ライフサイエンスコーパス: Methanobacterium

1 MthK is a Ca2+-gated K+ channel from Methanobacterium autotrophicum.

2 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

3 archaeal histones (rHFoB from the mesophile Methanobacterium formicicum, and rHMfA, rHMfB, and rHPyA

4 t archaeal histone rHFoB, from the mesophile Methanobacterium formicicum, has been determined by two-

5 le Methanothermus fervidus and the mesophile Methanobacterium formicicum, respectively, have been ide

6 ee archael histones: hFoB from the mesophile Methanobacterium formicicum; hMfB from the thermophile M

7 d cdhD genes, has 29% identity to NifH2 from Methanobacterium ivanovii.

8 The 381-amino acid Methanobacterium RNA ligase (MthRnl) catalyzes intramole

9 Chimeric holoenzymes, reconstituted from the Methanobacterium RNase P RNA and the Bacillus subtilis R

10 or a "nitrogen regulon" in Methanococcus and Methanobacterium species containing genes of nitrogen me

11 n images and metagenome results suggest that Methanobacterium spp. may work synergistically with Geob

12 iofilm anode dominated by Geobacter spp. and Methanobacterium spp. using carbon-fiber electrodes as t

13 . horikoshii ligase resembles the ligases of Methanobacterium thermautotrophicum and Sulfolobus shiba

14 a class carbonic anhydrase from the archaeon Methanobacterium thermoautotrophicum (Cab) has been dete

15 a-class carbonic anhydrase from the archaeon Methanobacterium thermoautotrophicum (Cab) was structura

16 ribonucleoside diphosphate reductase gene of Methanobacterium thermoautotrophicum (Mth RIR1 intein),

17 An ATP-dependent RNA ligase from Methanobacterium thermoautotrophicum (MthRnl) catalyzes

18 equencing using thermostable RNA ligase from Methanobacterium thermoautotrophicum (MthRnl).

19 om Methanosarcina acetivorans (NifB(Ma)) and Methanobacterium thermoautotrophicum (NifB(Mt)), which c

20 ethod can also generate a ready state of the Methanobacterium thermoautotrophicum (strain Marburg) MC

21 genomes of other archaeal species, including Methanobacterium thermoautotrophicum and Archaeoglobus f

22 es from the moderately thermophilic archaeon Methanobacterium thermoautotrophicum and demonstrate tha

23 e have adapted a leucyl-tRNA synthetase from Methanobacterium thermoautotrophicum and leucyl tRNA der

24 signed functions in the methanogenic archaea Methanobacterium thermoautotrophicum and Methanococcus j

25 eading frames of unassigned function in both Methanobacterium thermoautotrophicum and Methanococcus j

26 archaeal nucleosomes have been isolated from Methanobacterium thermoautotrophicum and Methanothermus

27 Extracts from H2-CO2-grown Methanobacterium thermoautotrophicum cells catalyzed eit

28 and the two protein Pyrococcus furiosus and Methanobacterium thermoautotrophicum clamp loaders, and

29 ic sequences of Methanococcus jannaschii and Methanobacterium thermoautotrophicum contain a structura

30 The archaea Methanobacterium thermoautotrophicum contains a single M

31 he corresponding ORF open reading frame from Methanobacterium thermoautotrophicum Delta H (MTH1152; r

32 The archaeon Methanobacterium thermoautotrophicum Delta H contains a

33 and 5-phospho-alpha-D-ribosyl diphosphate by Methanobacterium thermoautotrophicum delta(H), a member

34 s (at least six) in eukaryotes, the archaeon Methanobacterium thermoautotrophicum DeltaH (mth) genome

35 The Methanobacterium thermoautotrophicum DeltaH cab gene was

36 rrelated with changes in the supply of H2 to Methanobacterium thermoautotrophicum deltaH cells growin

37 obes to clone the homologous region from the Methanobacterium thermoautotrophicum deltaH genome.

38 e of the genome of the thermophilic archaeon Methanobacterium thermoautotrophicum deltaH has been det

39 RNA polymerase (RNAP) purified from Methanobacterium thermoautotrophicum DeltaH has been sho

40 In Methanococcus thermophila and Methanobacterium thermoautotrophicum deltaH, it has been

41 IMP in three members of the domain Archaea, Methanobacterium thermoautotrophicum deltaH, M. thermoau

42 omologues of RFC and PCNA from the archaeon, Methanobacterium thermoautotrophicum DeltaH.

43 type DNA polymerase (PolB) from the archaeon Methanobacterium thermoautotrophicum DeltaH.

44 Methanobacterium thermoautotrophicum has a single MCM ge

45 e entire genome of the thermophilic archaeon Methanobacterium thermoautotrophicum has allowed us to i

46 Archae such as Methanococcus jannaschii and Methanobacterium thermoautotrophicum has been difficult

47 ree-dimensional structure of the enzyme from Methanobacterium thermoautotrophicum has revealed that t

48 Using the Methanobacterium thermoautotrophicum homologue (MthK) an

49 stal structure of a K(+) channel (MthK) from Methanobacterium thermoautotrophicum in the Ca(2+)-bound

50 NA formation in Methanococcus jannaschii and Methanobacterium thermoautotrophicum is still unknown.

51 cture aligns with most major features of the Methanobacterium thermoautotrophicum LSm protein structu

52 Methanobacterium thermoautotrophicum MCM (mtMCM) is a he

53 oli to analyze residues that are critical to Methanobacterium thermoautotrophicum potassium channel (

54 iguration hypothesized for the related MthK (Methanobacterium thermoautotrophicum potassium) channel,

55 We discovered that Methanobacterium thermoautotrophicum strain DeltaH posse

56 h the cobY gene of the methanogenic archaeon Methanobacterium thermoautotrophicum strain DeltaH, but

57 erium cutirubrum, Halobacteriurn trapanicum, Methanobacterium thermoautotrophicum strains deltaH and

58 glycosylase from the thermophilic bacterium, Methanobacterium thermoautotrophicum THF.

59 y of the thermophilic RNA ligase MthRnl from Methanobacterium thermoautotrophicum to recognize and mo

60 The gene encoding GGGP synthase from Methanobacterium thermoautotrophicum was cloned using pr

61 985 constructs, of which 740 are drawn from Methanobacterium thermoautotrophicum, 123 from Saccharom

62 oli K12, 6% of Archaeoglobus fulgidus, 8% of Methanobacterium thermoautotrophicum, 23% of Arabidopsis

63 s found on a cryptic plasmid of the archaeon Methanobacterium thermoautotrophicum, a thermophile with

64 ons based on fusion links are shown here for Methanobacterium thermoautotrophicum, and another 661 pr

65 es can be found in Methanococcus jannaschii, Methanobacterium thermoautotrophicum, and Archaeoglobus

66 rchaeal genomes of Methanococcus jannaschii, Methanobacterium thermoautotrophicum, and Archaeoglobus

67 sarcina thermophila, Methanosarcina barkeri, Methanobacterium thermoautotrophicum, Archaeoglobus fulg

68 uenced completely (Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Archaeoglobus fulg

69 ly uncharacterized hypothetical protein from Methanobacterium thermoautotrophicum, has been determine

70 al product that was chemically identified in Methanobacterium thermoautotrophicum, M. thermophila, an

71 In the archaeon Methanobacterium thermoautotrophicum, MTH1669 encodes a

72 ublicly available: Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Pyrococcus horikos

73 In Methanobacterium thermoautotrophicum, this predicted sup

74 Using cell extracts from Methanobacterium thermoautotrophicum, we found that this

75 the euryarchaea Methanococcus jannaschii and Methanobacterium thermoautotrophicum, which do not encod

76 similar to the putative protein Prp31p from Methanobacterium thermoautotrophicum, while the 193-aa p

77 n RNA ligase from the thermophilic archaeon, Methanobacterium thermoautotrophicum.

78 he beta-class enzyme (Cab) from the archaeon Methanobacterium thermoautotrophicum.

79 ligase encoded by the thermophilic archaeon Methanobacterium thermoautotrophicum.

80 n the methane-metabolism functional group in Methanobacterium thermoautotrophicum.

81 ccus furiosus, Methanococcus jannaschii, and Methanobacterium thermoautotrophicum.

82 um-dependent potassium channel isolated from Methanobacterium thermoautotrophicum.

83 ng genes have been cloned and sequenced from Methanobacterium thermoformicicum Z-245.