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1 nt to 3' end, at conventional position 71 of tRNA(Thr).
2 ectively editing the misacylated species Ser-tRNA(Thr).
3 activity that also generates mischarged Ser-tRNA(Thr).
4 onor to methylate t(6)A to form m(6)t(6)A in tRNA(Thr).
5 (C182 in Escherichia coli) to hydrolyze Ser-tRNA(Thr).
6 Thr and to lack editing activity against Ser-tRNAThr.
9 ting at position 32 of the anticodon loop of tRNA(Thr)(AGU) stimulates, but is not required for, the
11 s ThrRS-cat was shown to synthesize both Thr-tRNAThr and Ser-tRNAThr and to lack editing activity aga
12 shown to synthesize both Thr-tRNAThr and Ser-tRNAThr and to lack editing activity against Ser-tRNAThr
15 residue critical for editing, leading to Ser-tRNA(Thr) formation and protein mistranslation that impa
18 of auxiliary elements, such as HMR-I and the tRNA(Thr) gene, in enhancing the association of Sir sile
19 content of Escherichia coli tRNASer(VGA) and tRNAThr(GGU) as controls were measured as 2.03 and 2.84
20 analyses of E. coli tRNASer(VGA) and E. coli tRNAThr(GGU), unfractionated tRNA from E. coli and 23S r
23 Here we show that archaeal editing of Ser-tRNAThr is catalyzed by a domain unrelated to, and absen
25 in the anticodon loop of Trypanosoma brucei tRNA(Thr) is methylated to 3-methylcytosine (m(3)C) as a
26 showed that air oxidation increased the Ser-tRNA(Thr) level in the presence of elongation factor Tu.
27 otein in trans to hydrolyze specifically Ser-tRNAThr, or it can be fused to ThrRS-cat to provide the
28 rogen peroxide oxidizes C182, leading to Ser-tRNA(Thr) production and mistranslation of threonine cod
30 reonyl-tRNA synthetases, responsible for Thr-tRNA(Thr) synthesis: one accurate and constitutively exp
32 e, early hypoxia increases wobble cmo(5)U in tRNA(Thr(UGU)), which parallels translation of transcrip
33 r the expression and processing of the genes tRNA(Thr)(UGU), tRNA(Leu)(UAA), and tRNA(Phe) (GAA) ther
34 cant reduction of the steady-state levels in tRNA(Thr) was observed in cells carrying both the A15951
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