戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 minant fermentative bacteria, Geobacter, and Methanobacterium.
2 me, encompassing 515 microbial genera (e.g., Methanobacterium) and 417 microbial KEGG genes (e.g., K0
3 gens in the genus Candidatus Methanoflorens, Methanobacterium, and Methanoregula show the potential f
4         MthK is a Ca2+-gated K+ channel from Methanobacterium autotrophicum.
5 of the MEC fed 0.02 g FAN/L was dominated by Methanobacterium, but 0.18 and 0.37 g FAN/L led to Metha
6  archaeal histones (rHFoB from the mesophile Methanobacterium formicicum, and rHMfA, rHMfB, and rHPyA
7 t archaeal histone rHFoB, from the mesophile Methanobacterium formicicum, has been determined by two-
8 le Methanothermus fervidus and the mesophile Methanobacterium formicicum, respectively, have been ide
9 ee archael histones: hFoB from the mesophile Methanobacterium formicicum; hMfB from the thermophile M
10 d cdhD genes, has 29% identity to NifH2 from Methanobacterium ivanovii.
11  favored hydrogenotrophic methanogens (e.g., Methanobacterium) lacking the hgcA methylation gene over
12 clastic (Methanosaeta) and hydrogenotrophic (Methanobacterium) methanogens in the stable IBA treatmen
13                           The 381-amino acid Methanobacterium RNA ligase (MthRnl) catalyzes intramole
14 Chimeric holoenzymes, reconstituted from the Methanobacterium RNase P RNA and the Bacillus subtilis R
15 axonomic units (OTUs) were classified as the Methanobacterium sp.
16 or a "nitrogen regulon" in Methanococcus and Methanobacterium species containing genes of nitrogen me
17 n images and metagenome results suggest that Methanobacterium spp. may work synergistically with Geob
18 iofilm anode dominated by Geobacter spp. and Methanobacterium spp. using carbon-fiber electrodes as t
19 . horikoshii ligase resembles the ligases of Methanobacterium thermautotrophicum and Sulfolobus shiba
20 a class carbonic anhydrase from the archaeon Methanobacterium thermoautotrophicum (Cab) has been dete
21 a-class carbonic anhydrase from the archaeon Methanobacterium thermoautotrophicum (Cab) was structura
22 ribonucleoside diphosphate reductase gene of Methanobacterium thermoautotrophicum (Mth RIR1 intein),
23             An ATP-dependent RNA ligase from Methanobacterium thermoautotrophicum (MthRnl) catalyzes
24 equencing using thermostable RNA ligase from Methanobacterium thermoautotrophicum (MthRnl).
25 om Methanosarcina acetivorans (NifB(Ma)) and Methanobacterium thermoautotrophicum (NifB(Mt)), which c
26 ethod can also generate a ready state of the Methanobacterium thermoautotrophicum (strain Marburg) MC
27 genomes of other archaeal species, including Methanobacterium thermoautotrophicum and Archaeoglobus f
28 es from the moderately thermophilic archaeon Methanobacterium thermoautotrophicum and demonstrate tha
29 e have adapted a leucyl-tRNA synthetase from Methanobacterium thermoautotrophicum and leucyl tRNA der
30 signed functions in the methanogenic archaea Methanobacterium thermoautotrophicum and Methanococcus j
31 eading frames of unassigned function in both Methanobacterium thermoautotrophicum and Methanococcus j
32 archaeal nucleosomes have been isolated from Methanobacterium thermoautotrophicum and Methanothermus
33                   Extracts from H2-CO2-grown Methanobacterium thermoautotrophicum cells catalyzed eit
34  and the two protein Pyrococcus furiosus and Methanobacterium thermoautotrophicum clamp loaders, and
35 ic sequences of Methanococcus jannaschii and Methanobacterium thermoautotrophicum contain a structura
36                                  The archaea Methanobacterium thermoautotrophicum contains a single M
37 he corresponding ORF open reading frame from Methanobacterium thermoautotrophicum Delta H (MTH1152; r
38                                 The archaeon Methanobacterium thermoautotrophicum Delta H contains a
39 and 5-phospho-alpha-D-ribosyl diphosphate by Methanobacterium thermoautotrophicum delta(H), a member
40 s (at least six) in eukaryotes, the archaeon Methanobacterium thermoautotrophicum DeltaH (mth) genome
41                                          The Methanobacterium thermoautotrophicum DeltaH cab gene was
42 rrelated with changes in the supply of H2 to Methanobacterium thermoautotrophicum deltaH cells growin
43 obes to clone the homologous region from the Methanobacterium thermoautotrophicum deltaH genome.
44 e of the genome of the thermophilic archaeon Methanobacterium thermoautotrophicum deltaH has been det
45          RNA polymerase (RNAP) purified from Methanobacterium thermoautotrophicum DeltaH has been sho
46             In Methanococcus thermophila and Methanobacterium thermoautotrophicum deltaH, it has been
47  IMP in three members of the domain Archaea, Methanobacterium thermoautotrophicum deltaH, M. thermoau
48 omologues of RFC and PCNA from the archaeon, Methanobacterium thermoautotrophicum DeltaH.
49 type DNA polymerase (PolB) from the archaeon Methanobacterium thermoautotrophicum DeltaH.
50                                              Methanobacterium thermoautotrophicum has a single MCM ge
51 e entire genome of the thermophilic archaeon Methanobacterium thermoautotrophicum has allowed us to i
52  Archae such as Methanococcus jannaschii and Methanobacterium thermoautotrophicum has been difficult
53 ree-dimensional structure of the enzyme from Methanobacterium thermoautotrophicum has revealed that t
54                 Structures of closed MthK, a Methanobacterium thermoautotrophicum homolog of BK chann
55                                    Using the Methanobacterium thermoautotrophicum homologue (MthK) an
56 stal structure of a K(+) channel (MthK) from Methanobacterium thermoautotrophicum in the Ca(2+)-bound
57 NA formation in Methanococcus jannaschii and Methanobacterium thermoautotrophicum is still unknown.
58 cture aligns with most major features of the Methanobacterium thermoautotrophicum LSm protein structu
59                                              Methanobacterium thermoautotrophicum MCM (mtMCM) is a he
60 n, we report the X-ray crystal structures of Methanobacterium thermoautotrophicum NifB without (apo M
61 oli to analyze residues that are critical to Methanobacterium thermoautotrophicum potassium channel (
62 iguration hypothesized for the related MthK (Methanobacterium thermoautotrophicum potassium) channel,
63                           We discovered that Methanobacterium thermoautotrophicum strain DeltaH posse
64 h the cobY gene of the methanogenic archaeon Methanobacterium thermoautotrophicum strain DeltaH, but
65 erium cutirubrum, Halobacteriurn trapanicum, Methanobacterium thermoautotrophicum strains deltaH and
66 glycosylase from the thermophilic bacterium, Methanobacterium thermoautotrophicum THF.
67 y of the thermophilic RNA ligase MthRnl from Methanobacterium thermoautotrophicum to recognize and mo
68         The gene encoding GGGP synthase from Methanobacterium thermoautotrophicum was cloned using pr
69  985 constructs, of which 740 are drawn from Methanobacterium thermoautotrophicum, 123 from Saccharom
70 oli K12, 6% of Archaeoglobus fulgidus, 8% of Methanobacterium thermoautotrophicum, 23% of Arabidopsis
71 s found on a cryptic plasmid of the archaeon Methanobacterium thermoautotrophicum, a thermophile with
72 es can be found in Methanococcus jannaschii, Methanobacterium thermoautotrophicum, and Archaeoglobus
73 rchaeal genomes of Methanococcus jannaschii, Methanobacterium thermoautotrophicum, and Archaeoglobus
74 sarcina thermophila, Methanosarcina barkeri, Methanobacterium thermoautotrophicum, Archaeoglobus fulg
75 uenced completely (Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Archaeoglobus fulg
76 ly uncharacterized hypothetical protein from Methanobacterium thermoautotrophicum, has been determine
77 al product that was chemically identified in Methanobacterium thermoautotrophicum, M. thermophila, an
78                              In the archaeon Methanobacterium thermoautotrophicum, MTH1669 encodes a
79 ublicly available: Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Pyrococcus horikos
80 d MthK, a Ca(2+)-activated K(+) channel from Methanobacterium thermoautotrophicum, the SF has been pr
81                                           In Methanobacterium thermoautotrophicum, this predicted sup
82                     Using cell extracts from Methanobacterium thermoautotrophicum, we found that this
83 the euryarchaea Methanococcus jannaschii and Methanobacterium thermoautotrophicum, which do not encod
84  similar to the putative protein Prp31p from Methanobacterium thermoautotrophicum, while the 193-aa p
85 btaining structures of the MthK channel from Methanobacterium thermoautotrophicum-a purely calcium-ga
86 um-dependent potassium channel isolated from Methanobacterium thermoautotrophicum.
87 n RNA ligase from the thermophilic archaeon, Methanobacterium thermoautotrophicum.
88 he beta-class enzyme (Cab) from the archaeon Methanobacterium thermoautotrophicum.
89  ligase encoded by the thermophilic archaeon Methanobacterium thermoautotrophicum.
90 n the methane-metabolism functional group in Methanobacterium thermoautotrophicum.
91 ccus furiosus, Methanococcus jannaschii, and Methanobacterium thermoautotrophicum.
92 ng genes have been cloned and sequenced from Methanobacterium thermoformicicum Z-245.