ライフサイエンスコーパス: DNA-binding protein

1 of EBNA1, a viral encoded sequence-specific DNA binding protein.

2 A sliding clamp, and the RPA single-stranded DNA binding protein.

3 cation of RADX as an RPA-like, single-strand DNA binding protein.

4 ble to any type of yeast surface expressible DNA-binding protein.

5 c helix-loop-helix leucine zipper (bHLH-Zip) DNA-binding protein.

6 y resembling helix-turn-helix motif found in DNA binding proteins.

7 r chromatin remodelers, but not to unrelated DNA binding proteins.

8 , we discovered that cohesin SA1 and SA2 are DNA binding proteins.

9 A occupied by tandem arrays of high-affinity DNA binding proteins.

10 A (ssDNA) and interacting with several other DNA binding proteins.

11 ics on DNA in the presence of multiple other DNA binding proteins.

12 gests they do not block 1D searches by other DNA binding proteins.

13 to the superfamily of basic-helix-loop-helix DNA-binding proteins.

14 nots discovered so far are either enzymes or DNA-binding proteins.

15 sites, including potential roles of several DNA-binding proteins.

16 e researchers to use this method to identify DNA-binding proteins.

17 rules are developed to insert operators for DNA-binding proteins.

18 acterized demonstrating that Ml proteins are DNA-binding proteins.

19 oid in a way similar to exploration by other DNA-binding proteins.

20 interactions between regulatory elements and DNA-binding proteins.

21 been experimentally assayed for thousands of DNA-binding proteins.

22 target DNA by adjacently bound programmable DNA-binding proteins.

23 rning method for the effective prediction of DNA-binding proteins.

24 insight into the searching mechanism used by DNA-binding proteins.

25 activator of interferon regulatory factors/Z-DNA binding protein 1 (DAI/ZBP1) bound plasmid DNA in th

26 o-SMAD1/5 and the expression of inhibitor of DNA binding protein 1 (ID1) were upregulated in HCV-infe

27 er, we identified the innate immune sensor Z-DNA binding protein 1 (ZBP1) as the apical sensor of fun

28 pts during acute and chronic infection was Z-DNA binding protein 1 (ZBP1).

29 Chd1 (Chromodomain Helicase DNA Binding Protein 1) is a conserved ATP-dependent chro

30 ntly identified chromodomain helicase/ATPase DNA binding protein 1-like (Chd1l) as a novel regulator

31 nduced down-regulation of immune regulator Z-DNA binding protein 1.

32 Here, we show that acidic nucleoplasmic DNA-binding protein 1 (And-1) forms complexes with CtIP

33 other remodelers, the chromodomain helicase DNA-binding protein 1 (Chd1) remodeler repositions nucle

34 For the chromodomain helicase DNA-binding protein 1 (Chd1) remodeler, nucleosome slidi

35 We demonstrate that damaged DNA-binding protein 1 (DDB1) and Cullin4, two core compo

36 Cullin 1 (CUL1), Cullin 4A (CUL4A), damaged DNA-binding protein 1 (DDB1), and S-phase kinase-associa

37 J-DNA-binding protein 1 (JBP1) contributes to the biosynth

38 We have recently identified Z-DNA-binding protein 1 (ZBP1) as an innate sensor of infl

39 Z-DNA-binding protein 1 (ZBP1) is an innate immune sensor

40 Z-DNA-binding protein 1 (ZBP1), initially reported as an i

41 dapter-inducing interferon-beta (TRIF) and Z-DNA-binding protein 1 (ZBP1)/DNA-dependent activator of

42 Z-DNA-binding protein 1 (ZBP1; also known as DAI or DLM-1)

43 We also identified inhibitor of DNA binding protein 2 (ID2) as a key upstream regulator

44 port that the XPE gene product DDB2 (damaged DNA binding protein 2), a nucleotide excision repair pro

45 Damaged DNA-binding protein 2 (DDB2), a nuclear protein, partici

46 litated in the genomic context by UV-damaged DNA-binding protein 2 (DDB2), which is part of a multipr

47 factor and the co-regulator single-stranded DNA-binding protein 3 (SSBP3) regulates the genes necess

48 We report that chromodomain helicase DNA binding protein 4 (CHD4), an ATP-dependent chromatin

49 Here we report that chromodomain helicase DNA-binding protein 4 (CHD4) physically interacts with a

50 Here, we show that Chromodomain Helicase DNA-binding protein 4 (CHD4), a major ATPase/helicase su

51 interacted with CHD4 (chromodomain helicase DNA-binding protein 4), which is a part of the NuRD comp

52 Mutations in the human RBPs TAR-DNA binding protein 43 (TDP-43) and RNA-binding protein

53 Another protein, TAR DNA binding protein 43 (TDP-43) has been identified in u

54 TAR DNA binding protein 43 (TDP-43) is a major disease-assoc

55 TAR DNA binding protein 43 (TDP-43) is another protein linke

56 asmic mislocalization and aggregation of TAR-DNA binding protein 43 (TDP-43) is found in the majority

57 Tar DNA binding protein 43 (TDP-43) is the principal compone

58 sia (svPPA), is strongly associated with TAR-DNA binding protein 43 (TDP-43) type C pathology.

59 ically characterized by transactive response DNA binding protein 43 kDa (TDP-43) accumulation.

60 Aggregation of TDP-43 (transactive response DNA binding protein 43 kDa) is a hallmark of certain for

61 cerebral infarcts, and transactive response DNA binding protein 43 kDa.

62 Aggregation of TAR-DNA-binding protein 43 (TDP-43) and of its fragments TDP

63 RBPs affected by excitotoxicity included TAR DNA-binding protein 43 (TDP-43) and, most robustly, fuse

64 usions of pathogenic deposits containing TAR DNA-binding protein 43 (TDP-43) are evident in the brain

65 Accumulation of TAR DNA-binding protein 43 (TDP-43) as toxic cytoplasmic inc

66 TAR DNA-binding protein 43 (TDP-43) has emerged as a key pla

67 icates a direct role of transactive-response DNA-binding protein 43 (TDP-43) in the pathology of ALS

68 TAR DNA-binding protein 43 (TDP-43) is a nucleic acid-bindin

69 The 43-kDa trans-activating response region DNA-binding protein 43 (TDP-43) is a product of a causat

70 The trans-activating response DNA-binding protein 43 (TDP-43) is a transcriptional rep

71 Transactivation response element (TAR) DNA-binding protein 43 (TDP-43) misfolding is implicated

72 gic processes, including AD and most had TAR DNA-binding protein 43 (TDP-43) neuropathology.

73 giopathy), Lewy bodies, transactive response DNA-binding protein 43 (TDP-43) pathology, and hippocamp

74 ymptoms, mutations in the DCTN1 gene and TAR DNA-binding protein 43 (TDP-43) pathology.

75 Transactive response DNA-binding protein 43 (TDP-43) performs multiple tasks

76 compared to transactivation response element DNA-binding protein 43 (TDP-43) proteinopathy patients w

77 ogies (cerebrovascular, transactive response DNA-binding protein 43 (TDP-43)) may also influence cogn

78 signature with numerous round, hyaline, TAR DNA-binding protein 43 (TDP-43)-positive inclusions.

79 is often associated with aggregation of TAR DNA-binding protein 43 (TDP-43).

80 ed with loss of nuclear transactive response DNA-binding protein 43 (TDP-43).

81 cellular aggregation of transactive response DNA-binding protein 43 (TDP-43).

82 Hyperphosphorylated transactive response DNA-binding protein 43 (TDP-43, encoded by TARDBP ) prot

83 ns, including fused in sarcoma (FUS) and TAR DNA-binding protein 43 (TDP-43, encoded by TARDBP), are

84 lpha-synuclein in Parkinson disease, and TAR DNA-binding protein 43 in amyotrophic lateral sclerosis.

85 s known to influence the accumulation of TAR DNA-binding protein 43 kDa (TDP-43) proteinopathy, and t

86 ular mislocalization of transactive response DNA-binding protein 43 kDa (TDP-43).

87 interaction with the RNA-binding protein TAR DNA-binding protein 43 kDa (TDP-43).

88 erosis expressing mutant forms of either Tar DNA-binding protein 43 or superoxide dismutase.

89 pathology, Lewy bodies, transactive response DNA-binding protein 43 pathology, hippocampal sclerosis,

90 ral sclerosis and related disorders with Tar DNA-binding protein 43 proteinopathy.

91 TDP-43 (TAR DNA-binding protein 43) and FUS (fused in sarcoma) are a

92 ion with and loss of function of TDP-43 (TAR DNA-binding protein 43), which we show interacts with al

93 pal sclerosis, 11.7% to transactive response DNA-binding protein 43, 8.1% to cerebral amyloid angiopa

94 ic mutations in the TARDBP gene encoding TAR DNA binding protein-43 (TDP-43) have been identified in

95 TAR-DNA binding protein-43 (TDP-43) proteinopathy is seen in

96 cally by the RNA binding protein TDP-43 (TAR DNA binding protein-43 kDa).

97 The cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) is a hallmark of degener

98 gregated proteins, the most common being TAR DNA-binding protein-43 (TDP-43), tau, and fused in sarco

99 Here, we show that Chromodomain Helicase DNA-binding protein 6 (CHD6), distinct to other CHD enzy

100 Here, we identify the Chromodomain Helicase DNA Binding Protein 7 (CHD7), which is frequently mutate

101 ing protein gene CHD7 (Chromodomain helicase DNA binding protein 7).

102 function mutations in chromodomain helicase DNA-binding protein 7 (CHD7(LOF)) and lysine (K) methylt

103 he chromatin remodeler chromodomain-helicase-DNA-binding protein 7 (CHD7) expanded phenotypic HSPCs,

104 n demonstrate that the chromodomain helicase DNA-binding protein 7 (Chd7), frequently associated with

105 tly, it was shown that chromodomain helicase DNA-binding protein-7 (CHD7) interacts with RUNX1 and su

106 for the protein CHD8 [chromodomain-helicase-DNA-binding protein 8]) are among the most common mutati

107 we found that ATPases chromodomain helicase DNA-binding protein 9 (CHD9) and Brahma homologue (BRM,

108 DNA binding protein A (DbpA) is a member of the human co

109 changes in the mitochondrial single-stranded DNA-binding protein, a crucial protein involved in mtDNA

110 nteracting with an ensemble of (multivalent) DNA-binding proteins able to switch between an "on" (bin

111 tibility, agt and Taf1 Both encode unrelated DNA-binding proteins, agt for an alkyl-cysteine-S-alkylt

112 hromocenter modules, consisting of satellite DNA binding proteins and their cognate satellite DNA, pa

113 cterize the cell-to-cell transmission of TAR DNA-binding protein and alpha-synuclein, involved in amy

114 be genetically encoded by binding sites for DNA-binding proteins and can also involve changes in chr

115 Both DNA-binding proteins and changes in chromatin structure

116 Like phage VP882, these phages encode DNA-binding proteins and partner antirepressors, suggest

117 of two MT-A70 proteins and two homeobox-like DNA-binding proteins and specifically methylates dsDNA.

118 quences of 1063 (518 DNA-binding and 545 non DNA-binding) proteins and using jackknife validation, St

119 ur selected genes: Actin (Act), Apicomplexan DNA-binding protein (Ap2), Rhomboid protein 1 (Rom 1), a

120 of the two DNA strands while multi-specific DNA binding proteins are generally biased towards one st

121 The experimental methods used to identify DNA-binding proteins are expensive and time consuming an

122 ting experimental techniques for identifying DNA-binding proteins are time-consuming and expensive.

123 gates of the RNA-binding protein TDP-43 (TAR DNA-binding protein) are a hallmark of the overlapping n

124 Our approach should be adaptable to other DNA-binding proteins as well as small proteins fused to

125 n of translin (trsn), a highly conserved RNA/DNA binding protein, as essential for starvation-induced

126 SATB1 is a DNA binding protein associated with Parkinson's disease.

127 sults demonstrate that YaaA is a new type of DNA-binding protein associated with the oxidative stress

128 monstrated to target a shared substrate, the DNA binding protein BAF, elucidating a signaling pathway

129 oteins that associate with the chromatin and DNA-binding protein Barrier-to-autointegration factor (B

130 t the role of intragenic DNA methylation and DNA binding protein BORIS in cancer-specific splicing an

131 dition of mitochondrial single-stranded (ss) DNA-binding protein both influences the ways Twinkle loa

132 hesis with the specificity of a programmable DNA-binding protein by using protein trans-splicing to l

133 otential target site, which may be how other DNA binding proteins can steer selection of advantageous

134 This sequence-specific DNA-binding protein can disrupt EBV latency by driving t

135 On the protein side, only DNA-binding proteins can perform rotation-coupled diffus

136 he high-mobility group protein B1 (HMGB1), a DNA-binding protein capable of inducing secretion of TNF

137 ed of DNA binding proteins, RUNXs, and a non-DNA binding protein, CBFB.

138 complex, incorporating the sequence-specific DNA-binding protein Cep3 together with regulatory subuni

139 sively assesses the influence on contacts of DNA-binding proteins, cis-regulatory elements and DNA co

140 zer of the complex, MSL2, and the ubiquitous DNA-binding protein CLAMP are key players in the specifi

141 partment requires a DNA-uptake pilus and the DNA-binding protein ComEA.

142 rane proteins and argue that a novel knotted DNA-binding protein constitutes a new fold.

143 modifiers, chromatin remodelers, and methyl-DNA binding proteins contribute to neurodevelopmental de

144 While TDP-43 is an essential RNA/DNA binding protein critical for RNA-related metabolism,

145 hysical tethers of loops are anchored by the DNA-binding protein CTCF and the cohesin ring complex.

146 ions between two sequence-specific satellite DNA-binding proteins, D1 and Prod, bound to their cognat

147 Although the fast association between DNA-binding proteins (DBPs) and DNA is explained by a fa

148 Here, we report that the damage-specific DNA-binding protein DDB2 is critical for beta-catenin-me

149 DNA-binding proteins decode the modification status of s

150 reveal that Death Effector Domain-containing DNA-binding protein (DEDD), which is overexpressed in >

151 Single-strand DNA binding protein did not affect PcrA translocation ve

152 Because DNA-binding proteins (DNA-BPs) play a vital role in all

153 excess heterogeneous DNA, sequence-specific DNA-binding proteins execute various translocation mecha

154 onstrated that Hop1 is a structure-selective DNA-binding protein exhibiting high affinity for the Hol

155 st chromatin, profoundly influencing the way DNA-binding proteins explore RCs.

156 atin remodeling proteins of the chromodomain DNA-binding protein family, CHD7 and CHD8, mediate early

157 Open chromatin provides access to DNA-binding proteins for the correct spatiotemporal regu

158 Here, we show that DNA-binding protein from starved cells (Dps) - the extre

159 of stress and starvation, an NAP called Dps (DNA-binding protein from starved cells) becomes highly u

160 Identification of DNA-binding proteins from only sequence information is o

161 Pred can be used for effective prediction of DNA-binding proteins from sequence alone.

162 Thus, prediction of DNA-binding proteins from sequences alone using computat

163 cterium Deinococcus radiodurans contains two DNA-binding proteins from starved cells (Dps): Dps1 (DR2

164 We show that the phosphorylation of the RNA-DNA binding protein fused in sarcoma (FUS) is higher in

165 ficity by binding cooperatively with 3 other DNA-binding proteins, Gcr1p, Gcr2p, and Rap1p.

166 lification requires only the single-stranded DNA-binding protein gp32 from bacteriophage T4 and a str

167 These sequence-specific DNA binding proteins have been primarily characterized a

168 Recent advances in the field of programmable DNA-binding proteins have led to the development of faci

169 inding and stabilizing the mRNA encoding the DNA binding protein HMGA1, a known oncogene.

170 The mean diffusion coefficients of the DNA-binding protein HU and the nonendogenous protein Kae

171 NA colocalized with the VACV single-stranded DNA binding protein I3 in multiple puncta throughout the

172 We found that the inhibitor of DNA binding protein Id4 is enriched in quiescent NSCs an

173 e results reveal the role of single-stranded DNA binding proteins in controlling Exo1-catalyzed resec

174 ion followed by sequencing (ChIP-Seq) of 104 DNA binding proteins in embryonic stem cell (ESC) lines.

175 ly organized and assembled with histones and DNA-binding proteins in three dimensions.

176 ow that dinoflagellate nuclei have recruited DNA-binding proteins in three distinct evolutionary wave

177 cleosomes occupy DNA targets for a subset of DNA-binding proteins, including CCCTC-binding factor (CT

178 The T7 single-stranded DNA binding protein increases primer formation and exten

179 Many DNA-binding proteins induce changes in the structure of

180 The papillomavirus (PV) E2 protein is a DNA binding, protein interaction platform that recruits

181 Here, we show that the Cut DNA binding protein is required for neuroblast death, re

182 viruses, 60 copies of the positively charged DNA binding protein J guide the single-stranded DNA geno

183 to the nucleus, where it associates with the DNA-binding protein LAG-1/CSL to activate target gene tr

184 g evidence suggests involvement of other RNA/DNA binding proteins, like FUS in DNA damage response (D

185 tingly, 5hmC colocalized with the methylated DNA binding protein MeCP2 and with the active chromatin

186 Once deposited, mCA is bound by the methyl-DNA-binding protein MECP2 and functions in a rheostat-li

187 we used bioinformatics to identify cellular DNA-binding protein motifs adjacent to either latent or

188 l cells in a manner that is dependent on the DNA-binding protein MRE11 and the antiviral factor IRF1

189 For small (<100 kDa) DNA-binding proteins, obtaining particle images with suf

190 2 protein (gp32) is the single-stranded (ss) DNA binding protein of the bacteriophage T4.

191 ral dementia (FTD) with transactive response DNA-binding protein of 43 kD (TDP-43)-positive inclusion

192 er the past decade, the transactive response DNA-binding protein of 43 kDa (TDP-43) has been recogniz

193 Insoluble, hyperubiquitylated TAR DNA-binding protein of 43 kDa (TDP-43) in the central ne

194 ical aggregation of the transactive response DNA-binding protein of 43 kDa (TDP-43) is associated wit

195 bnormalities in the transactivation response DNA-binding protein of 43 kDa (TDP-43), whose nucleo-cyt

196 egans, including dnc-1 mutants and human TAR DNA-binding protein of 43 kDa overexpressing worms.

197 Our results suggest that HTa, a DNA-binding protein of bacterial origin, has converged o

198 Here we identify CdbA, a DNA-binding protein of the ribbon-helix-helix family tha

199 1 was S313/S314 of AT-Hook-Like10 (AHL10), a DNA-binding protein of unclear function.

200 cisely orient objects-and use them to dock a DNA-binding protein on a double-helix stage that has use

201 ns enables them to diffuse more quickly than DNA-binding proteins on both biopolymers.

202 (WD repeat and high mobility group [HMG]-box DNA-binding protein), one of the genes that was upregula

203 nvolving nonstructural proteins, such as the DNA-binding protein P1 and the genome terminal protein (

204 A DNA-binding protein ParB nucleates on parS sites and mus

205 This system depends on a DNA-binding protein ParB, which binds specifically to th

206 starvation protein A (SspA) complex and the DNA-binding protein pathogenicity island gene regulator

207 An antibody specific to G4-DNA and the G4-DNA-binding protein PC4 bind to the Atg7 PQFS.

208 DNA-binding proteins play a very important role in the s

209 DNA-binding proteins play an important role in various b

210 of the lysine residues in histones and other DNA-binding proteins plays a major role in regulation of

211 This complex, comprised of the zinc finger DNA-binding protein PRDM9 and the SNF2 family chromatin

212 show that the chromatin remodeler HELLS and DNA-binding protein PRDM9 function together to open chro

213 In this paper, we present iDNAProt-ES, a DNA-binding protein prediction method that utilizes both

214 ic DNA-binding proteins while multi-specific DNA-binding proteins prefer helices.

215 The DNA-binding protein PU.1 is a myeloid lineage-determinin

216 o form t-loops or complex with single-strand DNA binding proteins, raising the question of the mechan

217 ching has been reported or proposed for many DNA-binding proteins, raising the question of how widesp

218 DNA binding proteins rapidly locate their specific DNA t

219 ier-to-autointegration factor (BAF), a small DNA-binding protein, rapidly localizes to nuclear ruptur

220 NA) screening, we identified single-stranded DNA binding protein replication protein A (RPA) as a reg

221 nted the accumulation of the single-stranded DNA binding protein replication protein A (RPA) on damag

222 o occupancy of mitochondrial single-stranded DNA binding protein reported previously and provide stro

223 nucleotide deaminases linked to programmable DNA-binding proteins represents a promising approach to

224 ComH is a DNA-binding protein required for the import of DNA into

225 a-helical protein; and LUX ARRYTHMO (LUX), a DNA-binding protein required to recruit the evening comp

226 DNA-binding activity of the single-stranded DNA-binding protein RPA, efficient DNA replication throu

227 alleviated by binding of the single-stranded DNA binding protein, RPA, to the excluded DNA strand.

228 Rsc1/2 isoforms both cooperate with the DNA-binding proteins Rsc3/30 and the HMG protein, Hmo1,

229 c transcription factor complexes composed of DNA binding proteins, RUNXs, and a non-DNA binding prote

230 the prototypic Escherichia coli HJ-specific DNA-binding protein RuvA could be functionally exchanged

231 ssion yeast cells carrying a mutation in the DNA-binding protein Sap1 show defects in DNA replication

232 DNA-binding proteins search for specific targets via fac

233 g specificity, we found that highly specific DNA-binding proteins show balanced hydrogen bonding with

234 nucleosomes can influence, or be altered by, DNA-binding proteins, single-molecule techniques are inc

235 The bacterial single-stranded DNA binding protein (SSB) acts as an organizer of DNA re

236 E. coli single strand (ss) DNA binding protein (SSB) is an essential protein that b

237 The single-stranded DNA binding protein (SSB) of Escherichia coli plays esse

238 rotein that binds to E. coli single-stranded DNA binding protein (SSB) to function as a recombination

239 During DNA replication, the single-stranded DNA binding protein (SSB) wraps single-stranded DNA (ssD

240 The herpes simplex virus (HSV) single-strand DNA binding protein (SSB), ICP8, is the central player i

241 richia coli RNase HI and the single-stranded DNA-binding protein (SSB) in this process.

242 Escherichia coli single-strand (ss) DNA-binding protein (SSB) is an essential protein that b

243 Single-stranded DNA-binding protein (SSB) is typically present at the ab

244 e prion-forming potential of single-stranded DNA-binding protein (SSB) of Campylobacter hominis Our f

245 Bacterial single-stranded (ss)DNA-binding proteins (SSB) are essential for the replica

246 of LMO2 and LDB1 as well as single-stranded DNA-binding protein (SSBP) cofactors and DNA-binding bas

247 However, while single-stranded DNA binding proteins (SSBs) readily promote replication

248 on protein A (RPA) and other single-stranded DNA binding proteins (SSBs).

249 Bacterial single-stranded DNA-binding proteins (SSBs) bind single-stranded DNA and

250 Single-stranded DNA-binding proteins (SSBs) play a key role in genome ma

251 a encode homooligomeric single-stranded (ss) DNA-binding proteins (SSBs) that coat and protect ssDNA

252 domain binding protein (LDB)-single-stranded DNA-binding protein (SSDP) (ChiLS) complex controls nume

253 DNA binding proteins such as chromatin remodellers, tran

254 NA specificity, outside of extremely modular DNA binding proteins such as TAL effectors, has generall

255 covariance between histone modifications and DNA binding proteins, such as the relationship between t

256 These functions are mediated by DNA-binding proteins, such as Cdc13 in Saccharomyces cer

257 RecBCD is able to displace DNA-binding proteins, suggesting that it generates high

258 DNA binding proteins, supercoiling, macromolecular crowd

259 equence-specific double- and single-stranded DNA-binding proteins, Taz1 and Pot1, respectively, bridg

260 tive beta-catenin at the dorsal midline, the DNA-binding protein TCF binds and actively represses gen

261 Dominant mutations in the RNA/DNA-binding protein TDP-43 have been linked to amyotroph

262 Analysis involved assessing 43 kDa Tar-DNA binding protein (TDP-43) accumulation in brain regio

263 egeneration (FTLD) with transactive response DNA-binding protein (TDP) inclusions in 40.5%, FTLD-tau

264 poral lobar degeneration (FTLD) with longTAR DNA-binding protein (TDP)-43-positive neuropil threads a

265 , expressing ALS-linked gene mutants for TAR DNA-binding protein (TDP-43) and superoxide dismutase 1

266 TAR DNA-binding protein (TDP-43) is a highly conserved and e

267 cluding the telomeric repeat single-stranded DNA-binding protein Teb1 and its heterotrimer partners T

268 p53 tumor suppressor is a sequence-specific DNA binding protein that activates gene transcription to

269 An example is MeCP2, an abundant methylated-DNA binding protein that is mutated in the neurological

270 otein A and Escherichia coli single-stranded DNA binding protein that the magnitude of the Cy3 enhanc

271 ator-like effectors (TALEs) are repeat-based DNA binding proteins that can serve as probes for the di

272 This system provides a model for any DNA-binding protein that can be posttranslationally modi

273 PR-Cas9 genetic screen ZNF410, a pentadactyl DNA-binding protein that in human erythroid cells direct

274 ng et al., 2019) identify hnRNPA2B1 as a new DNA-binding protein that initiates and amplifies antivir

275 We show that ZC3H18 is a DNA-binding protein that interacts with an E2F site in t

276 EBNA1 is a sequence-specific DNA-binding protein that is consistently expressed in EB

277 In the absence of MatP, a DNA-binding protein that links ZapB to the chromosomal t

278 E STATEMENT CCCTC-binding factor (CTCF) is a DNA-binding protein that organizes nuclear chromatin top

279 PA over RPA (replication protein A), another DNA-binding protein that participates in the nucleotide

280 ication protein A (RPA) is a single-stranded DNA-binding protein that plays an essential role in DNA

281 tein AT-hook 2 (HMGA2) is a multi-functional DNA-binding protein that plays important roles in tumori

282 RADX is a mammalian single-stranded DNA-binding protein that stabilizes telomeres and stalle

283 Transcription factors are DNA-binding proteins that have key roles in gene regulat

284 occluding the underlying DNA sequences from DNA-binding proteins that must act on it.

285 ential to distinguish nucleosomes from other DNA-binding proteins that protect against MNase.

286 This is the case for DNA-binding proteins that undergo "facilitated dissociat

287 ase in accessibility allows Pol II and other DNA-binding proteins to repeatedly visit nearby DNA bind

288 er of the Ribbon-Helix-Helix (RHH) family of DNA-binding proteins, to transfer of DNA and protein sub

289 Most of the methods developed for predicting DNA-binding proteins use the information from the evolut

290 g DNA in the presence of other architectural DNA binding proteins using single-molecule fluorescence

291 DNA-binding proteins utilise different recognition mecha

292 specifically measuring target site search by DNA-binding proteins via intersegmental translocation.

293 WWP is a new family of minor groove-specific DNA-binding proteins, which improves our understanding o

294 secondary structure types in highly specific DNA-binding proteins while multi-specific DNA-binding pr

295 6.5- angstrom structure of BurrH, an 82-kDa DNA-binding protein whose helical pseudosymmetry prevent

296 sis of FTLD-Tau (n=24), transactive response DNA-binding protein with 43 kDa (FTLD-TDP) (n=25) or Alz

297 ng factor (CTCF) has been characterized as a DNA-binding protein with important functions in maintain

298 d to the overall binding specificity between DNA-binding proteins with different degrees of binding s

299 haeal gene expression, focusing on conserved DNA-binding proteins within the clade and the factors th

300 to various DNA-binding modules: full-length DNA binding proteins, zinc fingers (ZFs), transcription