ライフサイエンスコーパス: archaebacteria

1 acetyl-CoA biosynthesis in the methanogenic archaebacteria.

2 oximately 50 degrees C) of thermoacidophilic archaebacteria.

3 nd translation factors is largely unknown in archaebacteria.

4 onserved proteins in other eukaryotes and in archaebacteria.

5 lar to genes found in diverse eukaryotes and archaebacteria.

6 abditis elegans, mammals and four species of archaebacteria.

7 her members in fission yeast, nematodes, and archaebacteria.

8 cident with the divergence of eukaryotes and archaebacteria.

9 ound in various prokaryotes, eukaryotes, and archaebacteria.

10 early equidistant from metazoans, fungi, and Archaebacteria.

11 tor that was retained by both eubacteria and archaebacteria.

12 organization as seen in other eukaryotes and Archaebacteria.

13 sted primarily with data from eubacteria and archaebacteria [6-8].

14 Many bacteria and archaebacteria also express viperin-like enzymes with co

15 Here it is shown that archaebacteria also possess FtsZ and that it is biochemi

16 es (phlACB) conserved between eubacteria and archaebacteria and a gene (phlD) encoding a polyketide s

17 However, in some archaebacteria and chloroplasts, the corresponding seque

18 les corresponding to the smaller subunits of archaebacteria and chloroplasts.

19 e domain that is conserved among eukaryotes, archaebacteria and eubacteria.

20 tected in the complete genomes of only a few archaebacteria and eubacteria.

21 olution, and simpler forms are even found in archaebacteria and eubacteria.

22 esis is present in the other domains of life-Archaebacteria and Eukaryota.

23 ide similarity with orthologous sequences in Archaebacteria and eukaryotes.

24 uctural model of the RNase P holoenzyme from archaebacteria and higher organisms.

25 Z(S)) is the only one found in bacteria and archaebacteria and is also present in some eukaryotes.

26 or 2 that is conserved in all eukaryotes and archaebacteria and is the target of diphtheria toxin, is

27 ich seems to be the ancestral metabolism for archaebacteria and methanogenesis (which somehow then de

28 tionally encoded in the tRNAs of eukaryotes, archaebacteria and some bacteria and must be added by a

29 tified recently as an essential gene in many archaebacteria and some pathogenic eubacteria.

30 e (GlnRS) which other Bacteria, the Archaea (archaebacteria), and organelles apparently lack.

31 te synthase (GGPPS) of fungi, yeast, plants, archaebacteria, and eubacteria, respectively.

32 all three domains of organisms: eubacteria, archaebacteria, and eukaryotes.

33 across the membrane barriers of eubacteria, archaebacteria, and eukaryotes.

34 tiple enzyme homologues found in eubacteria, archaebacteria, and eukaryotes.

35 t in the last common ancestor of eubacteria, archaebacteria, and eukaryotes.

36 red across the major kingdoms of eubacteria, archaebacteria, and eukaryotes.

37 e species of the eukaryotes, prokaryotes and archaebacteria, and from mitochondrial and chloroplast o

38 n all species of eubacteria, eukaryotes, and archaebacteria, and in eukaryotic organelles.

39 Complete genomes of yeast, gram eubacteria, archaebacteria, and mitochondria do not contain paralogo

40 In eukaryotes, archaebacteria, and some bacteria, IPP is synthesized fr

41 Like eubacteria, archaebacteria are prokaryotes, although they are phylog

42 gram-positive bacteria, and eight species of archaebacteria are specifically related in terms of gene

43 heir placement in a separate domain; (v) the archaebacteria are specifically related to one another b

44 a as one group and within the eukaryotes and archaebacteria as a second group, but compared between t

45 This supports archaebacteria as founding ancestors of the eukaryotic n

46 arate mono/holophyly of the domains Archaea (archaebacteria), Bacteria (eubacteria) and Eucarya (euka

47 edicted to encode proteins related to D10 in archaebacteria, bacteriophages and in viruses known to i

48 3p exist in Drosophila, in nematodes, and in archaebacteria but not in eubacteria.

49 ve been identified in certain eubacteria and archaebacteria but, in each case, the proteasome-contain

50 eubacteria are more abundant than those from archaebacteria, but the latter are functionally more imp

51 Among archaebacteria, coenzyme M (2-mercaptoethanesulfonic aci

52 The archaebacteria constitute a kingdom of life separate fro

53 Archaea (archaebacteria) constitute a domain of life that is dist

54 yze a diverse array of DNA rearrangements in archaebacteria, eubacteria, and yeast and belongs to the

55 pyridoxine genes, but are found in the same archaebacteria, eubacteria, fungi, and plants that conta

56 In Gram-positive bacteria and archaebacteria FGAR-AT is a complex of three proteins: P

57 ttributable to particle-associated bacteria, archaebacteria, fungi, and viruses.

58 Now it has been discovered that archaebacteria had been doing a related kind of "experim

59 equencing of the complete genomes of several archaebacteria has shown that MCM proteins are also pres

60 50 S subunit of Haloarcula marismortui, the archaebacteria homolog of yeast YL37a, L37ae, coordinate

61 structural analysis of a Rad50 homolog from archaebacteria illuminated the catalytic core of the enz

62 ort for the notion that protein synthesis in archaebacteria is initiated with methionine and not with

63 ein synthesis in eukaryotic cytoplasm and in archaebacteria is initiated with methionine, whereas, th

64 third domain of life, the Archaea (formerly Archaebacteria), is populated by a physiologically diver

65 rhodopsin-I (SRI), a phototaxis receptor of archaebacteria, is a retinal-binding protein that exists

66 Until recently all archaebacteria isolated conformed to one of three basic

67 e thermophilic cenancestor of eukaryotes and archaebacteria (jointly called neomurans), radically mod

68 eIF-5A is the only protein in eukaryotes and archaebacteria known to contain hypusine.

69 Archaebacteria lack glutaminyl-tRNA synthetase and utili

70 Archaebacteria lack ubiquitin and 26 S proteasomes but d

71 g of introns in eukaryotes, and 11 predicted archaebacteria-like Sm and like-Sm core peptides, which

72 ast Sik1p/Nop56p, and putative homologues in archaebacteria, plants, and human.

73 otic proteasomes are different from those in archaebacteria proteasomes.

74 Transcription initiation in Archaea (archaebacteria) resembles the eucaryotic process, having

75 dentified pyridoxine biosynthesis pathway of archaebacteria, some eubacteria, fungi, and plants.

76 o archaebacterial ThrRSs after the eukaryote/archaebacteria split.

77 Many archaebacteria, such as Methanococcus jannaschii, also c

78 Experimental findings obtained with MPC from archaebacteria suggest that degradation of proteins by t

79 fraction E (PLFE) from the thermoacidophilic archaebacteria Sulfolobus acidocaldarius have been studi

80 The eubacteria-archaebacteria symbiosis became permanent as the nucleus

81 Plants, lower eukaryotes, bacteria, and archaebacteria synthesise L-histidine (His) in a similar

82 g evidence that methane is being consumed by archaebacteria that are phylogenetically distinct from k

83 Two methyltransferases from archaebacteria that catalyze methylation of mercaptoetha

84 st that the mevalonate pathway is germane to archaebacteria, that the DXP pathway is germane to eubac

85 ophilic and mesophilic eubacteria as well as archaebacteria, the human-disease pathogens Treponema pa

86 had been acquired by sulfidogenic wall-less archaebacteria (thermoplasmas) after aerotolerant cytopl

87 Archaebacteria thrive in environments characterized by a

88 ble-strand breaks, in organisms ranging from archaebacteria to humans.

89 conserved component of DNA replication from archaebacteria to humans.

90 that is conserved in organisms ranging from archaebacteria to yeast and that suggests a model for in

91 views of the Tree of Life which cluster the archaebacteria with eukaryotes.

92 ound in bacteriophage T4 and T5, eubacteria, archaebacteria, yeast, Drosophila, mouse and man.