ライフサイエンスコーパス: Eucarya

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1 al recognition particle (SRP) in Archaea and Eucarya.

2 hree domains of life: Bacteria, Archaea, and Eucarya.

3 ervation of SRP assembly between archaea and eucarya.

4 group's phylogenetic association within the Eucarya.

5 quisition of NH4+/NH3 in bacteria as well as eucarya.

6 highly conserved among Bacteria, Archaea and Eucarya.

7 sduction proteins from Bacteria, Archaea and Eucarya.

8 homologous recombination was extended to the Eucarya.

9 ss groups or domains: Archaea, Bacteria, and Eucarya.

10 n Bacteria, but is not present in Archaea or Eucarya.

11 cteria and Archaea, and a topology rooted in Eucarya.

12 hree domains of life (Archaea, Bacteria, and Eucarya) (1) as well as from mitochondria and chloroplas

13 iption-associated proteins from Bacteria and Eucarya (a total of 4,147), we have identified their hom

14 The presence of endonuclease in Eucarya and Archaea suggests an ancient origin for the t

15 tion pre-initiation complex assembly in both eucarya and archaea.

16 ing of transfer RNA precursors is similar in Eucarya and Archaea.

17 arity with other known OASS enzymes from the Eucarya and Bacteria domains.

18 wn to occur with GTP cyclohydrolase I in the Eucarya and Bacteria, but rather by two or more enzymes.

19 t extreme environments, inhospitable to most Eucarya and Bacteria.

20 synthesis, has been previously identified in eucarya and Escherichia coli.

21 apped around a nucleosome, in the genomes of Eucarya and the histone-containing Euryarchaeota, but no

22 cover all three taxonomic domains (bacteria, eucarya, and archaea) revealed that the sequences are di

23 oss all three taxonomic domains (Eubacteria, Eucarya, and Archaea) reveals that the sequences are div

24 s only in Bacteria, 51 have homologs only in Eucarya, and the remaining 61 have homologs in both phyl

25 at are conserved among Bacteria, Archaea and Eucarya are important detectors of common signals detect

26 ve been identified in Bacteria, Archaea, and Eucarya, as well as organelles.

27 These are proteins conserved in eucarya, bacteria and archaea, acting by a unique reacti

28 phate isomerase (TIM) is a dimeric enzyme in eucarya, bacteria and mesophilic archaea.

29 Comparisons with Eucarya-, Bacteria-, and Archaea-specific databases reve

30 tially universal in the domains Bacteria and Eucarya but has no counterparts in Archaea, probably ref

31 Within the Eucarya domain, plant homologues proved to be substantia

32 g compounds in organisms of the Bacteria and Eucarya domains.

33 se genes appear to have been acquired by the Eucarya during the endosymbiosis that gave rise to the m

34 (archaebacteria), Bacteria (eubacteria) and Eucarya (eukaryotes) and the placement of extreme thermo

35 bout the occurrence of GlnRS genes among the Eucarya (eukaryotes) outside of the "crown" taxa (animal

36 t is distinct from Bacteria (eubacteria) and Eucarya (eukaryotes).

37 Perhaps the Archaea and Eucarya have compensated for their lack of L36 by mainta

38 at the origin and initial diversification of Eucarya occurred in the late Archaean or Proterozoic Eon

39 me than that determined for RNase P of other Eucarya or Archaea.

40 t between the domains Bacteria, Archaea, and Eucarya or laterally transferred between Bacteria and Ar

41 hree primary domains, Archaea, Bacteria, and Eucarya-originally proposed by myself and others--be aba

42 As compared with homologs in other Eucarya, plant SBTs are more closely related to archaeal

43 sely related to GlnRS and GluRS genes of the Eucarya than to those of Bacteria.

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