ライフサイエンスコーパス: Archaeoglobus fulgidus

1 ermoautotrophicum, Pyrococcus horikoshii and Archaeoglobus fulgidus.

2 ing Methanobacterium thermoautotrophicum and Archaeoglobus fulgidus.

3 i, Methanobacterium thermoautotrophicum, and Archaeoglobus fulgidus.

4 al structure of a representative CDP-AP from Archaeoglobus fulgidus.

5 subunits in replication factor C (RFC) from Archaeoglobus fulgidus.

6 he three Amt orthologs from the euryarchaeon Archaeoglobus fulgidus.

7 e fraction of the hyperthermophilic archaeon Archaeoglobus fulgidus.

8 tested using CopA, a model Cu(+)-ATPase from Archaeoglobus fulgidus.

9 onsisting of a stand-alone macro domain from Archaeoglobus fulgidus.

10 jannaschii and the sulfate-reducing archaeon Archaeoglobus fulgidus.

11 its of the RFC homologue of the euryarchaeon Archaeoglobus fulgidus.

12 hyperthermophilic sulfate-reducing anaerobe Archaeoglobus fulgidus.

13 components of the hyperthermophilic archaeon Archaeoglobus fulgidus.

14 describe a UDG from the extreme thermophile Archaeoglobus fulgidus.

15 ia pestis, 5% of Escherichia coli K12, 6% of Archaeoglobus fulgidus, 8% of Methanobacterium thermoaut

16 ypic WrbA protein from E. coli and WrbA from Archaeoglobus fulgidus, a hyperthermophilic species from

17 Archaeoglobus fulgidus, a hyperthermophilic sulfate-redu

18 Archaeoglobus fulgidus, a hyperthermophilic, archaeal su

19 structure of the chromatin protein Alba from Archaeoglobus fulgidus, a substrate for the Sir2 protein

20 The splicing endonuclease from Archaeoglobus fulgidus (AF) belongs to the homodimeric f

21 an Aer HAMP model based on the structure of Archaeoglobus fulgidus Af1503-HAMP, the closest residue

22 member of this family, an FBPase/IMPase from Archaeoglobus fulgidus (AF2372), has been solved.

23 the crystal structure of a Piwi protein from Archaeoglobus fulgidus (AfPiwi) in complex with a small

24 his publication investigates the enzyme from Archaeoglobus fulgidus (Afu Pol-D).

25 e solved structures of a UBIAD1 homolog from Archaeoglobus fulgidus, AfUbiA, in an unliganded form an

26 cosylase from the hyperthermophilic organism Archaeoglobus fulgidus (AFUDG) is responsible for the re

27 The crystal structure of an Archaeoglobus fulgidus ammonium transporter (AMT) sugges

28 yperthermophilic, sulphate-reducing archaeon Archaeoglobus fulgidus and characterised its in vitro ac

29 (420)-0:gamma-glutamyl ligase (CofE-AF) from Archaeoglobus fulgidus and its complex with GDP at 2.5 A

30 ned the performance of the FEN1 enzymes from Archaeoglobus fulgidus and Methanococcus jannaschii and

31 omonas aeruginosa) and two archaeal species (Archaeoglobus fulgidus and Pyrococcus horikoshii).

32 rom the archaea Methanococcus jannaschii and Archaeoglobus fulgidus, and from the bacterium Thermotog

33 ulfovibrio vulgaris, Pseudomonas aeruginosa, Archaeoglobus fulgidus, and Methanocaldocococcus jannasc

34 rkeri, Methanobacterium thermoautotrophicum, Archaeoglobus fulgidus, and Mycobacterium smegmatis show

35 smodium falciparum, Tetrahymena thermophila, Archaeoglobus fulgidus, and Mycobacterium tuberculosis.

36 schii, Methanobacterium thermoautotrophicum, Archaeoglobus fulgidus, and Pyrococcus horikoshii) revea

37 barkeri and the closely related euryarchaeon Archaeoglobus fulgidus appeared to be of the Escherichia

38 rate species including Borrelia burgdorferi, Archaeoglobus fulgidus, Arabidopsis thaliana, and Homo s

39 crystal structure of the wild-type mIPS from Archaeoglobus fulgidus at 1.7 A, as well as the crystal

40 S from the hyperthermophilic sulfate reducer Archaeoglobus fulgidus at 1.9 A resolution.

41 lytic domain (P-domain, residues 415-621) of Archaeoglobus fulgidus B-type Lon protease (wtAfLonB) an

42 -based mutational analysis of RNase HII from Archaeoglobus fulgidus, both with and without a bound me

43 pothetical proteins from M. tuberculosis and Archaeoglobus fulgidus, but FGD showed no significant ho

44 n the Bacteria and Archaea domains (Af3 from Archaeoglobus fulgidus, Cd1 from Clostridium difficile,

45 The previous crystal structure of the Archaeoglobus fulgidus complex revealed a symmetric dime

46 wo crystal structures of a SIR2 homolog from Archaeoglobus fulgidus complexed with NAD have been dete

47 The hyperthermophilic archaeon Archaeoglobus fulgidus contains an L-Ala dehydrogenase (

48 The thermophilic, sulfur metabolizing Archaeoglobus fulgidus contains two genes, AF0473 and AF

49 utation) T. maritima CopA, comparing it with Archaeoglobus fulgidus CopA and Ca(2+) ATPase.

50 ansmembrane Cu(+) transport sites present in Archaeoglobus fulgidus CopA.

51 Archaeoglobus fulgidus CopB is a member of this subfamil

52 esting both models, the delivery of Cu(+) by Archaeoglobus fulgidus Cu(+) chaperone CopZ to the corre

53 Here, using Archaeoglobus fulgidus Cu(+)-ATPase CopA and the C-termi

54 tions of amino acids in these regions of the Archaeoglobus fulgidus Cu(+)-ATPase CopA do not affect A

55 ue SRP19 from the hyperthermophilic archaeon Archaeoglobus fulgidus, designated as Af19, was determin

56 CopA, a thermophilic membrane ATPase from Archaeoglobus fulgidus, drives the outward movement of C

57 The genome of the hyperthermophile Archaeoglobus fulgidus encodes a putative CopZ copper ch

58 The euryarchaeote Archaeoglobus fulgidus encodes two genes with homology t

59 Cocrystal structures of the class I archaeal Archaeoglobus fulgidus enzyme, poised for addition of C7

60 der range of substrates than the homodimeric Archaeoglobus fulgidus enzyme.

61 allographic studies of the highly homologous Archaeoglobus fulgidus enzyme.

62 microbial genomes (Saccharomyces cerevisiae, Archaeoglobus fulgidus, Escherichia coli, Haemophilus in

63 Archaeoglobus fulgidus ferritin (AfFtn) is the only tetr

64 fferences, we refined a crystal structure of Archaeoglobus fulgidus fibrillarin-Nop5p binary complex

65 Tfu-FNO were highly similar to those of the Archaeoglobus fulgidus FNO (Af-FNO).

66 gans (GenBankTM accession number Z69637) and Archaeoglobus fulgidus (GenBankTM accession number AE000

67 AF-Est2, from the hyperthermophilic archaeon Archaeoglobus fulgidus has been cloned, over-expressed i

68 i, Methanobacterium thermoautotrophicum, and Archaeoglobus fulgidus, implying the existence of unreco

69 The atomic structure of archaeal Hel308 from Archaeoglobus fulgidus in complex with DNA was recently

70 of an NAD kinase from the archaeal organism Archaeoglobus fulgidus in complex with its phosphate don

71 the crystal structure of reverse gyrase from Archaeoglobus fulgidus in the presence and absence of nu

72 A gene putatively identified as the Archaeoglobus fulgidus inositol-1-phosphate synthase (IP

73 uaporin AfAQP from sulfide reducing bacteria Archaeoglobus fulgidus into planar membranes and by moni

74 CopA from Archaeoglobus fulgidus is a hyperthermophilic ATPase res

75 CopA from Archaeoglobus fulgidus is a hyperthermophilic member of

76 Archaeoglobus fulgidus is the first sulphur-metabolizing

77 In the sulfate-reducing archaeon Archaeoglobus fulgidus it is a metal-dependent thermozym

78 the three polypeptide domains were found in Archaeoglobus fulgidus, Methanopyrus kandleri, Methanosa

79 hown not only that Methanococcus jannaschii, Archaeoglobus fulgidus, Methanosarcina acetivorans, and

80 acillus subtilis; four anaerobic regulons in Archaeoglobus fulgidus (NarL, NarP, Fnr, and ModE); and

81 that from the protein Af1503 of the archaeon Archaeoglobus fulgidus or the Tsr receptor.

82 characterized the interactions of human and Archaeoglobus fulgidus PCNA trimer with double-stranded

83 Here we report the crystal structure of Archaeoglobus fulgidus Piwi protein bound to double-stra

84 ynthetase variants that recognize engineered Archaeoglobus fulgidus prolyl-tRNAs (Af-tRNA(Pro)) with

85 rom Thermus aquaticus, Thermus thermophilus, Archaeoglobus fulgidus, Pyrococcus furiosus, Methanococc

86 Archaeoglobus fulgidus RbcL2, a form III ribulose-1,5-bi

87 organism, strain VC-16 (tentatively called "Archaeoglobus fulgidus") reduces sulphate--the only arch

88 igated some of the biochemical properties of Archaeoglobus fulgidus reverse gyrase.

89 Crystal structures of Archaeoglobus fulgidus Rio1 and Rio2 have shown that whe

90 Here, we report the crystal structures of Archaeoglobus fulgidus RNase HII in complex with PCNA, a

91 A protein component of the Archaeoglobus fulgidus RNase P was expressed in Escheric

92 sequences and crystal structures of LamR and Archaeoglobus fulgidus S2p, a non-laminin-binding orthol

93 y scattering (SAXS) solution analyses of the Archaeoglobus fulgidus secretion superfamily ATPase, afG

94 A crystal structure of the Archaeoglobus fulgidus SepCysS apoenzyme provides inform

95 ibosylation of acetyllysine is solved for an Archaeoglobus fulgidus sirtuin (Af2Sir2).

96 Archaeoglobus fulgidus SRP proteins also bound to full-l

97 k response of the hyperthermophilic archaeon Archaeoglobus fulgidus strain VC-16 was studied using wh

98 vate, closely resembles that of the archaeon Archaeoglobus fulgidus, strongly suggesting a common ori

99 the glycine betaine-binding protein ProX of Archaeoglobus fulgidus; the resultant model indicated th

100 ere we describe the crystal structure of the Archaeoglobus fulgidus tRNA nucleotidyltransferase in co

101 9 from the sulfate-reducing hyperthermophile Archaeoglobus fulgidus was determined at 1.7 A resolutio

102 conserved in archaeal homologs, AfAmt-2 from Archaeoglobus fulgidus was expressed in yeast.

103 oprotein) encoded by AF1518 in the genome of Archaeoglobus fulgidus was produced in Escherichia coli

104 The Af1503 HAMP domain from Archaeoglobus fulgidus was recently shown to be a four-h

105 A gene sequences from Thermovirga lienii and Archaeoglobus fulgidus were cloned and used to generate

106 zymes from Methanocaldococcus jannaschii and Archaeoglobus fulgidus were not.

107 rs of FENs derived from T5 bacteriophage and Archaeoglobus fulgidus were studied with a range of sing

108 sequences, from Methanococcus jannaschii and Archaeoglobus fulgidus, were analyzed in order to ascert

109 ute in many hyperthermophilic archaea (e.g., Archaeoglobus fulgidus) when the cells are grown above 8

110 o deduced sequences in Bacillus subtilis and Archaeoglobus fulgidus, which also lack some typical Rub

111 Here, we determined crystal structures of an Archaeoglobus fulgidus XPB homolog (AfXPB) that characte