ライフサイエンスコーパス: methanothermobacter

1 , phylogenetically affiliated with the genus Methanothermobacter family.

2 Methyl-coenzyme M reductase (MCR) from Methanothermobacter marburgensis (Mtm), catalyses the fi

3 tions, catalyzed by the enzyme isolated from Methanothermobacter marburgensis .

4 etics to study the reaction between MCR from Methanothermobacter marburgensis and a series of bromina

5 Methanothermobacter marburgensis is a methanogenic archa

6 brane channel protein AqpM from the archaeon Methanothermobacter marburgensis, we determined the stru

7 In this study, the reaction of MCR from Methanothermobacter marburgensis, with its native substr

8 of the cathodic microbiota suggested that a Methanothermobacter-related methanogen and synergistetes

9 Methanothermobacter thermautotrophicus (M.t.) RNAP is su

10 individual DNA helicases from the archaeons Methanothermobacter thermautotrophicus (Mth) and Thermoc

11 from two organisms identified in the search, Methanothermobacter thermautotrophicus (MTH) and Thermop

12 onated extracts of the thermophilic archaeon Methanothermobacter thermautotrophicus (Mth).

13 sed on the 6-fold symmetry of the N-terminal Methanothermobacter thermautotrophicus (mtMCM) hexamer s

14 Only one MCM is found in the archaeon Methanothermobacter thermautotrophicus (mtMCM), and this

15 n k(cat) and k(cat)/K(M) for the OMPDCs from Methanothermobacter thermautotrophicus (MtOMPDC) and Sac

16 That the OMPDCs from Methanothermobacter thermautotrophicus (MtOMPDC) and Sac

17 ue loop at the ortholog from the thermophile Methanothermobacter thermautotrophicus (MtOMPDC).

18 portion of the MCM complex from the archaeon Methanothermobacter thermautotrophicus (N-mtMCM) in the

19 y, the enzyme DapL (MTH52) was identified in Methanothermobacter thermautotrophicus and shown to belo

20 ed methanobacterial and pyrococcal tRNA, the Methanothermobacter thermautotrophicus AspRS acylated ap

21 ic archaea Methanocaldococcus jannaschii and Methanothermobacter thermautotrophicus contain a dual-sp

22 pen reading frame 48 (ORF48) in the archaeon Methanothermobacter thermautotrophicus encodes a putativ

23 We show here that Methanothermobacter thermautotrophicus GatD acts as a gl

24 The Methanothermobacter thermautotrophicus GatDE is slightly

25 We show that the Methanothermobacter thermautotrophicus GluRS is active t

26 n GlnRS S1/L1/L2 and the naturally occurring Methanothermobacter thermautotrophicus GluRS(ND), which

27 vergently transcribed fpaA-rlp-rub operon in Methanothermobacter thermautotrophicus in addition to tr

28 tivity of an MCM homologue from the archaeon Methanothermobacter thermautotrophicus is inhibited in t

29 ve established that the trpEGCFBAD operon in Methanothermobacter thermautotrophicus is transcribed di

30 nal analysis of the interactions between the Methanothermobacter thermautotrophicus MCM and the two C

31 of DNA and ATP on the thermostability of the Methanothermobacter thermautotrophicus MCM protein was d

32 Methanothermobacter thermautotrophicus minichromosomal m

33 acterization of the N-terminal region of the Methanothermobacter thermautotrophicus minichromosome ma

34 nichromosome maintenance (MCM) helicase from Methanothermobacter thermautotrophicus move along duplex

35 Over 90% of Methanothermobacter thermautotrophicus mutants isolated

36 t two-hybrid screen for interactions between Methanothermobacter thermautotrophicus proteins using pr

37 osome maintenance helicase from the archaeon Methanothermobacter thermautotrophicus required only ATP

38 The results reported establish the fate of Methanothermobacter thermautotrophicus TBP and TFB follo

39 milar complex for Gln-tRNA(Gln) formation in Methanothermobacter thermautotrophicus that allows the m

40 roRS) and leucyl-tRNA synthetases (LeuRS) in Methanothermobacter thermautotrophicus that enhances tRN

41 In Methanothermobacter thermautotrophicus the N-terminal po

42 he RPAs in Methanocaldococcus jannaschii and Methanothermobacter thermautotrophicus through fusions o

43 The Cdc6 proteins from the archaeon Methanothermobacter thermautotrophicus were previously s

44 Species close to Methanosarcina barkeri and Methanothermobacter thermautotrophicus were the two main

45 Modeling of the Methanothermobacter thermautotrophicus Z245 ACS (MT-ACS1

46 ylase (OMPDC) from Saccharomyces cerevisiae, Methanothermobacter thermautotrophicus, and Escherichia

47 he genomes of Methanocaldococcus jannaschii, Methanothermobacter thermautotrophicus, and Methanopyrus

48 he archaea Methanocaldococcus jannaschii and Methanothermobacter thermautotrophicus, from the eukaryo

49 identified in Methanocaldococcus jannaschii, Methanothermobacter thermautotrophicus, or Methanopyrus

50 In Methanothermobacter thermautotrophicus, oxaloacetate syn

51 e ability of an archaeal RNAP, purified from Methanothermobacter thermautotrophicus, to transcribe DN

52 were found only in Methanopyrus kandleri and Methanothermobacter thermautotrophicus, two strictly hyd

53 Focusing on the OMPDC from Methanothermobacter thermautotrophicus, we find the "rem

54 hybrid screen was performed for the archaeon Methanothermobacter thermautotrophicus.

55 ganization with Methanococcus jannaschii and Methanothermobacter thermoautotrophicum.

56 the RNase P enzyme from the archaebacterium Methanothermobacter thermoautotrophicus (Mth).

57 Methanothermobacter thermoautotrophicus RNA ligase (MthR

58 e structure of the MTH1020 gene product from Methanothermobacter thermoautotrophicus was previously s

59 e found in Methanocaldococcus jannaschii and Methanothermobacter thermoautotrophicus, and homologues

60 Methanosarcinales, in Thermoplasmatales and Methanothermobacter thermoautotrophicus, and in Halobact

61 mthCdc6-2) with the replication origin from Methanothermobacter thermoautotrophicus.