ライフサイエンスコーパス: Methanococcus jannaschii

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

2 plasma genitalium, Synechocystis PCC6803 and Methanococcus jannaschii).

3 was characterized from the hyperthermophile Methanococcus jannaschii.

4 ecognized in the complete genome sequence of Methanococcus jannaschii.

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

6 ng methanoarchaea M. thermoautotrophicum and Methanococcus jannaschii.

7 recombinant RNAP subunits from the archaeon Methanococcus jannaschii.

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

9 t FtsZ from the hyperthermophilic methanogen Methanococcus jannaschii.

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

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

12 tion with their counterparts in the archaeon Methanococcus jannaschii.

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

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

15 col challenge, and syntrophic coculture with Methanococcus jannaschii.

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

17 ethanoarchaea Methanosarcina thermophila and Methanococcus jannaschii.

18 tified in the hyperthermophilic euryarchaeon Methanococcus jannaschii.

19 ative RNA helicase from the hyperthermophile Methanococcus jannaschii.

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

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

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

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

24 The methanarchaeon, Methanococcus jannaschii, a hyperthermophilic, autotroph

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

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

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

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

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

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

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

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

33 for highly similar proteins were detected in Methanococcus jannaschii and Bacillus stearothermophilus

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

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

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

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

38 The genomic sequences of Methanococcus jannaschii and Methanobacterium thermoauto

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 The hyperthermophilic archaeon Methanococcus jannaschii encodes two putative transcript

72 The hyperthermophilic archaeon Methanococcus jannaschii encodes two putative transcript

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

74 The Methanococcus jannaschii gene MJ0671 was cloned and over

75 The Methanococcus jannaschii gene MJ1392 was cloned, and its

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

77 Comparisons with the Methanococcus jannaschii genome data underline the exten

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

79 The interpretation of the Methanococcus jannaschii genome will inevitably require

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

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

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

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

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

85 The hyperthermophilic euryarchaeon Methanococcus jannaschii has no recognizable homologues

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 Two putative Methanococcus jannaschii isocitrate dehydrogenase genes,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 Methanococcus jannaschii MJ0936 is a hypothetical protei

127 The Methanococcus jannaschii MJ109 gene product, the sequenc

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

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

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

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

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

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

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

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

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

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

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

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

140 Methanococcus jannaschii partially retains the superoper

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

142 Both the Methanococcus jannaschii phosphoenolpyruvate synthase an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 The Methanococcus jannaschii tyrosyl-transfer-RNA synthetase

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

171 Methanococcus jannaschii tyrosyl-tRNA synthetase is a mi

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

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

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

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

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

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

178 MVP, a Methanococcus jannaschii voltage-gated potassium channel

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

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

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

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

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

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

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

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

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

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

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

190 rium Haemophilus influenzae and the archaeon Methanococcus jannaschii, which had been previously misi

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

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