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

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

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

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

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

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

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

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

8 red a Fyn kinase domain with light-inducible nuclear localization signal.

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

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

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

12 Its N-terminus harbors a nuclear localization signal.

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

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

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

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

17 n-fluorescent-protein (CFP), with or without nuclear localization signal.

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

19 n, and (3) in sequence pattern searching for nuclear localization signal.

20 of the importin beta family, via a conserved nuclear localization signal.

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

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

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

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

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

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

27 were achieved by selectively mutating virion nuclear localization signals.

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

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

30 trast, has little effect on KPNA7 binding to nuclear localization signals.

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

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

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

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

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

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

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

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

39 owed us to identify a structurally conserved nuclear localization signal and amino acids involved in

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

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

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

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

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

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

46 The Rf4 gene product contains a nuclear localization signal and is likely to not interac

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

48 thin the catalytic domain of PfCCT acts as a nuclear localization signal and its deletion decreases t

49 TRKIN contains a nuclear localization signal and localizes to knobs earli

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

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

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

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

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

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

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

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

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

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

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

61 Deacetylation sites in Msh3 overlap a nuclear localization signal, and we show that localizati

62 , in which TAL effectors harbor their T3 and nuclear localization signals, and activation domain.

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

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

65 E344Q substitution reduces KPNA7 binding to nuclear localization signals, and that this limits KPNA7

66 region 2 of ZO-2, and S261 located within a nuclear localization signal, are critical for the intera

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

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

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

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

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

72 ha, a nuclear-import receptor; this required nuclear localization-signal binding.

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

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

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

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

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

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

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

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

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

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

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

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

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

86 Depletion of KPNA4 attenuated nuclear localization signal-dependent transport activity

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

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

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

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

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

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

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

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

95 ncharacterized region of Dnmt3a1 including a nuclear localization signal, has very low activity in TK

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

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

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

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

100 Mutations in the nuclear localization signal in EEEV capsid protein have

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

102 a7p-chimaerin localizes to the nucleus via a nuclear localization signal in its N terminus.

103 ed function of PHLPP1 depends on a bipartite nuclear localization signal in its unique N-terminal ext

104 We identified a nuclear localization signal in NAMPT and amino acid subs

105 A nuclear localization signal in ORF2 was necessary for in

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

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

108 capsid protein, which is positioned within a nuclear localization signal in the cyclophilin A-binding

109 trafficking elements, including a canonical nuclear localization signal in the extreme C terminus an

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

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

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

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

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

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

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

117 tinct host import factors that interact with nuclear localization signals in the Gag MA and NC domain

118 These features include enhancement of the nuclear localization signals in the nucleocapsid protein

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

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

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

122 intrinsically disordered domains containing nuclear localization signals into the central channel fo

123 A nuclear localization signal is embedded between PRR and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

151 A nuclear localization signal (NLS) knock-out mutant N did

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 The 3D(pol) N terminus encodes a nuclear localization signal (NLS) sequence,MRKTKLAPT, im

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 d that the ring component anillin contains a nuclear localization signal (NLS) that binds to importin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

188 at CRWN4 is coimported into the nucleus with nuclear localization signal (NLS)-bearing paralogues in

189 Here, we developed nuclear localization signal (NLS)-conjugated polymersome

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 plasma membrane and modulates its binding to nuclear localization signal (NLS)-containing proteins th

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

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

198 leoside triphosphohydrolase (dNTPase) with a nuclear localization signal (NLS).

199 f individual amino acids of the FMDV 3D(pol) nuclear localization signal (NLS).

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

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

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

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

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

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

206 However, M protein mutants with weakened nuclear localization signals (NLS) and deficient nuclear

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

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

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

210 d the nuclear translocation of CEBPD through nuclear localization signals (NLS) to activate PRKDC-med

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

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

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

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

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

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

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

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

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

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

221 karyopherins that engage the two independent nuclear localization signals (NLSs) in Gag.

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

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

224 The specific interaction of importins with nuclear localization signals (NLSs) of cargo proteins no

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

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

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

228 ngaged via the EHM-targeting signals and the nuclear localization signals (NLSs), as well as the nucl

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

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

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

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

233 Nuclear-import receptors (NIRs) bind nuclear-localization signals (NLSs) of protein cargo in

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

251 Mutation of the nuclear localization signal prevented detectable levels

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

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

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

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

256 rtin beta1- and 2-dependent proline-tyrosine nuclear localization signal (PY-NLS), which has a unique

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

275 However, because hDNA2 lacks the nuclear localization signal that is found in its yeast h

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

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

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

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

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

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

282 eered a Fyn biosensor with a light-inducible nuclear localization signal to demonstrate that the Fyn

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

284 Using a Giardia nuclear localization signal to target dCas9 to both nucl

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 ICAP1 contains a nuclear localization signal within an unstructured, N-te

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