ライフサイエンスコーパス: ethylmaleimide

1 3 degrees C) (i.e. 10-20 times faster than N-ethylmaleimide).

2 teines by oxidation and reaction with NEM (N-ethylmaleimide).

3 blocking the S-nitrosylation reaction with N-ethylmaleimide.

4 to be predominantly modified by thiols or N-ethylmaleimide.

5 e-sensitive factor attachment protein, and N-ethylmaleimide.

6 -nitrosoglutathione, hydrogen peroxide, or N-ethylmaleimide.

7 atment of cells with low concentrations of N-ethylmaleimide (10 microM), suggesting that enrichment w

8 e the newly formed intermediate selenol by N-ethylmaleimide; (3) deproteinization.

9 ctivity, and the activity was sensitive to N-ethylmaleimide, a sulfhydryl-modifying reagent.

10 sol-dependent fashion that is sensitive to N-ethylmaleimide and dependent on Sar1 and sec22B.

11 10-kDa molecular mass that is resistant to N-ethylmaleimide and heat inactivation.

12 s prevented by the SNARE protein inhibitor N-ethylmaleimide and the calcium chelator BAPTA.

13 residues to the membrane-permeant reagent N-ethylmaleimide and the membrane-impermeant reagent polye

14 N-Ethylmaleimide and thimerosal were able to simulate the

15 bited by sodium vanadate, sodium fluoride, N-ethylmaleimide, and phenylglyoxal but was not significan

16 species are trapped by cycloaddition with N-ethylmaleimide, and the reactions are traced by high res

17 ve been shown to be covalently modified by N-ethylmaleimide, and this treatment was found to block th

18 ns for activity, was potently inhibited by N-ethylmaleimide, and was labile at temperatures above 40

19 Furthermore, both N-ethylmaleimide- and H(2)O(2)-induced TRPC6 activations w

20 calcium-dependent Syt1 binding to soluble N-ethylmaleimide attachment protein receptor (SNARE) and v

21 on of Gbetagamma subunits with the soluble N-ethylmaleimide attachment protein receptor (SNARE) compl

22 Although FAK inhibition decreased soluble N-ethylmaleimide attachment protein receptor (SNARE)-media

23 a Golgi-localized target membrane-soluble N-ethylmaleimide attachment protein receptor (t-SNARE) pro

24 nt modification of its free cysteines with N-ethylmaleimide blocked binding to UL11 but not UL21.

25 the membrane-permeable sulfhydryl blocker, N-ethylmaleimide, by the RGD peptide, and by anti-alphaIIb

26 Preventing RyR cross-linking with N-ethylmaleimide decreased the propensity of Ca(2+) waves

27 odification of free cysteines in UL16 with N-ethylmaleimide does in fact prevent binding.

28 ed the role of a vesicle-residing, soluble N-ethylmaleimide factor attachment protein receptor (v-SNA

29 semolina protein (g protein) or 13.8 mumol N-ethylmaleimide/g protein reduces gliadin-glutenin cross-

30 trometry after derivatization to yield GSH-N-ethylmaleimide (GSNEM).

31 f the completely conserved Cys353) through N-ethylmaleimide modification or mutagenesis to alanine ab

32 e redox states of both the as purified and N-ethylmaleimide-modified forms, using the combination of

33 ent of muscle cells with the NSF inhibitor N-ethylmaleimide, mutation of NSF, or suppression of NSF e

34 Sensitivity to N-ethylmaleimide (NEM) and methanethiosulfonate reagents w

35 at was inhibited by the vesicle inhibitors N-ethylmaleimide (NEM) and monensin.

36 Chemical labeling with N-ethylmaleimide (NEM) and tandem mass spectrometry experi

37 e have investigated the mechanism by which N-ethylmaleimide (NEM) enhances transporter activity using

38 erythrocytes, the cysteine-modifying agent N-ethylmaleimide (NEM) has been shown to inhibit system y(

39 of the protein thiol groups on the MPI by N-ethylmaleimide (NEM) markedly reduced this rate constant

40 ns isolated in the presence and absence of N-ethylmaleimide (NEM), a chemical that reacts irreversibl

41 rate and effect of Cys-159 modification by N-ethylmaleimide (NEM), a cysteine-selective alkylating ag

42 ridine, a known Isomerase I inhibitor, and N-ethylmaleimide (NEM), a known LRAT inhibitor, significan

43 d unfolding (CIU), chemical labeling using N-ethylmaleimide (NEM), and both bottom-up and top-down pr

44 N-ethylmaleimide (NEM), and to a lesser extent, dithio(bis

45 lytes ((310)GSH and (616)GSSG), along with N-ethylmaleimide (NEM), and treated with acetonitrile to s

46 s cGMP independent but could be blocked by N-ethylmaleimide (NEM), indicating that NO acted via an S-

47 Pretreatment with N-ethylmaleimide (NEM), which occludes S-nitrosylation, or

48 e unmodified free thiols are blocked using N-ethylmaleimide (NEM).

49 ation by treatment with the thiol reagent, N-ethylmaleimide (NEM).

50 re more modest with a slight inhibition in N-ethylmaleimide (NEM, 1 mm)-treated RBCs and stimulation

51 current generated by the alkylating agent, N-ethylmaleimide, occluded the effect of H(2)O(2) The H(2)

52 y (2-aminoethyl)-methane thiosulfonate and N-ethylmaleimide of cysteine mutant proteins were measured

53 hemical labeling by isotope-coded forms of N-ethylmaleimide or succinic anhydride to site-specificall

54 es (c = 8 mmol L(-1)), photoligations with N-ethylmaleimide (possible for lambda </= 390 nm) are idea

55 bove their optimums and by Ca(2+), Zn(2+), N-ethylmaleimide, propranolol, and the sphingoid bases sph

56 ganine) lipids, nucleotides (ATP and CTP), N-ethylmaleimide, propranolol, phenylglyoxal, and divalent

57 affinity utilizing iodoacetamide (IAM) and N-ethylmaleimide reagents.

58 f reactive electrophiles: glyoxalase I and N-ethylmaleimide reductase.

59 ally inhibits NSF/Sec18 activity than does N-ethylmaleimide, requiring the administration of only low

60 aturating concentrations of the activator, N-ethylmaleimide-S1.

61 -type at near-saturating concentrations of N-ethylmaleimide-S1.

62 release machinery, this assay incorporates N-ethylmaleimide sensitive factor (NSF) and alpha-SNAP, wh

63 ecule binds our two model His(6) proteins, N-ethylmaleimide sensitive factor (NSF) and O(6)-alklyguan

64 reover, we provided evidence for a role of N-ethylmaleimide sensitive factor (NSF) in regulating MuSK

65 related to the single N domains in p97 and N-ethylmaleimide sensitive factor (NSF); N1 of Pex1 is mob

66 We find that lotus encodes N-ethylmaleimide sensitive factor 2 (NSF2), whereas wheezy

67 ion, enabling cooperation with the soluble N-ethylmaleimide sensitive factor adaptor protein receptor

68 significantly reduced formation of soluble n-ethylmaleimide sensitive factor adaptor protein receptor

69 Evolutionarily conserved SNARE (soluble N-ethylmaleimide sensitive factor attachment protein recep

70 Phosphorylation of this t-soluble N-ethylmaleimide sensitive factor attachment protein recep

71 nct combinations of Munc18 and the soluble N-ethylmaleimide sensitive factor attachment protein recep

72 Sec1/Munc18 (SM) proteins and soluble N-ethylmaleimide sensitive factor attachment protein recep

73 Soluble N-ethylmaleimide sensitive factor attachment protein recep

74 s study identifies the function of soluble N-ethylmaleimide sensitive factor attachment protein recep

75 a role for tethering complexes in soluble N-ethylmaleimide sensitive factor attachment protein recep

76 main, which likely participates in soluble N-ethylmaleimide sensitive factor attachment protein recep

77 tudy pinpoints the pivotal role of soluble N-ethylmaleimide sensitive factor attachment protein recep

78 in, complexin, and neuronal SNARE (soluble N-ethylmaleimide sensitive factor attachment protein recep

79 SNARE (soluble N-ethylmaleimide sensitive factor attachment protein recep

80 ining lipid bilayers as well as to soluble N-ethylmaleimide sensitive factor receptors (SNAREs) and p

81 N-Ethylmaleimide sensitive factor recycles SNAREs after fu

82 NSF (N-ethylmaleimide sensitive factor) and its yeast counterpa

83 The ATPase NSF (N-ethylmaleimide sensitive factor), together with SNAPs (s

84 The exocytic vesicular soluble N-ethylmaleimide sensitive fusion protein attachment prote

85 the packaging of a SNARE protein (soluble N-ethylmaleimide-sensitive attachment protein receptor) oc

86 ty to tomosyn that are outside the soluble N-ethylmaleimide-sensitive attachment receptor motif.

87 on secretion without altering its soluble N-ethylmaleimide-sensitive attachment receptor pairing wit

88 -1 (stabilizes assembled SNARE complexes), N-ethylmaleimide-sensitive factor (NSF) (disassembles SNAR

89 A soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

90 AAA domain-containing protein 1), soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

91 uires membrane fusion mediated by soluble N -ethylmaleimide-sensitive factor (NSF) attachment protein

92 Soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

93 is directly involved in regulating soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

94 main and modulate the affinity for soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

95 oforms to directly regulate SNARE (soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

96 In eukaryotic cells, the soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

97 Soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

98 Sec17 [soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein

99 N-Ethylmaleimide-sensitive factor (NSF) is a homo-hexameri

100 ptor molecule for the SNARE-priming enzyme N-ethylmaleimide-sensitive factor (NSF) is known to be cru

101 ovel synaptic interaction between Arr1 and N-ethylmaleimide-sensitive factor (NSF) that is enhanced i

102 nhibits exocytosis by chemically modifying N-ethylmaleimide-sensitive factor (NSF), a key component o

103 kinase Cepsilon (PKCepsilon) regulates the N-ethylmaleimide-sensitive factor (NSF), an ATPase critica

104 hepatic secretion of VLDL-TAG by targeting N-ethylmaleimide-sensitive factor (NSF), both in vivo and

105 N-ethylmaleimide-sensitive factor (NSF), first discovered

106 te a core complex of proteins comprised of N-ethylmaleimide-sensitive factor (NSF), soluble NSF attac

107 x is disassembled by an AAA+ ATPase called N-ethylmaleimide-sensitive factor (NSF).

108 iPSC-derived human neurons, among them the N-ethylmaleimide-sensitive factor (NSF).

109 iverse cellular activities (AAA+) protein, N-ethylmaleimide-sensitive factor (NSF/Sec18), and its co-

110 ts, whereas further incubation with p97 or N-ethylmaleimide-sensitive factor (two AAA ATPases involve

111 presence of LPC as opposed to cholesterol, N-ethylmaleimide-sensitive factor + adenosine triphosphate

112 vely to the predicted syntaxin and soluble N-ethylmaleimide-sensitive factor accessory protein recept

113 r to prevent the completion of the soluble N-ethylmaleimide-sensitive factor activating protein recep

114 r C-terminus domain and the SNARE (soluble N-ethylmaleimide-sensitive factor activating protein recep

115 Soluble N-ethylmaleimide-sensitive factor activating protein recep

116 of the Rab GTPase Sec4 to promote soluble N-ethylmaleimide-sensitive factor adaptor protein receptor

117 of the Sec4 Rab GTPase to promote soluble N-ethylmaleimide-sensitive factor adaptor protein receptor

118 ined whether genetic disruption of soluble N-ethylmaleimide-sensitive factor attached protein (SNARE)

119 Syntaxin (STX)-5 and alpha-soluble N-ethylmaleimide-sensitive factor attachment protein (alph

120 The assembly of the three neuronal soluble N-ethylmaleimide-sensitive factor attachment protein (SNAP

121 Trans-soluble N-ethylmaleimide-sensitive factor attachment protein (SNAP

122 ARE) complexes in conjunction with soluble N-ethylmaleimide-sensitive factor attachment protein (SNAP

123 gnate acceptor compartments before soluble N-ethylmaleimide-sensitive factor attachment protein (SNAR

124 (SNAP-25) is a key molecule in the soluble N-ethylmaleimide-sensitive factor attachment protein (SNAR

125 s study, we identify the vesicular soluble N-ethylmaleimide-sensitive factor attachment protein recep

126 ar machines that are essential for soluble N-ethylmaleimide-sensitive factor attachment protein recep

127 llular transport vesicles requires soluble N-ethylmaleimide-sensitive factor attachment protein recep

128 abnormal expression or function of soluble N-ethylmaleimide-sensitive factor attachment protein recep

129 Although epsinR is known to be an N-ethylmaleimide-sensitive factor attachment protein recep

130 tro by arresting the late steps of soluble N-ethylmaleimide-sensitive factor attachment protein recep

131 an open conformation to accelerate soluble N-ethylmaleimide-sensitive factor attachment protein recep

132 ansmitters and hormones depends on soluble N-ethylmaleimide-sensitive factor attachment protein recep

133 from beta-cells, specifically the soluble N-ethylmaleimide-sensitive factor attachment protein recep

134 ice expressing a dominant-negative soluble N-ethylmaleimide-sensitive factor attachment protein recep

135 Neuronal exocytosis is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein recep

136 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

137 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

138 The soluble N-ethylmaleimide-sensitive factor attachment protein recep

139 t work suggested that ER-localized soluble N-ethylmaleimide-sensitive factor attachment protein recep

140 depends on efficient formation of soluble N-ethylmaleimide-sensitive factor attachment protein recep

141 Mast cell degranulation requires N-ethylmaleimide-sensitive factor attachment protein recep

142 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

143 ved increase in K(+) currents is a soluble N-ethylmaleimide-sensitive factor attachment protein recep

144 We identified a member of the soluble N-ethylmaleimide-sensitive factor attachment protein recep

145 ther at the plasma membrane before soluble N-ethylmaleimide-sensitive factor attachment protein recep

146 tic vesicles, including the SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

147 aliana, include complexes, such as soluble N-ethylmaleimide-sensitive factor attachment protein recep

148 tate the formation of trans-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

149 ric levels with its cognate target-soluble N-ethylmaleimide-sensitive factor attachment protein recep

150 in membrane fusion events are the soluble N-ethylmaleimide-sensitive factor attachment protein recep

151 Membrane fusion is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein recep

152 depends on the disassembly of cis-soluble N-ethylmaleimide-sensitive factor attachment protein recep

153 r release and vesicle recycling in soluble N-ethylmaleimide-sensitive factor attachment protein recep

154 4 vesicle fusion reaction requires soluble N-ethylmaleimide-sensitive factor attachment protein recep

155 ganelles involves the formation of soluble N-ethylmaleimide-sensitive factor attachment protein recep

156 ctural relationships among SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein recep

157 Munc18c binds to the trans-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

158 fusogens from vesicle trafficking (soluble N-ethylmaleimide-sensitive factor attachment protein recep

159 s requires the concerted action of soluble N-ethylmaleimide-sensitive factor attachment protein recep

160 istence of the unproductive target soluble N-ethylmaleimide-sensitive factor attachment protein recep

161 oteins are important components of soluble N-ethylmaleimide-sensitive factor attachment protein recep

162 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

163 nsulin granules, is carried out by soluble N-ethylmaleimide-sensitive factor attachment protein recep

164 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

165 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

166 Platelet exocytosis is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein recep

167 the fusion pore induced by SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

168 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

169 e is comparable fusion of 4-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

170 general membrane fusion machinery-soluble N-ethylmaleimide-sensitive factor attachment protein recep

171 exocytosis by interacting with the soluble N-ethylmaleimide-sensitive factor attachment protein recep

172 synaptic proteins from the soluble SNARE (N-ethylmaleimide-sensitive factor attachment protein recep

173 .1 is postulated to be involved in soluble N-ethylmaleimide-sensitive factor attachment protein recep

174 le marker proteins, glutamate, the soluble N-ethylmaleimide-sensitive factor attachment protein recep

175 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

176 abeled vesicle-associated v-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

177 The soluble N-ethylmaleimide-sensitive factor attachment protein recep

178 that syt1 might facilitate SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

179 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

180 ediated by the formation of SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

181 c syntaxin 1A, and it can activate soluble N-ethylmaleimide-sensitive factor attachment protein recep

182 etween subsets of so-called SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

183 Arabidopsis (Arabidopsis thaliana) soluble N-ethylmaleimide-sensitive factor attachment protein recep

184 epeated release requires cycles of soluble N-ethylmaleimide-sensitive factor attachment protein recep

185 verexpression of ER/Golgi arginine soluble N-ethylmaleimide-sensitive factor attachment protein recep

186 components: vacuolar lipids, four soluble N-ethylmaleimide-sensitive factor attachment protein recep

187 The soluble N-ethylmaleimide-sensitive factor attachment protein recep

188 ies of membrane fusion mediated by soluble N-ethylmaleimide-sensitive factor attachment protein recep

189 C2 domains, and the neuronal core soluble N-ethylmaleimide-sensitive factor attachment protein recep

190 eins that regulate the activity of soluble N-ethylmaleimide-sensitive factor attachment protein recep

191 ion is mediated by the concerted action of N-ethylmaleimide-sensitive factor attachment protein recep

192 The role of soluble N-ethylmaleimide-sensitive factor attachment protein recep

193 ctivity on one of the three SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

194 s derived from target- and vesicle-soluble N-ethylmaleimide-sensitive factor attachment protein recep

195 ularly involving small G proteins, soluble N-ethylmaleimide-sensitive factor attachment protein recep

196 a Gbetagamma interaction with the soluble N-ethylmaleimide-sensitive factor attachment protein recep

197 /Munc18 (SM) proteins bind cognate soluble N-ethylmaleimide-sensitive factor attachment protein recep

198 d botulinum neurotoxin C to cleave soluble N-ethylmaleimide-sensitive factor attachment protein recep

199 th purified yeast vacuolar SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein recep

200 Yeast vacuole fusion requires soluble N-ethylmaleimide-sensitive factor attachment protein recep

201 tter release requires three SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

202 e transport of the plasma membrane soluble N-ethylmaleimide-sensitive factor attachment protein recep

203 ulinum neurotoxins cleave specific soluble N-ethylmaleimide-sensitive factor attachment protein recep

204 do not contain the t-SNARE (target-soluble N-ethylmaleimide-sensitive factor attachment protein recep

205 and vacuole protein sorting), and soluble N-ethylmaleimide-sensitive factor attachment protein recep

206 The soluble N-ethylmaleimide-sensitive factor attachment protein recep

207 ediated selective concentration of soluble N-ethylmaleimide-sensitive factor attachment protein recep

208 elta) for the Tlg2 target membrane-soluble N-ethylmaleimide-sensitive factor attachment protein recep

209 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

210 inds to and cleaves syntaxin 17, a soluble N-ethylmaleimide-sensitive factor attachment protein recep

211 specific fusion proteins [such as soluble N-ethylmaleimide-sensitive factor attachment protein recep

212 c13-4 is a Ca(2+)-dependent SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

213 y GTPases, their effector tethers, soluble N-ethylmaleimide-sensitive factor attachment protein recep

214 The soluble N-ethylmaleimide-sensitive factor attachment protein recep

215 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

216 and activation of (phago)lysosomal soluble N-ethylmaleimide-sensitive factor attachment protein recep

217 ane protein 4 (VAMP4), a vesicular soluble N-ethylmaleimide-sensitive factor attachment protein recep

218 Whereas SNARE (soluble N -ethylmaleimide-sensitive factor attachment protein recep

219 ich, in turn, interacts with the lysosomal N-ethylmaleimide-sensitive factor attachment protein recep

220 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

221 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

222 vitro and to separate the roles of soluble N-ethylmaleimide-sensitive factor attachment protein recep

223 Synaptic soluble N-ethylmaleimide-sensitive factor attachment protein recep

224 l by cooperating with the neuronal soluble N-ethylmaleimide-sensitive factor attachment protein recep

225 release requires the formation of soluble N-ethylmaleimide-sensitive factor attachment protein recep

226 interact with the vacuolar SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

227 NSF disassembles soluble N-ethylmaleimide-sensitive factor attachment protein recep

228 er with syntaxin-3 and syntaxin-1A soluble N-ethylmaleimide-sensitive factor attachment protein recep

229 component of the synaptic vesicle soluble N-ethylmaleimide-sensitive factor attachment protein recep

230 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein recep

231 Soluble N-ethylmaleimide-sensitive factor attachment protein recep

232 ituted with the target (t)-SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein recep

233 it a polarized distribution of the soluble N-ethylmaleimide-sensitive factor attachment protein recep

234 e Dawley rats, 4 dominant-negative soluble N-ethylmaleimide-sensitive factor attachment protein recep

235 ted by the formation of functional soluble N-ethylmaleimide-sensitive factor attachment protein recep

236 the Rab GTPase Ypt7p, four SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein recep

237 anosine 5'-3-O-(thio)triphosphate, soluble N-ethylmaleimide-sensitive factor attachment protein, and

238 protein receptor (SNARE) proteins soluble N-ethylmaleimide-sensitive factor attachment protein-25 (S

239 590 (a predicted alpha-SNAP [alpha-soluble N-ethylmaleimide-sensitive factor attachment protein]).

240 le of the fusion proteins, SNAREs (soluble N-ethylmaleimide-sensitive factor attachment proteins), in

241 ine triphosphate-binding proteins, soluble N-ethylmaleimide-sensitive factor attachment proteins, and

242 In neurons, soluble N-ethylmaleimide-sensitive factor attachment receptor (SNA

243 ytosis relies on assembly of three soluble N-ethylmaleimide-sensitive factor attachment receptor (SNA

244 ysosomes for degradation following soluble N-ethylmaleimide-sensitive factor attachment receptor (SNA

245 We discovered soluble N-ethylmaleimide-sensitive factor attachment receptor (SNA

246 Syntaxin 1a is a plasma membrane soluble N-ethylmaleimide-sensitive factor attachment receptor prot

247 ns homologous to eukaryotic SNARE (soluble N-ethylmaleimide-sensitive factor attachment receptor) dom

248 yt 1 using a reconstituted, SNARE (soluble N-ethylmaleimide-sensitive factor attachment receptor)-med

249 tail-anchored proteins, including soluble N-ethylmaleimide-sensitive factor attachment receptors (SN

250 ence in the NSF gene, encoding the protein N-Ethylmaleimide-Sensitive Factor essential for synaptic v

251 biting the binding of SNAREs to Sec18p, an N-ethylmaleimide-sensitive factor homologue responsible fo

252 ing the trimerized alphaSNAP, we find that N-ethylmaleimide-sensitive factor hydrolyzes 10 ATP molecu

253 712) or by inhibiting exocytosis (TAT-NSF, N-ethylmaleimide-sensitive factor inhibitor).

254 e-resident syntaxin-like glutamine-soluble N-ethylmaleimide-sensitive factor protein attachment prote

255 ;5 are regulated by the SNARE (for soluble N-ethylmaleimide-sensitive factor protein attachment prote

256 SNARE (soluble N-ethylmaleimide-sensitive factor protein attachment prote

257 R-SNAREs (soluble N-ethylmaleimide-sensitive factor receptor), Q-SNAREs, and

258 complex is disassembled by the AAA-ATPase N-ethylmaleimide-sensitive factor that requires the cofact

259 The ATPase NSF (N-ethylmaleimide-sensitive factor) and the adaptor protein

260 an essential component of the soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein rece

261 alpha-SNAP [soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein] and

262 attachment protein, and NSF is defined as N-ethylmaleimide-sensitive factor) complexes catalyze syna

263 SNARE bundles are reactivated by hexameric N-ethylmaleimide-sensitive factor, vesicle-fusing ATPase (

264 SNX27-independent recycling may involve N-ethylmaleimide-sensitive factor, which binds both PDZ in

265 tructures, and here we examine the role of N-ethylmaleimide-sensitive factor-activating protein recep

266 al membrane transporters, ATPases, soluble N-ethylmaleimide-sensitive factor-activating protein recep

267 uring synaptic vesicle fusion, the soluble N-ethylmaleimide-sensitive factor-attachment protein recep

268 The soluble N-ethylmaleimide-sensitive factor-attachment protein recep

269 enetic approach to identify target soluble N-ethylmaleimide-sensitive factor-attachment protein recep

270 nd retromer and another possibly involving N-ethylmaleimide-sensitive factor.

271 E hybrid complex cannot be disassembled by N-ethylmaleimide-sensitive factor.

272 cular synapses through cleavage of soluble N-ethylmaleimide-sensitive fusion (NSF) attachment protein

273 NT-CT interaction is further disrupted by N-ethylmaleimide-sensitive fusion ATPase (NSF), which asso

274 ment of Ca(2+) for the assembly of soluble N-ethylmaleimide-sensitive fusion attachment protein recep

275 sicle (DCV) exocytosis is a SNARE (soluble N-ethylmaleimide-sensitive fusion attachment protein recep

276 lates SNAP-23, the target membrane soluble N-ethylmaleimide-sensitive fusion factor attachment protei

277 We identified a direct interaction between N-ethylmaleimide-sensitive fusion protein (NSF), an ATPase

278 Here we identified Drosophila N-ethylmaleimide-sensitive fusion protein 2 (dNSF2) and so

279 Soluble N-ethylmaleimide-sensitive fusion protein attachment prote

280 integral membrane proteins called soluble N-ethylmaleimide-sensitive fusion protein attachment prote

281 The current model requires soluble N-ethylmaleimide-sensitive fusion protein attachment prote

282 mbrane associated proteins SNAREs (soluble N-ethylmaleimide-sensitive fusion protein attachment prote

283 The soluble N-ethylmaleimide-sensitive fusion protein attachment prote

284 s between synaptotagmin and SNARE (soluble N-ethylmaleimide-sensitive fusion protein attachment recep

285 dependent on GluA2 not GluA1, sensitive to N-ethylmaleimide-sensitive fusion protein interaction, and

286 and specific cleavage of neuronal soluble N-ethylmaleimide-sensitive fusion protein-attachment prote

287 sicles in the brain harbor several soluble N-ethylmaleimide-sensitive-factor attachment protein recep

288 ery ECs, depletion of Galpha12 and soluble N-ethylmaleimide-sensitive-fusion factor attachment protei

289 Similarly, l-cysteine and N-ethylmaleimide significantly attenuated the inhibition c

290 , glutathione was derivatized in-situ with N-ethylmaleimide to block the cysteine residue and to enha

291 g of untreated, Cytochalasin B treated and N-Ethylmaleimide treated MCF-7 breast cancer cells demonst

292 n when HMM was mixed with ATP-insensitive, N-ethylmaleimide-treated HMM (NEM-HMM; 25-30%).

293 The binding of N-ethylmaleimide-treated myosin subfragment 1 (NEM-S1) to

294 either functionally impaired by trypsin or N-ethylmaleimide treatments or with protein-free liposomes

295 e nonspecific small molecule DUB inhibitor N-ethylmaleimide was 16.2+/-3.2 muM and can be used as a q

296 The thiol-blocking agent N-ethylmaleimide was applied in order to inhibit formation

297 minoethyl methanethiosulfonate, but not by N-ethylmaleimide, was fully protected in the presence of s

298 the kinase inhibitor staurosporine and by N-ethylmaleimide, whereas KCC2(WT), KCC2(T934A), and KCC2(

299 ion of its only free cysteine residue with N-ethylmaleimide), which causes significant reduction in i

300 ith either 20mM added NaCl (WPI+NaCl), 5mM N-ethylmaleimide (WPI+NEM) or 20mM added NaCl and 5mM NEM