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