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1 tone in L. luteus, suggesting involvement of methionyl-tRNA synthetase.
2 ine concentration, suggesting involvement of methionyl-tRNA synthetase.
3 f the anticodon in aminoacylation of tRNA by methionyl-tRNA synthetase.
4 a similar base-pair uncoupling when bound to methionyl-tRNA synthetase.
5 em alone can be aminoacylated by the class I methionyl-tRNA synthetase.
6 cylated with methionine by overproduction of methionyl-tRNA synthetase.
7 ve identified mutations in the mitochondrial methionyl-tRNA synthetase, Aats-met, the homologue of hu
9 Previously, we demonstrated that the class I methionyl-tRNA synthetase aminoacylates RNA microhelices
11 ective at creating negative determinants for methionyl tRNA synthetase and positive determinants for
12 itroso-Hcy is in fact transferred to tRNA by methionyl-tRNA synthetase and incorporated into protein
13 plication of the carboxyl-terminal domain of methionyl-tRNA synthetase and may direct tRNA to the act
16 ere we describe a rationally designed mutant methionyl-tRNA synthetase containing two point substitut
18 both of which are activated by an engineered methionyl-tRNA synthetase (designated NLL-MetRS), are ex
19 istakenly selected in place of methionine by methionyl-tRNA synthetase during protein biosynthesis, w
20 NA microarrays and filter retention that the methionyl-tRNA synthetase enzyme from Escherichia coli (
21 n is our finding that the plant Oryza sativa methionyl-tRNA synthetase, expressed in Escherichia coli
23 identical to the carboxyl-terminal domain of methionyl-tRNA synthetase from Caenorhabditis elegans, a
24 ort that heterologous expression of a mutant methionyl-tRNA synthetase from Escherichia coli permits
28 e-recombinase-induced expression of a mutant methionyl-tRNA synthetase (L274G) enables the cell-type-
29 In one case, the C-terminal disruption of methionyl-tRNA synthetase (MetG) results in a 10,000-fol
30 a strain carrying a single genomic copy of a methionyl-tRNA synthetase (MetRS) gene, metG*, engineere
31 x with glutamyl-tRNA synthetase (GluRSc) and methionyl-tRNA synthetase (MetRS) in the cytoplasm to re
33 aturation mutagenesis library of the E. coli methionyl-tRNA synthetase (MetRS) led to the discovery o
34 chains was used to identify a diverse set of methionyl-tRNA synthetase (MetRS) mutants that allow eff
36 he centerpiece of the AND gate is a bisected methionyl-tRNA synthetase (MetRS) that charges the Met s
40 dified to lysidine to prevent recognition by methionyl-tRNA synthetase (MRS) and production of a chim
41 ogate, azidohomoalanine, is activated by the methionyl-tRNA synthetase of Escherichia coli and replac
42 siological buffer conditions with wheat germ methionyl-tRNA synthetase, required mutation of the anti
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