ライフサイエンスコーパス: Archaeoglobus

1 on structure of an isolated HAMP domain from Archaeoglobus, Aer HAMP is proposed to fold into a four-

2 hyperthermophilic, sulfate-reducing archaeon Archaeoglobus fulgidis.

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

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

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

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

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

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

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

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

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

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

13 (420)-0:gamma-glutamyl ligase (CofE-AF) from Archaeoglobus fulgidus and its complex with GDP at 2.5 A

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

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

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

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

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

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

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

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

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

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

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

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

26 Archaeoglobus fulgidus CopB is a member of this subfamil

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

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

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

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

31 The euryarchaeote Archaeoglobus fulgidus encodes two genes with homology t

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

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

34 allographic studies of the highly homologous Archaeoglobus fulgidus enzyme.

35 Archaeoglobus fulgidus ferritin (AfFtn) is the only tetr

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

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

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

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

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

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

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

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

44 CopA from Archaeoglobus fulgidus is a hyperthermophilic ATPase res

45 CopA from Archaeoglobus fulgidus is a hyperthermophilic member of

46 Archaeoglobus fulgidus is the first sulphur-metabolizing

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

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

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

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

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

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

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

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

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

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

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

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

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

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

61 Archaeoglobus fulgidus SRP proteins also bound to full-l

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

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

64 9 from the sulfate-reducing hyperthermophile Archaeoglobus fulgidus was determined at 1.7 A resolutio

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

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

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

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

69 zymes from Methanocaldococcus jannaschii and Archaeoglobus fulgidus were not.

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

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

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

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

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

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

76 Archaeoglobus fulgidus, a hyperthermophilic sulfate-redu

77 Archaeoglobus fulgidus, a hyperthermophilic, archaeal su

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 ermoautotrophicum, Pyrococcus horikoshii and Archaeoglobus fulgidus.

100 ing Methanobacterium thermoautotrophicum and Archaeoglobus fulgidus.

101 i, Methanobacterium thermoautotrophicum, and Archaeoglobus fulgidus.

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

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

104 e fraction of the hyperthermophilic archaeon Archaeoglobus fulgidus.

105 he three Amt orthologs from the euryarchaeon Archaeoglobus fulgidus.

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

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

108 jannaschii and the sulfate-reducing archaeon Archaeoglobus fulgidus.

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

110 hyperthermophilic sulfate-reducing anaerobe Archaeoglobus fulgidus.

111 components of the hyperthermophilic archaeon Archaeoglobus fulgidus.

112 describe a UDG from the extreme thermophile Archaeoglobus fulgidus.

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

114 ciled with available transcriptomics data in Archaeoglobus, Halobacterium, and Thermococcus spp.

115 uryarchaeota (Methanosarcina, Methanococcus, Archaeoglobus, Thermoplasma), with multiple genes in som

116 o be resolved, including the relationship of Archaeoglobus to the methanogens studied.