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1 hromosomally encoded organellar (apicoplast) isoleucyl-tRNA synthetase.
2 parasites had a mutation in the cytoplasmic isoleucyl-tRNA synthetase.
3 were investigated with an editing-defective isoleucyl-tRNA synthetase.
4 yl adenylates by editing synthetases such as isoleucyl-tRNA synthetase.
5 m with p43, as well as cross-reactivity with isoleucyl-tRNA synthetase.
6 ase of the particle and maps the location of isoleucyl-tRNA synthetase.
7 mary structure of Mycobacterium tuberculosis isoleucyl-tRNA synthetase.
8 aryote cytoplasmic than to other eubacterial isoleucyl-tRNA synthetases.
9 Administration of mupirocin, an inhibitor of isoleucyl-tRNA synthetase activity, resulted in changes
11 ied small molecules that inhibit recombinant isoleucyl-tRNA synthetase and that are lethal to the par
12 , which are also conserved in the homologous isoleucyl-tRNA synthetase and valyl-tRNA synthetase edit
14 by bacterial-type but not by eukaryotic-type isoleucyl-tRNA synthetases and might also be a determina
16 or of Escherichia coli and other eubacterial isoleucyl-tRNA synthetases, but not of eukaryote cytopla
17 as demonstrated by its ability to complement isoleucyl-tRNA synthetase-deficient mutants of E. coli.
18 s reliance on post-transfer editing, whereas isoleucyl-tRNA synthetase differs in retaining a distinc
19 ese eukaryote-like features, M. tuberculosis isoleucyl-tRNA synthetase exhibited highly specific cros
21 y halted before isoleucine codon by reducing isoleucyl-tRNA synthetase from reaction mixture of in vi
22 Methanosarcina species by mutagenesis of the isoleucyl-tRNA synthetase gene (ileS) from Methanosarcin
26 ity determinant for proper aminoacylation by isoleucyl tRNA synthetase (IleRS) and codon recognition
32 milar amino acids, valine and isoleucine, by isoleucyl-tRNA synthetase (IleRS) results, in part, from
33 he rate of activation of 5TFI by the E. coli isoleucyl-tRNA synthetase (IleRS) yielded a specificity
36 he Staphylococcus aureus ileS gene, encoding isoleucyl-tRNA synthetase (IleRS), contains a long mRNA
40 We showed by RNAi knockdown that T. brucei isoleucyl-tRNA synthetase is essential for the parasites
44 Valyl-tRNA synthetase, a close homolog of isoleucyl-tRNA synthetase, misactivates threonine, alpha
45 Substitution of a homologous CP1 domain from isoleucyl-tRNA synthetase or mutation within the LeuRS C
46 Here we report that a specific mutation in isoleucyl-tRNA synthetase prevents editing by blocking t
48 mutations in a presumptive "hinge region" of isoleucyl-tRNA synthetase that is situated between the t
49 eukaryote-like features, and unlike E. coli isoleucyl-tRNA synthetase, the M. tuberculosis enzyme ch
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