ライフサイエンスコーパス: elongation factor

1 iated with hyper-phosphorylation of the Spt5 elongation factor.

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

3 esis activities that required initiation and elongation factors.

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

5 anslation initiation factors and translation elongation factors.

6 Here, we focused on the elongation factor 1 (EF1) family of viral translational

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

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

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

10 beta-actin (Actin), beta-tubulin (Tubulin), elongation factor 1 alpha (EF1alpha), glyceraldehyde-3 p

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

12 s have indicated that eukaryotic translation elongation factor 1 delta (eEF1D) may associate with RNP

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

14 ted and disulfide-bonded proteins, including elongation factor 1-alpha1 and mouse serum albumin, and

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

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

17 drial fission factor (Mff) and mitochondrial elongation factor 1/2 (MIEF1/2) interact with and recrui

18 Stretching the GUVs in the range of elongation factors 1-1.3 led to an overall decrease in c

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

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

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

22 -like 13) dimethylation of eEF1A (eukaryotic elongation factor 1A) lysine 55 (eEF1AK55me2) is utilize

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

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

25 re we show that, when acetylated, eukaryotic elongation factor 1A1 (eEF1A1) negatively regulates PNS

26 We discovered that a C parvum translation elongation factor 1alpha (CpEF1alpha) was discharged fro

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

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

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

30 by phosphorylating its substrate, eukaryotic elongation factor 2 (eEF-2), thereby reducing its affini

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

32 through inhibition of eukaryotic translation elongation factor 2 (eEF2) via adenosine diphosphate (AD

33 ssociated hyperphosphorylation of eukaryotic elongation factor 2 (eEF2) was blunted with selective AM

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

35 is in a mouse liver by targeting translation elongation factor 2 (eEF2) with RNAi.

36 In the periphery, OXT activates eukaryotic elongation factor 2 (eEF2), an essential mediator of pro

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

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

39 lation of mRNA translation factor eukaryotic elongation factor 2 (eEF2), which results in inhibition

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

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

42 ), beta actin (ACTB), eukaryotic translation elongation factor 2 (EF2), glyceraldehyde-3-phosphate de

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

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

45 ed diphtheria toxin (DT), which binds to the elongation factor 2 and blocks protein synthesis, can sp

46 Eukaryotic elongation factor 2 kinase (eEF-2K), an atypical calmodu

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

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

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

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

51 Eukaryotic elongation factor 2 kinase (eEF2K) negatively regulates

52 protein synthesis by inactivating eukaryotic elongation factor 2 kinase (eEF2K), which, when active,

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

54 modification of histidine 715 in eukaryotic elongation factor 2, resulted in tagraxofusp resistance.

55 inhibition at the fungal protein eukaryotic elongation factor 2.

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

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

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

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

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

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

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

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

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

65 tein 5 (WBP5), also known as Transcriptional Elongation Factor A like 9 (TCEAL9) has been proposed as

66 Brain Expressed X-Linked (Bex)/Transcription elongation factor A-like (Tceal) superfamily members Bex

67 iator complex and the positive transcription elongation factor (Abstract figure).

68 transcription regulation shapes translation elongation factor activity and exposes how eEF2 is integ

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

70 ation factors MYC, BRD4, PAF1, and the super elongation factors AFF4 and ELL2.

71 the translation initiation factor initiation elongation factor alpha (eIF2alpha).

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

73 stitutively evicts Spt5, a key transcription elongation factor and TC-NER repressor, from the chromat

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

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

76 n DNA damage repair factors, transcriptional elongation factors and E3 ubiquitin ligases.

77 teins upon heat shock, including translation elongation factors and histones.

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

79 fication enzymes, translation-initiation and elongation factors, and ribosomal proteins.

80 ion initiation, whether cellular translation elongation factors are responsive to inflammation and in

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

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

83 -neurons, we focus here on the role of actin elongation factors as potential regulators of developmen

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

85 Transcript elongation factors associate with elongating RNA polymer

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

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

88 by additional loss of positive transcription elongation factor b (P-TEFb) activity, a key factor in p

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

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

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

92 The Positive Transcription Elongation Factor b (P-TEFb) phosphorylates Ser2 residue

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

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

95 ity by activating the positive transcription elongation factor b (P-TEFb) via its release from the in

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

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

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

99 The positive transcription elongation factor b (P-TEFb), composed of CDK9 and cycli

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

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

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

103 ) to recruit the host positive transcription elongation factor b (pTEFb) complex onto the viral trans

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

105 with both 7SK RNA and positive transcription elongation factor b are critical for HEXIM1 subdiffusion

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

107 f Pol II pausing, and positive transcription elongation factor b releases (P-TEFb) paused complex aft

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

109 tion with the P-TEFb (positive transcription elongation factor b) kinase complex and for its recruitm

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

111 c A1 subunit (Stx2A1) binds to the conserved elongation factor binding C-terminal domain (CTD) of rib

112 he Arc gene, facilitating increased negative elongation factor binding to the Arc promoter and decrea

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

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

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

116 Elongation factor-catalyzed GTP hydrolysis is a key reac

117 ivators BRD4 and MED1, and the transcription elongation factor CDK9 for transcription.

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

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

120 Transcription elongation factors dramatically affect RNAP pausing in v

121 ngation complex, EC*, encompassing the human elongation factors DSIF, PAF1 complex (PAF) and SPT6.

122 involving p300-mediated acetylation of a key elongation factor during genotoxic stress.

123 al P-stalk stimulates the GTPase activity of elongation factors during translation, we propose that t

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

125 ognostic value, we have developed a Negative Elongation Factor E (NELFE)-Dependent MYC Target (NDMT)

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

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

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

129 A2, encoding the tissue-specific translation elongation factor eEF1A2, have been shown to cause neuro

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

131 Elongation factor eEF2 with a GTP analog stabilizes the

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

133 phosphorylation of the critical translation elongation factor eEF2, which catalyzes the protein synt

134 beak, two binding regions of the eukaryotic elongation factor eEF2.

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

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

137 ne, coding for the mitochondrial translation elongation factor EF-Ts.

138 s is enhanced by surface-exposed translation elongation factor EF-Tu carrying a Lys-5 trimethylation,

139 each aminoacyl-tRNA that is delivered by the elongation factor EF-Tu(1).

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

141 the nucleotide-dependent switch mechanism of elongation factor (EF) Tu as a prototypical molecular sw

142 facilitated by the guanosine triphosphatase elongation factor (EF)-Tu.

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

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

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

146 of regulating stability and functions of key elongation factor ELL for expression of diverse sets of

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

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

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

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

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

152 und that regrowth in vivo requires the actin elongation factors Ena and profilin, but not the formins

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

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

155 complex (CTK complex) is known as a positive elongation factor for many inducible genes by releasing

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

157 84% sequence identity with the corresponding elongation factor from Escherichia coli Interestingly, t

158 Thus, we show that different linear actin elongation factors function in distinct contexts even wi

159 ly contain mutations in the gene encoding an elongation factor, FusA1.

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

161 led into subunits by two conserved proteins, elongation factor G (EF-G) and the ribosome recycling fa

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

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

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

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

166 In elongation factor G (EF-G), a highly conserved protein c

167 , ribosome-recycling factor (RRF) and GTPase elongation factor G (EF-G), synergistically split 100S r

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

169 The elongation factor G (EF-G)-catalyzed translocation of mR

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

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

172 ly of proteins that bind to the drug target (Elongation factor G [EF-G]) and promote dissociation of

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

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

175 ve dissected early folding events of nascent elongation factor G, a multi-domain protein that require

176 n, encompassing the first 293 amino acids of elongation factor G.

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

178 some in complex with the human mitochondrial elongation factor G1 (EF-G1(mt)) in three distinct confo

179 s or through the inhibition of mitochondrial elongation factor G1 (mEF-G1) progressively compromised

180 Transcription elongation factor GreA efficiently blocked Nun cross-lin

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

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

183 of one gene, lepA, a translation-associated elongation factor, increased rifampicin tolerance in all

184 Negative elongation factor is essential for endometrial function.

185 This universally conserved transcription elongation factor is known as Spt5 in archaeal and eukar

186 ation defect is explained by the loss of the elongation factors LEO1 and CDC73, part of PAF1 complex,

187 Bodian-Diamond syndrome that cooperates with elongation factor-like GTPase 1 (EFL1) to catalyze relea

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

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

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

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

192 t polypeptides, the guanosine triphosphatase elongation factors mtEF-Tu and mtEF-G1, and the Oxa1L tr

193 and enrichment of the positive transcription elongation factors MYC, BRD4, PAF1, and the super elonga

194 did not impact the recruitment of other key elongation factors, namely, Spt5, Spt6, and the FACT com

195 Negative elongation factor (NELF) and DRB sensitivity inducing fa

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

197 is marked by co-localization of the negative elongation factor (NELF) complex and facilitated by PU.1

198 arly transcription, mediated by the negative elongation factor (NELF) complex, allows cells to coordi

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

200 II and prevents the release of the negative elongation factor (NELF), thus stabilizing Pol II promot

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

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

203 function has been attributed to the negative elongation factor (NELF).

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

205 pre-termination complex" (PTC) with RNAP and elongation factors NusA and NusG, which stabilize the PT

206 The transcription elongation factor NusG facilitates this termination proc

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

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

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

210 (RNAP), the ribosome, and the transcription elongation factors NusG and NusA.

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

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

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

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

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

216 intenance and to have a strong dependence on elongation factor P (EFP).

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

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

219 interaction with the positive transcription elongation factor P-TEFb.

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

221 ion is independent of positive transcription elongation factor P-TEFb.

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

223 evating levels of the positive transcription elongation factor (P-TEFb), instating a large proliferat

224 Elongation factor Paf1C regulates several stages of the

225 These data indicate that elongation factors play an important role in promoter es

226 ngation factors suggests that both conserved elongation factors play important roles in transcription

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

228 Although elongation factors promote pause release leading to tran

229 as temporary backtracking and transcription elongation factor S-II (TFIIS)-dependent RNA cleavage, o

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

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

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

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

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

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

236 Binding of labeled elongation factor Spt4/5 to DNA typically followed RNApI

237 ancy and high occupancy of the transcription elongation factor Spt4/Spt5 suppresses TC-NER in Rad26-d

238 ain bound to early ECs, while levels of core elongation factors Spt4-Spt5, Paf1C, Spt6-Spn1, and Elf1

239 histone H2B (H2Bub1) and phosphorylation of elongation factor Spt5 by cyclin-dependent kinase 9 (Cdk

240 The transcription elongation factor Spt5 is conserved from bacteria to hum

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

242 The transcription elongation factor Spt6 and the H3K36 methyltransferase S

243 that the histone chaperone and transcription elongation factor Spt6 spatially and temporarily coincid

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

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

246 essentiality of both conserved transcription elongation factors suggests that both conserved elongati

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

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

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

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

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

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

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

254 e used a mutant version of the transcription elongation factor TFIIS (TFIIS(mut)), aiming to specific

255 The elongation factor TFIIS stimulates the intrinsic transcr

256 the vRNAP subunit Rpo30 resembles the Pol II elongation factor TFIIS, and that NPH-I resembles chroma

257 By recruiting elongation factor TFIIS, Med25 also facilitates transcri

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

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

260 L1 (also known as ELL) is the only bona fide elongation factor that directly stimulates transcription

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

262 age and remodel nucleosomes or transcription elongation factors that facilitate Pol II nucleosome byp

263 Ena/VASP tetramers are processive actin elongation factors that localize to diverse F-actin netw

264 translation elongation requires an essential elongation factor, the ABCF ATPase eEF3.

265 majority of organisms possess transcription elongation factors, the functionally similar bacterial G

266 In this study, we identified elongation factor thermo-unstable (EF-Tu), l-lactate deh

267 sion are aminoacyl-tRNA synthetases (aaRSs), elongation factor thermo-unstable (EF-Tu), the ribosome,

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

269 istone-based chromatin and thus must rely on elongation factors to accelerate transcription through c

270 stone-modification enzymes and transcription elongation factors to aid transcription through nucleoso

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

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

273 terminal domain (CTD) of Pol II and negative elongation factors to release Pol II from promoter-proxi

274 concentration dependent interactions between elongation factors, tRNAs, ribosomes, and other factors

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

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

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

278 osomal translation, the translational GTPase elongation factor Tu (EF-Tu) delivers a transfer RNA (tR

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

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

281 ed with a ternary complex (TC) consisting of elongation factor Tu (EF-Tu), aminoacyl tRNA and GTP, an

282 in protein synthesis is a ternary complex of elongation factor Tu (EF-Tu), aminoacyl-tRNA (aa-tRNA),

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

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

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

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

287 n by binding and stabilizing the translation elongation factor Tu (EF-Tu).

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

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

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

291 The elongation factor Tu GTP binding domain-containing prote

292 Elongation factor Tu seems to compete with the RNA degra

293 uginosa methyltransferase EftM trimethylates elongation factor-Tu (EF-Tu) on lysine 5 to form a post-

294 the long-term effects of Onc112 on ribosome, elongation factor-Tu (EF-Tu), and DNA spatial distributi

295 ultiple receptor-like kinases, including the ELONGATION FACTOR-TU RECEPTOR (EFR) and PEP1 RECEPTOR1 (

296 l genomes, and here we demonstrate that both elongation factors, via different mechanisms, can accele

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

298 d 30S ribosomal protein subunit variants and elongation factors were positively correlated with hour

299 SCAF8 is an RNAPII elongation factor, whereas SCAF4 is required for correct

300 s long been considered to be a transcription elongation factor whose ability to destabilize nucleosom