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1                                              T. thermophilus EF-Ts functions only as a homodimer.
2                                              T. thermophilus HB8 RNA polymerase (RNAP) recognizes mid
3                                              T. thermophilus Kt-23 has two further non-Watson-Crick b
4                                              T. thermophilus NDH-1 contains at most nine putative iro
5                                              T. thermophilus showed no such transition within the tem
6 ed the three proteins with 8His tags using a T. thermophilus expression system.
7        Paradoxically, the dimeric Arg-to-Ala T. thermophilus mutant enzyme packs as a hexamer in the
8 s of three primary proteins from E. coli and T. thermophilus 30S subunits that bind early in the asse
9                                  E. coli and T. thermophilus have evolved very different mechanisms f
10 rather similar dnaX sequences in E. coli and T. thermophilus lead to very different mechanisms of exp
11                          For the E. coli and T. thermophilus proteins, strong agreement is obtained b
12 urvey the folding stabilities of E. coli and T. thermophilus proteomes at various temperatures and pr
13 ults of the binding of RecA from E. coli and T. thermophilus show adaptation to pressure and temperat
14 of labeled membranes of P. denitrificans and T. thermophilus established photoaffinity labeling of th
15 on the crystal structures of human DIPP1 and T. thermophilus Ndx1, were generated using homology mode
16                       In the absence of ATP, T. thermophilus RuvB protein bound to linear double-stra
17 bility of key translation components between T. thermophilus and E. coli, and the functional conserva
18  did not inhibit transcription initiation by T. thermophilus RNAP in vitro or shorten the lifetimes o
19     Methylation of 30S ribosomal subunits by T. thermophilus KsgA is more efficient at low concentrat
20 ia coli catabolite activator protein (CAP)], T. thermophilus RNAP sigma(A) holoenzyme, a class II TAP
21 e lifetimes of promoter complexes containing T. thermophilus RNAP, in contrast to the conclusion in t
22 : Lys+Arg is 18.7% for E. coli and 21.2% for T. thermophilus.
23 acting residues: 39% for E. coli and 46% for T. thermophilus.
24  wider range of pressure and temperature for T. thermophilus compared to E. coli RecA, suggesting a c
25 ell below the minimal growth temperature for T. thermophilus.
26 ing the physiological growth temperature for T. thermophilus.
27 eratures, the heat capacity of unfolding for T. thermophilus RNase H is lower, resulting in a smaller
28 nus of its bacterial homolog (subunit C from T. thermophilus) stabilized the yeast subunit d mutant 3
29 elenomethione-substituted apical domain from T. thermophilus was determined to a resolution of 1.78 A
30                   In this work, laccase from T. thermophilus was produced in E. coli, and the effect
31 nd characterized the NO reductase (NOR) from T. thermophilus.
32 y crystal structures of PRODH and P5CDH from T. thermophilus, a model was built for a proposed PRODH-
33 m18-negative tRNA with recombinant trmH from T. thermophilus abolished its IFN-alpha inducing potenti
34 ure of the dimerization domain of EF-Ts from T. thermophilus refined to 1.7 A resolution.
35 se that the primary role of TtAgo is to help T. thermophilus disentangle the catenated circular chrom
36                                           In T. thermophilus ribosomal frameshifting is not required:
37 t of N-terminal PilQ deletion derivatives in T. thermophilus HB27.
38 e identified a novel transcription factor in T. thermophilus and T. aquaticus that shares a high degr
39 zation of protein translation and folding in T. thermophilus.
40                   Of these, 20 were found in T. thermophilus 16 S rRNA, 44 in H. marismortui 23 S rRN
41             Inactivation of the tlyA gene in T. thermophilus does not affect its sensitivity to capre
42 hat the transcriptional regulation of mer in T. thermophilus is both similar to, and different from,
43 ion of long range mechanochemical motions in T. thermophilus leucyl-tRNA synthetase.
44 ate and spectrum of spontaneous mutations in T. thermophilus resembled those of the thermoacidophilic
45 ralogous maltose transport operon present in T. thermophilus.
46 the shuttle vector's ability to replicate in T. thermophilus.
47 mulated over 20 single-base substitutions in T. thermophilus 16S and 23S rRNA, in the decoding site a
48 favoring menaquinone for charge transport in T. thermophilus.
49                                     Instead, T. thermophilus relies on the high temperatures of its e
50 s of new chimeric proteins reveals that like T. thermophilus RNase H, the folding core of C. tepidum
51 ibute to an overall reduction in activity of T. thermophilus ribonuclease H compared to its mesophili
52 stimulate the intrinsic cleavage activity of T. thermophilus RNA polymerase, and increase the k(app)
53 cterizing the intrinsic cleavage activity of T. thermophilus RNA polymerase, we have identified, clon
54 imentally observed conformational changes of T. thermophilus leucyl-tRNA synthetase upon substrate bi
55 e PutA PRODH domain, the FAD conformation of T. thermophilus PRODH is remarkably different and likely
56      The mutation in the hydrophobic core of T. thermophilus IPMDH resulted in a cavity of 32 A3, but
57 -like particles that contain trimers each of T. thermophilus DnaK, DnaJ, and DafA.
58                             Also, the FAD of T. thermophilus PRODH is highly solvent-exposed compared
59      To test whether the homodimeric form of T. thermophilus EF-Ts is necessary for catalyzing nucleo
60                        Affinity isolation of T. thermophilus HB8 RNAP from P23-45-infected cells iden
61 t in the genomes of the closest relatives of T. thermophilus.
62 e, employing the latest crystal structure of T. thermophilus complex I, we have used microsecond-scal
63  clear evidence that the pilus structures of T. thermophilus are not essential for natural transforma
64    Here we report five crystal structures of T. thermophilus enzyme in complex with NADH or quinone-l
65  sequencing as known hydrophilic subunits of T. thermophilus complex I.
66 idum RNase H is more restricted than that of T. thermophilus.
67 gion and comparisons with similar studies on T. thermophilus RNase H, identify new residues involved
68 ganism E. coli and the thermophilic organism T. thermophilus.
69  domain) of ba(3)-type cytochrome c oxidase (T. thermophilus) (pI = 6.0) exhibit optimal voltammetric
70  in vitro methylation by cloned and purified T. thermophilus PrmA.
71                        When gyrase, the sole T. thermophilus type II topoisomerase, is inhibited, TtA
72                 Finally, we demonstrate that T. thermophilus PRODH reacts with O(2) producing superox
73 ion complex provide compelling evidence that T. thermophilus RNA polymerase can bind to DNA containin
74                  In particular, we find that T. thermophilus CuA assembles more rapidly than reported
75                  These results indicate that T. thermophilus RNase H is stabilized in a delocalized f
76 ant shows no growth defects, indicating that T. thermophilus PrmA, like its E. coli homolog, is dispe
77              MALDI-TOF MS also revealed that T. thermophilus L11 contains a total of 12 methyl groups
78  a broad phylogenetic range, suggesting that T. thermophilus may be an ideal model system for the stu
79  the UV-sensitive phenotype, suggesting that T. thermophilus RuvB protein has a function similar to t
80                  This evidence suggests that T. thermophilus RNAP possesses less intrinsic binding en
81                                          The T. thermophilus analogs of Arg103, Asn106, Thr134, and L
82                                          The T. thermophilus NQO2 subunit displayed much higher stabi
83                                          The T. thermophilus NQO2 subunit was expressed in Escherichi
84          Like other characterized cNORs, the T. thermophilus cNOR consists of two subunits, NorB and
85 ition of ATP or gamma-S-ATP destabilized the T. thermophilus RuvB-DNA complexes.
86                            We determined the T. thermophilus V/A-ATPase structure by cryo-EM at 6.4 A
87  within the dimer interface that disrupt the T. thermophilus EF-Ts dimer but not the tertiary structu
88 ithin 3-4 A of the ppGpp binding site in the T. thermophilus cocrystal.
89 e is inserted after position 80 to mimic the T. thermophilus protein reproduce the differences in con
90 teins, relative binding free energies of the T. thermophilus 30S proteins to the 16S RNA were studied
91 deled on the known crystal structures of the T. thermophilus acyl-CoA synthetase with remarkably high
92                 The thermal stability of the T. thermophilus apical domain (Tm>100 degrees C as evalu
93 te that mutations increasing activity of the T. thermophilus enzyme at mesophilic temperatures do so
94 e basis of the higher thermostability of the T. thermophilus enzyme.
95          Here we report the structure of the T. thermophilus Gfh1 at 2.4 A resolution revealing a two
96        In the X-ray crystal structure of the T. thermophilus HB8 30 S subunit, the mutated residues a
97 enzyme to the microaerobic conditions of the T. thermophilus HB8 species.
98 es, we have developed an atomic model of the T. thermophilus ribosome using a homology modeling appro
99    In accordance, we find that growth of the T. thermophilus strain with an inactivated C1942 methylt
100 mparing the membrane-embedded regions of the T. thermophilus V/A-ATPase and eukaryotic V-ATPase from
101           We have also demonstrated that the T. thermophilus enzyme is allosterically regulated by UD
102 the III-B system the result implies that the T. thermophilus III-B system must elicit a more efficien
103      These results strongly suggest that the T. thermophilus NDH-1 is similar to other NDH-1 enzyme c
104   With the advantage of thermostability, the T. thermophilus NDH-1 provides a great model system to i
105     By mapping significant DNA motifs to the T. thermophilus HB8 genome, we identify potentially regu
106 of the antibiotic telithromycin bound to the T. thermophilus ribosome reveals a lactone ring with a c
107                                   Unlike the T. thermophilus transamidosome, the archaeal complex doe
108 rganisms, and the contacts observed with the T. thermophilus ribosome are consistent with biochemical
109 at there may be multiple pathways within the T. thermophilus cNOR.
110 riophage PH75, which infects the thermophile T. thermophilus, assembles in vivo at 70 degrees C and i
111 e factor GreA from the extreme thermophiles, T. thermophilus and Thermus aquaticus.
112 show that binding of a Thermus thermophilus (T. thermophilus) Csm (TthCsm) to a nascent transcript in
113                   Expression of thermostable T. thermophilus RuvB protein in the E. coli ruvB recG mu
114 e-stranded DNA endonuclease activity of this T. thermophilus domain is activated not by magnesium but
115 e X-ray crystal structure revealed that this T. thermophilus glucose binding protein (ttGBP) is struc
116 rily found in mesophilic bacteria related to T. thermophilus.
117 thermore, the interdomain angle of wild-type T. thermophilus goes from 81 degrees to 118 degrees wher
118                           Finally, wild-type T. thermophilus outcompetes an otherwise isogenic strain

 
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