ライフサイエンスコーパス: carboxyl terminus

1 as by a stretch of basic residues within its carboxyl terminus.

2 al Trp residues near either the amino or the carboxyl terminus.

3 main but not the actin-binding motifs in its carboxyl terminus.

4 signals from the Abl SH2 domain but not the carboxyl terminus.

5 tracellular loop and GFP was attached to the carboxyl terminus.

6 y a mutant Col XVII protein truncated at its carboxyl terminus.

7 in D1a and D1b proteins that differ in their carboxyl terminus.

8 t the amino terminus and a VWA domain at the carboxyl terminus.

9 main that precedes the proteasome-activating carboxyl terminus.

10 t the amino terminus and a SPRY motif at the carboxyl terminus.

11 , as well as global changes extending to its carboxyl terminus.

12 residues in the third intracellular loop and carboxyl terminus.

13 sphorylation on two tyrosine residues of its carboxyl terminus.

14 ylation of specific tyrosine residues in the carboxyl terminus.

15 second loop, the first loop, and lastly the carboxyl terminus.

16 binding site of the opposite protomer at its carboxyl terminus.

17 the exposure of neutralizing epitopes in the carboxyl terminus.

18 nters on a single residue serine 829, in the carboxyl terminus.

19 cytoplasmic amino terminus and a periplasmic carboxyl terminus.

20 a functional serine/threonine kinase at its carboxyl terminus.

21 e sequences revealed a 60% similarity at the carboxyl terminus.

22 ptides with proline or hydroxyproline at the carboxyl terminus.

23 alpy reduced by 50% following removal of the carboxyl-terminus.

24 -range interactions with the extramembranous carboxyl-terminus.

25 uctural roles for the bacteriorhodopsin (bR) carboxyl-terminus.

26 the first extracellular loop domain and its carboxyl-terminus.

27 to the specific LLKIL motif found within the carboxyl terminus (1).

28 otein between cells is mediated by the Eomes carboxyl terminus (456-692).

29 gerin retains a farnesyl lipid anchor at its carboxyl terminus, a modification that is thought to be

30 rring forms that differ in the length of the carboxyl terminus: a full-length receptor consisting of

31 n pumping, however, truncation of the entire carboxyl-terminus accelerated the rates of M-state decay

32 le interactions near the active site and the carboxyl terminus account for functional differences bet

33 hree NSP family members, binds the p130(cas) carboxyl terminus, adjacent to a bipartite p130(cas) Src

34 )R) functionality, we screened the GABA(B)R2 carboxyl terminus against a recently created proteomic a

35 The extended carboxyl terminus allows for regulatory input by scaffol

36 tion of a helix extending toward the peptide carboxyl terminus and docking within the receptor amino

37 g T. cruzi topoisomerase-II truncated at the carboxyl terminus and examined activity at centromeres a

38 ibrary with the rat AT(1A) receptor (AT(1)R) carboxyl terminus and identified GABARAP, a protein invo

39 We generated antisera to this carboxyl terminus and identified immunoreactivity in fai

40 on and alanine substitution mutations in the carboxyl terminus and identify critical residues between

41 pe serine peptidase inhibitory domain at the carboxyl-terminus and one or more unique N-domains prece

42 terminus), MsgB (middle portion) and MsgC1 (carboxyl terminus), and to three variations of MsgC1 (Ms

43 ane helices followed by a long intracellular carboxyl terminus, and earlier work demonstrated that th

44 hat G alpha subunit sequences outside of the carboxyl terminus are important for cell movement and de

45 revealed that Phe residues within the UL20p carboxyl terminus are involved in the regulation of cyto

46 id binding domain-like II (SBDL II) near the carboxyl terminus, as the site of [125I]IACoc insertion.

47 h full-length CaSR, suggesting that the CaSR carboxyl terminus between residues Thr(868) and Arg(898)

48 y receptor phosphorylation, primarily in the carboxyl terminus but also in the cytoplasmic loops, and

49 n potential phosphorylation sites within its carboxyl terminus but their role on desensitization, bet

50 ocess is initiated by phosphorylation of its carboxyl terminus by G protein-coupled receptor kinase 1

51 Phosphorylation of serine 369 in the KOR carboxyl terminus by G-protein receptor kinase 3 (GRK3)

52 a cluster of numerous serine residues in its carboxyl terminus by protein kinase A and subsequently b

53 r samples treated in (18)O-water, two at the carboxyl terminus by trypsin during hydrazide coupling a

54 ind that the interaction of STIM1 with Orai1 carboxyl terminus (C terminus) and the STIM1 K-domain ar

55 intrinsically disordered region (IDR) at the carboxyl-terminus (C-tail) executes its functions.

56 n is the class I binding domain, whereas the carboxyl terminus can be referred to as the degradation

57 The Na(v)1.2 carboxyl terminus caused faster inactivation in the Na(v

58 n in the Na(v)1.3 backbone, and the Na(v)1.3 carboxyl terminus caused slower inactivation in the Na(v

59 Calmodulin directly binds the AQP4 carboxyl terminus, causing a specific conformational cha

60 e tetratricopeptide motifs, and involves the carboxyl terminus coiled coil in survivin with critical

61 er characterize the role of the Vt strap and carboxyl terminus (CT) in actin binding, Vt self-associa

62 The carboxyl terminus (CT) of connexin 32 has been reported

63 n of either the full-length (FL) or just the carboxyl terminus (CT) of p130Cas in mammary epithelial

64 as increased in A2BR chimeras where the A2BR carboxyl terminus (CT) was replaced or fused with the A2

65 tion between Nedd4 (WW1-3 domains) and Cx43 (carboxyl terminus (CT)).

66 nders GBM cells resistant to TMZ through its carboxyl terminus (CT).

67 Interactions of the carboxyl-terminus (CT) and cytoplasmic loop (CL) domains

68 enaturation demonstrated that removal of the carboxyl-terminus decreased protein stability.

69 A 179-amino-acid region spanning the carboxyl terminus (designated EC; amino acids 192 to 394

70 We progressively deleted the distal carboxyl terminus domain (CTD) of the cold-activated mel

71 BA(B)R and requires the GABA(B)(1a) proximal carboxyl terminus domain to inhibit Cav2.2 channels.

72 o variants within its functionally important carboxyl terminus domain: E287K and G297S.

73 deletion mutation occurring within the EGFR carboxyl-terminus domain (CTD), in addition to identifyi

74 no terminus (NTD), catalytic core (CCD), and carboxyl terminus domains (CTD).

75 Moreover, Kunitz-2 and the carboxyl-terminus domains mediate interaction of Desmola

76 nsible for processing Atg8 proteins near the carboxyl terminus, exposing a conserved glycine.

77 lated protein 4 (NEDD4), homologous to E6-AP Carboxyl Terminus family E3 ubiquitin ligase, is a novel

78 e identify the HECT (homologous to the E6-AP carboxyl terminus) family E3 ubiquitin ligase, UBR5, as

79 ntial serologic responses to recombinant Msg carboxyl terminus fragments (MsgC1, MsgC3, MsgC8, and Ms

80 plex virus 1 (HSV-1) viral glycoproteins gD (carboxyl terminus), gE, gK, and gM, the membrane protein

81 to the amino terminus (GFP-GluR3) or to the carboxyl terminus (GluR3-GFP).

82 Removal of the distal half of the carboxyl-terminus had no effect on light-activated proto

83 Deletion of the carboxyl-terminus had no effect on purple membrane (PM)

84 the tumor suppressor Homologous to the E6-AP Carboxyl Terminus (HECT) domain and Ankyrin repeat conta

85 ere we show that the Homologous to the E6-AP Carboxyl Terminus (HECT) domain containing ubiquitin lig

86 demonstrate that the Homologous to the E6-AP Carboxyl Terminus (HECT) domain E3 ubiquitin ligase, Hec

87 with an E3 ubiquitin ligase homology to E6AP carboxyl terminus (HECT) domain.

88 teracting domains in KLF5 were mapped to its carboxyl terminus, including the PY motif of KLF5 and it

89 ere detected: an antiparallel amino terminus-carboxyl terminus interaction between alpha-synuclein mo

90 that trypsin-catalyzed (18)O exchange at the carboxyl terminus is in many instances inhomogeneous/inc

91 d V166E rClC-K1 demonstrated that the distal carboxyl terminus is necessary for slow cooperative gati

92 es with NAD(+) binding affinity and that the carboxyl terminus is required for assembly of a dimer of

93 binding and protection assays in vitro, the carboxyl terminus is required for important functions in

94 (v)1.2 and Na(v)1.3, we demonstrate that the carboxyl terminus is responsible for the differences.

95 The CaSR carboxyl terminus is the chief determinant of intracellu

96 lts indicate that Cx43, and specifically its carboxyl terminus, is crucial for signaling mechanisms p

97 type II membrane protein with its catalytic carboxyl terminus located in the Golgi lumen.

98 A CaSR chimera containing the mGluR1alpha carboxyl terminus matures completely (half-time of appro

99 required for degradation, while the helical carboxyl terminus mediates its attachment to proteins.

100 To describe how the carboxyl terminus modifies the regulation by barttin we

101 am from the nucleotide sequence encoding the carboxyl terminus (nucleotides 637-1149).

102 either as fused domains (IbetaH(Asp)) at the carboxyl terminus of a nonribosomal peptide synthetase (

103 rrying abgAB with a hexahistidine tag on the carboxyl terminus of AbgB and subsequent metal affinity

104 or an interaction between a residue near the carboxyl terminus of alpha-factor (position 11) and one

105 Purified Nedd4 recognizes the carboxyl terminus of alpha-synuclein (residues 120-133)

106 Because GAPDH binds to the carboxyl terminus of alpha-tubulin, we characterized the

107 een the proline and the phenylalanine at the carboxyl terminus of Ang II.

108 molecular interaction assay reveals that the carboxyl terminus of APC interacts with the matrix regio

109 vel ceramide binding domain (C20zeta) in the carboxyl terminus of aPKC.

110 tiary structure predictions suggest that the carboxyl terminus of Asp2 resembles the catalytic region

111 ophagosome targeting sequence] domain at the carboxyl terminus of Barkor.

112 in vivo and in vitro work has implicated the carboxyl terminus of BRCA1 in transcriptional stimulatio

113 n as a binding partner for the intracellular carboxyl terminus of CaR.

114 These established that the carboxyl terminus of CCK resides at the external surface

115 , an interaction with Cak1 is needed via the carboxyl terminus of Cdc28.

116 uggest that the di-arginine motif within the carboxyl terminus of Cdc42 is necessary for this GTPase

117 ptide motifs found within the intracellular, carboxyl terminus of chemokine receptor CXCR2 has been s

118 but also exposes a degron-like region at the carboxyl terminus of Chk1 to an Fbx6-containing SCF (Skp

119 This finding suggests that the carboxyl terminus of chromatin-loaded MCM3 may be seques

120 8-RFC that is produced by interaction of the carboxyl terminus of Ctf18 with the Ctf8 and Dcc1 subuni

121 soform of protein kinase C (PKCdelta) to the carboxyl terminus of Cx43.

122 the type 1 PDZ-binding motif (QDTRL) in the carboxyl terminus of cystic fibrosis transmembrane regul

123 The carboxyl terminus of DACH1 was necessary and sufficient

124 tion that is mediated through binding of the carboxyl terminus of DHHC5 and the PDZ3 domain of PSD-95

125 in bacterial proteasomal ATPases, buries the carboxyl terminus of each protomer in the central channe

126 4) 62+/-8%), and Cys(5) labeled those in the carboxyl terminus of ECL2 and ECL3 (Gln(348), 100%; Ile(

127 ng adaptor molecule (STAM)] was fused to the carboxyl terminus of EGFR, was generated.

128 Inducible expression of the carboxyl terminus of either Set1A or Set1B decreases ste

129 re we demonstrate that 35 amino acids of the carboxyl terminus of flagellin triggered inflammasome ac

130 GAL)); Gal80p, a repressor that binds to the carboxyl terminus of Gal4p and inhibits transcription; a

131 A weaker interaction site within the carboxyl terminus of gamma-ENaC (K(d) ~800 mum) was also

132 Deletion of 28 aa from the carboxyl terminus of gB (gBDelta28syn) caused extensive

133 infectious on 293 cells, indicating that the carboxyl terminus of gB is not essential for either viri

134 These results show that the carboxyl terminus of gD and the full-length gE, either a

135 chanistically, a proline-rich segment in the carboxyl terminus of GILZ physically binds the p65 subun

136 etween specific receptor residues within the carboxyl terminus of GLP1 and its receptor as normally d

137 y investigate the relative importance of the carboxyl terminus of glycoprotein D (gD) in the presence

138 altered by Gbetagamma sequestration with the carboxyl terminus of GRK2.

139 Our results demonstrate that the carboxyl terminus of hClC-Kb is not part of the binding

140 t result in truncations of the intracellular carboxyl terminus of hClC-Kb.

141 Lastly, we show that either the amino or the carboxyl terminus of HDAC7 is sufficient for transcripti

142 The carboxyl terminus of highly Ca(2+)-permeable CNGA3 expre

143 ains and to an intracellular domain near the carboxyl terminus of HR2.

144 We investigated the role of the E3 ligase carboxyl terminus of Hsc70-interacting protein (CHIP) in

145 Proteomic analysis reveals that the carboxyl terminus of Hsc70-interacting protein (CHIP) in

146 Carboxyl terminus of Hsc70-interacting protein (CHIP) is

147 ession of two distinct ubiquitin E3 ligases, carboxyl terminus of HSC70-interacting protein (CHIP) or

148 The carboxyl terminus of hsc70-interacting protein (CHIP) ub

149 -chaperone HSP70 and the ubiquitin E3 ligase carboxyl terminus of HSC70-interacting protein (CHIP).

150 Using the carboxyl terminus of Hsc70-interacting protein as a mode

151 Using an engineered version of the carboxyl terminus of Hsc70-interacting protein ubiquitin

152 dular human E3 ubiquitin ligase called CHIP (carboxyl terminus of Hsc70-interacting protein) by repla

153 CHIP (carboxyl terminus of Hsc70-interacting protein) is a U-b

154 Here, we show that CHIP (carboxyl terminus of Hsc70-interacting protein), a U-box

155 In addition, we demonstrate that an E3 CHIP (carboxyl terminus of Hsp70 interacting protein) interact

156 Here we show that the carboxyl terminus of HSP70-interacting protein (CHIP) bi

157 of ubiquitin-protein isopeptide ligase (E3) carboxyl terminus of Hsp70-interacting protein (CHIP) we

158 The carboxyl terminus of Hsp70-interacting protein (CHIP), a

159 colleagues show that a cochaperone protein, carboxyl terminus of Hsp70-interacting protein (CHIP), i

160 Our previous studies have implicated CHIP (carboxyl terminus of Hsp70-interacting protein) as a co-

161 ified ubiquitinating system containing CHIP (carboxyl terminus of Hsp70-interacting protein) as the E

162 The ubiquitin ligase CHIP (carboxyl terminus of Hsp70-interacting protein) regulate

163 ffect of a potent molecular chaperone, CHIP (carboxyl terminus of Hsp70-interacting protein), on alph

164 ains that bind a common acceptor site at the carboxyl terminus of Hsp90.

165 Certain mutations in the carboxyl terminus of HSV-1 glycoprotein B (gB) and in th

166 in the identification of key regions in the carboxyl terminus of IglE that are required for intracel

167 a3.1 by phosphorylating histidine 358 in the carboxyl terminus of KCa3.1.

168 The carboxyl terminus of LANA interacts with the F-box and W

169 Further, the carboxyl terminus of Lin28 is necessary for interaction

170 he tryptophan-rich lipid-binding loop in the carboxyl terminus of LPL prevents homodimer formation an

171 n adhesin recognition site is present in the carboxyl terminus of LR.

172 om malaria and circulating antibodies to the carboxyl terminus of merozoite surface protein 1 (MSP1).

173 reated a rat monoclonal antibody against the carboxyl terminus of mouse GPIHBP1 and used that antibod

174 The carboxyl terminus of MPER has the sequence LWYIK and app

175 orylation sites (Ser-725 and Ser-732) in the carboxyl terminus of murine MCM3 (mMCM3) and that ATM ph

176 he Na channel, the IQ-CaM interaction in the carboxyl terminus of Na(V)1.5 is latent under physiologi

177 We identify an ER-targeting sequence at the carboxyl terminus of native WLS that is critical for ER

178 Thus, the carboxyl terminus of NK1R is the structural basis for di

179 ntified an actin retroposon insertion at the carboxyl terminus of one of the ancestral POTE paralogs.

180 Furthermore, deletion of the conserved carboxyl terminus of ORF45 in the KSHV genome drasticall

181 The carboxyl terminus of p17 is necessary for interaction wi

182 Two discrete regions within the carboxyl terminus of p53 are essential for nucleolar loc

183 abilized cells requires sequences within the carboxyl terminus of p53.

184 variations in the details of docking of the carboxyl terminus of peptide ligands within this cleft,

185 have identified an invariant residue in the carboxyl terminus of PKC that mediates the binding to Hs

186 nts revealed that amino acids 686-726 in the carboxyl terminus of plakophilin-1 are required for its

187 n together, this study demonstrates that the carboxyl terminus of podocin/MEC-2 has to be placed at t

188 the LCMT-1 active-site pocket recognizes the carboxyl terminus of PP2A, and, interestingly, the PP2A

189 ACE edited the carboxyl terminus of proteasome-produced MHC class I pep

190 und by yeast two-hybrid analysis to bind the carboxyl terminus of protocadherin 15 CD3, a tip link pr

191 s implicate TM3 and a second region near the carboxyl terminus of PS1 aminoterminal fragment in media

192 m cells, involved two helical domains at the carboxyl terminus of Ric-8A.

193 ith viral protein kinases phosphorylates the carboxyl terminus of RNA polymerase II (Pol II) in vitro

194 ted through a direct interaction between the carboxyl terminus of sdk-1 and specific PDZ domains of M

195 In the best model, the carboxyl terminus of secretin was found to bind in a gro

196 The carboxyl terminus of SPAK (amino acids 316-548) pulls do

197 amino terminus of CNGA3 specifically to the carboxyl terminus of stereocilia tip-link protein CDH23

198 Notably, the cytosolic carboxyl terminus of STIM1 is sufficient to activate SOC

199 that this action of Gbetagamma requires the carboxyl terminus of the 25-kDa synaptosome-associated p

200 luorescent protein (YFP) was tethered to the carboxyl terminus of the alpha2A adrenergic receptor (al

201 The structural models showed that the carboxyl terminus of the ancestral sequence is more heli

202 which the C domain of EiAPR was fused to the carboxyl terminus of the APS reductase from Pseudomonas

203 a common polymorphism, positioned within the carboxyl terminus of the Bbeta-chain of the molecule.

204 tted from the PDZ-associated scaffold in the carboxyl terminus of the beta(1)-AR to Ser(312) in the 3

205 KAP79, and PKA form a ternary complex at the carboxyl terminus of the beta(1)-AR.

206 ntified tyrosine residues 292 and 422 at the carboxyl terminus of the beta-chain as the principal sit

207 he tyrosine kinase c-Src associated with the carboxyl terminus of the beta3 cytosolic tail.

208 (2+) sensing EF hand-like (EFL) motif in the carboxyl terminus of the channel.

209 protein (PfCSP), were fused in frame to the carboxyl terminus of the ClyA gene (clyA::t-csp) in gene

210 nstrated that fusing the heptapeptide to the carboxyl terminus of the FSHbeta subunit resulted in an

211 f Gbetagamma-specific scavengers-namely, the carboxyl terminus of the G protein-coupled receptor kina

212 us and discovered that removing the proximal carboxyl terminus of the GABA(B)(1a) subunit significant

213 Four RXXR motifs are present at the carboxyl terminus of the HBeAg precursor, with the first

214 The carboxyl terminus of the Hsc70-interacting protein (CHIP

215 acid residues Ser(895) and Val(1075) in the carboxyl terminus of the human calcium receptor (hCaR),

216 ction network crucial for recognition of the carboxyl terminus of the KDEL signal.

217 These experiments demonstrate that the carboxyl terminus of the LHX3 transcription factor is no

218 entification of phosphorylation sites in the carboxyl terminus of the minichromosome maintenance prot

219 Cleavage of the intracellular carboxyl terminus of the N-methyl-d-aspartate (NMDA) rec

220 a homologous 60-amino acid region within the carboxyl terminus of the Na(v)1.2 and the Na(v)1.3 chann

221 66 whereas residues in the center and at the carboxyl terminus of the peptide interact only weakly if

222 Amino acids are transferred to the carboxyl terminus of the peptide through adenosine triph

223 l step in this pathway is methylation of the carboxyl terminus of the prenylated protein by isoprenyl

224 traproline sequence (Pro293-Pro296) near the carboxyl terminus of the protein.

225 the protein is located 16 residues from the carboxyl terminus of the pyruvoyl-containing alpha chain

226 the presence of phosphorylation sites on the carboxyl terminus of the receptor; kinase activity of G

227 A highly immunogenic region in the carboxyl terminus of the rhBZLF1 protein containing over

228 To investigate the role of the carboxyl terminus of the UL20 protein (UL20p) in cytopla

229 Insertions in the carboxyl terminus of the UL28 protein were found to inte

230 ial signaling properties attributable to the carboxyl terminus of this receptor by using stably trans

231 MD), which leads to partial unwinding of the carboxyl terminus of transmembrane helix 6 and induces a

232 dition of this 19-amino acid sequence to the carboxyl terminus of Trf confers full acceptor activity

233 show that phenylalanine residues within the carboxyl terminus of UL20p are involved in the regulatio

234 The deletion of six amino acids from the carboxyl terminus of UL20p caused an approximately 1-log

235 he addition of an ER retention signal at the carboxyl terminus of UL20p forced the ER retention of gK

236 o amino acid changes cause retraction of the carboxyl terminus of UL20p from the intracellular space.

237 he role of phenylalanine residues within the carboxyl terminus of UL20p, since aromatic and hydrophob

238 found the second WW domain of SMURF1 and the carboxyl terminus of USP9X critical for this interaction

239 We additionally found that the carboxyl terminus of Vps32/CHMP4B plays a key role in re

240 However, the role of the carboxyl-terminus of ADAMTS13 in substrate recognition r

241 The findings indicate that the distal carboxyl-terminus of alpha1C plays an important role in

242 Although it is known that the carboxyl-terminus of bound-form Lpp is located in the pe

243 al domain of Cx32, and palmitoylation at the carboxyl-terminus of Cx32.

244 ing Cx43 with ACT1, a peptide mimetic of the carboxyl-terminus of Cx43, accelerates fibroblast migrat

245 tivity, and lentiviral overexpression of the carboxyl-terminus of G-protein-coupled receptor kinase 2

246 urs at two distinct cysteine clusters in the carboxyl-terminus of GluN2A and GluN2B subunits that dif

247 a cluster of cysteines in the middle of the carboxyl-terminus of GluN2A and GluN2B, leads to an incr

248 sackievirus-adenovirus receptor fused to the carboxyl-terminus of human IgG) efficiently neutralizes

249 yubiquitin) chains are formed by linking the carboxyl-terminus of one Ub (ubiquitin) subunit to eithe

250 interact directly in mammalian cells via the carboxyl-terminus of p53 and the DNA-binding domain of D

251 ed of the amino-terminus of Rem and the core/carboxyl-terminus of Rad inhibited L-type current withou

252 the amino-terminus of Rad fused to the core/carboxyl-terminus of Rem inhibited L-type current with a

253 a cyan fluorescent protein, as a tag at the carboxyl-terminus of the murine TRPC6 protein.

254 somal activity, suggesting that the extended carboxyl-terminus of this cofactor confers suboptimal bi

255 The effects of mutating the GABA(B)R2 carboxyl terminus on receptor stability and signaling we

256 g specific charged residues in the channel's carboxyl terminus or in the PDZ domain converts the sele

257 e limiting membrane of the endosome with its carboxyl terminus oriented to the cytoplasm.

258 ragment (A1-F92) as well as multiple smaller carboxyl-terminus peptides ranging from 17 to 26 amino a

259 on to substrates, ADP-ribosylation of the Ub carboxyl terminus precludes ubiquitylation.

260 spheres with Cx43 mutants revealed that Cx43 carboxyl terminus prevents neuronal maturation.

261 the amino-terminus in close proximity to the carboxyl-terminus produced similar FRET ratios.

262 more pronounced after the truncation of the carboxyl terminus proximal to the IQ motif (Na(V)1.5(Del

263 an unexpected sequence located near the Bim carboxyl-terminus (residues 181-192).

264 Intriguingly, the truncation of the PafE carboxyl-terminus resulted in the robust binding of PafE

265 utionarily conserved serine residue near the carboxyl terminus (Ser-883 in Xenopus).

266 ted approximately in the middle of the UL20p carboxyl terminus substantially enhanced cytoplasmic env

267 ductase, which has a joint Trx domain at the carboxyl terminus, termed NTRC.

268 TFPI is associated with lipoproteins and its carboxyl terminus (TFPIct) has been shown to be a ligand

269 esidue PDZ-ligand binding motif (PBM) at the carboxyl terminus that can function as a virulence deter

270 s contains a four-amino-acid sequence at its carboxyl terminus that is termed the PDZ-binding motif (

271 fied a novel phosphorylation site in the CBP carboxyl terminus that mediated association with AP-1 si

272 nt mutations also identified residues in the carboxyl terminus that regulated recovery from channel d

273 An intracellular mutation in the carboxyl terminus that slowed recovery of P2X1 receptor

274 mically to identify residues in the receptor carboxyl terminus that were phosphorylated upon agonist

275 Both of the IAP variants lacked the 2 carboxyl terminus thrombospondin type 1 repeat (TSR) and

276 en targeting the intracellular loops and the carboxyl terminus to investigate how specificity is enco

277 mino terminus to Orai1 enabled access of its carboxyl terminus to Orai1 and activation of Ca(2+) infl

278 rent F box protein that uses a domain at the carboxyl terminus to recognize substrates [1, 2].

279 observed when LBR-TD is extended toward its carboxyl terminus, to include an area rich in Ser-Arg re

280 D) and glutamic acid (E) as well as the free carboxyl terminus, to their corresponding methyl esters.

281 In summary, the carboxyl terminus TSR sequence is important for cleaving

282 g new gene) and HECT (homologous to the E6AP carboxyl terminus) types shed light on their enzymatic a

283 nstrate that a HECT (homologous to the E6-AP carboxyl terminus) ubiquitin ligase, Smurf2, is required

284 Interaction of GABARAP with the AT(1)R carboxyl terminus was further substantiated using GST pu

285 The carboxyl terminus was subject to the most change and may

286 Substitution of the carboxyl terminus was sufficient for converting Nox4 int

287 The extramembranous and intracellular carboxyl-terminus was deleted by insertion of premature

288 antigenic epitopes from either the amino- or carboxyl terminus were characterized with Als2cr4 recomb

289 h an unexpected epsilon-glycinylglycinyl-Lys carboxyl terminus when the site of linkage is Lys48.

290 g sequence that is involved in orienting the carboxyl terminus, which binds the catalytic iron.

291 p53 is subject to lysine methylation at its carboxyl terminus, which has been shown to repress p53's

292 ue fragment of the Ca(V)1.2 alpha(1) subunit carboxyl terminus, which includes a tandem of the pre-IQ

293 s it has an exceptionally long intracellular carboxyl terminus, which is predicted to be mainly disor

294 t would generate a unique 34 amino acid (aa) carboxyl terminus while maintaining the remaining struct

295 a cholesterol through the interaction of its carboxyl terminus with lipoproteins and heparan sulfate

296 n 2 (D-AKAP2/AKAP10), which interacts at its carboxyl terminus with protein kinase A and PDZ domain p

297 h the exclusion of exon 3 generates a unique carboxyl terminus with specific anti-apoptotic functions

298 a, a self- and tumor Ag, was modified at its carboxyl terminus with the invariant chain-derived Ii-Ke

299 sphorylation of AQP2 at various sites in its carboxyl terminus, with Ser-256 phosphorylation critical

300 P processing of CCL16-(1-97) in its extended carboxyl terminus yields two products, CCL16-(8-77) and