ライフサイエンスコーパス: Thermus thermophilus

1 h-resolution crystal structures of KsgA from Thermus thermophilus.

2 lity in the extremely thermophilic bacterium Thermus thermophilus.

3 uctures of PrmA from the extreme thermophile Thermus thermophilus.

4 re synthesized and evaluated with IDI-2 from Thermus thermophilus.

5 bunits and intact 2.3 MDa 70S ribosomes from Thermus thermophilus.

6 e from the extremely thermophilic bacterium, Thermus thermophilus.

7 of phiYS40, a lytic tailed bacteriophage of Thermus thermophilus.

8 A, was identified in the extreme thermophile Thermus thermophilus.

9 esistant mutants of the extreme thermophile, Thermus thermophilus.

10 a protein that has some homology to DafA of Thermus thermophilus.

11 somal proteins of Haloarcula marismortui and Thermus thermophilus.

12 aticivorans, Rhodopseudomonas palustris, and Thermus thermophilus.

13 H, but not the closely related protein from Thermus thermophilus.

14 mplex with elongation factor Tu (EF-Tu) from Thermus thermophilus.

15 rmination of the 30 S ribosomal subunit from Thermus thermophilus.

16 n was obtained from thermophilic eubacterium Thermus thermophilus.

17 ded by a single gene in Escherichia coli and Thermus thermophilus.

18 scherichia coli and one from the thermophile Thermus thermophilus.

19 pe cytochrome oxidase from Bacillus spp. and Thermus thermophilus.

20 We have purified a novel DNA polymerase from Thermus thermophilus.

21 ansformation and kanamycin (Km) selection in Thermus thermophilus.

22 ely similar to those reported for MnSOD from Thermus thermophilus.

23 n the ribosome of the thermophilic bacterium Thermus thermophilus.

24 by GdmCl using the Hsp104 homolog ClpB from Thermus thermophilus.

25 ixed valence states of cytochrome ba(3) from Thermus thermophilus.

26 site-directed mutants of the protein S6 from Thermus thermophilus.

27 2 of the ba(3)-type cytochrome oxidase from Thermus thermophilus.

28 charges from the 101-residue protein S6 from Thermus thermophilus.

29 rolases (dNTPases) from Escherichia coli and Thermus thermophilus.

30 RecA and RecA from a thermophilic bacteria, Thermus thermophilus.

31 was first described for the latter system in Thermus thermophilus.

32 There are two K-turns in the structure of Thermus thermophilus 16S rRNA, and the structures of U4

33 In Thermus thermophilus 16S rRNA, this RNA fold is directly

34 rize the modifications of C1942 and C1962 in Thermus thermophilus 23 S rRNA as 5-methylcytidines (m(5

35 cleotide geometries were calculated from the Thermus thermophilus 30 S subunit X-ray structure and co

36 In the atomic structure of the Thermus thermophilus 30 S subunit, 16 amino acids in S17

37 tion data and by the atomic structure of the Thermus thermophilus 30 S subunit, which has the S17 rec

38 he high-resolution crystal structures of the Thermus thermophilus 30S and Haloarcula marismortui 50S

39 ecently determined crystal structures of the Thermus thermophilus 30S and Haloarcula marismortui 50S

40 of streptomycin on the decoding site of the Thermus thermophilus 30S ribosomal subunit in complexes

41 otein complex from the central domain of the Thermus thermophilus 30S ribosomal subunit was solved at

42 A-pactamycin bound to its target site on the Thermus thermophilus 30S ribosomal subunit.

43 ct agreement with the X-ray structure of the Thermus thermophilus 30S subunit, A site binding was wea

44 nsional cryo-electron microscopic map of the Thermus thermophilus 30S-Era complex.

45 t the crystal structure of EF-P bound to the Thermus thermophilus 70S ribosome along with the initiat

46 crystal structure at 2.6-A resolution of the Thermus thermophilus 70S ribosome bound to EF-4 with a n

47 ranslation termination complex formed by the Thermus thermophilus 70S ribosome bound with release fac

48 present two X-ray crystal structures of the Thermus thermophilus 70S ribosome containing 16S rRNA ra

49 ere, we present the crystal structure of the Thermus thermophilus 70S ribosome containing a model mRN

50 scribe the crystal structure of the complete Thermus thermophilus 70S ribosome containing bound messe

51 nt high-resolution crystal structures of the Thermus thermophilus 70S ribosome in complex with each o

52 cture of the rescue factor YaeJ bound to the Thermus thermophilus 70S ribosome in complex with the in

53 ere we describe the crystal structure of the Thermus thermophilus 70S ribosome in complex with the re

54 Recently, two crystal structures of the Thermus thermophilus 70S ribosome in the same functional

55 We have solved the structures of the Thermus thermophilus 70S ribosome with A-, P-, and E-sit

56 in and two oncocin derivatives, bound to the Thermus thermophilus 70S ribosome.

57 in isolation (2.5 A) and bound to programmed Thermus thermophilus 70S ribosomes before (3.3 A) and af

58 Recently, the genes of cytochrome ba3 from thermus thermophilus, a homolog of the heme-copper oxida

59 nstrate that the ba(3) oxygen reductase from Thermus thermophilus, a representative of the B-family,

60 ants of the extremely thermophilic bacterium Thermus thermophilus, a species which has featured promi

61 report on structures of ternary complexes of Thermus thermophilus Ago catalytic mutants with 5'-phosp

62 with that of azide bound to Mn(III)SOD from Thermus thermophilus and by visible absorption spectra s

63 erties of the Na(+)/H(+) exchanger NapA from Thermus thermophilus and compare this to the prototypica

64 odification states of several S12 mutants of Thermus thermophilus and conclude that beta-methylthiola

65 The P5CDHs from Thermus thermophilus and Deinococcus radiodurans form tr

66 ine triphosphatases (ATPases)/synthases from Thermus thermophilus and Enterococcus hirae can be maint

67 rans, and the small ribosomal subunit RNA of Thermus thermophilus and identified a total of 97 ribose

68 chrome c oxidase from the plasma membrane of Thermus thermophilus and is the preferred terminal enzym

69 (3,3) states of the homologous enzymes from Thermus thermophilus and Lactobacillus plantarum using a

70 attributed to incomplete denitrification by Thermus thermophilus and related bacterial species.

71 ansmembrane proton channel domain of TH from Thermus thermophilus and the 6.9 A crystal structure of

72 onucleases H (RNases H) from the thermophile Thermus thermophilus and the mesophile Escherichia coli

73 onucleases H from the thermophilic bacterium Thermus thermophilus and the mesophile Escherichia coli

74 )-NO complex formed in cytochrome ba(3) from Thermus thermophilus and the product of its low-temperat

75 the highly divergent thermophilic eubacteria Thermus thermophilus and Thermotoga maritima were cloned

76 nd the recently determined structures of the Thermus thermophilus and Thermus aquaticus varsigma(70)-

77 ses from Thermus aquaticus, Thermus oshimai, Thermus thermophilus and Thermus brockianus.

78 genus Thermus (Taq (Thermus aquaticus), Tth (Thermus thermophilus) and Tfl (Thermus flavus)) and comp

79 om Haloarcula morismortui, Escherichia coli, Thermus thermophilus, and Deinococcus radiodurans.

80 tructures in the 30 S ribosomal subunit from Thermus thermophilus, and their interactions with 16 S R

81 X-ray crystal structures of the full-length Thermus thermophilus apo IF2 and its complex with GDP pr

82 -exonuclease enzymes from Thermus aquaticus, Thermus thermophilus, Archaeoglobus fulgidus, Pyrococcus

83 Ribosomes from the extreme thermophile Thermus thermophilus are capable of translation in a cou

84 the coupled reaction of PRODH and P5CDH from Thermus thermophilus are consistent with a substrate cha

85 Major centers of motion in the rRNAs of Thermus thermophilus are identified by alignment of crys

86 undertaken a systematic structural study of Thermus thermophilus Argonaute (TtAgo) ternary complexes

87 Here we report on the crystal structure of Thermus thermophilus argonaute bound to a 5'-phosphoryla

88 structure of a ternary complex of wild-type Thermus thermophilus argonaute bound to a 5'-phosphoryla

89 d the structure of the entire complex I from Thermus thermophilus at 4.5 A resolution.

90 novirus) grows in the thermophilic bacterium Thermus thermophilus at 70 degrees C.

91 ucture of the entire, intact complex I (from Thermus thermophilus) at 3.3 A resolution.

92 ucture of a Na(+)/H(+) antiporter, NapA from Thermus thermophilus, at 3 A resolution, solved from cry

93 Spo0J of the Gram-negative hyperthermophile Thermus thermophilus belong to the conserved ParAB famil

94 Here, we show that PilN and PilO from Thermus thermophilus can be isolated as a complex with P

95 We determined the X-ray crystal structure of Thermus thermophilus CarD, allowing us to generate a str

96 Here we present crystal structures of Thermus thermophilus CarH in all three relevant states:

97 mes, we determined crystal structures of two Thermus thermophilus Cas6 enzymes both alone and bound t

98 Here we report the crystal structure of Thermus thermophilus CasA.

99 B)Mb/Cu(+) complex are analogous to those in Thermus thermophilus CcO (TtCcO) but distinct from those

100 By electron cryo-tomography of whole Thermus thermophilus cells, we determined the in situ st

101 at the tedradecamer structure of the 800 kDa Thermus thermophilus chaperonin GroEL is preserved in aq

102 A study of the Thermus thermophilus chorismate mutase (TtCM) is describ

103 Molecular dynamics (MD) simulations of Thermus thermophilus chorismate mutase substrate complex

104 We have determined the structure of Thermus thermophilus ClpB (TClpB) using a combination of

105 the thermophilic ribonuclease HI enzyme from Thermus thermophilus, compared to its mesophilic homolog

106 crystal structure of the hydrophilic part of Thermus thermophilus complex I recently became available

107 us virus PH75, which infects the thermophile Thermus thermophilus, consists of a closed DNA strand of

108 m expression of the "signal peptide-lacking" Thermus thermophilus cycA gene in the cytoplasm of Esche

109 bility parameters for individual residues in Thermus thermophilus cysteine-free RNase H were determin

110 from the dinuclear heme a(3)/Cu(B) center in Thermus thermophilus cytochrome ba(3) oxidase.

111 e corresponding to amino acids 44-168 of the Thermus thermophilus cytochrome ba3 subunit II.

112 We have investigated the folding dynamics of Thermus thermophilus cytochrome c(552) by time-resolved

113 terminal signal sequence) structural gene of Thermus thermophilus cytochrome c(552) in the cytoplasm

114 and GluRS2s, to the crystal structure of the Thermus thermophilus D-GluRS:tRNA(Glu) complex, a diverg

115 complete modification map for SSU rRNA from Thermus thermophilus, determined primarily by HPLC/elect

116 d, herein we report the ligation fidelity of Thermus thermophilus DNA ligase at a range of temperatur

117 oligonucleotides were used as substrates for Thermus thermophilus DNA ligase, on a M13mp18 ssDNA temp

118 erse transcription of the RNA by recombinant Thermus thermophilus DNA polymerase (rTth pol), the resu

119 the well characterized DNA polymerase I-like Thermus thermophilus DNA polymerase.

120 show that cleavage by Thermus aquaticus and Thermus thermophilus DNA polymerases can be precise and

121 of the NBD of the bacterial Hsp70 homologue Thermus thermophilus DnaK in the ADP-bound state.

122 al NMR study of a prokaryotic Hsp70 homolog, Thermus thermophilus DnaK, using a 54kDa construct conta

123 sed it as a probe to isolate the full length Thermus thermophilus dnaX gene.

124 ysis showed that Deinococcus radiodurans and Thermus thermophilus do not possess asparagine synthetas

125 report the 2.5-A resolution structure of the Thermus thermophilus EC; the structure reveals the post-

126 Thermus thermophilus EF-Ts exists as a stable dimer in s

127 experimental analyses have demonstrated that Thermus thermophilus EF-Tu does not bind Asp-tRNA (Asn)

128 nty amino acids in the tRNA binding cleft of Thermus Thermophilus EF-Tu were each mutated to structur

129 nteraction of tRNA with Escherichia coli and Thermus thermophilus EF-Tu.

130 In some bacteria such as Thermus thermophilus, efficient delivery of misacylated

131 eport the 3.0-A resolution structures of the Thermus thermophilus elongation complex (EC) with a non-

132 tems of Saccharomyces cerevisiae tRNA Phe to Thermus thermophilus elongation factor Tu (EF-Tu) reveal

133 scherichia coli elongator aminoacyl-tRNAs to Thermus thermophilus elongation factor Tu (EF-Tu) were d

134 or valine and assayed for their affinity to Thermus thermophilus elongation factor Tu (EF-Tu)*GTP by

135 he affinities of these misacylated tRNAs for Thermus thermophilus elongation factor Tu (EF-Tu).GTP we

136 In order to identify amino acids in Thermus thermophilus elongation factor Tu which contribu

137 an RNA polymerase, the bacterial enzyme from Thermus thermophilus, engaged in reiterative transcripti

138 using the known structure of the homologous Thermus thermophilus enzyme.

139 stability of the seven-iron ferredoxin from Thermus thermophilus (FdTt), we investigated its chemica

140 structure of the anticodon-binding domain of Thermus thermophilus FRS and exhibited circular dichrois

141 totriose-binding protein identified from the Thermus thermophilus genome sequence.

142 einococcus radiodurans, D. geothermalis, and Thermus thermophilus genomes for nucleotide replacement

143 tRNA bound to glutamyl-tRNA synthetase from Thermus thermophilus (Glu-tRNA(Glu)) are considered.

144 from the extremely thermophilic eubacterium Thermus thermophilus has been cloned and expressed at hi

145 structure of the soluble Rieske protein from Thermus thermophilus has been determined at a resolution

146 in the hydrophilic domain of complex I from Thermus thermophilus has been determined with the use of

147 ic domain (peripheral arm) of complex I from Thermus thermophilus has been solved at 3.3 angstrom res

148 smortui and the small ribosomal subunit from Thermus thermophilus has permanently altered the way pro

149 alog, Gfh1, present in Thermus aquaticus and Thermus thermophilus, has the opposite effect on elongat

150 The two heme-copper terminal oxidases of Thermus thermophilus have been shown to catalyze the two

151 part (NDH-1) in Paracoccus denitrificans and Thermus thermophilus HB-8 consists of 14 subunits.

152 ating NADH-quinone oxidoreductase (NDH-1) of Thermus thermophilus HB-8 is composed of 14 subunits (de

153 eductase (NDH-1) of a thermophilic bacterium Thermus thermophilus HB-8 were cloned and sequenced.

154 DNA translocator secretin complex, PilQ, in Thermus thermophilus HB27 comprising a stable cone and c

155 A Thermus thermophilus HB27 strain was constructed in whic

156 Recombinant type II IPP isomerase from Thermus thermophilus HB27 was purified by Ni2+ affinity

157 50, CYP175A1 from the thermophilic bacterium Thermus thermophilus HB27, has been solved to 1.8-A reso

158 lus biogenesis and natural transformation of Thermus thermophilus HB27.

159 ne product complex crystal structures of the Thermus thermophilus (HB27) U3S protein.

160 results of experiments with Tth ligase from Thermus thermophilus HB8 and a series of nucleoside anal

161 We report sequence of Thermus thermophilus HB8 DNA containing the gene (cycA)

162 Thermus thermophilus HB8 DNA ligase (Tth DNA ligase) dif

163 e (complex I) from the thermophilic organism Thermus thermophilus HB8 has been purified and character

164 Here, we report that family 5 UDGb from Thermus thermophilus HB8 is not only a uracil DNA glycos

165 This Thermus ligase is similar to Thermus thermophilus HB8 ligase with respect to pH, salt

166 ring infection of the thermophilic bacterium Thermus thermophilus HB8 with the bacteriophage P23-45 w

167 presented by Thermus aquaticus YT1, Japan by Thermus thermophilus HB8, New Zealand by Thermus filifor

168 RNA polymerase (RNAP) from the thermophile, Thermus thermophilus HB8, was purified to electrophoreti

169 stal structure of the HD domain of Cas3 from Thermus thermophilus HB8.

170 B)-type ATPases are present in the genome of Thermus thermophilus (HB8 and HB27): the TTC1358, TTC137

171 ontaneous, erythromycin-resistant mutants of Thermus thermophilus IB-21 were isolated and found to ca

172 endent mutants of the thermophilic bacterium Thermus thermophilus IB-21.

173 OPP and allene 2-OPP were not substrates for Thermus thermophilus IDI-2 or Escherichia coli IDI-1 but

174 During studies with Thermus thermophilus IDI-2, we discovered that the olefi

175 reduction by ba(3) cytochrome c oxidase from Thermus thermophilus in the absence and presence of CO u

176 on NMR study of the 44-kDa NBD of Hsp70 from Thermus thermophilus in the ADP and AMPPNP states.

177 rase I homologues from Thermus aquaticus and Thermus thermophilus in the invasive signal amplificatio

178 We reconstituted protein translation of Thermus thermophilus in vitro from purified ribosomes, t

179 structed a mutant of the extreme thermophile Thermus thermophilus in which the prmA gene has been dis

180 nation of the crystal structure of CinA from Thermus thermophilus, in complex with several ligands.

181 rome oxidase from the thermophilic bacterium Thermus thermophilus, induced by guanidine hydrochloride

182 Gfh1, a transcription factor from Thermus thermophilus, inhibits all catalytic activities

183 Gfh1, a GreA homolog from Thermus thermophilus, inhibits rather than activates RNA

184 The ba3-type cytochrome c oxidase from Thermus thermophilus is a membrane-bound protein complex

185 Kt-23 in the 30S ribosomal subunit of Thermus thermophilus is a rare exception in which the bu

186 Thermus thermophilus is a thermophilic model organism di

187 The secretin complex of Thermus thermophilus is an oligomer of the 757-residue P

188 structure of the subunit from the bacterium Thermus thermophilus is presented.

189 The V/A-ATPase from the eubacterium Thermus thermophilus is similar in structure to the euka

190 matically invert the coenzyme specificity of Thermus thermophilus isopropylmalate dehydrogenase from

191 m the thermophilic Gram-negative eubacterium Thermus thermophilus; it is homologous to various multid

192 mployed experimental electrochemical data on Thermus thermophilus laccase as benchmarks to validate o

193 ined in the ba(3)-type oxygen reductase from Thermus thermophilus, leading from the propionates of he

194 We investigated the collective motion in Thermus thermophilus leucyl-tRNA synthetase by studying

195 ation of a different binding mode for N3- in Thermus thermophilus Mn-SOD than Fe-SOD.

196 e the 2.7-A X-ray structure of heterodimeric Thermus thermophilus multidrug resistance proteins A and

197 However, we have shown previously that the Thermus thermophilus N1c fragment containing this motif

198 rate dehydrogenase and the distantly related Thermus thermophilus NAD-dependent isopropylmalate dehyd

199 ution, since they are unchanged in bacteria (Thermus thermophilus, PDB entry 2J01) and archaea (Haloa

200 Gp39, a small protein encoded by Thermus thermophilus phage P23-45, specifically binds th

201 saminoacyl-tRNA is synthesized in nature (by Thermus thermophilus phenylalanyl-tRNA synthetase), and

202 ports that bisphenylalanyl-tRNA is formed by Thermus thermophilus phenylalanyl-tRNA synthetase.

203 Here we report the crystal structure of Thermus thermophilus PheRS (TtPheRS) at 2.6 A resolution

204 Starting with the crystal structure of Thermus thermophilus PheRS without bound ligand, HierDoc

205 The 2.0-A resolution structure of Thermus thermophilus PRODH reveals a distorted (betaalph

206 The 1.9 A resolution structure of Thermus thermophilus proline dehydrogenase inactivated b

207 he crystal structure of the 30S subunit from Thermus thermophilus, refined to 3 A resolution.

208 etween thermorubin and the 70S ribosome from Thermus thermophilus reported here shows that thermorubi

209 shown that S15 from the extreme thermophile Thermus thermophilus represses the translation of its ow

210 rmation of DNA in the thermophilic bacterium Thermus thermophilus requires a unique secretin complex

211 he 16S and 23S rRNAs of Escherichia coli and Thermus thermophilus revealed that most BPh interactions

212 f the recently determined genome sequence of Thermus thermophilus revealed the presence of more than

213 we have characterized the folding process of Thermus thermophilus ribonuclease H using circular dichr

214 we populated the folding intermediate of the Thermus thermophilus ribonuclease H, which forms before

215 s on multiple time scales in a cysteine-free Thermus thermophilus ribonuclease HI mutant (ttRNH(*)) a

216 We used the three-dimensional structure of Thermus thermophilus ribosomal protein S11, a bacterial

217 sembles the fold of the N-terminal domain of Thermus thermophilus ribosomal protein S3.

218 ok on the challenge of developing a detailed Thermus thermophilus ribosomal structure computationally

219 We solved the structure of the Thermus thermophilus ribosome bound to mRNA and three tR

220 n factor IF3 bound to the 30S subunit of the Thermus thermophilus ribosome has been determined by cry

221 re of EF4-guanosine diphosphate bound to the Thermus thermophilus ribosome with a P-site tRNA at 2.9

222 al structure at 3 angstrom resolution of the Thermus thermophilus ribosome with a tRNA in the hybrid

223 Examination of the crystal structures of Thermus thermophilus ribosomes in the pre- and post-tran

224 The high stability of the soluble Thermus thermophilus Rieske protein permits chemical red

225 e quinol and the inhibitor stigmatellin, the Thermus thermophilus Rieske protein was reacted with die

226 The 2.7 A resolution structure of the Thermus thermophilus RNA polymerase (RNAP) holoenzyme in

227 ranscription initiation complexes comprising Thermus thermophilus RNA polymerase, sigma(A), and a pro

228 he intrinsic transcript cleavage activity of Thermus thermophilus RNA polymerase.

229 erivative of myxopyronin B--complexed with a Thermus thermophilus RNAP holoenzyme.

230 rifabutin and rifapentin complexed with the Thermus thermophilus RNAP holoenzyme.

231 The 2.4 A resolution structure of the Thermus thermophilus RNAP-Stl complex showed that, in fu

232 Molecular modeling of Thermus thermophilus RNAP-substrate NTP complex identifi

233 ay structure defined a ppGpp binding site on Thermus thermophilus RNAP.

234 ause sites are conserved between E. coli and Thermus thermophilus RNAPs, but are not recognized by Sa

235 directed mutagenesis and gene replacement of Thermus thermophilus rpsL to assess the importance of si

236 rophobic pocket between domains 1 and 2, and Thermus thermophilus RRF (ttRRF) with and without a muta

237 Upon binding of either E. coli or Thermus thermophilus RRF to the E. coli ribosome, the ti

238 CR) assay using the recombinant thermostable Thermus thermophilus (rTth) enzyme was developed to dete

239 he 2.8 A resolution crystal structure of the Thermus thermophilus SecA protein (TtSecA).

240 isolation and characterization of mutants of Thermus thermophilus selected for resistance to the tube

241 , onto a stable coiled-coil base provided by Thermus thermophilus seryl-tRNA synthetase and tested th

242 in the cocrystal structure of tRNA(Ser) and Thermus thermophilus seryl-tRNA synthetase.

243 es and oxygenases from A. baumannii and from Thermus thermophilus (similar to the P. aeruginosa syste

244 The genomes of two closely related lytic Thermus thermophilus siphoviruses with exceptionally lon

245 ngatus photosystem II (<3-A diffraction) and Thermus thermophilus small ribosomal subunit bound to th

246 e of the myxopyronin-bound RNA polymerase of Thermus thermophilus suggests a binding mode of these in

247 enicol in complex with the 70S ribosome from Thermus thermophilus suggests a model for chloramphenico

248 A is dispensable in Deinococcus radiodurans, Thermus thermophilus, Synechocystis PCC6803 and Streptoc

249 raphic and biochemical analyses of RuvC from Thermus thermophilus (T.th. RuvC).

250 nthetase of the distantly related bacterium, Thermus thermophilus, than to that of the membrane-bound

251 se with reverse transcriptase activity (from Thermus thermophilus) that is selective by up to 18-fold

252 unction of the proton pump in complex I from Thermus thermophilus The simulations suggest that proton

253 In the RNase H from Thermus thermophilus, the low DeltaC degrees (P) has bee

254 of the closely related bacterial enzyme from Thermus thermophilus, the quinone is thought to bind in

255 ype III-B CRISPR-Cas system of the bacterium Thermus thermophilus, the TtCmr complex, is composed of

256 mplex of the Type III-A CRISPR-Cas system of Thermus thermophilus: the Csm complex (TtCsm).

257 lly truncated Spo0J (amino acids 1-222) from Thermus thermophilus to 2.3 A resolution by multiwavelen

258 were aligned to the programmed ribosome from Thermus thermophilus, to provide a common reference fram

259 The structure comprises Thermus thermophilus transcription activator protein TTH

260 d by the refined structure of the homologous Thermus thermophilus tRNA(Ser)-SerRS complex that Cusack

261 e recently found that NO and O(2) binding in Thermus thermophilus (Tt) ba(3) is ~10 times faster than

262 ere we demonstrate that Ago of the bacterium Thermus thermophilus (TtAgo) acts as a barrier for the u

263 d for four related thermostable DNA ligases, Thermus thermophilus ( Tth ) ligase, Thermus sp. AK16D l

264 The DNA ligase from Thermus thermophilus (Tth DNA ligase) seals single-stran

265 rom the Thermus species, including that from Thermus thermophilus (Tth pol).

266 Thermus thermophilus (Tth) DNA ligase is unable to join

267 (FRET), that homodimeric bacterial SSB from Thermus thermophilus (Tth) is able to diffuse spontaneou

268 We wanted to investigate whether Thermus thermophilus (Tth) NusG can be used as a model f

269 Here we present a crystal structure of Thermus thermophilus (Tth) RbfA and a three-dimensional

270 ly of the minimal functional holoenzyme from Thermus thermophilus (Tth), an extreme thermophile.

271 rimers, with three thermostable DNA ligases: Thermus thermophilus (Tth), Thermus scotoductus (Ts), an

272 mo-stable NAD(+)-dependent DNA ligases, from Thermus thermophilus (Tth), Thermus scotoductus (Ts), Rh

273 hilic eubacteria Thermus aquaticus (Taq) and Thermus thermophilus (Tth).

274 eins in Schizosaccharomyces pombe (Atl1) and Thermus thermophilus (TTHA1564) protect against the adve

275 The homocitrate synthase from Thermus thermophilus (TtHCS) is a metal-activated enzyme

276 nine-xanthine phosphoribosyltransferase from Thermus thermophilus (TtHGXPRT).

277 ymerases from Thermus aquaticus (TaqPol) and Thermus thermophilus (TthPol) reveals two regions, in th

278 that the PolX from the heat-stable organism Thermus thermophilus (TthPolX) inserts the four dNTPs wi

279 RNH proteins from Thermus thermophilus (ttRNH) and Escherichia coli (ecRNH

280 The Rieske protein from Thermus thermophilus (TtRp) and a truncated version of t

281 nd reduced states of the Rieske protein from Thermus thermophilus (TtRp) as determined by NMR spectro

282 ke protein from the cytochrome bc complex of Thermus thermophilus (TtRp) undergoes modest redox-state

283 coccus denitrificans and cytochrome ba3 from Thermus thermophilus, two distinct members of the heme-c

284 ed over interacting regions of the tRNA in a Thermus thermophilus TyrRS/tRNA(Tyr) cocrystal structure

285 Conversion of EG doublet in family 4 Thermus thermophilus UDGa to QD doublet increases the ca

286 The crystal structure of Thermus thermophilus UvrB reveals a core that is structu

287 substeps were resolved, as was the case with Thermus thermophilus V1-ATPase (TtV1).

288 permutants of the ribosomal protein S6 from Thermus thermophilus was analyzed.

289 of the hydrophilic domain of complex I from Thermus thermophilus was determined.

290 mains of complex I from Escherichia coli and Thermus thermophilus, we show that the pattern of cross-

291 of the bacteria Rhodobacter sphaeroides and Thermus thermophilus were demonstrated to be involved in

292 e tRNA from Escherichia coli Nissle 1917 and Thermus thermophilus were non-immunostimulatory.

293 ctive-site structure of cytochrome ba 3 from Thermus thermophilus, which is considered to be both nec

294 T and single-mutant Cu(A) redox centers from Thermus thermophilus, which shows that thermal fluctuati

295 rmational dynamics of the intact ATPase from Thermus thermophilus with those of its membrane and solu

296 sible surface of the rRNA calculated for the Thermus thermophilus X-ray crystal structures shows exte