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1 or associate into multifunctional complexes (Aquifex aeolicus).
2 hromosome of the hyperthermophilic bacterium Aquifex aeolicus.
3 roteins from the hyperthermophilic bacterium Aquifex aeolicus.
4 and purified LpxC from the hyperthermophile Aquifex aeolicus.
5 e traffic in the hyperthermophilic bacterium Aquifex aeolicus.
6 mbranes of the hyperthermophilic eubacterium Aquifex aeolicus.
7 of TatC from the hyperthermophilic bacterium Aquifex aeolicus.
8 enzyme from the hyperthermophilic bacterium, Aquifex aeolicus.
9 e of the leucine transporter (LeuT(Aa)) from Aquifex aeolicus.
10 ure of the C-terminal domain of sigma54 from Aquifex aeolicus.
11 e NtrC1 protein from the extreme thermophile Aquifex aeolicus.
12 tG6PDH) from the hyperthermophilic bacterium Aquifex aeolicus.
13 Delta 67) from the extreme hyperthermophile Aquifex aeolicus.
14 he hyperthermophiles Thermotoga maritima and Aquifex aeolicus.
15 cation apparatus of the extreme thermophile, Aquifex aeolicus.
18 re, we present new structures of FtsZ from47 Aquifex aeolicus,47 Bacillus subtilis, Methanococcus jan
19 tion structure of a leucine transporter from Aquifex aeolicus, a bacterial member of the SLC6 transpo
20 out the active site environment of LpxC from Aquifex aeolicus, a heat-stable orthologue that displays
22 -bound forms of the DBD of NtrC4 (4DBD) from Aquifex aeolicus, a member of the NtrC family of sigma(5
23 ss I BPL from the hyperthermophilic bacteria Aquifex aeolicus (AaBPL) in its ligand-free form and in
24 rom the hyperthermophilic, ancient bacterium Aquifex aeolicus (Aacpn10) has a 25-residue C-terminal e
25 deep-branching, hyperthermophilic bacterium Aquifex aeolicus (Aacpn10) shows high homology with meso
26 atured cpn10 from Homo sapiens (hmcpn10) and Aquifex aeolicus (Aacpn10) were monitored by far-UV circ
27 meric co-chaperonin proteins 10 (cpn10) from Aquifex aeolicus (Aacpn10-del25) and human mitochondria
28 al structure of the leucine transporter from Aquifex aeolicus (aaLeuT) has provided significant insig
29 end, we investigated a thermostable LS from Aquifex aeolicus (AaLS) and found that it also forms cag
30 empted to convert the capsid-forming LS from Aquifex aeolicus (AaLS) into pentamers through a small n
31 l, 60-subunit capsid, lumazine synthase from Aquifex aeolicus (AaLS), to act as a container for nucle
34 CAK dynamics with those of hyperthermophilic Aquifex aeolicus AK (AAAK), our results provide strong e
35 crystal structures of an active fragment of Aquifex aeolicus alanyl-tRNA synthetase complexed, separ
36 crystal structure of a catalytic fragment of Aquifex aeolicus AlaRS and additional data suggest how t
39 ral gene fliA was exchanged with homologs of Aquifex aeolicus (an extreme thermophile) and Chlamydia
40 of the free and CMP-bound forms of WaaA from Aquifex aeolicus, an ancient Gram-negative hyperthermoph
42 of intact NtrC4 (a sigma(54) activator from Aquifex aeolicus, an extreme thermophile), as well as it
45 ed the MpgII genes from T. maritima and from Aquifex aeolicus and found that both genes could restore
46 similar studies done with SPS orthologs from Aquifex aeolicus and humans, we propose a catalytic mech
49 ture of NusB from the thermophilic bacterium Aquifex aeolicus and studied the interaction of NusB and
50 rt the kinetic characterization of LpxK from Aquifex aeolicus and the crystal structures of LpxK in c
51 terized aldolases of Helicobacter pylori and Aquifex aeolicus and to the group that comprises the Cal
52 n from Escherichia coli, a KtrB protein from Aquifex aeolicus, and a Trk1,2 protein from Schizosaccha
53 studies of NtrC4, a sigma-54 activator from Aquifex aeolicus, and compare it with NtrC1 (a paralog)
54 e LpxC deacetylase from the hyperthermophile Aquifex aeolicus, and it has excellent antibiotic activi
55 L27, was cloned from the extreme thermophile Aquifex aeolicus, and the protein was overexpressed and
56 Escherichia coli and the metallo KDO8PS from Aquifex aeolicus are the best characterized members of e
57 erichia coli, Agrobacterium tumefaciens, and Aquifex aeolicus, as well as the ADAT2-ADAT3 proteins fr
59 charomyces cerevisiae, and from the bacteria Aquifex aeolicus, Borrelia burgdorferi, Clostridium stic
60 d of CTP and ATP; we transformed the related Aquifex aeolicus CC- and A-adding enzymes into UU- and G
62 GatCAB from the hyperthermophilic bacterium Aquifex aeolicus, complexed with glutamine, asparagine,
63 KDO8PS) from the hyperthermophilic bacterium Aquifex aeolicus differs from its Escherichia coli count
64 was used to probe conformational changes of Aquifex aeolicus dihydroorotase (DHO), which catalyzes t
66 solution that the ATP-dependent assembly of Aquifex aeolicus DnaA into a spiral oligomer creates a c
74 ly homologous and structurally characterized Aquifex aeolicus ferredoxin 4 (AaeFd4) using EPR, UV-vis
75 nanomolar concentrations, including that of Aquifex aeolicus, for which structural information is av
76 e E/G homologs from phylogenetically distant Aquifex aeolicus, Haemophilus influenzae Rd, and Synecho
78 conserved hypothetical protein, Aq1575, from Aquifex aeolicus has been determined by using x-ray crys
79 ecent NMR and X-ray studies of the LpxC from Aquifex aeolicus have provided the first structural info
80 tulosonate 8-phosphate (KDO8P) synthase from Aquifex aeolicus in complex with phosphoenolpyruvate (PE
82 of the alpha2beta2 GlyRS from the bacterium Aquifex aeolicus is able to perform the first step of th
83 have investigated the mechanism of action of Aquifex aeolicus IspH [E-4-hydroxy-3-methyl-but-2-enyl d
87 us ( Tth ) ligase, Thermus sp. AK16D ligase, Aquifex aeolicus ligase and the K294R mutant of the Tth
88 mains from heterologous organisms, including Aquifex aeolicus, localized to septal rings when produce
89 h amino acid was altered in both E. coli and Aquifex aeolicus LpxC and the catalytic activities of th
90 k(cat)/Km catalyzed by Escherichia coli and Aquifex aeolicus LpxC displayed a bell-shaped curve (EcL
91 h the wild type (WT) and the H265A mutant of Aquifex aeolicus LpxC, each in the absence of substrate
92 ctures of apo- and ADP/Mg(2+)-bound forms of Aquifex aeolicus LpxK to a resolution of 1.9 A and 2.2 A
93 e present the crystal structure of MraY from Aquifex aeolicus (MraYAA) at 3.3 A resolution, which all
94 e present the crystal structure of MraY from Aquifex aeolicus (MraYAA) in complex with its naturally
95 ared and studied, His42, His124, and Glu126 (Aquifex aeolicus numbering), with particular attention p
98 4Fe-3S] cluster in hydrogenase (Hase) I from Aquifex aeolicus performs two redox transitions within a
100 D structure of the central domain from NtrC1 Aquifex aeolicus protein into our 3D model; we propose t
103 and genetic approaches that CCA addition in Aquifex aeolicus requires collaboration between two rela
105 gnetic resonance (NMR) analysis of SmpB from Aquifex aeolicus revealed an antiparallel beta-barrel st
106 [2Fe-2S] cluster containing ferredoxin from Aquifex aeolicus reveals a thioredoxin-like fold that is
107 crystal structure of the nuclease domain of Aquifex aeolicus RNase III, the E41, D114, and E117 side
108 Here, we present two crystal structures of Aquifex aeolicus SD, including a ternary complex with bo
109 previously determined crystal structures of Aquifex aeolicus SelA complexed with tRNA(Sec) revealed
110 tal structures of GAF regulatory domains for Aquifex aeolicus sigma(54) activators NifA-like homolog
111 We identified a minimal construct of the Aquifex aeolicus sigma(54) AID that consists of two pred
113 e same affinity for the Escherichia coli and Aquifex aeolicus SmpB proteins as the intact E. coli tmR
115 protein from the hyperthermophilic bacterium Aquifex aeolicus suggested that this protein functions s
116 mologue from the hyperthermophilic bacterium Aquifex aeolicus, that shares 35.2% identity with human
117 mily members, we determined the structure of Aquifex aeolicus ThiL (AaThiL) with nonhydrolyzable AMP-
120 ligase from the hyperthermophilic bacterium Aquifex aeolicus was cloned, expressed in Escherichia co
121 homologue from the thermophilic eubacterium Aquifex aeolicus was cloned, overexpressed, and purified
123 namide ribonucleotide synthetase (GARS) from Aquifex aeolicus were expressed in Escherichia coli, and
124 and ATP; however, we recently found that in Aquifex aeolicus, which lies near the deepest root of th
125 we report the crystal structure of LpxC from Aquifex aeolicus, which reveals a new alpha+beta fold re
126 , including one from the extreme thermophile Aquifex aeolicus, which suggests that RusA may be of anc
127 avorably with the -tolerant hydrogenase from Aquifex aeolicus, which we use here as a benchmark.
128 y RNase P in the hyperthermophilic bacterium Aquifex aeolicus: Without an RNA subunit and the smalles
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