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4 tion during coded protein synthesis requires lysyl-tRNA(Lys), which is synthesized by lysyl-tRNA synt
5 resence of Nepsilon-(5-azido-2-nitrobenzoyl)-lysyl-tRNA, photoreactive lysine residues would be incor
6 ynthetases (LysRS1 and LysRS2) together form lysyl-tRNA(Pyl), a potential intermediate to pyrrolysyl-
8 RNA, we discovered that the Escherichia coli lysyl tRNA synthetase was responsible for misacylating t
10 stem eliminated misacylation by the E. coli lysyl tRNA synthetase, and led to the development of a f
12 hydrolyze lysyl-adenylate generated by human lysyl-tRNA synthetase (hLysRS) by proceeding through an
15 is, p.Tyr173SerfsX7, and p.Ile302Met) in the lysyl-tRNA synthetase (KARS) gene in two patients from t
17 e identified at highly conserved residues of lysyl-tRNA synthetase (KARS): the c.1129G>A (p.Asp377Asn
19 an methionyl-tRNA synthetase (MRS) and human lysyl-tRNA synthetase (KRS) were expressed in human-deri
21 nscription primer via an interaction between lysyl-tRNA synthetase (LysRS) and the HIV-1 Gag polyprot
22 f the transcription factors MITF or USF2 and lysyl-tRNA synthetase (LysRS) are associated with human
23 into two unrelated structural classes, with lysyl-tRNA synthetase (LysRS) being the only enzyme repr
24 previously shown that the essential protein lysyl-tRNA synthetase (LysRS) exists in two unrelated fo
26 unrelated aminoacyl-tRNA synthetase classes, lysyl-tRNA synthetase (LysRS) is the only example known
29 Gag and GagPol, as well as host cell factor lysyl-tRNA synthetase (LysRS), are required for specific
32 The crystal structure of the constitutive lysyl-tRNA synthetase (LysS) from Escherichia coli has b
35 69 base pair to G4:C69 and overproduction of lysyl-tRNA synthetase and methionyl-tRNA transformylase
36 jeK, encoding truncated homologs of class II lysyl-tRNA synthetase and of lysine-2,3-aminomutase, res
37 r results on recognition of tRNAs by E. coli lysyl-tRNA synthetase and on competition in cells among
40 , our analysis points to the extant forms of lysyl-tRNA synthetase being preceded in evolution by the
42 lso encode G73, the motif 2 loop sequence of lysyl-tRNA synthetase differs at multiple positions from
43 r, the capacity of tRNA3Lys to interact with lysyl-tRNA synthetase does not entirely explain the enha
49 udies have demonstrated that the presence of lysyl-tRNA synthetase in HIV-1 virions might account for
52 ases, we report here that the class II human lysyl-tRNA synthetase is relatively insensitive to the n
53 d a trans pQTL relationship between the KARS lysyl-tRNA synthetase locus and levels of the DIDO1 prot
54 Crystals of the thermo-inducible E. coli lysyl-tRNA synthetase LysU which diffract to 2.1 A resol
57 the sequence of the loop of motif 2 of human lysyl-tRNA synthetase specifies a structural variation t
58 syl-AMP generated by either E. coli or human lysyl-tRNA synthetase were partially transferable by C-t
59 ural classes, the only known exception being lysyl-tRNA synthetase which exists in both classes I (Ly
60 gene lies immediately adjacent to the cKARS (lysyl-tRNA synthetase) gene with the two genes in a head
63 molar inhibitor of the Plasmodium falciparum lysyl-tRNA synthetase, and exhibits activity against bot
64 lysis of B. burgdorferi mRNA showed that the lysyl-tRNA synthetase-encoding gene is highly expressed,
79 ination factor Rho, bacterial and eukaryotic lysyl-tRNA synthetases, bacteriophage T4 endonuclease VI
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