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1 structures of NikR from Escherichia coli and Pyrococcus horikoshii .
2 archaeal species (Archaeoglobus fulgidus and Pyrococcus horikoshii).
3 Trichoderma viride, Thermogata maritima, and Pyrococcus horikoshii.
4 ed studies of the monofunctional ligase from Pyrococcus horikoshii.
5 aryotic glutamate transporter homologue from Pyrococcus horikoshii.
6 l-tRNA synthetase is from the achaebacterium Pyrococcus horikoshii.
7 fied in the genomes of Pyrococcus abyssi and Pyrococcus horikoshii.
8 zyme, an endoglucanase from the thermophilic Pyrococcus horikoshii.
9 the crystal structure of the gene product of Pyrococcus horikoshii 999 (PH999), a PZAase, and its com
11 of comparing domain graphs of two organisms, Pyrococcus horikoshii (an extremophile) and Haemophilus
12 on the homologous sequence from subunit B of Pyrococcus horikoshii, an organism that lacks an actin c
14 sulfur-reducing anaerobic hyperthermophiles Pyrococcus horikoshii and Pyrococcus furiosus; however,
16 of the structure of l-lysine complexed with Pyrococcus horikoshii class I LysRS (LysRS1) and homolog
17 ervation between P. furiosus and the related Pyrococcus horikoshii clearly delimited the gene start i
18 as been used to kinetically characterise the Pyrococcus horikoshii DNA adenine methyltransferase.
22 ation by showing that Archease and RtcB from Pyrococcus horikoshii function in tandem, with Archease
23 resolution structure of the transporter from Pyrococcus horikoshii (Glt(Ph)) in steered molecular dyn
24 nt of a glutamate transporter homologue from Pyrococcus horikoshii, Glt(Ph), which is trapped in the
26 mate transporter homologue from the archaeon Pyrococcus horikoshii, GltPh, showed that distinct trans
28 ase domain of the hyperthermophilic archaeon Pyrococcus horikoshii is strongly regulated by the nativ
30 tem Glt(Ph), an archaeal EAAT homologue from Pyrococcus horikoshii, limited trypsin proteolysis exper
32 ning to evaluate the interaction between the Pyrococcus horikoshii Nop5p domain and an L7Ae box C/D R
33 s (Escherichia coli, Heliobacter pylori, and Pyrococcus horikoshii) of NikR reveal large conformation
35 Our laboratory has recently showed that in Pyrococcus horikoshii (P. horikoshii), the first step us
37 eric serine protease, an oligopeptidase from Pyrococcus horikoshii (PhAAP), revealing a complex, self
39 eprogramming the anticodon-binding pocket of Pyrococcus horikoshii ProRS (PhProRS), we were able to i
40 moautotrophicum, Archaeoglobus fulgidus, and Pyrococcus horikoshii) revealed 1326 orthologous sets, o
41 Here, we report two crystal structures of Pyrococcus horikoshii RNA-splicing ligase RtcB in comple
43 reviously yielded a crystal structure of the Pyrococcus horikoshii RtcB protein containing a new prot
44 ate transporter homolog from archaebacterium Pyrococcus horikoshii, sodium/aspartate symporter GltPh,
45 r dynamics simulations of three forms of the Pyrococcus horikoshii species of NikR including two apo-
46 of diphthamide biosynthesis in the archaeon Pyrococcus horikoshii uses a novel iron-sulphur-cluster
48 endoglucanase EGPh from the hypothermophilic Pyrococcus horikoshii was transaminated with pyridoxal-5
49 hermophilic Archaea, Pyrococcus furiosus and Pyrococcus horikoshii, was assessed by analysis of compl
50 nes from both Mycobacterium tuberculosis and Pyrococcus horikoshii were cloned, and their protein pro
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