ライフサイエンスコーパス: N-terminal region

1 enetrating cation-dependent mechanism in its N-terminal region.

2 rom the presence of an acidic residue at its N-terminal region.

3 cent segment (positions 61-67) in the FLIL33 N-terminal region.

4 tremely transient helices are present in the N-terminal region.

5 rimental evidence of O-linked glycans in the N-terminal region.

6 binding protein C (cMyBP-C), focusing on the N-terminal region.

7 tructure of a stable domain (CHD4-N) in this N-terminal region.

8 activity, and a functionally uncharacterized N-terminal region.

9 clease domain, but instead binds to the EsaD N-terminal region.

10 es against Plasmodium should include the CSP N-terminal region.

11 Lhcb1 and Lhcb2 can be phosphorylated in the N-terminal region.

12 ike domain at the C terminus and an extended N-terminal region.

13 hanges of negatively charged residues of the N-terminal region.

14 ssociated with conformational changes in the N-terminal region.

15 Arnt-Sim (PAS) domain in their intracellular N-terminal region.

16 vivo through direct recognition of the MinD N-terminal region.

17 the sequence differences are located in the N-terminal region.

18 those of peptides corresponding to the CCR1 N-terminal region.

19 ding cytochrome domain is fused to the AfGDH N-terminal region.

20 ttributable to conformational changes in the N-terminal region.

21 the orientation of the helices (alpha1-3) in N-terminal region.

22 yte-binding domains were mapped within their N-terminal regions.

23 ects the nucleus to the cytoskeleton via its N-terminal region [5-7].

24 beta8.1, 8.2(+) immune T cells recognize the N-terminal region (aa 41-152) of dense granule protein 6

25 n fold has no impact on oligomerization, but N-terminal regions affect the dimer-tetramer equilibrium

26 Here, we report that the E1A N-terminal region also interacted with the cellular prot

27 P1BP3 to chromatin depends on both its C and N terminal regions and is affected by the cell cycle and

28 The DeltaN-LKB1 protein lacks the N-terminal region and a portion of the kinase domain.

29 onal analysis suggests the involvement of an N-terminal region and a proximal C-terminal region that

30 d of two monomers that each contain a folded N-terminal region and an intrinsically disordered C-term

31 c), has a CaM-binding peptide located in its N-terminal region and displays peculiar biochemical prop

32 Because the N-terminal region and first transmembrane domain of the

33 tional ensembles of the partially disordered N-terminal region and interhelical loop.

34 Effects on alpha6beta4 involve BARP's N-terminal region and IRE1alpha's splicing of XBP1 mRNA.

35 Hsc70 dynamically associated with the N-terminal region and Rac1 GEF domain of Trio.

36 these nuclear structures is mediated by the N-terminal region and requires prion-like activity.

37 mokine N-loop/beta3 region to the receptor's N-terminal region and subsequent insertion of the chemok

38 ed form higher-order oligomers through their N-terminal region and that the same AT-rich site is reco

39 king of the [4Fe-4S] cluster by the flexible N-terminal region and the associated inhibition of the a

40 The results show that the N-terminal region and the C-terminal unstructured loop u

41 Here we report that the Set1 N-terminal region and the COMPASS subunit Swd2, which in

42 location of the WWP2 isoforms containing the N-terminal region and their interaction with SMAD2.

43 tions in GNPTAB uncovered amino acids in the N-terminal region and within the DMAP domain involved in

44 ective groups of hnRNP proteins, through its N-terminal region, and directly regulates pre-mRNA splic

45 changes that affect the solvent exposure of N-terminal region, and hence the redox sensitivity of th

46 molecular rationale for the function of the N-terminal region, and support the idea that Cerberus co

47 ns a newly defined ILT7-binding surface, the N-terminal region appears to suppress ILT7 activation.

48 ric assemblies in which interactions between N-terminal regions are important.

49 itinating activity, revealing a role for the N-terminal region as a regulatory module in the control

50 f-mediated cleavage mechanism, featuring the N-terminal region as an anchor for at least one of the D

51 he structure and dynamics of the p150(Glued) N-terminal region, both free and in complex with polymer

52 i activation required not only the conserved N-terminal region but also permissive communication of t

53 a protein that may be cleaved in vivo at the N-terminal region by neutrophil proteases including elas

54 However, phosphorylation at the GarA N-terminal region by the protein kinase PknB or PknG tri

55 that serine phosphorylation within the ICAP1 N-terminal region can prevent nuclear ICAP1 accumulation

56 linear extension of the filament, while the N-terminal region can serve as a branch-point.

57 ased rates of MT polymerization, whereas the N-terminal region cannot bind to MT plus ends but can ac

58 is the presence of two conserved regions: an N-terminal region codifying for signal peptide and a C-t

59 rin homology (PH) domains interacts with the N-terminal region comprising ARL8- and kinesin-1-binding

60 allographic structure of the Arabidopsis TPL N-terminal region comprising the LisH and CTLH (C-termin

61 ed missense mutations in the RING domain and N-terminal region compromise its activity, and therefore

62 We also show that the N-terminal region, conserved across all group 4 LEA prot

63 the C-terminal region rather than the nearby N-terminal region, consistent with an allosteric effect

64 for DNA binding and, in combination with the N terminal region, constitute a functional transactivato

65 with a C-terminal RING domain and disordered N-terminal region containing SUMO Interactions Motifs (S

66 of a C-terminal helical bundle and a dynamic N-terminal region containing two disulfide linkages.

67 he three-dimensional structure of the Xyn10C N-terminal region, containing the xylan-binding CBM22-1-

68 Here, we demonstrate that this N-terminal region contains a ubiquitin (Ub)-associated (

69 The results revealed that the chemokine N-terminal region contributes significantly to binding a

70 Mutations in the whirlin N-terminal region disrupted FL-whirlin isoform in the in

71 rthermore, we found that deletion of the F1L N-terminal region does not impede F1L antiapoptotic acti

72 activate ILT7, whereas substitutions in its N-terminal region enhance activation.

73 by leucine-rich repeats (LRRs) and having an N-terminal region enriched in alternating lysine and glu

74 an intrinsically disordered, low-complexity N-terminal region flanking the coil-coiled self-associat

75 nd the gelatin-binding domains of the 70-kDa N-terminal region (FN70K).

76 ball and tether, consisting of a disordered N-terminal region followed by a compact globular C-termi

77 The N-terminal region formed a solvent-exposed patch located

78 CYP1A2, containing the N-terminal regions from CYP1A1, no longer localized in o

79 and release the processed Nrf1 (lacking its N-terminal region) from the ER, which allows it to enter

80 When not phosphorylated, this N-terminal region functions as an autoinhibitory domain

81 ngement of RNA-binding sites, although these N-terminal regions have only limited sequence conservati

82 phosphorylation sites and truncations of the N-terminal region highlighted reduced lipid accumulation

83 f leucine-rich repeats domain also binds the N-terminal region, highlighting a possible mechanism for

84 munodominant B cell epitope derived from the N-terminal region I and to repeat sequences representing

85 ogous Glu-to-Lys substitutions in alphaSyn's N-terminal region (i.e. E35K and E61K).

86 Nase R, whereas the Walker B motif is in its N-terminal region implying that the two parts of the pro

87 to regulate DNA-damage responses through its N-terminal region in a poly(ADP-ribose) polymerase-depen

88 demonstrate that the established role of the N-terminal region in dimerization is not conserved; inst

89 LDL binding in vitro requires a disordered N-terminal region in PCSK9's prodomain.

90 er are partially understood, the role of the N-terminal region in the metazoan replicative mtDNA heli

91 or to a lesser extent at Ser-25, within this N-terminal region inhibit ICAP1 nuclear accumulation.

92 on and subsequent insertion of the chemokine N-terminal region into the transmembrane helical bundle

93 folded side of the main barrier in which the N-terminal region is disordered.

94 site-directed mutagenesis, we show that the N-terminal region is essential for ADP-ribosylating acti

95 ed chromatin-stimulated ATPase activity, the N-terminal region is required for ATP-dependent chromati

96 A highly conserved N-terminal region is required to bind dynein and kinesin

97 conserved membrane-proximal amino-terminal (N-terminal) region, is distinct from other lipid-activat

98 pper-dependent conformational changes in the N-terminal region lead to hyperphosphorylation at C-term

99 While loss of the N-terminal region leads to enhanced chromatin-stimulated

100 he best-scoring receptor structures have the N-terminal region lid region bound in a helical conforma

101 channel that otherwise binds ppGpp, and its N-terminal region, like the coiled-coil tip of DksA, eng

102 alyses over the N terminus revealed that the N-terminal region may also harbor a subfamily recognitio

103 ther RALF peptides that share this conserved N-terminal region may be perceived by LLG proteins in a

104 ngal or bacterial GEs, with a large inserted N-terminal region neighboring the active site and a diff

105 Although the N-terminal region normally localizes to podocyte foot pr

106 Notably, an extended N-terminal region (NTR) consisting of 11 amino acids was

107 nd to sites within the enigmatic, disordered N-terminal region (NTR) of HspB1.

108 e of an auto-regulatory motif, AutoN, in the N-terminal region (NTR) of ISWI, indicating that AutoN d

109 In contrast, the N-terminal region (NTR) of PARP-1 is over 500 residues a

110 kinetic techniques to show that the myosin-I N-terminal region (NTR) plays a critical role in tuning

111 ure shows the stalk region and the essential N-terminal region (NTR) previously unseen in our DNA unb

112 In the human sHSP HSPB1, the disordered N-terminal region (NTR) represents nearly 50% of the seq

113 revealed that PA2588 has a novel fold at the N-terminal region (NTR), and its C-terminal HTH (helix-t

114 ), a central Trp-Gly-Arg (WGR) domain and an N-terminal region (NTR).

115 ly spliced isoforms, differing only in their N-terminal regions (NTRs).

116 at serine 8 causes structural changes in the N-terminal region of Abeta aggregates in favor of less c

117 and other biological events that involve the N-terminal region of Abeta aggregates.

118 ough sequential truncation, we show that the N-terminal region of Abeta contributes to the enhanced f

119 stigated metal ions bind specifically to the N-terminal region of Abeta, forming a dynamic, partially

120 tively inhibited by antibodies targeting the N-terminal region of Abeta42.

121 Using biochemical assays, we found that the N-terminal region of AKAP8L binds to mTORC1 in the cytop

122 terdomain region (CIDR) domains found in the N-terminal region of all PfEMP1.

123 modeling revealed that two residues near the N-terminal region of alpha-helix 1 in GPPrP might mediat

124 Moreover, we showed that the N-terminal region of alpha-syn is important for PLK2-med

125 Glycation affected primarily the N-terminal region of alpha-synuclein, reducing membrane

126 ions to refine structure and topology of the N-terminal region of alphaS bound to the surface of syna

127 on is a rare example of a replacement in the N-terminal region of amylin.

128 Surprisingly, the N-terminal region of Asl is not required for centriole d

129 ATXN7L3B shares 74% identity with the N-terminal region of ATXN7L3, but the functions of ATXN7

130 B0238, which specifically interacts with the N-terminal region of BB0323.

131 h ankyrin repeats (ANK) 1, 6, and 7, and the N-terminal region of Bcl-3.

132 The N-terminal region of BubR1 binds to both Cdc20 and Mad2,

133 by binding of the Hsp90 middle domain to an N-terminal region of Caenorhabditis elegans Cdc37 (CeCdc

134 We further identified a conserved N-terminal region of CDH23-C that binds to the CKK domai

135 We also show that the N-terminal region of CHD2, which contains tandem chromod

136 We also show that the N-terminal region of CHD4, although not CHD4-N alone, is

137 activation of myocardial contraction by the N-terminal region of cMyBP-C in its different phosphoryl

138 t a structural description of the Fn binding N-terminal region of CshA, derived from a combination of

139 Heat shock protein 90 (HSP90) binds to the N-terminal region of CTA1 and facilitates its ER-to-cyto

140 ational analysis predicted that the extended N-terminal region of CYP144A1-FLV is largely unstructure

141 activation is surprisingly derived from the N-terminal region of DgcB itself.

142 The N-terminal region of DNA-binding domain of STAT3 is resp

143 ion at Y102 disrupts the helical fold of the N-terminal region of E2 and its interaction with key cel

144 re we show that the intrinsically disordered N-terminal region of E7 from high-risk HPV16 binds the T

145 In this study, we discovered that the N-terminal region of Efb (Efb-N) promotes platelet bindi

146 e non-synonymous substitution (A120G) in the N-terminal region of eIF2Bbeta was responsible for the T

147 The peptide derived from the N-terminal region of Evasin-4 possessed nanomolar affini

148 the C terminus of Evasin-1, but through the N-terminal region of Evasin-4.

149 le played by a stretch of 17 residues in the N-terminal region of EZH2, we call the activation loop,

150 p57 and found that Cys(6) and Cys(23) in the N-terminal region of ficolin-3 form the intermolecular d

151 t Lsm11, in addition to interacting with the N-terminal region of FLASH, also contacts the C-terminal

152 A-MVD-causing mutations are clustered in the N-terminal region of FLNA.

153 Thus, the N-terminal region of FMDV 3D that acts as a nuclear loca

154 The N-terminal region of GPR107 is critical for its biologic

155 l characterization of the previously unknown N-terminal region of HAI-1, we provide new insight into

156 tation experiments, we demonstrated that the N-terminal region of HNF6 was responsible for its inhibi

157 An N-terminal region of HopK1 shares similarity with the co

158 nd sedimentation analysis, we found that the N-terminal region of Hsp27 and the terminal regions of a

159 Here, we present the structure of the N-terminal region of human BCAP and show that it possess

160 -L in the endoplasmic reticulum (ER) via the N-terminal region of human invariant chain p33, with or

161 to be important for biological activity: the N-terminal region of human neuropeptide Y (NPY1-9, Tyr(1

162 e rate of amyloid formation, even though the N-terminal region of IAPP is believed to be flexible in

163 During early mitosis, the N-terminal region of INCENP forms a three-helix bundle w

164 ombine the CsgG nanopore with the 35-residue N-terminal region of its extracellular interaction partn

165 We conclude that Delta-JDBD, and not the N-terminal region of JBP1 alone, is a distinct folding u

166 P interacts extensively with the N-terminal region of L, burying more than 4,016 angstrom

167 -interacting motif 2 (PAM2w) featured in the N-terminal region of LARP4A was found to be important fo

168 Accordingly, the N-terminal region of LEAP2 is able to inhibit ghrelin-in

169 munoprecipitated the recombinantly expressed N-terminal region of LRP2.

170 ng interface to a few acidic residues in the N-terminal region of MAD1, and point mutations in this s

171 the interaction domain with Mec3 within the N-terminal region of Mcm10 and demonstrate that its trun

172 TFAM tethers the N-terminal region of mtRNAP to recruit the polymerase to

173 sharp contrast, recombinant proteins of the N-terminal region of MUC5B (D1-D2-D'-D3 domains, NT5B),

174 These results show that the N-terminal region of MyBP-C stabilizes the ON state of t

175 h muscle cells through direct binding to the N-terminal region of myocardin.

176 The N-terminal region of Ndfip1 binds to UbcH7, whereas the

177 shallow pocket adjacent to the groove in the N-terminal region of NHR trimer as a new drug target, an

178 ion is mediated by the J domain of Hsp40 and N-terminal region of NP.

179 Difference densities suggest that the N-terminal region of NS1 forms globular lobes that media

180 the SHFV PLP1s cleaving at sites within the N-terminal region of nsp1beta were produced in the in vi

181 ons involve the intrinsically disordered and N-terminal region of NUP98 with over 30 partner genes.

182 Alterations in the N-terminal region of OsDGAT1-1 gene revealed its regulat

183 However, how the N-terminal region of PDZD11 interacts with the N-termina

184 alysis suggested at least one epitope on the N-terminal region of PEDV/TGEV N protein that contribute

185 structure of the complex between PcrH and an N-terminal region of PopB (residues 51-59), which reveal

186 interacts directly with pUL96; however, the N-terminal region of pp150 and the C-terminal region of

187 The N-terminal region of prion protein (residues 23-90) is r

188 1 cleaved eight amino acid residues from the N-terminal region of Prx1 inside the matrix, without int

189 d by TSP1, which directly interacts with the N-terminal region of PTX3.

190 y binding to polar residues in the conserved N-terminal region of PulG, we propose that PulM acts as

191 A conserved N-terminal region of RALF23 is sufficient for the bioche

192 The 76 amino acid N-terminal region of Ref is positively charged (25/76 am

193 The putative role of the N-terminal region of rhodopsin-like 7 transmembrane biog

194 Here we show that, although the N-terminal region of RNF4 bears no secondary structure,

195 The N-terminal region of RTA is required for the reduction o

196 The long N-terminal region of RTN3 contains several newly identif

197 Scc2 binds to Scc1 through an N-terminal region of Scc1 that overlaps with its Pds5-bi

198 an artificial fusion substrate in which the N-terminal region of securin was linked to an APC/C core

199 The N-terminal region of simian hemorrhagic fever virus (SHF

200 icroscopy, we demonstrate that the conserved N-terminal region of SPR1 and its GGG motif are necessar

201 We demonstrated that the glycine-rich N-terminal region of SPS is crucial for the SelA-tRNA(Se

202 Expression of the N-terminal region of SS4 alone did not alter the ss4 mut

203 Interestingly, the N-terminal region of SS4 alone or when fused to GS confe

204 ted versions of SS4 and a fusion between the N-terminal region of SS4 and GS in the Arabidopsis ss4 m

205 The N-terminal region of SS4 is unique among SS isoforms and

206 Remarkably, fusion of the N-terminal region of SS4 to A. tumefaciens GS restored t

207 ion mutants, we further demonstrate that the N-terminal region of TALEs is required for the initial n

208 Recent data demonstrate that the N-terminal region of tau (aa 2-18), termed the "phosphat

209 Overall, in addition to the N-terminal region of the B-chain, which was shown to ser

210 f SH2D5 and an NxxF motif located within the N-terminal region of the breakpoint cluster region.

211 ever, addition of dynactin together with the N-terminal region of the cargo adaptor BICD2 (BICD2N) gi

212 between the PTEN C-tail and a segment in the N-terminal region of the catalytic domain.

213 ssed in eukaryotic cells, the TMH-containing N-terminal region of the CbuD1884 protein trafficked to

214 e observed that HCV1, a bNAb recognizing the N-terminal region of the CD81bs, bound a soluble E2 core

215 me families revealed two insertions into the N-terminal region of the CYP125 family (residues 58-67 a

216 ear localization signal (NLS) located at the N-terminal region of the foot-and-mouth disease viral po

217 The N-terminal region of the foot-and-mouth disease virus (F

218 While the N-terminal region of the G-patch always folds into an al

219 nonneutralizing CD4-induced epitopes in the N-terminal region of the HIV-1 gp120 (A32-like epitopes)

220 d we identified a distinct domain within the N-terminal region of the HSP-16.48 protein that specifie

221 sulfide bonds, a structure homologous to the N-terminal region of the human granulin protein.

222 riggered by a polyglutamine expansion in the N-terminal region of the huntingtin (HTT) protein.

223 r caused by a polyglutamine expansion in the N-terminal region of the huntingtin protein (N17).

224 ant toxicity of the polyglutamine-containing N-terminal region of the huntingtin protein encoded by e

225 Polyglutamine expansion within the N-terminal region of the huntingtin protein results in t

226 The N-terminal region of the huntingtin protein, encoded by

227 The N-terminal region of the longer encoded peptide directs

228 The sequence-variable N-terminal region of the M protein defines the M type an

229 ntibodies reported thus far to recognize the N-terminal region of the membrane-proximal external regi

230 Here, we show that phosphorylation at the N-terminal region of the mitochondrial calcium uniporter

231 any of these sera reacted to epitopes in the N-terminal region of the molecule.

232 The N-terminal region of the protein allows the interaction

233 by a polyglutamine (polyQ) expansion in the N-terminal region of the protein huntingtin (HTT).

234 novel RNA recognition features involving the N-terminal region of the protein that exists in a semi-d

235 over that the major ATRX RBR lies within the N-terminal region of the protein, distinct from its PHD

236 o, mediated by the coiled-coil domain at the N-terminal region of the protein.

237 in cultured cells, primarily mediated by the N-terminal region of the protein.

238 rts this activity even in the absence of the N-terminal region of the protein.

239 sted to occur via the product binding to the N-terminal region of the protein.

240 ch reveals that FliD is pentameric, with the N-terminal region of the protomer forming an extensive s

241 in the RNA-binding motif 2 interact with the N-terminal region of the RS domain (RS1).

242 tudy, we found that a 197-aa deletion in the N-terminal region of the S protein did not alter virus (

243 is enhanced by the presence of the unfolded N-terminal region of the sequence and by destabilization

244 Using the disordered N-terminal region of the Sic1 protein as a test case, we

245 o characterise the mechano-sensitive compact N-terminal region of the talin rod, and show that the th

246 with double cysteine substitutions near the N-terminal region of the TMD to study the effect of alte

247 critical for the inhibitory function of the N-terminal region of the V protein.

248 Transgenic mice lacking the N-terminal region of the WWP2 protein show improved card

249 es in the juxtaposition of the less ordered, N-terminal region of their capsid proteins, VP1/2/3.

250 An unstructured N-terminal region of Tim10 is necessary and sufficient t

251 PrS-YjhX specifically interacts with the N-terminal region of TopA (TopA67) but not full-TopA in

252 tudies, we identified a critical role of the N-terminal region of UBXD1 (UBXD1-N).

253 The N-terminal region of vIRF-1 interacts directly with memb

254 he in vivo assembled particles involving the N-terminal region of VP1.

255 vo missense variants predicted to affect the N-terminal region of WDR37-p.Ser119Phe, p.Thr125Ile, p.S

256 In addition, we show that the N-terminal region of WNK1 binds to the UV radiation resi

257 o evaluate pairwise interactions between the N-terminal regions of CESA1, CESA3, CESA5, CESA6 and the

258 gnition of acetylated lysine residues in the N-terminal regions of histones.

259 ng the presence of RNA structures within the N-terminal regions of its coding sequences.

260 ghly conserved amino acid differences in the N-terminal regions of Pgamma isoforms, demonstrating for

261 Antibodies to the N-terminal regions of the IT4var09 PfEMP1 variant (NTS-D

262 The N-terminal regions of these variants were essential for

263 mponent of the peripheral stalk binds to the N-terminal regions of two alpha-subunits.

264 s, however, additionally have low-complexity N-terminal regions of unknown function.

265 redictions in the C-terminal, but not in the N-terminal, region of Hhat.

266 The N-terminal region ofSdGluc5_26A protrudes into the activ

267 Although the extended transmembrane Orai N-terminal region (Orai1 amino acids 73-91; Orai3 amino

268 ts viral membrane fusion by lifting the MPER N-terminal region out of the viral membrane, mandating t

269 ese results confirm the influential roles of N-terminal region (positions 7 and 8) and the loop 40-60

270 h cMyBP-C antibody against the actin-binding N-terminal region reduced ADP sensitivity, indicative of

271 rotein is composed of a largely unstructured N-terminal region (residues 1-71) and a well-folded C-te

272 ight binding interaction with LcrV while the N-terminal region (residues 7-51) shows weaker interacti

273 ing CyRPA and RIPR, and contains a conserved N-terminal region (RH5Nt) of unknown function that is cl

274 Ahnak, through its N-terminal region, scaffolds the L-type pore-forming alp

275 paramagnetic lanthanide ion attached to its N-terminal region shows a decrease in alignment as the d

276 C) has a highly disordered conformation, its N-terminal region shows resonance broadening consistent

277 osine A3 receptor (A3AR) having an identical N-terminal region shows similar biological profiles to T

278 he formation of an AcAS-Cu(I) complex at the N-terminal region stabilizes local conformations with al

279 s CH1 to bind actin aided by an unstructured N-terminal region that becomes alpha-helical upon bindin

280 of troponin I (cTnI) has a unique 31-residue N-terminal region that binds cardiac troponin C (cTnC) t

281 whereas reintroduction of AKAP8L missing the N-terminal region that confers the interaction with mTOR

282 combination and identify regions of the RAG1 N-terminal region that control nucleolar association and

283 AFF4 consists of an intrinsically disordered N-terminal region that interacts with other super-elonga

284 ubiquitin E3 ligase activity, located in an N-terminal region that is not strictly required for the

285 localization signal within an unstructured, N-terminal region that is rich in serine and threonine r

286 ends on the presence of a basic unstructured N-terminal region that tethers SpaI to the membrane.

287 ly, the structures contain a large, flexible N-terminal region that was investigated by gel-filtratio

288 human FLASH can be directly joined with its N-terminal region through alternative splicing.

289 es refolding of the short, unstructured MDM2 N-terminal region to achieve its high affinity.

290 n Nrd1 can partially substitute for the Set1 N-terminal region to restore CTD interactions and histon

291 se, yet two-state folding and binding of the N-terminal region to the p53 receptor site.

292 hoGAP domain, induces strong binding of that N-terminal region to the RhoGAP domain, converting DLC1

293 kappaB activation by vFLIP only requires the N-terminal region up to the transition between the regis

294 Solution analysis of the F1L N-terminal regions using small angle x-ray scattering in

295 e from the proline-glutamine-rich repetitive N-terminal region was identified as the immunodominant I

296 he T-tubule membrane through their cytosolic N-terminal region, which contains 8 lipid-binding (MORN)

297 erminal catalytic domain but differ in their N-terminal region, which is composed of 4 repeats of sca

298 has RNA methyltransferase activities at its N-terminal region, which is responsible for capping the

299 associates with LDs through its hydrophobic N-terminal region, which is sufficient to demarcate site

300 tions, an extended 38-amino acid-long unique N-terminal region with still unknown functions.