ライフサイエンスコーパス: ribosomal protein

1 hosphorylated 4E-binding protein 1, and p-S6 ribosomal protein.

2 protein (RNP) complexes containing rRNAs and ribosomal proteins.

3 tags for the recombinant production of human ribosomal proteins.

4 Hel2-dependent regulatory ubiquitylation of ribosomal proteins.

5 e limited to fewer "core" genes, such as the ribosomal proteins.

6 f multiple nuclear DNA-encoded mitochondrial ribosomal proteins.

7 ukaryotic translation initiation factors and ribosomal proteins.

8 ensity, which affected mostly mRNAs encoding ribosomal proteins.

9 gger site-specific ubiquitination on several ribosomal proteins.

10 karyotic ribosomes are composed of rRNAs and ribosomal proteins.

11 mal proteins competes with production of non-ribosomal proteins.

12 d down-regulation of genes encoding rRNA and ribosomal proteins.

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

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

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

16 els and translation efficiencies for several ribosomal proteins.

17 anscripts with high initiation rates such as ribosomal proteins.

18 the LSU, as well as previously unidentified ribosomal proteins.

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

20 -dependent upregulation of mitochondrial 37S ribosomal protein 1/ATP-binding cassette subfamily C mem

21 Using ribosomal protein 24 hypomorphic mice (Rpl24(Bst/+) ) as

22 Our structures further uncover how specific ribosomal proteins act as chaperones to correctly fold t

23 We find that cells produce excess ribosomal proteins, amounting to a constant approximatel

24 iption and translation such as sigma factor, ribosomal protein and tRNA genes.

25 The galactosamine moiety bound to ribosomal proteins and blocked cellular translation, whi

26 nd selectively enhanced translation of other ribosomal proteins and cell cycle regulators.

27 by TGF-beta1 were characterised by increased ribosomal proteins and dysregulated proteins involved in

28 The majority of ribosomal proteins and enzymes synthesizing the storage

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

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

31 rocess that involves the ordered assembly of ribosomal proteins and numerous RNA structural rearrange

32 UBE2O recognized ribosomal proteins and other substrates directly, target

33 dules thus obtained reveals an enrichment of ribosomal proteins and pathways likely central to inheri

34 In muscle from older persons, ribosomal proteins and proteins related to energetic met

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

36 Selection pressure led to the loss of two ribosomal proteins and removal of essentially all eukary

37 le of phase separation by NPM1 in organizing ribosomal proteins and RNAs within the nucleolus.

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

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

40 ent of specific protein families such as the ribosomal proteins and the DEAD box helicases, we identi

41 e nuclear import of approximately 80 nascent ribosomal proteins and the elimination of excess amounts

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

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

44 osine [m(7)G] cap of TOP mRNAs, which encode ribosomal proteins and translation factors.

45 bly chaperones recognize nascent unassembled ribosomal proteins and transport them together with kary

46 stic insights into the complex dynamics of a ribosomal protein, and it proposes a previously underapp

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

48 d iPSS in the polycistronic operons encoding ribosomal proteins, and the majority upstream and proxim

49 Astrocyte ribosomal proteins are found adjacent to synapses in viv

50 The long unstructured domains of unassembled ribosomal proteins are highly prone to misfolding and of

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

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

53 f pre-rRNA, and assembly of mature rRNA with ribosomal proteins are the linchpins of ribosome biogene

54 Ribosomal proteins are translated in the cytoplasm and i

55 -transcriptional rRNA modifications and some ribosomal proteins are underrepresented in the accumulat

56 sequence regions 33-52 and 72-82 of the S16 ribosomal protein as proteotypic peptide markers.

57 mplex and heterogeneous process during which ribosomal proteins assemble on the nascent rRNA during t

58 and family composition (e.g. with GAPDH and ribosomal proteins being the largest families).

59 Bacteria missing ribosomal protein bL9 are known to exhibit a reduction i

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

61 ble for import can maintain the stability of ribosomal proteins by neutralizing unfavorable positive

62 control that involves the ubiquitination of ribosomal proteins by the E3 ubiquitin ligase Hel2/RQT1.

63 However, the production of human ribosomal proteins can be challenging.

64 logical culture, nucleic acid amplification, ribosomal protein characterization, and genome sequencin

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

66 dia-specific and several repurposed existing ribosomal proteins compensate for the extensive rRNA red

67 osomes drive cell growth, but translation of ribosomal proteins competes with production of non-ribos

68 Silva investigates how ribosomal protein complexes are regulated by K63 ubiquit

69 onsistent with general translation shutdown, ribosomal proteins contacting the mRNA showed decreased

70 A new study shows that splitting ribosomal protein content into many small, similarly siz

71 RNA molecules dominate the mass and why the ribosomal protein content is divided into 55-80 small, s

72 ing thioredoxin as a fusion protein, soluble ribosomal protein could be obtained directly from cell l

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

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

75 on and metabolism, as well as those encoding ribosomal proteins, DNA and histone-modifying enzymes an

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

77 gulates nutrient-dependent downregulation of ribosomal protein encoding RNAs, leading to the redistri

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

79 cation of CD4(+) T cell responses to defined ribosomal protein epitopes expands the range of antigeni

80 dings suggest that the monoubiquitination of ribosomal protein eS7A plays a crucial role in translati

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

82 Accordingly, approximately 25% of ribosomal proteins expressed in rapidly growing cells do

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

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

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

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

87 oning the assembly site, and dissociation of ribosomal proteins from karyopherins.

88 ignature, which is associated with defective ribosomal protein function and linked to the erythroid l

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

90 latory complex spatial organization at yeast ribosomal protein genes and yeast tRNA genes.

91 ted by translational repression, while HiToP ribosomal protein genes are regulated posttranslationall

92 t of cells appears to decouple expression of ribosomal protein genes from the environmental stress re

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

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

95 bundant class of intron-containing RNAs (the ribosomal protein genes) to Mer1-regulated transcripts.

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

97 dates identified in this search included two ribosomal protein genes, RPL35a and RPL23, and ferredoxi

98 pes can withstand genetic lesions of certain ribosomal protein genes, some of which are linked to div

99 p of human disorders most commonly caused by ribosomal protein haploinsufficiency or defects in ribos

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

101 Variants in genes encoding ribosomal proteins have thus far been associated with Di

102 In addition, as excessive heme could amplify ribosomal protein imbalance, prematurely lower GATA1, an

103 ; and the first report of a prokaryotic-type ribosomal protein in a eukaryotic virus.

104 dysplasia, and we highlight the role of this ribosomal protein in bone development.

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

106 Among 79 ribosomal proteins in yeast, only a few are identified w

107 ng rRNA variants and rRNA modifications, and ribosomal proteins, including their stoichiometry, compo

108 er acetylation occupancy and lower levels of ribosomal proteins, including those involved in ribosome

109 ncing of Rps19, but not several other tested ribosomal proteins, indicating distinct cellular respons

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

111 ribosomes by delaying the release of nascent ribosomal proteins into the cytosol.

112 od about the recombinant production of human ribosomal proteins involved the recovery of proteins fro

113 on that explains how integration of the last ribosomal proteins is coupled to release of the nuclear

114 f mRNAs encoding cytosolic and mitochondrial ribosomal proteins is substantially repressed by HRI dur

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

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

117 fiers of F508del-CFTR biogenesis, from which ribosomal protein L12 (RPL12/uL11) emerged as a molecula

118 d identified, namely enolase, cyclophilin-A, ribosomal protein L13 and actin-1.

119 mic distribution of box C/D snoRNAs from the ribosomal protein L13a (Rpl13a) locus.

120 echanism of inflammation control directed by ribosomal protein L13a and "GAIT" (Gamma Activated Inhib

121 een and a pull-down assay identified plastid ribosomal protein L15, uL15c (formerly RPL15), as intera

122 conventional organelles, colocalize with the ribosomal protein L22, and cluster the WNK signaling pat

123 Extra-ribosomal functions of human ribosomal protein L3 (uL3) may affect DNA repair, cell c

124 In addition, we identified RIBOSOMAL PROTEIN L30 (RPL30) as a prime SMT7 target and

125 We report the crystal structure of ribosomal protein L4 (RpL4) bound to its dedicated assem

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

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

128 We show that 60S ribosomal proteins L6 (RPL6) and RPL28, which are adjace

129 ooperativity of the C-terminal domain of the ribosomal protein L9 in the pressure-temperature plane u

130 Conversely, ribosomal protein large P0 (Rplp0), non-POU domain conta

131 iptomic analyses show progressive changes in ribosomal protein levels and mitochondrial function as e

132 ities were also correlated with the cellular ribosomal protein levels, thereby suggesting that mRNA p

133 This tsRNA binds at least two ribosomal protein mRNAs (RPS28 and RPS15) to enhance the

134 a C. neoformans ccr4Delta mutant, stabilized ribosomal protein mRNAs are retained in the translating

135 ion is accompanied by Ccr4-mediated decay of ribosomal protein mRNAs.

136 elevates the expression of a large subset of ribosomal protein mRNAs.

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

138 ppressed the expression of the mitochondrial ribosomal protein MRPS10 and reduced 12S ribosomal RNA (

139 tivity of specific cells and tissue types to ribosomal protein mutations.

140 enin/MMP signaling and a YY1/lncRNA ESCCAL-1/ribosomal protein network are uncovered and validated as

141 ng the context-independent downregulation of ribosomal proteins observed in blood neutrophils.

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

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

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

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

146 In addition to downregulating ribosomal proteins, p17 reduces mTORC2 assembly and disr

147 Eukaryotic-specific ribosomal protein paralogues eRpL22 and eRpL22-like are

148 Human ribosomal proteins play important structural and functio

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

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

151 LARP4 is a posttranscriptional regulator of ribosomal protein production in mammalian cells and sugg

152 cluding multiple aminoacyl tRNA synthetases, ribosomal proteins, protein chaperones, and the Clp syst

153 ocesses: RNA processing; gene transcription; ribosomal proteins; protein degradation; and metabolism

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

155 owth, cells must manage a massive economy of ribosomal proteins (r-proteins) and RNAs (rRNAs) to prod

156 ) of the rplM-rpsI operon, which encodes the ribosomal proteins (r-proteins) L13 and S9.

157 s mediated by an interaction with a specific ribosomal protein, RACK1, and that an increase in cytopl

158 showed robust translational upregulation of ribosomal proteins relative to other proteins.

159 hly charged proteins, such as histone H1 and ribosomal proteins, requires a dimer of two transport re

160 duration of feast and the allocation of the ribosomal protein reserve to maximize the overall gain i

161 To visualize co-transcriptional assembly of ribosomal protein-RNA complexes in real time, we develop

162 Ribosomal protein (RP) gene mutations, mostly associated

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

164 Variants in ribosomal protein (RP) genes drive Diamond-Blackfan anem

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

166 r in strains in which deletion of individual ribosomal protein (RP) genes leads to globally increased

167 Ribosomal protein (RP) genes must be coordinately expres

168 most often due to heterozygous mutations in ribosomal protein (RP) genes that lead to defects in rib

169 ve results from a detailed analysis of human Ribosomal Protein (RP) levels in normal and cancer sampl

170 h cell-type-specific pathologies and reduced ribosomal protein (RP) levels.

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

172 As with concomitant stabilization, including ribosomal protein (RP) mRNAs.

173 henotype is less severe than that of 2 other ribosomal protein (RP) mutant genes.

174 on and the tissue-specific variations of the ribosomal protein (RP) pool.

175 ght coordination of ribosomal RNA (rRNA) and ribosomal protein (RP) production.

176 stence of eukaryotic ribosomes with distinct ribosomal protein (RP) stoichiometry and regulatory role

177 To determine the contribution of the ribosomal protein (RP)-murine double minute 2 (MDM2)-p53

178 congenital disorders caused by mutations in ribosomal proteins (RP) or assembly factors and are char

179 gested that MYC drives the overexpression of ribosomal proteins (RP)L5 and RPL11, which bind and inhi

180 occurs in the cytoplasm by insertion of the ribosomal protein Rpl10 (uL16).

181 ockade of TAK1 was prevented by depletion of ribosomal protein RPL11.

182 In lymphoma, both p19ARF and ribosomal proteins RPL11 and RPL5 respond to c-MYC activ

183 novo splice variants in RPL13, which encodes ribosomal protein RPL13 (also called eL13), in four unre

184 munoprecipitates with RNA polymerase I, with ribosomal proteins RPL26 and RPL24, and with components

185 Here, we show that a largely uncharacterized ribosomal protein, RPL26, is the principal target of UFM

186 lncNB1 binds to the ribosomal protein RPL35 to enhance E2F1 protein synthesi

187 Among these genes ribosomal protein RPL35A, putative RNA helicase DDX24, a

188 In these screens, we identified ribosomal proteins RPLP1 and RPLP2 (RPLP1/2) to be among

189 ribosomal RNA (rRNA) expansion segments and ribosomal proteins (rProtein).

190 folding and local autonomy of assembly with ribosomal proteins (rProteins), and that the rProtein an

191 omozygotes lacking any of the five different ribosomal proteins (RPs) can produce fully functional fi

192 ow cells that lack one of the highly similar ribosomal proteins (RPs) often display distinct phenotyp

193 ation in eukaryotes created paralog pairs of ribosomal proteins (RPs) that show high sequence similar

194 s-acting factors and the incorporation of 79 ribosomal proteins (RPs).

195 components of translation machinery, such as ribosomal proteins (RPs).

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

197 oval of ubiquitin from an internal lysine of ribosomal protein RPS27a/eS31.

198 Yeast ribosomal protein Rps3/uS3 resides in the mRNA entry cha

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

200 binds within the carboxy-terminal domain of ribosomal protein S1 (RpsA) and inhibits trans-translati

201 30S subunits and ribosomal protein S1 alone display high-affinity binding

202 Ribosomal protein S1 forms a wall of the tunnel between

203 Ribosomal protein S1 is essential for standby, as 30Delt

204 Ribosomal protein S1 plays important roles in the transl

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

206 no sequence and is facilitated by a putative ribosomal protein S1-binding site.

207 r complex, allowing the refolded CTD to bind ribosomal protein S10.

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

209 t identified NBP35 and DRE2 (Derepressed for Ribosomal protein S14 Expression).

210 that interact with Geobacillus kaustophilus ribosomal protein S15.

211 Ribosomal protein s15a (RPS15A) plays a promotive role i

212 that ectopic expression of the mitochondrial ribosomal protein S18-2 (MRPS18-2) led to immortalizatio

213 rt novel immunosuppressive properties of the ribosomal protein S19 (RPS19), which is upregulated in h

214 Here, we report that AtPRMT3 interacts with Ribosomal Protein S2 (RPS2), facilitating processing of

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

216 Specifically, human growth hormone 1, murine ribosomal protein S27, and murine ATP synthase H(+) tran

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

218 40S ribosomal protein S28 (RPS28) knockdown increases total

219 sphate feeding, generate less phosphorylated ribosomal protein S6 (P-S6) than the WT.

220 nduce an up-regulation of phosphorylated (p)-ribosomal protein S6 (rpS6) (namely, p-rpS6-S235/S236) a

221 hypochromic skin patches, we identified the ribosomal protein S6 (RPS6) p.R232H variant, present as

222 ns involved in translational control, namely ribosomal protein S6 (rS6) and 4E-BP1.

223 ted protein kinase (AMPK) alpha (Thr172) and ribosomal protein S6 (Ser235/Ser236) was performed using

224 -LTD, through a mechanism involving mTOR and ribosomal protein S6 activation.

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

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

227 was associated with decreased phosphorylated ribosomal protein S6 immunoreactivity.

228 IL-7 treatment increased levels of phospho-ribosomal protein S6 in HIV-specific CD8 T cells, sugges

229 e genes Nr4a1 and Irf8 and activation of the ribosomal protein S6 is also conserved across stimuli.

230 The Ser/Thr kinase 90 kDa ribosomal protein S6 kinase 1 (p90RSK) belongs to a prot

231 e, we show that multisite phosphorylation of ribosomal protein S6 kinase 1 (S6K1) alters target selec

232 rget of rapamycin complex 1 (mTORC1) and p70 ribosomal protein S6 kinase 1 (S6K1) axis.

233 Ribosomal protein S6 kinase 1 (S6K1) is a major downstre

234 of mammalian target of rapamycin complex 1, ribosomal protein S6 kinase 1, and eukaryotic translatio

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

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

237 We investigated regulation of ribosomal protein S6 kinase B1 (RPS6KB1) by AURKA and th

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

239 age proinflammatory activation by catalyzing ribosomal protein S6 kinase beta-1 (S6K1) O-GlcNAcylatio

240 lular signal-regulated kinase) and S6K-RPS6 (ribosomal protein S6 kinase-ribosomal protein S6) axes.

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

242 es expressed higher levels of phosphorylated ribosomal protein S6 than paired fibroblasts from normal

243 1(Thr412) , 19%; p70 S6K1(Thr389) , 58%) and ribosomal protein S6(Ser235/236) (37%), greater rested-s

244 e) and S6K-RPS6 (ribosomal protein S6 kinase-ribosomal protein S6) axes.

245 B (trkB), namely, phosphorylation of Akt and ribosomal protein S6, in SN neurons.

246 horylation of a downstream target of mTORC1, ribosomal protein S6, was inhibited by EAD1.

247 EPRS, but not canonical S6K1 targets, e.g., ribosomal protein S6.

248 Ribosomal protein S6K (S6K) messenger RNA (mRNA) levels

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

250 hyde-3 phosphate dehydrogenase (GAPDH), 40 S ribosomal protein S9 (RpS9) and ubiquitin-conjugating pr

251 Ribosomal proteins scored among the most significantly d

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

253 global folds, including similarity to early ribosomal proteins, similar small molecule ligand bindin

254 ity may arise from factors other than simply ribosomal protein stoichiometry.

255 tors of RAN translation and identified small ribosomal protein subunit 25 (RPS25), presenting a poten

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

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

258 ons in the expression of the large and small ribosomal protein subunits (RPL and RPS, respectively) i

259 ssion of specific isoforms of genes encoding ribosomal proteins, suggesting that alterations in prote

260 lision in vivo resulted in ubiquitination of ribosomal proteins, suggesting that collision is sensed

261 nsity at their C-terminus are overwhelmingly ribosomal proteins, suggesting the possibility that this

262 olecular dynamics simulations show that each ribosomal protein switches the 16S conformation and damp

263 ional regulation is a potential mechanism of ribosomal protein synthesis and stoichiometry.

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

265 RPS3 is a small ribosomal protein that also has extraribosomal functions

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

267 protein complex comprises specific rRNAs and ribosomal proteins that are organized into functional do

268 We identified two specific ribosomal proteins that are strictly required for flaviv

269 probable only in the presence of additional ribosomal proteins that bind upstream and downstream of

270 osomes involves the hierarchical addition of ribosomal proteins that progressively stabilize the fold

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

272 studies using human marrow erythroid cells, ribosomal protein transcripts and proteins increase, and

273 ells (CD71(+)Ter119(neg-lo)), heme increases ribosomal protein transcripts, suggesting that heme, in

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

275 ms reveal the importance of stalling-induced ribosomal protein ubiquitination by Hel2/ZNF598 for both

276 o-terminal amphipathic helix of SecA and the ribosomal protein uL23 form a composite binding site for

277 linking indicated that F399 in SecA contacts ribosomal protein uL29, and binding to nascent chains di

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

279 e suggest that altering the conformations of ribosomal protein uL6 and rRNA helix H69, which interact

280 We also identified ribosomal proteins under relaxed or neutral selection.

281 th growth, including many encoding cytosolic ribosomal proteins, underwent distinct histone modificat

282 ere we report that ubiquitination of the 40S ribosomal protein uS10 by the E3 ubiquitin ligase Hel2 (

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

284 within the ribosomal S11 domain in the yeast ribosomal protein uS11 shows impaired growth and defecti

285 nking of aldehyde derivatives of RNAs to the ribosomal protein uS3 through its peptide 55-64 located

286 Here we examined function of the small ribosomal protein uS3/Rps3, earlier shown to interact wi

287 le molecule FRET to show how combinations of ribosomal proteins uS4, uS17 and bS20 in the 16S 5' doma

288 For example, the 40S ribosomal protein uS5 (RPS2) is known to form an extrari

289 etween A-3 and the conserved beta-hairpin of ribosomal protein uS7 fails to diminish the contribution

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

291 that encode translation machinery, including ribosomal proteins, was upregulated during the T cell cl

292 By knocking down each of the 80 ribosomal proteins, we identified proteins that modulate

293 Numerous ribosomal proteins were identified, confirming the work

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

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

296 oteins of a cell, comprise ribosomal RNA and ribosomal proteins, which coassemble hierarchically duri

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

298 y (LC-MS/MS) enable direct quantification of ribosomal proteins with high specificity, accuracy, and

299 ransferase center, and stable association of ribosomal proteins with rRNA surrounding the polypeptide

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