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1 We have previously shown that limitation for isoleucyl-tRNA can initiate a ribosome bypass when an AU
2 t less error-prone and kinetically optimized isoleucyl-tRNA(Ile) synthesis under cellular conditions.
3 olo-form while MupM is a mupirocin-resistant isoleucyl tRNA synthase, preventing self-poisoning.
4 d mutations in the P. falciparum cytoplasmic isoleucyl tRNA synthetase (cIRS).
5 ity determinant for proper aminoacylation by isoleucyl tRNA synthetase (IleRS) and codon recognition
6  orf, whose function is unknown; divIVA; and isoleucyl tRNA synthetase (ileS).
7                         In cattle, cytosolic isoleucyl-tRNA synthetase (IARS) missense mutations caus
8              For example, the close homologs isoleucyl-tRNA synthetase (IleRS) and valyl-tRNA synthet
9                       Using Escherichia coli isoleucyl-tRNA synthetase (IleRS) as a model enzyme, we
10                                              Isoleucyl-tRNA synthetase (IleRS) catalyzes transfer of
11                             Escherichia coli isoleucyl-tRNA synthetase (IleRS) exploits both the tRNA
12                                              Isoleucyl-tRNA synthetase (IleRS) is an aminoacyl-tRNA s
13                                              Isoleucyl-tRNA synthetase (IleRS) is unusual among amino
14 milar amino acids, valine and isoleucine, by isoleucyl-tRNA synthetase (IleRS) results, in part, from
15 he rate of activation of 5TFI by the E. coli isoleucyl-tRNA synthetase (IleRS) yielded a specificity
16              Leucyl-tRNA synthetase (LeuRS), isoleucyl-tRNA synthetase (IleRS), and valyl-tRNA synthe
17              Leucyl-tRNA synthetase (LeuRS), isoleucyl-tRNA synthetase (IleRS), and valyl-tRNA synthe
18 he Staphylococcus aureus ileS gene, encoding isoleucyl-tRNA synthetase (IleRS), contains a long mRNA
19        We show that in the synthetic site of isoleucyl-tRNA synthetase (IleRS), Nva and Val are activ
20                       Here, it is shown that isoleucyl-tRNA synthetase (IleRS), which occasionally mi
21 e analog that inhibits the essential enzyme, isoleucyl-tRNA synthetase (IleRS).
22 ereas mupirocin targets the essential enzyme isoleucyl-tRNA synthetase (IleRS).
23 electively inhibiting eukaryotic cytoplasmic isoleucyl-tRNA synthetase (IleRS).
24 Administration of mupirocin, an inhibitor of isoleucyl-tRNA synthetase activity, resulted in changes
25                             Here I show that isoleucyl-tRNA synthetase aminoacylates CoA-SH with vali
26 ied small molecules that inhibit recombinant isoleucyl-tRNA synthetase and that are lethal to the par
27 , which are also conserved in the homologous isoleucyl-tRNA synthetase and valyl-tRNA synthetase edit
28              Together with prior analyses of isoleucyl-tRNA synthetase and valyl-tRNA synthetase, the
29                                        Using isoleucyl-tRNA synthetase as an example, we placed mutat
30 s reliance on post-transfer editing, whereas isoleucyl-tRNA synthetase differs in retaining a distinc
31 ese eukaryote-like features, M. tuberculosis isoleucyl-tRNA synthetase exhibited highly specific cros
32             As an example, discrete sites in isoleucyl-tRNA synthetase for amino acid activation and
33 y halted before isoleucine codon by reducing isoleucyl-tRNA synthetase from reaction mixture of in vi
34 Methanosarcina species by mutagenesis of the isoleucyl-tRNA synthetase gene (ileS) from Methanosarcin
35              In this study, a novel group of isoleucyl-tRNA synthetase gene (ileS) T box leader seque
36               The monomeric Escherichia coli isoleucyl-tRNA synthetase has a zinc-containing peptide
37   We showed by RNAi knockdown that T. brucei isoleucyl-tRNA synthetase is essential for the parasites
38                             Escherichia coli isoleucyl-tRNA synthetase is one of five closely related
39                                 For example, isoleucyl-tRNA synthetase misactivates valine (to produc
40                      In the absence of tRNA, isoleucyl-tRNA synthetase misactivates valine, while val
41 Substitution of a homologous CP1 domain from isoleucyl-tRNA synthetase or mutation within the LeuRS C
42   Here we report that a specific mutation in isoleucyl-tRNA synthetase prevents editing by blocking t
43             Recent mutational analysis of an isoleucyl-tRNA synthetase showed that discrimination of
44 mutations in a presumptive "hinge region" of isoleucyl-tRNA synthetase that is situated between the t
45    Valyl-tRNA synthetase, a close homolog of isoleucyl-tRNA synthetase, misactivates threonine, alpha
46  eukaryote-like features, and unlike E. coli isoleucyl-tRNA synthetase, the M. tuberculosis enzyme ch
47                                          For isoleucyl-tRNA synthetase, these errors are reduced by t
48 as demonstrated by its ability to complement isoleucyl-tRNA synthetase-deficient mutants of E. coli.
49 hromosomally encoded organellar (apicoplast) isoleucyl-tRNA synthetase.
50  parasites had a mutation in the cytoplasmic isoleucyl-tRNA synthetase.
51  were investigated with an editing-defective isoleucyl-tRNA synthetase.
52 yl adenylates by editing synthetases such as isoleucyl-tRNA synthetase.
53 m with p43, as well as cross-reactivity with isoleucyl-tRNA synthetase.
54 ase of the particle and maps the location of isoleucyl-tRNA synthetase.
55 mary structure of Mycobacterium tuberculosis isoleucyl-tRNA synthetase.
56                       Vertebrate cytoplasmic isoleucyl-tRNA synthetases (IARS1s) have an uncharacteri
57 by bacterial-type but not by eukaryotic-type isoleucyl-tRNA synthetases and might also be a determina
58                             Examples include isoleucyl-tRNA synthetases whose acquisition from eukary
59 or of Escherichia coli and other eubacterial isoleucyl-tRNA synthetases, but not of eukaryote cytopla
60 aryote cytoplasmic than to other eubacterial isoleucyl-tRNA synthetases.