ライフサイエンスコーパス: elongation factor Tu

1 e 2) and a gene from the plastid genome (the elongation factor Tu).

2 ibosomal peptidyl transferase center and the elongation factor Tu.

3 t is unable to substitute for either EF-G or elongation factor Tu.

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

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

6 d further ensured through collaboration with elongation factor Tu.

7 ding to either the 50 S ribosomal subunit or elongation factor Tu.

8 and the presence and the absence of AMP and elongation factor Tu.

9 nd presence of inorganic pyrophosphatase and elongation factor Tu.

10 second domain in the eukaryotic translation elongation factor-Tu.

11 y cleaves the host translation factor EF-Tu (elongation factor Tu) after it has formed a weak complex

12 e tmRNA enters the ribosome with the help of elongation factor Tu and a protein factor called small p

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

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

15 is comprised of the cognate aminoacyl-tRNA, elongation factor Tu and GTP.

16 yl-tRNA (aa-tRNA), in a ternary complex with elongation factor-Tu and GTP, enters the aminoacyl (A) s

17 During protein synthesis, the two elongation factors Tu and G alternately bind to the 50S

18 The process is normally catalyzed by the elongation factors Tu and G; however, the reactions can

19 ture of the complex between Escherichia coli elongation factors Tu and Ts (EF-Tu.Ts) and subsequent m

20 d include type IV secretion system proteins, elongation factor Tu, and members of the MSP2 superfamil

21 ree beta-lactamases, three thioredoxins, one Elongation Factor Tu, and one RuBisCO, all of them theor

22 associated with the S1 subunit, site II with elongation factor Tu, and polymerization with the viral

23 ted molecular patterns, including Flagellin, Elongation Factor Tu, and the plant phytocytokine Golven

24 stal structure of a tmRNA fragment, SmpB and elongation factor Tu bound to the ribosome at 3.2 angstr

25 ts decoding site, to accelerate the rates of elongation factor-Tu-catalyzed GTP hydrolysis and riboso

26 e can position either elongation factor G or elongation factor Tu complexed with an aminoacylated tra

27 te (A site) of the ribosome via a multistep, elongation factor-Tu dependent process.

28 protein of choice is possible by exploiting elongation factor Tu-dependent reassignment of UAG codon

29 earlier that surface-localized M. pneumoniae elongation factor Tu (EF-Tu(Mp)) mediates binding to the

30 6-kDa protein as mitochondrial translational elongation factor Tu (EF-Tu(mt)).

31 In plants, the bacterial MAMPs flagellin and elongation factor Tu (EF-Tu) activate distinct, phylogen

32 s as a nucleotide-exchange factor by binding elongation factor Tu (EF-Tu) and accelerating the GDP di

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

34 is critical for triggering GTP hydrolysis on elongation factor Tu (EF-Tu) and elongation factor G (EF

35 lying the orderly, sequential association of elongation factor Tu (EF-Tu) and elongation factor G (EF

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

37 anslating ribosome in a ternary complex with elongation factor Tu (EF-Tu) and GTP.

38 some in a ternary complex with the G-protein elongation factor Tu (EF-Tu) and GTP.

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

40 5 and the 30 kDa proteins identified them as elongation factor Tu (EF-Tu) and pyruvate dehydrogenase

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

42 Elongation factor Tu (EF-Tu) binds all elongator aminoac

43 Elongation factor Tu (EF-Tu) binds and loads elongating

44 Elongation factor Tu (EF-Tu) binds to all standard amino

45 r-cognate tRNAs delivered to the ribosome by Elongation Factor Tu (EF-Tu) can follow divergent pathwa

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

47 Elongation factor Tu (EF-Tu) delivers aminoacyl-tRNA to

48 The crystal structure of intact elongation factor Tu (EF-Tu) from Escherichia coli in GD

49 The elongation factor Tu (EF-Tu) from Pseudomonas aeruginosa

50 ydroxyl groups in stabilizing a complex with elongation factor Tu (EF-Tu) from Thermus thermophilus.

51 Recent evidence indicates that translation elongation factor Tu (EF-Tu) has a role in the cell in a

52 It was long known that elongation factor Tu (EF-Tu) is N-terminally acetylated,

53 faciens microbe-associated molecular pattern elongation factor Tu (EF-Tu) is perceived by orthologs o

54 Elongation factor Tu (EF-Tu) is responsible for the deli

55 In translation, elongation factor Tu (EF-Tu) molecules deliver aminoacyl

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

57 rvations of cross-reactivity with the 45-kDa elongation factor Tu (EF-Tu) protein from Chlamydia trac

58 cerevisiae tRNA Phe to Thermus thermophilus elongation factor Tu (EF-Tu) revealed that much of the s

59 The universally conserved His-66 of elongation factor Tu (EF-Tu) stacks on the side chain of

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

61 ator aminoacyl-tRNAs to Thermus thermophilus elongation factor Tu (EF-Tu) were determined.

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

63 As (aa-tRNAs) have evolved to bind bacterial elongation factor Tu (EF-Tu) with uniform affinities, mu

64 d for their affinity to Thermus thermophilus elongation factor Tu (EF-Tu)*GTP by using a ribonuclease

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

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

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

68 By analogy to elongation factor Tu (EF-Tu), SelB is expected to contro

69 he cellular levels of alanine synthetase and elongation factor TU (EF-Tu), the amount of tRNA and the

70 e ribosome is limited by its poor binding to elongation factor Tu (EF-Tu), the yield of incorporation

71 ein synthesis is promoted by two G proteins, elongation factor Tu (EF-Tu), which delivers aminoacyl t

72 e triphosphatase (GTPase) factors, including elongation factor Tu (EF-Tu), which delivers aminoacyl-t

73 inoacyl-tRNA is delivered to the ribosome by elongation factor Tu (EF-Tu), which hydrolyzes guanosine

74 ne cluster responsible for production of the elongation factor Tu (EF-Tu)-targeting 29-member thiazol

75 stimulates the activity of Escherichia coli elongation factor Tu (EF-Tu).

76 sfer RNA to the ribosome is catalysed by the elongation factor Tu (EF-Tu).

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

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

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

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

81 e is energized by the GTPase reaction of the elongation factor Tu (EF-Tu).

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

83 inal part binds GTP and tRNA in analogy with elongation factor Tu (EF-Tu).

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

85 e misacylated tRNAs for Thermus thermophilus elongation factor Tu (EF-Tu).GTP were determined using a

86 ported that surface-associated M. pneumoniae elongation factor Tu (EF-Tu, also called MPN665) serves

87 at overexpressed Hsp33 specifically binds to elongation factor-Tu (EF-Tu) and targets it for degradat

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

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

90 pattern recognition receptors (PRRs) such as ELONGATION Factor-TU (EF-TU) RECEPTOR (EFR) and FLAGELLI

91 s GTPase activating protein (RasGAP) and the elongation factor-Tu (EF-Tu) with a 1 W mechanism is sti

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

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

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

95 '-yl imidodiphosphate) but not [14C]Phe-tRNA.elongation factor Tu.GDP.kirromycin increased labeling o

96 The elongation factor Tu GTP binding domain-containing prote

97 s as good as between elongation factor G and elongation factor Tu-guanosine-5'(beta,gamma-imido)triph

98 he co-crystal structure of Thermus aquaticus elongation factor Tu.guanosine 5'- [beta,gamma-imido]tri

99 Binding of the ternary complex [14C]Phe-tRNA-elongation factor Tu.guanyl-5'-yl imidodiphosphate) but

100 Elongation factor Tu in Chlamydomonas reinhardtii is a c

101 tation, driven by a conformational change in elongation factor Tu involving GTP hydrolysis, transorie

102 For example, Elongation Factor Tu is predominantly single copy, and 9

103 eEF1A, the eukaryotic homologue of bacterial elongation factor Tu, is a well characterized translatio

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

105 to a mechanistic model for GTP hydrolysis on elongation factor Tu mediated by aa-tRNA.

106 Glucose 6-phospatase, alcohol dehydrogenase, elongation factor-TU, methylglutaryl coenzyme A (CoA), a

107 Reducing levels of translation elongation factor Tu or slowing translation initiation o

108 major antigenic outer membrane protein MgPa, elongation factor Tu, pyruvate dehydrogenase E1alpha, an

109 Using the LRR-RK ELONGATION FACTOR TU RECEPTOR (EFR) as a model, we set o

110 Previous studies have shown that bacterial elongation factor Tu receptor (EFR), a pattern-recogniti

111 h repeat (LRR)-RK subfamily XIIa member EFR (elongation factor Tu receptor) and phosphorylation-depen

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

113 A similar approach with swaps between the Elongation factor-Tu receptor and BAK1 also resulted in

114 f26 corresponding to bacterial flagellin and elongation factor Tu, respectively.

115 Elongation factor Tu seems to compete with the RNA degra

116 -kDa protein was 100% identical to bacterial elongation factor Tu, suggesting a role as a possible ch

117 mpete for aminoacyl-tRNAs in the presence of elongation factor Tu, suggesting that YbaK acts before r

118 Cleavage of SRL slightly affected binding of elongation factor Tu ternary complex (EF-Tu*GTP*tRNA) to

119 Addition of elongation factor Tu to the aaRS.tRNA complex stimulates

120 70-80% in levels of mRNA for the chloroplast elongation factor Tu (tufA) in asynchronously growing Ch

121 Levels of mRNA for the chloroplast-encoded elongation factor Tu (tufA) showed a dramatic daily osci

122 Elongation factor Tu variants with rarely occurred amino

123 e of the most abundant proteins in the cell, elongation factor Tu, was found to be more oxidatively m

124 1, glutamate dehydrogenase, gamma-actin, and elongation factor Tu were identified as increasingly car

125 identify amino acids in Thermus thermophilus elongation factor Tu which contribute to its specificity