ライフサイエンスコーパス: C terminus

1 from S. coelicolor WhiD (ScWhiD) only at the C terminus.

2 ame-shifted protein product with an extended C terminus.

3 interaction by sequestering copper from the C terminus.

4 leavage about 450 residues upstream from the C terminus.

5 ing the recruitment of a key loop by the XIP C terminus.

6 road set of chimeric GPCRs harboring the V2R C terminus.

7 l as a novel Art v 3-specific epitope at the C terminus.

8 tion, S6 kinase undergoes acetylation at the C terminus.

9 range and increasing rigidity from the N to C terminus.

10 ing a coreceptor-mimetic sulfopeptide to its C terminus.

11 tion and reveal a dimer mediated by the Ku80 C terminus.

12 uences in eukaryotes, including the Hedgehog C terminus.

13 ne with 16 histidines and 2 cysteines at its C terminus.

14 cated N terminus and cytoplasmically located C terminus.

15 nts that have been fused onto the receptor's C terminus.

16 ing to truncation of ~300 amino acids in the C terminus.

17 ia evolutionarily conserved sequences in its C-terminus.

18 m, P2RX7E, which in addition has a truncated C-terminus.

19 to mimic constitutive acetylation of the p53 C-terminus.

20 and trimers, each including SpyTag at their C-terminus.

21 tetratricopeptide repeat (TPR) domain at the C-terminus.

22 tion to the polarity requires an intact RecA C-terminus.

23 viously proposed to be auto-inhibited by its C-terminus.

24 r CyRPA), with SnoopTagJr fused at the N- or C-terminus.

25 horylation of either Ser396 or Ser404 in the C-terminus.

26 the PDZ domain and its interaction with DVL C-terminus.

27 hich contained an aromatic tryptophan at its C-terminus.

28 ctural feature upstream of the ebolavirus NP C-terminus.

29 t Bif-1 interacted with prohibitin-2 via its C-terminus.

30 d in DBLepsilon and DBLzeta domains near the C-terminus.

31 ylate specific serine sites located near its C-terminus.

32 horylation of serine 261 residue on the AQP2 C-terminus.

33 mon N-terminus with P and V but has a unique C-terminus.

34 ith Vac14 in a manner that requires the Fig4 C-terminus.

35 sed with a double (V5-HA) epitope tag at the C-terminus.

36 quential folding pathway initiating from the C-terminus.

37 zone targeting depended on the intracellular C-terminus.

38 factors, while the GAIP interacting protein C-terminus 1 (GIPC1, aka Synectin) interacts with the ne

39 vaccination (p < 0.001), higher in NANP than C-terminus (2855 vs 1297 proportional change between mea

40 (2-(diphenylphosphanyl)phenyl)methanol as a C-terminus activator has been demonstrated at simple and

41 ta suggest that overexpression of the Spc110 C terminus acts as a dominant-negative mutant that titra

42 At the C terminus, additional residues outside of the affinity-

43 We find that the Fig4 C-terminus alone interacts with Vac14 in vivo and retain

44 approximately 18 domains further towards the C terminus along titin.

45 of the GAL4 DNA-binding domain to the BRCA1 C terminus (amino acids 1396-1863), we assessed the func

46 RM peptide externalizes from the capsid, its C-terminus (amino acids 28-40) anchors into the membrane

47 s moved the linker closer to the tropomyosin C terminus, an effect that was more pronounced in the pr

48 and 4R isoforms, underrepresentation of the C terminus, an increase in negative charge in the prolin

49 l nuclear localization signal in the extreme C terminus and a nuclear retention element (NRE) in the

50 the cell, proteins are synthesized from N to C terminus and begin to fold during translation.

51 agenesis, we map phosphorylation to the Env7 C terminus and confirm that Ser-331 is a primary and pre

52 Alternative splicing of Shtn1 at the C terminus and downstream of the WH2-PRR domain produces

53 d in the gp120 trimer association domain and C terminus and in the gp41 heptad repeat 1 (HR1) region.

54 tabilized by a helix-loop-helix motif at the C terminus and interactions between the beta-sheets of t

55 FFA4-L phosphorylation occurs on the distal C terminus and is directly responsible for recruitment a

56 It has a conserved PPIase domain at the C-terminus and a highly charged N-terminal stretch, whic

57 indlin plus-tip localization depended on the C-terminus and a putative EB1-interaction motif (hxxPTxh

58 two different catcher domains at the N- and C-terminus and by combining two corresponding Tag-fused

59 osphopeptide analogues of the GPCR rhodopsin C-terminus and determine the ability of these peptides t

60 eceptor phyB interacts with SPA1 through its C-terminus and enhances the recruitment of PIF1 for phos

61 This dual mechanism is mediated by the CB1R C-terminus and involves the Helix 9 (H9) domain.

62 a/delta'-residues associated with the alpha2 C-terminus and the clamp-binding loop.

63 The single biotin moiety at the C-terminus and the small size of the nanobody (15 kDa) e

64 ke cytoplasmic kinase phosphorylates RBOHD's C-terminus and two phosphorylated residues (S862 and T91

65 phosphorylate different residues in the AQP2 C-terminus, and suggest new strategies to target distinc

66 te that specific residues within the tatM2NX C terminus are required to confer antagonism on TRPM2.

67 on site and the last five amino acids in the C-terminus are necessary for deposition.

68 the highest positive charge density at their C-terminus are overwhelmingly ribosomal proteins, sugges

69 th the Ku-binding motif (KBM) at the extreme C-terminus are required for end joining.

70 ed transmembrane region closest to the APOL1 C terminus as the pore-lining segment of this novel chan

71 d of an invariant domain and a hypervariable C terminus, as a key component of self-recognition.

72 NuMA's C terminus binds DNA in vitro and chromosomes in interph

73 The extracellular C terminus binds the adhesion GPCR Latrophilin, forming

74 Additionally, they show that the Galpha C-terminus binds to a highly-conserved patch on the conc

75 es CcrM degradation by Lon and that the CcrM C terminus both binds to its DNA substrate and is recogn

76 the central region of the cavity and has its C terminus bound in an allosteric pocket of domain IV th

77 Meanwhile, MKT1L resembles MKT1 at the C terminus but additionally features an N-terminal exten

78 sphorylation at Ser(424) and Ser(429) in the C terminus by cyclin-dependent kinase 5 (Cdk5).

79 We further show that the ATG16L1 C-terminus can compensate for WIPI2 depletion to sustain

80 , with arginine (Arg) or lysine (Lys) at the C-terminus, can be analyzed using the HECD method.

81 us with a carboxybenzyl group (Z) and at the C-terminus carried either a carboxylic acid or an isopht

82 At its C terminus, CENP-C harbors a conserved cupin domain that

83 in the middle of the alphaE, positioning its C terminus closer to the active site.

84 residues (S325/S328/S330) in the regulatory C-terminus contributes to multiple features of the cardi

85 -interacting protein kinase 1 (RIPK1) to its C terminus (CT), independent of its ion-conducting funct

86 tg8-interacting motifs (AIMs) located at the C-terminus, cytoplasmic loop, and within the transmembra

87 ding an N terminus-derived heavy chain and a C terminus-derived light chain.

88 In the monomer the extended C terminus destabilizes the core domain to produce highl

89 in part through its intrinsically disordered C terminus, directly binds to WT cTnC, and we find that

90 In the Ca(2+)-saturated state, the TnI C-terminus dissociates from actin and binds in part to T

91 n, which persists for ~90 s following Galpha C terminus dissociation.

92 While the C-terminus does not appear to be a limiting step in musc

93 The breast cancer 1 and -2 C terminus domains of XRCC1 are essential for formation

94 nding partner proteins on its N-terminus and C-terminus domains and creating a supercomplex that prom

95 finity Ca(2+)-binding sites contained in the C-terminus domains, RCK1 and RCK2, contribute equally to

96 ed in negatively charged residues near their C-terminus eject the fastest, while nascent chains enric

97 Truncating alpha-catenin's C-terminus eliminates force-activated F-actin binding, a

98 in wound around the thin filaments, with its C-terminus embedded within the Z-disk and its N-terminus

99 M1 variants with enhanced flexibility in the C terminus failed to support its store-independent activ

100 interactions evidently involve both the Ras C terminus for lipid anchoring and its G-protein domain.

101 dition to covalent thioester linkage to Ub's C terminus for Ub transfer reactions, conjugation enzyme

102 binding/tetramerization element whereas the C-terminus forms an intrinsically disordered linker (IDL

103 e rotation of the helix switch dislodges the C-terminus from the regulatory region, activating the fl

104 ylases NEIL1 and NEIL2, Xenopus laevis NEIL3 C terminus has two highly conserved zinc finger motifs c

105 While nebulin's C-terminus has been implicated in both sarcomeric struct

106 R), phosphorylation of multiple sites on the C-terminus has been recognized as a critical step underl

107 re specifically, a 0.58 kbp deletion, at the C-terminus has been reported in high frequencies in Sene

108 hat the binding of calcium-calmodulin to the C-terminus has long-range allosteric effects on the extr

109 features are a catalytic homologous to E6AP C terminus (HECT) domain and 3 central WW domains that b

110 , revealed that the residues at the HIV-1 MA C terminus help stabilize protein-protein interactions w

111 e data also suggest the participation of the C terminus in membrane localization, which is generally

112 nduces a conformational heterogeneity at the C terminus in the fibril state, whereas the overall fibr

113 -S781R or a CGEP variant with an unprocessed C-terminus in a cgep clpr2-1 background was used to demo

114 chitecture and suggests a role for the Ctf19 C-terminus in mediating CPC-binding and accurate chromos

115 ity of the N-terminus and cationicity of the C-terminus in temporin B improves its membrane activity

116 Deletion of 25 amino acids (aa) from the C terminus inactivated MGAT4D-L, but deletion of 20 aa d

117 mutant protein bearing an alteration in the C-terminus indicated that light stabilizes ACS5 by inhib

118 Overexpression of the Spc110 C terminus induces SPB defects and disrupts microtubule

119 PC1 C terminus inhibited Kv4.3 currents to the same degree a

120 he N-terminus of aSyn occurs upon release of C-terminus interactions when calcium binds, but the leve

121 Following integration of the SCC C terminus into the TIM23 complex, amino acids 141 to 14

122 s of truncated Inp1 variants showed that the C terminus is important for association to the peroxisom

123 The Sss1p/Sec61gamma C terminus is juxtaposed to the key gating module of Sec

124 Further, the HigA structure reveals that the C terminus is ordered and does not transition between di

125 ompact state and an extended state where the C terminus is primed for activation.

126 The C terminus is required for functional binding to signali

127 One role of the multifunctional KCNQ C terminus is to mediate subtype-specific assembly of he

128 binding, demonstrating that alpha-catenin's C-terminus is a modular detector of F-actin tension.

129 Prph2 (termed RRCT), we find that the Prph2 C-terminus is necessary and sufficient for the initiatio

130 ggested that a charge carrier residue at the C-terminus is promoting the formation of diagnostic w io

131 We therefore propose that melanopsin's C-terminus is proximal to intracellular loop 3, and C-te

132 Additionally, the C-terminus is reported to contribute to muscle hypertrop

133 Farnesylation at the C-terminus is required for hGBP1's activity against micr

134 Expressing the Epe1 C-terminus is sufficient to disrupt heterochromatin by o

135 g an additional 25-45 amino acids at the Rca C terminus, known as the C-terminal extension (CTE).

136 nding through a compensatory mutation in the C-terminus leads to improved function.

137 ing protein calmodulin (CaM) to the proximal C-terminus leads to the boosting of channel activity and

138 This mislocalization and its unique C terminus led to increased degradation, as shown by gre

139 The Spc110 C terminus links the gamma-tubulin complex to the centra

140 domain (Lys-525, Lys-639, and Lys-725), and C terminus (Lys-800).

141 l stability assays, we demonstrated that the C terminus maintains ACLY tetramerization, a conserved a

142 Furthermore, interactions at the peptide C terminus modulated DM-binding affinity, suggesting dis

143 omain (Ala-Ser-Lys) within the intracellular C terminus of 5-HT(2A)R severely diminished internalizat

144 We further show that ArnA binds to the C terminus of ArnB, which harbors all the phosphorylatio

145 vented when the Gbetagamma sink betaARK1-ct (C terminus of beta-adrenergic receptor kinase-1) was coe

146 y probed the effects of substitutions in the C terminus of BRCA1: the N- and C-terminal borders of it

147 Y102E are similar in that neither binds the C terminus of Brd4, but in all other aspects the mutant

148 Peptide fragments derived from the C terminus of C5a can still interact with the receptor,

149 of the N terminus and palmitoylation of the C terminus of CB(2).

150 emonstrate this utility, we fused TTR to the C terminus of conatumumab, an antibody that targets tumo

151 ternative interface comprising beta6 and the C terminus of CRD and beta2 of RBD.

152 RAS alpha4-alpha5 while state B involved the C terminus of CRD, beta3-5 of RBD, and part of KRAS alph

153 Red) cassette was inserted in-frame with the C terminus of CSF1R, separated by a T2A-cleavable linker

154 We propose that the intrinsically disordered C terminus of cTnT directly interacts with the regulator

155 In this study, we tagged mEGFP to C terminus of dishevelled2 gene using CRISPR/Cas9-induce

156 previously ambiguous N terminus of DRC4 and C terminus of DRC5.

157 highly-conserved histidine residues near the C terminus of each microtubule-binding repeat are pH sen

158 t stem cells, we show that a mutation at the C terminus of eIF2gamma impairs CDC123 promotion of eIF2

159 Multiple residues in the C terminus of eIF6 are phosphorylated by GSK3 in a seque

160 ites for all four proteases are found in the C terminus of HC2.

161 to 40) of p17 and the Gly-rich region of the C terminus of hnRNP A1.

162 The ubiquitin ligase CHIP (C terminus of HSC70-interacting protein) promoted SIRT6

163 The PDZ domain binds to the C terminus of its proposed natural ligand, CXXC repeat-c

164 uced conformational fit to both the proximal C terminus of KCNQ4 channels and CaM, likely underlying

165 Q or the 25-aa C terminus of MGAT4D-L to the C terminus of MGAT1.

166 transferred by attaching PSLFQ or the 25-aa C terminus of MGAT4D-L to the C terminus of MGAT1.

167 tions of all 11 phosphorylation sites on the C terminus of MORs almost completely abolished desensiti

168 natively spliced gag RNA, interacts with the C terminus of mouse APOBEC3 and prevents its packaging w

169 ectroscopy, show that the interaction of the C terminus of Neuroligin-2 with Collybistin-2 induces a

170 Mutations that truncate the C terminus of neuronal Kv7/KCNQ channels are linked to a

171 ative splicing and show that the full-length C terminus of p73 is essential for hippocampal developme

172 43, the two cysteine residues closest to the C terminus of pejvakin, for reactive oxygen species-indu

173 via several PxDLS-like motifs located at the C terminus of Piccolino, which can connect multiple RIBE

174 ld allowed cryo-EM tomography mapping of the C terminus of protein A to the apical lobe, which correl

175 ng studies on the role of the H2 alpha-helix C terminus of PrP, we found that deletion of the highly

176 e first 3 aa linked to N-fMet as well as the C terminus of PSMalpha2 in promoting FPR2 to recruit bet

177 ed 69-residue (Asn(81)-Asn(149)) fragment at C terminus of Rhi o 2 was identified as crucial for IgE-

178 The C terminus of RPGR(1-19) that contains the prenylation s

179 Here, we show that the C terminus of RRS1-R but not RRS1-S is phosphorylated.

180 Here, we show that overexpression of the C terminus of Spc110 is toxic to cells and correlates wi

181 We propose the extreme C terminus of Sss1p/Sec61gamma is an essential component

182 in vinculin through a specific domain at the C terminus of TarP.

183 identified a short conserved sequence at the C terminus of the Acm1 D-box that was necessary and suff

184 etin/TonB, short N-terminal subdomain at the C terminus of the CCSSD, a previously unobserved topolog

185 k, including D165 in motif F and R416 at the C terminus of the FMDV 3D(pol) and RNA template-primer.

186 observed that when mim6 was appended to the C terminus of the heavy chains of bNAbs, this sulfopepti

187 ith the exception of a 1 aa extension at the C terminus of the longer peptide.

188 Phosphorylation of sites on the C terminus of the mu-opioid receptor (MOR) results in th

189 ed that the degree of phosphorylation on the C terminus of the mu-opioid receptor alters acute desens

190 he disordered N terminus and the hydrophobic C terminus of the peptide.

191 Key regions of M1, particularly in the C terminus of the protein, remain poorly characterized.

192 ling is terminated by phosphorylation of the C terminus of the receptor by GPCR kinases (GRKs) and by

193 th most of the pore-forming domain (PFD) and C terminus of the Serum Resistance Associated-interactin

194 ocus on the mechanism by which the cytosolic C terminus of the synaptic cell adhesion protein Neuroli

195 on the exposure of a cryptic epitope on the C terminus of the transmembrane portion of pro-TNF on cl

196 identified a 49-amino-acid-long motif in the C terminus of the two channels that regulates expression

197 uggest that the WT linker runs alongside the C terminus of tropomyosin.

198 al, backbone-extended monomers at the N- and C- terminus of peptides using wild-type and engineered r

199 noncanonical amino acid either at the N- or C-terminus of a protein or microprotein of interest for

200 tRNA ligase (PEARL) adds amino acids to the C-terminus of a small peptide scaffold in an ATP- and tR

201 degradation mechanism that acts through the C-terminus of ACS5.

202 e end-to-end bonds formed between the N- and C-terminus of adjacent Tpm molecules define Tpm continui

203 Further mechanistic probing revealed that C-terminus of c-Cbl interacted with the cytoplasmic tail

204 into the CENP-H/K complex by binding to the C-terminus of CENP-H, leading to formation of the ternar

205 ions that completely or partially remove the C-terminus of CFTR at the same time as keeping an intact

206 s of W1282X-CFTR, whose PTC is closer to the C-terminus of CFTR, suggest the presence of both C-termi

207 a hemagglutinin tag (HA) was attached to the C-terminus of either alpha9 or alpha10 proteins.

208 tandem affinity tag was conjugated with the C-terminus of endogenous HSP90beta protein over the pare

209 The C-terminus of Epe1 directly interacts with Swi6(HP1), an

210 The C-terminus of Galpha is ejected from its beta sheet core

211 ies reveal that the engagement of the distal C-terminus of Galphai/o with the receptor differentiates

212 The unique distal C-terminus of GIRK1, G1-dCT, was important but insuffici

213 tional binding region was revealed to be the C-terminus of helix B of IL-7, highlighting the value of

214 uitination by the Hsp70-associated E3 ligase c-terminus of Hsp70-interacting protein (CHIP) and subse

215 The heat shock protein 70 (Hsp70):c-terminus of Hsp70-interacting protein (CHIP) complex f

216 ltaneously to H3S10ph and the phosphorylated C-terminus of Hst2.

217 Fusion of the peptide to either the N- or C-terminus of IN results in maximal stimulation of conce

218 inds to a phosphorylated serine motif on the C-terminus of Kv1.2; and that loss of this interaction i

219 Thus, the processed C-terminus of lacritin that is deficient or absent in dr

220 The C-terminus of Mad1 directly interacts with PML, and this

221 BRCA2 binds to the C-terminus of MEILB2, resulting in the formation of the

222 patially-restricted delivery of PP1 near the C-terminus of Ndc80, a core kinetochore-microtubule link

223 acts with both subunits, especially near the C-terminus of p51.

224 rotein comprised of the body of Rom1 and the C-terminus of Prph2 (termed RRCT), we find that the Prph

225 hough post-translational modification of the C-terminus of RAS has been studied extensively, little i

226 e S4-S5 linker (S4-S5(L)) interacts with the C-terminus of S6 (S6(T)) to stabilize the gate in the op

227 ions are located in the extended cytoplasmic C-terminus of Slack channels and result in increased Sla

228 Previous experiments have shown that the C-terminus of Slack channels binds a number of cytoplasm

229 onnative structure in a peptide model of the C-terminus of SOD1, a sequence that might serve as a pot

230 This suggests that the extracellular C-terminus of SosA is required both for cell division in

231 onal binding site was identified between the C-terminus of SOST and the LRP6 E2 domain.

232 HDC2, a human E3 that recognizes the extreme C-terminus of substrates.

233 -binding peptide (DSARGFKKPGKR) fused to the C-terminus of superfolder green fluorescent protein (sfG

234 izes several important residues close to the C-terminus of TglA to perform its activity and is tolera

235 eadthrough-reducing mutations at the extreme C-terminus of the a/Tif32 subunit of eIF3 either suppres

236 contains a five-amino acid insertion at the C-terminus of the C-terminal zinc finger and has no obse

237 we inserted an endogenous 3X-FLAG tag at the C-terminus of the canonical DISC1 gene in human induced

238 uced a luciferase reporter in-frame with the C-terminus of the dystrophin gene in mice.

239 used to attach an EGFP coding module to the C-terminus of the endogenous NME1 gene in melanoma cell

240 y the plant homeodomain (PHD) present at the C-terminus of the five ING proteins.

241 ple Gdf11 deletion alleles that modified the C-terminus of the GDF11 protein.

242 We find that the C-terminus of the HigA antitoxin is required for dimeriz

243 osomes and adds an ssrA tag or degron to the C-terminus of the incomplete protein, which directs degr

244 erved phosphorylated Ser/Thr residues at the C-terminus of the nucleolar phosphoprotein Treacle.

245 y site of the enzyme that normally binds the C-terminus of the peptide substrate.

246 RL that catalyzes the addition of Cys to the C-terminus of the peptide TglA in the biosynthesis of 3-

247 preferential membrane orientation, where the C-terminus of the peptide traverses the plasma membrane

248 An AfsA-like domain at the C-terminus of the PKS was shown to catalyze condensation

249 fied protease (P3) first removes the extreme C-terminus of the prodomain.

250 seven transmembrane helices, with the N- and C-terminus of the protein located at the extracellular s

251 ons to the intermediate state, the hand-like C-terminus of the VSD-pore linker (S4-S5L) interacts wit

252 t target the two adjacent PPXY motifs at the C-terminus of the Warts polypeptide and additional WW do

253 the first of two WD40 propellers located on C-terminus of TPL.

254 ontaining a tetrazole-derived warhead at the C-terminus of ubiquitin and employed a cyclic polyargini

255 The C-terminus of UNC80 contains a domain that interacts wit

256 ction between LvgA and a linear motif in the C-terminus of VpdB.

257 y also in vivo Furthermore, we show that the C terminus, only in the context of the full-length enzym

258 ell-penetrating peptide to their N-terminus, C-terminus, or stapling unit.

259 The location of this interaction on the C terminus overlaps with the sites of human pathogenic m

260 At the C-terminus, PALB2 variants p.L947F [c.2841G>T], p.L947S

261 Our data show C terminus peptides of Galpha(s), Galpha(i), and Galpha(

262 , and between its hydrophobic region and the C terminus, prevent self-association.

263 Deletion of the C terminus prevents tubule formation but not viral repli

264 find that the intrinsically disordered SIRT6 C-terminus promotes binding at the higher affinity site

265 Protonation of the C-terminus promotes helicity and pore size.

266 rectly with CypD via its acidic proline-rich C-terminus region and binding at the putative ligand bin

267 eract with the alternatively spliced channel C-terminus regulating gating of Ca(V)1.3 channels.

268 acidic N-terminus (residues 1-40) and basic C-terminus (residues 264-303), whereas NMR signals from

269 s a conformational change that dislodges the C terminus, resulting in a cis-to-trans switch that is l

270 Docking of the tetraspanin 33 C terminus revealed that it fits into the hydrophobic ho

271 Proteins with a functionalized C-terminus such as a C-terminal thioester are key to the

272 TMIE point mutations in the C terminus that are linked to deafness disrupt phospholi

273 The long isoform (BRD4L) has an extended C terminus that binds transcription cofactors, while the

274 in both the third intracellular loop and the C terminus that may promote this interaction.

275 fluorescent protein attached directly to the C-terminus that is similar to fusions used in previous s

276 a-helical assembly at the nucleoprotein (NP) C-terminus that was conserved through half a century of

277 udied responses to the repeat region and the C-terminus, the antibody response against the N-terminal

278 erminus is a toxic effector regulated by the C terminus, there is an emerging consensus that this cis

279 the NLRP1B N terminus and freeing the NLRP1B C terminus to activate caspase-1.

280 nt-associated protein, localized through its C terminus to distinct regions (C-zones) of the sarcomer

281 e that ACLY forms a homotetramer through the C terminus to facilitate CoA binding and acetyl-CoA prod

282 vivo screen for molecules that link the Brp C terminus to SVs.

283 cur following initial binding of the peptide C-terminus to the ECD.

284 and photo-manipulation of the crucial Galpha C terminus, to demonstrate the temporal coupling of cogn

285 The W1282X mutation results in both C-terminus truncated and read-through proteins that are

286 rminus of CFTR, suggest the presence of both C-terminus truncated CFTR proteins that are poorly funct

287 g of melanopsin mutants including a proximal C-terminus truncation (at residue 365) and proline mutat

288 rd cytoplasmic loop, which is increased upon C-terminus truncation, supporting the idea that these tw

289 otein (AKAP) 79/150, which binds to the LTCC C-terminus via a modified leucine-zipper (LZ) interactio

290 hate (PIP(2)) binding domains, or the entire C terminus, was without effect on the forskolin response

291 To study the functions of nebulin's C-terminus, we generated a mouse model deleting the fina

292 xposed on the cytoplasmic face of the folded C terminus, where it might interact with other channel p

293 ible regions of the gH N terminus and the gL C terminus, while the fifth was placed around gL residue

294 eracted with COMA in vitro through the Ctf19 C-terminus whose deletion affected chromosome segregatio

295 ss and facilitates the interaction of RRS1's C terminus with its TIR domain.

296 of three tyrosine residues in the alpha-dbn C terminus with phenylalanine compromising the alphakap-

297 ed its interaction through its intracellular C terminus with Rab4, which was increased by l-PGDS.

298 n to site-specifically label proteins at the C-terminus with a variety of cysteine-lysine dipeptide c

299 onfocal microscopy of the Glbs tagged at the C-terminus with green fluorescent protein was used to de

300 d by the viral protein Gag and tagged at its C-terminus with the fluorescent protein Dendra2 have the