ライフサイエンスコーパス: carboxyl-terminal

1 ys indicate that BKIP-1 interacts with SLO-2 carboxyl terminal.

2 e of substrate delivery, which begins at the carboxyl-terminal.

3 Further analysis suggests that the carboxyl-terminal 100 amino acids of Cpr6 and Cpr7 are c

4 hesis, isopropylmalate synthase, missing the carboxyl-terminal 160 amino acids.

5 ORF33-binding domain to the highly conserved carboxyl-terminal 19 amino acids (aa) of ORF45 and the U

6 equires protein synthesis, the presence of a carboxyl-terminal 27-amino acid region of UVR8, and the

7 nduced cell fusion caused by deletion of the carboxyl-terminal 28 amino acids of gB or the dominant s

8 pe of the mutant virus gBDelta28 lacking the carboxyl-terminal 28 amino acids of gB.

9 recombinant virus carrying a deletion of the carboxyl-terminal 29 amino acids of gD (gDDeltact) and t

10 that differ only in the region encoding the carboxyl-terminal 36-40-amino acid residues.

11 reports, RNPs with N truncations lacking the carboxyl-terminal 43-residues harboring the MoRE domain

12 Deletion of the carboxyl-terminal 66 amino acids of BGLF2 reduced the ab

13 time, was concentrated within the functional carboxyl-terminal activating regions 2 and 3 (CTAR2 and

14 This study reveals that LMP1, through its carboxyl-terminal activation domain 1 (LMP1-CTAR1), acti

15 ppaB binding to the RON promoter through its carboxyl-terminal activation region 1 to induce expressi

16 n between the amino-terminal FXXLF motif and carboxyl-terminal AF-2 domain (N/C interaction) prevente

17 modifies the nascent polypeptide by adding a carboxyl-terminal alanine and threonine (CAT) tail throu

18 vivin by interacting with Glu-126 within its carboxyl-terminal alpha helix.

19 inesterase (AChE) family, ChEL possesses two carboxyl-terminal alpha-helices.

20 eviates from the canonical 5 beta-strand and carboxyl-terminal alpha-helix topology of all other CsrA

21 In particular, the carboxyl-terminal amino acid Arg of the inhibitor is coo

22 p (ubiquitin-like) domains (D2 and D3) and a carboxyl-terminal amphipathic helix, a domain arrangemen

23 nstraining its position and sequestering the carboxyl-terminal amphipathic helix.

24 orrect disulfide bonds in the noncollagenous carboxyl-terminal and amino-terminal propeptides.

25 The histone variant macroH2A1 contains a carboxyl-terminal approximately 30-kDa domain called a m

26 meabilized ATP7A(P1386S) fibroblasts bound a carboxyl-terminal ATP7A antibody, consistent with reloca

27 4, (ii) the amino-terminal cysteine-rich and carboxyl-terminal basic domains of ORF31 mediate the ORF

28 s complex are the OMP BamA [which contains a carboxyl-terminal beta-barrel and an amino-terminal peri

29 Truncation of the Uba1 carboxyl-terminal beta-grasp domain reduces cognate Ubc2

30 Carboxyl-terminal binding protein 1 (CtBP1) has been sho

31 Carboxyl-terminal-binding protein-1 (CtBP1) is a transcr

32 dergoes both amino terminal (N-terminal) and carboxyl terminal (C-terminal) proteolytic modifications

33 t for normal growth and directly targets the carboxyl-terminal (C-terminal) domain of Rpt1 of the Rpt

34 ries of posttranslational modifications at a carboxyl-terminal CaaX motif: prenylation at cysteine, p

35 s-associated speck-like protein containing a carboxyl-terminal caspase recruitment domain- and NLRP3-

36 s-associated speck-like protein containing a carboxyl-terminal caspase-recruitment domain, and caspas

37 e guiding hypothesis of this study is that a carboxyl-terminal cleavage product of the cardiac L-type

38 es its proapoptotic function and generates a carboxyl-terminal cleavage product, acCED-8, that promot

39 pendent ubiquitination of Ret51, whereas the carboxyl-terminal coiled-coil domain of CD2AP was dispen

40 esylated progerin (Lmna(csmHG)) in which the carboxyl-terminal -CSIM motif was changed to -CSM.

41 gerin (Lmna(nHG/+) mice, in which progerin's carboxyl-terminal -CSIM motif was changed to -SSIM) also

42 A peptide mimetic of the carboxyl terminal (CT) of Cx43, incorporating a postsyna

43 ect interaction of protein partners with the carboxyl-terminal (CT) domain.

44 nnels are characterized by the presence of a carboxyl-terminal cyclic nucleotide-binding domain (CNBD

45 such as addition of an isoprenyl lipid to a carboxyl-terminal cysteine in proteins that terminate wi

46 n is the posttranslational modification of a carboxyl-terminal cysteine residue of proteins that term

47 Here, we show that the carboxyl-terminal cysteine-rich (CCR) domain of this pro

48 eceptor is unique in having an intracellular carboxyl-terminal cysteine-rich region (Ccys).

49 erved, 10-residue sequence in the receptor's carboxyl-terminal cytoplasmic tail.

50 Importantly, a carboxyl terminal deletion mutant of Lin28 that retains

51 The carboxyl-terminal di-arginine motif (Arg-186 and Arg-187

52 7A and that binding is mediated in part by a carboxyl-terminal di-leucine motif.

53 356 of cdAE1) lacking the amino-terminal and carboxyl-terminal disordered regions, produced at physio

54 at phosphorylation of tyrosine Tyr253 in the carboxyl terminal domain, confirmed by Western blot, act

55 e amino terminal, the tandem repeat, and the carboxyl terminal domain, with each domain having unique

56 , PyrD and PyrR; PyrR proteins have an extra carboxyl-terminal domain (COG3236) of unknown function.

57 between the phosphorylated RNA polymerase II carboxyl-terminal domain (CTD) and cellular capping enzy

58 hosphorylates the RNA polymerase II (Pol II) carboxyl-terminal domain (CTD) and the processivity fact

59 (5)P(6)S(7) repeats of the RNA polymerase II carboxyl-terminal domain (CTD) comprise an informational

60 (5)P(6)S(7) repeats of the RNA polymerase II carboxyl-terminal domain (CTD) convey information about

61 Mutational analyses have indicated that the carboxyl-terminal domain (CTD) of hepadnavirus core prot

62 Mutational analyses have suggested that the carboxyl-terminal domain (CTD) of hepadnavirus core prot

63 BRD4 is an atypical kinase that binds to the carboxyl-terminal domain (CTD) of RNA polymerase II and

64 The carboxyl-terminal domain (CTD) of the largest subunit of

65 The carboxyl-terminal domain (CTD) of the largest subunit of

66 We found that TRPV1 with the carboxyl-terminal domain (CTD) of TRPV3 retained heat ac

67 ell division, alters RNA polymerase (Pol) II carboxyl-terminal domain (CTD) phosphorylation, and repr

68 egulatory domain for Brd4 in addition to the carboxyl-terminal domain (CTD) that interacts with pTEFb

69 ping enzymes, the RNA polymerase II (Pol II) carboxyl-terminal domain (CTD), elongation factor Spt5,

70 oes not absolutely require the non-conserved carboxyl-terminal domain (CTD), which is necessary for r

71 el-forming transmembrane domain (TMD), and a carboxyl-terminal domain (CTD).

72 d a SPOUT methyltransferase family catalytic carboxyl-terminal domain (CTD).

73 Structural elements in both the distal carboxyl-terminal domain and channel core were identifie

74 gating process, channels lacking the distal carboxyl-terminal domain are no longer regulated by the

75 .5 interacts with IKKalpha/beta, whereas the carboxyl-terminal domain binds to protein phosphatase 1.

76 il-attachment domain, a slender shaft, and a carboxyl-terminal domain composed of several nodules.

77 bind to tissues in a manner dependent on the carboxyl-terminal domain containing short consensus repe

78 ence of P3H1: an amino-terminal domain and a carboxyl-terminal domain corresponding to the 2-oxogluta

79 ctor receptor-1 binding site but lacking the carboxyl-terminal domain encoding the heparin-binding do

80 ding and catalytic motifs, the isolated TlyA carboxyl-terminal domain exhibits no detectable affinity

81 importance of conformational changes in the carboxyl-terminal domain for catalysis.

82 genes encoding the full-length VgrG1 and its carboxyl-terminal domain in HeLa Tet-Off cells disrupted

83 ally occurring DLX3 mutant that disrupts the carboxyl-terminal domain leading to tricho-dento-osseous

84 the present study we identify Tyr-610 in the carboxyl-terminal domain of BAK1 as a major site of auto

85 These results suggest that the carboxyl-terminal domain of Cav2.1 is not essential for

86 one H3 at Ser(10) In addition, targeting the carboxyl-terminal domain of CS-GRP78 with a mAb suppress

87 Here, we biophysically characterize the carboxyl-terminal domain of Cx45 (Cx45CT).

88 binds to eIF3a indirectly via binding to the carboxyl-terminal domain of eIF3b.

89 dentity of the 20-kDa segment as part of the carboxyl-terminal domain of full-length Cx43.

90 Antibodies directed against the carboxyl-terminal domain of GRP78 are antagonists that b

91 2M* antagonist antibody directed against the carboxyl-terminal domain of GRP78 blocks these alpha2M*-

92 An antibody against the carboxyl-terminal domain of GRP78 may have important app

93 3-kinase, mTORC, or an antibody against the carboxyl-terminal domain of GRP78.

94 ced phosphorylation of multiple sites in the carboxyl-terminal domain of p300 by protein kinase Hipk2

95 , Cdk7 phosphorylates serines 5 and 7 of the carboxyl-terminal domain of RNA polymerase II and can al

96 p binds the citrus thioredoxin CsTdx and the carboxyl-terminal domain of RNA polymerase II and is a d

97 n with CsTdx and that CsCyp binds the citrus carboxyl-terminal domain of RNA polymerase II YSPSAP rep

98 dk9-mediated serine 2 phosphorylation in the carboxyl-terminal domain of RNA polymerase II.

99 Expression of the carboxyl-terminal domain of Rpn11 partially suppressed t

100 C99 is the transmembrane carboxyl-terminal domain of the amyloid precursor protei

101 of CsCYP, a cyclophilin associated with the carboxyl-terminal domain of the citrus RNA Pol II that f

102 It demonstrates that the carboxyl-terminal domain of the heavy chains determines

103 Xanthomonas citri, known as PthAs, bind the carboxyl-terminal domain of the sweet orange (Citrus sin

104 ein interaction between the highly conserved carboxyl-terminal domain of the V protein and the helica

105 ts revealed that the Ssu72 RNA polymerase II carboxyl-terminal domain phosphatase, a critical determi

106 ical signals manifested by RNA polymerase II carboxyl-terminal domain phosphorylation status.

107 IV-1 STC and a higher-order form that adopts carboxyl-terminal domain rearrangements.

108 The nuclease lobe also contains a carboxyl-terminal domain responsible for the interaction

109 In this study, we identified carboxyl-terminal domain RNA polymerase II polypeptide A

110 ) and PHD (plant homeo domain) fingers and a carboxyl-terminal domain that directly binds the largest

111 m-type DNA sites and via its large, compound carboxyl-terminal domain to core-type DNA sites, where D

112 the amino-terminal domain and Glu-255 in the carboxyl-terminal domain, referred to as apoE4 domain in

113 In the distal carboxyl-terminal domain, residue Q404 was identified as

114 me interface includes the RNAP subunit alpha carboxyl-terminal domain, which is required for RNAP-rib

115 ical calcium binding loops in the calmodulin carboxyl-terminal domain.

116 omain, an AGP-like domain, and a hydrophobic carboxyl-terminal domain.

117 nd this interaction required the SLY1 or SNE carboxyl-terminal domain.

118 SK-3 serine phosphorylation sites within the carboxyl-terminal domain.

119 ransition coupled the phosphorylation of the carboxyl-terminal-domain (CTD) of RNA polymerase II (RNA

120 otubule-binding properties of the amino- and carboxyl-terminal domains of CENP-F as well as the carbo

121 served common docking (CD) domain within the carboxyl-terminal domains of ERK3 and ERK4 and the conse

122 TH directly binds the substrate binding and carboxyl-terminal domains of Hsc70.

123 When the carboxyl-terminal domains of TcdB012 and TcdB027 are swa

124 that the HD together with the DLX3 amino- or carboxyl-terminal domains was required for maximal inhib

125 and Q653, which are sites in the amino- and carboxyl-terminal domains, respectively.

126 rove the existence of endogenously expressed carboxyl-terminal domains, which may serve as valuable t

127 ic domain, but differ conspicuously in their carboxyl-terminal domains.

128 tes, resulting in nuclear translocation of a carboxyl-terminal EIN2 fragment (EIN2-C').

129 abilize a short triple helix attached at the carboxyl-terminal end and allows for the proper oxidatio

130 inantly labeling only single residues in the carboxyl-terminal end of ECL2 and the amino-terminal end

131 This intermediate, which retains the carboxyl-terminal end of the pro-domain, had antimicrobi

132 Here we show that a Cdk9 carboxyl-terminal extension, distinct from the catalytic

133 aking place at the amino-terminal (FERM) and carboxyl-terminal (FAT) domains and that both domains ar

134 lerostin and does not involve the amino- and carboxyl-terminal flexible arm regions.

135 ed APP ectodomain (sAPPbeta), membrane bound carboxyl terminal fragment (CTF), levels of beta-amyloid

136 rough the intramembrane cleavage of the beta-carboxyl-terminal fragment (betaCTF) of beta-amyloid pre

137 Expression of a MyoGEF carboxyl-terminal fragment (residues 501-790) decreased

138 , we expressed, purified, and crystallized a carboxyl-terminal fragment comprising residues 371-553.

139 with Astn2 TM2 leads to the appearance of a carboxyl-terminal fragment consistent with intramembrane

140 The BACE1 carboxyl-terminal fragment contains a di-leucine sorting

141 The carboxyl-terminal fragment of the toxin heavy chain (Hc)

142 , which cleaves the channel to form a 95-kDa carboxyl-terminal fragment that includes the transmembra

143 capn-InsP(3)R1) corresponding to the stable, carboxyl-terminal fragment to examine the functional con

144 Purified full-length UL37 and its carboxyl-terminal fragment were sufficient to deamidate

145 g as well as generation of a cell-associated carboxyl-terminal fragment with potential oncogenic func

146 the interaction of signals present in their carboxyl-terminal fragment with specific trafficking mol

147 ve demonstrated the functional importance of carboxyl terminal fragments of MUC16 in multiple tumor t

148 Carboxyl-terminal fragments (CTFs) of TDP-43 aggregate t

149 inal RD4 domain of RIP140 interacts with the carboxyl-terminal gate-keeping domain of the IP3R.

150 these GTPases is due in large part to their carboxyl-terminal geranylgeranyl moiety.

151 RavZ hydrolyzed the amide bond between the carboxyl-terminal glycine residue and an adjacent aromat

152 ediates posttranslational glycosylation of a carboxyl-terminal glycosylation site in an unfolded prot

153 antiviral function of tetherin requires the carboxyl-terminal GPI anchor, while the GPI anchor delet

154 als are distinctive for subfamilies, and the carboxyl-terminal granulin domain occurs in two PLCP sub

155 hiols with a length of 11 carbon atoms and a carboxyl terminal group can efficiently block the charge

156 Cys(6)-sec labeling multiple residues in the carboxyl-terminal half of ECL2 and throughout ECL3, Cys(

157 witches, not continuously, in the amino- and carboxyl-terminal halves of the bundle and the linker do

158 with monomeric AChE, proving exposure of the carboxyl-terminal helices within the larger context of T

159 is selectively destabilized by removing the carboxyl-terminal helix in the native structure to produ

160 th the phosphoinositide-binding loop and the carboxyl-terminal helix of Vps34 mediate catalysis on me

161 the keg-4 mutation, which is located in the carboxyl-terminal HERC2-like repeats, and deletion of th

162 HBeAg from different patients exhibits minor carboxyl-terminal heterogeneity.

163 strong elevation of mRNA levels of ubiquitin carboxyl-terminal hydrolase (CYLD), a known mediator of

164 quitin specific peptidase (USP) 14/ubiquitin carboxyl-terminal hydrolase (UCH) L5 deubiquitinases of

165 main shared with two regulators of ubiquitin carboxyl-terminal hydrolase 37 (Uch37), namely adhesion

166 in termination and 5 affecting its ubiquitin carboxyl-terminal hydrolase domain.

167 Ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1) has been implica

168 Ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1) is an example of

169 The enzyme ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1) is one of the mo

170 ect polyubiquitinated proteins and ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1) protein levels.

171 Here, we show that ubiquitin carboxyl-terminal hydrolase-L5 (UCHL5 or UCH37) de-ubiqu

172 after ectopic cell surface expression of the carboxyl-terminal immunoglobulin variable-like N2 domain

173 of melanoma antigen-A11 on the AR NH(2)- and carboxyl-terminal interaction amplify the androgen-depen

174 otif in the androgen-dependent AR NH(2)- and carboxyl-terminal interaction and binding MAGE-A11 and f

175 ages in the androgen-dependent AR NH(2)- and carboxyl-terminal interaction, whereas the second FXXLF

176 l activity associated with the AR NH(2)- and carboxyl-terminal interaction.

177 r (CL-II) in the juxtamembrane region of Smo carboxyl-terminal intracellular tail (C-tail).

178 fusion process, we focused on these acylated carboxyl-terminal intravirion tails.

179 Type B Ggamma subunits, lacking a carboxyl-terminal isoprenylation motif, are found only i

180 In addition to the classic carboxyl-terminal KDEL motif, a variety of sequence vari

181 so lost when ER residence is achieved with a carboxyl-terminal KDEL or KSEL instead of a KTEL motif.

182 tifs within these proteins revealed that the carboxyl-terminal KEN box and D-boxes of Tos4 are import

183 or CDX2, only the highly conserved wild-type carboxyl-terminal KTEL motif results in the appropriate

184 ivators that are recruited by PR through the carboxyl-terminal ligand binding domain have been studie

185 T1/2-PIX-NCK-PAK complex), LD5, and all four carboxyl-terminal LIM domains (that bind tubulin and PTP

186 for APAF1, Resistance genes, and CED4]), and carboxyl-terminal LRR domain have undergone distinct evo

187 ne variant harboring an approximately 25-kDa carboxyl-terminal macrodomain.

188 omain involved in protein interactions and a carboxyl-terminal membrane domain that carries out the t

189 by a variety of mechanisms, one of which is carboxyl-terminal methylation of the catalytic subunit b

190 Both FFAs and TNF induce an Akt inhibitor, carboxyl-terminal modulator protein (CTMP).

191 of MUC16 are ascribed to the cell-associated carboxyl-terminal MUC16 (MUC16-Cter), the exact biochemi

192 ed progerin to elicit disease depends on the carboxyl-terminal mutation used to eliminate protein pre

193 erminal region that regulates the NH(2)- and carboxyl-terminal (N/C) interaction enables direct bindi

194 We recently showed that the second carboxyl-terminal non-collagenous domain (NC2) of homotr

195 yl-terminal domains of CENP-F as well as the carboxyl-terminal (non-kinesin) domain of CENP-E.

196 Through binding of Erk2 to the second of its carboxyl-terminal NPXY motifs, LRP1 beta-chain positivel

197 The carboxyl terminal of [Ru(bpy)(2)PICH(2)](2+) (fluorescen

198 action with the cochaperone ubiquitin ligase carboxyl terminal of Hsp70/Hsp90 interacting protein (CH

199 on of surface electrostatic potential at the carboxyl terminal of the alpha1-helix of HLA class I all

200 s of a single glutamic acid residue near the carboxyl terminal of TorsinA.

201 of the scissile sites near the amino- versus carboxyl-terminal of the lambdaN protein to the proteoly

202 only the lambda3 protein associates with the carboxyl-terminal one-third of microNS and that viral RN

203 lomavirus E6, were found to encode a related carboxyl-terminal PDZ domain-binding motif (PBM) that me

204 arkers for collagen I and III synthesis, the carboxyl terminal peptide from pro-collagen I (PICP) and

205 The carboxyl-terminal peptide of AtABP1 induced an auxin-lik

206 , a process that does not depend on the more carboxyl-terminal PHD-2.

207 ated the in vivo phosphorylation of multiple carboxyl-terminal phosphate acceptor sites, including th

208 sitive transcription factor b (pTEFb), Ser-2 carboxyl-terminal phosphorylation, and polyadenylation f

209 60 is an integral thylakoid protein, and its carboxyl-terminal portion is distantly related to prokar

210 eat domain of O-GlcNAc transferase binds the carboxyl-terminal portion of an HCF-1 proteolytic repeat

211 study, the data demonstrate that within the carboxyl-terminal portion of mouse TG, T3 is formed de n

212 Previous studies suggest that the carboxyl-terminal portion of the pUL56 subunit interacts

213 to confirm that two different domains in the carboxyl-terminal portion of TRIP8b--the tetratricopepid

214 s of bacterial serine proteases known as the carboxyl-terminal processing proteases (CTPs).

215 ng proteins, including E2f, interact through carboxyl-terminal protein interaction domains, but genet

216 posed of an amino-terminal clip domain and a carboxyl-terminal proteinase domain.

217 Deleting the carboxyl-terminal PTH1R PDZ-recognition domain did not a

218 protein lacking N-terminal myristoylation, a carboxyl-terminal pX extension of VP1, VP2 late domains

219 The carboxyl-terminal RD4 domain of RIP140 interacts with th

220 termination codon results in deletion of the carboxyl terminal region of the LHX3 protein, which is c

221 The variable carboxyl terminal region of topoisomerase-II has a major

222 palmitylated at two cysteine residues in its carboxyl terminal region.

223 een the DH domain (residues 162-351) and the carboxyl-terminal region (501-790) of MyoGEF can inhibit

224 uster of five surface alpha-helices, and the carboxyl-terminal region (CTR), and cooperative interact

225 and in vivo pulldown assays showed that the carboxyl-terminal region (residues 501-790) of MyoGEF co

226 ys showed that phosphorylation of the MyoGEF carboxyl-terminal region by aurora B kinase interfered w

227 owed that exogenous expression of the MyoGEF carboxyl-terminal region decreased the invasion activity

228 one RNA recognition motif (RRM) domain and a carboxyl-terminal region enriched in serine/arginine dip

229 Furthermore, expression of the MyoGEF carboxyl-terminal region interfered with RhoA localizati

230 peptide repeats in conserved positions and a carboxyl-terminal region known as the thioredoxin-like d

231 We used a peptide of the carboxyl-terminal region of AtABP1 as a tool.

232 TRIP8b interacts with the carboxyl-terminal region of HCN channels and regulates t

233 ther deletion analysis demonstrated that the carboxyl-terminal region of HDA6 and the bromo-adjacent

234 Unexpectedly, we found that the unstructured carboxyl-terminal region of Mps1 plays an essential role

235 er, our findings suggest that binding of the carboxyl-terminal region of MyoGEF to its DH domain acts

236 revious genetic analysis showed that a short carboxyl-terminal region of Nab3 is functionally importa

237 While it is evident that the carboxyl-terminal region of natural peptide ligands bind

238 of the peptide-binding domain located at the carboxyl-terminal region of the avian HSPA2.

239 ipitation studies showed the alpha-actinin-4 carboxyl-terminal region specifically interacted with th

240 rmed by circumscribed regions of Sestd1 (the carboxyl-terminal region) and Dact1 (the amino-terminal

241 mong known TRP structures, together with the carboxyl-terminal region, forms a large two-layered cyto

242 of COP1, which is known to interact with the carboxyl-terminal region.

243 c-Jun specifically at the chromatin via its carboxyl-terminal region.

244 teract with two different regions of the HCN carboxyl-terminal region: the carboxyl-terminal three am

245 The carboxyl-terminal regions of these peptides are thought

246 We determined the role of carboxyl-terminal regulation of NOPR (nociceptin, orphan

247 Masking the targeting signal by carboxyl-terminal reporter fusion led to cytoplasmic loc

248 Transient expression of a carboxyl-terminal reporter gene construct directed SaB4H

249 Therefore, we have identified a homologous carboxyl-terminal residue that regulates the kinetics an

250 ly reported molecular approximations between carboxyl-terminal residues 24 and 35 within GLP1 and its

251 and a mutation (p.Phe557Ter) lacking the 31 carboxyl-terminal residues also had normal or enhanced a

252 molecular approximations between amino- and carboxyl-terminal residues of GLP1 and its receptor.

253 rates an amino-terminal (residues 1-816) and carboxyl-terminal (residues 817-1314) fragment, each con

254 n of full-length Cx43, endogenously produced carboxyl-terminal segments of Cx43 have been described a

255 , however, behind the separate generation of carboxyl-terminal segments of Cx43 have remained elusive

256 Covalently linked carboxyl-terminal segments of the beta-amyloid peptide (

257 Conserved carboxyl-terminal sequence motifs with class-specific pa

258 In particular the highly cationic carboxyl-terminal sequence of melittin, is consistently

259 However, replacement of a longer carboxyl-terminal sequence with termini from either a fo

260 In addition, substitution of the native carboxyl-terminal sequence with the last few dissimilar

261 t kinase to demonstrate that residues on the carboxyl-terminal side of the EspB transmembrane domain

262 these variants, MOR-1A, an intron-retention carboxyl terminal splice variant identical to MOR-1 exce

263 determine the function(s) of a 32-amino acid carboxyl-terminal tail (Mgm101(238-269)) conserved in th

264 ation within the Homer binding region in the carboxyl-terminal tail (P1148L) does not alter the intra

265 Contrary to speculation, the divergent carboxyl-terminal tail domain (CTD) is dispensable, but

266 he amino-terminal region of the protein, and carboxyl-terminal tail identity both contribute to MLO a

267 e segment, preventing proper position of the carboxyl-terminal tail in a proportion of mutant molecul

268 ons and that alterations affecting the ATP7A carboxyl-terminal tail induce release of the copper tran

269 receptor (GPCR) family because it lacks the carboxyl-terminal tail involved in GPCR desensitization.

270 ld type and mutant kinases indicate that the carboxyl-terminal tail is largely dispensable for autoph

271 The carboxyl-terminal tail of 5-HT2AR encodes a motif that m

272 beta-Arrestin binding to the carboxyl-terminal tail of beta(1)-ARs promotes a conform

273 gered by one or two tyrosines located in the carboxyl-terminal tail of EAT-2 but not found in SAP.

274 ein interaction interface in the cytoplasmic carboxyl-terminal tail of Gpr161.

275 in the RIIbeta subunit, which docks onto the carboxyl-terminal tail of the adjacent C subunit, thereb

276 The carboxyl-terminal tail of the CRFR1 terminates in a PDZ-

277 ld interact with the intracellular loops and carboxyl-terminal tail of the GPCR.

278 lymerase and an electrostatic binding of the carboxyl-terminal tail of the helicase to a basic patch

279 ction with a beta2-adrenoceptor fused to the carboxyl-terminal tail of the vasopressin type 2 recepto

280 of the Mps1 kinase domain revealed that the carboxyl-terminal tail region of Mps1 is unstructured, r

281 (362), Ser(363) and Thr(366) residues at the carboxyl-terminal tail were primarily responsible for ss

282 ared with AVR1, A-L is shorter and lacks the carboxyl-terminal tail, the T-region that is crucial for

283 ct PDZ-binding motif at the end of the CRFR1 carboxyl-terminal tail.

284 promised by genetic perturbations within the carboxyl-terminal tail.

285 ons of the HCN carboxyl-terminal region: the carboxyl-terminal three amino acids (SNL) and the cyclic

286 at its narrow end, which are connected to a carboxyl-terminal three-blade beta-propeller tip domain

287 AcV5 epitope tags, fused carboxyl terminal to the inactive GUS- proteins, enabled

288 USP19, the only DUB containing a carboxyl-terminal transmembrane domain, was proposed to

289 s537Stop, results in a truncation within the carboxyl-terminal transmembrane helix.

290 cer of conformational flexibility within the carboxyl-terminal transmembrane region.

291 In addition to binding to the carboxyl-terminal tripeptide of HCN channels, TRIP8b als

292 V-1(F) gBDelta28syn mutant virus, encoding a carboxyl-terminal truncated gB, causes extensive cell fu

293 idylinositol 4,5-bisphosphate binding of the carboxyl-terminal Tubby domain attaches these proteins t

294 Twist1, through its carboxyl-terminal Twist-box, binds to the Sox9 high mobi

295 HcCNL contained a carboxyl-terminal type 1 peroxisomal targeting signal ma

296 In this article, we show that a carboxyl-terminal tyrosine-based sorting motif (YxxPhi)

297 interacting and trafficking domains and the carboxyl-terminal VSL domain.

298 The Vta1 carboxyl-terminal Vta1 SBP1 Lip5 (VSL) domain stimulates

299 The carboxyl-terminal Vta1/SBP-1/Lip5 (VSL) domain of Vta1 b

300 protein-SlGGB1 fusion protein as well as the carboxyl-terminal yellow fluorescent protein-SlGGB1/amin