ライフサイエンスコーパス: COOH terminus

1 ains two breast cancer susceptibility gene 1 COOH terminus (BRCT) motifs, which are present in severa

2 Competition of TNP-ATP binding to the Kir1.1 COOH terminus by MgATP was complex with both Mg(2+) and

3 rm the extracellular orientation of the PV-1 COOH terminus.

4 F hands in the proximal region of the NaV1.5 COOH terminus.

5 and encodes a variant protein that carries a COOH terminus different from that of IIp45 due to a fram

6 e single baculovirus iap repeat (BIR) and a -COOH-terminus coiled domain instead of a RING finger.

7 roteolytic activity that liberates the Abeta COOH terminus from the beta-amyloid precursor protein is

8 al activity was the cationic and amphipathic COOH-terminus.

9 using antibodies specific for the NH(2) and COOH terminus of Sec61alpha was used to map the location

10 H2 terminus, and intracellular loops 3-8 and COOH terminus in the 17-transmembrane model.

11 fragments that we termed truncated EAAT2 and COOH terminus of EAAT2 (CTE).

12 except in their third intracellular loop and COOH terminus, domains thought to be involved in signal

13 se mutations in the NH2 terminus (W236R) and COOH terminus (Y856H) of sMyBP-C have been causally link

14 ing domains reside in the central region and COOH-terminus of OspA.

15 tion also results in an unmasking of the ARF COOH terminus, suggesting that redistribution disrupts a

16 on of HIV accessory protein Vpr, which binds COOH terminus of hHR23A/B.

17 tein 1 (TopBP1) protein contains eight BRCA1 COOH terminus motifs and shares similarities with Cut5,

18 this single amino acid deletion in the BRCA1 COOH terminus (BRCT) domain affects the function of the

19 amely activation domain 1, and the two BRCA1 COOH terminus (BRCT) repeats.

20 Here, we show that the Xenopus BRCA1 COOH terminus repeat-containing Xmus101 protein is requi

21 Overexpression in plants of the CBF1 COOH-terminus as a fusion with the yeast GAL4 DNA bindin

22 PP2A can physically associate with the CFTR COOH terminus.

23 monstrate a novel role of the sodium channel COOH terminus structure in the control of channel inacti

24 tic cleavage of tubulin's negatively charged COOH terminus or by high salt concentrations.

25 protein-crystal interaction, and the charged COOH terminus is often implicated in this function.

26 logenin protein), which contains the charged COOH terminus of the full protein, on the HAP surface.

27 domains requires sequences within the coilin COOH terminus.

28 alytic kinase domain of the highly conserved COOH terminus of the protein.

29 antibody (mAb), TnI-1, against the conserved COOH terminus of TnI.

30 otein kinase (PKA) or truncation of the Cx43 COOH terminus (CT).

31 The cytosolic COOH terminus of alphaENaC contained a strongly interact

32 The DACH1 COOH terminus was required for binding to PELP1.

33 Homologous to E6AP COOH terminus (HECT) ubiquitin ligases have been implica

34 Removal of the entire COOH terminus by truncation (c'973 and c'991) abrogated

35 s abolished nucleotide binding to the entire COOH terminus or to the first 49 amino acid residues of

36 on proteins in cancer cells contains the EWS COOH terminus.

37 The exposed COOH terminus of protein kinase C provides the primary i

38 Moreover, fusion of p53 extreme COOH terminus to a completely unrelated transcriptional

39 e, serine 1244 (Ser(1244)), near the extreme COOH terminus of NR2C, which is phosphorylated by both c

40 In contrast, loss of the extreme COOH terminus rendered the protein unstable and led to r

41 and Slo1(QEERL), which differ at the extreme COOH terminus, show markedly different steady-state expr

42 sease-causing mutation truncates the extreme COOH-terminus and induces a closed gating conformation.

43 ignal of synaptotagmin 1 lies at the extreme COOH-terminus of the protein and can function in the abs

44 med to assess the effect of loss of the FLI1 COOH terminus on transcriptional modulation of EWS/FLI1

45 se amyloid peptide Abeta has a heterogeneous COOH terminus, as variants 40 and 42 residues long are f

46 e site (RTRR), a ZP domain and a hydrophobic COOH-terminus with a 3' UTR of only 10 nucleotides.

47 gnizes the COOH terminus indicates an intact COOH terminus.

48 to inside-out signaling, whereas the intact COOH terminus is important for outside-in signaling.

49 Its COOH terminus is composed of two potential protein-prote

50 with its NH2 terminus in the matrix and its COOH terminus in the cytosol.

51 ts NH(2) terminus facing the cytosol and its COOH terminus in the intermembrane space.

52 ecretion and to a cell-binding domain at its COOH terminus for receptor-mediated internalization.

53 At its COOH terminus, mACF7 contains two putative EF-hand calci

54 5/Disc-large/ZO-1 (PDZ)-binding motif at its COOH terminus, the identity of the PDZ domain protein(s)

55 s a membrane-spanning segment located at its COOH terminus.

56 intermediate filament-binding domain at its COOH terminus.

57 Because FAK function is regulated by its COOH terminus (FAK-CD), we used FAK-CD as a target to id

58 potentially novel interactions involving its COOH terminus as sites for early DNA damage and stress-m

59 R7BP is palmitoylated near its COOH terminus, which targets the protein to the plasma m

60 n, and a pleckstrin homology domain near its COOH terminus.

61 more easily because the conformation of its COOH terminus against the membrane is altered.

62 regulated through the phosphorylation of its COOH terminus.

63 r Akt to be fully activated, Ser(473) on its COOH terminus needs to be phosphorylated.

64 d muscle myosin II motor domain fused on its COOH terminus to a thermal stable, fast folding variant

65 VCP is phosphorylated at Ser784 within its COOH terminus, a region previously shown to target VCP t

66 RF NH2-terminus that bound to SYK, or at its COOH-terminus motif that binds to MERLIN, the product of

67 gating enzyme Ubc13 and the ubiquitin ligase COOH terminus of Hsp70 interacting protein (CHIP) as bei

68 on and interaction with the ubiquitin ligase COOH terminus of Hsp70-interacting protein.

69 The intact RING finger domain at the Mdm2 COOH terminus (amino acids 399-489) was necessary and su

70 iruses expressing F proteins with a modified COOH terminus.

71 quence of the 19 amino acids at the myopodin COOH terminus.

72 agment containing residues 194 to the native COOH terminus at position 319 was solved by x-ray diffra

73 several analyzed motifs present in the NKCC2 COOH terminus, only those required for ER exit and surfa

74 context of the last 11 residues of the NR2b COOH terminus.

75 tion element, each labeled near the NH(2) or COOH terminus with fluorescent probes.

76 ab5c, or Rab5a truncated at the NH(2) and/or COOH terminus.

77 es virus fusion protein at either the NH2 or COOH terminus linked via a four-residue turn sequence (G

78 ppropriate targeting sequences to the NH2 or COOH terminus of CKAR.

79 scent protein (YFP) were fused to the NH2 or COOH terminus of MRAP such that YFP fluorescence could o

80 assettes fused with either NH(2) terminus or COOH terminus of DNA polymerases broaden the salt concen

81 hRAD54 bound directly to the p53 COOH terminus in vitro without a nucleic acid intermedia

82 because of differential splicing of the p63 COOH terminus.

83 to activation, but whether the palmitoylated COOH terminus participates in signaling, especially when

84 trinsic affinity of PDK-1 for phosphorylated COOH terminus is over an order of magnitude greater than

85 he gene, corresponding to the phosphorylated COOH terminus of Gsy2p.

86 on proteins, and its tyrosine-phosphorylated COOH terminus binds Nck, a host adaptor protein critical

87 breast cancer susceptibility gene 1 product COOH terminus domain of XRCC1.

88 G-protein signaling-GAIP-interacting protein COOH terminus (GIPC) is involved in protein trafficking,

89 ecific peptide motifs followed by a required COOH-terminus.

90 cells the recombinant 393-amino acid residue COOH terminus of C19ORF5 (C19ORF5C) exhibited four types

91 e globular Cks domain and the glutamine-rich COOH terminus.

92 ology (SH) 3 domains binding to the Pro-rich COOH terminus of Cbl.

93 aC) mice express a protein lacking the Runx2 COOH terminus, which integrates several cell proliferati

94 domain of PYK2 and an LD motif in gelsolin's COOH terminus.

95 We observe that appending GFP to Pex7p's COOH terminus shifts Pex7p's intracellular distribution

96 Thus, the Sec2p COOH terminus functions in targeting vesicles, however,

97 to-substrate ratios near the betaII spectrin COOH-terminus.

98 t activation potential appended to the Stat1 COOH terminus could substitute for the wild-type protein

99 idues in loop alpha2 or in the alpha-subunit COOH terminus (alphaCT).

100 cysteine to the long disordered beta-subunit COOH terminus (betaCT) enabled it to become cross-linked

101 The COOH terminus of Aux1p/Swa2p contains a J-domain that is

102 The COOH terminus of EEA1 contains a FYVE domain that intera

103 The COOH terminus of menin mediates binding to DNA, but MEN1

104 The COOH terminus of p53 modulates the transcriptional and a

105 The COOH terminus of periplakin was shown to have a strong a

106 The COOH terminus of the peptide main chain is tugged toward

107 The COOH terminus of the STATs acts as a transcriptional act

108 The COOH terminus of YAP65 is necessary and sufficient to me

109 In addition, the COOH terminus of PTEN has a typical PDZ domain-binding m

110 Using a novel antibody directed against the COOH terminus of SUR1 (ABCC8), we show that this K(ATP)

111 inus is highly homologous to Poleta, and the COOH terminus is highly homologous to the S. cerevisiae

112 A direct interaction between F-actin and the COOH terminus of alpha-ENaC was further corroborated by

113 peptide identified by phage display, and the COOH terminus of FAK was detected by in vitro and in viv

114 close proximity to helices 11 and 12 and the COOH terminus of tubulin.

115 bonds, which bring the sialylmotifs and the COOH terminus within close proximity, is critical for th

116 s, we conclude that the NH2 terminus and the COOH terminus, as well as the major portion of a large c

117 peptide binding groove is widened around the COOH terminus of the alpha 1 helix, which contains resid

118 f factor Va contains an acidic region at the COOH terminus (residues 680-709).

119 evealed the juxtaposition of epitopes at the COOH terminus and near the proline-rich region, and of t

120 wever, extension of the kinase domain at the COOH terminus by inclusion of the 36 residue linker regi

121 ine in sialylmotif L and the cysteine at the COOH terminus form a second disulfide bridge.

122 res the presence of a conserved D-box at the COOH terminus of Aurora B.

123 The PDZ binding motif located at the COOH terminus of CFTR interacts preferentially with the

124 roduced, and this truncation occurred at the COOH terminus of Cx45.6.

125 n R205A exhibited altered specificity at the COOH terminus of fMLF, with R205A binding fMLF-O-butyl >

126 kinase domains, SK1 and SK2, present at the COOH terminus of giant obscurin-B.

127 ingle-chain antibody against EGFRvIII at the COOH terminus of H and containing the marker green fluor

128 unctional nuclear localization signal at the COOH terminus of HIP1, which contributes to the nuclear

129 d hMAST205 and the PDZ binding domain at the COOH terminus of MMAC1/PTEN.

130 tion, the presence of the VEDEC motif at the COOH terminus of Slo1 channels is sufficient to confer a

131 ddition of green fluorescence protein at the COOH terminus of ST8Sia IV did not render the enzyme ina

132 A similar complex formed at the COOH terminus of the peptide shows no sign of DM-specifi

133 The role of a LXXLL motif at the COOH terminus of this sequence has now been analyzed by

134 other thin filament proteins is found at the COOH terminus of TnI, truncations of the last 19-23 amin

135 dependent on the conserved tryptophan at the COOH terminus of VCA.

136 essive or individual EC domains fused at the COOH terminus to an Fc domain, were analyzed using a bea

137 pha (1-68) undergoes processing first at the COOH terminus to produce SDF-1alpha 1-67 and then at the

138 he His-tag plus two extra amino acids at the COOH terminus when expressed in Escherichia coli generat

139 ificantly when using a PfR4 truncated at the COOH terminus, suggesting the involvement of COOH-termin

140 Serum processing of SDF-1alpha at the COOH terminus, which has not been previously reported, r

141 ne-rich linker domain and SH3 domains at the COOH terminus.

142 ne in sialylmotif S, and one cysteine at the COOH terminus.

143 arge alpha-helical-coiled coil domain at the COOH terminus.

144 ture of human p23 lacking 35 residues at the COOH terminus.

145 ng sequence called the CAP-Gly domain at the COOH terminus.

146 tion leads to a conformational change at the COOH terminus.

147 and a talin-like actin-binding domain at the COOH terminus.

148 Both of these residues are well beyond the COOH terminus predicted previously by two independent st

149 RSK2 binds the COOH terminus of PEA-15 and does not interact with its N

150 ve form is monomeric and is regulated by the COOH terminus of beta-catenin, which selectively compete

151 In turn, this allows SpoIVB to cleave the COOH terminus of SpoIVFA an event pivotal to activating

152 mbrane and the fusion protein containing the COOH terminus of Cx45.6.

153 ghout the chase; no fragments containing the COOH terminus were detected.

154 us mutation in the c-rel region encoding the COOH terminus of c-Rel (c-relDeltaCT/DeltaCT) display ma

155 A retrovirus encoding the COOH terminus of growth arrest and DNA damage gene (GADD

156 This bonding spatially fixes the COOH terminus of the subunit in the correct context for

157 pe, thus excluding an essential role for the COOH terminus domain of Par-4 in embryogenesis and devel

158 8 mutation truncated three residues from the COOH terminus and resulted in the loss of severing activ

159 -S) and a synthetic peptide derived from the COOH terminus of Galphaq abolished mechanically evoked 5

160 wo minimal peptides were identified from the COOH terminus of the fusion protein.

161 passing amino acid sequence 695-699 from the COOH terminus of the heavy chain of factor Va (Asp-Tyr-A

162 at amino acid region (695)DYDY(698) from the COOH terminus of the heavy chain of factor Va regulates

163 X derivative containing 25 residues from the COOH terminus of the proteinase domain of human X.

164 portion between 39 and 51 residues from the COOH terminus of the rat oxytocin receptor is required f

165 yeast two-hybrid screen that identified the COOH terminus of the Hsp70-interacting protein (CHIP) as

166 We identify the COOH terminus of menin as the domain that mediates the s

167 A, but MEN1 disease-derived mutations in the COOH terminus abolish the ability of menin to bind DNA.

168 ys-15 in the NH2 terminus and Cys-622 in the COOH terminus also reacted with MTS reagents.

169 VEGF-Ax has a 22-amino-acid extension in the COOH terminus and has been reported to function as a neg

170 deletion of the phosphorylation site in the COOH terminus domain of Rb abrogates phosphorylation of

171 ion, whereas tyrosine phosphorylation in the COOH terminus influences interaction with E-cadherin.

172 at there is an internalization signal in the COOH terminus of CFTR that consists of Tyr(1424)-X-X-Ile

173 n of the internalization motif SSXXIL in the COOH terminus of CXCR4 resulted in B cells that constitu

174 P was dependent on a sequence (PPPXY) in the COOH terminus of each subunit.

175 ce of the membrane interactive domain in the COOH terminus of gammaENaC was established with whole-ce

176 ) phosphorylates four serine residues in the COOH terminus of glycogen synthase.

177 y active and possesses a chromodomain in the COOH terminus of its IN.

178 ified a nuclear localization sequence in the COOH terminus of NCoA62/SKIP and showed that NCoA62/SKIP

179 ephosphorylation of Ser/Thr-Pro sites in the COOH terminus of S6K, including Thr(412), a residue esse

180 ion of a predicted coiled-coil region in the COOH terminus of SNX1 also abolished vesicle localizatio

181 y a novel role for a structural motif in the COOH terminus of the heart NaV1.5 sodium channel in dete

182 ine 950 residue and serines 1280-1283 in the COOH terminus of the receptor are required for IGF-I-ind

183 2 to induce phosphorylation of Ser375 in the COOH terminus of the receptor, to induce association of

184 constructs containing point mutations in the COOH terminus that impair Rab5 but not PtdIns-3-P bindin

185 autophosphorylation at two positions in the COOH terminus, the turn motif, and the hydrophobic motif

186 carbohydrate recognition domain motif in the COOH terminus.

187 suppressor protein as well as regions in the COOH terminus.

188 yr at residues Tyr(992) and Tyr(1068) in the COOH terminus.

189 xpressing a Par-4 mutant protein lacking the COOH terminus domain.

190 ) was raised against a peptide mimicking the COOH terminus of hirudin.

191 (2)-terminal half, whereas residues near the COOH terminus are required for binding to claudins.

192 In contrast, the conserved tyrosine near the COOH terminus is dispensable and the pleckstrin homology

193 nd that a clearly delineated region near the COOH terminus of both proteins is necessary for both the

194 entified and characterized a region near the COOH terminus of PB1-F2 that is necessary and sufficient

195 We report here that a region near the COOH terminus of PIAS1 (amino acids 392-541) directly in

196 , resulting in an amino acid change near the COOH terminus of the protein.

197 ubulin that encompasses alpha379 is near the COOH terminus that has been proposed as a site of intera

198 Acting as a dominant negative, the COOH terminus of Pyk2 fused to a Tat peptide (Tat-CT), b

199 n of these cells targets the NH2 but not the COOH terminus of IkappaBalpha.

200 residues from the NH(2)-terminal side of the COOH terminus abolished nucleotide binding to the entire

201 ata indicate that the central portion of the COOH terminus is not essential for lymphoid transformati

202 nd reveal that one important function of the COOH terminus is to stabilize the v-Abl protein in lymph

203 tate NMR to determine the orientation of the COOH terminus of an amelogenin splice variant, LRAP (leu

204 essential function of polyglycylation of the COOH terminus of beta-tubulin can be transferred to alph

205 t with earlier observations, deletion of the COOH terminus of BRCA1 did not affect significantly the

206 Deletion of the last six residues of the COOH terminus of either PMCA2b or PMCA4b did not alter t

207 We searched for binding partners of the COOH terminus of kinesin light chain, which contains tet

208 Deletion of the COOH terminus of SLAP-2 blocked function and abrogated i

209 The location of the interaction of the COOH terminus of the bacteriophage T4 DNA polymerase wit

210 These cleavages result in the release of the COOH terminus of the molecule and the production of a M(

211 ery little effect on the conformation of the COOH terminus of TnI as indicated by the unaffected mAb

212 Studies with constructs of the COOH terminus reveal that the intrinsic affinity of PDK-

213 sing a v-Abl protein lacking portions of the COOH terminus were compared for their ability to transfo

214 of amino acids in the central region of the COOH terminus, including those implicated in JAK interac

215 highly conserved juxtamembrane region of the COOH terminus, where p120(ctn) also binds.

216 r to the first 49 amino acid residues of the COOH terminus.

217 localized to the last 21 amino acids of the COOH terminus.

218 gh affinity to integrin alpha(v)beta3 on the COOH terminus of the viral attachment (H) protein and re

219 opic expression of the PBS mutant and/or the COOH terminus of actopaxin in HeLa cells resulted in sub

220 linker attached to either the NH(2)- or the COOH terminus of an antigenic peptide that is tightly bo

221 (N0) epitope-tagged at either the NH2 or the COOH terminus showed their localization to the mitochond

222 al antibody that specifically recognizes the COOH terminus indicates an intact COOH terminus.

223 full-length Sec2 proteins, implying that the COOH terminus does not alter the exchange rate.

224 The results provide evidence that the COOH terminus is an essential structure in TnI and parti

225 inding and motility assays, we show that the COOH terminus mediates binding of sMyBP-C to thick filam

226 We recently showed that the COOH terminus of the cystic fibrosis transmembrane condu

227 These results demonstrate that the COOH terminus of the DNA polymerase is inserted into the

228 These results suggest that the COOH terminus of the inhibitory region of TnI (residues

229 ing of this fusion protein revealed that the COOH terminus of Tir, by itself, is sufficient to initia

230 pic staining of myofibrils indicate that the COOH terminus of TnI forms an exposed structure in the m

231 f p18(INK4c) regulation mediated through the COOH terminus and suggest that functional differences mi

232 onstrated that TRP bound to INAD through the COOH terminus, and this interaction was required for loc

233 tivity and, notably, when transferred to the COOH terminus of a warm-adapted (rabbit) PEPT1, it confe

234 ss a spore membrane, binding in trans to the COOH terminus of another SpoIVB molecule.

235 cking site for TSG101 has been mapped to the COOH terminus of Bcr, indicating that this interaction m

236 Armadillo (Arm) repeat 10 to the COOH terminus of beta-catenin is involved in binding to

237 Specifically, SpoIVB binds to the COOH terminus of BofA.

238 Binding of this mAb to the COOH terminus of cardiac TnI induced extensive conformat

239 inal 15 aa RepA tag, when it is fused to the COOH terminus of GFP.

240 ition tag, plasmid P1 RepA, was fused to the COOH terminus of green fluorescent protein (GFP).

241 "A" and "B" sites and maps primarily to the COOH terminus of its alpha 5 helix.

242 e docking of Cdc2-cyclin B1 complexes to the COOH terminus of Myt1 facilitates the phosphorylation of

243 have now produced a specific antibody to the COOH terminus of NGEP-L and showed that it detects an ap

244 se-binding region of p16(INK4a) fused to the COOH terminus of p18(INK4c) is active in all known bioch

245 es a series of plakin repeats similar to the COOH terminus of plakins such as plectin and BPAG1e.

246 equence (AAL) derived from DOC-2/DAB2 to the COOH terminus of R11, we showed that R11PPL but not R11

247 ia binding of the PDZ domain of PTPH1 to the COOH terminus of TACE.

248 l three known K(ATP) channels but not to the COOH terminus of the ATP-insensitive channel, Kir2.1.

249 Proximate to the COOH terminus of the BRCA2 protein, a conserved and DNA

250 MMP-7 had another cleavage site close to the COOH terminus of the cysteine-rich domain.

251 A peptide corresponding to the COOH terminus of the DNA polymerase was labeled with a f

252 evealed interaction of MLCK-147 close to the COOH terminus of the first actin and near residues 228-2

253 es the NH(2) terminus of the EWS gene to the COOH terminus of the FLI1 transcription factor.

254 Small espin is identical in sequence to the COOH terminus of the larger ( approximately 110-kD) espi

255 two conserved tyrosines located close to the COOH terminus of the protein-tyrosine kinase Syk.

256 e start of the nearby TnI helix 1 and to the COOH terminus of the TnT-TnI coiled-coil.

257 two PAM residues (Arg(126)-His(127)) to the COOH terminus of VEK30 (VEK32) maintained a monomeric pe

258 alytic domain (Deltacap, residues 433 to the COOH terminus) clamp tightly around the DNA helix to for

259 the oligonucleotide was oriented toward the COOH terminus of the helix.

260 NH(2) terminus of p63 represses, whereas the COOH terminus activates hsp70 transcription.

261 e in nascent lambda transcripts, whereas the COOH terminus binds RNA polymerase and contacts DNA temp

262 To elucidate whether the COOH terminus is important in the binding and orientatio

263 cloned as a protein that interacts with the COOH terminus of adenomatous polyposis coli (APC).

264 bstrate and that CaMKII interaction with the COOH terminus of alpha1C is essential for CDF of L-type

265 riched PDZ protein) that associates with the COOH terminus of GCC in biochemical assays and by co-imm

266 tion that CLNX physically interacts with the COOH terminus of SERCA2b and that after dephosphorylatio

267 4a/b, Ddb1, and Crbn, and interacts with the COOH terminus of the ACR via Crbn.

268 ranslocation is indeed directional, with the COOH terminus of the substrate protein entering ClpP fir

269 electrostatic tethering interaction with the COOH terminus of tubulin.

270 t has been proposed that elements within the COOH terminus may determine substrate specificity of the

271 nsitive sites had been identified within the COOH terminus of aggrecan, demonstration that aggrecanas

272 To localize the ATP-binding site within the COOH terminus of Kir1.1, we produced and purified maltos

273 endosomal membranes via a domain within the COOH terminus of Vps27.

274 ugh all mutants lacking sequences within the COOH terminus were compromised for lymphoid transformati

275 dence that this 13-amino acid segment at the COOH-terminus of alpha-spectrin is crucial to the stabil

276 as the LIM domain, which is localized in the COOH-terminus is dispensable for this phenomenon.

277 We report that the last 3 amino acids in the COOH-terminus of CFTR (T-R-L) comprise a PDZ-interacting

278 and four potential SH3-binding motifs in the COOH-terminus.

279 ng a monoclonal antibody that recognizes the COOH-terminus of hNIS revealed a band with a molecular w

280 It was found that the COOH-terminus of FPC and the NH2-terminus of PC2 interac

281 Mutational analysis through the COOH-terminus using truncation and alanine-substitution

282 sisting of a short degron, CL1, fused to the COOH-terminus of green fluorescent protein (GFPu).

283 sing synthetic peptides corresponding to the COOH-terminus of human complement C5a we demonstrated th

284 Mutations within the COOH-terminus of Tra1p disrupted its interaction with ac

285 K506-binding protein (FKBP) domains at their COOH terminus.

286 rminus and one or three LIM domains at their COOH terminus.

287 other members of the SLC12A family, of their COOH terminus.

288 domain, triggering EZH2 degradation through COOH terminus of Hsp70-interacting protein (CHIP)-mediat

289 HDX of the TnI COOH terminus indicated that its known role in regulatio

290 Most of the TnI COOH terminus was protected from H/D exchange, implying

291 Da RGMc to a 40 kDa protein with a truncated COOH-terminus.

292 interacts electrostatically with the tubulin COOH terminus to permit diffusional translocation of MCA

293 COOH terminus was replaced by the wild-type COOH terminus of beta-tubulin.

294 Among >40 rab proteins, rab38 has a unique COOH terminus which would allow posttranslational farnes

295 wn forms of MyBP-C slow, but it has a unique COOH terminus.

296 cking or function of GCC, we used the unique COOH terminus of GCC as the "bait" to screen a human int

297 etal myofibers with antibodies to the unique COOH terminus of variant-1 demonstrated that, unlike oth

298 itude greater than that for unphosphorylated COOH terminus, contrasting with the finding that PDK-1 d

299 via two PSDP motifs present within the Vps27 COOH terminus.

300 transformed with an alpha-tubulin gene whose COOH terminus was replaced by the wild-type COOH terminu