ライフサイエンスコーパス: C-terminal portion

1 able" distal helix may be valid only for the C-terminal portion.

2 ation of wild-type gene 37 inserted into its C-terminal portion.

3 NA polymerases (RdRps) in its nonoverlapping C-terminal portion.

4 2 peptide, whereas Rcf1 is homologous to the C-terminal portion.

5 r domain, and a DNA polymerase domain in the C-terminal portion.

6 id sequence identity to known cyclins in the C-terminal portion.

7 near the conserved CxxC or RHR motif in the C-terminal portion.

8 the E3 ligase activity and integrity of the C-terminal portion.

9 rylation sites and a more ordered and folded C-terminal portion.

10 N terminus of the MC160 protein but not the C-terminal portion.

11 e-homeobox domain of DUX4 but splice-out the C-terminal portion.

12 ess a conserved cis-proline located in their C-terminal portions.

13 ndependent genes corresponding to the N- and C-terminal portions.

14 Importantly, the Rad52 C-terminal portion alone can promote Rad51 presynaptic f

15 This interaction was refined to the C-terminal portion (amino acids 348-588) of ATDC and the

16 kely corresponding to the cytoplasmic N- and C-terminal portions, and a more compact domain, correspo

17 , whereas none of the lysine residues in the C-terminal portion are protected.

18 motifs in the membrane-distal, nonstructural C-terminal portions are required for the exit from the E

19 Its C-terminal portion (CNK(C-term)) directly binds to RAF.

20 ORF57 interacts directly with the RBM15 C-terminal portion containing the SPOC domain to reduce

21 The C-terminal portion contributes further to hTAP's nuclear

22 The third antibody recognizes the C-terminal portion (deleted in NPM-ALK) and reacts only

23 ombinant human Slit-2 protein and the N- and C-terminal portions generated by in vivo proteolytic pro

24 hobic amino acid residues in the core of the C-terminal portion generates a protein with enhanced sta

25 iffers mainly in the presence of an extended C-terminal portion incorporating four closely spaced O-l

26 st large areas of p101 including both N- and C-terminal portions interact with the N-terminal half of

27 sted antiparallel beta-barrel with the N and C-terminal portions interacting with adjacent subunits.

28 ef heart mitochondrial F(1)-ATPase where the C-terminal portion is arranged as a two-alpha-helix hair

29 of CD151 we established that the cytoplasmic C-terminal portion is critical for activity of CD151 tow

30 to the C-terminus during secretion, and the C-terminal portion is critical to the co-dependent secre

31 We conclude that the intracellular Ctp1 C-terminal portion is essential for clipping, while the

32 hat the conserved T-box domain, with a small C-terminal portion, is required for recruiting histone m

33 Within the C-terminal portion, modification of four amino acids in

34 inuclear zinc center that is situated at the C-terminal portion of a "TIM" barrel motif.

35 The nucleotide is situated at the C-terminal portion of a five-stranded parallel beta-shee

36 UNC-96 and LIM-8 also bind to the C-terminal portion of a myosin heavy chain (MHC), MHC A,

37 e report that UNC-98 also interacts with the C-terminal portion of a myosin heavy chain.

38 The C-terminal portion of Aap contains a 135-aa-long, prolin

39 elength anomalous dispersion, shows that the C-terminal portion of AhpF (residues 210-521) is structu

40 pended substrate, first being reduced by the C-terminal portion of AhpF, and subsequently reducing Ah

41 Deletion mutants showed the C-terminal portion of apoptosis signal-regulating kinase

42 Missense mutations in the C-terminal portion of ATP7A have also been shown to caus

43 iction algorithm suggest that the functional C-terminal portion of AvrRpt2 is a cysteine protease.

44 The C-terminal portion of Bcd(A57-61) is required to mediate

45 anslational modifications in the lysine-rich C-terminal portion of beta.

46 ibitors of the interaction between BRCT (the C-terminal portion of BRCA1, a key tumor suppressor prot

47 Exclusion of the C-terminal portion of CALM from the fusion protein, whic

48 We also show that PBP interacts with the C-terminal portion of CAR, suggesting that PBP is involv

49 r HHV-6 receptor activity reside outside the C-terminal portion of CD46.

50 ing and primarily consist of residues in the C-terminal portion of CheY.

51 One residue in the C-terminal portion of CNT2 was found to significantly co

52 complement cascade, primarily recognize the C-terminal portion of DEK protein and exhibit higher aff

53 complement cascade, primarily recognize the C-terminal portion of DEK protein, and exhibit higher af

54 Second, we observed that the C-terminal portion of delta, which forms a jelly-roll be

55 rly postnatal, but not adult induction, of a C-terminal portion of DISC1 in mice results in a cluster

56 3-prime fragments that encode the conserved C-terminal portion of DUX4 and (iii) capped and polyaden

57 CCR5 ECL2-derived peptides, we show that the C-terminal portion of ECL2 (2C, comprising amino acids C

58 The C-terminal portion of EiAPR, expressed separately, exhib

59 is located in an unstructured region of the C-terminal portion of eIF4G1 that coordinates assembly o

60 Mutant mice in which the C-terminal portion of EphB2 is truncated had an intermed

61 is the autonomously expressed, noncatalytic C-terminal portion of FAK.

62 shorter segments of FGF-1 sequences into the C-terminal portion of FGF-7 or FGF-10 revealed that subs

63 one hybrid experiments demonstrated that the C-terminal portion of FL functions in transcriptional ac

64 The C-terminal portion of FSA shares a striking sequence sim

65 ant in a priA mutant by mutating dif and the C-terminal portion of ftsK.

66 ine-binding domain of FRS2alpha fused to the C-terminal portion of Gab1, the region including the bin

67 DE5Delta1-465 contained the C domain and the C-terminal portion of GAF-B; and PDE5Delta1-534 containe

68 Exposed residues in the C-terminal portion of GCAP1, including EF-hand 4 and the

69 ther, these data suggest that targets in the C-terminal portion of Gln3 required for the Gln3-Tor1 in

70 f in fork binding and the interaction of the C-terminal portion of gp59 with helicase and SSB.

71 he duplex DNA ahead of the fork, whereas the C-terminal portion of gp59 would provide the docking sit

72 In addition, the C-terminal portion of gp7 shows conformational flexibili

73 dicate that the peptide corresponding to the C-terminal portion of GpIbalpha and the entire extracell

74 We further discovered that the C-terminal portion of hCCCAP is identical to the human c

75 The C-terminal portion of helix 3, which connects to the COR

76 in shows a close association of helix-1, the C-terminal portion of helix-2 and the N-terminal portion

77 the START domain present in the cytoplasmic C-terminal portion of human MLN64.

78 Here we present the crystal structure of the C-terminal portion of human POT1 (POT1C) complexed with

79 We studied the C-terminal portion of human TSP2 from the third EGF-like

80 that two additional forms consisting of the C-terminal portion of ICP34.5 are generated in infected

81 involved in binding of IFN-alpha2b while the C-terminal portion of IFN is critical for antiproliferat

82 IKKgamma-binding domain (NBD/gammaBD) in the C-terminal portion of IKKbeta in MEFs deficient in IKKbe

83 Abs that recognized epitopes located in the C-terminal portion of LAGE-1, which is distinct from NY-

84 structure at 1.5 A of the immunosuppressive C-terminal portion of Lassa virus NP and illustrate that

85 binding of LPL to GPIHBP1 requires only the C-terminal portion of LPL and does not depend on full-le

86 LPL binding to GPIHBP1, suggesting that the C-terminal portion of LPL is important for GPIHBP1 bindi

87 The C-terminal portion of M13 becomes alpha-helical and deve

88 The C-terminal portion of maize CENPC shares similarity with

89 y and exhibit structural similarity with the C-terminal portion of major group 1 allergens.

90 other autotransporter proteins, whereas the C-terminal portion of MapA resembled the translocation d

91 sites) in the first 294 residues, while the C-terminal portion of MeCP2 (residues 295 to 486) contai

92 ant vaccine, bvMSP1(42), based on the 42-kDa C-terminal portion of MSP1, was expressed as a secreted

93 olved single-amino-acid substitutions in the C-terminal portion of nsP2, the viral helicase-protease.

94 Finally, modeling the remaining C-terminal portion of Nup157 shows that it projects as a

95 stitutively turned on due to the loss of the C-terminal portion of p100.

96 ightly regulated by sequences located at the C-terminal portion of p100.

97 Although the C-terminal portion of P2X7 is thought to be essential fo

98 that the C-terminal part of Vpr binds to the C-terminal portion of p300/CBP within amino acids 2045 t

99 structure of the p55 domain extends into the C-terminal portion of p33.

100 immature HRI, but not with Hsp90, while the C-terminal portion of p50(cdc37) interacted with Hsp90.

101 We now report that deletion of the C-terminal portion of p69, which encodes the highly basi

102 s H3 and H4 interact preferentially with the C-terminal portion of PARP1 protein and that the N-termi

103 nd C/H3 domains of CBP and p300 and with the C-terminal portion of PBP that encompasses amino acids 1

104 Moreover, the data indicate that the unique C-terminal portion of perilipin A is responsible for its

105 technique revealed the interface between the C-terminal portion of Pgamma and AIPL1-TPR.

106 mAb102.1F10 bound the C-terminal portion of Phl p 7 in a calcium-dependent man

107 also requires pXI, which is identical to the C-terminal portion of pI.

108 The C-terminal portion of pIII, termed the "C" domain, is re

109 milk a malaria vaccine candidate, the 42-kDa C-terminal portion of Plasmodium falciparum merozoite su

110 An apoptotic function was localized to the C-terminal portion of PR3.

111 Thus, the C-terminal portion of PSD-95 serves a dual function.

112 human T-cell lymphomas, and we show that the C-terminal portion of RAG2 is required for this.

113 The co-localization did not occur when the C-terminal portion of RetGC1, containing its regulatory

114 etention signal is likely present within the C-terminal portion of RyR, a region that contains four p

115 use of GPS-linker scanning mutagenesis, the C-terminal portion of SadB was shown to be dispensable f

116 eral regulators have been shown to contact a C-terminal portion of sigma(70) that harbors conserved r

117 ed by SIKE phosphorylation, clustered in the C-terminal portion of SIKE (Ser-133, -185, -187, -188, -

118 at least 4 LIM domains in FHL2, whereas the C-terminal portion of SK1 mediates the binding of FHL2 i

119 gest that glypican binding to the releasable C-terminal portion of Slit may serve as a mechanism for

120 We show that the C-terminal portion of Sox10 is sufficient to mediate thi

121 P16-PRLBD and VP16-GRLBD interacted with the C-terminal portion of steroid receptor coactivator-1, th

122 Expression of the C-terminal portion of STIM1 with Orai1 was sufficient to

123 A sequence motif within the C-terminal portion of Streptococcus gordonii SspB (AgI/I

124 xpressing high levels of HSPGs mapped to the C-terminal portion of SU.

125 and peptides corresponding to the conserved C-terminal portion of T. maritima FliF.

126 Here, we show that the C-terminal portion of TG2 directly interacted with the G

127 ry module" and specific sequences within the C-terminal portion of the "regulatory module" of HSL (am

128 moves one residue from an alpha-helix in the C-terminal portion of the AAA+ domain.

129 of TraR contributing to TraM binding to the C-terminal portion of the activator protein.

130 zation of the TfR binding site on HFE to the C-terminal portion of the alpha1 domain helix and an adj

131 high-affinity binding to DR6 requires a more C-terminal portion of the APP ectodomain.

132 30-amino acid peptides corresponding to the C-terminal portion of the beta- and/or gamma-rat epithel

133 required for activity are positioned at the C-terminal portion of the beta-barrel.

134 n bacterial intimin-like proteins and on the C-terminal portion of the BsaB protein.

135 f norepinephrine leads to an ordering of the C-terminal portion of the C-terminal domain into an alph

136 ch other and highlight the importance of the C-terminal portion of the C-terminal lobe in this intera

137 lmodulin and alpha-actinin bind to the short C-terminal portion of the C0 region of NR1.

138 DRBMs) of ADAR1 while the second maps to the C-terminal portion of the catalytic domain.

139 The C-terminal portion of the chain plays an important role

140 nt changes in structure were detected in the C-terminal portion of the channel upon activation of the

141 In contrast, the C-terminal portion of the checkpoint protein RAD9p is es

142 omain from Gly8 to Gly44 (domain 2), and the C-terminal portion of the collagen-like domain from Gly4

143 of a 111-amino acid peptide derived from the C-terminal portion of the cystic fibrosis transmembrane

144 functions of LIN-3 in all tissues, while the C-terminal portion of the cytoplasmic domain is involved

145 region (residues 34 and 43), and one in the C-terminal portion of the ectodomain (residue 277).

146 coiled coils via interactions throughout the C-terminal portion of the ectodomain.

147 on, possibly by chemical modification of the C-terminal portion of the enzyme containing the TIMP-1 b

148 We further demonstrate that the C-terminal portion of the enzyme is disordered and not e

149 ers encodes an Arg to Cys replacement in the C-terminal portion of the extracellular domain of neurol

150 Expression of the region encoding the C-terminal portion of the FCV ORF1 (amino acids 942 to 1

151 The C-terminal portion of the fibrin alpha chain extends int

152 Site-directed mutagenesis indicated that the C-terminal portion of the first transmembrane domain was

153 ition from alpha-helix to 3(10) helix in the C-terminal portion of the fourth transmembrane helix.

154 A peptide containing the C-terminal portion of the FtsA divisome protein is a sub

155 ort that the SCAN domain is derived from the C-terminal portion of the gag capsid (CA) protein from t

156 acid residue extension corresponding to the C-terminal portion of the Gag p10 protein, has been dete

157 Internal deletion of the C-terminal portion of the Gag p10 region resulted in the

158 tide, Gly-Pro-Arg-Pro-Pro, that binds to the C-terminal portion of the gamma-chain of fibrin can dete

159 -chain, N-terminal peptide that binds to the C-terminal portion of the gamma-chain of fibrin has been

160 high level of endogenous proteolysis at the C-terminal portion of the GFP-Spf1 molecule that abolish

161 the minimal PY-NLS in yeast consists of the C-terminal portion of the human consensus, R/H/KX(2-5)PY

162 LR, viable M. genitalium and the recombinant C-terminal portion of the immunogenic protein MG309 (rMG

163 Finally, we demonstrate that the C-terminal portion of the inv(16) fusion protein contain

164 escribed by a "two-site" model, in which the C-terminal portion of the ligand interacts with the N-te

165 obes located on the C-terminal helix and the C-terminal portion of the linker increased further as a

166 asparagine for glutamine at codon 322 of the C-terminal portion of the LMP1 gene.

167 sus AvrRpm1 specificity is determined by the C-terminal portion of the LRR domain.

168 (2+) is characterized by condensation of the C-terminal portion of the metal-binding loops with monod

169 ltiprotein-binding scaffold exhibited by the C-terminal portion of the MICALs represents a unique com

170 4 to bind peptide sequences derived from the C-terminal portion of the MIIA rod with submicromolar af

171 Many mutations affecting the C-terminal portion of the molecule block the pre-B-trans

172 On A. fumigatus, PTX3 exposed the C-terminal portion of the molecule, probably resulting i

173 ding solid-supported synthesis to access the C-terminal portion of the molecule.

174 The C-terminal portion of the Mus308 polypeptide encodes a D

175 Truncation of the C-terminal portion of the N protein by protease digestio

176 t the C terminus of CD2AP interacts with the C-terminal portion of the nephrin cytoplasmic domain.

177 The C-terminal portion of the NG2 cytoplasmic domain, theref

178 hat CheZ localization requires the truncated C-terminal portion of the P1 domain present in CheA(S).

179 resides within a 70-amino acid domain in the C-terminal portion of the p10 region of Gag, and in vitr

180 ow mapped the nuclear export activity to the C-terminal portion of the p10 sequence and identified th

181 ripts expressed a p8 minicore containing the C-terminal portion of the p21 core protein and lacking t

182 o-acid truncated protein containing only the C-terminal portion of the passenger domain and the entir

183 the present study, we demonstrated that the C-terminal portion of the PB1-F2 protein binds to MAVS i

184 g synthetic peptides derived from the active C-terminal portion of the PB1-F2 protein from those two

185 subunit is homologous to the I subunit, the C-terminal portion of the pea D was used for antigen pro

186 The conserved C-terminal portion of the peptide is biochemically stabl

187 I20 are in agreement with a location of the C-terminal portion of the peptide near the lipid/water i

188 l-l-phenylalanine (Bpa) in position 8 of the C-terminal portion of the peptide was identified previou

189 Ca(2+) is to increase the interaction of the C-terminal portion of the peptide with the N-terminal lo

190 a transmembrane fusion protein encoding the C-terminal portion of the PKD1 cytoplasmic tail, PKD1(11

191 The cytoplasmic C-terminal portion of the polycystin-1 polypeptide (PKD1

192 Our results suggest that the C-terminal portion of the pore region within the alpha-s

193 In contrast, the C-terminal portion of the predicted PerA protein that co

194 onserved domains have been identified in the C-terminal portion of the preToc75 transit peptide from

195 ot appear to require its PH domain since the C-terminal portion of the protein (CRAC-DeltaPH) can sub

196 In particular, the C-terminal portion of the protein (Met-135-Gly-248) is s

197 fied an insertion (hap2-1) that disrupts the C-terminal portion of the protein and tags mutant pollen

198 il of LDLR, and that conserved motifs in the C-terminal portion of the protein bind to clathrin and t

199 ndicate that fragments of Hrs containing the C-terminal portion of the protein can potently inhibit H

200 s, but work by others had suggested that the C-terminal portion of the protein contains a single surf

201 The C-terminal portion of the protein has homology to glutat

202 kinase A of the beta-subunit of eIF2 in the C-terminal portion of the protein increased the guanine

203 In contrast, the C-terminal portion of the protein that harbors at least

204 ns of the illness, antibody responses to the C-terminal portion of the protein were more prominent.

205 Six highly conserved residues in the C-terminal portion of the protein were mutated to alanin

206 generated against an epitope in the deleted, C-terminal portion of the protein, these antibodies did

207 ominant negative form of PYK2 containing the C-terminal portion of the protein, which binds paxillin

208 334 and 504 that is apparently masked by the C-terminal portion of the protein, which includes six re

209 N-terminal portion and the LIM domain in the C-terminal portion of the protein.

210 ange from valine to glutamic acid within the C-terminal portion of the protein.

211 o-acceptor sites in HDAC2 are located in the C-terminal portion of the protein.

212 s identified a transactivation domain in the C-terminal portion of the protein.

213 poA-I cysteine substitution mutations in the C-terminal portion of the protein.

214 ted that the cleavage site is located in the C-terminal portion of the protein.

215 domain for ligand at a site adjacent to the C-terminal portion of the RGD triad.

216 re and sequence optimization to redesign the C-terminal portion of the RGS14 GoLoco motif peptide so

217 ain (residues 198-227)] and C-terminal [RS2: C-terminal portion of the RS domain (residues 228-248)]

218 y N-terminal domains, phosphorylation of the C-terminal portion of the RS domain (RS2) by the nuclear

219 novel ETS-interacting subdomain (EID) in the C-terminal portion of the Runt homology domain (RHD) in

220 in two distinct cytoplasmic M3R regions, the C-terminal portion of the second intracellular loop (i2)

221 n of small varphi-values for residues in the C-terminal portion of the sequence (residues 35-76), cou

222 Remarkably, the C-terminal portion of the sequence in the protease domai

223 AsiA binds tightly within the C-terminal portion of the sigma70 subunit of RNA polymer

224 the surprising finding that swapping a small C-terminal portion of the tail between IIA and IIB inver

225 teract with amino acids contained within the C-terminal portion of the third extracellular domain (ED

226 tracellular loop and a second Cys within the C-terminal portion of the third intracellular loop, at p

227 erol-binding region is located partly at the C-terminal portion of the TMD and partly in the first am

228 fied by site-directed mutagenesis within the C-terminal portion of the tNOX protein corresponding to

229 nce of a dileucine recognition signal in the C-terminal portion of the tyrosinase molecule.

230 ur isoforms that differ in the length of the C-terminal portion of their extracellular domains.

231 ion mutants revealed that the 141-amino-acid C-terminal portion of this protein was capable of target

232 l features indicative of active kinases, the C-terminal portion of this segment sterically restricts

233 The C-terminal portion of titin is closely associated with t

234 n induces a major rotational movement of the C-terminal portion of TM VII and increases the proximity

235 E6 requires the same C-terminal portion of TNF R1 for binding as does TNF R1-

236 and mutations in residues 160 and 163 in the C-terminal portion of TNT1 adjacent to the cTnT H1-H2 li

237 ch contained one Cys substitution within the C-terminal portion of transmembrane domain (TM) VII (Val

238 nsmembrane domain 1 (M1) and domain 2 in the C-terminal portion of transmembrane domain 2 (M2) and th

239 Deletion of the C-terminal portion of TRIM56 abrogated the TRIM56-TRIF i

240 a virus (MLV), whereas overexpression of the C-terminal portion of TSG101 (TSG-3') potently disrupts

241 Furthermore, overexpression of the C-terminal portion of TSG101 (TSG-3') potently inhibits

242 The crystal structure for the C-terminal portion of Tup1 has been solved and, when seq

243 The C-terminal portion of Ty3 RT encodes a functional RNase

244 Internal deletions of either the C-terminal portion of UCR1 or the N-terminal portion of

245 S-transferase (GST) fused to the cytoplasmic C-terminal portion of UhpB, results in complete blockage

246 ssing the RCC1 homology domain followed by a C-terminal portion of variable lengths and sequences.

247 In contrast, high deuteration levels in the C-terminal portion of Vif indicated that this region was

248 Mutational analysis showed that the C-terminal portion of Vpr, known to harbor its cell cycl

249 In contrast, MT binding masked the C-terminal portion of WHAMM and prevented it from promot

250 The C-terminal portion of XPC (residues 492-940; XPC-C) has

251 NF reacts with antibodies to both the N- and C-terminal portions of actin on Western blots and migrat

252 Mainly the C-terminal portions of both CcmI and apocytochrome c(2)

253 quence analysis predicts that regions in the C-terminal portions of both MPs and MPt have high probab

254 The C-terminal portions of both toxins are composed of 20 an

255 phorylated fragments representing the N- and C-terminal portions of DMP1 have been identified, appare

256 half of dynamin-2 PRD but to both the N- and C-terminal portions of dynamin-1 PRD.

257 sion of FH, miniFH, contains only the N- and C-terminal portions of FH linked by an optimized peptide

258 ts of SNV and ANDV NPcore exclude the N- and C-terminal portions of full polypeptide to obtain stable

259 N- and C-terminal portions of mammalian G(i2) and G(16) were su

260 QSTM1 (sequestosome)-Nup214, both containing C-terminal portions of Nup214.

261 Mutants with alterations in both the N- and C-terminal portions of p12 exhibited a distinct phenotyp

262 ding frames that are predicted to encode the C-terminal portions of sensor kinases.

263 conclude that domains located in the N- and C-terminal portions of the Ac45 protein direct its traff

264 demarcation of the roles between the N- and C-terminal portions of the antibiotic was determined as

265 ns in ubiquitin and E6AP, both in the N- and C-terminal portions of the catalytic domain, that are im

266 The structure shows that the N- and C-terminal portions of the GAP homologous regions togeth

267 Env function when inserted in the center or C-terminal portions of the hypervariable domain.

268 ins encompassing the N-terminal, middle, and C-terminal portions of the keratin 14 protein.

269 ins homologous with either the N-terminal or C-terminal portions of the M. bovis FbiC.

270 stabilize the monomer through contacts with C-terminal portions of the motor or recruit other compon

271 amined, only peptides representing the N-and C-terminal portions of the protein had the ability to so

272 of an interaction between the N-terminal and C-terminal portions of the protein that is required for

273 Significant N- and C-terminal portions of the protein were found to be disp

274 Here we demonstrate that the SIX domains and C-terminal portions of the SO and OPTIX proteins are req

275 r procedure contained the N-terminal and the C-terminal portions of the tagged luciferase.

276 Alanine substitutions in the N-terminal and C-terminal portions of the tail had no effect on either

277 there exist important functional domains in C-terminal portions of the Tbx3 protein that affect its

278 s suggested that sequences in both the N and C-terminal portions of the VP5 sequence contribute to th

279 Interestingly, the C-terminal portions of these H-N-H phage endonucleases c

280 that a direct interaction between the N- and C-terminal portions of UL9 might exist and serve to modu

281 The C-terminal portion (p55 domain) of wild-type p88 VacA co

282 lar growth in macrophages, where the Mh3881c C-terminal portion plays a critical role.

283 A binding domains (stau-RBD) but lacking the C-terminal portion potentially involved in dendritic tar

284 nstitute the prion domain, and the remaining C-terminal portion regulates nitrogen catabolism.

285 nal region (residues 1-71) and a well-folded C-terminal portion (residues 72-159).

286 n elongation results as a consequence of the C-terminal portion separating from the rest of the molec

287 t the site of interaction may lie within the C-terminal portion that is common to all NfeD homologues

288 g of two C2 domains and a core domain in the C-terminal portion that is homologous to the A domain fo

289 inding to the full-length protein and to the C-terminal portion that is released from the cell membra

290 MotA interact with region 4 of sigma70, the C-terminal portion that normally contacts -35 DNA and th

291 s necessary for RNA editing events include a C-terminal portion that shares structural characteristic

292 ion activity, which can be suppressed by its C-terminal portion via an intramolecular interaction.

293 Six CHFI mutants lacking different N- and C-terminal portions were generated.

294 bunits associate with alpha primarily in its C-terminal portion, which has a unique structure and the

295 targeting of the long isoform of TSLP at the C-terminal portion, which is common to both isoforms, mi

296 ntromere localization of SYCP2L requires its C-terminal portion, which is missing in truncated varian

297 erminal RING domain and the integrity of its C-terminal portion, while the restriction of HCoV-OC43 r

298 ns, and a > or =200 amino acid intracellular C-terminal portion with several phosphorylation signalin

299 ges that alter the interaction of the mobile C-terminal portion with the active site.

300 TUSP are localized in the cytoplasm but the C-terminal portion with the two NLSs produced distinct d