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 structure of the beta2AR in complex with the carboxyl terminal 14 amino acids from Galphas along with

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

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

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

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

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

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

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

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

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

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

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

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

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

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

21 tically, ARID1A interacted with EZH2 via its carboxyl terminal and antagonized EZH2-mediated IFN resp

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

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

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

25 4, (ii) the amino-terminal cysteine-rich and carboxyl-terminal basic domains of ORF31 mediate the ORF

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

46 7A and that binding is mediated in part by a carboxyl-terminal di-leucine motif.

47 356 of cdAE1) lacking the amino-terminal and carboxyl-terminal disordered regions, produced at physio

48 ssociates with CPL2, a plant-specific Pol II carboxyl terminal domain (CTD) phosphatase, to form the

49 The RNA polymerase II carboxyl terminal domain (RNAPII CTD) kinase complex (CT

50 se 9 (CDK9)-that phosphorylates NELF and the carboxyl terminal domain of Pol II-and enrichment of the

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

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

53 ansmembrane domain M3, and the intracellular carboxyl terminal domain.

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

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

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

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

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

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

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

61 pendent kinase 12 (CDK12) phosphorylates the carboxyl-terminal domain (CTD) of RNA polymerase II (pol

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

63 In endoplasmic reticulum (ER) membranes, the carboxyl-terminal domain (CTD) of SREBPs binds to the CT

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

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

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

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

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

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

70 ivator with glutamic acid/aspartic acid-rich carboxyl-terminal domain 2 (CITED2) as a critical intrin

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

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

73 .5 interacts with IKKalpha/beta, whereas the carboxyl-terminal domain binds to protein phosphatase 1.

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

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

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

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

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

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

80 LANA with point mutations in the carboxyl-terminal domain identified an MCM6 binding doma

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

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

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

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

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

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

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

88 2M* antagonist antibody directed against the carboxyl-terminal domain of GRP78 blocks these alpha2M*-

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

90 3-kinase, mTORC, or an antibody against the carboxyl-terminal domain of GRP78.

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

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

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

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

95 The carboxyl-terminal domain of STN1 interacts with CTC1 at

96 We show that the carboxyl-terminal domain of TaiP exposes a mimic of an e

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

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

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

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

101 ylates p53, or with an acetylation mimicking carboxyl-terminal domain p53 mutant.

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

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

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

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

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

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

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

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

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

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

112 ARRDC3 on a conserved tyrosine (Y382) in the carboxyl-terminal domain.

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

114 eractions bridge to the acidic intracellular carboxyl-terminal domain.

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

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

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

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

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

120 ain, while MCM6 bound to both the amino- and carboxyl-terminal domains of LANA.

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

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

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

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

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

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

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

128 slational termination impairment and protein carboxyl terminal extension), which mechanistically link

129 imerization is stimulated by the lysine-rich carboxyl-terminal extension of UBE2S that is also requir

130 It also disclosed a carboxyl-terminal extension that forms a helix-helix int

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

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

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

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

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

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

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

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

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

140 that STAT3 interacts with a calpain-cleaved carboxyl-terminal fragment of FLNA.

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

142 al analysis, and CRISPR editing identified a carboxyl-terminal fragment of thrombospondin-1 as an une

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

144 ino-terminal domains of NLRP1B, liberating a carboxyl-terminal fragment that is a potent caspase-1 ac

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

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

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

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

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

150 d APPswe mutant variant upregulates APP, APP carboxyl terminal fragments, and Abeta levels.

151 ulting metabolites, both alpha- and beta-APP carboxyl-terminal fragments and APP intracellular domain

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

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

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

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

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

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

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

159 pensable for the interaction with P, and the carboxyl-terminal half of P is sufficient for the intera

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

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

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

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

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

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

166 immunosensors for the detection of Ubiquitin carboxyl-terminal hydrolase (UCHL-1) biomarker of brain

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

168 oleucine, l-valine, l-aspartic and ubiquitin carboxyl-terminal hydrolase involved in protein degradat

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

170 e the serum levels of tau protein, ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1), neurofilament l

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

172 Ubiquitin carboxyl-terminal hydrolases (UCHs) belong to an enzymat

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

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

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

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

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

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

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

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

186 e Golgi is the pH-dependent recognition of a carboxyl-terminal Lys-Asp-Glu-Leu (KDEL) signal by the K

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 ifference between the isoforms with the same carboxyl-terminal microtubule-binding domain repeats, is

191 Recent research indicates a role of carboxyl-terminal modulator protein (CTMP) in Akt-signal

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

193 In conclusion, our findings identify carboxyl-terminal multisite phosphorylation as key step

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

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

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

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

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

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

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

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

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

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

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

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

206 raction with beta-arrestins is controlled by carboxyl-terminal phosphorylation.

207 trates via phosphopeptide recognition by its carboxyl-terminal polo-box domain (PBD) is poorly unders

208 60 is an integral thylakoid protein, and its carboxyl-terminal portion is distantly related to prokar

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

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

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

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

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

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

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

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

217 luding an extended transmembrane helix 5 and carboxyl-terminal receptor tail that interacts with G pr

218 ive EF-hand-like Ca(2+) binding motif in the carboxyl terminal region of BTV nonstructural phosphopro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

239 uncations of the highly charged and flexible carboxyl-terminal region.

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

241 The carboxyl-terminal regions of these peptides are thought

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

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

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

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

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

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

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

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

250 omain and to the mitochondrial membrane by a carboxyl-terminal sequence (CTS).

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

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

253 e of S generates a polybasic Arg-Arg-Ala-Arg carboxyl-terminal sequence on S1, which conforms to a C-

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

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

256 r phosphorylation occurred primarily at four carboxyl-terminal serine (Ser) and threonine (Thr) resid

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

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

259 NSs bound to the carboxyl-terminal SPRY subdomain of TRIM21, enhancing p6

260 enhanced the interaction of PTPN22 with the carboxyl-terminal Src kinase (CSK), an interaction that

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

276 todomain, a transmembrane helix, and a short carboxyl-terminal tail, or as a soluble ectodomain that

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

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

279 through palmitoylation of the GLP-1R at its carboxyl-terminal tail.

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

281 % (95% CI: 0% to 6%; p = 0.04) and increased carboxyl-terminal telopeptide of collagen type I by 4% (

282 sue inhibitor of matrix metalloproteinase 1, carboxyl-terminal telopeptide of collagen type I, and so

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

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

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

286 Recent research has demonstrated that the carboxyl-terminal transmembrane domain (TMD) of some Bcl

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

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

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

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

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

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

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

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

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

296 5-associated seven transmembrane full-length carboxyl terminal variants, MOR-1B1, MOR-1B2, MOR-1B3, M

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