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1 nitial amber suppressor version of the yeast tryptophanyl tRNA.
2 tion catalyzed by wild-type Escherichia coli tryptophanyl-tRNA synthe-tase (TrpRS) have now been inve
5 ted induction of the gene encoding the human tryptophanyl tRNA synthetase (WRS) results in the produc
6 netic codes, we have developed an orthogonal tryptophanyl tRNA synthetase and tRNA pair, derived from
7 aromatic amino acids; and cells harboring a tryptophanyl tRNA synthetase mutation conferring tempera
8 UAAs) into proteins using engineered E. coli tryptophanyl-tRNA synthetase (EcTrpRS)-tRNA(Trp) pairs.
11 es the first step of protein synthesis-human tryptophanyl-tRNA synthetase (T2-TrpRS) has potent anti-
12 ccus radiodurans NOS (deiNOS) and an unusual tryptophanyl-tRNA synthetase (TrpRS II) catalyzes the re
13 al structures of Bacillus stearothermophilus tryptophanyl-tRNA synthetase (TrpRS) afford evidence tha
14 r example, an alternative splice fragment of tryptophanyl-tRNA synthetase (TrpRS) and a similar natur
17 c.770A > G (p.His257Arg), in the cytoplasmic tryptophanyl-tRNA synthetase (TrpRS) gene (WARS) that co
21 by contemporary Bacillus stearothermophilus tryptophanyl-tRNA synthetase (TrpRS) over that of TrpRS
25 the aromatic amino acid permease (aroP) and tryptophanyl-tRNA synthetase (trpS) contained several am
29 We deleted the anticodon binding domain from tryptophanyl-tRNA synthetase and fused the discontinuous
31 an activation by Bacillus stearothermophilus tryptophanyl-tRNA synthetase falls asymptotically to a p
32 The crystal structure of a highly homologous tryptophanyl-tRNA synthetase from Bacillus stearothermop
33 ption of the auxiliary, antibiotic-resistant tryptophanyl-tRNA synthetase gene (trpRS1) in Streptomyc
35 la embryonic salivary gland, we identified a tryptophanyl-tRNA synthetase gene that maps to cytologic
36 uss the potential noncanonical activities of tryptophanyl-tRNA synthetase in immune response and regu
38 id activation by Bacillus stearothermophilus tryptophanyl-tRNA synthetase involves three allosteric s
40 e our preliminary description of the class I tryptophanyl-tRNA synthetase minimal catalytic domain wi
41 subtilis containing a temperature-sensitive tryptophanyl-tRNA synthetase produce elevated levels of
45 ions were mapped to the trpS locus (encoding tryptophanyl-tRNA synthetase) have been previously isola
46 enzymes, tyrosyl-tRNA synthetase (TyrRS) and tryptophanyl-tRNA synthetase, connect protein synthesis
47 ining a temperature-sensitive mutant form of tryptophanyl-tRNA synthetase, encoded by the trpS1 allel
50 with an engineered Saccharomyces cerevisiae tryptophanyl tRNA-synthetase (Trp-RS):suppressor tRNA pa
51 an orthogonal promoter and to reengineer the tryptophanyl tRNA-synthetase:suppressor tRNA pair from S
53 Recent work suggests that human tyrosyl- and tryptophanyl-tRNA synthetases (TrpRS) link protein synth
54 he possibility that present day tyrosyl- and tryptophanyl-tRNA synthetases appeared after the separat
55 Ij particular, the eukaryotic tyrosyl- and tryptophanyl-tRNA synthetases are more related to each o
56 s shared by all tyrosyl-tRNA synthetases and tryptophanyl-tRNA synthetases for amino acid discriminat
57 ts of the closely related human tyrosyl- and tryptophanyl-tRNA synthetases were discovered to be acti
58 (another antibiotic that inhibits bacterial tryptophanyl-tRNA synthetases) and that its transcriptio
59 reptomyces coelicolor has two genes encoding tryptophanyl-tRNA synthetases, one of which (trpRS1) is