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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 of the respective gene products alanyl- and methionyl-tRNA synthetase.
8 re, we identify alanyl-tRNA synthetase 1 and methionyl-tRNA synthetase 1 variants as new gene defects
9 ve identified mutations in the mitochondrial methionyl-tRNA synthetase, Aats-met, the homologue of hu
11 Previously, we demonstrated that the class I methionyl-tRNA synthetase aminoacylates RNA microhelices
13 ective at creating negative determinants for methionyl tRNA synthetase and positive determinants for
14 itroso-Hcy is in fact transferred to tRNA by methionyl-tRNA synthetase and incorporated into protein
15 plication of the carboxyl-terminal domain of methionyl-tRNA synthetase and may direct tRNA to the act
18 modifications formed via a pathway involving methionyl-tRNA synthetase-catalyzed metabolic conversion
19 ere we describe a rationally designed mutant methionyl-tRNA synthetase containing two point substitut
21 both of which are activated by an engineered methionyl-tRNA synthetase (designated NLL-MetRS), are ex
22 istakenly selected in place of methionine by methionyl-tRNA synthetase during protein biosynthesis, w
23 NA microarrays and filter retention that the methionyl-tRNA synthetase enzyme from Escherichia coli (
24 n is our finding that the plant Oryza sativa methionyl-tRNA synthetase, expressed in Escherichia coli
26 identical to the carboxyl-terminal domain of methionyl-tRNA synthetase from Caenorhabditis elegans, a
27 ort that heterologous expression of a mutant methionyl-tRNA synthetase from Escherichia coli permits
31 e-recombinase-induced expression of a mutant methionyl-tRNA synthetase (L274G) enables the cell-type-
32 In one case, the C-terminal disruption of methionyl-tRNA synthetase (MetG) results in a 10,000-fol
33 a strain carrying a single genomic copy of a methionyl-tRNA synthetase (MetRS) gene, metG*, engineere
34 x with glutamyl-tRNA synthetase (GluRSc) and methionyl-tRNA synthetase (MetRS) in the cytoplasm to re
36 aturation mutagenesis library of the E. coli methionyl-tRNA synthetase (MetRS) led to the discovery o
37 chains was used to identify a diverse set of methionyl-tRNA synthetase (MetRS) mutants that allow eff
40 he centerpiece of the AND gate is a bisected methionyl-tRNA synthetase (MetRS) that charges the Met s
44 s, aminoacyl-tRNA synthetases, including the methionyl-tRNA synthetases MetRS1 and MetRS2, are attrac
46 dified to lysidine to prevent recognition by methionyl-tRNA synthetase (MRS) and production of a chim
47 (ERS), glutaminyl-tRNA synthetase (QRS), and methionyl-tRNA synthetase (MRS), which were specifically
48 ogate, azidohomoalanine, is activated by the methionyl-tRNA synthetase of Escherichia coli and replac
49 siological buffer conditions with wheat germ methionyl-tRNA synthetase, required mutation of the anti