ライフサイエンスコーパス: Methanococcus

1 n the antibiotic-insensitive archaebacterium Methanococcus.

2 proteolipid type found in eukaryotes and in Methanococcus.

3 ty between an adjacent upstream sequence and Methanococcus 16S rRNA.

4 synthase (AHAS) was cloned from the archaeon Methanococcus aeolicus.

5 consecutive helices (alpha-alpha-alpha), and Methanococcus, alternating helix-strand structures (beta

6 and function of the predicted exosome in the Methanococcus and Halobacterium lineages.

7 rent gene loss complementary to that seen in Methanococcus and Halobacterium, Thermoplasma acidophilu

8 present evidence for a "nitrogen regulon" in Methanococcus and Methanobacterium species containing ge

9 eropyrum) and euryarchaeota (Methanosarcina, Methanococcus, Archaeoglobus, Thermoplasma), with multip

10 dies of the mesophiles in the archaeal genus Methanococcus have become commonplace following the rece

11 tions found in yeast fibrillarin Nop1 to the Methanococcus homologue structure reveals that many of t

12 trophicus (MTH), and the extreme thermopiles Methanococcus igneus (MIG) and Methanococcus jannaschii

13 perthermophiles Methanococcus jannaschii and Methanococcus igneus were studied to determine whether m

14 ol to generate DIP has also been detected in Methanococcus igneus.

15 ng candidate enzymes previously evolved from Methanococcus janaschii Tyr synthetase for unnatural ami

16 hose of Haemophilus influenzae (a bacteria), Methanococcus jannaschii (an archaeon), and yeast (a euk

17 ted from ribosomes and whole-cell lysates of Methanococcus jannaschii (approximately 1,800 genes) usi

18 The crystal structure of eIF-5A from Methanococcus jannaschii (MJ eIF-5A) has been determined

19 The small heat-shock protein (sHSP) from Methanococcus jannaschii (Mj HSP16.5) forms a homomeric

20 motetrameric tRNA splicing endonuclease from Methanococcus jannaschii (MJ), indicating its role in ca

21 n of C8-substituted-nucleotides by FtsZ from Methanococcus jannaschii (Mj-FtsZ) and Bacillus subtilis

22 with that of a previously solved enzyme from Methanococcus jannaschii (MJ0109).

23 e thermopiles Methanococcus igneus (MIG) and Methanococcus jannaschii (MJA)) were characterized for t

24 a hyperthermophilic piezophilic methanogen, Methanococcus jannaschii (Mja).

25 MAT from the hyperthermophilic archaeon Methanococcus jannaschii (MjMAT) is a prototype of the n

26 from the thermophilic methanogenic archaeon Methanococcus jannaschii (Mjpri).

27 a(+)/Ca(2+)-exchange function of an NCX from Methanococcus jannaschii (NCX_Mj) and report its 1.9 ang

28 and 31 open reading frames including one in Methanococcus jannaschii .

29 teria such as Escherichia coli, archaea like Methanococcus jannaschii and animal viruses.

30 for three other I-1-Pases (from the archaea Methanococcus jannaschii and Archaeoglobus fulgidus, and

31 udy, these potential RubisCO sequences, from Methanococcus jannaschii and Archaeoglobus fulgidus, wer

32 aea Methanobacterium thermoautotrophicum and Methanococcus jannaschii and in Bacillus subtilis.

33 synthetase in the genomes of Archae such as Methanococcus jannaschii and Methanobacterium thermoauto

34 he only known exceptions are the euryarchaea Methanococcus jannaschii and Methanobacterium thermoauto

35 the mechanism of cysteinyl-tRNA formation in Methanococcus jannaschii and Methanobacterium thermoauto

36 The genomic sequences of Methanococcus jannaschii and Methanobacterium thermoauto

37 residing in the transcription factor IIB of Methanococcus jannaschii and Methanocaldococcus vulcaniu

38 thermolithotrophicus, and hyperthermophiles Methanococcus jannaschii and Methanococcus igneus were s

39 s and, in part, its operon organization with Methanococcus jannaschii and Methanothermobacter thermoa

40 dehydrogenase genes, MJ1425 and MJ0490, from Methanococcus jannaschii and one from Methanothermus fer

41 rom47 Aquifex aeolicus,47 Bacillus subtilis, Methanococcus jannaschii and Pseudomonas aeruginosa that

42 screening for GC-rich regions in the AT-rich Methanococcus jannaschii and Pyrococcus furiosus genomes

43 ied in the hyperthermophilic marine archaeon Methanococcus jannaschii and shown to catalyze the final

44 FEN1 enzymes from Archaeoglobus fulgidus and Methanococcus jannaschii and the DNA polymerase I homolo

45 om several archaea, including the methanogen Methanococcus jannaschii and the sulfate-reducing archae

46 binant versions of the F and P subunits from Methanococcus jannaschii and used them in in vitro and i

47 Escherichia coli, Haemophilus influenzae and Methanococcus jannaschii are involved in 64 unique fusio

48 s of two adjacent genes in the chromosome of Methanococcus jannaschii are similar to the amino and ca

49 stal structure of a specificity subunit from Methanococcus jannaschii at 2.4-A resolution.

50 rt the crystal structure of the complex from Methanococcus jannaschii at a resolution of 3.2 A.

51 oth Methanobacterium thermoautotrophicum and Methanococcus jannaschii but is unrelated to canonical L

52 derived from the tyrosyl-tRNA synthetase of Methanococcus jannaschii can be used to genetically enco

53 The complete genomic sequencing of Methanococcus jannaschii cannot identify the gene for th

54 family, the archaeal Sulfolobus shibatae and Methanococcus jannaschii CCA-adding enzymes, are also ca

55 f the hyperthermophiles Aquifex aeolicus and Methanococcus jannaschii complement enteric amtB mutants

56 sequence of the hyperthermophilic methanogen Methanococcus jannaschii contains homologs of most genes

57 rial S. typhimurium CorA and by the archaeal Methanococcus jannaschii CorA, which bear only 12% ident

58 the structure of the DNA-binding core of the Methanococcus jannaschii DNA topoisomerase VI A subunit

59 The hyperthermophilic archaeon Methanococcus jannaschii encodes two putative transcript

60 The hyperthermophilic archaeon Methanococcus jannaschii encodes two putative transcript

61 a, Saccharomyces cerevisiae for Eukarya, and Methanococcus jannaschii for Archaea, provide the basis

62 The Methanococcus jannaschii gene MJ0671 was cloned and over

63 The Methanococcus jannaschii gene MJ1392 was cloned, and its

64 In comparisons of the entire set of Methanococcus jannaschii genes with their orthologs from

65 Comparisons with the Methanococcus jannaschii genome data underline the exten

66 One of the ORFs in the Methanococcus jannaschii genome possesses high similarit

67 The interpretation of the Methanococcus jannaschii genome will inevitably require

68 From homology searching of the Methanococcus jannaschii genome, a gene coding for an en

69 asma genitalium, Haemophilus influenzae, and Methanococcus jannaschii genomes for unidentified or mis

70 but homologous enzymes, the hyperthermophile Methanococcus jannaschii has an enzyme, DCD-DUT, that ha

71 beta-semialdehyde dehydrogenase (ASADH) from Methanococcus jannaschii has been determined to 2.3 angs

72 ble 8-oxoguanine (oxoG) DNA glycosylase from Methanococcus jannaschii has been expressed in Escherich

73 The hyperthermophilic euryarchaeon Methanococcus jannaschii has no recognizable homologues

74 The hyperthermophilic archaeon Methanococcus jannaschii has two members of this gene fa

75 Cell extracts of Methanococcus jannaschii have been shown to readily conv

76 Analyses of the F(420)s present in Methanococcus jannaschii have shown that these cells con

77 lactate synthase encoded by the ComA gene in Methanococcus jannaschii have suggested that ComA, which

78 lutionary distant alpha-crystallin domain in Methanococcus jannaschii heat-shock protein 16.5 reveals

79 ontrast to the syn conformation reported for Methanococcus jannaschii homoserine kinase.

80 The high-resolution structures of Methanococcus jannaschii HSK ternary complexes with its

81 vergence, we induced the ordered oligomer of Methanococcus jannaschii Hsp16.5 to transition to either

82 y studies of five different sHSP assemblies: Methanococcus jannaschii HSP16.5, human alphaB-crystalli

83 the complete genome sequence of the archaeon Methanococcus jannaschii in 1996.

84 We have polymerized FtsZ1 from Methanococcus jannaschii in the presence of millimolar c

85 le cassette of known structure, MJ0796, from Methanococcus jannaschii indicates that at least two bin

86 AdoMetDC from the Archaea Methanococcus jannaschii is a prototype for a recently d

87 mple, a previous putative gene (MJ1604) from Methanococcus jannaschii is now annotated as a phosphofr

88 Whereas ProRS from Methanococcus jannaschii is similar to E. coli in its ab

89 Two putative Methanococcus jannaschii isocitrate dehydrogenase genes,

90 The genome of the archaeon Methanococcus jannaschii lacks the gene for a normal cys

91 ative third catalytic residue from a related Methanococcus jannaschii LonB, also faces the solvent an

92 hosphate (in a reaction analogous to that of Methanococcus jannaschii MJ0044).

93 similarity to that of the recently reported Methanococcus jannaschii Mj0226 protein.

94 The protein product of the Methanococcus jannaschii MJ0503 gene aksA (AksA) was fou

95 old classes have been proposed: one based on Methanococcus jannaschii MJ0577 (1MJH) that binds ATP, a

96 The protein product of the Methanococcus jannaschii MJ0768 gene has been expressed

97 We studied a prototypical ABC NBD, the Methanococcus jannaschii MJ0796, using spectroscopic tec

98 h are typified by Bacillus subtilis YqeV and Methanococcus jannaschii Mj0867, and we predict that Rim

99 Methanococcus jannaschii MJ0936 is a hypothetical protei

100 The Methanococcus jannaschii MJ109 gene product, the sequenc

101 The protein product of the Methanococcus jannaschii MJ1256 gene has been expressed

102 Here,Methanococcus jannaschii MR-ATPgammaS-DNA structure reve

103 recognition model based on the structures of Methanococcus jannaschii Mre11 (MjMre11) bound to longer

104 The archaeal NCX_Mj (Methanococcus jannaschii NCX) system was used to resolve

105 onsense codon, TAG, together with orthogonal Methanococcus jannaschii or Escherichia coli tRNA/synthe

106 Methanococcus jannaschii partially retains the superoper

107 e forms part of a multidomain protein, as in Methanococcus jannaschii peptidyl-prolyl cis/trans isome

108 Both the Methanococcus jannaschii phosphoenolpyruvate synthase an

109 The protein translation apparatus of Methanococcus jannaschii possesses the unusual enzyme pr

110 The archaeal Methanococcus jannaschii ProRS is a member of the eukary

111 Studies with human and Methanococcus jannaschii ProRS, which lack a post-transf

112 A solution NMR study of a model ABC, Methanococcus jannaschii protein MJ1267, reveals that AD

113 The phylogenetic distribution of Methanococcus jannaschii proteins can provide, for the f

114 uence of the extremely thermophilic archaeon Methanococcus jannaschii provides a wealth of data on pr

115 he hyperthermophiles Thermotoga maritima and Methanococcus jannaschii resulted in fivefold higher T.

116 vely high similarity to the sequences of the Methanococcus jannaschii reverse gyrase (48% overall ide

117 y the recently solved X-ray structure of the Methanococcus jannaschii SecY complex, is a matter of co

118 changer (NCX) antiporter NCX_Mj protein from Methanococcus jannaschii shows an outward-facing conform

119 We have solved the structure of the Methanococcus jannaschii Spt4/5 complex by X-ray crystal

120 coli, and their ability to bind to human and Methanococcus jannaschii SRP RNA were determined in vitr

121 genes from the thermophilic archaeabacterium Methanococcus jannaschii that code for the putative cata

122 nucleotide triphosphate pyrophosphatase from Methanococcus jannaschii that shows a preference for pur

123 oded by bacterial genomes ranged from 8% for Methanococcus jannaschii to 37% for Mycoplasma pneumonia

124 For Methanococcus jannaschii tRNA(Pro), accuracy is difficul

125 he crystal structures of two substrate-bound Methanococcus jannaschii tyrosyl aminoacyl-tRNA syntheta

126 o alter or expand the genetic code, only the Methanococcus jannaschii tyrosyl tRNA synthetase and tRN

127 The Methanococcus jannaschii tyrosyl-transfer-RNA synthetase

128 ocedure, we apply it to the design of mutant Methanococcus jannaschii tyrosyl-tRNA synthetase (M.jann

129 Methanococcus jannaschii tyrosyl-tRNA synthetase is a mi

130 The small size of the archaebacterial Methanococcus jannaschii tyrosyl-tRNA synthetase may giv

131 We synthesized 1 and evolved a Methanococcus jannaschii tyrosyl-tRNA synthetase/tRNA(CU

132 The hyperthermophilic euryarchaeon Methanococcus jannaschii uses coenzyme M (2-mercaptoetha

133 , we demonstrate that the Thi4 ortholog from Methanococcus jannaschii uses exogenous sulfide and is c

134 of subunit H, in solution, from the archaeon Methanococcus jannaschii using multidimensional nuclear

135 MVP, a Methanococcus jannaschii voltage-gated potassium channel

136 ucture of the endonuclease from the archaeon Methanococcus jannaschii was determined to a resolution

137 In the work presented here, aIF2beta from Methanococcus jannaschii was expressed in Escherichia co

138 ease (FEN) of the hyperthermophilic archaeon Methanococcus jannaschii was expressed in Escherichia co

139 for observed IMP cyclohydrolase activity in Methanococcus jannaschii was purified and sequenced: its

140 monella serovar Typhimurium and the archaeon Methanococcus jannaschii were purified and shown to reta

141 e have investigated three such proteins from Methanococcus jannaschii with the strongest overall sequ

142 udy, a conserved archaeal gene (gi1500322 in Methanococcus jannaschii) was identified as the best can

143 Cd1 from Clostridium difficile, and Mj2 from Methanococcus jannaschii) were overproduced in Escherich

144 plasma genitalium, Synechocystis PCC6803 and Methanococcus jannaschii).

145 structure of the fibrillarin homologue from Methanococcus jannaschii, a hyperthermophile, at 1.6 A r

146 A sHSP homologue of Methanococcus jannaschii, a hyperthermophilic Archaeon,

147 structure of a small heat-shock protein from Methanococcus jannaschii, a hyperthermophilic archaeon.

148 The methanarchaeon, Methanococcus jannaschii, a hyperthermophilic, autotroph

149 the genomic sequence of the hyperthermophile Methanococcus jannaschii, addressing questions of its ph

150 Many archaebacteria, such as Methanococcus jannaschii, also contain a gene (S4) that

151 for chorismate mutase (CM) from the archaeon Methanococcus jannaschii, an extreme thermophile, was su

152 In contrast, the IMPase from Methanococcus jannaschii, an organism in which DIP does

153 tyrosyl-tRNA synthetases from S. cerevisiae, Methanococcus jannaschii, and Bacillus stearothermophilu

154 genome sequence of an autotrophic archaeon, Methanococcus jannaschii, and its 58- and 16-kilobase pa

155 Archaeoglobus fulgidus, Pyrococcus furiosus, Methanococcus jannaschii, and Methanobacterium thermoaut

156 neumoniae, Synechocystis sp. strain PCC6803, Methanococcus jannaschii, and Pyrobaculum aerophilum).

157 lap endonuclease from Archaeglobus fulgidus, Methanococcus jannaschii, and Pyrococcus furiosus, respe

158 en purified to homogeneity from the archaeon Methanococcus jannaschii, and the gene encoding it has b

159 In this report, it is shown not only that Methanococcus jannaschii, Archaeoglobus fulgidus, Methan

160 ch protein, MJ0577, from a hyperthermophile, Methanococcus jannaschii, at 1.7-A resolution.

161 The MJ1149 gene from the Archaeon, Methanococcus jannaschii, has been cloned and expressed

162 t variations were observed in (G+C)% and, in Methanococcus jannaschii, in the frequency of the dinucl

163 rophosphatase gene from the archaebacterium, Methanococcus jannaschii, introduced into E. coli, incre

164 isolated from the hyperthermophilic Archaea Methanococcus jannaschii, is a member of the small heat-

165 hose genomes have been sequenced completely (Methanococcus jannaschii, Methanobacterium thermoautotro

166 no orthologs for these genes can be found in Methanococcus jannaschii, Methanobacterium thermoautotro

167 letely sequenced and are publicly available: Methanococcus jannaschii, Methanobacterium thermoautotro

168 is sp. genome nor in the archaeal genomes of Methanococcus jannaschii, Methanobacterium thermoautotro

169 ately halophilic and non-halophilic Archaea (Methanococcus jannaschii, Methanosarcina mazei, Methanob

170 structure of the corresponding protein from Methanococcus jannaschii, MJ0158.

171 segment, RCK domain-containing channel from Methanococcus jannaschii, MjK2, by testing its general f

172 Haemophilus influenzae, Helicobacter pylori, Methanococcus jannaschii, Mycoplasma pneumoniae, M. geni

173 ations for 81 gel patterns for Homo sapiens, Methanococcus jannaschii, Pyro coccus furiosus, Shewanel

174 d metal ion, which is different from that of Methanococcus jannaschii, strongly supports an active ro

175 habditis elegans, Methanopyrus kandleri, and Methanococcus jannaschii, suggesting a conservation of i

176 ynthetic organisms, viz. the archaebacterium Methanococcus jannaschii, the eubacterium Escherichia co

177 Applied to the complete genome of Methanococcus jannaschii, the method recognized the fold

178 nd with the exception of the archaebacterium Methanococcus jannaschii, the numbers of multidrug efflu

179 ingle polypeptide of 645 amino acids, as for Methanococcus jannaschii, the Sulfolobus solfataricus SS

180 bound to full-length SRP RNA of the archaeon Methanococcus jannaschii, to eukaryotic human SRP RNA, a

181 signed open reading frame from the genome of Methanococcus jannaschii, viz., MJ0757.

182 available archaeal genome sequence, that of Methanococcus jannaschii, were analysed using the BLAST2

183 For the prolyl-tRNA synthetase (ProRS) of Methanococcus jannaschii, which activates both proline a

184 esolution (1.5-1.9 A) structures of PSP from Methanococcus jannaschii, which define the open state pr

185 of the orthogonal tyrosine pair derived from Methanococcus jannaschii, which has been used to selecti

186 ethanoarchaea Methanosarcina thermophila and Methanococcus jannaschii.

187 tified in the hyperthermophilic euryarchaeon Methanococcus jannaschii.

188 ative RNA helicase from the hyperthermophile Methanococcus jannaschii.

189 -) with phosphoserine phosphatase (PSP) from Methanococcus jannaschii.

190 was characterized from the hyperthermophile Methanococcus jannaschii.

191 ecognized in the complete genome sequence of Methanococcus jannaschii.

192 etected and purified from one such organism, Methanococcus jannaschii.

193 ng methanoarchaea M. thermoautotrophicum and Methanococcus jannaschii.

194 recombinant RNAP subunits from the archaeon Methanococcus jannaschii.

195 esence of a homolog in the archaeal organism Methanococcus jannaschii.

196 t FtsZ from the hyperthermophilic methanogen Methanococcus jannaschii.

197 characterization of the SSB of an archaeon, Methanococcus jannaschii.

198 tion with their counterparts in the archaeon Methanococcus jannaschii.

199 chocystis PCC 6803, as well as one Archaeon, Methanococcus jannaschii.

200 search open reading frames in the genome of Methanococcus jannaschii.

201 a bacterial regulatory protein, GlnK1, from Methanococcus jannaschii.

202 col challenge, and syntrophic coculture with Methanococcus jannaschii.

203 ng two 36.2-kDa subunits from the methanogen Methanococcus jannaschii.

204 was recently shown that Methanocaldococcus (Methanococcus) jannaschii and other anaerobic archaea sy

205 Although Methanocaldococcus (Methanococcus) jannaschii was the first archaeon to have

206 tor the conformations of the PAN ATPase from Methanococcus jannischii.

207 ion would predict that it would, between the Methanococcus lineage (which is the deepest of the metha

208 closely related homologue from the mesophile Methanococcus maripaludis (Mma) is nearly inert as a tra

209 e that L7Ae coelutes with partially purified Methanococcus maripaludis (Mma) RNase P activity.

210 cci, we isolated nine conditional mutants of Methanococcus maripaludis after transformation of the wi

211 An acetate-requiring mutant of Methanococcus maripaludis allowed efficient labeling of

212 Methanococcus maripaludis and Methanocaldococcus jannasc

213 ions with alternative methanogenic partners, Methanococcus maripaludis and Methanospirillum hungatei,

214 s of H(2) metabolism in the model methanogen Methanococcus maripaludis and using formate as an additi

215 equence of the 8,285-bp plasmid pURB500 from Methanococcus maripaludis C5 was determined.

216 The methanogenic archaean Methanococcus maripaludis can use ammonia, alanine, or d

217 ble, mesophilic, hydrogenotrophic methanogen Methanococcus maripaludis contains 1,722 protein-coding

218 Here we show that ThiI from the archaeon Methanococcus maripaludis contains a [3Fe-4S] cluster th

219 oacylation of the same tRNA with cysteine by Methanococcus maripaludis cysteinyl-tRNA synthetase.

220 or switch-off, in the methanogenic archaeon Methanococcus maripaludis does not involve detectable co

221 The Methanococcus maripaludis energy-conserving hydrogenase

222 Although the Methanococcus maripaludis genome lacks a gene that can b

223 roscopy, we show that an archaeal pilus from Methanococcus maripaludis has a structure entirely diffe

224 Among the archaea, Methanococcus maripaludis has the unusual ability to use

225 Here we report the crystal structure of a Methanococcus maripaludis homologue of Rce1, whose endop

226 d structures of the archaeal chaperonin from Methanococcus maripaludis in both a peptide acceptor (op

227 al structure of the archaeal chaperonin from Methanococcus maripaludis in several nucleotides bound s

228 Methanococcus maripaludis is a mesophilic archaeon that

229 Mma10b from the euryarchaeote Methanococcus maripaludis is a mesophilic member of the

230 Methanococcus maripaludis is a mesophilic species of Arc

231 Methanococcus maripaludis is a methanogenic archaeon tha

232 Methanococcus maripaludis is a strictly anaerobic, metha

233 Methanococcus maripaludis is a strictly anaerobic, metha

234 en assimilation in the methanogenic archaeon Methanococcus maripaludis is regulated by transcriptiona

235 The Methanococcus maripaludis MMP0352 protein belongs to an

236 in Hildenborough growing syntrophically with Methanococcus maripaludis on lactate were used to develo

237 d, at 3.2-A resolution, the structure of the Methanococcus maripaludis phosphoseryl-tRNA synthetase (

238 t has recently been reported for an archaeal Methanococcus maripaludis pili filament and an archaeal

239 or switch-off, in the methanogenic archaeon Methanococcus maripaludis requires both nifI(1) and nifI

240 the hydrogenotrophic, methanogenic archaeon Methanococcus maripaludis S2 using a derivative of the T

241 narum NRC-1), a hydrogenotrophic methanogen (Methanococcus maripaludis S2), an acidophilic and aerobi

242 addition, SerRS was expressed from a cloned Methanococcus maripaludis serS gene.

243 a mutational analysis of Sec biosynthesis in Methanococcus maripaludis strain Mm900.

244 We showed previously that in Methanococcus maripaludis switch-off requires at least o

245 ) in the aminoacylation reaction for the two Methanococcus maripaludis synthetases SepRS (forming Sep

246 ere we report the construction of mutants of Methanococcus maripaludis that are defective in each put

247 In Methanococcus maripaludis the electrons for this reactio

248 philic methanogens, Methanococcus voltae and Methanococcus maripaludis This could indicate that the n

249 evels were used to determine the response of Methanococcus maripaludis to leucine limitation.

250 We have used genetic methods in Methanococcus maripaludis to study nitrogen metabolism a

251 and tRNA(Ser), we introduced mutations into Methanococcus maripaludis tRNA(Sec) to investigate how M

252 Agmatidine is also present in Methanococcus maripaludis tRNA2(Ile) and in Sulfolobus s

253 we report that during continuous culture of Methanococcus maripaludis under defined nutrient conditi

254 a source of hydrogen gas for the methanogen, Methanococcus maripaludis using a capillary assay with a

255 gar-biosynthetic proteins were identified in Methanococcus maripaludis using phylogenetic and gene cl

256 rium Desulfovibrio vulgaris and the archaeon Methanococcus maripaludis were established and followed

257 Cells of Methanococcus maripaludis were grown by using continuous

258 hod, eight independent acetate autotrophs of Methanococcus maripaludis were isolated.

259 h canonical LysRS activity was purified from Methanococcus maripaludis, and the gene that encodes thi

260 In the methanogenic archaeon Methanococcus maripaludis, growth with ammonia results i

261 y of apbC/NBP35 homologs from three archaea: Methanococcus maripaludis, Methanocaldococcus jannaschii

262 cture of FlaK, a preflagellin peptidase from Methanococcus maripaludis, solved at 3.6 A resolution.

263 omplex from the hydrogenotrophic methanogen, Methanococcus maripaludis, that contains heterodisulfide

264 two crystal structures of an APC member from Methanococcus maripaludis, the alanine or glycine:cation

265 Transfer RNAs from Methanococcus vannielii, Methanococcus maripaludis, the thermophile Methanococcus

266 Using the methanogenic archaeon Methanococcus maripaludis, we show that deletion of ThiI

267 This was proven for Methanococcus maripaludis, where deletion of the SepRS-e

268 ween the nif and glnK(1) promoter regions of Methanococcus maripaludis, where two operators are prese

269 disrupted the cysS gene (encoding CysRS) of Methanococcus maripaludis.

270 oup II chaperonin from methanogenic archaeon Methanococcus maripaludis.

271 anogenesis in a hydrogenotrophic methanogen, Methanococcus maripaludis.

272 expression vectors was developed for use in Methanococcus maripaludis.

273 n) gene cluster in the methanogenic archaeon Methanococcus maripaludis.

274 unction of glnA in the methanogenic archaeon Methanococcus maripaludis.

275 onal regulation in the methanogenic Archaeon Methanococcus maripaludis.

276 , and tungsten on the diazotrophic growth of Methanococcus maripaludis.

277 to syntrophic conditions with the methanogen Methanococcus maripaludis.

278 hose of Escherichia, but some are closest to Methanococcus or to Synechocystis.

279 compared with their homologs from mesophilic Methanococcus species.

280 strates the utility of genetic approaches in Methanococcus that have not been widely used in the meth

281 e Methanococcus voltae (MVO), the thermopile Methanococcus thermolithotrophicus (MTH), and the extrem

282 es of adenylate kinases from the thermophile Methanococcus thermolithotrophicus and the mesophile Met

283 , Methanococcus maripaludis, the thermophile Methanococcus thermolithotrophicus, and hyperthermophile

284 In Methanococcus thermophila and Methanobacterium thermoaut

285 These organisms, Methanococcus vannielii and Clostridium sticklandii, pro

286 A source of the recombinant monofunctional Methanococcus vannielii PR-AMP cyclohydrolase has been d

287 A selenium-binding protein (SeBP) from Methanococcus vannielii was recently identified, and its

288 ctions of these cysteines in the enzyme from Methanococcus vannielii, a series of biochemical studies

289 Transfer RNAs from Methanococcus vannielii, Methanococcus maripaludis, the

290 In Methanococcus vannielii, selenium transport in the cell

291 Strain PS of Methanococcus voltae (a methanogenic, anaerobic archaeba

292 ogenic members of the Archaea: the mesophile Methanococcus voltae (Mv), the thermophile M. thermolith

293 ogenic members of the Archaea (the mesophile Methanococcus voltae (MVO), the thermopile Methanococcus

294 chaellins of related mesophilic methanogens, Methanococcus voltae and Methanococcus maripaludis This

295 occus thermolithotrophicus and the mesophile Methanococcus voltae have been solved to resolutions of

296 integrative expression vectors contained the Methanococcus voltae histone promoter and multiple cloni

297 ructural analysis shows that archaebacterial Methanococcus voltae RadA(D302K) (MvRAD51(D302K)) and Hs

298 pDLT44 did not replicate in Methanococcus voltae.

299 have created an insertion in the smc gene of Methanococcus voltae.

300 l genes are most closely related to those of Methanococcus, whereas the majority of operational genes