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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.
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
12 A new carboxyl esterase, AF-Est2, from the hyperthermophilic archaeon Archaeoglobus fulgidus has be
14 structure of the 104 residue SRP19 from the hyperthermophilic archaeon Archaeoglobus fulgidus, desig
17 ctures, to our knowledge, of an ACD from the hyperthermophilic archaeon Candidatus Korachaeum cryptof
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
33 an endonuclease III homolog, PaNth, from the hyperthermophilic archaeon Pyrobaculum aerophilum, whose
34 ation of a putative DNA glycosylase from the hyperthermophilic archaeon Pyrobaculum aerophilum, whose
39 transcarbamoylase (OTCase) from the deep sea hyperthermophilic archaeon Pyrococcus abyssi demonstrate
40 ned the solution structure of RPP21 from the hyperthermophilic archaeon Pyrococcus furiosus ( Pfu) us
41 which beta-strand sequences of Rds from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) and
42 ate ferredoxin oxidoreductase (POR) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) cata
43 ngle cubane cluster ferredoxin (Fd) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) have
44 ngle cubane cluster ferredoxin (Fd) from the hyperthermophilic archaeon Pyrococcus furiosus (Pf) poss
45 es from Escherichia coli (EcMetAP-I) and the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-
46 ng for the methionyl aminopeptidase from the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-
47 tic studies were conducted on the POP of the hyperthermophilic archaeon Pyrococcus furiosus (Pfu) 85
48 protons of perdeuterated rubredoxin from the hyperthermophilic archaeon Pyrococcus furiosus and the m
50 ylase was identified in cell extracts of the hyperthermophilic archaeon Pyrococcus furiosus by its ab
51 ified from cell extracts of the proteolytic, hyperthermophilic archaeon Pyrococcus furiosus by multis
53 shed membrane preparations from cells of the hyperthermophilic archaeon Pyrococcus furiosus contain h
59 The maltose-regulated mlr-2 gene from the hyperthermophilic archaeon Pyrococcus furiosus having ho
61 The cytoplasmic hydrogenase (SHI) of the hyperthermophilic archaeon Pyrococcus furiosus is an NAD
65 ed intracellular proteolytic activity in the hyperthermophilic archaeon Pyrococcus furiosus was found
68 a tungstopterin-containing protein from the hyperthermophilic archaeon Pyrococcus furiosus, have bee
69 coding a thermostable endoglucanase from the hyperthermophilic archaeon Pyrococcus furiosus, was clon
76 homogeneity from crude cell extracts of the hyperthermophilic archaeon Pyrococcus furiosus: a beta-g
77 A intein located in the ATPase domain of the hyperthermophilic archaeon Pyrococcus horikoshii is stro
78 (POR) has been previously purified from the hyperthermophilic archaeon, Pyrococcus furiosus, an orga
82 class of small chromosomal proteins from the hyperthermophilic archaeon Sulfolobus acidocaldarius and
84 domain of life, with the discovery that the hyperthermophilic archaeon Sulfolobus has three replicat
86 II chaperonins known as rosettasomes in the hyperthermophilic archaeon Sulfolobus shibatae, are not
87 -glycosidase (clan GH-1A, family 1) from the hyperthermophilic archaeon Sulfolobus solfataricus at 2.
91 ce of a global gene regulatory system in the hyperthermophilic archaeon Sulfolobus solfataricus is de
97 gh mutagenesis of the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7
98 ily DNA replication polymerase (Dpo1) in the hyperthermophilic archaeon, Sulfolobus solfataricus, is
100 structure of TIM from Thermoproteus tenax, a hyperthermophilic archaeon that has an optimum growth te
101 cture of the ribosomal protein L30e from the hyperthermophilic archaeon Thermococcus celer determined
102 that ribonucleotides are incorporated by the hyperthermophilic archaeon Thermococcus kodakarensis bot
103 magnetic, four-iron ferredoxin (Fd) from the hyperthermophilic archaeon Thermococcus litoralis (Tl) h
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