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1  distinct active site structures to catalyze tRNA aminoacylation.
2 ases had the same two complementary modes of tRNA aminoacylation.
3  stem and is directly responsible for proper tRNA aminoacylation.
4 tural mechanisms ensuring the selectivity of tRNA aminoacylation.
5 the tRNA during amino acid activation and/or tRNA aminoacylation.
6 the peptide is not important for the kcat of tRNA aminoacylation.
7  the catalytic efficiency and specificity of tRNA aminoacylation.
8  synthetic and native tRNA and in inhibiting tRNA aminoacylation.
9 o each other in playing an important role in tRNA aminoacylation.
10 ucines in the leucine heptad repeats reduced tRNA aminoacylation.
11 nylate synthesis and the transition state of tRNA aminoacylation.
12 acids is highly sensitive to the kinetics of tRNA aminoacylation.
13 ative to tyrosine, and significantly reduces tRNA aminoacylation.
14 ll function, requires accurate transfer RNA (tRNA) aminoacylation.
15 t motif 2 loop residues are not critical for tRNA aminoacylation activity of the human enzyme.
16                Herein, it is documented that tRNA aminoacylation also occurs in yeast nuclei and is i
17 catalyzing aminoacyl-adenylate formation and tRNA aminoacylation and a second editing or proofreading
18 N-acylphosphoramidates, are useful probes of tRNA aminoacylation and enzyme mechanism, and have poten
19 lar ATP is utilized in protein synthesis via tRNA aminoacylation and guanosine triphosphate regenerat
20  assays show that m(1)G37 deficiency reduces tRNA aminoacylation and in some cases peptide-bond forma
21                           Reports of nuclear tRNA aminoacylation and its role in tRNA nuclear export
22 os1p, is also unessential, we tested whether tRNA aminoacylation and Los1p operate in alternative tRN
23  Protein translation is orchestrated through tRNA aminoacylation and ribosomal elongation.
24 rd a platform for the synthesis by enzymatic tRNA aminoacylation and ribosomal translation of cyclic
25 s protocol provides robust quantification of tRNA aminoacylation and we provide an end-to-end method
26 Thus, association in a MARS complex enhances tRNA-aminoacylation and contributes to parasite fitness.
27 these two sites lead to rigorous accuracy in tRNA aminoacylation, and both activities are essential t
28 ty of both CysRS and tRNA(Cys) for efficient tRNA aminoacylation, and highlight the energetic costs o
29  tRNA function by enhancing tRNA maturation, tRNA aminoacylation, and translation, thereby improving
30 A modifying enzymes enhance tRNA maturation, tRNA aminoacylation, and tRNA function during protein sy
31 onsible for amino acid supply, transfer RNA (tRNA) aminoacylation, and protein folding.
32                   Recognition strategies for tRNA aminoacylation are ancient and highly conserved, ha
33 understanding the efficiency and fidelity of tRNA aminoacylation as a function of tRNA sequence, modi
34 term evolution of amino acid specificity and tRNA aminoacylation, both essential for expanding the ge
35 ginine residue (R144) that was essential for tRNA aminoacylation but played no role in amino acid act
36 h LeuRS improves the catalytic efficiency of tRNA aminoacylation by both LysRS and ProRS.
37 ssion of the genetic code depends on precise tRNA aminoacylation by cognate aminoacyl-tRNA synthetase
38 tion of the genetic code depends on accurate tRNA aminoacylation by cognate aminoacyl-tRNA synthetase
39 butes to translational fidelity by enhancing tRNA aminoacylation by ProRS.
40                       Accurate transfer RNA (tRNA) aminoacylation by aminoacyl-tRNA synthetases contr
41 hat association in the MARS complex enhances tRNA-aminoacylation efficiency, which is in part depende
42                                    Assays of tRNA aminoacylation established the specific attachment
43 tion, editing mechanisms evolved to maintain tRNA aminoacylation fidelity.
44  and provides insights into protein-mediated tRNA aminoacylation, folding, localization, trafficking,
45 ases to improve the anticodon specificity of tRNA aminoacylation from bacteria to humans, possibly to
46 indicating the evolution of determinants for tRNA aminoacylation from E. coli to yeast to human and t
47 ough many aaRS CMT mutants result in loss of tRNA aminoacylation function, animal genetics studies de
48                              We propose that tRNA aminoacylation functions in one of at least two par
49 he availability of nutrients to cells and by tRNA aminoacylation in the nucleus.
50                              The accuracy of tRNA aminoacylation in vivo is uncertain, however, and m
51   These results indicate that suppression of tRNA aminoacylation is able to inhibit p70(s6k) activity
52                                      Because tRNA aminoacylation is fundamental to cell growth, these
53 d by deacylated tRNA, which accumulates when tRNA aminoacylation is limited by lack of substrates or
54 he cells are viable, indicating that nuclear tRNA aminoacylation is not required for all tRNA nuclear
55 rming that the rate of the chemical step for tRNA aminoacylation (k(chem)) exceeds the steady-state r
56 ts global translation in this organism; that tRNA aminoacylation levels exert, at most, weak control
57  and glycine codons through the reduction of tRNA aminoacylation levels.
58             Our understanding of the complex tRNA aminoacylation machinery in metazoans also remains
59  confirmed the dysfunction in amino acid and tRNA aminoacylation metabolic processes, and highlighted
60            During the first chemical step of tRNA aminoacylation, noncognate amino acids that are sma
61 ion of the unnatural base pair into mRNA and tRNA, aminoacylation of the tRNA with a non-canonical am
62 emonstrate a potential role for the indirect tRNA aminoacylation pathway in regulating translational
63 ular aminoacyl-tRNA synthetases and promotes tRNA aminoacylation, polysome formation, and protein syn
64 ssion promotes sarcomagenesis by stimulating tRNA aminoacylation, protein synthesis, and tumor cell g
65 erization of the baseline landscape of plant tRNA aminoacylation rates and demonstrates an approach f
66               The limited selectivity in the tRNA aminoacylation reaction appears to be due to ineffi
67 thetic aminoacyl-adenylates as substrates in tRNA aminoacylation reaction may provide a way for incor
68  the transition states for both steps of the tRNA aminoacylation reaction.
69          Most mutants are less attenuated in tRNA aminoacylation than in adenylate synthesis, suggest
70 onformation transitions in various stages of tRNA aminoacylation that are associated with catalysis.
71 erminal domain for amino acid activation and tRNA aminoacylation through a domain-domain interaction.
72 diol contribution affects steps ranging from tRNA aminoacylation to peptide bond formation.
73                  A highly sensitive assay of tRNA aminoacylation was developed that directly measures
74                                      Nuclear tRNA aminoacylation was proposed to provide a proofreadi
75            A synthetic active site catalyzes tRNA aminoacylation, while an editing active site hydrol