ライフサイエンスコーパス: archaeal protein

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1 iously undetected functions of bacterial and archaeal proteins and in the identification of novel pro

2 There were relatively few (15)N-enriched archaeal proteins, and all showed low atom% enrichment,

3 life in hypersaline environments, halophilic archaeal proteins are enriched in acidic amino acids.

4 Candidate twin-arginine signal peptides from archaeal proteins as well as plant thylakoid-targeting s

5 d that CHDL domains in various bacterial and archaeal proteins confer carbohydrate binding activity t

6 The fraction of bacterial and archaeal proteins containing regions conserved over long

7 The amino acid sequence of the archaeal protein contains a putative zinc-binding domain

8 tically distinct and coherent group of these archaeal proteins [designated aIF2Bs (archaeal initiatio

9 In vitro, the assembled archaeal protein efficiently uses H2O2 to oxidize Fe(II)

10 rs to depend on domain of life, with the two archaeal proteins existing as higher-order oligomers.

11 their apparent phylogenetic affinities, the archaeal protein families split into bacterial and eukar

12 vel, and the other (catalytic) domain in the archaeal protein has a new fold.

13 e previous report that more than half of the archaeal proteins have no homologues and shows that, wit

14 the protein-protein interactions between the archaeal proteins have not yet been determined.

15 matic analysis identified an uncharacterized archaeal protein in the Methanocaldococcus jannaschii ge

16 gth differences of eukaryotic, bacterial and archaeal proteins in relation to function, conservation

17 nitiate its association with the duplex, the archaeal protein initiated its transit along dsDNA in th

18 The central feature of this archaeal protein is a sheet of six antiparallel beta-str

19 Thus, the archaeal protein is called replication protein A (RPA),

20 For the archaeal protein it was shown that the N-terminal portio

21 This new archaeal protein kinase displayed no catalytic activity

22 The archaeal protein kinase utilized purine nucleotides as p

23 tein L16, which is shown to be homologous to archaeal protein L10e, cluster to the same region as the

24 nas aeruginosa predicted that Ser-309 of the archaeal protein lies within the substrate binding site.

25 One residue unique to archaeal proteins (Met-295) was of particular interest b

26 Both archaeal proteins, overexpressed in Escherichia coli and

27 Most archaeal proteins participating in DNA replication are m

28 the PP1/2A/2B superfamily, the gene for the archaeal protein phosphatase PP1-arch2 was identified, c

29 the crystal structure of an atypical Sm-like archaeal protein (SmAP3) in which the conserved Sm domai

30 ences and have sequences in common with many archaeal proteins, some of which are involved in methion

31 A conserved archaeal protein, ssArd1, was cloned and expressed in Es

32 study channeling in bienzyme complexes to an archaeal protein synthesis pathway featuring the misamin

33 parallel experiments using (2)H2O, extensive archaeal protein synthesis was detected in all condition

34 1.75-A crystal structure of SmAP, an Sm-like archaeal protein that forms a heptameric ring perforated

35 allosteric site, the low sensitivity of the archaeal protein to serine is consistent with phosphoser

36 Likely DNA-binding domains in archaeal proteins were analyzed using sequence profile m

37 the bacterial proteins and about 70% of the archaeal proteins were predicted with varying precision.

38 to the N termini of 810 eubacterial and 175 archaeal proteins, which are rarely acetylated.

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