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1 provides a wealth of data on proteins from a thermophile.
2 es from the thermophilic fungus Sporotrichum thermophile.
3 t and below the optimal temperature for this thermophile.
4 esence of more than 30 putative PBPs in this thermophile.
5 ncrease in highly connected residues in this thermophile.
6 from Thermus thermophilus (Tth), an extreme thermophile.
7 stent pattern of signature differences among thermophiles.
8 lyses, as well as protein engineering within thermophiles.
9 e homologous protein structures from extreme thermophiles.
10 and psychrophiles, but not within the GAPDH thermophiles.
11 tudy of the mechanism of protein splicing in thermophiles.
12 found to be analogous to those occurring in thermophiles.
13 branch, the protein is found exclusively in thermophiles.
14 upon folding is higher in mesophiles than in thermophiles.
15 derstanding the evolution of mesophiles from thermophiles.
16 ure or compactness of the denatured state in thermophiles.
17 is greatly diverged from that of homologs in thermophiles.
18 haracterizations than those from prokaryotic thermophiles.
19 urrently cultivated are sulphur-metabolizing thermophiles.
20 ncode a novel DNA repair system conserved in thermophiles.
21 ing psychrophiles, from mesophiles, and from thermophiles.
22 superfamily, which typically are missing in thermophiles.
23 ence, tapirins are specific to these extreme thermophiles.
24 halophiles, or ('sulphur-dependent') extreme thermophiles.
25 microbial communities that include anaerobic thermophiles.
26 ies have been shown to be present in several thermophiles [6][7][8], no sequences have been found tha
28 pulate Chaetomium thermophilum, a eukaryotic thermophile, along with various biochemical applications
31 izes the native L-shaped fold in the extreme thermophile and which has been incorporated into much la
36 bic effects allow for discrimination between thermophiles and psychrophiles, but not within the GAPDH
38 ith homologs of Aquifex aeolicus (an extreme thermophile) and Chlamydia trachomatis (an obligate intr
41 eria that hosted these particular genes were thermophiles, and neither hyperthermophiles nor mesophil
43 nit protein L27, was cloned from the extreme thermophile Aquifex aeolicus, and the protein was overex
44 erse species, including one from the extreme thermophile Aquifex aeolicus, which suggests that RusA m
48 yses and experimental data suggest that both thermophiles are capable of hydrolyzing all major polysa
51 ults support the hypothesis that proteins of thermophiles are subject to unusually strong purifying s
52 esult in more stable proteins (i.e. those of thermophiles) are also tuned to have a higher tolerance
53 Our technique allows exploiting eukaryotic thermophiles as source for purifying thermostable native
54 tal gene transfer, resulted in trees showing thermophiles as the earliest evolved bacterial lineage.
55 activator from Aquifex aeolicus, an extreme thermophile), as well as its ATPase domain alone, and re
57 haracterization of recombinant PyrR from the thermophile Bacillus caldolyticus and the crystal struct
58 5N-edited TROSY NMR spectra of TRAP from the thermophile Bacillus stearothermophilus over an extended
59 , L10(L12) 4 was expressed from the moderate thermophile Bacillus stearothermophilus to quantitativel
60 ermal stability of adenylate kinase from the thermophile Bacillus stearothermophilus were monitored d
62 forming the S4-5' domain rRNA complex from a thermophile, Bacillus stearothermophilus, and points out
65 lity is prevalent in prokaryotes, especially thermophiles, but uncommon in eukaryotic organisms, ther
66 e dismutase (SOD) to test if this eukaryotic thermophile can provide insights into macromolecular mec
69 enabling the same approach to be amenable to thermophile-derived cellulases or to the separation of m
72 ucleotide CpG=CG is underrepresented in many thermophiles (e.g., M. jannaschii, Sulfolobus sp., and M
74 sed on the solution structure of an isolated thermophile HAMP domain in which G235 defines a critical
76 ies most correlated with the proteins of the thermophile include higher residue volume, higher residu
77 cal to those of cultivated chemolithotrophic thermophiles, including the hydrogen-oxidizing Calderoba
78 d to those of other saccharolytic, anaerobic thermophiles is most similar to that of Caldicellulosiru
79 cterium animalis subsp Lactis, Streptococcus thermophiles, Lactobacillus bulgaricus, and Lactococcus
80 the mesophile Methanococcus voltae (Mv), the thermophile M. thermolithotrophicus (Mt) and the hyperth
81 in substrates and that metabolism in extreme thermophiles may use sugars in both ring and straight ch
82 ate modeling of helix-rich proteins found in thermophiles, mesophiles, and organisms that flourish ne
83 tal structures of adenylate kinases from the thermophile Methanococcus thermolithotrophicus and the m
84 us vannielii, Methanococcus maripaludis, the thermophile Methanococcus thermolithotrophicus, and hype
85 e nine-residue loop at the ortholog from the thermophile Methanothermobacter thermautotrophicus (MtOM
86 show that Ptr2 and a Lrp homologue from the thermophile Methanothermococcus thermolithotrophicus (Mt
87 e Methanobacterium formicicum; hMfB from the thermophile Methanothermus fervidus; and hPyA1 from the
88 e use of enzymes from extremophiles, such as thermophiles or alkaliphiles, offers the potential to in
89 her cellobiose dehydrogenase from Corynascus thermophiles or bilirubin oxidase from Myrothecium verru
91 at O-2'-ribose methylation in this bacterial thermophile plays a reduced role in thermostabilization
92 in threonyl-transfer RNA synthetase from the thermophile Pyrococcus abyssi that forms complementary v
94 of cellobiose dehydrogenase from Corynascus thermophiles (recDHCtCDH) expressed recombinantly in Esc
95 ic effect is particularly strong for extreme thermophiles, since the spontaneous deamination reaction
96 omplexes show structural similarity with the thermophile-specific enzyme reverse gyrase, which cataly
97 ndole-3-glycerol phosphate synthase from the thermophile Sulfolobus solfataricus (sIGPS) and the alph
98 re very different from those of the archaeal thermophile Sulfolobus solfataricus growing in the same
99 renarchaeal DNA polymerases from the extreme thermophiles Sulfolobus acidocaldarius and Pyrodictium o
100 maripaludis S2), an acidophilic and aerobic thermophile (Sulfolobus solfataricus P2), and an anaerob
103 entous bacteriophage PH75, which infects the thermophile T. thermophilus, assembles in vivo at 70 deg
104 script cleavage factor GreA from the extreme thermophiles, T. thermophilus and Thermus aquaticus.
105 XXA motif is enhanced to a greater extent in thermophiles than in mesophiles, suggesting that helical
106 he gain in enthalpy upon folding is lower in thermophiles than in mesophiles, whereas the loss in ent
107 stability is significantly more favorable in thermophiles than in mesophiles, whereas the maximal sta
108 ous substitutions was significantly lower in thermophiles than in nonthermophiles, and this effect wa
109 rulating, sulfate-reducing, chemoautotrophic thermophile that can fix its own nitrogen and carbon by
110 ents of the highly active mannanase from the thermophile Thermoanaerobacterium polysaccharolyticum.
112 nism of the citrate synthase from a moderate thermophile, Thermoplasma acidophilum (TpCS), are compar
113 oplasmic region of a sensor HK, one from the thermophile Thermotoga maritima in complex with ADPbetaN
114 from the mesophile Escherichia coli and the thermophile Thermotoga maritima, subunit dissociation ac
116 phate dehydrogenase (GAPDH) from the extreme thermophile Thermus aquaticus has been solved at 2.5 Ang
118 acterial ribonucleases H (RNases H) from the thermophile Thermus thermophilus and the mesophile Esche
120 We have constructed a mutant of the extreme thermophile Thermus thermophilus in which the prmA gene
121 We have shown that S15 from the extreme thermophile Thermus thermophilus represses the translati
122 he filamentous virus PH75, which infects the thermophile Thermus thermophilus, consists of a closed D
127 DNA-dependent RNA polymerase (RNAP) from the thermophile, Thermus thermophilus HB8, was purified to e
131 that MUG-K68N, UNG-N123 and family 5 Thermus thermophiles UDGb-A111N can form bidentate hydrogen bond
132 base excision repair pathway, suggests that thermophiles use a mechanism similar to that used by mes
133 rchaeon Methanococcus jannaschii, an extreme thermophile, was subcloned and expressed in Escherichia
134 the universal tree of life, suggesting that thermophiles were among the first forms of life on earth
135 the recombinant enzymes that originated from thermophiles were expressed in Escherichia coli and puri
136 roved in the cores of proteins isolated from thermophiles when compared to proteins from mesophiles.
137 role of modifications contained in RNA from thermophiles, which is to reduce regional RNA flexibilit
138 aeon Methanobacterium thermoautotrophicum, a thermophile with an optimal growth temperature of 65 deg
139 logs for structural biology; yet, eukaryotic thermophiles would provide more similar macromolecules p
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