ライフサイエンスコーパス: maritima

1 etabolic network of the bacterium Thermotoga maritima.

2 (A), obtained for components from Thermotoga maritima.

3 racterized an ExoVII homolog from Thermotoga maritima.

4 and purified untagged MreB1 from Thermotoga maritima.

5 II in all bacteria and, in particular, in T. maritima.

6 ns differ substantially between yeast and T. maritima.

7 nd P3P4 from the hyperthermophile Thermotoga maritima.

8 ply in the geophilomorph centipede Strigamia maritima.

9 idges and in compactness for proteins from T.maritima.

10 Bacillus caldotenax and UvrC from Thermotoga maritima.

11 re of most of the FliN protein of Thermotoga maritima.

12 f the hyperthermophilic bacterium Thermotoga maritima.

13 f the C-terminal 70% of FliG from Thermotoga maritima.

14 he group I NifS-like protein from Thermotoga maritima.

15 on in the geophilomorph centipede, Strigamia maritima.

16 rkers in a myriapod, the centipede Strigamia maritima.

17 ng of a sigma70-like subunit from Thermotoga maritima.

18 sis of the genome of the centipede Strigamia maritima.

19 ome of the thermophilic bacterium Thermotoga maritima.

20 Mycoplasma genitalium, and 23% in Thermotoga maritima.

21 arine hyperthermophilic bacterium Thermotoga maritima.

22 proteins from the model bacterium Thermotoga maritima.

23 m the hyperthermophilic bacterium Thermotoga maritima.

24 the hydrogen-producing bacterium Thermotoga maritima.

25 es of chemoreceptor and CheW from Thermotoga maritima.

26 tic diversity in the sister species Oxyrrhis maritima.

27 ome in the thermophilic bacterium Thermotoga maritima.

28 train RQ2 is probably a strain of Thermotoga maritima.

29 P4-P5 fragment of CheA, both from Thermotoga maritima.

30 e activity in endonuclease V from Thermotoga maritima.

31 licobacter pullorum and WecA from Thermatoga maritima.

32 flavinated FDP (deflavo-FDP) from Thermotoga maritima.

33 by DHFR from the hyperthermophile Thermotoga maritima.

34 hate transport system regulator PhoU from T. maritima (a 235-residue mainly alpha-helical protein), w

35 ethylation of chemoreceptors from Thermotoga maritima, a hyperthermophile that has served as a useful

36 In the case of T. maritima, a three-step serine degradation pathway was in

37 Met-DCs are structurally conserved in the T. maritima AdoMetDC despite very limited primary sequence

38 The x-ray structure of the Thermatoga maritima AdoMetDC proenzyme reveals a dimeric protein fo

39 The biomass of Puccinellia maritima also had a positive influence on elevation, whi

40 characterization of an IscU from Thermatoga maritima, an evolutionarily ancient hyperthermophilic ba

41 ot yet been analysed: the myriapod Strigamia maritima and a representative of an outgroup to the euar

42 , including the hyperthermophiles Thermotoga maritima and Aquifex aeolicus.

43 uiring alkaline phosphatases from Thermotoga maritima and Bacillus subtilis have a His and a Trp at t

44 osphatases from organisms such as Thermotoga maritima and Bacillus subtilis require cobalt for maxima

45 roperties of a TF:S7 complex from Thermotoga maritima and determined its crystal structure.

46 heA binds CheY with identical affinity in T. maritima and E. coli at the vastly different temperature

47 Here we show that MreB from both T. maritima and E. coli binds directly to cell membranes.

48 ecies in two halophyte seed oils from Cakile maritima and Eryngium maritimum.

49 We have created a series of Thermotoga maritima and Escherichia coli pseudouridine 55 synthase

50 In vitro and in vivo analyses of mutant T. maritima and Escherichia coli RodZ validate the structur

51 generated based on the structures of the T. maritima and human AdoMetDCs.

52 al structure of the PanK-III from Thermotoga maritima and identified it as a member of the "acetate a

53 tivation of the hyperthermophiles Thermotoga maritima and Methanococcus jannaschii resulted in fivefo

54 o from the Gram-negative bacteria Thermotoga maritima and Pseudomonas aeruginosa.

55 Sequence comparisons establish that the T. maritima and Slr0387 proteins have loops of similar leng

56 terized the ECF transporters from Thermotoga maritima and Streptococcus thermophilus.

57 on cumulative GC skew analysis, both the T. maritima and T. neapolitana lineages contain one or two

58 igand-free SAICAR synthetase from Thermatoga maritima and the adenine nucleotide complexes of the syn

59 ubtilis, Sulfolobus tokodaii, and Thermotoga maritima) and two eukaryotic (Saccharomyces cerevisiae a

60 gene homologues from the centipede Strigamia maritima, and document a detailed time series of express

61 lies against the entire genome of Thermotoga maritima, and make over a 100 new fold predictions.

62 ctory receptor gene family is absent from S. maritima, and olfaction in air is likely effected by exp

63 llulases from Trichoderma viride, Thermogata maritima, and Pyrococcus horikoshii.

64 , the hyperthermophilic bacterium Thermotoga maritima, and those of close homologs from mesophilic ba

65 mational differences between the E. coli, T. maritima, and yeast synthetases suggest the possibility

66 1 domain of the NusA protein from Thermotoga maritima, another cold-shock associated RNA-binding prot

67 om a four-helix protein-TM1526 of Thermatoga maritima archaea bacteria-which maintains the topologica

68 the hyperthermophilic eubacterium Thermotoga maritima are shown here to differ significantly from tho

69 g domains of HemK from E.coli and Thermotoga maritima are structurally similar, despite the fact that

70 he hydrogenase maturase HydE from Thermotoga maritima as a template, we obtained several unusual form

71 structure of lysine bound to the Thermotoga maritima asd lysine riboswitch ligand-binding domain.

72 scriptional repressor, HrcA, from Thermotoga maritima at 2.2A resolution.

73 synthase complex (YaaD-YaaE) from Thermotoga maritima at 2.9 A resolution.

74 oteins from a variety of sources (Thermotoga maritima, Bacillus subtilis, Acinetobacter baylyi, and N

75 of the FliY catalytic domain from Thermotoga maritima bears strong resemblance to the middle domain o

76 ere help clarifying evolution in Poaceae, S. maritima being a part of the poorly-known Chloridoideae

77 The open reading frame TM1643 of Thermotoga maritima belongs to a large family of proteins, with hom

78 In Thermotoga maritima both candidate genes (in an originally misannot

79 d during chloramphenicol challenge and in T. maritima bound in exopolysaccharide aggregates during me

80 distance was also revealed for O. repens/O. maritima, but not for O. spinosa/O. intermedia.

81 onformational states of CorA from Thermotoga maritima by determining which residues support the penta

82 the CheA-receptor interaction in Thermotoga maritima by NMR spectroscopy and validate the identified

83 of unknown activity, Tm0936 from Thermotoga maritima, by docking high-energy intermediate forms of t

84 ow here that the Cmr complex from Thermotoga maritima can cleave an ssRNA target that is complementar

85 show that both RimO and MiaB from Thermotoga maritima catalyze methyl transfer from SAM to an acid/ba

86 Intriguingly, the Thermatoga maritima CCA-adding enzyme groups with the A-adding enzy

87 us jannaschii resulted in fivefold higher T. maritima cell densities when compared with monoculture a

88 re, we present the crystal structure of a T. maritima cellobiose-binding protein (tm0031) that is hom

89 T. maritima cellobiose-binding protein binds a variety of l

90 Transcriptional analysis of T. maritima cells from these aggregates using a whole genom

91 soluble ternary complex formed by Thermotoga maritima CheA (TmCheA), CheW, and receptor signaling dom

92 the two ATP-binding sites of the Thermotoga maritima CheA dimer (TmCheA) and the single site of the

93 uces the subunit dissociation rate of the T. maritima CheA dimer by interacting with the regulatory d

94 The structure of Thermotoga maritima CheA domain P2 in complex with CheY reveals a d

95 ide binding to the active site of Thermotoga maritima CheA was investigated using stopped-flow fluore

96 phospho-accepting His (His-45) in Thermotoga maritima CheA.

97 The crystal structures of T. maritima CheC and CheX reveal a common fold unlike that

98 T. maritima CheC, as well as CheX, dephosphorylate CheY, al

99 the cytoplasmic domains of four different T. maritima chemoreceptors.

100 ient methylation, the interaction between T. maritima CheR and T. maritima MCPs is of relatively low

101 nalyses utilizing S. enterica and Thermotoga maritima CheR proteins and MCPs indicate that MCP methyl

102 ystal structure of the homologous Thermotoga maritima class III RNR, showing its architecture and the

103 f the putative laminarinase, Lam16A, from T. maritima comprise a highly thermostable family 4 CBM tha

104 ctures of a fragment of MetH from Thermotoga maritima comprising the domains that bind Hcy and CH(3)-

105 A specific feature of T. maritima CopA is ATP utilization in the absence of coppe

106 T and mutated (NMBD deletion or mutation) T. maritima CopA, comparing it with Archaeoglobus fulgidus

107 The copper transport ATPase from Thermotoga maritima (CopA) provides a useful system for mechanistic

108 Thermotoga maritima CorA (TmCorA) is the only member of this protei

109 The crystal structures of Thermotoga maritima CorA provide an excellent structural framework

110 The crystal structure of Thermotoga maritima CorA shows a homopentamer with two transmembran

111 A/ParC CTD with the GyrA CTD from Thermotoga maritima creates an enzyme that negatively supercoils DN

112 These observations suggest that T. maritima DAHP synthase is a metalloenzyme.

113 The activity of T. maritima DAHP synthase is inhibited by two of the three

114 Crystals of DAHPS from Thermotoga maritima (DAHPS(Tm)) were grown in the presence of PEP a

115 hosphate dehydrogenase (Gpd) from Thermotoga maritima, demonstrated robust activity over a range of t

116 studies of thermostable CheA from Thermotoga maritima determine that the His-containing substrate dom

117 of Mycobacterium tuberculosis and Thermotoga maritima did not.

118 ived from Thermus species Z05 and Thermotoga maritima DNA polymerases.

119 ogenase that was previously purified from T. maritima does not use either reduced ferredoxin or NADH

120 A resolution crystal structure of Thermotoga maritima DrrB, providing a second structure of a multido

121 n from the thermophilic bacteria, Thermotoga maritima, enabled an NMR-based site-specific analysis of

122 The gene buk2 from Thermotoga maritima encodes a member of the ASKHA (acetate and suga

123 idues D43, E89, D110, and H214 in Thermotoga maritima endonuclease V catalysis.

124 ed in nine conserved positions of Thermotoga maritima endonuclease V to identify amino acid residues

125 served motifs of the thermostable Thermotoga maritima endonuclease V to probe for residues that affec

126 , a small cold-shock protein from Thermotoga maritima, engineered to contain a single tryptophan resi

127 Thermotoga maritima exo-beta-fructosidase (BfrA) secreted by a reco

128 amilies based on EDTA resistance and that T. maritima ExoVII is the first member of the branch that i

129 Nevertheless, both E. coli and T. maritima ExoVII share a similar putative active site mot

130 re essential for the nuclease activity of T. maritima ExoVII.

131 that FMN-free diferrous FDP from Thermotoga maritima exposed to 1 equiv NO forms a stable diiron-mon

132 single enzyme 'model system', the Thermotoga maritima family 1 beta-glucosidase, TmGH1.

133 rmophilic and anaerobic bacterium Thermotoga maritima ferments a wide variety of carbohydrates, produ

134 ng to the conserved C-terminal portion of T. maritima FliF.

135 between the N-terminal domain of Thermotoga maritima FliG (FliG(N)) and peptides corresponding to th

136 We find that T. maritima FliG(N) is homodimeric in the absence of the Fl

137 in oligomeric state occurs in full-length T. maritima FliG, as well.

138 Furthermore, we show that Thermotoga maritima FliM and FliN form a 1:3 complex structurally e

139 liN is primarily a dimer in solution, and T. maritima FliN and FliM together form a stable FliM(1)-Fl

140 T. maritima FliN is primarily a dimer in solution, and T. m

141 Lys81 (equivalent to Lys150 and Lys82 in T. maritima) for the Bacillus subtilis enzyme suggesting th

142 The centipede Strigamia maritima forms all of its segments during embryogenesis.

143 rom a hyperthermophilic bacterium Thermotoga maritima from its natural coenzyme NADP(+) to NAD(+).

144 tly confirmed for the purified product of T. maritima gene dipA cloned and expressed in Escherichia c

145 Numerous improvements to T. maritima genome annotations were proposed, including the

146 his work represents the first overview of S. maritima genome regarding the respective coding and repe

147 rbohydrate-active proteins encoded in the T. maritima genome was followed using a targeted cDNA micro

148 ences (BESs), representing 26.7 Mb of the S. maritima genome.

149 chain release factor 1 (RF1) from Thermotoga maritima (gi 4981173) at 2.65 Angstrom resolution by sel

150 The crystal structures of Thermotoga maritima GTase and its complex with the inhibitor acarbo

151 he observation that the smallest donor for T.maritima GTase is maltotetraose, the smallest chain tran

152 while other salt marsh species (e.g. Suaeda maritima) had no influence or a negative impact on eleva

153 m the hyperthermophilic bacterium Thermotoga maritima has been cloned and expressed in Escherichia co

154 Despite the fact that T. maritima has been phylogenetically characterized as a pr

155 For some genes S. maritima has evolved paralogues to generate coding seque

156 wo plant species where the outcrosser Cakile maritima has replaced an earlier, inbreeding, colonizer

157 ladenosine of tRNA in E. coli and Thermotoga maritima, has been demonstrated to harbor two distinct [

158 its response regulator RR468 from Thermotoga maritima, here we report a pH-mediated conformational sw

159 horetic mobility shift analyses show that T. maritima HU (TmHU) binds double-stranded DNA with high a

160 the hyperthermophilic eubacterium Thermotoga maritima HU bends DNA and constrains negative DNA superc

161 We suggest that T. maritima HU serves an architectural function when associ

162 ludes approximately 35 bp, association of T. maritima HU with DNA of sufficient length to accommodate

163 We then show that in S. maritima, hunchback and Kruppel are expressed in subsets

164 2.3-kb locus with similarity to a Thermotoga maritima hypothetical protein, while another is part of

165 ed products can be further metabolized by T. maritima in a previously uncharacterized SAH degradation

166 e crystal structures of ThiI from Thermotoga maritima in complex with a truncated tRNA.

167 nsor HK, one from the thermophile Thermotoga maritima in complex with ADPbetaN at 1.9 A resolution.

168 sly produced the NfnAB complex of Thermotoga maritima in Escherichia coli, provided kinetic evidence

169 Thermotoga sp. RQ2 differs from T. maritima in its genes involved in myo-inositol metabolis

170 the 6-phospho-beta-glycosidase, BglT, from T.maritima in native and complexed (NAD(+) and Glc6P) form

171 rting the reticulate origin of samples of T. maritima in southwestern France and T. sinuatocollis/T.

172 ferent structures of FGAR-AT from Thermotoga maritima in the presence of substrates, a substrate anal

173 of the GH10 xylanase Xyl10B from Thermotoga maritima in transplastomic plants and demonstrate except

174 Thermotoga maritima is a marine hyperthermophilic microorganism tha

175 The geophilomorph centipede Strigamia maritima is an emerging model for studies of development

176 Spartina maritima is an Old-World species distributed along the E

177 ucture of the PurLQS complex from Thermotoga maritima is described revealing a 2:1:1 stoichiometry of

178 the fold of sigma1.1 from the thermophile T. maritima is distinctly different.

179 an 100,000 alternate splice forms, but in S. maritima is encoded by over 100 paralogues.

180 a putative signaling peptide and tmRNA in T. maritima is intriguing, since this overlapping arrangeme

181 T. maritima is unable to grow on myo-inositol as a single c

182 Structural characterization of Thermotoga maritima IscU by CD and high resolution NMR yielded data

183 ize the molten globule characteristics of T. maritima IscU by near-ultraviolet circular dichroism, 1-

184 ism studies of the D40A protein show that T. maritima IscU coordinates a [2Fe-2S]2+ cluster.

185 denaturation experiments demonstrate that T. maritima IscU is a thermally stable protein with a therm

186 on for IscU-type proteins, we demonstrate T. maritima IscU-mediated reconstitution of human apoferred

187 -nucleotide sensing domain of the Thermotoga maritima lysine riboswitch in the lysine-bound (1.9 angs

188 Here we report that Thermotoga maritima MazG protein (Tm-MazG), the product of the TM09

189 interaction between T. maritima CheR and T. maritima MCPs is of relatively low affinity.

190 /154/157A triple variant forms of Thermotoga maritima MiaB have revealed the presence of two distinct

191 gh structural homology of their monomers, T. maritima MreB and actin filaments display different asse

192 urthermore, the biophysical properties of T. maritima MreB filaments, including high rigidity and pro

193 mbly and mechanical properties of Thermotoga maritima MreB in the presence of different nucleotides i

194 Here, we studied the assembly of Thermotoga maritima MreB triggered by ATP in vitro and compared it

195 At the optimal growth temperature of T. maritima, MreB assembly proceeded much faster than that

196 A whole-genome alignment of Thermotoga maritima MSB8 and Thermotoga neapolitana NS-E has reveal

197 f the hyperthermophilic bacterium Thermotoga maritima MSB8 presents evidence for lateral gene transfe

198 The hyperthermophilic bacterium Thermotoga maritima MSB8 was grown on a variety of carbohydrates to

199 nine Thermotoga strains to the sequenced T. maritima MSB8.

200 Molecular replacement with the Thermotoga maritima NifS model was used to determine phasing, and t

201 cture of E.coli IscS is similar to that of T.maritima NifS with nearly identical secondary structure

202 and MCPs indicate that MCP methylation in T. maritima occurs independently of a pentapeptide-binding

203 The genome of S. maritima offers us a unique glimpse into the ancestral a

204 f the hyperthermophilic bacterium Thermotoga maritima on 14 monosaccharide and polysaccharide substra

205 Growth of T. maritima on monosaccharides was found to be slower than

206 dies demonstrate that TM1635 from Thermotoga maritima, originally annotated as a putative nuclease, i

207 a type III PanK, the enzyme from Thermotoga maritima (PanK(Tm)), solved at 2.0-A resolution.

208 The extremophile Thermotoga maritima possesses a remarkable array of carbohydrate-pr

209 Endonuclease V obtained from Thermotoga maritima preferentially cleaves purine mismatches in cer

210 DXMS analysis was attempted on 24 Thermotoga maritima proteins with varying crystallization and diffr

211 amphipathic helix in vitro using Thermotoga maritima proteins.

212 re, we report the analysis of the Thermotoga maritima proteome, in which we compare the proteins that

213 proteins define a distinct subset of the T. maritima proteome.

214 s for 432 proteins, comprising 23% of the T. maritima proteome.

215 A new crystal structure of the T. maritima Psi55S Y67F mutant in complex with a 5FU-RNA at

216 The crystal structures of Thermotoga maritima Psi55S, and its complex with RNA, have been det

217 Thus, S. maritima raises evolutionary and ecological interests.

218 er recolonized a hot environment (Thermotoga maritima) relied in their evolutionary strategy of therm

219 The results indicate that T. maritima relies extensively on ABC transporters for carb

220 cillus casei, and 23 and 40% with Thermotoga maritima, respectively.

221 is C-terminal domain of FliN from Thermotoga maritima revealed a saddle-shaped dimer formed mainly fr

222 FliM middle domain (FliM(M)) from Thermotoga maritima reveals a pseudo-2-fold symmetric topology simi

223 rom the chemotaxis kinase CheA of Thermotoga maritima reveals a remarkable degree of structural heter

224 esolution of the RNA component of Thermotoga maritima ribonuclease P.

225 R89) are essential for efficient Thermotoga maritima RNase P activity.

226 port the crystal structure of the Thermotoga maritima RNase P holoenzyme in complex with tRNA(Phe).

227 plasmic helix-turn-helix motif of Thermotoga maritima RodZ directly interacts with monomeric as well

228 The 1.6 A crystal structure of Thermotoga maritima RuvB together with five mutant structures revea

229 Unlike endonuclease V from Thermotoga maritima, Salmonella endonucleae V can only turnover deo

230 we report a crystal structure of Thermotoga maritima SecA at 1.9 A resolution.

231 Here, we present the crystal structure of T. maritima SecA in isolation, determined in its ADP-bound

232 e recent crystal structure of the Thermotoga maritima SecA-SecYEG complex shows the ATPase in a confo

233 port the in vivo relevance of the Thermotoga maritima SecA.SecYEG crystal structure that visualized S

234 In gynodioecious Beta vulgaris ssp. maritima, sex determination involves cytoplasmic male st

235 published data for DHFR from E. coli and T. maritima shows a decreasing trend in efficiency of hydri

236 We describe several examples where S. maritima shows different solutions from insects to simil

237 modating RNAP in the DNA channel, whereas T. maritima sigma1.1 must be rearranged to fit therein.

238 texts, including the structure of Thermotoga maritima sigmaA region 4 described herein.

239 g to potently inhibited Sirt1 and Thermotoga maritima Sir2 and to moderately inhibited Sirt3 requires

240 sirtuin, the Sir2 homologue from Thermatoga maritima (Sir2Tm).

241 nd C-terminal globular domains of Thermotoga maritima SMC in Escherichia coli by replacing the approx

242 resolution crystal structure of a Thermotoga maritima soluble receptor (Tm14) reveals distortions in

243 richia coli in complex with RNAP and from T. maritima solved free in solution.

244 The novel catabolic pathway in T. maritima starts as the conventional route using the myo-

245 herichia coli and the thermophile Thermotoga maritima, subunit dissociation activates at temperatures

246 de ranging collection of such networks in T. maritima suggests that this organism is capable of adapt

247 X-ray structures of Thermatoga maritima TA have been determined as the apo-enzyme at 1.

248 e and L-allo-threonine are substrates for T. maritima TA, enzymatic assays revealed a strong preferen

249 ) and tetraploid (2n=4x=60; O. repens and O. maritima) taxa exist.

250 osa/O. intermedia (diploid) and O. repens/O. maritima (tetraploid) plants.

251 ly found also in bacteria such as Thermotoga maritima that do not utilise a PEP-PTS system, require b

252 ce for chemoreceptor methylation sites in T. maritima that is distinct from the previously identified

253 hich are analogous to residues in Thermotoga maritima that mediate cross-talk.

254 Beyond the information obtained for T. maritima, the present study illustrates how expression-b

255 a pathway for polysaccharide formation in T. maritima, these results point to the existence of peptid

256 the structures of hTK1 and of the Thermotoga maritima thymidine kinase (TmTK) in complex with the bis

257 ructures of complexes between the Thermotoga maritima (Tm) NadA K219R/Y107F variant and (i) the first

258 T. maritima (Tm) RNase III catalytic activity exhibits a br

259 first X-ray crystal structure of Thermatoga maritima (Tm) ThyX in complex with a nonsubstrate analog

260 The Thermotoga maritima TM0065 gene codes for a protein (TM-IclR) that

261 m the hyperthermophilic bacterium Thermotoga maritima (TM0322).

262 echanistic studies of a FDTS from Thermotoga maritima (TM0449) are presented here.

263 f the hyperthermophilic bacterium Thermotoga maritima, TM0504 encodes a putative signaling peptide im

264 mensional structure of GK-II from Thermotoga maritima (TM1585; PDB code 2b8n) revealed a new fold dis

265 Thermotoga maritima (Tma) EndoV recognizes and primarily cleaves he

266 lus caldotenax (Bca)and UvrC from Thermatoga maritima (Tma), and recombinant proteins were overexpres

267 ucture, that from the eubacterium Thermatoga maritima (Tma).

268 ductase from the hyperthermophile Thermotoga maritima (TmDHFR) are presented.

269 ductase from the hyperthermophile Thermotoga maritima (TmDHFR) has been examined by enzyme isotope su

270 dimeric, thermophilic enzyme from Thermotoga maritima (TmDHFR).

271 of GH36 alpha-galactosidase from Thermotoga maritima (TmGalA).

272 nt inhibitor (Ki = 8.2 nM) of the Thermotoga maritima TmGH1 beta-glucosidase.

273 g substance A protein (NusA) from Thermotoga maritima (TmNusA), a protein involved in transcriptional

274 EcfS subunit for riboflavin from Thermotoga maritima, TmRibU.

275 complex of the YjeQ protein from Thermotoga maritima (TmYjeQ), a member of the YjeQ GTPase subfamail

276 TrpB from Pyrococcus furiosus and Thermotoga maritima to generate a suite of catalysts for the synthe

277 The transcriptional response of T. maritima to specific carbohydrate growth substrates indi

278 is, we have utilized the centipede Strigamia maritima to study the correspondence between the express

279 The gene for the Thermotoga maritima Trk potassium transporter component TrkA was or

280 zyme, as well as the structure of Thermotoga maritima TruB in complex with RNA.

281 In Thermotoga maritima, two PhoU homologues have been identified bioin

282 f the hyperthermophilic bacterium Thermotoga maritima was analyzed using purified recombinant enzyme.

283 om the thermophilic microorganism Thermotoga maritima was cloned, and the enzyme was overexpressed in

284 m the hyperthermophilic bacterium Thermotoga maritima was determined at 1.2-A resolution by using x-r

285 d recombinant tagaturonate epimerase from T. maritima was directly confirmed and kinetically characte

286 uronate to mannonate catabolic pathway in T. maritima was reconstituted in vitro using a mixture of r

287 es, we found that the protein subunit from T.maritima was responsible for the comparative thermal sta

288 Previously, Tm0936 from Thermotoga maritima was shown to catalyze the deamination of S-aden

289 NagA from Thermotoga maritima was shown to require a single divalent cation f

290 om a hyperthermophilic bacterium, Thermotoga maritima, was cloned and expressed in Escherichia coli.

291 P from a thermophilic bacterium, Thermotoga maritima, was overexpressed in and purified from Escheri

292 2-residue alpha+beta protein from Thermotoga maritima), we predicted the complete, topologically corr

293 hypothetical protein TM0979 from Thermotoga maritima, we demonstrate the capabilities of this microc

294 it using the simple microorganism Thermotoga maritima, we show our model accurately simulates variati

295 inked transcriptional networks in Thermotoga maritima, we used full-genome DNA microarray analysis of

296 meric ABC exporter TM287/288 from Thermotoga maritima, which contains a non-canonical ATP binding sit

297 fragment of the FliG protein from Thermotoga maritima, which encompasses the middle and C-terminal pa

298 trast to the optimal growth temperature of T.maritima, which is near 80 degrees C.

299 ctions between FliM and FliG from Thermotoga maritima with X-ray crystallography and pulsed dipolar E

300 Thermotoga maritima XseA/B homologs TM1768 and TM1769 were co-expre