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1 ution assay of homologous recombination in a hyperthermophilic archaeon.
2  evolution, have not been determined for any hyperthermophilic archaeon.
3 st description of a nitrate reductase from a hyperthermophilic archaeon.
4 ock protein from Methanococcus jannaschii, a hyperthermophilic archaeon.
5 ifies a putative primordial Orai sequence in hyperthermophilic archaeons.
6                                          The hyperthermophilic archaeon Acidianus ambivalens expresse
7                                          The hyperthermophilic archaeon Aeropyrum pernix (A. pernix)
8 m chain alcohol dehydrogenase (ADH) from the hyperthermophilic archaeon Aeropyrum pernix has been sol
9 he Aeropyrum coil-shaped virus (ACV), of the hyperthermophilic archaeon Aeropyrum pernix, with a viri
10 ncovered a putative MIG protein from another hyperthermophilic archaeon, Aeropyrum pernix.
11                                          The hyperthermophilic archaeon Archaeoglobus fulgidus contai
12   A new carboxyl esterase, AF-Est2, from the hyperthermophilic archaeon Archaeoglobus fulgidus has be
13               The heat shock response of the hyperthermophilic archaeon Archaeoglobus fulgidus strain
14  structure of the 104 residue SRP19 from the hyperthermophilic archaeon Archaeoglobus fulgidus, desig
15 homogeneity from the soluble fraction of the hyperthermophilic archaeon Archaeoglobus fulgidus.
16 ed, expressed and purified components of the hyperthermophilic archaeon Archaeoglobus fulgidus.
17 ctures, to our knowledge, of an ACD from the hyperthermophilic archaeon Candidatus Korachaeum cryptof
18 ed by an intron in the 23 S rRNA gene of the hyperthermophilic archaeon Desulfurococcus mobilis.
19 HSP homologue of Methanococcus jannaschii, a hyperthermophilic Archaeon, forms a homogeneous multimer
20 Sulfolobus acidocaldarius is so far the only hyperthermophilic archaeon in which genetic recombinatio
21 ted Box C/D RNAs from Pyrococcus furiosus, a hyperthermophilic archaeon, into the nuclei of oocytes f
22            DNA in Methanothermus fervidus, a hyperthermophilic archaeon, is constrained into archaeal
23                                          The hyperthermophilic archaeon Methanocaldococcus jannaschii
24                                 MAT from the hyperthermophilic archaeon Methanococcus jannaschii (MjM
25                                          The hyperthermophilic archaeon Methanococcus jannaschii enco
26                                          The hyperthermophilic archaeon Methanococcus jannaschii enco
27                                          The hyperthermophilic archaeon Methanococcus jannaschii has
28           The flap endonuclease (FEN) of the hyperthermophilic archaeon Methanococcus jannaschii was
29                                 However, the hyperthermophilic archaeon Methanopyrus kandleri harbors
30               This 12.7-kDa protein from the hyperthermophilic archaeon Pyrobaculum aerophilum adopts
31 lectron transfer flavoprotein (ETF) from the hyperthermophilic archaeon Pyrobaculum aerophilum The Et
32                                          The hyperthermophilic archaeon Pyrobaculum aerophilum used 2
33                 The nitrate reductase of the hyperthermophilic archaeon Pyrobaculum aerophilum was pu
34 an endonuclease III homolog, PaNth, from the hyperthermophilic archaeon Pyrobaculum aerophilum, whose
35 ation of a putative DNA glycosylase from the hyperthermophilic archaeon Pyrobaculum aerophilum, whose
36 is of intracellular disulfide bonding in the hyperthermophilic archaeon Pyrobaculum aerophilum.
37 ORFs of the recently sequenced genome of the hyperthermophilic archaeon Pyrobaculum aerophilum.
38 strom and 2 angstrom, respectively, from the hyperthermophilic archaeon Pyrobaculum calidifontis.
39                                          The hyperthermophilic archaeon Pyrobaculum islandicum uses t
40 odABC transport system, was predicted in the hyperthermophilic archaeon Pyrobaculum.
41 transcarbamoylase (OTCase) from the deep sea hyperthermophilic archaeon Pyrococcus abyssi demonstrate
42 ned the solution structure of RPP21 from the hyperthermophilic archaeon Pyrococcus furiosus ( Pfu) us
43  which beta-strand sequences of Rds from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) and
44 ate ferredoxin oxidoreductase (POR) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) cata
45 ngle cubane cluster ferredoxin (Fd) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) have
46 ngle cubane cluster ferredoxin (Fd) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) poss
47 echanism of the H(+)-dependent MATE from the hyperthermophilic archaeon Pyrococcus furiosus (PfMATE).
48 es from Escherichia coli (EcMetAP-I) and the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-
49 ng for the methionyl aminopeptidase from the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-
50 tic studies were conducted on the POP of the hyperthermophilic archaeon Pyrococcus furiosus (Pfu) 85
51 protons of perdeuterated rubredoxin from the hyperthermophilic archaeon Pyrococcus furiosus and the m
52                    The LrpA protein from the hyperthermophilic archaeon Pyrococcus furiosus belongs t
53 ylase was identified in cell extracts of the hyperthermophilic archaeon Pyrococcus furiosus by its ab
54 ified from cell extracts of the proteolytic, hyperthermophilic archaeon Pyrococcus furiosus by multis
55            Cell extracts of the proteolytic, hyperthermophilic archaeon Pyrococcus furiosus contain h
56 shed membrane preparations from cells of the hyperthermophilic archaeon Pyrococcus furiosus contain h
57        The original genome annotation of the hyperthermophilic archaeon Pyrococcus furiosus contained
58         Previous studies have shown that the hyperthermophilic archaeon Pyrococcus furiosus contains
59                                          The hyperthermophilic archaeon Pyrococcus furiosus genome en
60                                          The hyperthermophilic archaeon Pyrococcus furiosus grows opt
61           Crystal structures of SOR from the hyperthermophilic archaeon Pyrococcus furiosus have been
62    The maltose-regulated mlr-2 gene from the hyperthermophilic archaeon Pyrococcus furiosus having ho
63                          Ferredoxin from the hyperthermophilic archaeon Pyrococcus furiosus is a mono
64     The cytoplasmic hydrogenase (SHI) of the hyperthermophilic archaeon Pyrococcus furiosus is an NAD
65 ss of PfMATE, a proton-coupled MATE from the hyperthermophilic archaeon Pyrococcus furiosus Pairs of
66             Identification of operons in the hyperthermophilic archaeon Pyrococcus furiosus represent
67                                          The hyperthermophilic archaeon Pyrococcus furiosus uses carb
68         The reverse gyrase gene rgy from the hyperthermophilic archaeon Pyrococcus furiosus was clone
69 ed intracellular proteolytic activity in the hyperthermophilic archaeon Pyrococcus furiosus was found
70          Here, the beta-glucosidase from the hyperthermophilic archaeon Pyrococcus furiosus was recom
71         Iron is an essential element for the hyperthermophilic archaeon Pyrococcus furiosus, and many
72  a tungstopterin-containing protein from the hyperthermophilic archaeon Pyrococcus furiosus, have bee
73 coding a thermostable endoglucanase from the hyperthermophilic archaeon Pyrococcus furiosus, was clon
74  proton and sodium transport in Mbh from the hyperthermophilic archaeon Pyrococcus furiosus.
75 nder anaerobic, reducing conditions from the hyperthermophilic archaeon Pyrococcus furiosus.
76 e rare biological form of RNA circles in the hyperthermophilic archaeon Pyrococcus furiosus.
77 vate synthetase (PpsA) was purified from the hyperthermophilic archaeon Pyrococcus furiosus.
78 nsferase at resolutions up to 1.2 A from the hyperthermophilic archaeon Pyrococcus furiosus.
79 oreductase (NROR) has been purified from the hyperthermophilic archaeon Pyrococcus furiosus.
80 e report random insertion mutagenesis in the hyperthermophilic archaeon Pyrococcus furiosus.
81  homogeneity from crude cell extracts of the hyperthermophilic archaeon Pyrococcus furiosus: a beta-g
82 A intein located in the ATPase domain of the hyperthermophilic archaeon Pyrococcus horikoshii is stro
83  (POR) has been previously purified from the hyperthermophilic archaeon, Pyrococcus furiosus, an orga
84              The ferredoxin (7.5 kDa) of the hyperthermophilic archaeon, Pyrococcus furiosus, contain
85                                          The hyperthermophilic archaeon, Pyrococcus furiosus, was gro
86 leaves the 5' side of deoxyinosine, from the hyperthermophilic archaeon, Pyrococcus furiosus.
87 class of small chromosomal proteins from the hyperthermophilic archaeon Sulfolobus acidocaldarius and
88                                          The hyperthermophilic archaeon Sulfolobus acidocaldarius exc
89  domain of life, with the discovery that the hyperthermophilic archaeon Sulfolobus has three replicat
90                                       In the hyperthermophilic archaeon Sulfolobus shibatae the two c
91  II chaperonins known as rosettasomes in the hyperthermophilic archaeon Sulfolobus shibatae, are not
92 -glycosidase (clan GH-1A, family 1) from the hyperthermophilic archaeon Sulfolobus solfataricus at 2.
93                                          The hyperthermophilic archaeon Sulfolobus solfataricus emplo
94                                          The hyperthermophilic archaeon Sulfolobus solfataricus grows
95                   The Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus is an
96 ce of a global gene regulatory system in the hyperthermophilic archaeon Sulfolobus solfataricus is de
97 noncatalytic subunit, denoted PriX, from the hyperthermophilic archaeon Sulfolobus solfataricus.
98 eavage of mRNA from an invading virus in the hyperthermophilic archaeon Sulfolobus solfataricus.
99 gh mutagenesis of the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus.
100 ral modules of the homomultimeric MCM of the hyperthermophilic archaeon Sulfolobus solfataricus.
101 in chromatin structure and regulation in the hyperthermophilic archaeon Sulfolobus solfataricus.
102 gh mutagenesis of the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7
103 ily DNA replication polymerase (Dpo1) in the hyperthermophilic archaeon, Sulfolobus solfataricus, is
104                     Pyrococcus furiosus is a hyperthermophilic archaeon that grows optimally at 100 d
105 structure of TIM from Thermoproteus tenax, a hyperthermophilic archaeon that has an optimum growth te
106 cture of the ribosomal protein L30e from the hyperthermophilic archaeon Thermococcus celer determined
107 that ribonucleotides are incorporated by the hyperthermophilic archaeon Thermococcus kodakarensis bot
108                                          The hyperthermophilic archaeon Thermococcus kodakarensis enc
109 magnetic, four-iron ferredoxin (Fd) from the hyperthermophilic archaeon Thermococcus litoralis (Tl) h
110                                          The hyperthermophilic archaeon Thermococcus litoralis strain
111                     Pyrococcus furiosus is a hyperthermophilic archaeon which grows optimally near 10

 
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