ライフサイエンスコーパス: ribosomal subunit

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

2 in IIId(1) is crucial for recruiting the 40S ribosomal subunit.

3 and delivers the initiator tRNA to the small ribosomal subunit.

4 ribosome includes that of the isolated small ribosomal subunit.

5 PS15, a gene encoding a component of the 40S ribosomal subunit.

6 conserved role in the maturation of the 60S ribosomal subunit.

7 appears to be an essential core of the small ribosomal subunit.

8 protein uL23 at the tunnel exit on the large ribosomal subunit.

9 and the start codon in the P site of the 30S ribosomal subunit.

10 to the aminoacyl-tRNA site on the small 30S ribosomal subunit.

11 ructure around and within the developing 40S ribosomal subunit.

12 the peptidyltransferase center of the large ribosomal subunit.

13 the peptidyl transferase center of the large ribosomal subunit.

14 rearrangements of the head domain in the 30S ribosomal subunit.

15 e conditions, BipA associates with the small ribosomal subunit.

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

17 ng of eIF4G and the recruitment of the small ribosomal subunit.

18 nd is required for the assembly of the small ribosomal subunit.

19 large, multiprotein eIF3 complex to the 40S ribosomal subunit.

20 the decoding center of the A site of the 40S ribosomal subunit.

21 RPS19, which encodes a component of the 40S ribosomal subunit.

22 binding interface that clashes with the 40S ribosomal subunit.

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

24 rt fully into the P decoding site on the 40S ribosomal subunit.

25 RNA mapped the AMI binding site to the small ribosomal subunit.

26 RNA codon present in the A site of the small ribosomal subunit.

27 of the nuclear export adapter from the large ribosomal subunit.

28 TS2 rRNA processing and synthesis of the 60S ribosomal subunit.

29 an in vivo assembly landscape for the larger ribosomal subunit.

30 target site on the Thermus thermophilus 30S ribosomal subunit.

31 makes up the major mass and shape of the 60S ribosomal subunit.

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

33 of the 28S ribosomal RNA (rRNA) in the large ribosomal subunit.

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

35 Pase required for the formation of the large ribosomal subunit.

36 ory region located on the surface of the 60S ribosomal subunit.

37 t penetrates deep into the core of the large ribosomal subunit.

38 complex (TC), which is recruited to the 40S ribosomal subunit.

39 is also present within the highly conserved ribosomal subunits.

40 esulting in a reduction in the number of 40S ribosomal subunits.

41 al step during cytoplasmic maturation of 40S ribosomal subunits.

42 al structures of EF-G bound and EF-G unbound ribosomal subunits.

43 c factors required for the maturation of 60S ribosomal subunits.

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

45 tivity and the dissociation and recycling of ribosomal subunits.

46 binding specificity from ribosomes to small ribosomal subunits.

47 mRNA associating with polysomes versus free ribosomal subunits.

48 as components of precursors to 60S (pre-60S) ribosomal subunits.

49 eins to the RNAs forming the small and large ribosomal subunits.

50 yield the 18S ribosomal RNA component of 40S ribosomal subunits.

51 replenish the pool of translation-competent ribosomal subunits.

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

53 uses the aggregation of both small and large ribosomal subunits.

54 interdependence of the biogenesis of the two ribosomal subunits.

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

56 tructure that binds to 80S ribosomes and 60S ribosomal subunits.

57 ture of the RQC complex bound to stalled 60S ribosomal subunits.

58 s the rRNA components of the large and small ribosomal subunits.

59 r with Ltn1 and the AAA-ATPase Cdc48, to 60S ribosomal subunits.

60 and maturation steps for construction of 60S ribosomal subunits.

61 three reactions but also re-associated yeast ribosomal subunits.

62 ive roles of tRNA and RRF in dissociation of ribosomal subunits.

63 ting the assembly of the mitochondrial small ribosomal subunits.

64 are converted to translation-competent large ribosomal subunits.

65 espiratory chain complexes and mitochondrial ribosomal subunits.

66 nsequences of deficiency for small and large ribosomal subunits.

67 n translation and genetically interacts with ribosomal subunits.

68 r the interactions between both of the small ribosomal subunits.

69 binds ribosomes and isolated large and small ribosomal subunits.

70 NA and nascent chain destruction and recycle ribosomal subunits.

71 we demonstrate the engineering of the small-ribosomal subunit (16S) RNA of Mycoplasma mycoides, by c

72 Methylation of the bacterial small ribosomal subunit (16S) rRNA on the N1 position of A1408

73 inal processing step to produce mature small ribosomal subunit 18S rRNA.

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

75 s of ribosome biogenesis in mammals, the two ribosomal subunits 40S and 60S are produced via splittin

76 somal Entry Site (CrPV-IRES) binds the small ribosomal subunit (40S) and the translocation intermedia

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

78 ociation factor eIF6 from the surface of the ribosomal subunit 60S.

79 presence of expansion segments in the large ribosomal subunit (60S) of Trypanosoma brucei.

80 nformation compatible with binding the large ribosomal subunit (60S).

81 Upon joining of the large and small ribosomal subunits, a 100-nt long expansion segment of t

82 80S ribosome after the joining of individual ribosomal subunits-a process that is catalysed by this u

83 noncoding ribosome, proto-mRNA and the small ribosomal subunit acted as cofactors, positioning the ac

84 change the folding or dynamics of the large ribosomal subunit, altering the rate of GTP hydrolysis a

85 factors (eIFs) in conjunction with the 40 S ribosomal subunit and (initiator) tRNA(i).

86 etween the Cy3-labeled L1 stalk of the large ribosomal subunit and a Cy5-labeled tRNA(Lys) in the rib

87 or L9), an essential component of the large ribosomal subunit and a putative tumor suppressor, was i

88 site (IRES) that can autonomously bind a 40S ribosomal subunit and accurately position it at the init

89 lants, besides being a component of the 40 S ribosomal subunit and acting as a target of TOR.

90 RPS29 is a component of the small 40S ribosomal subunit and essential for rRNA processing and

91 of EF-G moves toward the A site of the small ribosomal subunit and facilitates the movement of peptid

92 estration of the early assembly of the large ribosomal subunit and in faithful protein production.

93 delivering initiator Met-tRNAiMet to the 40S ribosomal subunit and in selecting the translation initi

94 s LTO1; required for biogenesis of the large ribosomal subunit and initiation of translation in oxyge

95 which encodes a component (S20) of the small ribosomal subunit and is a new colon cancer predispositi

96 e A/U-tail enables mRNA binding to the small ribosomal subunit and is essential for translation.

97 and most variable ES of the eukaryotic large ribosomal subunit and is located at the surface of the r

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

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

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

101 n the three-dimensional structure of the 30S ribosomal subunit and probably act directly by compensat

102 tablishes how Ltn1 associates with the large ribosomal subunit and properly positions its E3-catalyti

103 2.5-A structure of the Trypanosoma cruzi 60S ribosomal subunit and propose a model for the stepwise a

104 nd initiator transfer RNA bound to the small ribosomal subunit and provide insights into the details

105 the closed and open conformations of the 30S ribosomal subunit and requires disruption of the interfa

106 vious in vitro assembly studies of the small ribosomal subunit and six 50S assembly groups that clear

107 nt the near-atomic structures of the Mtb 50S ribosomal subunit and the complete Mtb 70S ribosome, sol

108 M mediates an rRNA modification in the small ribosomal subunit and thus plays a role analogous to Ksg

109 ng that AROS selectively associates with 40S ribosomal subunits and also with polysomes.

110 (eIF6) is essential for the synthesis of 60S ribosomal subunits and for regulating the association of

111 ting with the 70S ribosome, may also bind to ribosomal subunits and form TF-polypeptide complexes tha

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

113 SRP9/14, CSDE1, DHX36, and PABPC1 with both ribosomal subunits and polysomal RNA, an association not

114 f trans-acting enzymes to produce functional ribosomal subunits and secure the translational capacity

115 gnificant role in the binding of Ltn1 to 60S ribosomal subunits and that NTD mutations causing defect

116 elongation', 'translation factor activity', 'ribosomal subunit' and 'phosphorelay signal transduction

117 eveal extensive solvation of the small (30S) ribosomal subunit, and interactions with A-site and P-si

118 A-binding subunit of the small mitochondrial ribosomal subunit, and is required for the assembly of t

119 ates with translation-initiating factors and ribosomal subunits, and in vitro binding assays revealed

120 astid ribosomes, a specific depletion in 30S ribosomal subunits, and reduced activity of plastid prot

121 directly tracked the CrPV IRES, 40S and 60S ribosomal subunits, and tRNA using single-molecule fluor

122 nce dedicated assembly factors keep immature ribosomal subunits apart and prevent them from translati

123 ce only occurs when both ppGpp and the small ribosomal subunit are present.

124 chromosomal DNA segregate, while 30S and 50S ribosomal subunits are able to penetrate the nucleoids.

125 te that structural domains of eukaryotic 60S ribosomal subunits are formed in a hierarchical fashion.

126 adopts a distinct conformation in which the ribosomal subunits are in a semirotated orientation and

127 However, this mechanism requires that free ribosomal subunits are not excluded from the nucleoid.

128 ropose that rRNAs not packaged into complete ribosomal subunits are polyadenylated by the poly(A) pol

129 bosomes and target mRNAs suggest that both I-ribosomal subunits are required for the preferential tra

130 ngle-molecule methods, fluorescently labeled ribosomal subunits are required.

131 Initial recruitment of the small ribosomal subunit as well as two translocation steps bef

132 w that this protein interacts with the large ribosomal subunit as well as with a series of non-riboso

133 The small ribosomal subunit assembles cotranscriptionally on the n

134 tated iPSCs exhibited defects in 40S (small) ribosomal subunit assembly and production of 18S ribosom

135 assembly factors during the final stages of ribosomal subunit assembly and visualize structural feat

136 the protein composition of various yeast 60S ribosomal subunit assembly intermediates has been studie

137 utated iPSCs exhibited defective 60S (large) ribosomal subunit assembly, accumulation of 12S pre-rRNA

138 t proteins to organize RNA structure for 40S ribosomal subunit assembly.

139 eukaryotic translation initiation, the small ribosomal subunit, assisted by initiation factors, locat

140 In eukaryotes, the large ribosomal subunit-associated quality control complex (RQ

141 d 43 ms and have determined 3D structures of ribosomal subunit association intermediates.

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

143 e rapid accumulation of immature 30S and 50S ribosomal subunits at 15 degrees C.

144 iciency of late steps in biogenesis of large ribosomal subunits at low temperatures, presumably while

145 The drug binds to both small and large ribosomal subunits at nine independent sites.

146 ate in their maturation, nascent small (40S) ribosomal subunits bind 60S subunits to produce 80S-like

147 yeast homolog Mbf1 revealed a conserved 40S ribosomal subunit binding site at the mRNA entry channel

148 the eIF3c RNA-binding motif also reduce 40S ribosomal subunit binding to eIF3, and inhibit eIF5B-dep

149 nslation initiation in eukaryotes, the small ribosomal subunit binds messenger RNA at the 5' end and

150 According to the canonical mechanism, 40S ribosomal subunit binds to the 5'-end of messenger RNA (

151 Nop9 is a conserved small ribosomal subunit biogenesis factor, essential in yeast.

152 ases (Rio1, Rio2 and Rio3) function in small ribosomal subunit biogenesis.

153 s an RRM protein that is essential for large ribosomal subunit biogenesis.

154 diffraction) and Thermus thermophilus small ribosomal subunit bound to the antibiotic paromomycin at

155 ults in transcriptional upregulation of most ribosomal subunits, but no alternative transporters, and

156 e characterized rRNA of the H. sapiens large ribosomal subunit by computation, circular dichroism, UV

157 ganizes the assembly of the eukaryotic small ribosomal subunit by coordinating the folding, cleavage,

158 s recruited or stabilized on translating 40S ribosomal subunits by interactions with 18S rRNA and Asc

159 e show that stable rRNA domains of the small ribosomal subunit can independently recruit their own bi

160 The eukaryotic small ribosomal subunit carries only four ribosomal (r) RNA me

161 oli cells to determine the fractions of free ribosomal subunits, classify individual subunits as free

162 bundances of modified residues in incomplete ribosomal subunits compared to a mature (15)N-labeled rR

163 ys, shikimate derivative dependent pathways, ribosomal subunit composition, hormone signaling, wound

164 omain V of the 23S/25S/28S rRNA of the large ribosomal subunit constitutes the active center for the

165 The resulting ribosomal subunits could be specifically labeled in livi

166 the hypervariable domains D1/D2 of the large ribosomal subunit (D1/D2 LSU) as a barcoding marker for

167 Although ribosomal subunit dissociation and nascent peptide degra

168 nteract with both the ribosome and the small ribosomal subunit during stress response.

169 utward movement of the L1 stalk of the large ribosomal subunit during the subunit-joining step of tra

170 Association of the two ribosomal subunits during the process of translation ini

171 tein (EGFP) reporter fused to the L10a large ribosomal subunit (EGFPL10a).

172 -initiation complex (PIC) containing the 40S ribosomal subunit, eIF1, eIF1A, eIF3, ternary complex (e

173 A selective autophagic pathway for 60S ribosomal subunits elicited by nitrogen starvation in ye

174 this process, the protein Rqc2 and the large ribosomal subunit elongate stalled polypeptides with car

175 ient peptide segments from the cores of both ribosomal subunits enhance RNA polymerase ribozyme (RPR)

176 rsally conserved rRNA structure of the small ribosomal subunit essential for protein synthesis.

177 ion complex (43S PIC), consisting of the 40S ribosomal subunit, eukaryotic initiation factors (eIFs)

178 tments with reported roles in transcription, ribosomal subunit export, and translation; however, the

179 factor for bulk mRNA and also contributes to ribosomal subunit export.

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

181 enabling the factor to engage the 40S small ribosomal subunit for translation initiation.

182 ases ubiquitinated nascent proteins from 60S ribosomal subunits for proteasomal degradation.

183 chanism of inhibition of a key step in large ribosomal subunit formation.

184 e present the crystal structure of the large ribosomal subunit from Staphylococcus aureus, a versatil

185 We examined 50 S ribosomal subunits from 10 species and found a clear dis

186 Assembly of 30S ribosomal subunits from their protein and RNA components

187 onset UVR-induced melanoma was linked to the ribosomal subunit gene Rrp15.

188 f the L1 stalk, a mobile domain of the large ribosomal subunit, have been shown to accompany the elon

189 ilis that facilitate the assembly of the 50S ribosomal subunit, however their roles in this process a

190 omes in persisters exist largely as inactive ribosomal subunits, (ii) rRNAs and tRNAs are mostly degr

191 crystal structures of the eubacterial large ribosomal subunit in complex with them.

192 KRIPP1 and KRIPP8 as components of the small ribosomal subunit in mammalian and insect forms, but als

193 the entire 3' domain of the bacterial small ribosomal subunit in real time.

194 We found that L13a is released from the 60S ribosomal subunit in response to infection by respirator

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

196 20A-eGFP fusion proteins comigrated with 50S ribosomal subunits in Suc density gradients, even after

197 RNA and causing abnormal accumulation of 50S ribosomal subunits in the high-molecular-mass fraction o

198 initiation factor (eIF) 4F and recruits 40S ribosomal subunits in the presence of active helicase fa

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

200 Binding of Met-tRNAi to the small (40S) ribosomal subunit, in a ternary complex (TC) with eIF2-G

201 pseudouridine modifications within the small ribosomal subunit, in RAS-induced senescence in vivo.

202 PL15, which encodes a component of the large ribosomal subunit, increased metastatic growth in multip

203 e, 50S, ribosomal subunit to the small, 30S, ribosomal subunit initiation complex (IC) during bacteri

204 initiation, 43S complexes, comprising a 40S ribosomal subunit, initiator transfer RNA and initiation

205 mechanism, which licenses entry of the large ribosomal subunit into translation.

206 The binding interface on the large ribosomal subunit is buried by the small subunit during

207 t the timely removal of ERAL1 from the small ribosomal subunit is essential for the efficient maturat

208 study shows that nuclear export of the large ribosomal subunit is regulated by a GTPase that blocks r

209 ltiple proteins of the small and large yeast ribosomal subunits is suppressed.

210 h-resolution structures for eukaryotic large ribosomal subunits, it remained unclear how these ribonu

211 efects in these individuals include impaired ribosomal subunit joining and attenuated global protein

212 data highlight the dynamics of IF2-dependent ribosomal subunit joining and the role played by the N t

213 Ribosomal subunit joining is a key checkpoint in the bac

214 on by selectively increasing the rate of 50S ribosomal subunit joining to 30S initiation complexes (I

215 3S pre-initiation complex (PIC) assembly, to ribosomal subunit joining.

216 Maturation of the large ribosomal subunit (LSU) in eukaryotes is a complex and h

217 of pre-ribosomal RNA (pre-rRNA) and to large ribosomal subunit (LSU) pre-rRNA processing independent

218 ve cleavage sites of the kinetoplastid large ribosomal subunit (LSU) rRNA chain, which is known to be

219 whose absence impairs formation of the large ribosomal subunit (LSU).

220 ins, associates with the mitochondrial large ribosomal subunit (mt-LSU).

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

222 In the small ribosomal subunit of budding yeast, on the 18S rRNA, two

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

224 translation enhancers (3'CITEs) that bind to ribosomal subunits or translation factors thought to ass

225 TPase activity of eIF5B after the joining of ribosomal subunits prevented the dissociation of eIF5B f

226 rrant nascent-chains obstructing large (60S) ribosomal subunits-products of ribosome stalling during

227 insufficiency of Mrpl40 (mitochondrial large ribosomal subunit protein 40) as a contributor to abnorm

228 Large ribosomal subunit protein bL31, which forms intersubunit

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

230 he yeast Saccharomyces cerevisiae, the large ribosomal subunit protein Rpl3p is methylated at histidi

231 tomatitis virus (VSV), we identify the large ribosomal subunit protein rpL40 as requisite for VSV cap

232 o catalyze prolyl-hydroxylation of the small ribosomal subunit protein RPS23.

233 cer is ribosome-dependent and that the small ribosomal subunit protein S1 interacts with the enhancer

234 green fluorescent protein (eGFP)-tagged L10a ribosomal subunit protein under control of the collagen1

235 The small ribosomal subunit protein uS9 (formerly called rpS16 in

236 serine/threonine residues in the human small ribosomal subunit protein, receptor for activated C kina

237 We visualize ribosomal subunit proteins and show that the large subun

238 NAs and monoubiquitination of distinct small ribosomal subunit proteins.

239 CP activity resulted in aggregation of large ribosomal subunit proteins.

240 linked the evolution of the large and small ribosomal subunits, proto-mRNA, and tRNA.

241 n assembly of bacterial and eukaryotic large ribosomal subunits, providing insights into how these RN

242 factors required for maturation of the small ribosomal subunit (Rcl1, Fcf1/Utp24, Utp23) and the larg

243 f PABP-eIF4G on cap binding to promote small ribosomal subunit recruitment.

244 During translation, the two eukaryotic ribosomal subunits remain associated through 17 intersub

245 on and inhibit the nuclear export of the 60S ribosomal subunit, respectively.

246 ple EF-G catalysed translocation from normal ribosomal subunit reverse-rotation, leaving the ribosome

247 al surveillance, acts as an inhibitor of 60S ribosomal subunit ribophagy and is antagonized by Ubp3.

248 ide bond is formed, a reaction that requires ribosomal subunit rotation and is catalyzed by the guano

249 rmation that favors an intermediate state of ribosomal subunit rotation.

250 ecovered from cells expressing both a tagged ribosomal subunit, Rpl10a, and the bacterial biotin liga

251 e proteins depends on interactions with both ribosomal subunits, some portion of 30S and 50S assembly

252 omal protein L13a is released from the large ribosomal subunit soon after infection and inhibits the

253 rRNA) processing as a component of the small ribosomal subunit (SSU) processome.

254 KsgA, a universally conserved small ribosomal subunit (SSU) rRNA methyltransferase, has rece

255 be required for the generation of the small ribosomal subunit (SSU).

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

257 nce to linezolid (and a variety of other 50S ribosomal subunit-targeted antibiotics) but not to tediz

258 Multiple interactions between the ribosomal subunits, termed intersubunit bridges, keep th

259 L27 is a component of the eubacterial large ribosomal subunit that has been shown to play a critical

260 e structures of three complexes of the small ribosomal subunit that represent distinct steps in mamma

261 tion conditions, they accumulated incomplete ribosomal subunits that we named 45SYphC and 44.5SYsxC p

262 neighboring proline residue resulting in 40S ribosomal subunits that were blocked from polysome forma

263 he model explains the evolution of the large ribosomal subunit, the small ribosomal subunit, tRNA, an

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

265 G3BP interacts with 40S ribosomal subunits through its RGG motif, which is also

266 ves the tightly regulated joining of the 50S ribosomal subunit to an initiator transfer RNA (fMet-tRN

267 factors involved in the recruitment of a 40S ribosomal subunit to an mRNA.

268 nitiation factors needed to recruit the 40 S ribosomal subunit to an mRNA.

269 ding of initiator tRNA and mRNA to the small ribosomal subunit to form the initiation complex, which

270 sively in the cytoplasm and binds to the 40S ribosomal subunit to gain access to translating mRNAs, M

271 mplex and stimulates its assembly to the 50S ribosomal subunit to make the 70S ribosome.

272 eIF4A modulates the conformation of the 40S ribosomal subunit to promote mRNA recruitment.

273 e array of initiation factors onto the small ribosomal subunit to select an appropriate mRNA start co

274 he 5'-UTR, allowing eIF4F to recruit the 40S ribosomal subunit to the 5'-end.

275 Joining of the large, 50S, ribosomal subunit to the small, 30S, ribosomal subunit i

276 t is active translation that normally allows ribosomal subunits to assemble on nascent mRNAs througho

277 ether with eIF3 and eIF4A/4B, eIF4G recruits ribosomal subunits to mRNAs and facilitates 5' untransla

278 bitors are enhanced by the limited access of ribosomal subunits to nascent mRNAs in the compacted nuc

279 action with a 5' proximal hairpin to deliver ribosomal subunits to the 5' end for translation initiat

280 Ltn1 binds to 60S ribosomal subunits to ubiquitylate nascent polypeptides

281 y a process mediated specifically by the 30S ribosomal subunit, to degrade defective 70S ribosomes bu

282 of human 40S subunits, we characterized pre-ribosomal subunits trapped on RIOK1 by mass spectrometry

283 on of the large ribosomal subunit, the small ribosomal subunit, tRNA, and mRNA.

284 aled a direct interaction of cpSRP54 and the ribosomal subunit uL4, which is not located at the tunne

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

286 The L1 stalk of the large ribosomal subunit undergoes large-scale movements couple

287 cation, relative to protein S12 of the small ribosomal subunit using single-molecule FRET.

288 peptidyl-tRNA enters the P site of the small ribosomal subunit via reversible, swivel-like motions of

289 The expression of these ribosomal subunits was also associated with susceptibili

290 ntial protein Era in the assembly of the 30S ribosomal subunit, we analyzed assembly intermediates th

291 both function during maturation of the small ribosomal subunit, we show here that Rrp5 provides speci

292 f chloroplast ribosomal RNAs and assembly of ribosomal subunits were disrupted by reduced expression

293 c are defective in the maturation of the 60S ribosomal subunit, whereas maturation of the 40S subunit

294 The creation of orthogonal large and small ribosomal subunits, which interact with each other but n

295 iquitinated polypeptides associated with 60S ribosomal subunits, while Dom34-Hbs1 generate 60S-associ

296 the nascent peptide exit tunnel of the large ribosomal subunit with comparable affinities, the bacter

297 Here, we labeled human 40S ribosomal subunits with a fluorescent SNAP-tag at riboso

298 sly unexplored labile complexes of human 40S ribosomal subunits with RNAs, whose formation is manifes

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

300 ract with each other but not with endogenous ribosomal subunits, would extend our capacity to create