ライフサイエンスコーパス: Thermus thermophilus

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

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

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

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

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

6 lity in the extremely thermophilic bacterium Thermus thermophilus.

7 uctures of PrmA from the extreme thermophile Thermus thermophilus.

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

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

10 o, an Argonaute protein from the Eubacterium Thermus thermophilus.

11 e from the extremely thermophilic bacterium, Thermus thermophilus.

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

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

14 esistant mutants of the extreme thermophile, Thermus thermophilus.

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

16 somal proteins of Haloarcula marismortui and Thermus thermophilus.

17 aticivorans, Rhodopseudomonas palustris, and Thermus thermophilus.

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

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

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

21 n was obtained from thermophilic eubacterium Thermus thermophilus.

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

23 scherichia coli and one from the thermophile Thermus thermophilus.

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

25 n the ribosome of the thermophilic bacterium Thermus thermophilus.

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

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

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

29 2 of the ba(3)-type cytochrome oxidase from Thermus thermophilus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

46 t the crystal structure of a posttermination Thermus thermophilus 70S ribosome complexed with EF-G, R

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

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

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

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

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

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

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

54 A crystal structure of the Thermus thermophilus 70S ribosome with a tRNA(Phe) bound

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 rystal structure of sarecycline bound to the Thermus thermophilus 70S ribosome.

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

59 ype III spacer acquisition in phage-infected Thermus thermophilus, a bacterium that lacks either a st

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

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

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

63 show herein that a glycosynthase mutant of a Thermus thermophilus alpha-glycosidase can react with un

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

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

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

67 The P5CDHs from Thermus thermophilus and Deinococcus radiodurans form tr

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

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

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

71 (3,3) states of the homologous enzymes from Thermus thermophilus and Lactobacillus plantarum using a

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

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

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

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

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

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

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

79 bind adjacent to the active site of Ddl from Thermus thermophilus and used a combined biochemical and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

95 flow-flash experiments on the fully reduced Thermus thermophilus ba(3) (Tt ba(3)) cytochrome oxidase

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

97 for a thermostable bacteriophage, P23-45 of Thermus thermophilus Both the unexpanded procapsid and t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 Complex I from Thermus thermophilus encases 16 subunits with nine iron-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 r operon of the deeply branching thermophile Thermus thermophilus HB27 encodes for, an O-acetyl-l-hom

154 A Thermus thermophilus HB27 strain was constructed in whic

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

156 50, CYP175A1 from the thermophilic bacterium Thermus thermophilus HB27, has been solved to 1.8-A reso

157 lus biogenesis and natural transformation of Thermus thermophilus HB27.

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

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

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

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

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

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

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

165 We demonstrate that, in Thermus thermophilus HB8, the uncharacterized protein TT

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

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

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

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

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

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

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

173 e of the prototypical SEDS protein RodA from Thermus thermophilus in complex with its cognate bPBP at

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

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

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

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

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

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

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

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

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

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

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

185 Thermus thermophilus is a thermophilic model organism di

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

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

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

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

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

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

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

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

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

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

196 which cation/proton antiporters (CPAs), like Thermus thermophilus NapA (TtNapA) and Escherichia coli

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

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

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

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

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

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

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

204 mass spectrometry to show that the bacterium Thermus thermophilus produces two forms of type IV pilus

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

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

207 f a related Na(+)/H(+) antiporter, NapA from Thermus thermophilus, renders the transporter electroneu

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 the Fpr loop K61~I72 with a longer loop from Thermus thermophilus RuvC (E71~A87) endows Fpr with an e

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

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

242 We found Thermus thermophilus sensitive to lysis D (SlyD) and The

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

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

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

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

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

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

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

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

251 Here, we show that binding of a Thermus thermophilus (T. thermophilus) Csm (TthCsm) to a

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

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

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

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

256 In the eubacterium Thermus thermophilus, the DNA-guided Argonaute TtAgo def

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

258 e of the hyperthermophilic laccase HB27 from Thermus thermophilus, the physiologic role of which is u

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

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

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

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

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

264 The structure comprises Thermus thermophilus transcription activator protein TTH

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

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

267 nical interest Via DNA-Guided Argonaute from Thermus thermophilus (TtAgo).

268 s demonstrated that the sole bactofilin from Thermus thermophilus (TtBac) forms constitutive filament

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

270 in's binding to the 70S ribosomal subunit of Thermus thermophilus (Tth) has been unambiguously determ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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