ライフサイエンスコーパス: elongation factor

1 me O-GlcNAcase (OGA) as an RNA polymerase II elongation factor.

2 are aided by a collection of proteins called elongation factors.

3 anslation initiation factors and translation elongation factors.

4 ion of ribosomal proteins and initiation and elongation factors.

5 o both nucleotide and replication initiation/elongation factors.

6 nown about the role of lysine methylation on elongation factors.

7 the translation elongation factor eukaryotic elongation factor 1 alpha (eEF1A) is necessary for AID c

8 The human elongation factor 1 alpha (EEF1A1) promoter fragment int

9 NA), as well as fragments of the translation elongation factor 1 alpha (EF-1alpha) and actin (Act) ge

10 rometry (LC-MS/MS)-based proteomics revealed elongation factor 1 alpha (EF1a) as a protein binding to

11 ion by at least 100-fold with the use of the elongation factor 1 alpha (EF1alpha) promoter and a stro

12 bosomal DNA and fragments of the translation elongation factor 1 alpha (Tef1), endochitinase CHI18-5

13 re we discovered that eukaryotic translation elongation factor 1 alpha 1 (eEF1A1) interacted with PpI

14 of these proteins, the actin-binding protein elongation factor 1 alpha 1 (EF1alpha1), blocks neural c

15 portions of the beta-tubulin and translation elongation factor 1-alpha genes indicated that the isola

16 enes, such as actin, alpha/beta-tubulin, and elongation factor 1-alpha.

17 s of the potential of therapeutics targeting elongation factor 1.

18 class of novel cyclic lactone inhibitors of elongation factor 1.

19 The essential eukaryotic elongation factor 1A (eEF1A) delivers aminoacyl tRNAs to

20 he mTOR pathway such as eIF4E and eukaryotic elongation factor 1A (eEF1A) early during L-LTP causing

21 anslation elongation, eukaryotic translation elongation factor 1A (eEF1A) has been shown to interact

22 d cellular WW domain proteins and eukaryotic elongation factor 1A (eEF1A) in control of activation of

23 Eukaryotic elongation factor 1A (EEF1A), is encoded by two distinct

24 During elongation, eukaryotic elongation factor 1A (eEF1A; EF-Tu in bacteria) delivers

25 taining axonal particles are associated with elongation factor 1A, a component of the protein transla

26 We conclude that the eukaryotic elongation factor-1A and its ternary complex with GTP an

27 -affinity probe, we identify the translation elongation factor-1A ternary complex (eEF1A.GTP.aminoacy

28 The eukaryotic elongation factor 1A2 (EEF1A2) was identified as an upst

29 oaches identified the eukaryotic translation elongation factor 1alpha (EF-1alpha) as the primary targ

30 -largest subunit (RPB2), and the translation elongation factor 1alpha (EF-1alpha) gene.

31 e to an enhanced interaction with Eukaryotic Elongation Factor 1alpha (EF1alpha), whose protein level

32 Tef1/2 (the yeast form of translation elongation factor 1alpha [eEF1A]) aids the specificity o

33 ransfer RNA synthetase, elongation factor 2, elongation factor 1delta, and eukaryotic translation and

34 regions of endogenous eukaryotic translation elongation factor 2 (eEF-2) gene] using the Clustered Re

35 thesis through phosphorylation of eukaryotic elongation factor 2 (eEF-2).

36 Furthermore, we found that eukaryotic elongation factor 2 (eEF2) and its kinase eEF2K are key

37 an target of rapamycin (mTOR) and eukaryotic elongation factor 2 (eEF2) in the mPFC, effects recently

38 Translocation of the IRES by elongation factor 2 (eEF2) is required to bring the firs

39 diphthamide on human eukaryotic translation elongation factor 2 (eEF2) is the target of ADP ribosyla

40 A catalyzes the trimethylation of eukaryotic elongation factor 2 (eEF2) on Lys-525.

41 ing protein (Tbp) and eukaryotic translation elongation factor 2 (Eef2) were not affected by inflamma

42 n this study, we demonstrate that eukaryotic elongation factor 2 (eEF2), which catalyzes the GTP-depe

43 controlled by phosphorylation of eukaryotic elongation factor 2 (eEF2), which inhibits its activity

44 ar target has been identified as translation elongation factor 2 (eEF2), which is responsible for the

45 ein kinase and phosphorylation of eukaryotic elongation factor 2 (eEF2).

46 the translocation intermediate stabilized by elongation factor 2 (eEF2).

47 longation factor G (EF-G) in prokaryotes and elongation factor 2 (EF-2) in eukaryotes].

48 osttranslational modification on translation elongation factor 2 (EF2) in archaea and eukaryotes.

49 ication in archaeal and eukaryal translation elongation factor 2 (EF2).

50 chanism of action, inhibition of translation elongation factor 2 (PfEF2), led to progression of 2 (DD

51 reduced phosphorylation levels of eukaryotic elongation factor 2 and also requires the presence of el

52 catalyzed the ADP-ribosylation of eukaryotic elongation factor 2 and inhibited protein synthesis.

53 Calmodulin (CaM)-dependent eukaryotic elongation factor 2 kinase (eEF-2K) impedes protein synt

54 Eukaryotic elongation factor 2 kinase (eEF-2K), the only calmodulin

55 We also used eukaryotic elongation factor 2 kinase (eEF2K) (also known as CaMKII

56 plitudes by reducing postsynaptic eukaryotic elongation factor 2 kinase (eEF2K) activity subsequent t

57 Eukaryotic elongation factor 2 kinase (eEF2K) is a Ca(2+)/calmoduli

58 Eukaryotic elongation factor 2 kinase (eEF2K) is the best-character

59 Eukaryotic elongation factor 2 kinase (eEF2K), an atypical calmodul

60 Here, we demonstrate that elongation factor 2 kinase (eEF2K), an evolutionarily co

61 ch is controlled by the Ca(2+)/CaM-dependent elongation factor 2 kinase (eEF2K).

62 d higher levels of phosphorylated eukaryotic elongation factor 2 kinase than were observed in Mtm1 p.

63 des the activation of eukaryotic translation elongation factor 2 kinase with a consequent inhibition

64 ivation and downregulation of the eukaryotic elongation factor 2 kinase, which normally inhibits tran

65 n factor 2 and also requires the presence of elongation factor 2 kinase.

66 ot inhibit the phosphorylation of eukaryotic elongation factor 2 or augment subsequent expression of

67 kills by ADP-ribosylation of the translation elongation factor 2, but many of the host factors requir

68 esent on archaeal and eukaryotic translation elongation factor 2, diphthamide represents one of the m

69 thetase, glutaminyl-transfer RNA synthetase, elongation factor 2, elongation factor 1delta, and eukar

70 synthesis by ADP-ribosylation of eukaryotic elongation factor 2.

71 ible for the trimethylation of lysine 509 on elongation factor 2.

72 ulin-dependent phosphorylation of eukaryotic elongation factor-2 (eEF-2) by eukaryotic elongation fac

73 induced the phosphorylation of a eukaryotic elongation factor-2 (eEF-2) kinase, radiation sensitivit

74 We report here that eukaryotic elongation factor-2 kinase (eEF-2K), a negative regulato

75 ic elongation factor-2 (eEF-2) by eukaryotic elongation factor-2 kinase (EF2K), which inhibits elonga

76 required protein translation and eukaryotic elongation factor-2 kinase activity.

77 cells via ADP-ribosylation of the eukaryotic elongation factor-2.

78 itting of ribosomes, catalyzed by eukaryotic elongation factor 3 (eEF3) and ATP.

79 apl-C) consisting of eight HEAT (Huntingtin, Elongation factor 3, A subunit, and target of rapamycin)

80 in the LYST ARM/HEAT (armadillo/huntingtin, elongation factor 3, protein phosphatase 2A, and the yea

81 the N-terminal HEAT (named after Huntingtin, elongation factor 3, protein phosphatase 2A, and yeast k

82 domains, consisting of six (A-F) Huntingtin, elongation factor 3, protein phosphatase 2A, target of r

83 Despite numerous studies, the function of elongation factor 4 (EF-4/LepA), a highly conserved tran

84 Elongation factor 4 (EF4) is a member of the family of r

85 Elongation factor 4 (EF4/LepA) is a highly conserved gua

86 h the regulated binding of the transcription elongation factor AFF3 between a DMR and an enhancer.

87 A, a stop codon reassigned by a Sec-specific elongation factor and a distinctive RNA structure.

88 al. (2015) describe a connection between an elongation factor and a repressive complex to prevent tr

89 EAD to regulate binding of the NELF negative elongation factor and block SMAD2,3 induction of ME gene

90 phosphate group to the essential translation elongation factor and GTPase, elongation factor (EF)-Tu.

91 , which recruits the selenocysteine specific elongation factor and tRNA(Sec) needed to reassign the U

92 action of the sarcin ricin loop with the two elongation factors and (iii) networked information excha

93 so that it can serve as a platform for other elongation factors and maintain its association with RNA

94 By phosphorylating negative elongation factors and the C-terminal domain of RNA poly

95 of DRB sensitivity-inducing factor, negative elongation factor, and C-terminal domain (CTD) serine-2

96 ocalization of SBP2, selenocysteine-specific elongation factor, and L30 recoding factors from the cyt

97 Spt5, a transcription elongation factor, and Rpb4, a subunit of RNA polymerase

98 otational status determines its affinity for elongation factors, and hence translational fidelity and

99 However, RNAPII is decorated with elongation factors as it transcribes the genome.

100 e identified transcription pause-release and elongation factors as one set of in vivo-specific cancer

101 Here, we identify TFIIS.h, a transcription elongation factor, as a new transcriptional target of p5

102 ed Atf4 binding regulated the association of elongation factors at both the promoter and the enhancer

103 de in the specialized positive transcription elongation factor b (P-TEFb) activation mechanism that i

104 ons in an Arabidopsis positive transcription elongation factor b (P-TEFb) complex and influences glob

105 Pol II release, that positive transcription elongation factor b (P-TEFb) directly regulates the init

106 es the release of the positive transcription elongation factor b (P-TEFb) from the 7SK snRNP in a man

107 tor of transcription)-positive transcription elongation factor b (P-TEFb) interaction allowed for loc

108 icular members of the positive transcription elongation factor b (P-TEFb) involved in the release of

109 ription elongation by positive transcription elongation factor b (P-TEFb) plays a central role in det

110 The positive transcription elongation factor b (P-TEFb) promotes transcription elon

111 d Tat protein hijacks positive transcription elongation factor b (P-TEFb) to phosphorylate and activa

112 Positive transcription elongation factor b (P-TEFb), a complex of Cdk9 and cycl

113 s and inactivates the positive transcription elongation factor b (P-TEFb), an essential eukaryotic mR

114 es its binding to the positive transcription elongation factor b (P-TEFb), and potentiates its transc

115 The positive transcription elongation factor b (P-TEFb), comprised of cyclin-depend

116 CDK9, a component of positive transcription elongation factor b (P-TEFb), to target gene promoters,

117 lymerase II (RNAPII), positive transcription elongation factor b (P-TEFb), which is composed of CycT1

118 s CDK13 and CDK11 and positive transcription elongation factor b (P-TEFb).

119 e nuclear activity of positive transcription elongation factor b (P-TEFb).

120 ion by inhibiting the positive transcription elongation factor b (P-TEFb, a complex of CDK9 and cycli

121 y reported effects on positive transcription elongation factor b and HMBA inducible protein-1.

122 DK9, the component of positive transcription elongation factor b complex responsible for Ser2 phospho

123 reased recruitment of positive transcription elongation factor b to the LTR promoter.

124 tiation and P-TEFb (positive transcriptional elongation factor b) events during elongation.

125 regulatory subunit of positive transcription elongation factor b, a complex that inhibits OL maturati

126 ms a complex with the positive transcription elongation factor b, which controls phosphorylation of R

127 al regulated kinase/positive transcriptional elongation factor-b and NF-kappaB.

128 ecruiting the P-TEFb (positive transcription elongation factor-b) (CycT1:CDK9) C-terminal domain (CTD

129 This general transcription elongation factor binds to RNA polymerase (RNAP) soon af

130 endent kinase 9 (CDK9), that regulates these elongation factors, blocked induction of the AA-responsi

131 ects by suggesting that codon recognition by elongation factor-bound aminoacyl-tRNA is initiated by h

132 Elongation factor-catalyzed GTP hydrolysis is a key reac

133 NusG/Spt5 is the only elongation factor conserved in all domains of life.

134 ion to revealing insights into how these two elongation factors cooperate to promote RNAPII elongatio

135 We found that loop 3 affects two discrete elongation factor-dependent steps in the IRES initiation

136 The actin elongation factors Diaphanous and Enabled both promote b

137 activation of a top candidate RBP, negative elongation factor E (NELFE), via somatic copy-number alt

138 n of a subset of proteins by ubiquitin chain elongation factors (E4), represented by Ufd2p in Sacchar

139 d seedlings recovered eukaryotic translation elongation factor (eEF) 1B (alpha-, beta-, and gamma-sub

140 Translation elongation factor eEF1A has a well-defined role in prote

141 e mutations in the gene encoding translation elongation factor eEF1A2 have recently been found to giv

142 ires diphthamide modification of translation elongation factor eEF2 and wobble uridine modifications

143 Elongation factor eEF2 with a GTP analog stabilizes the

144 decreased phosphorylation of the eukaryotic elongation factor eEF2, reminiscent of the effects of ke

145 ated region, Sec-tRNA(Sec), the Sec-specific elongation factor eEFSec, and SECIS binding protein 2.

146 A specialized translation elongation factor, eEFSec in eukaryotes and SelB in prok

147 through the ribosome, a process catalyzed by elongation factor EF-G, is a crucial step in protein syn

148 tively; (iii) deletion of efp, which encodes elongation factor EF-P that assists the translation of p

149 parameters and the mechanistic strategies of elongation factor (EF) Ts-catalyzed nucleotide exchange

150 al translation elongation factor and GTPase, elongation factor (EF)-Tu.

151 some is catalyzed by a universally conserved elongation factor (EF-G in prokaryotes and EF-2 in eukar

152 AbDsbA and the highly conserved prokaryotic elongation factor, EF-Tu.

153 tin, RNA polymerase (Pol) II associates with elongation factors (EFs).

154 s is facilitated by protein complexes called elongation factors (EFs).

155 entral domain of Nmd3 mimics the translation elongation factor eIF5A, inserting into the E site of th

156 tional modification of essential translation elongation factor eIF5A, mediated by deoxyhypusine synth

157 The transcription elongation factor eleven nineteen lysine-rich leukemia g

158 mplex (LEC)-which contains the transcription elongation factor ELL/EAF-was found to be required for t

159 affold proteins AFF1/4 and the transcription elongation factors ELL1/2 are core components of the sup

160 vating Ell2 (which encodes the transcription-elongation factor ELL2).

161 EPOP interacts with the transcription elongation factor Elongin BC and the H2B deubiquitinase

162 The RNA polymerase II (Pol II) transcription elongation factor, Elongin A (EloA), is methylated by PR

163 tention and demonstrate that the translation elongation factor eukaryotic elongation factor 1 alpha (

164 Targeting JMJD6 or other identified elongation factors extends survival in orthotopic xenogr

165 an easy passage for pol II, and the negative elongation factor facilitates termination at the end of

166 suggesting that nucleoprotein represents an elongation factor for the viral RNA polymerase.

167 ing lumen formation, the actin nucleator and elongation factor, formin-like 3 (fmnl3), localizes to E

168 84% sequence identity with the corresponding elongation factor from Escherichia coli Interestingly, t

169 The antibiotic fusidic acid (FA) targets elongation factor G (EF-G) and inhibits ribosomal peptid

170 nt crystal structures of G proteins, such as elongation factor G (EF-G) bound to the ribosome, as wel

171 bits bacterial protein synthesis by blocking elongation factor G (EF-G) catalyzed translocation of me

172 The universally conserved GTPase elongation factor G (EF-G) catalyzes the translocation o

173 ersally conserved ribosome-dependent GTPase [elongation factor G (EF-G) in prokaryotes and elongation

174 Elongation factor G (EF-G) is a universally conserved tr

175 ation step of prokaryotic protein synthesis, elongation factor G (EF-G), a guanosine triphosphatase (

176 rotated state is not a proper substrate for elongation factor G (EF-G), thus inhibiting translocatio

177 We observed significantly slower elongation factor G (EF-G)-catalyzed translocation throu

178 anied by large interdomain rearrangements of elongation factor G (EF-G).

179 of the small subunit head domain within the elongation factor G (GDP)-bound ribosome complex.

180 ent translational GTPase factors, along with elongation factor G and BPI-inducible protein A.

181 The translation factors, elongation factor G and ribosome recycling factor, are k

182 ional ribosome complexes and to compete with elongation factor G for interaction with pretranslocatio

183 compensated by mutations in the translation elongation factor G.

184 ational GTPase (trGTPase) factors along with elongation factors G and 4 (EF-G and EF4).

185 Transcription elongation factor GreA efficiently blocked Nun cross-lin

186 ng elongation pauses and their resolution by elongation factor GreA.

187 e loop, acting in concert with initiation or elongation factors, guides the nontemplate DNA in transc

188 genic region (HBS1L-MYB) between GTP-binding elongation factor HBS1L and myeloblastosis oncogene MYB

189 Our results show that Spt4/5 is a general elongation factor in archaea as its presence on all gene

190 herichia coli, sigma(70), can function as an elongation factor in vivo by loading directly onto the t

191 s circumstance, DksA acts as a transcription elongation factor in vivo.

192 the phosphorylation states of initiation and elongation factors in the core translation machinery.

193 or indirectly through IWS1, a transcription elongation factor involved in BR-regulated gene expressi

194 biochemical methods and identified the actin elongation factor Mena as a novel GRASP65-binding protei

195 ning protein member X1)-TUFM (Tu translation elongation factor mitochondrial) protein complex, promot

196 which is exacerbated by TEFM (transcription elongation factor mitochondrial).

197 these genes include the conserved cell wall elongation factors MreC and MreD(2,6,7), as well as a me

198 and vertebrates, DSIF together with negative elongation factor (NELF) associates with RNA polymerase

199 gation by acting as a decoy for the negative elongation factor (NELF) complex upon induction of immed

200 The role of the negative elongation factor (NELF) in maintaining HIV latency was

201 PARP-1 ADP-ribosylates and inhibits negative elongation factor (NELF), a protein complex that regulat

202 identify two new factors (BRD4 and negative elongation factor (NELF)-E) and to define their sites an

203 l) II, which requires the 4-subunit negative elongation factor (NELF).

204 sly characterized genes (e.g., transcription elongation factor NusA and tumor necrosis factor alpha-i

205 Furthermore, we show that the elongation factor NusA cooperates with UvrD in coupling

206 The bacterial transcription elongation factor, NusA, functions as an antiterminator

207 The transcription elongation factor NusG facilitates this termination proc

208 The bacterial transcription elongation factor NusG stimulates the Rho-dependent tran

209 lier upon the binding of unrelated bacterial elongation factor NusG, suggesting that this may be a ge

210 it is fully responsive to the transcription elongation factor NusG.

211 preclude the binding of tRNA and translation elongation factors on the ribosome.

212 Elongation factor P (EF-P) accelerates diprolyl synthesi

213 Elongation factor P (EF-P) binds to ribosomes requiring

214 Translation elongation factor P (EF-P) in Bacillus subtilis is requi

215 Elongation factor P (EF-P) is a conserved ribosome-bindi

216 Elongation factor P (EF-P) is a universally conserved ba

217 Strikingly, we show that elongation factor P (EF-P), traditionally known to allev

218 nship, we examined the bacterial translation elongation factor P (EF-P), which plays a critical role

219 ling at poly-Pro motifs is alleviated by the elongation factor P (EF-P).

220 ia, stalling at PPP motifs is rescued by the elongation factor P (EF-P).

221 nd MePCE captures the positive transcription elongation factor P-TEFb and prevents phosphorylation of

222 In contrast, the positive transcription elongation factor P-TEFb is a local explorer that oversa

223 orks by activating the human transcriptional elongation factor P-TEFb, a CDK9-cyclin T1 heterodimer t

224 block is associated with recruitment of the elongation factor P-TEFb, the co-activator GRIP1, the ch

225 er, and blockage of the assembly of the host elongation factor P-TEFb.

226 translation is carried out in the absence of elongation factor P.

227 evealed roles for the positive transcription elongation factor (P-TEFb) component Cyclin T1 (Ccnt1).

228 The positive transcription elongation factor (P-TEFb) is required for the transcrip

229 and late-stage transcription initiation and elongation factors, plus the capping and methylating enz

230 structures, whereas Enabled (Ena), an actin elongation factor, preferentially localizes to those in

231 Although elongation factors promote pause release leading to tran

232 y recruiting the host positive transcription elongation factor (pTEFb) to the RNA polymerase II trans

233 subunits AF4/FMR2 family member 4 (AFF4) and elongation factor RNA polymerase II 2 (ELL2) were recrui

234 bromo-adjacent homology and transcriptional elongation factor S-II domain, which we named REPRESSOR

235 dependent upon binding of the Sec-dedicated elongation factor SelB to a Sec insertion sequence (SECI

236 coding the UGA opal codon with a specialized elongation factor (SelB in bacteria) and an RNA structur

237 phosphate synthetase (SelD, SPS), a specific elongation factor (SelB), and a specific mRNA sequence k

238 pled chromatin changes mediated by conserved elongation factors Set2, Clr6CII, Spt6 and FACT.

239 Moreover, FPS and rubber elongation factor/small rubber particle protein gene fam

240 A striking expansion of the REF/SRPP (rubber elongation factor/small rubber particle protein) gene fa

241 of factors, including mRNA capping enzymes, elongation factors, splicing factors, 3'-end-processing

242 We found that targeting the transcription elongation factor Spt4 selectively decreased production

243 nes by binding a repeating domain within the elongation factor Spt5 (suppressor of Ty).

244 CTD) repeats of RNA polymerase II (Pol2) and elongation factor Spt5 are thought to orchestrate cotran

245 th Rpb1 (the largest RNAPII subunit) and the elongation factor Spt5 on their respective C-terminal do

246 the known RNA polymerase II (pol II) pausing/elongation factors SPT5 and TRIM28-KAP1-TIF1beta, and a

247 ing as a histone chaperone and transcription elongation factor, Spt6 counteracts repression by opposi

248 nalyze interactions of the EGFP and negative elongation factor subunit E (NELF-E) proteins with their

249 fic to S. pombe, that requires the conserved elongation factor subunit Spt4 and resembles promoter-pr

250 that targeted reduction in the transcription elongation factor SUPT4H1/SUPT5H reduces both sense and

251 ed sequence-specific synthetic transcription elongation factors (Syn-TEFs).

252 otein designated T. brevicorniculatum rubber elongation factor (TbREF) by using mass spectrometry to

253 using mycological culture, while translation elongation factor (TEF)-1alpha analysis of Fusarium isol

254 ound that interaction of human transcription elongation factor TEFM with mitochondrial RNA polymerase

255 show to be independent of the transcription elongation factor TEFM.

256 Transcript elongation factors (TEFs) are a heterogeneous group of p

257 transcripts is coordinated by transcription elongation factors (TEFs) such as polymerase-associated

258 slation (ribosomal proteins, initiation, and elongation factors), temperature-regulated transcription

259 cerevisiae RNAP II that a cleavage-deficient elongation factor TFIIS (TFIIS(AA)) enhances backtracked

260 By recruiting elongation factor TFIIS, Med25 also facilitates transcri

261 he interactions of RNAPII with transcription elongation factors TFIIS and TFIIF, which affect these p

262 NusG/Spt5 is a transcription elongation factor that assists in DNA-templated RNA synt

263 niversally conserved bacterial transcription elongation factor that binds RNA polymerase (RNAP).

264 DSIF or Spt4/5) is a conserved transcription elongation factor that both inhibits and stimulates tran

265 establish UvrD as a bona fide transcription elongation factor that contributes to genomic integrity

266 We now show that RECQL5 is a general elongation factor that is important for preserving genom

267 s of the roles of translation initiation and elongation factors that assist the ribosome in binding t

268 is mechanism of action is similar to that of elongation factors that enhance the processivity of mult

269 s of ATP synthase and its relatives, and the elongation factor thermo unstable.

270 the peptide elf18 derived from the bacterial elongation factor thermo-unstable.

271 ve opportunistic pathogen that trimethylates elongation factor-thermo-unstable (EF-Tu) on lysine 5.

272 omain-containing proteins, and transcription elongation factors to mediate chromatin remodeling and r

273 requires the recruitment of transcriptional elongation factors to rapidly induce innate response gen

274 In the cell, the binding of two translation elongation factors to the same general region of the rib

275 tations that alter the coiled-coil domain of elongation factor Ts (EF-Ts) and confer resistance to th

276 e presence of the nucleotide exchange factor elongation factor Ts (EF-Ts).

277 The process requires the GTPase factors elongation factor Tu (EF-Tu) and EF-G.

278 programmed ribosome in ternary complex with elongation factor Tu (EF-Tu) and GTP and then, again, in

279 receptor (EFR) recognizes the bacterial PAMP elongation factor Tu (EF-Tu) and its derived peptide elf

280 We identify elongation factor Tu (EF-Tu) as a PPHD substrate, which

281 We show Elongation factor Tu (Ef-Tu) moonlights on the surface o

282 ontained within a similar PGH motif found in elongation factor Tu (EF-Tu) that is required for GTP hy

283 We find that CdiA-CT(EC869) binds to elongation factor Tu (EF-Tu) with high affinity and this

284 GTP hydrolysis by elongation factor Tu (EF-Tu), a translational GTPase tha

285 essential housekeeping protein, translation elongation factor Tu (EF-Tu).

286 lecting cognate aminoacyl-tRNAs delivered by elongation factor Tu (EF-Tu).

287 phosphorylation of the universally conserved elongation factor Tu (EF-Tu).

288 AG amber codon--inserts Sec depending on the elongation factor Tu (EF-Tu).

289 omplex with its cognate immunity protein and elongation factor Tu (EF-Tu).

290 f bacterial flagellin (flg22) or translation elongation factor Tu (elf18).

291 roteins were downregulated and identified as elongation factor Tu and GAPDH.

292 n of aminoacyl-tRNAs in ternary complex with elongation factor Tu and GTP on messenger RNA-programmed

293 The elongation factor Tu GTP binding domain-containing prote

294 ves the elf18 peptide derived from bacterial elongation factor Tu, is activated upon ligand binding b

295 d the Ser-tRNA(Thr) level in the presence of elongation factor Tu.

296 gests a common GTPase mechanism for EF-G and elongation factor Tu.

297 During protein synthesis, elongation factor-Tu (EF-Tu) bound to GTP chaperones the

298 ith peptides derived from flagellin (flg22), elongation factor-Tu (elf18), or an endogenous protein (

299 XPD and TUFM, a mitochondrial Tu translation elongation factor was detected to be physically interact

300 kinesin-1 adaptor protein, Fasiculation and Elongation Factor zeta 1 (FEZ1).