positively charged amino acids frequent in ribosomal proteins on ribosome progression.

152 y, coordinated translational upregulation of ribosomal proteins only occurred in the liver but not in

153 equences that follow genetic knockout of the ribosomal proteins RPS25 or RACK1 in a human cell line,

154 ient mutants, NMD-susceptible transcripts of ribosomal proteins that are known for their role as nonc

155 enhanced the levels of ubiquitination of the ribosomal proteins uS10, uS3 and eS7.

156 transcription, recovery of transcription of ribosomal proteins, and initiation of wound healing and

157 oroplast protein chaperone machinery and 70S ribosomal proteins, but other parts of the proteostasis

158 rganisms live longer when they lack specific ribosomal proteins, especially of the large 60S subunit

159 mes; to accomplish this task, ribosomes make ribosomal proteins, polymerases, enzymes, and signaling

160 ession of pre-ribosomal RNAs (pre-rRNAs) and ribosomal proteins, pre-rRNA processing, and subunit ass

161 tide and thioamide backbone substitutions in ribosomal proteins, the former likely conserved in all d

162 avoidance of host transcripts encoding host ribosomal proteins, which are required by IAV for replic

163 n the phylogenies of both 16S rRNA genes and ribosomal proteins, which we propose to name (U)Petromon

164 osomal ubiquitylation (RRub) on distinct 40S ribosomal proteins, yet the cellular role and fate of ub

165 , as well as a reduction in transcription of ribosomal proteins.

166 ation-initiation and elongation factors, and ribosomal proteins.

167 many mRNAs, although not with those encoding ribosomal proteins.

168 els and translation efficiencies for several ribosomal proteins.

169 th a specific decrease in the translation of ribosomal proteins.

170 The abundance of ribosomal (r)-proteins (around 6% of the proteome; 10(7)

171 o remodeling of ribosomes, in which multiple ribosomal (r-) proteins containing the zinc-binding CXXC

172 s a less-known function to induce eukaryotic ribosomal readthrough of PTCs to produce a full-length p

173 grity of the base pair helps to modulate the ribosomal response to regulatory nascent peptides, deter

174 terized them by partially sequencing the 16s ribosomal ribonucleic acid (rrs), flagellin (flaB), and

175 microbial composition was explored using 16S ribosomal ribonucleic acid sequencing.

176 16S ribosomal-ribonucleic acid polymerase chain reaction (PC

177 ucturally conserved domain that binds the 5S ribosomal RNA (rRNA) and allows its incorporation into r

178 that directly mediate the expression of the ribosomal RNA (rRNA) components of ribosomes.

179 We reanalyzed raw 16S ribosomal RNA (rRNA) gene sequences and metadata from pu

180 Post-transcriptional ribosomal RNA (rRNA) modifications are present in all or

181 : see text] bound to the ribosome reveal 23S ribosomal RNA (rRNA) nucleotide A1913 positional changes

182 side chain of macrolides interacts with 23S ribosomal RNA (rRNA) nucleotides A752 and U2609, that we

183 ng residue networks (sectors) within the 23S ribosomal RNA (rRNA) of the large ribosomal subunit.

184 we found reduced pseudouridine levels in the ribosomal RNA (rRNA) of the patients.

185 ol gene regulation, but regulatory roles for ribosomal RNA (rRNA) remain largely unexplored.

186 Ribosomal RNA (rRNA) transcription by RNA polymerase I (

187 duced small RNA (tiRNA) and transcription of ribosomal RNA (rRNA), respectively.

188 A-seq requires efficient physical removal of ribosomal RNA (rRNA), which otherwise dominates transcri

189 tudy, we evaluated two methods for preparing ribosomal RNA (rRNA)-depleted sequencing libraries for R

190 rects 2'-O-methylation at uridine 116 of 18S ribosomal RNA (rRNA).

191 Shotgun and 16S ribosomal RNA amplicon sequencing were performed on fece

192 Bacterial 16S ribosomal RNA analyses were performed on stool samples f

193 Virgin Islands, amplifying the large-subunit ribosomal RNA and psbA protein D1 marker genes, revealed

194 ize the upper airway microbiome, we used 16S ribosomal RNA and shotgun metagenomic sequencing.

195 faceted transcription factor in enhancer and ribosomal RNA biology.

196 We conclude that use of a standard ribosomal RNA depletion method for library preparation c

197 roviding a thermodynamic basis for vectorial ribosomal RNA flux out of the nucleolus.

198 sic sites in nascent RNA, messenger RNA, and ribosomal RNA from yeast and human cells.

199 o evaluate the diagnostic performance of 16S ribosomal RNA gene (rRNA) polymerase chain reaction (PCR

200 We used 16S ribosomal RNA gene amplicon sequencing to profile microb

201 Faecal 16S ribosomal RNA gene analysis was undertaken.

202 ing profiles from COI, cytochrome b, and 16S ribosomal RNA gene PCR products.

203 Using faecal 16S ribosomal RNA gene sequences and host genotype data from

204 Feces were collected and analyzed by 16S ribosomal RNA gene sequencing and bacterial community an

205 lysis of fecal microbiota composition by 16S ribosomal RNA gene sequencing and fecal/urinary metaboli

206 tool sub-Operational Taxonomic Units from16S ribosomal RNA gene sequencing data.

207 We conducted 16S ribosomal RNA gene sequencing to characterize intestinal

208 16S ribosomal RNA gene sequencing was performed on DNA extra

209 16S ribosomal RNA gene sequencing was performed on sputum fr

210 We applied 16S ribosomal RNA gene sequencing, shotgun metagenomic seque

211 Feces were collected and analyzed by 16S ribosomal RNA gene sequencing.

212 ntitative polymerase chain reaction, and 16S ribosomal RNA gene sequencing; lamina propria and mesent

213 position was evaluated by sequencing the 16S ribosomal RNA gene V1-V3 region.

214 associates with RNA polymerase I transcribed ribosomal RNA gene, Rn45s.

215 hibitor of RNA polymerase I transcription of ribosomal RNA genes (rDNA), induces replication stress a

216 rearrangements among the protein-coding and ribosomal RNA genes could be inferred across the phyloge

217 d includes 13 protein-coding genes (PCGs), 2 ribosomal RNA genes, 22 transfer RNA genes and an 834 bp

218 ut microbiome composition sequenced from 16S ribosomal RNA genes.

219 enes such as that encoding the small subunit ribosomal RNA has revealed the extensive diversity of ba

220 ultiple genes impacting protein synthesis: a ribosomal RNA helicase gene, tRNA biosynthesis genes, an

221 mbled NPET, including an aberrantly flexible ribosomal RNA helix 74, resulting in at least three diff

222 and Nog1 work together in the maturation of ribosomal RNA helix 74, which is required to ensure prop

223 NSP1 binds to 18S ribosomal RNA in the mRNA entry channel of the ribosome

224 Here we used amplicon sequencing of the ribosomal RNA internal transcribed spacer region to exam

225 antitative polymerase chain reaction and 16S ribosomal RNA metagenomic sequencing.

226 de resistance determinants including a novel ribosomal RNA methyltransferase situated in a CRISPR (cl

227 Our knowledge about the repertoire of ribosomal RNA modifications and the enzymes responsible

228 ent classes, enables identification of novel ribosomal RNA processing factors and sites, and suggests

229 th ribosomes and that EBP1 silencing hinders ribosomal RNA processing.

230 By using V4 and full-length 16S ribosomal RNA sequencing of a series of fecal samples, w

231 spectroscopy for metabolic profiling and 16S ribosomal RNA sequencing to assess the gut microbiome.

232 Samples were analyzed by 16S ribosomal RNA sequencing, and diet-related metabolites w

233 esence of collagenolytic colonies and by 16S ribosomal RNA sequencing, which determined the anatomic

234 Microbiota data were obtained using 16S ribosomal RNA sequencing.

235 rs the integrity of the nucleolus, impairing ribosomal RNA synthesis and evoking the ribosomal protei

236 n the nucleoli is required for inhibition of ribosomal RNA synthesis and nucleolar segregation in res

237 ARF plays a significant role in regulating ribosomal RNA synthesis and processing, ribosome export

238 MYC mediates ribosomal RNA transcription in 2-cell embryos, supportin

239 s were mostly identified on transfer RNA and ribosomal RNA until the last decade, when they have been

240 occus were assessed by DNA sequencing of 16S ribosomal RNA, and absolute S. aureus abundance was meas

241 e cells and in muscles of mice without NO66, ribosomal RNA, pre-rRNA, and protein synthesis all incre

242 habitual low dietary fiber intake using 16S ribosomal RNA-based approaches.

243 U-alpha is also needed for clustering of 6/7 ribosomal RNA-encoding loci.

244 such as the structure and maturation of its ribosomal RNA.

245 s measured by metagenomic sequencing and 16s ribosomal RNA.

246 the nascent chain and the negatively charged ribosomal-RNA lining the exit tunnel, and for quickly ej

247 olus, involves coordinated expression of pre-ribosomal RNAs (pre-rRNAs) and ribosomal proteins, pre-r

248 rial DNAs of two kinds: maxicircles encoding ribosomal RNAs (rRNAs) and proteins and minicircles bear

249 Ribosomal RNAs (rRNAs) are essential components of the r

250 by auxiliary factors that process and modify ribosomal RNAs (rRNAs) or are involved in ribosome assem

251 f GLTSCR2 impairs maturation of 18S and 5.8S ribosomal RNAs (rRNAs), and Nop53 is required for matura

252 r certain non-coding RNAs (ncRNAs) including ribosomal RNAs (rRNAs), transfer RNAs (tRNAs), small nuc

253 ient enzyme specialized in synthesizing most ribosomal RNAs.

254 is widespread and found in messenger (mRNA), ribosomal (rRNA), and noncoding RNAs.

255 were evaluated for their ability to inhibit ribosomal s6 kinase (RSK) activity and cancer cell proli

256 The p90 ribosomal S6 kinase (RSK) is one of these kinases, altho

257 Here, we demonstrate that RSK2 (p90 ribosomal S6 kinase 2) plays a critical role in ER stres

258 egulatory ribosomal binding and to defective ribosomal scanning of ORFs outside periods of productive

259 of a transmembrane domain upstream from the ribosomal slip site generates a force on the nascent pol

260 g site affects the long-term distribution of ribosomal species between 30S and 50S subunits versus 70

261 The ribosomal stalk proteins, RPLP1 and RPLP2 (RPLP1/2), whi

262 t the polypeptide exit tunnel (PET), and the ribosomal stalk, respectively.

263 and RPLP2 (RPLP1/2), which form the ancient ribosomal stalk, were discovered decades ago but their f

264 d cryogenic electron microscopy to reveal 33 ribosomal states after the delivery of aminoacyl-tRNA by

265 translation factors to sense and communicate ribosomal states.

266 p53-mutant cells, suggesting involvement of ribosomal stress in the response.

267 tead required ANAC082, a recently identified ribosomal stress response mediator.

268 s required for Mdn1 to transmit force to its ribosomal substrates, but it is not currently understood

269 the final maturation steps of the two large ribosomal subunit (50S) rRNAs, 23S and 5S pre-rRNAs, are

270 h C-terminal tails in the absence of a small ribosomal subunit and mRNA has remained unknown.

271 e of Staphylococcus aureus RsfS to the large ribosomal subunit and present a 3.2 angstrom resolution

272 S) that binds to uL14 protein onto the large ribosomal subunit and prevents its association with the

273 Amicetin's binding to the 70S ribosomal subunit of Thermus thermophilus (Tth) has been

274 Large ribosomal subunit protein bL31, which forms intersubunit

275 oximal tubule-specific expression of an L10a ribosomal subunit protein fused with enhanced green fluo

276 ysosomal ribosomal degradation and perturbed ribosomal subunit stoichiometry, both of which were resc

277 hich forms intersubunit bridges to the small ribosomal subunit, assumes different conformations in th

278 ial fast binding step of the IRES to the 40S ribosomal subunit, followed by a slow unimolecular react

279 evious work revealed that rps28bDelta (small ribosomal subunit-28B) mutants do not form PBs under nor

280 located in the decoding center of the small ribosomal subunit.

281 l protein genes of either the small or large ribosomal subunit.

282 in the 23S ribosomal RNA (rRNA) of the large ribosomal subunit.

283 involved in the generation of the human 40S ribosomal subunit.

284 IF5B in concert with components of the large ribosomal subunit.

285 the peptidyl transferase center of the large ribosomal subunit.

286 n partners identified 2 functional clusters: ribosomal subunits and nucleolar proteins including the

287 in the late stages of the biogenesis of 50S ribosomal subunits in plastids, a role that presumably e

288 20A-eGFP fusion proteins comigrated with 50S ribosomal subunits in Suc density gradients, even after

289 t mycobacterial HflX associates with the 50S ribosomal subunits in vivo and can dissociate purified 7

290 Aborted translation produces large ribosomal subunits obstructed with tRNA-linked nascent c

291 composition and structure of assembling 60S ribosomal subunits undergo numerous changes as pre-ribos

292 g of biochemically active complexes, such as ribosomal subunits within the nucleolus.

293 roduces a selective homeostatic reduction in ribosomal subunits, thereby offering a mechanism for the

294 sure proper construction of the NPET and 60S ribosomal subunits.

295 replenish the pool of translation-competent ribosomal subunits.

296 ve cytoplasmic step in the biogenesis of 40S ribosomal subunits.

297 l (NPET) is a major functional center of 60S ribosomal subunits.

298 ponse proteins included many associated with ribosomal synthesis and protein translation, suggesting

299 In each round of ribosomal translation, the translational GTPase elongati

300 control (RQC) pathway stimulates regulatory ribosomal ubiquitylation (RRub) on distinct 40S ribosoma