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1 ive mutant GSAT inhibited ALA formation from glutamyl-tRNA.
2 apicomplexans possess a unique heterodimeric glutamyl-tRNA amidotransferase consisting of GatA and Ga
3 acterial AspRS and the B subunit of archaeal glutamyl-tRNA amidotransferases, and another previously
6 LUCA by amidation of the mischarged species, glutamyl-tRNA(Gln) and aspartyl-tRNA(Asn), by tRNA-depen
8 when it was incubated with Escherichia coli glutamyl-tRNA(Glu) and purified recombinant Chlamydomona
10 verexpression of rHb1.1 and the hemA-encoded glutamyl-tRNA (GTR) reductase increased intracellular le
16 erted to a glutamate 1-semialdehyde (GSA) by glutamyl-tRNA reductase (GTR) in an NADPH-dependent reac
20 on is imposed on cultures of S. typhimurium, glutamyl-tRNA reductase (HemA) enzyme activity is increa
23 e first enzyme committed to ALA synthesis is glutamyl-tRNA reductase encoded in Arabidopsis by a smal
25 of CHLH and HEMA1 encoding Mg chelatase and glutamyl-tRNA reductase were increased in rfd1 and the A
28 ression of the HEMA1 and Lhcb genes encoding glutamyl-tRNA reductase, the first committed enzyme of 5
29 eflected in an enhanced level of the encoded glutamyl-tRNA reductase, which catalyzes one of the rate
30 ichia coli, the hemA gene encodes the enzyme glutamyl-tRNA reductase, which catalyzes the first commi
31 ichia coli, the hemA gene encodes the enzyme glutamyl-tRNA reductase, which catalyzes the first commi
35 ic screen reveals that the overexpression of glutamyl-tRNA synthetase (GltX) suppresses the toxicity
36 (Gln) is produced via an indirect pathway: a glutamyl-tRNA synthetase (GluRS) first attaches glutamat
38 ort the characterization of a well conserved glutamyl-tRNA synthetase (GluRS) paralog (YadB in Escher
39 in early eukaryotes from a nondiscriminating glutamyl-tRNA synthetase (GluRS) that aminoacylates both
40 nsplanting a conserved arginine residue from glutamyl-tRNA synthetase (GluRS) to glutaminyl-tRNA synt
41 the presence of AsnRS and GlnRS, as well as glutamyl-tRNA synthetase (GluRS), a discriminating and a
42 ved from the archaeal-type nondiscriminating glutamyl-tRNA synthetase (GluRS), an enzyme with relaxed
43 oshii class I LysRS (LysRS1) and homology to glutamyl-tRNA synthetase (GluRS), residues implicated in
44 Gln) is initially acylated with glutamate by glutamyl-tRNA synthetase (GluRS), then the glutamate moi
45 netic analyses predict that GlnRS arose from glutamyl-tRNA synthetase (GluRS), via gene duplication w
49 ompare the signaling pathways in a bacterial glutamyl-tRNA synthetase (GluRS):tRNA(Glu) and an archae
50 ng protein that forms a ternary complex with glutamyl-tRNA synthetase (GluRSc) and methionyl-tRNA syn
51 in a two-step process; a non-discriminating glutamyl-tRNA synthetase (ND-GluRS) forms Glu-tRNA(Gln),
53 e for essentially all of the glutaminyl- and glutamyl-tRNA synthetase activity detected in both the c
54 and asparaginyl-tRNA synthetase evolved from glutamyl-tRNA synthetase and aspartyl-tRNA synthetase, r
55 ase and utilize a two-step pathway involving glutamyl-tRNA synthetase and glutamine amidotransferase
56 t-transfer states with charged tRNA bound to glutamyl-tRNA synthetase from Thermus thermophilus (Glu-
57 rk identifies genes encoding glutaminyl- and glutamyl-tRNA synthetase in the closely related organism
59 lation pathway utilizes a non-discriminating glutamyl-tRNA synthetase to synthesize Glu-tRNA(Gln) and
60 C. trachomatis aspartyl-tRNA synthetase and glutamyl-tRNA synthetase were shown to be non-discrimina
70 RNA reductase (GluTR), converts glutamate of glutamyl-tRNA to glutamate 1-semialdehyde (GSA) which is
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