コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ite is much more extensive in the absence of SSB protein.
2 5'-strand is also elevated in the absence of SSB protein.
3 ffects the ssDNA binding mode preferences of SSB protein.
4 raction of RecR with RecO in the presence of Ssb protein.
5 action of a ssDNA translocase that pushes an SSB protein.
6 y an exonuclease and TG1 RDF is a functional SSB protein.
7 ' helicase, RecJ, a 5'-->3' exonuclease, and SSB protein.
8 change is greatly facilitated by the E. coli SSB protein.
9 occurs after formation of a 1:1 complex with SSB protein.
10 omplexes consisting of RecF, RecO, RecR, and Ssb proteins.
11 eractions of RecF protein with RecR and with Ssb proteins.
12 s the interaction of full-length Redbeta and SSB proteins.
13 tures may be shared among different types of SSB proteins.
14 DNA strand exchange in the presence of both SSB proteins.
15 ecies-specific or even specific to bacterial SSB proteins.
16 ntained within the N-terminal domains of the SSB proteins.
17 is unique to Deinococcus and Thermus species SSB proteins.
18 nesium ion, and single-stranded DNA-binding (SSB) protein.
19 tical location of single-strand DNA-binding (SSB) protein.
20 the presence of single-stranded DNA binding (SSB) protein.
21 nd the T7 Gp2.5 single-stranded DNA-binding (SSB) protein.
22 ochondrial single-stranded (ss) DNA-binding (SSB) proteins.
23 , RecQ, RecJ, and single-strand DNA binding (SSB) proteins.
24 ly protected by single-stranded DNA-binding (SSB) proteins.
25 d and protected by binding of ssDNA-binding (SSB) proteins.
26 vity of their cognate single strand binding (Ssb) proteins.
27 pitation, size-exclusion chromatography, and Ssb protein affinity chromatography in the absence of an
29 ases to chemo-mechanically push heterologous SSB proteins along ssDNA provides a potential mechanism
33 modulating the binding mode of a multimeric SSB protein and consequently, in generating the appropri
34 milarities to a single-stranded DNA binding (SSB) protein and an editing exonuclease, respectively.
35 binding protein encoded by Escherichia coli (SSB protein) and phage T4 (gene 32 protein) also have ac
36 of these two highly conserved homotetrameric SSB proteins, and these differences might be tailored to
37 RecBCD enzyme, single-stranded DNA-binding (SSB) protein, and LexA repressor respond to dsDNA breaks
38 eukaryotic-type RPA homologue, crenarchaeal SSB proteins appear much more similar to the bacterial p
39 Mutational studies demonstrated that the Ssb proteins are also required for phage replication, bo
40 roteins, and demonstrate that both SSAPs and Ssb proteins are essential for the life cycle of tempera
43 ence of E. coli single-stranded DNA binding (SSB) protein, arguing that LexA repressor affects the co
46 nsfer of the homotetrameric Escherichia coli SSB protein between ssDNA molecules was studied using st
50 richia coli single-stranded (ss)DNA binding (SSB) protein binds ssDNA in multiple binding modes and r
52 h degree of sequence homology with bacterial SSB proteins but differs in the composition of its C-ter
53 of the in vivo concentrations of the SSA and SSB proteins by deletion or overexpression affects HSF a
54 n on ssDNA introduces a new model for how an SSB protein can be redistributed, while remaining tightl
55 vations can be explained by a model in which SSB protein can undergo a temperature- and salt-dependen
56 RecQ helicase, in conjunction with RecA and SSB proteins, can initiate recombination events in vitro
59 ase activity is reduced in proportion to the SSB protein concentration; in its absence, ATPase activi
60 strand exchange reaction (especially at high SSB protein concentrations or when SSB protein is added
63 ecOR protein to ssDNA, which is inhibited by SSB protein despite the documented interaction between R
64 rnary structure analogous to that of E. coli SSB protein,despite possessing DNA-binding domains more
65 nown to stimulate RecO protein to facilitate SSB protein displacement by RecA protein, inhibits annea
67 s been established for the RecA(Ec) protein, SSB protein does not stimulate the RecA(Sp) protein-prom
68 We show here that single-strand binding (SSB) proteins enhance the unwinding processivity of both
69 d that overexpression of SSB-1 but not other SSB proteins enhanced the HGF-induced serum response ele
70 similarly, this improved ability to displace SSB protein for RecA P67W protein correlates with an inc
78 have determined the crystal structure of the SSB protein from the crenarchaeote Sulfolobus solfataric
79 Here, we show that the structurally similar SSB protein from the malarial parasite Plasmodium falcip
80 s represent the first analysis of paralogous SSB proteins from any bacterial species and provide a fo
82 the use of the single-stranded DNA binding (SSB) protein from Escherichia coli as a strong FP signal
84 trand DNA junctions in vitro, D. radiodurans SSB protein has a limited capacity to displace the short
88 RecA(Sp) protein from the ssDNA substrate by SSB protein, however, appears to limit the efficiency of
89 al role for either cellular or virus-encoded SSB protein in improving the processivity of the NS3 in
90 Quantitative estimates of D. radiodurans SSB protein in the D. radiodurans cell indicate approxim
91 nce, they offer new insight into the role of SSB protein in the initiation phase of recombination.
93 era highlights the evolutionary diversity of SSB proteins in an otherwise conserved transcription reg
94 ly to be relevant to the action of bacterial SSB proteins in double-strand break repair, acting at th
95 e present study, we explored the function of SSB proteins in the regulation of the hepatocyte growth
96 nhibition of DNA strand exchange activity is SSB protein-independent, suggesting that LexA S119A repr
99 y as reagents for investigating the roles of SSB/protein interactions in diverse DNA replication, rec
100 y at high SSB protein concentrations or when SSB protein is added to the ssDNA before RecA(Sp) protei
103 at very high concentrations, whereas E. coli SSB protein is highly inhibitory at relative low concent
104 E. coli single-stranded DNA-binding protein (SSB protein) is used to remove secondary structure from
107 promoted reaction, the stimulatory effect of SSB protein may be due entirely to this postsynaptic mec
108 radiodurans SSB and homotetrameric bacterial SSB proteins may confer a selective advantage to D. radi
109 richia coli single-stranded (ss)DNA binding (SSB) protein mediates genome maintenance processes by re
114 scherichia coli single-stranded DNA-binding (SSB) protein on the ability of gp4 to synthesize primers
115 rotein replaced the COOH terminus of E. coli SSB protein or T4 gene 32 protein cannot support the gro
118 ings and suggests the model that the SSA and SSB proteins perform distinct roles in the regulation of
119 in the presence of glucose, suggesting that Ssb proteins, perhaps through their interaction with Reg
122 scherichia coli single-stranded DNA-binding (SSB) protein plays a central role in DNA replication, re
123 erichia coli single strand (ss) DNA binding (SSB) protein protects ssDNA intermediates and recruits a
125 restart showed that the replisome-associated SSB protein remains associated with the blocked fork for
126 RecO, and RecR proteins prior to addition of Ssb protein resulted in the formation of complexes consi
129 ccus pneumoniae single-stranded DNA binding (SSB) proteins, SsbA and SsbB, to various dT(n) oligomers
130 ccus jannaschii, the Sulfolobus solfataricus SSB protein (SsoSSB) has a single DNA-binding domain in
134 t the identification of a novel crenarchaeal SSB protein that is distinctly different from its euryar
135 , the causative agent of malaria, encodes an SSB protein that localizes to the apicoplast and likely
136 eukaryotic single-stranded (ss) DNA-binding (SSB) protein that is essential for all aspects of genome
137 ir appeared unaffected by alterations in the SSB protein, the mutational analysis suggests a direct r
138 Furthermore, we show that, in the absence of SSB protein, the RecBCD enzyme is inhibited by the ssDNA
139 is coated with single-stranded DNA binding (SSB) protein, thereby accelerating DNA strand exchange.
140 approach relied on the unique ability of the SSB protein to bind the nucleic acid aptamer in its free
141 rved for the binding of the Escherichia coli SSB protein to single-stranded (ss) oligodeoxyadenylates
142 ic Escherichia coli single-stranded binding (SSB) protein to three single-stranded nucleic acids, pol
143 the release of preferentially bound Cl- from SSB protein upon binding nucleic acid, with the release
145 th E. coli single stranded (ss) DNA binding (SSB) protein via the last 9 amino acids of the C-termina
147 photocrosslinking, and when Escherichia coli SSB protein was added to the incubations, it bound the s
148 y members function as homotetramers, dimeric SSB proteins were recently discovered in a distinct bact
150 cherichia coli stranded DNA-binding protein (SSB) protein, which occurs through stabilizing of the bi