ライフサイエンスコーパス: N-terminal portion

1 ng either the entire L11 protein or just the N-terminal portion.

2 -binding domain was situated in the flexible N-terminal portion.

3 in with the virion components located in the N-terminal portion.

4 as a putative DNA helicase is encoded by the N-terminal portion.

5 mbrane NRG isoforms with this CRD within the N-terminal portion.

6 inding, one on the C-terminal and one on the N-terminal portion.

7 the presence of STIM1 and the conserved Orai N-terminal portion.

8 tion of the p21 core protein and lacking the N-terminal portion.

9 Previous NMR studies indicated that the N-terminal portion (1ADSGE5) of unphosphorylated fibrino

10 ptually subdividing 1 into three regions: an N-terminal portion, a central statine-containing core, a

11 ll as that of FHL, interacting with the LAF1 N-terminal portion and the HFR1 C-terminal region.

12 with truncated Prx1 proteins showed that the N-terminal portion and the homeodomain of Prx1 were nece

13 of proteins containing the PDZ domain in the N-terminal portion and the LIM domain in the C-terminal

14 ly targeted to the nucleus by signals in its N-terminal portion, and the full-length protein accumula

15 The N-terminal portion (codons 1 to 24) of the 5'-proximal o

16 ernal leader could function even if the most N-terminal portion contained negative charges in the fir

17 osed of two subdomains, a largely disordered N-terminal portion containing three known phosphorylatio

18 raged 55 +/- 2%, suggesting that the missing N-terminal portion contains most of the alpha-helical st

19 The N-terminal portion contains the methylated DNA binding d

20 nce of a VHS (Vps27p/Hrs/Stam) domain in the N-terminal portion followed by a GAT (GGA and Tom) domai

21 the levels of cellular LRP and releases its N-terminal portion in the extracellular milieu while the

22 MD simulations suggested that the remaining N-terminal portion in the non-functional Orai1 N-truncat

23 two sets of constructs were created in which N-terminal portions (including either VRI-IV or only VRI

24 Residues at the N-terminal portion, including the first helix, the seque

25 alone revealed low deuteration levels in the N-terminal portion, indicating that this region containe

26 cytoplasmic tail, PKD1(115-226), but not the N-terminal portion, induced a large, Ca(2+)-permeable ca

27 portion is essential for clipping, while the N-terminal portion is sufficient for DSB end-resection.

28 c(y) revealed that its signal sequence-like N-terminal portion is uncleaved; hence, it is anchored t

29 One, which is located in the N-terminal portion, is shorter than but similar in seque

30 al analyses it is shown that domain C of the N-terminal portion, located adjacent to the helicase cat

31 n in muscle and adipose tissues and that its N-terminal portion may be critical for APPL1 function.

32 either in small proteins, or it makes up the N-terminal portion of a larger protein, usually a protei

33 of our peptide sequences and represented the N-terminal portion of a protein containing a signal pept

34 Deletion of the N-terminal portion of Acf1 (or its homologue in yeast) a

35 of AHR transactivation by AHRR involves the N-terminal portion of AHRR; does not involve competition

36 Therefore, the role of the N-terminal portion of ALL-1 is to direct the protein to

37 myc gene was abolished after deletion of the N-terminal portion of alpha-enolase.

38 rt of the binding pocket that recognizes the N-terminal portion of alpha-factor and is involved in th

39 erminal tail (residues 1-9), followed by the N-terminal portion of alpha-helix 1 (residues Cys-11, Gl

40 The N-terminal portion of alphaL is predicted to contain a b

41 The N-terminal portion of AML1, which is retained in AML1/ET

42 of 60-77-residue components identical to the N-terminal portion of apolipoprotein A-I (Apo A-I).

43 a2NTD (the N-terminal portion of Atp6v0a2) and secreted chemokine-c

44 The N-terminal portion of AvrPtoB is sufficient for its viru

45 d region (sigma(70) NCR) and a region in the N-terminal portion of beta' that appears to functionally

46 study, we used a monoclonal antibody to the N-terminal portion of beta-APP to examine how the immuno

47 motif present in the PC1 CTT as well as the N-terminal portion of beta-catenin.

48 The N-terminal portion of BFCOL1 contains its DNA-binding do

49 es and a conserved hydrophobic region in the N-terminal portion of BovK sensor domain were important

50 n kinase domain and lacks the autoinhibitory N-terminal portion of BRAF.

51 monoclonal antibody we generated against the N-terminal portion of BRCA2.

52 -C/EBP-epsilon antibodies raised against the N-terminal portion of C/EBP-epsilon (amino acids 1 to 11

53 BPepsilon and fusion proteins containing the N-terminal portion of C/EBPepsilon, whereas PIASxalpha w

54 The complete HelX protein and the soluble N-terminal portion of Ccl2 (called Ccl2*) were overprodu

55 Herein, we show that the N-terminal portion of CNK (CNK(N-term)) strongly coopera

56 olypeptide of 24-25 kDa corresponding to the N-terminal portion of D1 that is unstable and appears to

57 The N-terminal portion of D2 is disordered, and this region

58 nd that mu1 autocleavage is regulated by the N-terminal portion of delta, which forms an alpha-helica

59 Like mammalian IRS proteins, the N-terminal portion of dIRS contains a pleckstrin homolog

60 ites are located in analogous regions of the N-terminal portion of each isozyme.

61 The N-terminal portion of ETO forms complexes with PLZF, whi

62 precursors demonstrated that the lack of the N-terminal portion of FE65, which includes part of the f

63 n-bond stabilised secondary structure in the N-terminal portion of fH module 16, and the number and t

64 by cell surface binding sites for the 70-kD N-terminal portion of fibronectin.

65 he frz genes as well as regions encoding the N-terminal portion of FrzCD.

66 around the fluorescein, suggesting that the N-terminal portion of galanin, which constitutes the bin

67 Thus, the N-terminal portion of GCLC may undergo a change that sta

68 MAbs (including H6 and 37S) reacted with the N-terminal portion of gH between amino acids 19 and 276.

69 a series of chimeric peptides combining the N-terminal portion of GLP-1 or Ex-4 and the C-terminal s

70 mbinant vaccinia viruses expressing only the N-terminal portion of gp160, containing P18 but not HP53

71 One neurovirulence determinant mapped to the N-terminal portion of gp7O, which contains the VRA and V

72 Several regions of the N-terminal portion of GroEL-bound mAAT are highly suscep

73 the STAT1 interaction domain resides in the N-terminal portion of HCV core (amino acids [aa] 1 to 23

74 oligomers in vitro and in vivo and that the N-terminal portion of HDAC3 is necessary for this proper

75 g site together with five differences in the N-terminal portion of helix I conferred S-mephenytoin 4'

76 1, the C-terminal portion of helix-2 and the N-terminal portion of helix-3, bounded by the intramolec

77 rkness, indicating that the COP1-interacting N-terminal portion of HFR1 is essential for COP1-mediate

78 This fragment interacts with the N-terminal portion of HIF-1alpha spanning amino acid res

79 the three-dimensional structure of a 22-kDa N-terminal portion of human eIF2alpha by x-ray diffracti

80 a protein shares sequencesimilarity with the N-terminal portion of human PCAF that is involved in bin

81 AT1aR replaced the HK of BKB2R, leaving the N-terminal portion of IC1 without a positively charged r

82 t two overlapping regions within the central N-terminal portion of ICP0 (residues 212 to 311) promote

83 n region I, termed Phos 1, which lies in the N-terminal portion of ICP0, impairs the E3 ubiquitin (Ub

84 Therefore, the N-terminal portion of ICP27 contains at least two functi

85 or binding to GC-rich sequences and that the N-terminal portion of ICP27 is highly flexible in struct

86 er, our results suggest a model in which the N-terminal portion of ICP27 mediates a nonessential acti

87 The N-terminal portion of ICP4 contains well-defined transac

88 is of IE1 regulatory domains, the M1 to T266 N-terminal portion of IE1 was subdivided (on the basis o

89 The proline-rich N-terminal portion of INSM1 is required for cyclin D1 bi

90 e describe a refined model of the alpha(IIb) N-terminal portion of integrin alpha(IIb)beta(3) obtaine

91 We determined that the N-terminal portion of IpaB is necessary for stable expre

92 s T-antigen binding was localized within the N-terminal portion of IRS-1 molecule, and the binding wa

93 lice variants which encode proteins with the N-terminal portion of K-bZIP but lacking the C-terminal

94 The N-terminal portion of K-bZIP is derived from the K8 open

95 In addition, we find that the N-terminal portion of Klar is also important for functio

96 Strains lacking only the N-terminal portion of L11 grew well at physiological tem

97 The lipid A-binding N-terminal portion of lactoferrin (residues 1-33) induce

98 erved amino acid residues indicated that the N-terminal portion of LasR is required for multimerizati

99 ate that a fusion protein of the ACD and the N-terminal portion of lethal factor from Bacillus anthra

100 ine a nuclear localization domain within the N-terminal portion of Lsh.

101 d and positively charged residues within the N-terminal portion of MA constitute the membrane-binding

102 LS (FUS) and the related gene EWS encode the N-terminal portion of many fusion oncoproteins involved

103 o an unanticipated trans-acting role for the N-terminal portion of matrix in the formation of stable

104 110 kDa extracellular protein represents the N-terminal portion of mature Hap (designated Haps).

105 ex reveals that 3A6 primarily recognizes the N-terminal portion of MBP, in contrast with antimicrobia

106 A PB1 domain is encoded within the N-terminal portion of MEKK2, MEKK3, and MEK5.

107 d the interacting regions were mapped to the N-terminal portion of menin and amino acids 43 to 171 of

108 We report that the N-terminal portion of migfilin can bind all three human

109 One of these is the N-terminal portion of motif F and the second is a large

110 pha-beta FAD-binding motif is present in the N-terminal portion of mPAO.

111 The N-terminal portion of mPar3 exhibits strong microtubule

112 The N-terminal portion of NBD1 structure has an extra beta-s

113 ding motifs, or of the basic residues in the N-terminal portion of NC, abrogated assembly.

114 tion occurs on the cytoplasmically localized N-terminal portion of NDR1 and that this interaction is

115 The N-terminal portion of NIL-16 interacts selectively with

116 The N-terminal portion of Notch(IC) inhibited p50 DNA bindin

117 izes to the nucleus and that a region in the N-terminal portion of Notch(IC), not the six ankyrin rep

118 rmal tissues, the two antibodies against the N-terminal portion of NPM labeled the cytoplasm of neopl

119 of which recognize, by Western blotting, the N-terminal portion of NPM present in the NPM-ALK fusion

120 sion domain (RepD1) to a small region at the N-terminal portion of NRIF3 (residues 20 to 50).

121 al locus is inhibited in cells producing the N-terminal portion of Nuc from a multicopy plasmid.

122 Protease p29, derived from the N-terminal portion of ORF A, functions as a suppressor o

123 encing, while protease p48, derived from the N-terminal portion of ORF B, is required for viral RNA r

124 The N-terminal portion of ORF9 was found to be similar to a

125 The p50 protein is incorporated within the N-terminal portion of p105 and is a unique product of pr

126 utant Cdc37 gene products indicated that the N-terminal portion of p50(cdc37) interacted with immatur

127 The N-terminal portion of p64 has several potential binding

128 The N-terminal portion of parathyroid hormone is critical fo

129 The N-terminal portion of PDE3 can be arbitrarily divided in

130 The N-terminal portion of phosphodiesterase (PDE) 3 was arbi

131 The N-terminal portion of PiTX-K alpha has three fewer resid

132 gests that TCR recognition is focused on the N-terminal portion of pMART-1.

133 An N-terminal portion of PP1G was cloned by RT-PCR, and dif

134 al assembly domain (the M domain) within the N-terminal portion of Pr55Gag mediates the interaction o

135 ing epitopes located within the unstructured N-terminal portion of PrP(C) and those recognizing epito

136 age and was localized to a region within the N-terminal portion of PspA.

137 overall data support the hypothesis that the N-terminal portion of PTH is alpha-helical when bound to

138 N-terminal cleavage fragment shows that the N-terminal portion of Rad9 localizes in the cytosol, bin

139 Since the N-terminal portion of RAD9p was previously demonstrated

140 Here we report that the N-terminal portion of RAG1 has a distinct enzymatic role

141 5 weakens the direct association between the N-terminal portion of RbC (RbC(N)) and the marked-box do

142 le proteolytic fragments accumulate from the N-terminal portion of RecE.

143 - or C-terminal deletions, we found that the N-terminal portion of RepA is required for recognition.

144 all of which are prenylated, as well as the N-terminal portion of retinitis pigmentosa GTPase regula

145 The N-terminal portion of Rhizobium FtsZ polymerized in Esch

146 The N-terminal portion of RP1 stimulates the formation of mi

147 ction with a 75-kD protein (p75) required an N-terminal portion of RPS2 that is smaller than the regi

148 Our data indicate that the N-terminal portion of RsiV from amino acid 1 to 60, whic

149 lowing cleavage by the unknown protease, the N-terminal portion of RsiV requires further processing,

150 ocation has 752 amino acids and contains the N-terminal portion of RUNX1 (also known as AML1, CBFalph

151 These observations suggest that the N-terminal portion of S(mu)bp-2 which encompasses severa

152 brid system, CCTeta was found to bind to the N-terminal portion of sGC.

153 have determined the crystal structure of the N-terminal portion of SHARPIN, which adopts the highly c

154 It is shown here that the N-terminal portion of sigma(E), residues 1-153, binds co

155 An N-terminal portion of Sir1 (residues 27 to 149 [Sir1(27-

156 The N-terminal portion of Sp110 was homologous to two previo

157 show that the coiled-coil region within the N-terminal portion of SS4 is involved in both processes.

158 Over-expression of the N-terminal portion of SSDP1 (N-SSDP1), which contains th

159 This analysis demonstrates that the N-terminal portion of TdT, including the BRCA-1 C-termin

160 The ASPL-TFE3 fusion replaces the N-terminal portion of TFE3 by the fused ASPL sequences,

161 ionic interactions was found to connect the N-terminal portion of the 8th helix to the nearby NPXXY

162 the endonuclease activity is mediated by the N-terminal portion of the A subunit.

163 The R- mutations were all located in the N-terminal portion of the A subunit.

164 D/H polymorphism at residue 216 falls in the N-terminal portion of the AAA+ domain near the sensor 1

165 y, WH2 shares structural similarity with the N-terminal portion of the actin monomer-sequestering thy

166 rypsin-resistant peptide did not include the N-terminal portion of the AhR against which the antibody

167 The N-terminal portion of the alpha subunit and the majority

168 rnal region of the donor which coded for the N-terminal portion of the alpha-lac gene.

169 t Anxa2 mediates HSC adhesion mainly via the N-terminal portion of the Anxa2 peptide.

170 ibe a small set of amino acid sites from the N-terminal portion of the basic helix-loop-helix (bHLH)

171 The most pronounced difference is in the N-terminal portion of the beta4-beta5 loop, which is str

172 The structure reveals that the N-terminal portion of the BPS region binds as a pseudosu

173 CBR inhibitors target a crevice between the N-terminal portion of the bridge helix and a surrounding

174 n appendage domain that is inserted into the N-terminal portion of the catalytic domain, and a C-term

175 nd sequence a PCR product that coded for the N-terminal portion of the CF-chitinase.

176 nt from Asn1 to Ala7 (denoted domain 1), the N-terminal portion of the collagen domain from Gly8 to G

177 gion or interchain disulfide linkage; 2) the N-terminal portion of the collagen-like domain is requir

178 o species, reveal that the EGF motif and the N-terminal portion of the cytoplasmic domain are importa

179 The proximal helix and the N-terminal portion of the distal helix are found to be i

180 Very slow NH exchange for the N-terminal portion of the distal helix suggest that an i

181 hydrophobic groove, which interacts with the N-terminal portion of the divergent IQ1 and IQ2 motifs.

182 The N-terminal portion of the enzyme was capable of only uri

183 genous protein that is highly related to the N-terminal portion of the FeLV envelope protein, which i

184 he CD44-binding site is localized within the N-terminal portion of the fibrin beta chains, including

185 CNS disease associated with the N-terminal portion of the Fr98 env gene was preceded by

186 p120, and molecular dynamics showed that the N-terminal portion of the fusion peptide can be solvent-

187 cell-cell fusion mechanism and show that the N-terminal portion of the gH cytotail is critical for th

188 op participates in communication between the N-terminal portion of the helicase and the C-terminal ca

189 Furthermore, an N-terminal portion of the herbicide resistance gene 5-en

190 e papain-like protease p29, derived from the N-terminal portion of the hypovirus CHV1-EP713-encoded o

191 n M3R dimer that was cross-linked within the N-terminal portion of the i3 loop (264C) was functionall

192 This association involves the N-terminal portion of the intracellular tail of DAT and

193 Q2N antibodies, directed against a conserved N-terminal portion of the KCNQ2 polypeptide, to localize

194 These results indicate that the N-terminal portion of the large subunit of MBP contained

195 esidue 19, contribute to the capacity of the N-terminal portion of the ligand to interact with the ju

196 ecular effects on secondary structure in the N-terminal portion of the ligand.

197 The binding was further localized to the N-terminal portion of the M molecule.

198 The N-terminal portion of the M. catarrhalis acid phosphatas

199 uggest that the delta subunit N terminus and N-terminal portion of the M1 domain are, at least in par

200 respect to amino acid residue charge in the N-terminal portion of the mature protein has occurred re

201 H/DX protection, and only locally within the N-terminal portion of the MBD.

202 we determined the solution structure of the N-terminal portion of the MCM complex from the archaeon

203 contact between Cdc6 and MCM occurs via the N-terminal portion of the MCM protein.

204 The PTP domain is located in the N-terminal portion of the molecule and shares approximat

205 ect ovarian Sf9 cells induced to express the N-terminal portion of the molecule form MT-rich processe

206 nic interactions, localized primarily in the N-terminal portion of the molecule, enhance the stabilit

207 pterin aldolase function is expressed as the N-terminal portion of the multifunctional folic acid syn

208 of the Rel homology domain (RHD) within the N-terminal portion of the NF-kappa B 1 protein is requir

209 , which normally generates p50, degrades the N-terminal portion of the NF-kappa B 1 protein when the

210 Itch binds to the N-terminal portion of the Notch intracellular domain via

211 encode one methyltransferase, located at the N-terminal portion of the NS5 protein, to catalyze both

212 st two-hybrid system indicated that only the N-terminal portion of the p-55 domain is required for p-

213 All lack the N-terminal portion of the p21 core.

214 The N-terminal portion of the Pem HD, which includes the fir

215 , in which the Bpa residue is located in the N-terminal portion of the peptide, was used to define fu

216 rther assess the functional relevance of the N-terminal portion of the perforin molecule in its lytic

217 These results suggest the N-terminal portion of the perforin molecule to be an imp

218 Even more unusually, the N-terminal portion of the polypeptide chain is pinned to

219 in of the scaffolding subunit resides in the N-terminal portion of the polypeptide chain.

220 38), Cys(48), Cys(70), and Cys(72)] with the N-terminal portion of the potyvirus-encoded helper compo

221 Post-translational processing of the N-terminal portion of the predicted gene product to give

222 om the membrane bilayer, suggesting that the N-terminal portion of the presequence is essential for m

223 ation of a fusion protein (PF-MC) made up of N-terminal portion of the protease inhibitor Trappin-2 (

224 onstrate that despite massive changes in the N-terminal portion of the protein and in the DNA upstrea

225 The presence of the N-terminal portion of the protein appeared to promote at

226 eral SHANK3 missense mutations affecting the N-terminal portion of the protein by expression of wild-

227 The N-terminal portion of the protein is important for inter

228 region of Rgt1 physically interacts with the N-terminal portion of the protein that includes the DNA-

229 IcmR was found to bind to the N-terminal portion of the protein thus providing a mecha

230 gnal and was secreted by the T4SS, while the N-terminal portion of the protein was not secreted.

231 n Methanothermobacter thermautotrophicus the N-terminal portion of the protein was shown to be involv

232 Substitution of leucine for Lys-61 in the N-terminal portion of the protein, however, abolished th

233 requires the Acidic blob (AB) region in the N-terminal portion of the protein, indicating that the A

234 on sites of ICP27 appeared to cluster in the N-terminal portion of the protein, such that a frameshif

235 Some of these mutations occur in the N-terminal portion of the protein, the Mad homology 1 (M

236 r the archaeal protein it was shown that the N-terminal portion of the protein, which is composed of

237 e for the non-functional segment at the most N-terminal portion of the protein.

238 closely spaced transmembrane domains in the N-terminal portion of the protein.

239 , but also present within the poorly defined N-terminal portion of the protein.

240 The N-terminal portion of the PstDNV coat protein adopts a "

241 The results demonstrate that the N-terminal portion of the PTHrP molecule is responsible

242 nist, a synthetic lipopeptide comprising the N-terminal portion of the putative Mycobacterium leprae

243 The N-terminal portion of the putative protein product prese

244 ve genitotropic serovars possessed an intact N-terminal portion of the putative toxin gene.

245 ently developed a shortened CFTR missing the N-terminal portion of the R domain (residues 708-759, CF

246 on interaction with vitronectin, whereas the N-terminal portion of the reactive loop does not experie

247 ased on TREM2 and TYROBP fusion to the C- or N-terminal portion of the Renilla luciferase gene.

248 8)] is further divided into N-terminal [RS1: N-terminal portion of the RS domain (residues 198-227)]

249 RPK1 has been shown to polyphosphorylate the N-terminal portion of the RS domain (RS1) of the SR prot

250 of approximately a dozen serines in only the N-terminal portion of the RS domain (RS1).

251 ion of a short stretch of amino acids in the N-terminal portion of the RS domain of ASF/SF2 while Clk

252 The N-terminal portion of the seatbelt contains a small disu

253 ct E36 cells, whereas vectors containing the N-terminal portion of the SSAV SU protein and C-terminal

254 transmembrane domain 5 (TM5) and within the N-terminal portion of the third intracellular loop (i3 l

255 The N-terminal portion of the Toc75 transit peptide is suffi

256 The Wld(s) protein consists of the N-terminal portion of the ubiquitination factor Ube4b fu

257 es and limited proteolysis revealed that the N-terminal portion of the unassembled subunit is meta-st

258 raised against a repetitive sequence in the N-terminal portion of the WND molecule detects an additi

259 breakdown was inhibited by TIMP-1 or by the N-terminal portion of TIMP-3, although FGF-2 did not aff

260 ) binds to ssRNA, our studies imply that the N-terminal portion of TLR7 triggers a yet to be identifi

261 e compatible with involvement in vivo of the N-terminal portion of troponin I in enhancing force prod

262 1 and a CD36 agonist antibody but not by the N-terminal portion of TSP1, suggesting that CD36 or a re

263 howed that the complete TUSP protein and the N-terminal portion of TUSP are localized in the cytoplas

264 either the C-terminal portion of UCR1 or the N-terminal portion of UCR2 abolishes dimerization of PDE

265 coimmunoprecipitation assay to show that the N-terminal portion of UL9 can indeed directly interact w

266 teract via their C-terminal domains with the N-terminal portion of UPL3.

267 formation is contained within the cytosolic, N-terminal portion of V-ATPase subunit a (Stv1p).

268 SU, amino acids 83 to 116, encompassing the N-terminal portion of variable region A (VRA).

269 Here, the degree of motion in the N-terminal portion of Vik1 highly correlated with that i

270 The N-terminal portion of WAX2 is homologous with members of

271 Because the N-terminal portion of Wld(S) (N70) localized to axons, w

272 A small region in the N-terminal portion of xSLBP1 is required to stimulate tr

273 t a characterization of the structure of the N-terminal portion of yeast Sac1, containing the conserv

274 A interaction are mapped, revealing that the N-terminal portion of YY1 (amino acids 1-300) and the DN

275 Therefore, the N-terminal portion of Zcchc11, which lacks nucleotidyltr

276 e yeast two-hybrid system indicates that the N-terminal portions of cotton fiber GhCesA1 and GhCesA2

277 Taken together, these results identify N-terminal portions of FGF8 protein isoform for having t

278 Kinetic and NMR studies thus reveal that the N-terminal portions of FXIII AP (28-37) (V34 and V34L) a

279 The N-terminal portions of HAP form a beta-strand that inser

280 When coupled to microspheres, N-terminal portions of human A beta (A beta 1-16, A beta

281 teristic of much of the protection-eliciting N-terminal portions of PspA and PspC.

282 thetic peptides encompassing the central and N-terminal portions of the alpha1 chain.

283 Considering that the N-terminal portions of the core histones constitute site

284 en fluorescent protein (GFP)- or FLAG-tagged N-terminal portions of the Htt protein containing either

285 S. pneumoniae ClpXP in vivo, even though the N-terminal portions of the tags differ significantly bet

286 -helix crosses the OM first, followed by the N-terminal portions of the virulence protein.

287 Little similarity is present in the N-terminal portions of these peptides, which might sugge

288 tion of p105 is rapidly degraded whereas the N-terminal portion (p50) is left intact.

289 ll-down assay suggests an association of the N-terminal portion (Phe(120)-Phe(187)) of the D2 loop wi

290 The N-terminal portion, PTHrP-(1-34), retains all the calcio

291 onal roles have not yet been assigned to the N-terminal portion (residues 1-491; XPC-N).

292 o the register of the heptad repeat from the N-terminal portion (S1 path) of the molecule.

293 We investigated the role of the N-terminal portion (SS1) of the S5-S6 linkers in channel

294 r membrane protein with a long extracellular N-terminal portion that bears several ligand-binding dom

295 hatase activity and a proteolytically labile N-terminal portion that functions to enhance the affinit

296 by proteins with distinct homology in their N-terminal portion to bacterial Type IV pilins.

297 partite architecture consisting of a soluble N-terminal portion (TprC(N)), presumably periplasmic and

298 gnal peptides, were identical; the remaining N-terminal portions were gene specific.

299 zed by a conserved tripartite motif in their N-terminal portion which comprises a canonical RING doma