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2 that there was generally sufficient H(2) for Methanocaldococcus growth at Axial but not at Endeavour.
3 we demonstrate that NifB from the methanogen Methanocaldococcus infernus is a radical SAM enzyme able
4 rystallographic structure of an Ogg2 member, Methanocaldococcus janischii Ogg, in complex with a DNA
9 discovery of an isopentenyl kinase (IPK) in Methanocaldococcus jannaschii (MJ) suggests a new variat
11 We also cloned the corresponding gene from Methanocaldococcus jannaschii (mj1022) and characterized
15 ed substrate-enzyme conjugate [pre-tRNA(Tyr)-Methanocaldococcus jannaschii (Mja) RPR] to investigate
16 e substitutions in the C-terminal stirrup of Methanocaldococcus jannaschii (Mja) TBP do not completel
17 f these RPRs, such as that from the archaeon Methanocaldococcus jannaschii (Mja), to catalyze precurs
18 rt that Argonaute from the archaeal organism Methanocaldococcus jannaschii (MjAgo) possesses two mode
19 ltransferase (CobY) enzyme from the archaeon Methanocaldococcus jannaschii (MjCobY) in complex with G
20 ctroneutral Na(+)/H(+) exchanger, NhaP1 from Methanocaldococcus jannaschii (MjNhaP1), a close homolog
22 o proteins in Escherichia coli using evolved Methanocaldococcus jannaschii aminoacyl-tRNA synthetase(
23 ed by borrelidin, whereas ThrRS enzymes from Methanocaldococcus jannaschii and Archaeoglobus fulgidus
24 s, to several orthogonal aaRSes derived from Methanocaldococcus jannaschii and Escherichia coli tyros
26 y recombinant ProRS enzymes from the archaea Methanocaldococcus jannaschii and Methanothermobacter th
28 r created two RPAs that mimicked the RPAs in Methanocaldococcus jannaschii and Methanothermobacter th
29 , Mj0400 and Mj1249, have been identified in Methanocaldococcus jannaschii as the enzymes involved in
30 In the case of the methanogenic archaeon Methanocaldococcus jannaschii as well as most methanogen
31 ntron (both linear and circular forms) using Methanocaldococcus jannaschii box C/D RNP core proteins.
32 ically active box C/D sRNP from the archaeon Methanocaldococcus jannaschii by single-particle electro
33 inity of PaNhaP and the related MjNhaP1 from Methanocaldococcus jannaschii can be attributed to an ad
34 crystal structures of FAICAR synthetase from Methanocaldococcus jannaschii complexed with various lig
35 found that the prototypical NBD MJ0796 from Methanocaldococcus jannaschii dimerizes in response to A
38 the hyperthermophilic, methanogenic archaeon Methanocaldococcus jannaschii encodes a CobY protein (Mj
39 Here, we report that the MJ0438 gene from Methanocaldococcus jannaschii encodes a novel S-adenosyl
43 pCysS (Cys(64), Cys(67), and Cys(272) in the Methanocaldococcus jannaschii enzyme) are essential for
44 1003 and MJ1271 proteins from the methanogen Methanocaldococcus jannaschii formed the first homoaconi
46 d an uncharacterized archaeal protein in the Methanocaldococcus jannaschii genome, MJ0887, which coul
48 mation of lactaldehyde and hydroxyacetone in Methanocaldococcus jannaschii have been established.
49 rystal structure of an engineered variant of Methanocaldococcus jannaschii Hsp16.5 wherein a 14 amino
50 ickel site distinct from that of zinc-loaded Methanocaldococcus jannaschii HypB as well as subtle cha
51 Here we present the structure of KsgA from Methanocaldococcus jannaschii in complex with several li
52 of the Nep1 homolog from the archaebacterium Methanocaldococcus jannaschii in its free form (2.2 A re
53 es that contrasted with the related organism Methanocaldococcus jannaschii included the absence of in
54 ification of the corresponding activity from Methanocaldococcus jannaschii indicated that tRNA(Cys) b
57 encoded by the MJ0619 gene in the methanogen Methanocaldococcus jannaschii is likely this missing met
58 report that the enzyme encoded by Mj0883 of Methanocaldococcus jannaschii is the archaeal counterpar
59 nases associated with isoprene biosynthesis, Methanocaldococcus jannaschii isopentenyl phosphate kina
60 ccharomyces cerevisiae, Escherichia coli and Methanocaldococcus jannaschii It presents the following
63 py, the first step of this transformation in Methanocaldococcus jannaschii occurs by the reaction of
64 s of the trefoil-knotted protein MJ0366 from Methanocaldococcus jannaschii on the operation of the Cl
65 ribosome-SecY channel complexes derived from Methanocaldococcus jannaschii or Escherichia coli show t
67 of these (Pyrococcus abyssi proabylysin and Methanocaldococcus jannaschii projannalysin), which are
69 Earlier we reported the structure of the Methanocaldococcus jannaschii PSTK (MjPSTK) complexed wi
70 cus maripaludis tRNA(Sec) to investigate how Methanocaldococcus jannaschii PSTK distinguishes tRNA(Se
71 y presents a biochemical characterization of Methanocaldococcus jannaschii PSTK, including kinetics o
73 we designate as PurP, is the product of the Methanocaldococcus jannaschii purP gene (MJ0136), which
74 ps in the biosynthesis of coenzyme F(420) in Methanocaldococcus jannaschii requires generation of 2-p
77 wo Methanocaldococcus strains from Axial and Methanocaldococcus jannaschii showed similar Monod growt
79 f a non-synthetase protein from the archaeon Methanocaldococcus jannaschii that was copurified with p
80 aracterized the genome-wide occupancy of the Methanocaldococcus jannaschii transcription machinery an
83 ding an amber suppressor tRNA derived from a Methanocaldococcus jannaschii tyrosyl-tRNA (MjtRNATyrCUA
85 G1PDH from the hyperthermophilic methanogen Methanocaldococcus jannaschii with bound substrate dihyd
86 aracterize here the MJ1541 gene product from Methanocaldococcus jannaschii, an enzyme that was annota
87 om three archaea: Methanococcus maripaludis, Methanocaldococcus jannaschii, and Sulfolobus solfataric
88 d biochemically, in the sequenced genomes of Methanocaldococcus jannaschii, Bacillus cereus ATCC 1098
89 of the ORFs had their highest Blastp hits in Methanocaldococcus jannaschii, lateral gene transfer or
91 ing this protein have not been identified in Methanocaldococcus jannaschii, Methanothermobacter therm
93 nit RNA polymerase from the hyperthermophile Methanocaldococcus jannaschii, we describe a functional
95 accharomyces cerevisiae, and archaebacterium Methanocaldococcus jannaschii, which encodes a protein w
96 ed for a GTP cyclohydrolase III protein from Methanocaldococcus jannaschii, which has no amino acid s
97 solution structure of the archaeal CorA from Methanocaldococcus jannaschii, which is a unique complet
98 its simplicity, we studied the Trx system of Methanocaldococcus jannaschii--a deeply rooted hyperther
111 ion reaction, and it was recently shown that Methanocaldococcus (Methanococcus) jannaschii and other
114 n factor IIB of Methanococcus jannaschii and Methanocaldococcus vulcanius, revealing a novel modified
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