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1 or associate into multifunctional complexes (Aquifex aeolicus).
2 cation apparatus of the extreme thermophile, Aquifex aeolicus.
3 hromosome of the hyperthermophilic bacterium Aquifex aeolicus.
4 roteins from the hyperthermophilic bacterium Aquifex aeolicus.
5  and purified LpxC from the hyperthermophile Aquifex aeolicus.
6 e traffic in the hyperthermophilic bacterium Aquifex aeolicus.
7 mbranes of the hyperthermophilic eubacterium Aquifex aeolicus.
8 of TatC from the hyperthermophilic bacterium Aquifex aeolicus.
9 enzyme from the hyperthermophilic bacterium, Aquifex aeolicus.
10 e of the leucine transporter (LeuT(Aa)) from Aquifex aeolicus.
11 ure of the C-terminal domain of sigma54 from Aquifex aeolicus.
12 e NtrC1 protein from the extreme thermophile Aquifex aeolicus.
13 tG6PDH) from the hyperthermophilic bacterium Aquifex aeolicus.
14  Delta 67) from the extreme hyperthermophile Aquifex aeolicus.
15 he hyperthermophiles Thermotoga maritima and Aquifex aeolicus.
16                                              Aquifex aeolicus 3-deoxy-D-manno-octulosonate 8-phosphat
17                                              Aquifex aeolicus 3-deoxy-d-manno-octulosonate 8-phosphat
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
21                              The enzyme from Aquifex aeolicus, a hyperthermophilic organism of ancien
22 -bound forms of the DBD of NtrC4 (4DBD) from Aquifex aeolicus, a member of the NtrC family of sigma(5
23 formed in vitro cleavage of dsRNAs by Ec and Aquifex aeolicus (Aa) enzymes and delineated their produ
24 ss I BPL from the hyperthermophilic bacteria Aquifex aeolicus (AaBPL) in its ligand-free form and in
25 rom the hyperthermophilic, ancient bacterium Aquifex aeolicus (Aacpn10) has a 25-residue C-terminal e
26  deep-branching, hyperthermophilic bacterium Aquifex aeolicus (Aacpn10) shows high homology with meso
27 atured cpn10 from Homo sapiens (hmcpn10) and Aquifex aeolicus (Aacpn10) were monitored by far-UV circ
28 meric co-chaperonin proteins 10 (cpn10) from Aquifex aeolicus (Aacpn10-del25) and human mitochondria
29 al structure of the leucine transporter from Aquifex aeolicus (aaLeuT) has provided significant insig
30  end, we investigated a thermostable LS from Aquifex aeolicus (AaLS) and found that it also forms cag
31 empted to convert the capsid-forming LS from Aquifex aeolicus (AaLS) into pentamers through a small n
32 l, 60-subunit capsid, lumazine synthase from Aquifex aeolicus (AaLS), to act as a container for nucle
33           The [2Fe-2S] ferredoxin (Fd4) from Aquifex aeolicus adopts a thioredoxin-like polypeptide f
34           We report the crystal structure of Aquifex aeolicus Ago (Aa-Ago) together with binding and
35 CAK dynamics with those of hyperthermophilic Aquifex aeolicus AK (AAAK), our results provide strong e
36  crystal structures of an active fragment of Aquifex aeolicus alanyl-tRNA synthetase complexed, separ
37 crystal structure of a catalytic fragment of Aquifex aeolicus AlaRS and additional data suggest how t
38  of the 453 amino acid catalytic fragment of Aquifex aeolicus AlaRS.
39 chaeum equitans, Pyrobaculum aerophilum, and Aquifex aeolicus (all hyperthermophiles).
40 ral gene fliA was exchanged with homologs of Aquifex aeolicus (an extreme thermophile) and Chlamydia
41 of the free and CMP-bound forms of WaaA from Aquifex aeolicus, an ancient Gram-negative hyperthermoph
42                                              Aquifex aeolicus, an extreme hyperthermophile, has neith
43  of intact NtrC4 (a sigma(54) activator from Aquifex aeolicus, an extreme thermophile), as well as it
44                                              Aquifex aeolicus, an organism that flourishes at 95 degr
45 teases from two different bacterial species, Aquifex aeolicus and B. subtilis.
46  (there termed PRORPs) and in some bacteria (Aquifex aeolicus and close relatives); both enzyme types
47 ed the MpgII genes from T. maritima and from Aquifex aeolicus and found that both genes could restore
48 similar studies done with SPS orthologs from Aquifex aeolicus and humans, we propose a catalytic mech
49       The amt genes of the hyperthermophiles Aquifex aeolicus and Methanococcus jannaschii complement
50 le for two different PGT domains, PBP1A from Aquifex aeolicus and PBP1A from Escherichia coli.
51 ture of NusB from the thermophilic bacterium Aquifex aeolicus and studied the interaction of NusB and
52 rt the kinetic characterization of LpxK from Aquifex aeolicus and the crystal structures of LpxK in c
53 terized aldolases of Helicobacter pylori and Aquifex aeolicus and to the group that comprises the Cal
54 n from Escherichia coli, a KtrB protein from Aquifex aeolicus, and a Trk1,2 protein from Schizosaccha
55  studies of NtrC4, a sigma-54 activator from Aquifex aeolicus, and compare it with NtrC1 (a paralog)
56 e LpxC deacetylase from the hyperthermophile Aquifex aeolicus, and it has excellent antibiotic activi
57 L27, was cloned from the extreme thermophile Aquifex aeolicus, and the protein was overexpressed and
58 Escherichia coli and the metallo KDO8PS from Aquifex aeolicus are the best characterized members of e
59 erichia coli, Agrobacterium tumefaciens, and Aquifex aeolicus, as well as the ADAT2-ADAT3 proteins fr
60                The ribosomal protein S8 from Aquifex aeolicus (AS8) is unique in that there is a 41-r
61 charomyces cerevisiae, and from the bacteria Aquifex aeolicus, Borrelia burgdorferi, Clostridium stic
62 e of the full-length WzmWzt transporter from Aquifex aeolicus bound to adenosine triphosphate (ATP) a
63 d of CTP and ATP; we transformed the related Aquifex aeolicus CC- and A-adding enzymes into UU- and G
64               A hemoglobin was identified in Aquifex aeolicus, cloned, recombinantly expressed, purif
65  GatCAB from the hyperthermophilic bacterium Aquifex aeolicus, complexed with glutamine, asparagine,
66 KDO8PS) from the hyperthermophilic bacterium Aquifex aeolicus differs from its Escherichia coli count
67  was used to probe conformational changes of Aquifex aeolicus dihydroorotase (DHO), which catalyzes t
68                      The X-ray structures of Aquifex aeolicus dihydroorotase in two space groups, C22
69  solution that the ATP-dependent assembly of Aquifex aeolicus DnaA into a spiral oligomer creates a c
70 d the structure of the conserved core of the Aquifex aeolicus DnaA protein to 2.7 A resolution.
71        Based on the structural similarity of Aquifex aeolicus DnaA to other AAA+ proteins that are ol
72 deled upon the crystallographic structure of Aquifex aeolicus DnaA, predicts a hydrogen bond between
73                 A 3.3 A crystal structure of Aquifex aeolicus DnaB, complexed with nucleotide, reveal
74                  The genome of the bacterium Aquifex aeolicus encodes a polypeptide which is related
75                             The phoU gene of Aquifex aeolicus encodes a protein called PHOU_AQUAE wit
76                   The deeply rooted organism Aquifex aeolicus encodes one type IIA topoisomerase conf
77            The thermophilic chemolithotroph, Aquifex aeolicus, expresses a gene product that exhibits
78 ly homologous and structurally characterized Aquifex aeolicus ferredoxin 4 (AaeFd4) using EPR, UV-vis
79  nanomolar concentrations, including that of Aquifex aeolicus, for which structural information is av
80 o-EM to determine 3D maps of the full-length Aquifex aeolicus FtsH protease.
81 e E/G homologs from phylogenetically distant Aquifex aeolicus, Haemophilus influenzae Rd, and Synecho
82       We determined the cryo-EM structure of Aquifex aeolicus HARP (Aq880) and two crystal structures
83              The hyperthermophilic bacterium Aquifex aeolicus has a MutL protein (Aae MutL) that poss
84 conserved hypothetical protein, Aq1575, from Aquifex aeolicus has been determined by using x-ray crys
85 ecent NMR and X-ray studies of the LpxC from Aquifex aeolicus have provided the first structural info
86 tulosonate 8-phosphate (KDO8P) synthase from Aquifex aeolicus in complex with phosphoenolpyruvate (PE
87     The placement of the extreme thermophile Aquifex aeolicus in the bacterial phylogenetic tree has
88  of the alpha2beta2 GlyRS from the bacterium Aquifex aeolicus is able to perform the first step of th
89  of unknown function family 507 protein from Aquifex aeolicus is reported (AaDUF507, UniProt O67633,
90 have investigated the mechanism of action of Aquifex aeolicus IspH [E-4-hydroxy-3-methyl-but-2-enyl d
91              We report the inhibition of the Aquifex aeolicus IspH enzyme (LytB, (E)-4-hydroxy-3-meth
92 bstrate permeation pathway in the homologous Aquifex aeolicus leucine transporter.
93 al structure of the leucine transporter from Aquifex aeolicus (LeuT).
94 us ( Tth ) ligase, Thermus sp. AK16D ligase, Aquifex aeolicus ligase and the K294R mutant of the Tth
95 mains from heterologous organisms, including Aquifex aeolicus, localized to septal rings when produce
96 h amino acid was altered in both E. coli and Aquifex aeolicus LpxC and the catalytic activities of th
97  k(cat)/Km catalyzed by Escherichia coli and Aquifex aeolicus LpxC displayed a bell-shaped curve (EcL
98 h the wild type (WT) and the H265A mutant of Aquifex aeolicus LpxC, each in the absence of substrate
99 ctures of apo- and ADP/Mg(2+)-bound forms of Aquifex aeolicus LpxK to a resolution of 1.9 A and 2.2 A
100 ling nanoparticles, including the 60-subunit Aquifex aeolicus lumazine synthase (LuS) and the 24-subu
101 e present the crystal structure of MraY from Aquifex aeolicus (MraYAA) at 3.3 A resolution, which all
102 e present the crystal structure of MraY from Aquifex aeolicus (MraYAA) in complex with its naturally
103 ared and studied, His42, His124, and Glu126 (Aquifex aeolicus numbering), with particular attention p
104                          Relative to EcNusG, Aquifex aeolicus NusG (AaNusG) and several other bacteri
105 doglycan glycosyltransferase (PGT) domain of Aquifex aeolicus PBP1A.
106 4Fe-3S] cluster in hydrogenase (Hase) I from Aquifex aeolicus performs two redox transitions within a
107                When introduced into purified Aquifex aeolicus PilT, substitutions in the AIRNLIRE mot
108 D structure of the central domain from NtrC1 Aquifex aeolicus protein into our 3D model; we propose t
109        Here, we demonstrate that KDO8PS from Aquifex aeolicus, representing only the second member of
110  fashion, whereas the Class II enzymes (e.g. Aquifex aeolicus) require metal ions for catalysis.
111  and genetic approaches that CCA addition in Aquifex aeolicus requires collaboration between two rela
112  enzymes from human, Myxococcus xanthus, and Aquifex aeolicus, respectively.
113 gnetic resonance (NMR) analysis of SmpB from Aquifex aeolicus revealed an antiparallel beta-barrel st
114  [2Fe-2S] cluster containing ferredoxin from Aquifex aeolicus reveals a thioredoxin-like fold that is
115  crystal structure of the nuclease domain of Aquifex aeolicus RNase III, the E41, D114, and E117 side
116   Here, we present two crystal structures of Aquifex aeolicus SD, including a ternary complex with bo
117  previously determined crystal structures of Aquifex aeolicus SelA complexed with tRNA(Sec) revealed
118 tal structures of GAF regulatory domains for Aquifex aeolicus sigma(54) activators NifA-like homolog
119     We identified a minimal construct of the Aquifex aeolicus sigma(54) AID that consists of two pred
120           We report here the structure of an Aquifex aeolicus sigma(54) domain (residues 69-198), whi
121 e same affinity for the Escherichia coli and Aquifex aeolicus SmpB proteins as the intact E. coli tmR
122                  Trbp111 is a 111 amino acid Aquifex aeolicus structure-specific tRNA-binding protein
123 protein from the hyperthermophilic bacterium Aquifex aeolicus suggested that this protein functions s
124 mologue from the hyperthermophilic bacterium Aquifex aeolicus, that shares 35.2% identity with human
125 mily members, we determined the structure of Aquifex aeolicus ThiL (AaThiL) with nonhydrolyzable AMP-
126                 Given the ancient lineage of Aquifex aeolicus, this observation provides the first in
127 n of the bacterial helicase loader DnaC from Aquifex aeolicus to 2.7 A resolution.
128 eport a 2.6 angstrom co-crystal structure of Aquifex aeolicus Trbp111 bound to tRNA(Ile), which revea
129  ligase from the hyperthermophilic bacterium Aquifex aeolicus was cloned, expressed in Escherichia co
130  homologue from the thermophilic eubacterium Aquifex aeolicus was cloned, overexpressed, and purified
131                                              Aquifex aeolicus was one of the earliest diverging, and
132 namide ribonucleotide synthetase (GARS) from Aquifex aeolicus were expressed in Escherichia coli, and
133 activity-based screen, two phosphatases from Aquifex aeolicus were identified that dephosphorylate AR
134  and ATP; however, we recently found that in Aquifex aeolicus, which lies near the deepest root of th
135 we report the crystal structure of LpxC from Aquifex aeolicus, which reveals a new alpha+beta fold re
136 , including one from the extreme thermophile Aquifex aeolicus, which suggests that RusA may be of anc
137 avorably with the -tolerant hydrogenase from Aquifex aeolicus, which we use here as a benchmark.
138 y RNase P in the hyperthermophilic bacterium Aquifex aeolicus: Without an RNA subunit and the smalles

 
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