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1 loenzyme from Thermus thermophilus (Tth), an extreme thermophile.
2 cid sequence, tapirins are specific to these extreme thermophiles.
3 extreme halophiles, or ('sulphur-dependent') extreme thermophiles.
4  from the homologous protein structures from extreme thermophiles.
5 h stabilizes the native L-shaped fold in the extreme thermophile and which has been incorporated into
6 cleotide-binding fold observed in PIMTs from extreme thermophiles and humans.
7 g caldarchaeol lipids that are found in some extreme thermophiles and methanogens.
8 hanged with homologs of Aquifex aeolicus (an extreme thermophile) and Chlamydia trachomatis (an oblig
9                         The placement of the extreme thermophile Aquifex aeolicus in the bacterial ph
10 mal subunit protein L27, was cloned from the extreme thermophile Aquifex aeolicus, and the protein wa
11 from diverse species, including one from the extreme thermophile Aquifex aeolicus, which suggests tha
12  of an activator, the NtrC1 protein from the extreme thermophile Aquifex aeolicus.
13  polymerase III replication apparatus of the extreme thermophile, Aquifex aeolicus.
14              Here we describe a UDG from the extreme thermophile Archaeoglobus fulgidus.
15                                   Viruses of extreme thermophiles are of great interest because they
16 igma(54) activator from Aquifex aeolicus, an extreme thermophile), as well as its ATPase domain alone
17 nd Eucarya (eukaryotes) and the placement of extreme thermophiles at the base of the Bacteria.
18  solubilized without any pretreatment by the extreme thermophile Caldicellulosiruptor bescii that has
19 ight chain substrates and that metabolism in extreme thermophiles may use sugars in both ring and str
20  mutagenic effect is particularly strong for extreme thermophiles, since the spontaneous deamination
21 th the crenarchaeal DNA polymerases from the extreme thermophiles Sulfolobus acidocaldarius and Pyrod
22 tic transcript cleavage factor GreA from the extreme thermophiles, T. thermophilus and Thermus aquati
23 e-3-phosphate dehydrogenase (GAPDH) from the extreme thermophile Thermus aquaticus has been solved at
24                           Ribosomes from the extreme thermophile Thermus thermophilus are capable of
25          We have constructed a mutant of the extreme thermophile Thermus thermophilus in which the pr
26              We have shown that S15 from the extreme thermophile Thermus thermophilus represses the t
27 we describe four structures of PrmA from the extreme thermophile Thermus thermophilus.
28 ng center of 16S rRNA, was identified in the extreme thermophile Thermus thermophilus.
29 o-dependent or class II FBP aldolase from an extreme thermophile, Thermus aquaticus (Taq).
30 aneous thiostrepton-resistant mutants of the extreme thermophile, Thermus thermophilus.
31 om the archaeon Methanococcus jannaschii, an extreme thermophile, was subcloned and expressed in Esch
32 whether this biochemical pathway is found in extreme thermophiles, we examined the published genome s
33 rk, we studied orphan receptor Alpo4 from an extreme thermophile worm Alvinella pompejana.