ライフサイエンスコーパス: archaebacterial

1 -tRNA synthase (ProRS) pairs derived from an archaebacterial ancestor for use in Escherichia coli.

2 E. coli rpoB and rpoC genes corresponding to archaebacterial and chloroplast split subunits were indi

3 Genes of archaebacterial and eubacterial ancestry tend to perform

4 sis, enabled independent escape of the first archaebacterial and eubacterial cells from their hydroth

5 whereas the much greater differences between archaebacterial and eubacterial sequences indicate these

6 ria, appeared in 1995 and other eubacterial, archaebacterial and eukaryotic genomes were soon sequenc

7 teases, while CAD-containing proteins in the archaebacterial and eukaryotic lineages appear to have d

8 esentatives of a diverse range of eukaryote, archaebacterial, and eubacterial taxa has revealed that

9 Many small bacterial, archaebacterial, and eukaryotic genomes have been sequen

10 llular Activities) are found in eubacterial, archaebacterial, and eukaryotic species and participate

11 ucture reveals an unexpected homology to two archaebacterial DNA binding proteins which are also invo

12 We show that archaebacterial DNA polymerases are strongly inhibited b

13 All six archaebacterial DNA polymerases tested were inhibited, w

14 40% when dUTP was used in place of dTTP for archaebacterial DNA polymerases.

15 cleus originated by recombination of eu- and archaebacterial DNA that remained attached to eubacteria

16 tive substrate specificity, tolerance of the archaebacterial enzymes for acidic pHs and elevated temp

17 Although the archaebacterial enzymes were inactive at temperatures be

18 Recent structural studies of a homologous archaebacterial exchanger, NCX_Mj, revealed its outward

19 milar architecture between the mammalian and archaebacterial exchangers.

20 sortium "Thiodendron latens." By eubacterial-archaebacterial genetic integration, the chimera, an ami

21 Archaebacterial halophiles (Haloarchaea) are oxygen-resp

22 stones H2B and H2A, respectively, and to the archaebacterial histone-like protein HMf-2.

23 e end of the acceptor stem in eukaryotic and archaebacterial initiator methionine tRNAs plays an impo

24 ophilic eubacterium Thermotoga maritima, the archaebacterial lyase contains unique features.

25 To define the barrier function of archaebacterial membranes and to examine the effects of

26 The small size of the archaebacterial Methanococcus jannaschii tyrosyl-tRNA sy

27 Structural analysis shows that archaebacterial Methanococcus voltae RadA(D302K) (MvRAD5

28 Here we show that the archaebacterial Methanosarcina mazei ThrRS efficiently m

29 alinarum bacteriorhodopsin, an alpha-helical archaebacterial MP with a single cofactor, and (iii, iv)

30 hat have no homologues in the mitochondrial, archaebacterial, or cytosolic ribosomal protein sequence

31 apparent homologs in bacterial, chloroplast, archaebacterial, or cytosolic ribosomes.

32 racterization of a simplified eubacterial or archaebacterial proteasome has been reported.

33 cterial RecA and separately among eukaryotic/archaebacterial Rad51/RadA.

34 The archaebacterial repertoire has a similar size in all euk

35 a and beta' subunits and their homologs from archaebacterial RNA polymerases, the eukaryotic RNA poly

36 a and beta' subunits and their homologs from archaebacterial RNAPs, eukaryotic RNAPs I-III, nuclear-c

37 g motif is conserved between eubacterial and archaebacterial SecY and eukaryotic Sec61.

38 Thus, the majority of the archaebacterial sequences are not consistent with curren

39 a common ancestor about 2 billion years ago, archaebacterial sequences being measurably more similar

40 Several distantly related archaebacterial sequences were designated as 'enolase-2'

41 n-like protein found in many eubacterial and archaebacterial species, appears to protect cells from o

42 e, by grouping upstream sequences from three archaebacterial species, we found a conserved motif that

43 PhoB, PurR, RpoH, and FhlA regulons in other archaebacterial species.

44 ced eukaryotic genomes contain more genes of archaebacterial than eubacterial affinity.

45 all alanyl-tRNA synthetases is missing from archaebacterial threonine enzymes.

46 e tree of life, and was most likely added to archaebacterial ThrRSs after the eukaryote/archaebacteri

47 M. mazei and most other archaebacterial ThrRSs have a domain, N2(A), fused to th

48 -3) that also shares significant homology to archaebacterial topoisomerase VI (TOP6) subunit A, where

49 Spo11p is related to a subunit of archaebacterial topoisomerase VI and appears to cleave D

50 represented by strain VC-16 arises from the archaebacterial tree precisely where such an interpretat

51 e 'multicorn' to indicate its analogy to the archaebacterial tricorn protease.

52 ane depolarization when transplanted from an archaebacterial voltage-activated potassium channel (KvA

53 In this study, we analyze KvAP, an archaebacterial voltage-dependent potassium channel, to

54 s a tarantula venom toxin which binds to the archaebacterial voltage-gated potassium channel KvAP.