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1 the single-stranded DNA binding protein RPA (replication protein A).
2 f HEL308 is specifically stimulated by human replication protein A.
3 atalytic, requires ATP, and is stimulated by replication protein A.
4 e the physical interaction of Mei5-Sae3 with replication protein A.
5 d by the single-stranded DNA-binding protein replication protein A.
6 This inhibition can be overcome by replication protein A.
7 tranded DNA bubbles that are stably bound by replication protein A.
8 trimeric single-stranded DNA binding protein replication protein A.
9 also requires checkpoint proteins Rad17 and replication protein A.
10 because it does not require interaction with replication protein A.
11 ning topoisomerase III alpha, RMI1, RMI2 and replication protein A.
12 structure containing multifunctional FHV RNA replication protein A.
15 rate of DNA break formation, as measured by replication protein A accumulation at the site of damage
17 racts physically with two cellular proteins, replication protein A and DNA polymerase alpha-primase (
18 nomic RNAs; RNA1 encodes multifunctional RNA replication protein A and RNA interference suppressor pr
19 SIRT6 depletion impaired the accumulation of replication protein A and single-stranded DNA at DNA dam
20 sphorylation of AID, which led to binding of replication protein A and subsequent propagation of the
21 completely lacked sequences similar to RPA (replication protein A) and DNA Helicases reported in oth
22 actor C, proliferating cell nuclear antigen, replication protein A, and DNA polymerase delta that sup
23 sociates with Cdc45, DNA polymerase epsilon, replication protein A, and two replication factor C comp
24 ne to bind the DNA-binding domain A of human replication protein A, and was as resistant to serum nuc
25 signaling and nucleotide excision repair is replication protein A, and we find that its accumulation
26 exhibited good specificity for XPA over RPA (replication protein A), another DNA-binding protein that
28 g because late G2 cells fail to recruit RPA (replication protein A), ATR (ataxia telangiectasia and R
29 to TIN2/TRF1/TRF2, POT1a is thought to block replication protein A binding to the single-stranded tel
30 ith single-stranded DNA-binding protein RPA (replication protein A) causes binding of Rad24-RFC via i
31 ctable Mcm2 phosphorylation in vivo, reduced replication protein A-ChIP signal at an origin, and dimi
32 We also observed a substantially reduced replication protein A- chromatin immunoprecipitation sig
34 ion by nucleating the Rad51 recombinase onto replication protein A-coated single-stranded DNA strands
35 ation mediator in enabling hRad51 to utilize replication protein A-coated ssDNA as recombination subs
36 , the oxidative deamination product of C, in replication protein A-coated ssDNA template and inhibits
38 e have recently characterized an alternative replication protein A complex (aRPA) that is unique to p
40 ion complexes (PICs) identified Sub1 and the replication protein A complex (RPA), both of which bind
41 a region of AGCT repeats targeted by the AID-replication protein A complex when transcribed in vitro.
42 imilarities to corresponding subunits in the replication protein A complex, further supporting an evo
44 protein similar to the second subunit of the replication protein A conserved from yeast to mammals.
46 g agents and display hyperphosphorylation of Replication Protein A due to increased activity of DNA2
47 tion sensitive genes, repaire related genes, replication protein A encoding gene, DNA replication ini
48 ts in RPA2, a homolog of yeast and mammalian replication protein A, exhibit loss of silencing at tran
50 damage as evidenced by increased gamma-H2AX, replication protein A foci, and Chk1 kinase phosphorylat
52 e isolation and characterization of multiple replication protein A homologs, RPA1, RPA2, and RPA3, fr
53 r, the single-stranded binding protein human replication protein A (hRPA) restricts sliding and enfor
56 p53 (p53TAD) and the 70 kDa subunit of human replication protein A (hRPA70) was investigated using he
57 ion by hMSH2-hMSH6 is not abrogated by human replication protein A (HsRPA) bound to the displaced sin
58 interactions between human RecQ proteins and Replication Protein A, identify SSB as a broadly conserv
59 he formation of intranuclear foci by ATR and replication protein A, implicating a functional role for
60 in conjunction with flap endonuclease 1 and replication protein A in DNA lagging strand replication
61 orthologs of the two OB fold/one zinc finger replication protein A in Methanosarcina acetivorans and
62 n in CD4+ lymphocytes is the accumulation of replication protein A in nuclear foci, an indication tha
64 on ataxia telangiectasia mutated, NBS1, and replication protein A, indicating it functions after DNA
66 ed DUE-B inhibited chromatin replication and replication protein A loading in the presence of endogen
67 tion, the multifunctional, transmembrane RNA replication protein A of the nodavirus flock house virus
68 bound by the single-stranded binding protein Replication Protein A or are targeted by cellular nuclea
69 inds duplex regions up to 500 bp; and either replication protein A or Escherichia coli single strande
70 d in HR-defective cells do not colocalize to replication protein A or gammaH2AX, excluding the possib
71 ng cellular DNA replication factors, such as replication protein A or polymerase alpha-primase, to re
72 duced phosphorylation of Chk1 and UV-induced replication protein A phosphorylation and chromatin bind
74 e TIM-Tipin complex to the 34 kDa subunit of replication protein A provides a biochemical explanation
75 tment and activation appeared independent of replication protein A, Rad17, and the Rad9-Hus1-Rad1 pro
76 igen (PCNA) by regulating the recruitment of replication protein A, Rad18, and helicase-like transcri
77 olog 2 (Msh2)-MutS homolog 6, Exonuclease 1, replication protein A, replication factor C-Delta1N, pro
78 Salpha, MutLalpha, exonuclease 1 (Exo1), and replication protein A (RPA) (in the absence or presence
79 to be single-stranded DNA (ssDNA), coated by replication protein A (RPA) and containing a primer-temp
81 strate that SMARCAL1 directly interacts with Replication protein A (RPA) and is recruited to sites of
82 binds directly to the ssDNA-binding protein Replication protein A (RPA) and is recruited to sites of
83 gle-stranded DNA, which are rapidly bound by replication protein A (RPA) and other single-stranded DN
84 studies indicate that WRN is associated with replication protein A (RPA) and p53 in vivo before and a
85 ingle-stranded DNA (ssDNA)-binding proteins, replication protein A (RPA) and protection of telomeres
89 single-stranded DNA (ssDNA)-binding complex replication protein A (RPA) and the checkpoint kinase CH
90 SB resection, and thereby for recruitment of replication protein A (RPA) and the protein kinase ATR t
92 entified single-stranded DNA binding protein replication protein A (RPA) as a regulator of the deposi
93 nover of the DSB-responsive factors MDC1 and replication protein A (RPA) at DNA damage sites and that
95 single-stranded DNA (ssDNA)-binding protein replication protein A (RPA) becomes phosphorylated perio
97 he yeast single-stranded DNA binding protein replication protein A (RPA) but not by a mutant form of
99 uclease inhibition impairs radiation-induced replication protein A (RPA) chromatin binding, suggestin
100 proteins, we show that Sgs1, Top3, Rmi1, and replication protein A (RPA) coordinate catenation and de
102 ing of complementary strands of DNA bound by replication protein A (RPA) during discrete repair pathw
103 hows that mutants first accumulate extensive replication protein A (RPA) foci, followed by increased
104 showed that HCV NS5A(S25-C447) and cellular replication protein A (RPA) functionally cooperate as a
106 vation-induced cytidine deaminase (AID) with replication protein A (RPA) has been proposed to promote
107 (PKA) and subsequent interaction of AID with replication protein A (RPA) have been proposed to play i
108 cribe a CCCH type of zinc finger domain in a replication protein A (RPA) homolog found in members of
111 demonstrate that MRN directly interacts with replication protein A (RPA) in unperturbed cells and tha
113 on with Mcm2-7 during S phase, and decreased replication protein A (RPA) interaction with origin DNA
116 The single-stranded DNA-binding protein replication protein A (RPA) interacts with several human
128 ly known as the DNA damage response, wherein replication protein A (RPA) is a key regulator playing m
139 ed whether the interaction of p53 with human replication protein A (RPA) is necessary for the regulat
147 ent and alignment of DNA processing factors, replication protein A (RPA) lies at the heart of dynamic
148 n of the single-stranded DNA binding protein replication protein A (RPA) on damaged chromatin and sev
149 SV40 T antigen (Tag) helicase actively loads replication protein A (RPA) on emerging single-stranded
151 t signaling but correlates with the level of replication protein A (RPA) recruited to chromatin.
152 n of the single-stranded DNA (ssDNA)-binding replication protein A (RPA) selectively restores XPF-ERC
153 using purified truncated Rad52 proteins and replication protein A (RPA) showed that annealing of oli
154 ion of the single-strand DNA-binding protein replication protein A (RPA) stimulated the helicase reac
156 e conserved eukaryotic ssDNA-binding protein replication protein A (RPA) suggest a novel mechanism by
157 with the single-stranded DNA-binding protein replication protein A (RPA) to displace BamHI-E111A boun
158 specifically required for the recruitment of replication protein A (RPA) to ICL-stalled replication f
159 ' overhangs and facilitating the switch from replication protein A (RPA) to protection of telomeres 1
160 ught to facilitate the handoff of ssDNA from replication protein A (RPA) to the RAD51 recombinase dur
163 TERRA and leads to persistent association of replication protein A (RPA) with telomeres after DNA rep
164 the expression of Bid and the association of replication protein A (RPA) with the ATR- interacting pr
167 o interact with the 32-kDa subunit (RPA2) of replication protein A (RPA), a heterotrimeric protein re
168 e), a novel protein interaction inhibitor of replication protein A (RPA), a protein involved in the A
169 ses that include the hyperphosphorylation of replication protein A (RPA), a protein that plays key ro
171 study, we have examined the ability of human replication protein A (RPA), a single-stranded DNA bindi
172 We report here that RFWD3 associates with replication protein A (RPA), a single-stranded DNA-bindi
173 ated the potential interaction of FANCJ with replication protein A (RPA), a single-stranded DNA-bindi
174 orylated on serine residue 38 interacts with replication protein A (RPA), a ssDNA binding protein, to
175 that the targeting activity of AID is due to replication protein A (RPA), a ssDNA-binding protein inv
182 ion, including DNA polymerase alpha-primase, replication protein A (RPA), and more recently, human to
183 ent of long flaps, coating of those flaps by replication protein A (RPA), and sequential cleavage of
184 the archaeal/eukaryotic functional homolog, replication protein A (RPA), are essential for most aspe
187 of the DNA damage sensor complex, including replication protein A (RPA), ataxia telangiectasia and R
189 other, the single-stranded binding protein, replication protein A (RPA), coats the flap, inhibits FE
191 coded T antigen and three cellular proteins, replication protein A (RPA), DNA polymerase alpha/primas
193 The single-stranded DNA-binding protein, replication protein A (RPA), governs cleavage activity.
194 nless it is destabilized by proteins such as replication protein A (RPA), GQ could interfere with DNA
196 er components of the repair complex, such as replication protein A (RPA), is controlled in part by a
197 e single strand DNA (ssDNA)-binding protein, replication protein A (RPA), is essential for DNA replic
198 aryotic single-stranded DNA-binding protein, replication protein A (RPA), is essential in DNA metabol
200 uman activities: MutSalpha, MutLalpha, EXOI, replication protein A (RPA), proliferating cell nuclear
201 revealed that chromosome-associated foci of replication protein A (RPA), RAD51 and DMC1 are less abu
203 2-Msh6 (or Msh2-Msh3), exonuclease 1 (Exo1), replication protein A (RPA), RFC, PCNA, and DNA polymera
204 ligase that interacts with and ubiquitylates replication protein A (RPA), show profound defects in IC
208 case, identified a physical interaction with replication protein A (RPA), the major cellular single-s
213 to replication forks via an interaction with replication protein A (RPA), the major ssDNA-binding pro
214 of the SOSS1 complex, containing SSB1, with Replication Protein A (RPA), the primary single-strand D
216 polymerase delta (pol delta) is assisted by replication protein A (RPA), the single-stranded DNA-bin
217 Using the eukaryotic ssDNA binding protein, Replication Protein A (RPA), we demonstrate that NMR spe
218 he previously characterized interaction with replication protein A (RPA), we found that SMARCAL1 form
219 roliferating Cell Nuclear Antigen (PCNA) and Replication Protein A (RPA), which are critical for DNA
222 tide or longer flap is envisioned to attract replication protein A (RPA), which inhibits flap endonuc
223 accumulation of single-stranded DNA bound by replication protein A (RPA), which triggers activation o
224 osphorylation of the Ser-15 site of p53 in a replication protein A (RPA)- and ATM and Rad3-related (A
228 AH2 catalyzes the ATP-dependent rewinding of replication protein A (RPA)-bound complementary single-s
230 tivated primarily through the persistence of replication protein A (RPA)-bound single-stranded DNA at
231 or APEX2), is required for the generation of replication protein A (RPA)-bound single-stranded DNA, t
233 e protein F (CENP-F), allowing ATR to engage replication protein A (RPA)-coated centromeric R loops.
235 processive with PCNA, over at least 5 kb, on Replication Protein A (RPA)-coated primed single strand
236 n addition, formation of irradiation-induced replication protein A (RPA)-coated single-stranded DNA (
237 regulatory partner of ATR, binds directly to replication protein A (RPA)-coated ssDNA and enables the
238 the binding interactions of human RAD52 with replication protein A (RPA)-coated ssDNA, and we monitor
242 the ATR-ATRIP heterodimer binds to naked or replication protein A (RPA)-covered DNAs with comparable
243 g partner ATR-interacting protein (ATRIP) to replication protein A (RPA)-covered single-stranded DNA
244 D3-related (ATR) signals the accumulation of replication protein A (RPA)-covered single-stranded DNA
275 -stranded DNA (ssDNA) that is complexed with replication protein A (RPA); the resulting nucleoprotein
276 epair and cell cycle arrest proteins such as replication protein A (RPA, a three subunit protein comp
277 lutionarily related to the 32-kDa subunit of replication protein A (RPA-32) and contains an oligonucl
278 on single-stranded DNA (ssDNA) protected by replication protein-A (RPA) and annealing of RPA-coated
279 ble-stranded DNA, enabling RAD51 to displace replication protein-A (RPA) from ssDNA and stabilizing R
282 ngle-stranded DNA-binding (SSB) proteins (or replication protein A, RPA, in eukaryotes) play a centra
283 ged DNA, promotes DNA end joining, regulates replication protein A (RPA2) phosphorylation and ubiquit
284 rminal domain of the intermediate subunit of replication protein A (RPA32C) was identified and charac
286 g properties of the Saccharomyces cerevisiae replication protein A (scRPA) using fluorescence titrati
288 Our results also indicate that the yeast replication protein A stimulated the ATPase activity of
292 soSSB dynamic behaviour is closer to that of Replication Protein A than to Escherichia coli SSB; a fe
293 nucleolin and is required for recruitment of replication protein A to DSBs, a marker of DSB processin
294 lication arrest, spontaneous accumulation of replication protein A to foci and chromatin, and a G2/M
296 on does not simply originate from binding of Replication Protein A to the flap and sequestering it.
297 aborates with the ssDNA-binding complex RPA (replication protein A) to induce the sumoylation of reco
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