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1 aRnl) from the radiation-resistant bacterium Deinococcus radiodurans.
2  the extremely radiation resistant bacterium Deinococcus radiodurans.
3  Shewanella oneidensis, Escherichia coli and Deinococcus radiodurans.
4 sensory core of the bacteriophytochrome from Deinococcus radiodurans.
5 r the ionizing radiation-resistant bacterium Deinococcus radiodurans.
6 ly: LutC protein, encoded by ORF DR_1909, of Deinococcus radiodurans.
7 m the ionizing radiation-resistant bacterium Deinococcus radiodurans.
8 i, and the extremely radioresistant organism Deinococcus radiodurans.
9 ccharomyces cerevisiae, Eschericia coli, and Deinococcus radiodurans.
10 trometry and compared to a tryptic digest of Deinococcus radiodurans.
11 for 50S subunit complexes of the eubacterium Deinococcus radiodurans.
12 r, using the bacteriophytochrome (BphP) from Deinococcus radiodurans.
13 the populations approached that exhibited by Deinococcus radiodurans.
14  Escherichia coli, Thermus thermophilus, and Deinococcus radiodurans.
15 e present the crystal structure of RecF from Deinococcus radiodurans.
16 dinary radiation resistance on the bacterium Deinococcus radiodurans.
17 sis-dependent DNA strand-annealing system of Deinococcus radiodurans.
18  structure of the large ribosomal subunit of Deinococcus radiodurans.
19                                              Deinococcus radiodurans, a highly radioresistant and str
20 used to measure in situ Mn(II) speciation in Deinococcus radiodurans, a radiation-resistant bacteria
21            A whole-genome restriction map of Deinococcus radiodurans, a radiation-resistant bacterium
22                                              Deinococcus radiodurans, a radiation-resistant bacterium
23    As an example, we use data on survival of Deinococcus radiodurans after high doses (thousands of G
24 rtholog enhances survival of the eubacterium Deinococcus radiodurans after ultraviolet irradiation.
25  certain other bacteria, such as E. coli and Deinococcus radiodurans, although the average mutation r
26 r analyzing mutations in Escherichia coli to Deinococcus radiodurans, an extremeophile with an astoni
27       We have purified the RecN protein from Deinococcus radiodurans and characterized its DNA-depend
28 ' from helix 40 of the large subunit rRNA in Deinococcus radiodurans and Escherichia coli, respective
29 einyl-tRNA synthetase from M. jannaschii and Deinococcus radiodurans and its characterization in vitr
30 herichia coli and to characterize DR_1025 of Deinococcus radiodurans and MM_0920 of Methanosarcina ma
31 ke proteins in two heterotrophic eubacteria, Deinococcus radiodurans and Pseudomonas aeruginosa.
32 proteins in the nonphotosynthetic eubacteria Deinococcus radiodurans and Pseudomonas aeruginosa.
33 coded by the radiation-resistant eubacterium Deinococcus radiodurans and show that DNA binding does n
34         In the radiation-resistant bacterium Deinococcus radiodurans and some eukaryotes, Ro has also
35 complex between the SF1B helicase RecD2 from Deinococcus radiodurans and ssDNA in the presence and ab
36 ts and genomic sequence analysis showed that Deinococcus radiodurans and Thermus thermophilus do not
37 l subunit RNAs of Haloarcula marismortui and Deinococcus radiodurans, and the small ribosomal subunit
38 e, by comparing RNAPs from Escherichia coli, Deinococcus radiodurans, and Thermus aquaticus, we show
39  present in Yersinia pestis and the other in Deinococcus radiodurans, appear to encode closely relate
40 te metabolism in the radiation-resistance of Deinococcus radiodurans are discussed.
41           When exponential-phase cultures of Deinococcus radiodurans are exposed to a 5000-Gray dose
42 taining polypeptides (Cys-polypeptides) from Deinococcus radiodurans as well as from mouse B16 melano
43   Here we show that in Synechocystis sp. and Deinococcus radiodurans, as in A. aeolicus, CCA is added
44 77) in the L1 loop of the non-discriminating Deinococcus radiodurans AspRS2 is required for tRNA(Asn)
45 crystal structure of the RecD2 helicase from Deinococcus radiodurans at 2.2-A resolution.
46 ome, using the chromophore-binding domain of Deinococcus radiodurans bacterial phytochrome assembled
47 ity by recombining the photosensor module of Deinococcus radiodurans bacterial phytochrome with the e
48 hore in the x-ray structure of a fragment of Deinococcus radiodurans bacteriophytochrome in the Pr fo
49 ino acids within the bilin-binding domain of Deinococcus radiodurans bacteriophytochrome with respect
50 hesis activity by a different bacterial NOS (Deinococcus radiodurans) but not by any of the three mam
51 MarR family, regulates uricase expression in Deinococcus radiodurans by binding a shared promoter reg
52                                              Deinococcus radiodurans can reconstitute its genome from
53 stal structures of this D207H variant of the Deinococcus radiodurans CBD, in which His-207 is observe
54 ynthase in the radiation-resistant bacterium Deinococcus radiodurans charges tRNA with tryptophan and
55      We show applications to the analysis of Deinococcus radiodurans chromosome I, of two strains of
56                             Gene Dr1184 from Deinococcus radiodurans codes for a Nudix enzyme (DR-CoA
57 ed open reading frames for the microorganism Deinococcus radiodurans, consistent with previous result
58 enome of the radiation-resistant eubacterium Deinococcus radiodurans contains an ortholog of an RNA-b
59  the extremely radiation resistant bacterium Deinococcus radiodurans contains genes for two SSB homol
60            The radiation-resistant bacterium Deinococcus radiodurans contains two DNA-binding protein
61 of Ro in the radiation-resistant eubacterium Deinococcus radiodurans contributes to survival of this
62 anges in gene expression as stationary phase Deinococcus radiodurans cultures recover from acute expo
63 ressed, and characterized a hemeprotein from Deinococcus radiodurans (D. radiodurans NO synthase, dei
64 ned nucleotide co-occurrence patterns in the Deinococcus radiodurans, D. geothermalis, and Thermus th
65 otein from the radiation-resistant bacterium Deinococcus radiodurans (deiNOS) associates with an unus
66                                              Deinococcus radiodurans (DEIRA) can survive very high do
67                                              Deinococcus radiodurans disproportionately favored TGA m
68 Taq DNA pol C is most closely related to the Deinococcus radiodurans DNA pol C.
69                                     However, Deinococcus radiodurans Dps-1, which binds DNA with high
70 e RecA proteins of Escherichia coli (Ec) and Deinococcus radiodurans (Dr) both promote a DNA strand e
71                            The resistance of Deinococcus radiodurans (Dr) to extreme doses of ionizin
72                                              Deinococcus radiodurans (Dr) withstands desiccation, rea
73 n enzyme from the amidohydrolase family from Deinococcus radiodurans (Dr-OPH) with homology to phosph
74 encoding prolyl-tRNA synthetase) or with the Deinococcus radiodurans DR0705 gene, the ortholog of the
75                                              Deinococcus radiodurans (Drad), a bacterium with an extr
76 h droplets of the bacterial phytochrome from Deinococcus radiodurans (DrBphP), which is weakly fluore
77                          The RecA protein of Deinococcus radiodurans (DrRecA) has a central role in g
78                       The RecQ helicase from Deinococcus radiodurans (DrRecQ) is unusual among RecQ f
79 otein from the radiation-resistant bacterium Deinococcus radiodurans (DrSSB) functions as a homodimer
80 viously shown that urate is a ligand for the Deinococcus radiodurans-encoded MarR homolog HucR (hypot
81        The mutY homolog gene (mutY(Dr)) from Deinococcus radiodurans encodes a 39.4-kDa protein consi
82 Q helicase from the radioresistant bacterium Deinococcus radiodurans encodes three "Helicase and RNas
83                       Four of these genomes (Deinococcus radiodurans, Escherichia coli, Haemophilus i
84 tridium sticklandii, Cytophaga hutchinsonii, Deinococcus radiodurans, Escherichia coli, Magnetospiril
85        Unlike the Haloarcula marismortui and Deinococcus radiodurans examples, the lower portion of h
86                                              Deinococcus radiodurans exhibits an extraordinary resist
87  of iron, Dps-1 from the radiation-resistant Deinococcus radiodurans fails to protect DNA from hydrox
88 imental data from gene expression studies on Deinococcus radiodurans following DNA damage using cDNA
89 ntial for preserving the genome integrity of Deinococcus radiodurans following treatment by gamma rad
90       New interpretations of the capacity of Deinococcus radiodurans for resistance to high doses of
91     The P5CDHs from Thermus thermophilus and Deinococcus radiodurans form trimer-of-dimers hexamers i
92 rnative sigma factors were identified in the Deinococcus radiodurans genome sequence and designated s
93 n this issue how the genome of the bacterium Deinococcus radiodurans gets reassembled after being sha
94                                              Deinococcus radiodurans has a remarkable capacity to sur
95 mparison with other Dps proteins, Dps-1 from Deinococcus radiodurans has an extended N terminus compr
96                 The MarR homolog, HucR, from Deinococcus radiodurans has been shown to repress expres
97 smidic and intrachromosomal recombination in Deinococcus radiodurans has been studied recently and ha
98 mic function-type heat shock sigma factor of Deinococcus radiodurans, has been shown to play a centra
99  genes from the radiation-resistant organism Deinococcus radiodurans have been cloned into vectors un
100 e we have identified, cloned and deleted the Deinococcus radiodurans HspR homologue, DR0934.
101 the structures of proline dehydrogenase from Deinococcus radiodurans in the oxidized state complexed
102 nformation on DXS, from Escherichia coli and Deinococcus radiodurans, in complex with the coenzyme th
103  We now show that a bacteriophytochrome from Deinococcus radiodurans, incorporating biliverdin as the
104        Here, we demonstrate that the RecF of Deinococcus radiodurans interacts with DNA as an ATP-dep
105                                              Deinococcus radiodurans is a highly radiation-resistant
106                                   RecD2 from Deinococcus radiodurans is a superfamily 1 DNA helicase
107                                              Deinococcus radiodurans is extraordinarily resistant to
108                                The bacterium Deinococcus radiodurans is extremely resistant to high l
109                                              Deinococcus radiodurans is extremely resistant to ionizi
110                                              Deinococcus radiodurans is highly resistant to radiation
111                                The bacterium Deinococcus radiodurans is resistant to extremely high l
112  from the extremely radioresistant bacterium Deinococcus radiodurans is the exact inverse of this est
113                                              Deinococcus radiodurans is unique in its ability to reco
114 by one particular family member, ISDra2 from Deinococcus radiodurans, is dramatically stimulated upon
115                                              Deinococcus radiodurans, known for its extraordinary DNA
116 aeal (Haloarcula marismortui) and bacterial (Deinococcus radiodurans) large ribosomal subunits have b
117 uman and two bacterial (Escherichia coli and Deinococcus radiodurans) MnSODs.
118           We report that the complex between Deinococcus radiodurans NOS (deiNOS) and an unusual tryp
119 otein in the radiation-resistant eubacterium Deinococcus radiodurans participates in ribosomal RNA (r
120  Shewanella putrefaciens, Synechocystis sp., Deinococcus radiodurans, Pasteurella multocida, and Acti
121 ructure of the chromophore-binding domain of Deinococcus radiodurans phytochrome assembled with its c
122 re of the chromophore-binding domains of the Deinococcus radiodurans phytochrome at 2.1 A resolution.
123 oreceptor through structural analysis of the Deinococcus radiodurans phytochrome BphP assembled with
124 ochemical, and computational analyses of the Deinococcus radiodurans phytochrome, we demonstrate that
125 ing (Pr) state, the bilin chromophore of the Deinococcus radiodurans proteobacterial phytochrome (DrB
126                                              Deinococcus radiodurans R1 (DEIRA) is a bacterium best k
127                                              Deinococcus radiodurans R1 and other members of this gen
128 e complete genome sequence of the bacterium, Deinococcus radiodurans R1 has been released.
129 ual ORFs from Shewanella oneidensis MR-1 and Deinococcus radiodurans R1 have been designed.
130 equence of the radiation-resistant bacterium Deinococcus radiodurans R1 is composed of two chromosome
131                                              Deinococcus radiodurans R1 is extremely resistant to bot
132 , developed to facilitate gene disruption in Deinococcus radiodurans R1, has been used to inactivate
133 in and Snf2/Rad54 helicase were reported for Deinococcus radiodurans R1, leading to the speculation t
134 e hypothetical uricase regulator (HucR) from Deinococcus radiodurans R1.
135                          The RecA protein of Deinococcus radiodurans (RecA(Dr)) is essential for the
136                            We show here that Deinococcus radiodurans RecD2 helicase inactivates Esche
137                                Intriguingly, Deinococcus radiodurans RecO does not bind SSB-Ct and we
138                                              Deinococcus radiodurans represents an organism in which
139  and 200 than those for Escherichia coli and Deinococcus radiodurans, respectively.
140                                              Deinococcus radiodurans RNA ligase (DraRnl) is a templat
141                                              Deinococcus radiodurans RNA ligase (DraRnl) is the found
142                                              Deinococcus radiodurans RNA ligase (DraRnl) seals 3-OH/5
143 hermophilic Thermus aquaticus and mesophilic Deinococcus radiodurans RNAPs and identify the FL as an
144                                              Deinococcus radiodurans single-stranded (ss) DNA binding
145                                          The Deinococcus radiodurans SSB protein has an occluded site
146 rmined a 1.8-A-resolution x-ray structure of Deinococcus radiodurans SSB.
147    IRS24 is a DNA damage-sensitive strain of Deinococcus radiodurans strain 302 carrying a mutation i
148 on usages are characterized in the genome of Deinococcus radiodurans (strain R1).
149 equence of the radiation-resistant bacterium Deinococcus radiodurans suggests the presence of both di
150 erization of HucR, a novel MarR homolog from Deinococcus radiodurans that demonstrates phenolic sensi
151 fication of the large ribosomal subunit from Deinococcus radiodurans that exploits its association wi
152 this instrument, we employ a model system of Deinococcus radiodurans that has been engineered to expr
153 velopment of bioremediation strategies using Deinococcus radiodurans, the most radiation resistant or
154 ive potential lateral transfer with archaea; Deinococcus radiodurans, the most radiation-resistant mi
155 truction and characterization of recombinant Deinococcus radiodurans, the most radiation-resistant or
156 onuclease A and the ICAT-labeled proteome of Deinococcus radiodurans, the presence of these label-spe
157     In both animal cells and the eubacterium Deinococcus radiodurans, the Ro autoantigen, a ring-shap
158               In the only studied bacterium, Deinococcus radiodurans, the Ro ortholog Rsr functions i
159 ersal in Bacteria as t(6)A is dispensable in Deinococcus radiodurans, Thermus thermophilus, Synechocy
160 response of the genomes of cyanobacteria and Deinococcus radiodurans to ionizing radiation.
161 mplex from the radiation-resistant bacterium Deinococcus radiodurans to protect protein epitopes from
162                               The ability of Deinococcus radiodurans to recover from extensive DNA da
163          The remarkable ability of bacterium Deinococcus radiodurans to survive extreme doses of gamm
164 re we report the 1.75-A crystal structure of Deinococcus radiodurans topoisomerase IB (DraTopIB), a p
165                                              Deinococcus radiodurans topoisomerase IB (DraTopIB), an
166 y identified peptides from the microorganism Deinococcus radiodurans was used for the training of the
167        The NOS gene from one such bacterium, Deinococcus radiodurans, was cloned and expressed (deiNO
168  member of the amidohydrolase superfamily in Deinococcus radiodurans, was cloned, expressed, and puri
169 weakly promiscuous PLL scaffold (Dr0930 from Deinococcus radiodurans ), we designed an extremely effi
170 siccation- and radiation-resistant bacterium Deinococcus radiodurans, we suggest that the extraordina
171 -one ionizing radiation-sensitive strains of Deinococcus radiodurans were evaluated for their ability
172 d based on the radiation-resistant bacterium Deinococcus radiodurans, which is being engineered to ex
173 we analyzed the sHsp system of the bacterium Deinococcus radiodurans, which is resistant against vari

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