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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  two archaeal species Haloferax volcanii and Thermococcus barophilus.
4 ential for S(0) respiration in Pyrococcus or Thermococcus but appears to participate in oxidative def
5 ein L30e from the hyperthermophilic archaeon Thermococcus celer determined at cryo-temperature.
6 taH and Marburg, Methanothermus fervidus and Thermococcus celer strain AL-1.
7                                      Because Thermococcus DNA polymerases incorporate as many as 1,00
8        Here, we report cryo-EM structures of Thermococcus gammatolerans McrB and McrBC, and E. coli M
9        Here we present the structures of the Thermococcus gammatolerans McrB DNA-binding domain (TgDe
10 thermophilus sensitive to lysis D (SlyD) and Thermococcus gammatolerans SlyD FK-506-binding protein (
11 gle-stranded DNA by the helicase Hel308 from Thermococcus gammatolerans.
12 ty family-B DNA polymerase from the archaeon Thermococcus gorgonarius (Tgo-Pol), able to replicate pa
13 tion describes an X-ray crystal structure of Thermococcus gorgonarius polymerase in complex with a DN
14 y crystal structure, at 2.8 A resolution, of Thermococcus gorgonarius polymerase in complex with a DN
15 cteriophage RB69 and the recently determined Thermococcus gorgonarius), but differ in their relative
16  In Tgo, the replicative DNA polymerase from Thermococcus gorgonarius, we identify a single mutation
17 determined the ability of RNAP purified from Thermococcus kodakaraensis (T.k.) to initiate transcript
18  oxygen compared to the previously described Thermococcus kodakaraensis and halophile proteins.
19 d the tRNA recognition of the discriminating Thermococcus kodakaraensis AspRS to that of a ND-AspRS b
20 d Tris buffer, the DNA primase isolated from Thermococcus kodakaraensis catalyzed the formation of dA
21 nterestingly, the genome of the euryarchaeon Thermococcus kodakaraensis contains two PCNA-encoding ge
22          Thermococcus kodakarensis (formerly Thermococcus kodakaraensis) strains have been constructe
23 eral proteins that co-purify with aIF2B from Thermococcus kodakaraensis, and these include aIF2alpha,
24 d protein, encoded by TK1252 in the archaeon Thermococcus kodakaraensis, was shown to stably interact
25 s have been constructed and transformed into Thermococcus kodakaraensis, which direct the constitutiv
26 e complex and its subunits from the archaeon Thermococcus kodakaraensis.
27 t encodes a nonessential beta-glycosidase in Thermococcus kodakaraensis.
28 entified in an atomic structure of RadB from Thermococcus kodakaraensis.
29                                              Thermococcus kodakarensis (formerly Thermococcus kodakar
30 promoter DNA ternary complexes from archaea, Thermococcus kodakarensis (Tko).
31  crystal structure of euryarchaeal RNAP from Thermococcus kodakarensis (Tko).
32                          Histone proteins in Thermococcus kodakarensis are sufficiently abundant to c
33 corporated by the hyperthermophilic archaeon Thermococcus kodakarensis both in vitro and in vivo and
34                Hydrogen (H(2)) production by Thermococcus kodakarensis compares very favourably with
35                           The model archaeon Thermococcus kodakarensis encodes 15 inteins, and we est
36               The hyperthermophilic archaeon Thermococcus kodakarensis encodes several enzymes to rep
37                              Atypically, the Thermococcus kodakarensis genome encodes three archaeal
38  this approach, we successfully enriched the Thermococcus kodakarensis mini-chromosome maintenance co
39 e report the biochemical characterization of Thermococcus kodakarensis Nat10 (TkNat10), an RNA acetyl
40 sion of Gms proteins from various archaea in Thermococcus kodakarensis results in the production of G
41           Here we report the construction of Thermococcus kodakarensis strains with mutations that de
42            Here we report the structure of a Thermococcus kodakarensis transcription pre-termination
43 rium Thermotoga maritima in a naive archaeon Thermococcus kodakarensis which naturally has positively
44 cement, we have isolated archaeal mutants of Thermococcus kodakarensis with the subunit F-encoding ge
45  in Thermotoga spp., Pyrococcus furiosus and Thermococcus kodakarensis, indicating the existence of a
46   Therefore, all DNA interactions in vivo in Thermococcus kodakarensis, the most genetically versatil
47 l protein, encoded by TK0808 in the archaeon Thermococcus kodakarensis, was shown to stably interact
48  from Pyrococcus horikoshii and Glt(Tk) from Thermococcus kodakarensis.
49  we map m(5)C in the model hyperthermophile, Thermococcus kodakarensis.
50 xin (Fd) from the hyperthermophilic archaeon Thermococcus litoralis (Tl) has been constructed on the
51 ides by the thermostable DNA polymerase from Thermococcus litoralis (Vent DNA polymerase).
52 Thermus aquaticus, family B polymerases from Thermococcus litoralis and Thermococcus 9(o)N-7, and the
53  values for DNA and dNTP similar to those of Thermococcus litoralis DNA polymerase.
54 ly thermostable glutamate dehydrogenase from Thermococcus litoralis has been determined at 2.5 A reso
55                                              Thermococcus litoralis is a strictly anaerobic archaeon
56               The hyperthermophilic archaeon Thermococcus litoralis strain NS-C, first isolated in 19
57 he hyperthermophiles Pyrococcus furiosus and Thermococcus litoralis whose optimal growth temperatures
58 uryarchaeota species Pyrococcus furiosus and Thermococcus litoralis, phosphoglucose isomerase (PGI) a
59 he proteolytic and hyperthermophilic archaea Thermococcus litoralis, Thermococcus sp. strain ES-1, Py
60 hermophilic Archaea, Pyrococcus furiosus and Thermococcus litoralis.
61 s the components required for the process in Thermococcus, Okazaki fragment maturation was reconstitu
62  undertaken cryo-EM studies on multi-subunit Thermococcus onnurineus Csm effector ternary complexes,
63           We report on cryo-EM structures of Thermococcus onnurineus Csm(crRNA) binary, Csm(crRNA)-ta
64 r structure-function studies have focused on Thermococcus onnurineus Csm6 to deduce mechanistic insig
65 espiratory formate hydrogen lyase complex of Thermococcus onnurineus was inserted into the P. furiosu
66 rotein from the type IV-C CRISPR cassette of Thermococcus onnurineus.
67          Here, we show which hydrogenases in Thermococcus paralvinellae are affected by added H2 duri
68  hyperthermophilic heterotrophs in the genus Thermococcus produce H2 in the absence of S degrees and
69 ncorporated ribonucleotides, archaea such as Thermococcus rely only upon RNaseH2 to initiate the path
70 to function as the replicative polymerase in Thermococcus replicating both the leading and the laggin
71 ssible plasmid identified in a Euryarchaeon, Thermococcus sp. 33-3.
72 anothermobacter thermautotrophicus (Mth) and Thermococcus sp. 9 degrees N (9 degrees N).
73 novel steric gate histidine residue (H931 in Thermococcus sp. 9 degrees N PolD) in the PolD s-motif b
74 e from the hyperthermophilic marine archaeon Thermococcus sp. 9 degrees N-7 (9 degrees N-7 pol) provi
75                                              Thermococcus sp. 9 degrees N-7 DNA polymerase exhibited
76      Of the five cloned DNA polymerases, the Thermococcus sp. 9 degrees N-7 DNA polymerase was chosen
77  to reduce the 3'-5' exonuclease activity of Thermococcus sp. 9 degrees N-7 DNA polymerase.
78  activity for a Family D DNA polymerase from Thermococcus sp. 9 degrees N.
79 s by randomly mutagenizing the gene encoding Thermococcus sp. JDF-3 DNA polymerase and screening muta
80 thermophilic archaea Thermococcus litoralis, Thermococcus sp. strain ES-1, Pyrococcus furiosus, and P
81 ituted in vitro using purified proteins from Thermococcus species 9 degrees N or cell extracts.
82  of dual-specificity ATP/NAD+ ligases in two Thermococcus species and Pyrococcus abyssi and an ATP/AD
83 fhl1 have a competitive advantage over other Thermococcus species in hot subsurface environments wher
84 cs data in Archaeoglobus, Halobacterium, and Thermococcus spp.
85                                          The Thermococcus strain PK could reduce elemental sulfur to
86                                   Therefore, Thermococcus that possess fhl1 have a competitive advant
87 st of the methanogen branchings) and that of Thermococcus (the deepest of all branchings on the metha
88      Inorganic pyrophosphatase (IPPase) from Thermococcus thioreducens is a large oligomeric protein