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1 and three groups corresponding to the genus Thermococcus.
2 polymerases from Thermococcus litoralis and Thermococcus 9(o)N-7, and the family X polymerase, human
3 ential for S(0) respiration in Pyrococcus or Thermococcus but appears to participate in oxidative def
7 ty family-B DNA polymerase from the archaeon Thermococcus gorgonarius (Tgo-Pol), able to replicate pa
8 tion describes an X-ray crystal structure of Thermococcus gorgonarius polymerase in complex with a DN
9 y crystal structure, at 2.8 A resolution, of Thermococcus gorgonarius polymerase in complex with a DN
10 cteriophage RB69 and the recently determined Thermococcus gorgonarius), but differ in their relative
11 In Tgo, the replicative DNA polymerase from Thermococcus gorgonarius, we identify a single mutation
12 determined the ability of RNAP purified from Thermococcus kodakaraensis (T.k.) to initiate transcript
14 d the tRNA recognition of the discriminating Thermococcus kodakaraensis AspRS to that of a ND-AspRS b
15 d Tris buffer, the DNA primase isolated from Thermococcus kodakaraensis catalyzed the formation of dA
16 nterestingly, the genome of the euryarchaeon Thermococcus kodakaraensis contains two PCNA-encoding ge
18 eral proteins that co-purify with aIF2B from Thermococcus kodakaraensis, and these include aIF2alpha,
19 d protein, encoded by TK1252 in the archaeon Thermococcus kodakaraensis, was shown to stably interact
20 s have been constructed and transformed into Thermococcus kodakaraensis, which direct the constitutiv
26 corporated by the hyperthermophilic archaeon Thermococcus kodakarensis both in vitro and in vivo and
30 cement, we have isolated archaeal mutants of Thermococcus kodakarensis with the subunit F-encoding ge
31 Therefore, all DNA interactions in vivo in Thermococcus kodakarensis, the most genetically versatil
32 l protein, encoded by TK0808 in the archaeon Thermococcus kodakarensis, was shown to stably interact
33 xin (Fd) from the hyperthermophilic archaeon Thermococcus litoralis (Tl) has been constructed on the
35 Thermus aquaticus, family B polymerases from Thermococcus litoralis and Thermococcus 9(o)N-7, and the
37 ly thermostable glutamate dehydrogenase from Thermococcus litoralis has been determined at 2.5 A reso
40 he hyperthermophiles Pyrococcus furiosus and Thermococcus litoralis whose optimal growth temperatures
41 uryarchaeota species Pyrococcus furiosus and Thermococcus litoralis, phosphoglucose isomerase (PGI) a
42 he proteolytic and hyperthermophilic archaea Thermococcus litoralis, Thermococcus sp. strain ES-1, Py
44 s the components required for the process in Thermococcus, Okazaki fragment maturation was reconstitu
45 espiratory formate hydrogen lyase complex of Thermococcus onnurineus was inserted into the P. furiosu
47 hyperthermophilic heterotrophs in the genus Thermococcus produce H2 in the absence of S degrees and
48 ncorporated ribonucleotides, archaea such as Thermococcus rely only upon RNaseH2 to initiate the path
49 to function as the replicative polymerase in Thermococcus replicating both the leading and the laggin
51 e from the hyperthermophilic marine archaeon Thermococcus sp. 9 degrees N-7 (9 degrees N-7 pol) provi
56 s by randomly mutagenizing the gene encoding Thermococcus sp. JDF-3 DNA polymerase and screening muta
57 thermophilic archaea Thermococcus litoralis, Thermococcus sp. strain ES-1, Pyrococcus furiosus, and P
59 of dual-specificity ATP/NAD+ ligases in two Thermococcus species and Pyrococcus abyssi and an ATP/AD
60 fhl1 have a competitive advantage over other Thermococcus species in hot subsurface environments wher
64 st of the methanogen branchings) and that of Thermococcus (the deepest of all branchings on the metha
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