ライフサイエンスコーパス: localization signal

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

2 ion, although AnkG lacks a predicted nuclear localization signal.

3 mediating ligand-induced exposure of nuclear localization signal.

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

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

6 hanges in the STAT3 dimer masked its nuclear localization signal.

7 rescent proteins sandwiched around a nuclear localization signal.

8 reas the N-terminus contains a mitochondrial localization signal.

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

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

11 e C-terminal basic stretch and basic nuclear localization signal.

12 omains, a proline-rich region, and a nuclear localization signal.

13 in mammalian Sun1, the SUN--nuclear envelope localization signal.

14 Its N-terminus harbors a nuclear localization signal.

15 n XPNPEP3 that was devoid of a mitochondrial localization signal.

16 ely spliced exon 3, encoding a mitochondrial localization signal.

17 inhibitor or by mutating a predicted nuclear localization signal.

18 a functional coiled-coil domain and nuclear localization signal.

19 serine 114, within a PKA site in the nuclear localization signal.

20 uclear export signal and an adjacent nuclear localization signal.

21 RAF3 to the nucleus via a functional nuclear localization signal.

22 -terminal transmembrane domain and a nuclear localization signal.

23 T (residues 16 to 24) that acts as a nuclear localization signal.

24 uclei after exposure of a C-terminal nuclear localization signal.

25 95-100 kDa, which lacked N-terminal nuclear localization signals.

26 oised for activation by calcium and membrane-localization signals.

27 ieved by selectively mutating virion nuclear localization signals.

28 is regulated by small GTPase activators and localization signals.

29 nucleoplasmic sequences and 12% for nuclear localization signals.

30 , a nuclear import factor that binds nuclear localization signals.

31 se R-motifs are found in canonical nucleolar localization signals.

32 clear import of viral genome via its nuclear localization signals.

33 rowing body of work on nuclear and nucleolar localization signals.

34 e 2 (AAV2) that act as nuclear and nucleolar localization signals.

35 ied, including a bipartite classical nuclear localization signal, a mitochondrial matrix targeting se

36 ontrol its localization, including a nuclear localization signal, a nuclear retention domain and a nu

37 Here, we show that the nuclear localization signal alone is not sufficient for lipin-1

38 uced to ablate a previously reported nuclear localization signal also resulted in a significant decre

39 to as pUL31, containing a bipartite nuclear localization signal, an intrinsically disordered region

40 r targeting sequences: two classical nuclear localization signals, an INM sorting motif, and a signal

41 2 separable functional signatures, a nuclear localization signal and a putative EDGE motif, that is c

42 Mutation analysis indicated that the nuclear localization signal and both the N- and C-terminal regio

43 t exons 5-15 of kazrin, encoding the nuclear localization signal and C-terminal domain, are not requi

44 of both a peptide-encoded N-terminal nuclear localization signal and C-terminal nuclear export signal

45 iced Set-beta transcript lacking the nuclear localization signal and demonstrated that the full-lengt

46 es to infection require a functional nuclear localization signal and DNA binding domain.

47 uncated Leo1(LA1186) protein lacks a nuclear localization signal and is distributed mostly in the cyt

48 e BAG6 sequence contains a canonical nuclear localization signal and is localized predominantly in th

49 of its isoforms, DNAJB6a, contains a nuclear localization signal and regulates beta-catenin signaling

50 ior requires coordinated action of a nuclear localization signal and reversible G protein (heterotrim

51 how that ICAP1 contains a functional nuclear localization signal and that nuclear localization impair

52 oteins contain a consensus bipartite nuclear localization signal and were found in the nucleus when i

53 ng, but specific Rbfox isoforms lack nuclear localization signals and accumulate in the cytoplasm.

54 inery that recognizes one class of dendritic localization signals and establish its role in the polar

55 transmembrane protein with multiple nuclear localization signals and no known domains or motifs.

56 argeting motif that is distinct from nuclear localization signals and that can be computationally pre

57 protein coding genes encode multiple protein-localization signals and that, in 20-d-old adult fly hea

58 conserved Myc box regions but lacks nuclear localization signals and the bHLHZ domain essential for

59 inally truncated PTBP3 isoforms lack nuclear localization signals and/or most of the RRM1 domain and

60 Rad51C has a functional nuclear localization signal, and although we found that the subc

61 sequence indicated the presence of a nuclear localization signal, and subcellular fractionation of LN

62 t NF-kappaB dimerization properties, nuclear localization signals, and binding to cytosolic IkappaBs

63 The NKD proteins have putative nuclear localization signals, and green fluorescent protein fusi

64 of selection, contain functional subcellular localization signals, and their readthrough is regulated

65 ending on TLRs' expression pattern, cellular localization, signaling, and deployment of inflammatory

66 c as well as endocytosis and a mitochondrial localization signal are required for these events.

67 For example, the NPIR and KDEL localization signals are distinctive for subfamilies, an

68 ivation domain at aa 31 to 185 and a nuclear localization signal at aa 23 to 29.

69 ue to the presence of a transferable nuclear localization signal at its C terminus.

70 oylation site at Lys(1172) or of the nuclear localization signal at Lys(1147) abolished L1-stimulated

71 495X FUS, which abrogates a putative nuclear localization signal at the C-terminus of FUS, in HEK-293

72 N-terminal DNA-binding domains, the nuclear localization signal becomes more highly exchanging.

73 derived mutant LT (MCV350) lacking a nuclear localization signal binds hVam6p but fails to inhibit hV

74 se substrate is fused to a bipartite nuclear localization signal (bNLS) and nuclear export signal (NE

75 dChIRP improves the RNA genomic localization signal by >20-fold relative to previous tec

76 CK1delta catalytic activity and centrosomal localization signal (CLS) are required to rescue cilia f

77 Here we identify a modular centrosomal localization signal (CLS) localizing cyclin A to centros

78 Deletion analysis mapped the centrosomal localization signal (CLS) of CK1delta to its C-terminal

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

80 port of proteins harboring a classic nuclear localization signal (cNLS) or the spontaneous nuclear im

81 revious studies linked the classical nuclear localization signal (cNLS) receptor, importin-alpha/Srp1

82 th with defects in M9- and classical nuclear localization signal (cNLS)-mediated protein import, nucl

83 soforms contains predicted classical nuclear localization signals (cNLS) within exons 7 and 11.

84 rtin alphas are import receptors for nuclear localization signal-containing proteins.

85 We found that targeting a nuclear localization signal-containing S6 variant [NLS-S6(Rpt1)]

86 r DCL4 transcript isoform encoding a nuclear localization signal, DCL4(NLS), is present in Arabidopsi

87 , and K376A) in conjunction with the nuclear localization signal deletion did not result in cytoplasm

88 verexpression of TEF3-1, but not its nuclear localization signal-deletion mutant (TEF3-DeltaNLS), ind

89 erexpressing exogenous FUS without a nuclear localization signal (DeltaNLS-FUS), which developed prog

90 9-Delta1/N60 fragment, which lacks a nuclear localization signal, displayed enhanced cytoplasmic vs.

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

92 A2 function for endosomal escape and nuclear localization signals for nuclear targeting and (ii) trig

93 d, nonactivating fatty acids inhibit nuclear localization signal formation by destabilizing this acti

94 d this localization is dictated by a nuclear localization signal found in the Adi3 T-loop extension,

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

96 s was restricted to the PM by fusing to a PM localization signal from the Rit GTPase, the resulting p

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

98 ET genes was investigated by pAtTET::NUCLEAR LOCALIZATION SIGNAL-GREEN FLUORESCENT PROTEIN/beta-GLUCU

99 amino acids of MxB to function as a nuclear localization signal; however, the ability of the N-termi

100 he interaction was mediated by two nucleolar localization signals identified by bioinformatics and mu

101 idues 11-27 and an isoleucine-lysine nuclear localization signal (IK-NLS) motif at residues 35-40.

102 ference, together with the lack of a nuclear localization signal in any of the AnkA orthologues, sugg

103 Mutation of the nuclear localization signal in CELF1 abolished the ability to do

104 s have been shown to deteriorate the nuclear localization signal in FUS and thereby facilitate cytopl

105 A nuclear localization signal in ORF2 was necessary for inhibiting

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

107 uch nonlinear processing generates an object-localization signal in the apical dendritic tuft of laye

108 ism whereby L takes advantage of the nuclear localization signal in the COOH region of 2A to enhance

109 essing human TDP-43 with a defective nuclear localization signal in the forebrain (hTDP-43-DeltaNLS),

110 Along with the known nuclear localization signal in the hinge domain, we identified a

111 GRs or those with a mutation in the nuclear localization signal in the muscle of MGRKO mice indicate

112 lization is mediated by a complex cis-acting localization signal in the nos 3' untranslated region th

113 We found putative nuclear localization signals in NEMO whose mutations disrupted s

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

115 sids, which leads to the exposure of nuclear localization signals in the C terminus of core protein a

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

117 in the nucleus through the action of nuclear localization signals in the repeated regions of the prot

118 ion studies identified and confirmed nuclear localization signals in XLG2 and XLG3 and a nuclear expo

119 Cdk5 has no intrinsic nuclear localization signal; in the absence of p27, two weak nuc

120 expressing full-length HDM-2 with a membrane-localization signal into untransformed MCF-10-2A cells n

121 reen fluorescent protein (GFP) and a nuclear localization signal is fused to the amino terminus of GF

122 -terminal region of NPM1 where its nucleolar localization signal is located.

123 tion of NRDE-3 requires a functional nuclear localization signal, is required for nuclear RNAi, and r

124 isoform, which lacks the N-terminal nuclear localization signal, is restricted to the cytoplasm.

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

126 P-43 protein, as a disruption of its nuclear localization signal leads to mislocalization and aggrega

127 tead, this ability is dependent on a nuclear localization signal located in its N-terminal 40 amino a

128 ption complexes through the use of targeting/localization signals may provide new avenues for designi

129 screen for novel factors associated with RNA localization signals mediating minus end-directed mRNA t

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

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

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

133 te thus acts as a widespread microtubule tip localization signal (MtLS).

134 ed with recombinant NEMO but not the nuclear localization signal mutant version and induced nuclear i

135 Utilizing a p53 nuclear localization signal mutant, whose nuclear import is comp

136 AP (AAP2) nuclear (NLS) and nucleolar (NoLS) localization signals near the carboxy-terminal region of

137 In these proteins, a nuclear localization signal (NLS) and an intrinsically disordere

138 st substrates that carry a classical nuclear localization signal (NLS) and bind to importin alpha1, S

139 nal region of FMDV 3D that acts as a nuclear localization signal (NLS) and in template binding is als

140 evidence that Cby harbors bona fide nuclear localization signal (NLS) and nuclear export signal (NES

141 on protein between RecA containing a nuclear localization signal (NLS) and the DNA-binding domain of

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

143 quence analyses revealed a potential nuclear localization signal (NLS) at the C terminus of IPSE/alph

144 P24 recognizes a unique nonclassical nuclear localization signal (NLS) binding site on KPNA5 that is

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

146 nction genetic approach, a bipartite nuclear localization signal (NLS) derived from the nucleoplasmin

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

148 ein domains, including the canonical nuclear localization signal (NLS) in the AR hinge region.

149 be the identification of a potential nuclear localization signal (NLS) in the C-terminal region of I2

150 translocate proteins that contain a nuclear localization signal (NLS) into the nucleus.

151 When a strong nuclear localization signal (NLS) is added to dia2 mutants lacki

152 thin the MeCP2 protein sequence, the nuclear localization signal (NLS) is reported to reside between

153 dy documents multifunctionality of a nuclear localization signal (NLS) located at the N-terminal regi

154 importin alpha/beta from a bipartite nuclear localization signal (NLS) located in the tail domain [14

155 analysis suggests that a monopartite nuclear localization signal (NLS) may reside in the N-terminal l

156 Consistent with the presence of a nuclear localization signal (NLS) motif within the GmHSP40.1 cod

157 on domain although it does possess a nuclear localization signal (NLS) motif, whilst Cry3 lacks both

158 hBVR nuclear export signal (NES) and nuclear localization signal (NLS) mutants demonstrated its criti

159 Here we show that mutation of the nuclear localization signal (NLS) of human Kinesin-14 HSET cause

160 acterized the importin-alpha binding nuclear localization signal (NLS) of rat ChREBP, identifying it

161 We found that, in addition to the nuclear localization signal (NLS) of XPA, importin-alpha4 or/and

162 26 and Ser828, located in a putative nuclear localization signal (NLS) on the Drosophila melanogaster

163 x virus 1 (HSV-1) mutant lacking the nuclear localization signal (NLS) on the ICP0 gene (0DeltaNLS) i

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

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

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

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

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

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

170 ed the structure and conservation of nuclear localization signal (NLS) sequences previously identifie

171 protein VP1-2 contains an N-terminal nuclear localization signal (NLS) that is critical for capsid ro

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

173 ting on RNA (ADAR1) carries a unique nuclear localization signal (NLS) that overlaps one of its doubl

174 SAP11 contains a bipartite nuclear localization signal (NLS) that targets this effector to

175 otein (GFP) reporter fusion assays a nuclear localization signal (NLS) that was mapped to a 23-amino-

176 of influenza virus A/WSN/33 when its nuclear localization signal (NLS) was disrupted by R101S and R10

177 nt mouse, nBmp2NLS(tm), in which the nuclear localization signal (NLS) was inactivated to prevent nuc

178 ear localization, and a nonclassical nuclear localization signal (NLS) was mapped to a short, highly

179 Ser238 neighbors a nuclear localization signal (NLS) whose function is blocked by p

180 port that Nurr1 contains a bipartite nuclear localization signal (NLS) within its DNA binding domain

181 Both HDAgs contain a nuclear localization signal (NLS), but only HDAg-L contains a CR

182 f topo IIalpha, while preserving the nuclear localization signal (NLS), enhances the decatenation che

183 a cell penetrating peptide (CPP), a nuclear localization signal (NLS), or a bifunctional CPP-NLS or

184 translocated into the nucleus via a nuclear localization signal (NLS), specific among keratins, wher

185 and threonine residues adjacent to a nuclear localization signal (NLS), thereby abrogating its NLS ac

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

187 s required in the nucleus to release nuclear localization signal (NLS)-containing cargo from import r

188 Notably, the PB2 nuclear localization signal (NLS)-containing domain translocates

189 mediate nuclear transport by linking nuclear localization signal (NLS)-containing proteins to importi

190 esmata, targeted to the nucleus in a nuclear localization signal (NLS)-dependent manner, where it loc

191 eterodimer alpha2beta1 in vitro in a nuclear localization signal (NLS)-dependent manner.

192 phate (RanGTP) gradient that imports nuclear localization signal (NLS)-specific cargoes (NLS-cargoes)

193 o the nucleus, it does not possess a nuclear localization signal (NLS).

194 otif which functions as an efficient nuclear localization signal (NLS).

195 volutionarily conserved multipartite nuclear localization signal (NLS).

196 boxy-terminal 143 residues contain a nuclear localization signal (NLS).

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

198 e-isoforms that contain a functional nuclear localization signal (NLS).

199 lasts harboring mutations in the FUS nuclear localization signal (NLS).

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

201 ortin alpha (Imp alpha), and variant nuclear localization signals (NLS) representing a range of bindi

202 0-nm diameter) and without (< 10 nm) nuclear localization signals (NLS), macroscopic transport rates

203 ied, with two overlapping one of two nuclear localization signals (NLS).

204 , proline/serine (PS) domain and two nuclear localization signals (NLS).

205 CAPN5 possesses two nuclear localization signals (NLS): an N-terminal monopartite NL

206 rminal residues (1-45) including the nuclear localization signal (NLS1) are dispensable.

207 Previous studies have described one nuclear localization signal (NLSI) in p53 and speculated on two

208 idues within the peptides containing nuclear localization signals (NLSs) 1 and 2 were non-acetylated,

209 ant pathogen Phytophthora sojae uses nuclear localization signals (NLSs) for translocation of protein

210 al nucleocytoplasmic import pathway, nuclear localization signals (NLSs) in cargo proteins are recogn

211 Importin alpha1 can bind classical nuclear localization signals (NLSs) in two NLS-binding sites, kn

212 l with mutations that inactivate the nuclear localization signals (NLSs) of Apc (Apc(mNLS)).

213 their bacterial homologues, possess nuclear localization signals (NLSs) to enter the cell nucleus du

214 proteins have been shown to contain nuclear localization signals (NLSs), although its biological rol

215 ospholipase A(2) (PLA(2)) domain and nuclear localization signals (NLSs).

216 ell nuclei and contains two putative nuclear localization signals (NLSs).

217 s of influenza A viruses contain two nuclear localization signals (NLSs): a well-studied monopartite

218 lpha and NRF-2beta contain intrinsic nuclear localization signals (NLSs): the Ets domain within NRF-2

219 tches of basic amino acids-nuclear/nucleolar localization signals (NLSs/NoLSs).

220 modular signals for nuclear import (nuclear localization signals, NLSs) and export (nuclear export s

221 Here, we show that NSs contains a nucleolar localization signal (NoLS) and induces disorganization o

222 to target the nucleolus through a nucleolar localization signal (NoLS) localized between residues 33

223 leolus, and deletion of a putative nucleolus localization signal (NoLS) within its N-terminal moiety

224 nce that is predicted to contain a nucleolar localization signal (NoLS), only p8 is found in the nucl

225 lus, suggesting that it contains a nucleolar localization signal (NoLS).

226 orylation at S659, which exposed the nuclear localization signal of ACSS2 for importin alpha5 binding

227 sphorylation sites reside around the nuclear localization signal of Alp7, and the phosphodeficient al

228 ith point mutations in the canonical nuclear localization signal of CMAS, which relocated the enzyme

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

230 redicted deleterious variants in the nuclear localization signal of Heterogeneous Nuclear Ribonucleop

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

232 Disruption of the nuclear localization signal of PHAPI caused a modest decrease of

233 glycerol medium, and removal of the nuclear localization signal of Rat1, the nuclear homolog of Xrn1

234 SBMA, we genetically manipulated the nuclear localization signal of the polyglutamine-expanded AR.

235 bic domain and a proximal C-terminal nuclear localization signal of VP4 were required for (i) cytolys

236 This is because the predicted nuclear localization signals of HMR are nonfunctional, and there

237 nd this reduction requires the mitochondrial localization signals of Opa3.

238 These data suggest that the subcellular localization signals of ORF45 have important functional

239 We identified two nuclear localization signals of Stp1 and found that the N-termin

240 ion sites: one (short form) with the nuclear localization signal only, exclusively localized in the n

241 BP12) fused to a cellular 'address' (nuclear localization signal or nuclear export sequence).

242 srupting Arl13b's palmitoylation site, cilia localization signal, or GTPase handling altered the Shh

243 trated via the assembly of stable QD-nuclear localization signal peptide bioconjugates that promoted

244 in its free form or in complex with nuclear localization signal peptides as the starting conformatio

245 Mutation of the nuclear localization signal prevented detectable levels of AtLAZ

246 not a truncated version lacking the nuclear localization signal protects from pathogenic TDP-43-medi

247 identified a novel proline-tyrosine nuclear localization signal (PY-NLS) in DJ-1, and we found that

248 portin recognizes a proline-tyrosine nuclear localization signal (PY-NLS) in the N-terminal tail of N

249 Mutations in the proline/tyrosine-nuclear localization signal (PY-NLS) of the Fused in Sarcoma pro

250 Here, we show that the PY-type nuclear localization signal (PY-NLS)/karyopherinbeta2 (Kapbeta2)

251 o species are due to gain/loss of cis-acting localization signals rather than to differences in the R

252 rins for Rrp6 nuclear import and the nuclear localization signals recognized by them.

253 go proteins, including the classical nuclear localization signals, recognized by the adaptor importin

254 e adaptor importin-alpha, and the PY nuclear localization signals, recognized by transportin-1.

255 -characterized basic amino acid-rich nuclear localization signal region at positions 101 to 105, M1 c

256 onstrate that the positively charged nuclear localization signal region in the tail in apo-OsCaM61 is

257 etylated lysine is in the N-terminal nuclear localization signal region.

258 ction as a nuclear export signal and nuclear localization signal, respectively.

259 r truncated Ptpmt1 lacking the mitochondrial localization signal restored the differentiation capabil

260 of mouse and human, and contained nucleolar localization signal, RNA-binding domain and several phos

261 nuc-ErbB3 possesses a functional nuclear localization signal sequence and binds to chromatin.

262 ls showed that all of them contain a nuclear localization signal sequence flanking to the K1 segment

263 rthermore, despite the presence of a nuclear localization signal sequence in Gag, we observed no foam

264 The C terminus encompassing the nuclear localization signal sequesters the enzyme in the nucleus

265 g proteins (EBs) through the microtubule tip localization signal SKIP, which lies N terminal to MCAK'

266 d to nuclei, through the fusion with nuclear localization signal, still exerts strong antiproliferati

267 last targeting signal and a putative nuclear localization signal, suggesting that they are dual targe

268 Overexpression of nuclear localization signal-tagged HSP27 also rescues mutant TBP

269 tor SP1, and coexpression of SP1 and nuclear localization signal-tagged HSP27 synergistically activat

270 playing an established mitochondria-specific localization signal targets mitochondria, and that an in

271 DP-43 variant with a mutation in the nuclear localization signal (TDP-43-NLS).

272 Orc6 and Orc1 each contain a single nuclear localization signal that is essential for nuclear locali

273 hat residues (20)KY(21) constitute a nuclear localization signal that is not required for the ability

274 -1314 possesses a conserved putative nuclear localization signal that may facilitate the nuclear targ

275 elements consists of a high-affinity nuclear localization signal that mediates indirect tethering to

276 with importin alpha via a classical nuclear localization signal that recruits importin alpha to the

277 Although different ER localization signals that exhibit varying affinities for

278 and restricting access to a primary nuclear localization signal through which the apoptogenic form i

279 by mutating Ser rich clusters of the nuclear localization signal to Ala abolished nuclear import and

280 termines whether AGR2 requires a specific ER localization signal to be functionally active.

281 have expressed KpnI fused to a mitochondrial localization signal to induce a specific mitochondrial d

282 rallels effects of the attachment of nuclear localization signal to Sis1, indicating that Cur1 acts o

283 very of potent Tat inhibitors that utilize a localization signal to target a dominant negative protei

284 ruction is also used in multipartite nuclear localization signals to provide broad substrate specific

285 fuse the ADAR2 domain, tagged with a nuclear localization signal, to an RNA binding peptide from bact

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

287 This novel TSS localization signal (TSLS), spanning amino acids 50 to 7

288 The localization signal was compared with ER-specific dyes.

289 n, which could be reversed after the nuclear localization signal was deleted.

290 inal 25 amino acids to function as a nuclear localization signal was not required for restriction.

291 1 (FHY1) and fhy1-like, an intrinsic nuclear localization signal was proposed to be involved in the n

292 PAD4 or PADV), the only PADI with a nuclear localization signal, was previously shown to act in myel

293 tNLS algorithm uncovered a potential nuclear localization signal, whereas the algorithm DBS-Pred retu

294 t in the shorter isoform, contains a nuclear localization signal, whereas the C terminus of B56epsilo

295 The Orc6 nuclear localization signal, which is essential for Orc6 functio

296 It also possesses a nuclear localization signal, which is required for its transloca

297 dreCmas1 was mediated by a bipartite nuclear localization signal, which seemed irrelevant for other e

298 both a nuclear export sequence and a nuclear localization signal, whose activities are regulated by p

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

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