ライフサイエンスコーパス: nuclear localization signal

1 were full length, containing the N-terminal nuclear localization signal.

2 way for mediating ligand-induced exposure of nuclear localization signal.

3 mutation is combined with the deletion of a nuclear localization signal.

4 by driving Esp1 into the nucleus with a SV40 nuclear localization signal.

5 tional changes in the STAT3 dimer masked its nuclear localization signal.

6 ed' fluorescent proteins sandwiched around a nuclear localization signal.

7 ains a nuclear export signal (NES) but not a nuclear localization signal.

8 uttling of Staufen1 into the nucleus via its nuclear localization signal.

9 -based domains, a proline-rich region, and a nuclear localization signal.

10 both the C-terminal basic stretch and basic nuclear localization signal.

11 Its N-terminus harbors a nuclear localization signal.

12 inase-2 inhibitor or by mutating a predicted nuclear localization signal.

13 ncluding a functional coiled-coil domain and nuclear localization signal.

14 rt, and serine 114, within a PKA site in the nuclear localization signal.

15 h-like nuclear export signal and an adjacent nuclear localization signal.

16 tandem zinc finger domain contains an active nuclear localization signal.

17 calize TRAF3 to the nucleus via a functional nuclear localization signal.

18 ot merely the consequence of expression of a nuclear localization signal.

19 d in the nucleus by the addition of an SV-40 nuclear localization signal.

20 rapid when the fusion includes an additional nuclear localization signal.

21 es its C-terminal transmembrane domain and a nuclear localization signal.

22 MRKTKLAPT (residues 16 to 24) that acts as a nuclear localization signal.

23 ted to nuclei after exposure of a C-terminal nuclear localization signal.

24 s induction, although AnkG lacks a predicted nuclear localization signal.

25 were achieved by selectively mutating virion nuclear localization signals.

26 y chosen nucleoplasmic sequences and 12% for nuclear localization signals.

27 ith Srp1, a nuclear import factor that binds nuclear localization signals.

28 d in the nucleus and identify two functional nuclear localization signals.

29 e the nuclear import of viral genome via its nuclear localization signals.

30 band at 95-100 kDa, which lacked N-terminal nuclear localization signals.

31 identified, including a bipartite classical nuclear localization signal, a mitochondrial matrix targ

32 c that control its localization, including a nuclear localization signal, a nuclear retention domain

33 Here, we show that the nuclear localization signal alone is not sufficient for

34 s introduced to ablate a previously reported nuclear localization signal also resulted in a significa

35 referred to as pUL31, containing a bipartite nuclear localization signal, an intrinsically disordered

36 has four targeting sequences: two classical nuclear localization signals, an INM sorting motif, and

37 ontains 2 separable functional signatures, a nuclear localization signal and a putative EDGE motif, t

38 Mutation analysis indicated that the nuclear localization signal and both the N- and C-termin

39 lude that exons 5-15 of kazrin, encoding the nuclear localization signal and C-terminal domain, are n

40 ivities of both a peptide-encoded N-terminal nuclear localization signal and C-terminal nuclear expor

41 vely spliced Set-beta transcript lacking the nuclear localization signal and demonstrated that the fu

42 responses to infection require a functional nuclear localization signal and DNA binding domain.

43 The truncated Leo1(LA1186) protein lacks a nuclear localization signal and is distributed mostly in

44 The BAG6 sequence contains a canonical nuclear localization signal and is localized predominant

45 al subunit (MUC1-C) is devoid of a classical nuclear localization signal and is targeted to the nucle

46 One of its isoforms, DNAJB6a, contains a nuclear localization signal and regulates beta-catenin s

47 is behavior requires coordinated action of a nuclear localization signal and reversible G protein (he

48 try to show that ICAP1 contains a functional nuclear localization signal and that nuclear localizatio

49 Both proteins contain a consensus bipartite nuclear localization signal and were found in the nucleu

50 e splicing, but specific Rbfox isoforms lack nuclear localization signals and accumulate in the cytop

51 type zinc finger domains (PS51024) and bears nuclear localization signals and highly conserved sequen

52 gle-pass transmembrane protein with multiple nuclear localization signals and no known domains or mot

53 ype of targeting motif that is distinct from nuclear localization signals and that can be computation

54 retains conserved Myc box regions but lacks nuclear localization signals and the bHLHZ domain essent

55 e N-terminally truncated PTBP3 isoforms lack nuclear localization signals and/or most of the RRM1 dom

56 Rad51C has a functional nuclear localization signal, and although we found that

57 The NH(2)-terminal transactivation domain, nuclear localization signal, and bHLH/LZ domain of N-Myc

58 protein sequence indicated the presence of a nuclear localization signal, and subcellular fractionati

59 at least three sites including T170 near the nuclear localization signal, and T170 was shown to deter

60 tains Golgi targeting information, a cryptic nuclear localization signal, and three caspase cleavage

61 show that NF-kappaB dimerization properties, nuclear localization signals, and binding to cytosolic I

62 The NKD proteins have putative nuclear localization signals, and green fluorescent prot

63 t, and DNA-dependent protein kinase kinases; nuclear localization signals; and a Zn finger domain.

64 onal activation domain at aa 31 to 185 and a nuclear localization signal at aa 23 to 29.

65 ucleus due to the presence of a transferable nuclear localization signal at its C terminus.

66 the sumoylation site at Lys(1172) or of the nuclear localization signal at Lys(1147) abolished L1-st

67 ion of R495X FUS, which abrogates a putative nuclear localization signal at the C-terminus of FUS, in

68 ion of adenovirus harboring cyclin D1 with a nuclear localization signal attenuated HF under PO in th

69 s to the N-terminal DNA-binding domains, the nuclear localization signal becomes more highly exchangi

70 , tumor-derived mutant LT (MCV350) lacking a nuclear localization signal binds hVam6p but fails to in

71 le-366-Ala-390, which includes the bipartite nuclear localization signal, binds to the p38alpha-docki

72 h a kinase substrate is fused to a bipartite nuclear localization signal (bNLS) and nuclear export si

73 TRAF6 does not possess a nuclear localization signal but enters the nucleus throu

74 a resistance is disrupted by mutation of the nuclear localization signal, but is restored upon coexpr

75 is of urothelial cell DNA is therefore not a nuclear localization signal, but its manipulation holds

76 leus, likely due to the insertion of cryptic nuclear localization signals by a frame shift caused by

77 In Ca(2+)-OsCaM61, the basic nuclear localization signal cluster adopts an extended c

78 utive import of proteins harboring a classic nuclear localization signal (cNLS) or the spontaneous nu

79 Previous studies linked the classical nuclear localization signal (cNLS) receptor, importin-al

80 cell death with defects in M9- and classical nuclear localization signal (cNLS)-mediated protein impo

81 elated isoforms contains predicted classical nuclear localization signals (cNLS) within exons 7 and 1

82 Importin alphas are import receptors for nuclear localization signal-containing proteins.

83 We found that targeting a nuclear localization signal-containing S6 variant [NLS-S

84 A longer DCL4 transcript isoform encoding a nuclear localization signal, DCL4(NLS), is present in Ar

85 A, K364A, and K376A) in conjunction with the nuclear localization signal deletion did not result in c

86 rther, overexpression of TEF3-1, but not its nuclear localization signal-deletion mutant (TEF3-DeltaN

87 mouse overexpressing exogenous FUS without a nuclear localization signal (DeltaNLS-FUS), which develo

88 he RanBP9-Delta1/N60 fragment, which lacks a nuclear localization signal, displayed enhanced cytoplas

89 form of pyruvate kinase protein fused with a nuclear localization signal enhanced cell proliferation

90 ) does not localize to nuclei, as it lacks a nuclear localization signal equivalent to that present i

91 ggesting that the motif may act as a general nuclear localization signal for cellular RNAs.

92 olipase A2 function for endosomal escape and nuclear localization signals for nuclear targeting and (

93 saturated, nonactivating fatty acids inhibit nuclear localization signal formation by destabilizing t

94 tein, and this localization is dictated by a nuclear localization signal found in the Adi3 T-loop ext

95 This N-terminus of FoxP3 with nuclear localization signals (FoxP3N/NLS) is able to sup

96 One isoform loses the putative nuclear localization signal, generating c-Drosha.

97 dopsis TET genes was investigated by pAtTET::NUCLEAR LOCALIZATION SIGNAL-GREEN FLUORESCENT PROTEIN/be

98 minal 25 amino acids of MxB to function as a nuclear localization signal; however, the ability of the

99 t at residues 11-27 and an isoleucine-lysine nuclear localization signal (IK-NLS) motif at residues 3

100 This difference, together with the lack of a nuclear localization signal in any of the AnkA orthologu

101 Mutation of the nuclear localization signal in CELF1 abolished the abili

102 mutations have been shown to deteriorate the nuclear localization signal in FUS and thereby facilitat

103 A nuclear localization signal in ORF2 was necessary for in

104 l in the hinge domain, we identified a novel nuclear localization signal in the A/B domain of thyroid

105 a mechanism whereby L takes advantage of the nuclear localization signal in the COOH region of 2A to

106 ice expressing human TDP-43 with a defective nuclear localization signal in the forebrain (hTDP-43-De

107 Along with the known nuclear localization signal in the hinge domain, we iden

108 on of WT GRs or those with a mutation in the nuclear localization signal in the muscle of MGRKO mice

109 We found putative nuclear localization signals in NEMO whose mutations dis

110 asmic shuttling protein, and it contains two nuclear localization signals in the basic region and one

111 ucleocapsids, which leads to the exposure of nuclear localization signals in the C terminus of core p

112 We identified two critical nuclear localization signals in the central, poorly char

113 was correlated with the retention of defined nuclear localization signals in the protein sequence, ex

114 inantly in the nucleus through the action of nuclear localization signals in the repeated regions of

115 ocalization studies identified and confirmed nuclear localization signals in XLG2 and XLG3 and a nucl

116 Cdk5 has no intrinsic nuclear localization signal; in the absence of p27, two

117 nus of green fluorescent protein (GFP) and a nuclear localization signal is fused to the amino termin

118 We demonstrate that the putative bipartite nuclear localization signal is not required, but the tet

119 distribution of NRDE-3 requires a functional nuclear localization signal, is required for nuclear RNA

120 shorter isoform, which lacks the N-terminal nuclear localization signal, is restricted to the cytopl

121 It contains a nuclear localization signal KRKR motif in the N-terminus

122 rt of TDP-43 protein, as a disruption of its nuclear localization signal leads to mislocalization and

123 Instead, this ability is dependent on a nuclear localization signal located in its N-terminal 40

124 LANA1(S) proteins lack an N-terminal nuclear localization signal motif, and some isoforms dif

125 nt manner through an atypical basic patch PY nuclear localization signal motif.

126 ORF57 correlates with the intact N-terminal nuclear localization signal motifs of ORF57 and takes pl

127 e these sequences do not correspond to known nuclear localization signal motifs, they represent a new

128 interacted with recombinant NEMO but not the nuclear localization signal mutant version and induced n

129 Utilizing a p53 nuclear localization signal mutant, whose nuclear import

130 In these proteins, a nuclear localization signal (NLS) and an intrinsically d

131 nlike most substrates that carry a classical nuclear localization signal (NLS) and bind to importin a

132 tified a highly conserved putative bipartite nuclear localization signal (NLS) and demonstrated that

133 N-terminal region of FMDV 3D that acts as a nuclear localization signal (NLS) and in template bindin

134 mpelling evidence that Cby harbors bona fide nuclear localization signal (NLS) and nuclear export sig

135 A fusion protein between RecA containing a nuclear localization signal (NLS) and the DNA-binding do

136 Anillin contains a conserved nuclear localization signal (NLS) at its C-terminus that

137 Sequence analyses revealed a potential nuclear localization signal (NLS) at the C terminus of I

138 plex, eVP24 recognizes a unique nonclassical nuclear localization signal (NLS) binding site on KPNA5

139 pathway is only the second to have a defined nuclear localization signal (NLS) consensus.

140 in-of-function genetic approach, a bipartite nuclear localization signal (NLS) derived from the nucle

141 ctional studies that UNE-S harbours a robust nuclear localization signal (NLS) directing SerRS to the

142 Deletion of a canonical nuclear localization signal (NLS) from pUL15 generated a

143 upstream of the helicase domain; however, no nuclear localization signal (NLS) has been identified by

144 AR protein domains, including the canonical nuclear localization signal (NLS) in the AR hinge region

145 e describe the identification of a potential nuclear localization signal (NLS) in the C-terminal regi

146 pha) can translocate proteins that contain a nuclear localization signal (NLS) into the nucleus.

147 When a strong nuclear localization signal (NLS) is added to dia2 mutan

148 Canonical nuclear localization signal (NLS) is identified in the n

149 Within the MeCP2 protein sequence, the nuclear localization signal (NLS) is reported to reside

150 The study documents multifunctionality of a nuclear localization signal (NLS) located at the N-termi

151 leasing importin alpha/beta from a bipartite nuclear localization signal (NLS) located in the tail do

152 uctural analysis suggests that a monopartite nuclear localization signal (NLS) may reside in the N-te

153 Consistent with the presence of a nuclear localization signal (NLS) motif within the GmHSP

154 nteraction domain although it does possess a nuclear localization signal (NLS) motif, whilst Cry3 lac

155 Here we have identified two novel nuclear localization signal (NLS) motifs in murine Nrf2,

156 ts with hBVR nuclear export signal (NES) and nuclear localization signal (NLS) mutants demonstrated i

157 Here we show that mutation of the nuclear localization signal (NLS) of human Kinesin-14 HS

158 e recharacterized the importin-alpha binding nuclear localization signal (NLS) of rat ChREBP, identif

159 We found that, in addition to the nuclear localization signal (NLS) of XPA, importin-alpha

160 at Ser826 and Ser828, located in a putative nuclear localization signal (NLS) on the Drosophila mela

161 s simplex virus 1 (HSV-1) mutant lacking the nuclear localization signal (NLS) on the ICP0 gene (0Del

162 Within this region, mutation of the putative nuclear localization signal (NLS) PGKMV diminished, but

163 used to probe the binding modes between the nuclear localization signal (NLS) polypeptide of NF-kapp

164 The nuclear localization signal (NLS) polypeptide of RelA, t

165 We show that importin alpha binds to a nuclear localization signal (NLS) present in the cytopla

166 Moreover, acetylation of Skp2 in the nuclear localization signal (NLS) promotes its cytoplasm

167 ING4 is known to bind p53 via its nuclear localization signal (NLS) region and to enhance

168 ition of the simian virus 40 large-T-antigen nuclear localization signal (NLS) results in the nuclear

169 Remarkably, this nuclear localization signal (NLS) sequence motif is also

170 cancers (L858R, EGFRvIII), or mutated in the nuclear localization signal (NLS) sequence.

171 e analyzed the structure and conservation of nuclear localization signal (NLS) sequences previously i

172 egument protein VP1-2 contains an N-terminal nuclear localization signal (NLS) that is critical for c

173 Here we identify a TIM nuclear localization signal (NLS) that is required for a

174 inase acting on RNA (ADAR1) carries a unique nuclear localization signal (NLS) that overlaps one of i

175 SAP11 contains a bipartite nuclear localization signal (NLS) that targets this effe

176 scent protein (GFP) reporter fusion assays a nuclear localization signal (NLS) that was mapped to a 2

177 protein into the hepatocyte cytoplasm and a nuclear localization signal (NLS) to enter its nucleus.

178 1 (M1) of influenza virus A/WSN/33 when its nuclear localization signal (NLS) was disrupted by R101S

179 In contrast, a dominant nuclear localization signal (NLS) was found in a small r

180 ted mutant mouse, nBmp2NLS(tm), in which the nuclear localization signal (NLS) was inactivated to pre

181 for nuclear localization, and a nonclassical nuclear localization signal (NLS) was mapped to a short,

182 ining a cell penetrating peptide (CPP) and a nuclear localization signal (NLS) were synthesized and t

183 Ser238 neighbors a nuclear localization signal (NLS) whose function is bloc

184 y, we report that Nurr1 contains a bipartite nuclear localization signal (NLS) within its DNA binding

185 Both HDAgs contain a nuclear localization signal (NLS), but only HDAg-L conta

186 he CTD of topo IIalpha, while preserving the nuclear localization signal (NLS), enhances the decatena

187 ntaining a cell penetrating peptide (CPP), a nuclear localization signal (NLS), or a bifunctional CPP

188 ents and translocated into the nucleus via a nuclear localization signal (NLS), specific among kerati

189 serine and threonine residues adjacent to a nuclear localization signal (NLS), thereby abrogating it

190 RanGTP is required in the nucleus to release nuclear localization signal (NLS)-containing cargo from

191 Notably, the PB2 nuclear localization signal (NLS)-containing domain tran

192 alpha's mediate nuclear transport by linking nuclear localization signal (NLS)-containing proteins to

193 o not support nuclear translocation of a p53 nuclear localization signal (NLS)-containing substrate p

194 plasmodesmata, targeted to the nucleus in a nuclear localization signal (NLS)-dependent manner, wher

195 pherin heterodimer alpha2beta1 in vitro in a nuclear localization signal (NLS)-dependent manner.

196 triphosphate (RanGTP) gradient that imports nuclear localization signal (NLS)-specific cargoes (NLS-

197 nantly to the nucleus, it does not possess a nuclear localization signal (NLS).

198 basic motif which functions as an efficient nuclear localization signal (NLS).

199 ify an evolutionarily conserved multipartite nuclear localization signal (NLS).

200 the carboxy-terminal 143 residues contain a nuclear localization signal (NLS).

201 ipogenic enzyme containing an NH(2)-terminal nuclear localization signal (NLS).

202 of splice-isoforms that contain a functional nuclear localization signal (NLS).

203 n Drosophila, GCLc, but not GCLm, contains a nuclear localization signal (NLS).

204 ontain a cysteine-rich region and a putative nuclear localization signal (NLS).

205 t fibroblasts harboring mutations in the FUS nuclear localization signal (NLS).

206 GALLS-FL and VirE2 contain nuclear localization signals (NLS) and secretion signals

207 Although lacking defined nuclear localization signals (NLS) M2-APC predominantly

208 nit, Importin alpha (Imp alpha), and variant nuclear localization signals (NLS) representing a range

209 with (30-nm diameter) and without (< 10 nm) nuclear localization signals (NLS), macroscopic transpor

210 identified, with two overlapping one of two nuclear localization signals (NLS).

211 urn (HT), proline/serine (PS) domain and two nuclear localization signals (NLS).

212 CAPN5 possesses two nuclear localization signals (NLS): an N-terminal monopa

213 importin Kap95, which functions on classical nuclear-localization signal (NLS)-bearing substrates.

214 amino-terminal residues (1-45) including the nuclear localization signal (NLS1) are dispensable.

215 Previous studies have described one nuclear localization signal (NLSI) in p53 and speculated

216 sine residues within the peptides containing nuclear localization signals (NLSs) 1 and 2 were non-ace

217 ycete plant pathogen Phytophthora sojae uses nuclear localization signals (NLSs) for translocation of

218 Although nuclear localization signals (NLSs) have been described,

219 classical nucleocytoplasmic import pathway, nuclear localization signals (NLSs) in cargo proteins ar

220 Importin alpha1 can bind classical nuclear localization signals (NLSs) in two NLS-binding s

221 use model with mutations that inactivate the nuclear localization signals (NLSs) of Apc (Apc(mNLS)).

222 destined for import into the nucleus contain nuclear localization signals (NLSs) that are recognized

223 , unlike their bacterial homologues, possess nuclear localization signals (NLSs) to enter the cell nu

224 karyotic proteins have been shown to contain nuclear localization signals (NLSs), although its biolog

225 to a phospholipase A(2) (PLA(2)) domain and nuclear localization signals (NLSs).

226 zed to cell nuclei and contains two putative nuclear localization signals (NLSs).

227 o proteins that contain arginine/lysine-rich nuclear localization signals (NLSs).

228 ivergent nuclear export signal (NES) and two nuclear localization signals (NLSs).

229 l strains of influenza A viruses contain two nuclear localization signals (NLSs): a well-studied mono

230 h NRF-2alpha and NRF-2beta contain intrinsic nuclear localization signals (NLSs): the Ets domain with

231 specific modular signals for nuclear import (nuclear localization signals, NLSs) and export (nuclear

232 ) phosphorylation at S659, which exposed the nuclear localization signal of ACSS2 for importin alpha5

233 Five phosphorylation sites reside around the nuclear localization signal of Alp7, and the phosphodefi

234 mouse with point mutations in the canonical nuclear localization signal of CMAS, which relocated the

235 manner that was dependent on the functional nuclear localization signal of ErbB4.

236 e novo predicted deleterious variants in the nuclear localization signal of Heterogeneous Nuclear Rib

237 of MxB to bind to HIV-1 capsid and (ii) the nuclear localization signal of MxB, which is important f

238 Disruption of the nuclear localization signal of PHAPI caused a modest dec

239 grow in glycerol medium, and removal of the nuclear localization signal of Rat1, the nuclear homolog

240 ccumulates in the nucleus with help from the nuclear localization signal of STAT3, activating a subse

241 leus in SBMA, we genetically manipulated the nuclear localization signal of the polyglutamine-expande

242 hydrophobic domain and a proximal C-terminal nuclear localization signal of VP4 were required for (i)

243 This is because the predicted nuclear localization signals of HMR are nonfunctional, a

244 We identified two nuclear localization signals of Stp1 and found that the

245 initiation sites: one (short form) with the nuclear localization signal only, exclusively localized

246 tein (FKBP12) fused to a cellular 'address' (nuclear localization signal or nuclear export sequence).

247 r demonstrated via the assembly of stable QD-nuclear localization signal peptide bioconjugates that p

248 tin-beta in its free form or in complex with nuclear localization signal peptides as the starting con

249 Mutation of the nuclear localization signal prevented detectable levels

250 BPN1 but not a truncated version lacking the nuclear localization signal protects from pathogenic TDP

251 We identified a novel proline-tyrosine nuclear localization signal (PY-NLS) in DJ-1, and we fou

252 or transportin recognizes a proline-tyrosine nuclear localization signal (PY-NLS) in the N-terminal t

253 Mutations in the proline/tyrosine-nuclear localization signal (PY-NLS) of the Fused in Sar

254 Here, we show that the PY-type nuclear localization signal (PY-NLS)/karyopherinbeta2 (K

255 ith the ability of VP24 to interact with the nuclear localization signal receptor for PY-STAT1, karyo

256 factor Nhp6Ap enters the nucleus via a novel nuclear localization signal recognized by calcium calmod

257 karyopherins for Rrp6 nuclear import and the nuclear localization signals recognized by them.

258 the cargo proteins, including the classical nuclear localization signals, recognized by the adaptor

259 ed by the adaptor importin-alpha, and the PY nuclear localization signals, recognized by transportin-

260 s a well-characterized basic amino acid-rich nuclear localization signal region at positions 101 to 1

261 data demonstrate that the positively charged nuclear localization signal region in the tail in apo-Os

262 B) of acetylated lysine is in the N-terminal nuclear localization signal region.

263 Microinjection of a nuclear localization signal reporter protein revealed th

264 Chk1 function as a nuclear export signal and nuclear localization signal, respectively.

265 am peptide, which might contain a functional nuclear localization signal(s).

266 nuc-ErbB3 possesses a functional nuclear localization signal sequence and binds to chroma

267 ed cereals showed that all of them contain a nuclear localization signal sequence flanking to the K1

268 Furthermore, despite the presence of a nuclear localization signal sequence in Gag, we observed

269 on the T-complex that have plant-functional nuclear localization signal sequences that may recruit i

270 The C terminus encompassing the nuclear localization signal sequesters the enzyme in the

271 targeted to nuclei, through the fusion with nuclear localization signal, still exerts strong antipro

272 chloroplast targeting signal and a putative nuclear localization signal, suggesting that they are du

273 Overexpression of nuclear localization signal-tagged HSP27 also rescues mu

274 tion factor SP1, and coexpression of SP1 and nuclear localization signal-tagged HSP27 synergistically

275 n of a TDP-43 variant with a mutation in the nuclear localization signal (TDP-43-NLS).

276 and that Orc6 and Orc1 each contain a single nuclear localization signal that is essential for nuclea

277 found that residues (20)KY(21) constitute a nuclear localization signal that is not required for the

278 gly, 817-1314 possesses a conserved putative nuclear localization signal that may facilitate the nucl

279 f these elements consists of a high-affinity nuclear localization signal that mediates indirect tethe

280 nteracts with importin alpha via a classical nuclear localization signal that recruits importin alpha

281 Since ZO-1 also has two nuclear localization signals, this study was undertaken

282 rization and restricting access to a primary nuclear localization signal through which the apoptogeni

283 uitment by mutating Ser rich clusters of the nuclear localization signal to Ala abolished nuclear imp

284 rions parallels effects of the attachment of nuclear localization signal to Sis1, indicating that Cur

285 ic construction is also used in multipartite nuclear localization signals to provide broad substrate

286 We fuse the ADAR2 domain, tagged with a nuclear localization signal, to an RNA binding peptide f

287 In addition to its nuclear localization signal, translocation of M1 to the

288 xpression, which could be reversed after the nuclear localization signal was deleted.

289 e N-terminal 25 amino acids to function as a nuclear localization signal was not required for restric

290 pocotyl 1 (FHY1) and fhy1-like, an intrinsic nuclear localization signal was proposed to be involved

291 o called PAD4 or PADV), the only PADI with a nuclear localization signal, was previously shown to act

292 e PredictNLS algorithm uncovered a potential nuclear localization signal, whereas the algorithm DBS-P

293 t present in the shorter isoform, contains a nuclear localization signal, whereas the C terminus of B

294 The Orc6 nuclear localization signal, which is essential for Orc6

295 It also possesses a nuclear localization signal, which is required for its t

296 ntry of dreCmas1 was mediated by a bipartite nuclear localization signal, which seemed irrelevant for

297 nvolves both a nuclear export sequence and a nuclear localization signal, whose activities are regula

298 a stage prior to the interaction of the Vp3 nuclear localization signal with importins, consistent w

299 the ligand-sensing beta2 loop and a tertiary nuclear localization signal within the alpha-helical cap

300 reintegration complex is further promoted by nuclear localization signals within the nucleocapsid and