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1 on structure of an isolated HAMP domain from Archaeoglobus, Aer HAMP is proposed to fold into a four-
2 t originated in Vulcanisaeta, independent of Archaeoglobus, by separate acquisition of qmoABC genes p
3 hyperthermophilic, sulfate-reducing archaeon Archaeoglobus fulgidis.
4  structures of XPB in complex with Bax1 from Archaeoglobus fulgidus (Af) and Sulfolobus tokodaii (St)
5               The splicing endonuclease from Archaeoglobus fulgidus (AF) belongs to the homodimeric f
6 member of this family, an FBPase/IMPase from Archaeoglobus fulgidus (AF2372), has been solved.
7 the crystal structure of a Piwi protein from Archaeoglobus fulgidus (AfPiwi) in complex with a small
8 his publication investigates the enzyme from Archaeoglobus fulgidus (Afu Pol-D).
9 cosylase from the hyperthermophilic organism Archaeoglobus fulgidus (AFUDG) is responsible for the re
10 gans (GenBankTM accession number Z69637) and Archaeoglobus fulgidus (GenBankTM accession number AE000
11 acillus subtilis; four anaerobic regulons in Archaeoglobus fulgidus (NarL, NarP, Fnr, and ModE); and
12  an Aer HAMP model based on the structure of Archaeoglobus fulgidus Af1503-HAMP, the closest residue
13                  The crystal structure of an Archaeoglobus fulgidus ammonium transporter (AMT) sugges
14 yperthermophilic, sulphate-reducing archaeon Archaeoglobus fulgidus and characterised its in vitro ac
15 (420)-0:gamma-glutamyl ligase (CofE-AF) from Archaeoglobus fulgidus and its complex with GDP at 2.5 A
16 ned the performance of the FEN1 enzymes from Archaeoglobus fulgidus and Methanococcus jannaschii and
17 omonas aeruginosa) and two archaeal species (Archaeoglobus fulgidus and Pyrococcus horikoshii).
18 barkeri and the closely related euryarchaeon Archaeoglobus fulgidus appeared to be of the Escherichia
19 crystal structure of the wild-type mIPS from Archaeoglobus fulgidus at 1.7 A, as well as the crystal
20 S from the hyperthermophilic sulfate reducer Archaeoglobus fulgidus at 1.9 A resolution.
21 lytic domain (P-domain, residues 415-621) of Archaeoglobus fulgidus B-type Lon protease (wtAfLonB) an
22        The previous crystal structure of the Archaeoglobus fulgidus complex revealed a symmetric dime
23 wo crystal structures of a SIR2 homolog from Archaeoglobus fulgidus complexed with NAD have been dete
24               The hyperthermophilic archaeon Archaeoglobus fulgidus contains an L-Ala dehydrogenase (
25        The thermophilic, sulfur metabolizing Archaeoglobus fulgidus contains two genes, AF0473 and AF
26 utation) T. maritima CopA, comparing it with Archaeoglobus fulgidus CopA and Ca(2+) ATPase.
27 ansmembrane Cu(+) transport sites present in Archaeoglobus fulgidus CopA.
28                                              Archaeoglobus fulgidus CopB is a member of this subfamil
29 esting both models, the delivery of Cu(+) by Archaeoglobus fulgidus Cu(+) chaperone CopZ to the corre
30                                  Here, using Archaeoglobus fulgidus Cu(+)-ATPase CopA and the C-termi
31 tions of amino acids in these regions of the Archaeoglobus fulgidus Cu(+)-ATPase CopA do not affect A
32           The genome of the hyperthermophile Archaeoglobus fulgidus encodes a putative CopZ copper ch
33                            The euryarchaeote Archaeoglobus fulgidus encodes two genes with homology t
34 Cocrystal structures of the class I archaeal Archaeoglobus fulgidus enzyme, poised for addition of C7
35 der range of substrates than the homodimeric Archaeoglobus fulgidus enzyme.
36 allographic studies of the highly homologous Archaeoglobus fulgidus enzyme.
37                                              Archaeoglobus fulgidus ferritin (AfFtn) is the only tetr
38 fferences, we refined a crystal structure of Archaeoglobus fulgidus fibrillarin-Nop5p binary complex
39  Tfu-FNO were highly similar to those of the Archaeoglobus fulgidus FNO (Af-FNO).
40 AF-Est2, from the hyperthermophilic archaeon Archaeoglobus fulgidus has been cloned, over-expressed i
41 The atomic structure of archaeal Hel308 from Archaeoglobus fulgidus in complex with DNA was recently
42  of an NAD kinase from the archaeal organism Archaeoglobus fulgidus in complex with its phosphate don
43 the crystal structure of reverse gyrase from Archaeoglobus fulgidus in the presence and absence of nu
44          A gene putatively identified as the Archaeoglobus fulgidus inositol-1-phosphate synthase (IP
45 uaporin AfAQP from sulfide reducing bacteria Archaeoglobus fulgidus into planar membranes and by moni
46                                    CopA from Archaeoglobus fulgidus is a hyperthermophilic ATPase res
47                                    CopA from Archaeoglobus fulgidus is a hyperthermophilic member of
48                                              Archaeoglobus fulgidus is the first sulphur-metabolizing
49             In the sulfate-reducing archaeon Archaeoglobus fulgidus it is a metal-dependent thermozym
50 that from the protein Af1503 of the archaeon Archaeoglobus fulgidus or the Tsr receptor.
51  characterized the interactions of human and Archaeoglobus fulgidus PCNA trimer with double-stranded
52      Here we report the crystal structure of Archaeoglobus fulgidus Piwi protein bound to double-stra
53 ynthetase variants that recognize engineered Archaeoglobus fulgidus prolyl-tRNAs (Af-tRNA(Pro)) with
54                                              Archaeoglobus fulgidus RbcL2, a form III ribulose-1,5-bi
55 igated some of the biochemical properties of Archaeoglobus fulgidus reverse gyrase.
56                        Crystal structures of Archaeoglobus fulgidus Rio1 and Rio2 have shown that whe
57    Here, we report the crystal structures of Archaeoglobus fulgidus RNase HII in complex with PCNA, a
58                   A protein component of the Archaeoglobus fulgidus RNase P was expressed in Escheric
59 sequences and crystal structures of LamR and Archaeoglobus fulgidus S2p, a non-laminin-binding orthol
60 y scattering (SAXS) solution analyses of the Archaeoglobus fulgidus secretion superfamily ATPase, afG
61                   A crystal structure of the Archaeoglobus fulgidus SepCysS apoenzyme provides inform
62 ibosylation of acetyllysine is solved for an Archaeoglobus fulgidus sirtuin (Af2Sir2).
63                                              Archaeoglobus fulgidus SRP proteins also bound to full-l
64 k response of the hyperthermophilic archaeon Archaeoglobus fulgidus strain VC-16 was studied using wh
65 ere we describe the crystal structure of the Archaeoglobus fulgidus tRNA nucleotidyltransferase in co
66 9 from the sulfate-reducing hyperthermophile Archaeoglobus fulgidus was determined at 1.7 A resolutio
67 conserved in archaeal homologs, AfAmt-2 from Archaeoglobus fulgidus was expressed in yeast.
68 oprotein) encoded by AF1518 in the genome of Archaeoglobus fulgidus was produced in Escherichia coli
69                  The Af1503 HAMP domain from Archaeoglobus fulgidus was recently shown to be a four-h
70 A gene sequences from Thermovirga lienii and Archaeoglobus fulgidus were cloned and used to generate
71 zymes from Methanocaldococcus jannaschii and Archaeoglobus fulgidus were not.
72 rs of FENs derived from T5 bacteriophage and Archaeoglobus fulgidus were studied with a range of sing
73  the DsrMKJOP complex of the sulfate reducer Archaeoglobus fulgidus works as a menadiol:DsrC-trisulfi
74 Here, we determined crystal structures of an Archaeoglobus fulgidus XPB homolog (AfXPB) that characte
75  organism, strain VC-16 (tentatively called "Archaeoglobus fulgidus") reduces sulphate--the only arch
76 ute in many hyperthermophilic archaea (e.g., Archaeoglobus fulgidus) when the cells are grown above 8
77  other archaea (e.g. Pyrococcus furiosus and Archaeoglobus fulgidus), and their corresponding genes w
78 ia pestis, 5% of Escherichia coli K12, 6% of Archaeoglobus fulgidus, 8% of Methanobacterium thermoaut
79 ypic WrbA protein from E. coli and WrbA from Archaeoglobus fulgidus, a hyperthermophilic species from
80                                              Archaeoglobus fulgidus, a hyperthermophilic sulfate-redu
81                                              Archaeoglobus fulgidus, a hyperthermophilic, archaeal su
82 structure of the chromatin protein Alba from Archaeoglobus fulgidus, a substrate for the Sir2 protein
83 e solved structures of a UBIAD1 homolog from Archaeoglobus fulgidus, AfUbiA, in an unliganded form an
84 rom the archaea Methanococcus jannaschii and Archaeoglobus fulgidus, and from the bacterium Thermotog
85 ulfovibrio vulgaris, Pseudomonas aeruginosa, Archaeoglobus fulgidus, and Methanocaldocococcus jannasc
86 rkeri, Methanobacterium thermoautotrophicum, Archaeoglobus fulgidus, and Mycobacterium smegmatis show
87 smodium falciparum, Tetrahymena thermophila, Archaeoglobus fulgidus, and Mycobacterium tuberculosis.
88 schii, Methanobacterium thermoautotrophicum, Archaeoglobus fulgidus, and Pyrococcus horikoshii) revea
89 rate species including Borrelia burgdorferi, Archaeoglobus fulgidus, Arabidopsis thaliana, and Homo s
90 -based mutational analysis of RNase HII from Archaeoglobus fulgidus, both with and without a bound me
91 pothetical proteins from M. tuberculosis and Archaeoglobus fulgidus, but FGD showed no significant ho
92 n the Bacteria and Archaea domains (Af3 from Archaeoglobus fulgidus, Cd1 from Clostridium difficile,
93 ue SRP19 from the hyperthermophilic archaeon Archaeoglobus fulgidus, designated as Af19, was determin
94    CopA, a thermophilic membrane ATPase from Archaeoglobus fulgidus, drives the outward movement of C
95 microbial genomes (Saccharomyces cerevisiae, Archaeoglobus fulgidus, Escherichia coli, Haemophilus in
96 i, Methanobacterium thermoautotrophicum, and Archaeoglobus fulgidus, implying the existence of unreco
97  the three polypeptide domains were found in Archaeoglobus fulgidus, Methanopyrus kandleri, Methanosa
98 hown not only that Methanococcus jannaschii, Archaeoglobus fulgidus, Methanosarcina acetivorans, and
99 rom Thermus aquaticus, Thermus thermophilus, Archaeoglobus fulgidus, Pyrococcus furiosus, Methanococc
100 vate, closely resembles that of the archaeon Archaeoglobus fulgidus, strongly suggesting a common ori
101 sequences, from Methanococcus jannaschii and Archaeoglobus fulgidus, were analyzed in order to ascert
102 o deduced sequences in Bacillus subtilis and Archaeoglobus fulgidus, which also lack some typical Rub
103 strains, as well as the piezophilic archaeon Archaeoglobus fulgidus.
104 he three Amt orthologs from the euryarchaeon Archaeoglobus fulgidus.
105  describe a UDG from the extreme thermophile Archaeoglobus fulgidus.
106 ermoautotrophicum, Pyrococcus horikoshii and Archaeoglobus fulgidus.
107 ing Methanobacterium thermoautotrophicum and Archaeoglobus fulgidus.
108 i, Methanobacterium thermoautotrophicum, and Archaeoglobus fulgidus.
109  subunits in replication factor C (RFC) from Archaeoglobus fulgidus.
110 e fraction of the hyperthermophilic archaeon Archaeoglobus fulgidus.
111 tested using CopA, a model Cu(+)-ATPase from Archaeoglobus fulgidus.
112 onsisting of a stand-alone macro domain from Archaeoglobus fulgidus.
113 al structure of a representative CDP-AP from Archaeoglobus fulgidus.
114 jannaschii and the sulfate-reducing archaeon Archaeoglobus fulgidus.
115 its of the RFC homologue of the euryarchaeon Archaeoglobus fulgidus.
116  hyperthermophilic sulfate-reducing anaerobe Archaeoglobus fulgidus.
117 components of the hyperthermophilic archaeon Archaeoglobus fulgidus.
118  the glycine betaine-binding protein ProX of Archaeoglobus fulgidus; the resultant model indicated th
119 ciled with available transcriptomics data in Archaeoglobus, Halobacterium, and Thermococcus spp.
120 s in response to elevated temperature in two Archaeoglobus species and the production of GMGTs with u
121 uryarchaeota (Methanosarcina, Methanococcus, Archaeoglobus, Thermoplasma), with multiple genes in som
122 o be resolved, including the relationship of Archaeoglobus to the methanogens studied.
123                                  Homologs of Archaeoglobus veneficus ECN are widespread among mesophi
124  bacteria carry out DSR, but in archaea only Archaeoglobus, which acquired DSR genes from bacteria, h

 
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