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2 rom Methanobacterium thermoautotrophicum and leucyl tRNA derived from Halobacterium sp. NRC-1 as an o
3 sma KIC enrichment most accurately predicted leucyl-tRNA enrichment, whereas plasma Leu enrichment wa
4 f E. coli TruA in complex with two different leucyl tRNAs in conjunction with functional assays and c
6 lytic turnover, thus inhibiting synthesis of leucyl-tRNA(Leu) and consequentially blocking protein sy
7 use HSPE71, Rat RhoGAP protein, S cerevisiae leucyl tRNA synthetase and S cerevisiae chromosome II OR
8 carboxy-terminal domain (Cterm) of human mt-leucyl tRNA synthetase rescues the pathologic phenotype
11 er the overexpression of human mitochondrial leucyl-tRNA synthetase (LARS2) in the cytoplasmic hybrid
14 c and editing activities of Escherichia coli leucyl-tRNA synthetase (LeuRS) demonstrate that the enzy
24 this biocontrol agent targets A. tumefaciens leucyl-tRNA synthetase (LeuRS), an essential enzyme for
28 a unique tRNA-dependent mechanism to inhibit leucyl-tRNA synthetase (LeuRS), while the TM84-producer
32 ulting from cancer-associated MTOR mutations.Leucyl-tRNA synthetase (LRS) is a leucine sensor of the
35 Binding of gold-labeled tRNA(Leu) places leucyl-tRNA synthetase and the bifunctional glutamyl-/pr
36 ein, different mutations in Escherichia coli leucyl-tRNA synthetase are combined to unmask the pretra
37 of onychomycosis, inhibits yeast cytoplasmic leucyl-tRNA synthetase by formation of a stable tRNA(Leu
38 he collective motion in Thermus thermophilus leucyl-tRNA synthetase by studying the low frequency nor
40 These mutations that altered or abolished leucyl-tRNA synthetase editing were introduced into comp
41 overcome this limitation, we have adapted a leucyl-tRNA synthetase from Methanobacterium thermoautot
42 n identified a mutation in the mitochondrial leucyl-tRNA synthetase gene (lrs-2) that impaired mitoch
45 rving cells of leucine or treating them with leucyl-tRNA synthetase inhibitors did not elicit nuclear
46 ted that the transfer of human mitochondrial leucyl-tRNA synthetase into the cybrid cells carrying th
47 cid editing active site for Escherichia coli leucyl-tRNA synthetase resides within the CP1 domain tha
48 tational analysis within yeast mitochondrial leucyl-tRNA synthetase showed that the enzyme has mainta
49 ed conformational changes of T. thermophilus leucyl-tRNA synthetase upon substrate binding and analyz
50 red the refolding of the human mitochondrial leucyl-tRNA synthetase variant H324Q to that of wild typ
51 hreonine-rich region of the Escherichia coli leucyl-tRNA synthetase's CP1 domain that is hypothesized
53 be aminoacylated by the human mitochondrial leucyl-tRNA synthetase, we examined the aminoacylation k
57 d mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase: homozygous c.1565C>A (p.Thr522As
58 y a constitutive protein complex composed of leucyl-tRNA-synthetase and folliculin, which regulates m
60 cluding a complex between prolyl-(ProRS) and leucyl-tRNA synthetases (LeuRS) in Methanothermobacter t
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