ライフサイエンスコーパス: N-ethylmaleimide

1 23 degrees C) (i.e. 10-20 times faster than N-ethylmaleimide).

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

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

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

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

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

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

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

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

10 tosol-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 was prevented by the SNARE protein inhibitor N-ethylmaleimide and the calcium chelator BAPTA.

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

14 N-Ethylmaleimide and thimerosal were able to simulate th

15 hibited by sodium vanadate, sodium fluoride, N-ethylmaleimide, and phenylglyoxal but was not signific

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

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

18 ions for activity, was potently inhibited by N-ethylmaleimide, and was labile at temperatures above 4

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

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

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

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

23 6, a Golgi-localized target membrane-soluble N-ethylmaleimide attachment protein receptor (t-SNARE) p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

42 pyridine, a known Isomerase I inhibitor, and N-ethylmaleimide (NEM), a known LRAT inhibitor, signific

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

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

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

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

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

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

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

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

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

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

53 chemical labeling by isotope-coded forms of N-ethylmaleimide or succinic anhydride to site-specifica

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

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

56 inganine) lipids, nucleotides (ATP and CTP), N-ethylmaleimide, propranolol, phenylglyoxal, and divale

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

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

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

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

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

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

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

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

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

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

67 ction, enabling cooperation with the soluble N-ethylmaleimide sensitive factor adaptor protein recept

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

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

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

71 tinct combinations of Munc18 and the soluble N-ethylmaleimide sensitive factor attachment protein rec

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

73 Soluble N-ethylmaleimide sensitive factor attachment protein rec

74 his study identifies the function of soluble N-ethylmaleimide sensitive factor attachment protein rec

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

76 domain, which likely participates in soluble N-ethylmaleimide sensitive factor attachment protein rec

77 study pinpoints the pivotal role of soluble N-ethylmaleimide sensitive factor attachment protein rec

78 gmin, complexin, and neuronal SNARE (soluble N-ethylmaleimide sensitive factor attachment protein rec

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

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

81 N-Ethylmaleimide sensitive factor recycles SNAREs after

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

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

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

85 requires membrane fusion mediated by soluble N -ethylmaleimide-sensitive factor (NSF) attachment prot

86 Whereas SNARE (soluble N -ethylmaleimide-sensitive factor attachment protein re

87 by the packaging of a SNARE protein (soluble N-ethylmaleimide-sensitive attachment protein receptor)

88 vity to tomosyn that are outside the soluble N-ethylmaleimide-sensitive attachment receptor motif.

89 ty on secretion without altering its soluble N-ethylmaleimide-sensitive attachment receptor pairing w

90 18-1 (stabilizes assembled SNARE complexes), N-ethylmaleimide-sensitive factor (NSF) (disassembles SN

91 A soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

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

93 Soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

94 t is directly involved in regulating soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

95 domain and modulate the affinity for soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

96 isoforms to directly regulate SNARE (soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

97 In eukaryotic cells, the soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

98 Soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

99 Sec17 [soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

100 N-Ethylmaleimide-sensitive factor (NSF) is a homo-hexame

101 daptor molecule for the SNARE-priming enzyme N-ethylmaleimide-sensitive factor (NSF) is known to be c

102 novel synaptic interaction between Arr1 and N-ethylmaleimide-sensitive factor (NSF) that is enhanced

103 inhibits exocytosis by chemically modifying N-ethylmaleimide-sensitive factor (NSF), a key component

104 n kinase Cepsilon (PKCepsilon) regulates the N-ethylmaleimide-sensitive factor (NSF), an ATPase criti

105 s hepatic secretion of VLDL-TAG by targeting N-ethylmaleimide-sensitive factor (NSF), both in vivo an

106 N-ethylmaleimide-sensitive factor (NSF), first discovere

107 cate a core complex of proteins comprised of N-ethylmaleimide-sensitive factor (NSF), soluble NSF att

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

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

110 diverse cellular activities (AAA+) protein, N-ethylmaleimide-sensitive factor (NSF/Sec18), and its c

111 ents, whereas further incubation with p97 or N-ethylmaleimide-sensitive factor (two AAA ATPases invol

112 e presence of LPC as opposed to cholesterol, N-ethylmaleimide-sensitive factor + adenosine triphospha

113 sively to the predicted syntaxin and soluble N-ethylmaleimide-sensitive factor accessory protein rece

114 cer to prevent the completion of the soluble N-ethylmaleimide-sensitive factor activating protein rec

115 lar C-terminus domain and the SNARE (soluble N-ethylmaleimide-sensitive factor activating protein rec

116 Soluble N-ethylmaleimide-sensitive factor activating protein rec

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

118 or of the Sec4 Rab GTPase to promote soluble N-ethylmaleimide-sensitive factor adaptor protein recept

119 amined whether genetic disruption of soluble N-ethylmaleimide-sensitive factor attached protein (SNAR

120 Syntaxin (STX)-5 and alpha-soluble N-ethylmaleimide-sensitive factor attachment protein (al

121 cognate acceptor compartments before soluble N-ethylmaleimide-sensitive factor attachment protein (SN

122 The assembly of the three neuronal soluble N-ethylmaleimide-sensitive factor attachment protein (SN

123 Trans-soluble N-ethylmaleimide-sensitive factor attachment protein (SN

124 SNARE) complexes in conjunction with soluble N-ethylmaleimide-sensitive factor attachment protein (SN

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

126 his study, we identify the vesicular soluble N-ethylmaleimide-sensitive factor attachment protein rec

127 ular machines that are essential for soluble N-ethylmaleimide-sensitive factor attachment protein rec

128 cellular transport vesicles requires soluble N-ethylmaleimide-sensitive factor attachment protein rec

129 h abnormal expression or function of soluble N-ethylmaleimide-sensitive factor attachment protein rec

130 Although epsinR is known to be an N-ethylmaleimide-sensitive factor attachment protein rec

131 vitro by arresting the late steps of soluble N-ethylmaleimide-sensitive factor attachment protein rec

132 o an open conformation to accelerate soluble N-ethylmaleimide-sensitive factor attachment protein rec

133 transmitters and hormones depends on soluble N-ethylmaleimide-sensitive factor attachment protein rec

134 se from beta-cells, specifically the soluble N-ethylmaleimide-sensitive factor attachment protein rec

135 mice expressing a dominant-negative soluble N-ethylmaleimide-sensitive factor attachment protein rec

136 Neuronal exocytosis is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec

137 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

138 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

139 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

140 ent work suggested that ER-localized soluble N-ethylmaleimide-sensitive factor attachment protein rec

141 is depends on efficient formation of soluble N-ethylmaleimide-sensitive factor attachment protein rec

142 Mast cell degranulation requires N-ethylmaleimide-sensitive factor attachment protein rec

143 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

144 erved increase in K(+) currents is a soluble N-ethylmaleimide-sensitive factor attachment protein rec

145 We identified a member of the soluble N-ethylmaleimide-sensitive factor attachment protein rec

146 tether at the plasma membrane before soluble N-ethylmaleimide-sensitive factor attachment protein rec

147 aptic vesicles, including the SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

148 thaliana, include complexes, such as soluble N-ethylmaleimide-sensitive factor attachment protein rec

149 litate the formation of trans-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

150 etric levels with its cognate target-soluble N-ethylmaleimide-sensitive factor attachment protein rec

151 rs in membrane fusion events are the soluble N-ethylmaleimide-sensitive factor attachment protein rec

152 Membrane fusion is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec

153 es depends on the disassembly of cis-soluble N-ethylmaleimide-sensitive factor attachment protein rec

154 ter release and vesicle recycling in soluble N-ethylmaleimide-sensitive factor attachment protein rec

155 UT4 vesicle fusion reaction requires soluble N-ethylmaleimide-sensitive factor attachment protein rec

156 organelles involves the formation of soluble N-ethylmaleimide-sensitive factor attachment protein rec

157 ructural relationships among SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec

158 at Munc18c binds to the trans-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

159 n fusogens from vesicle trafficking (soluble N-ethylmaleimide-sensitive factor attachment protein rec

160 sis requires the concerted action of soluble N-ethylmaleimide-sensitive factor attachment protein rec

161 existence of the unproductive target soluble N-ethylmaleimide-sensitive factor attachment protein rec

162 proteins are important components of soluble N-ethylmaleimide-sensitive factor attachment protein rec

163 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

164 insulin granules, is carried out by soluble N-ethylmaleimide-sensitive factor attachment protein rec

165 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

166 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

167 Platelet exocytosis is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec

168 of the fusion pore induced by SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

169 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

170 ere is comparable fusion of 4-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

171 he general membrane fusion machinery-soluble N-ethylmaleimide-sensitive factor attachment protein rec

172 f exocytosis by interacting with the soluble N-ethylmaleimide-sensitive factor attachment protein rec

173 ey synaptic proteins from the soluble SNARE (N-ethylmaleimide-sensitive factor attachment protein rec

174 v2.1 is postulated to be involved in soluble N-ethylmaleimide-sensitive factor attachment protein rec

175 icle marker proteins, glutamate, the soluble N-ethylmaleimide-sensitive factor attachment protein rec

176 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

177 labeled vesicle-associated v-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

178 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

179 st that syt1 might facilitate SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

180 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

181 mediated by the formation of SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

182 ric syntaxin 1A, and it can activate soluble N-ethylmaleimide-sensitive factor attachment protein rec

183 between subsets of so-called SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

184 e Arabidopsis (Arabidopsis thaliana) soluble N-ethylmaleimide-sensitive factor attachment protein rec

185 Repeated release requires cycles of soluble N-ethylmaleimide-sensitive factor attachment protein rec

186 -overexpression of ER/Golgi arginine soluble N-ethylmaleimide-sensitive factor attachment protein rec

187 ed components: vacuolar lipids, four soluble N-ethylmaleimide-sensitive factor attachment protein rec

188 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

189 udies of membrane fusion mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec

190 wo C2 domains, and the neuronal core soluble N-ethylmaleimide-sensitive factor attachment protein rec

191 oteins that regulate the activity of soluble N-ethylmaleimide-sensitive factor attachment protein rec

192 usion is mediated by the concerted action of N-ethylmaleimide-sensitive factor attachment protein rec

193 The role of soluble N-ethylmaleimide-sensitive factor attachment protein rec

194 activity on one of the three SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

195 ces derived from target- and vesicle-soluble N-ethylmaleimide-sensitive factor attachment protein rec

196 icularly involving small G proteins, soluble N-ethylmaleimide-sensitive factor attachment protein rec

197 ia a Gbetagamma interaction with the soluble N-ethylmaleimide-sensitive factor attachment protein rec

198 c1/Munc18 (SM) proteins bind cognate soluble N-ethylmaleimide-sensitive factor attachment protein rec

199 and botulinum neurotoxin C to cleave soluble N-ethylmaleimide-sensitive factor attachment protein rec

200 with purified yeast vacuolar SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec

201 Yeast vacuole fusion requires soluble N-ethylmaleimide-sensitive factor attachment protein rec

202 mitter release requires three SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

203 ade transport of the plasma membrane soluble N-ethylmaleimide-sensitive factor attachment protein rec

204 otulinum neurotoxins cleave specific soluble N-ethylmaleimide-sensitive factor attachment protein rec

205 a do not contain the t-SNARE (target-soluble N-ethylmaleimide-sensitive factor attachment protein rec

206 on and vacuole protein sorting), and soluble N-ethylmaleimide-sensitive factor attachment protein rec

207 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

208 -mediated selective concentration of soluble N-ethylmaleimide-sensitive factor attachment protein rec

209 2Delta) for the Tlg2 target membrane-soluble N-ethylmaleimide-sensitive factor attachment protein rec

210 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

211 binds to and cleaves syntaxin 17, a soluble N-ethylmaleimide-sensitive factor attachment protein rec

212 by specific fusion proteins [such as soluble N-ethylmaleimide-sensitive factor attachment protein rec

213 unc13-4 is a Ca(2+)-dependent SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

214 ily GTPases, their effector tethers, soluble N-ethylmaleimide-sensitive factor attachment protein rec

215 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

216 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

217 y and activation of (phago)lysosomal soluble N-ethylmaleimide-sensitive factor attachment protein rec

218 brane protein 4 (VAMP4), a vesicular soluble N-ethylmaleimide-sensitive factor attachment protein rec

219 which, in turn, interacts with the lysosomal N-ethylmaleimide-sensitive factor attachment protein rec

220 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

221 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

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

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

224 nal by cooperating with the neuronal soluble N-ethylmaleimide-sensitive factor attachment protein rec

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

226 11 interact with the vacuolar SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

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

228 nner with syntaxin-3 and syntaxin-1A soluble N-ethylmaleimide-sensitive factor attachment protein rec

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

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

231 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

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

233 loit a polarized distribution of the soluble N-ethylmaleimide-sensitive factor attachment protein rec

234 gue Dawley rats, 4 dominant-negative soluble N-ethylmaleimide-sensitive factor attachment protein rec

235 iated by the formation of functional soluble N-ethylmaleimide-sensitive factor attachment protein rec

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

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

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

239 02590 (a predicted alpha-SNAP [alpha-soluble N-ethylmaleimide-sensitive factor attachment protein]).

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

241 osine triphosphate-binding proteins, soluble N-ethylmaleimide-sensitive factor attachment proteins, a

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

243 ocytosis relies on assembly of three soluble N-ethylmaleimide-sensitive factor attachment receptor (S

244 lysosomes for degradation following soluble N-ethylmaleimide-sensitive factor attachment receptor (S

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

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

247 ions homologous to eukaryotic SNARE (soluble N-ethylmaleimide-sensitive factor attachment receptor) d

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

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

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

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

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

253 19712) or by inhibiting exocytosis (TAT-NSF, N-ethylmaleimide-sensitive factor inhibitor).

254 ane-resident syntaxin-like glutamine-soluble N-ethylmaleimide-sensitive factor protein attachment pro

255 P2;5 are regulated by the SNARE (for soluble N-ethylmaleimide-sensitive factor protein attachment pro

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

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

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

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

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

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

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

263 e 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

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

266 gral membrane transporters, ATPases, soluble N-ethylmaleimide-sensitive factor-activating protein rec

267 During synaptic vesicle fusion, the soluble N-ethylmaleimide-sensitive factor-attachment protein rec

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

269 ogenetic approach to identify target soluble N-ethylmaleimide-sensitive factor-attachment protein rec

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

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

272 uscular synapses through cleavage of soluble N-ethylmaleimide-sensitive fusion (NSF) attachment prote

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

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

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

276 rylates SNAP-23, the target membrane soluble N-ethylmaleimide-sensitive fusion factor attachment prot

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

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

279 Soluble N-ethylmaleimide-sensitive fusion protein attachment pro

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

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

282 Membrane associated proteins SNAREs (soluble N-ethylmaleimide-sensitive fusion protein attachment pro

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

284 ons between synaptotagmin and SNARE (soluble N-ethylmaleimide-sensitive fusion protein attachment rec

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

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

287 vesicles in the brain harbor several soluble N-ethylmaleimide-sensitive-factor attachment protein rec

288 rtery ECs, depletion of Galpha12 and soluble N-ethylmaleimide-sensitive-fusion factor attachment prot

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

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

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

292 een 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) t

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

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

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

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

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

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

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