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1 structures of NikR from Escherichia coli and Pyrococcus horikoshii .
2 archaeal species (Archaeoglobus fulgidus and Pyrococcus horikoshii).
3 zyme, an endoglucanase from the thermophilic 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 Trichoderma viride, Thermogata maritima, and 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 studies of the archeal homologs Glt(Ph) from Pyrococcus horikoshii and Glt(Tk) from Thermococcus koda
15 sulfur-reducing anaerobic hyperthermophiles Pyrococcus horikoshii and Pyrococcus furiosus; however,
17 of the structure of l-lysine complexed with Pyrococcus horikoshii class I LysRS (LysRS1) and homolog
18 ervation between P. furiosus and the related Pyrococcus horikoshii clearly delimited the gene start i
19 as been used to kinetically characterise the Pyrococcus horikoshii DNA adenine methyltransferase.
23 ation by showing that Archease and RtcB from Pyrococcus horikoshii function in tandem, with Archease
24 resolution structure of the transporter from Pyrococcus horikoshii (Glt(Ph)) in steered molecular dyn
25 nt of a glutamate transporter homologue from Pyrococcus horikoshii, Glt(Ph), which is trapped in the
27 mate transporter homologue from the archaeon Pyrococcus horikoshii, GltPh, showed that distinct trans
28 mini-intein that interrupts the DNA PolII of Pyrococcus horikoshii has a linker region in place of th
30 ase domain of the hyperthermophilic archaeon Pyrococcus horikoshii is strongly regulated by the nativ
31 h, a homotrimeric aspartate transporter from Pyrococcus horikoshii, is an archaeal homolog of mammali
33 tem Glt(Ph), an archaeal EAAT homologue from Pyrococcus horikoshii, limited trypsin proteolysis exper
35 ning to evaluate the interaction between the Pyrococcus horikoshii Nop5p domain and an L7Ae box C/D R
36 s (Escherichia coli, Heliobacter pylori, and Pyrococcus horikoshii) of NikR reveal large conformation
38 Our laboratory has recently showed that in Pyrococcus horikoshii (P. horikoshii), the first step us
40 eric serine protease, an oligopeptidase from Pyrococcus horikoshii (PhAAP), revealing a complex, self
41 Herein, we present a structure of NadA from Pyrococcus horikoshii (PhNadA) in complex with IA and sh
43 olog, Glt(Ph), an aspartate transporter from Pyrococcus horikoshii, presents the best structurally ch
44 eprogramming the anticodon-binding pocket of Pyrococcus horikoshii ProRS (PhProRS), we were able to i
45 moautotrophicum, Archaeoglobus fulgidus, and Pyrococcus horikoshii) revealed 1326 orthologous sets, o
46 Here, we report two crystal structures of Pyrococcus horikoshii RNA-splicing ligase RtcB in comple
48 reviously yielded a crystal structure of the Pyrococcus horikoshii RtcB protein containing a new prot
49 ate transporter homolog from archaebacterium Pyrococcus horikoshii, sodium/aspartate symporter GltPh,
50 r dynamics simulations of three forms of the Pyrococcus horikoshii species of NikR including two apo-
51 glutamate transporter homologue Glt(Ph) from Pyrococcus horikoshii suggested that the slow conformati
52 of diphthamide biosynthesis in the archaeon Pyrococcus horikoshii uses a novel iron-sulphur-cluster
54 endoglucanase EGPh from the hypothermophilic Pyrococcus horikoshii was transaminated with pyridoxal-5
55 hermophilic Archaea, Pyrococcus furiosus and Pyrococcus horikoshii, was assessed by analysis of compl
56 nes from both Mycobacterium tuberculosis and Pyrococcus horikoshii were cloned, and their protein pro