ライフサイエンスコーパス: cytosolic protein

1 somehow escape endocytic vesicles to contact cytosolic protein.

2 nding interactions with a folded or unfolded cytosolic protein.

3 emonstrated a dose-dependent increase in Ras cytosolic protein.

4 ing frame of unknown function that encodes a cytosolic protein.

5 n compared with the wild-type or exclusively cytosolic protein.

6 protein fractions compared with cell wall or cytosolic proteins.

7 brane proteins or diffusional entry of small cytosolic proteins.

8 belong to a small family of multifunctional cytosolic proteins.

9 alues close to the isoelectric point of many cytosolic proteins.

10 TRAP_Cy3) to trap and visualize dithiols in cytosolic proteins.

11 causes the loss of solubility intracellular cytosolic proteins.

12 s may result from more widespread effects on cytosolic proteins.

13 down IRF5 from a mixture of endothelial cell cytosolic proteins.

14 lucosamine (O-GlcNAc) to various nuclear and cytosolic proteins.

15 the less hydrophobic amino acid segments in cytosolic proteins.

16 domains that distinguish MLPs from potential cytosolic proteins.

17 re was little impact on Ag presentation from cytosolic proteins.

18 a more restricted role in the processing of cytosolic proteins.

19 lational modification of diverse nuclear and cytosolic proteins.

20 interaction and docking targets for various cytosolic proteins.

21 ity of the cytosolic domain to interact with cytosolic proteins.

22 of protein methylation in the regulation of cytosolic proteins.

23 ell might also be facilitated by target cell cytosolic proteins.

24 ctive lysosomal mechanism for degradation of cytosolic proteins.

25 partments for the sequestration of misfolded cytosolic proteins.

26 es, which may recognize membrane, nuclear or cytosolic proteins.

27 rimentally dissect cell surface-exposed from cytosolic proteins.

28 o efficient in preventing the aggregation of cytosolic proteins.

29 le in unconventional secretion of leaderless cytosolic proteins.

30 Our analysis unveiled lymphocyte cytosolic protein 1 (LCP1), a lymphocyte-specific target

31 OR], 2.54; P = 1.20 x 10(-6)) and lymphocyte cytosolic protein-1 (LCP1) (OR, 3.29; P = 2.96 x 10(-6))

32 m, MG formation and glycation and changes in cytosolic protein abundances, MG modification and proteo

33 Polymerization of the cytosolic protein actin is critical to cell movement and

34 tical for the capture of heat stress-induced cytosolic protein aggregates and their retention in the

35 Large cytosolic protein aggregates are removed by two main cel

36 Here we demonstrate that cytosolic protein aggregates can also behave as infectio

37 we show that HRI controls autophagy to clear cytosolic protein aggregates when the ubiquitin-proteaso

38 ases are associated with the accumulation of cytosolic protein aggregates.

39 eed by coupling an active transport model of cytosolic proteins along a two-dimensional microtubule (

40 The cytosolic protein alpha-catenin is a postulated force tr

41 atially distinguishable transport routes for cytosolic proteins: an IFT-dependent path along the axon

42 The ribonuclease inhibitor (RI) is a cytosolic protein and a potent inhibitor of bovine pancr

43 D66 encodes an approximately 30-kDa soluble, cytosolic protein and that the chymotrypsin-like activit

44 ded with the impaired turnover of long-lived cytosolic proteins and accumulation of autophagosomes.

45 ranslocation was enhanced by the addition of cytosolic proteins and ATP to the reaction mixture.

46 tions manifest themselves via scaffolding of cytosolic proteins and cytoskeletal networks to specific

47 ophagy (autophagy) is a process wherein bulk cytosolic proteins and damaged organelles are sequestere

48 ification is present on numerous nuclear and cytosolic proteins and has been implicated in essential

49 ophagy controls the degradation of selective cytosolic proteins and may protect neurons against degen

50 tabolic process, leads to the degradation of cytosolic proteins and organelles in the vacuole/lysosom

51 otes that utilizes small vesicles to traffic cytosolic proteins and organelles to the vacuole for bre

52 autophagy, a bulk degradation process of cytosolic proteins and organelles, is protective during

53 utophagy is a bulk degradation mechanism for cytosolic proteins and organelles.

54 omeostatic process responsible for recycling cytosolic proteins and organelles.

55 ise to nuclear chromosomal genes that encode cytosolic proteins and precursor proteins that are synth

56 e system by binding to peptides derived from cytosolic proteins and presenting them on the cell surfa

57 h altered ubiquitin-dependent degradation of cytosolic proteins and regulation of protein synthesis d

58 Entry into the microdomain is selective for cytosolic proteins and requires a binding pathway to Pop

59 densed chromatin decorated with granular and cytosolic proteins and they can trap extracellular patho

60 n be sensed by a growing number of host cell cytosolic proteins and TLR3, which contribute to the ind

61 lling, (vi) degradation of Mo and fibroblast cytosolic proteins, and (vii) promotion of survival of i

62 n-like GTPase Vps1p, V-ATPase pump activity, cytosolic proteins, and ATP and GTP hydrolysis.

63 encoding putative transporters, hypothetical cytosolic proteins, and macrolide efflux pumps.

64 ntified an interaction between NKCC2 and the cytosolic protein, annexin A2 (AnxA2).

65 Thus, nonpathogenic cytosolic proteins appear capable of transfer.

66 st-translational modification of nuclear and cytosolic proteins, appears causal for XLID.

67 e role of macroautophagy, a process in which cytosolic proteins are delivered to the lysosome by de n

68 Cysteine residues in cytosolic proteins are maintained in their reduced state

69 In vivo biochemical studies reveal that cytosolic proteins are organized into higher order struc

70 ittle is currently known about how misfolded cytosolic proteins are recognized by protein quality con

71 Many cytosolic proteins are recruited to the plasma membrane

72 elective type of autophagy by which specific cytosolic proteins are sent to lysosomes for degradation

73 An increasing number of cytosolic proteins are shown to interact with membrane l

74 We propose a model where cytosolic proteins are transported by dynamically assemb

75 riving programmed elimination of preexisting cytosolic proteins are unclear.

76 was accompanied by elevated myofibrillar and cytosolic protein as well as DNA synthesis.

77 Our observations establish misfolding of cytosolic proteins as an effect of aminoglycoside action

78 HSP90 also refolds some endogenous cytosolic proteins as part of a foldosome complex contai

79 expressed and prostate-specific membrane and cytosolic proteins, as well as RNA.

80 directly interacts with several membrane and cytosolic proteins at neuronal plasma membranes, leading

81 mics, electrical signaling, and diffusion of cytosolic proteins at unprecedented spatial resolution.

82 m a poly(Q) (polyglutamine) expansion in the cytosolic protein ataxin-2 (Atx2).

83 an expansion of polyglutamine tracts in the cytosolic protein ataxin-2 (Atx2).

84 somal ceramide that ultimately activates the cytosolic protein BAX.

85 st that they may be mediators of transfer of cytosolic proteins between motor neurons.

86 Herein, we report that cGAS is not a cytosolic protein but rather localizes to the plasma mem

87 ation of NUP62 attenuated the gated entry of cytosolic proteins but did not affect entry of membrane

88 osttranslational modification of nuclear and cytosolic proteins but is present also in mitochondria.

89 SOD1 is mostly a cytosolic protein, but a substantial portion is associat

90 Parkin is a mostly cytosolic protein, but is rapidly recruited to damaged m

91 osttranslational modification of nuclear and cytosolic proteins by O-linked beta-N-acetylglucosamine

92 chanism whereby overexpression of a specific cytosolic protein bypasses the essentiality of an inner

93 The cytosolic protein c-FLIP (cellular Fas-associated death

94 first demonstration that large fragments of cytosolic proteins can be accumulated in prematurely sen

95 We report that misfolded cytosolic proteins can be cleared from mammalian cells b

96 Cytosolic proteins can be selectively delivered to lysos

97 Thus, exosomal packaging and release of cytosolic proteins can modulate the activity of cellular

98 We show that diverse cytosolic proteins (CaVbeta, 14-3-3, calmodulin and CaMK

99 n induces pyroptosis, which is mediated by a cytosolic protein complex called the inflammasome that s

100 DAMPS result in the assembly of a cytosolic protein complex termed the inflammasome, which

101 LRP3) inflammasome is a caspase-1-containing cytosolic protein complex that is essential for processi

102 Compared with cytosolic protein complexes and with genome-wide retenti

103 uries trigger the assembly of inflammasomes, cytosolic protein complexes that activate caspase-1, lea

104 strictly controlled by several lysosomal or cytosolic protein complexes that directly detect and tra

105 Inflammasomes are cytosolic protein complexes that regulate caspase-1 acti

106 Inflammasomes are cytosolic protein complexes that respond to diverse dang

107 Inflammasomes are cytosolic protein complexes that serve as platforms for

108 Inflammasomes are cytosolic protein complexes, which orchestrate the matur

109 A cytosolic protein, Complexin (Cpx), binds the SNARE comp

110 A cytosolic protein, complexin (Cpx), binds to the SNARE b

111 Clathrin, a cytosolic protein composed of heavy and light chain subu

112 TrkH assembles with TrkA, a cytosolic protein comprising two RCK (regulate the condu

113 or IRE1alpha kinase activity using wild-type cytosolic protein constructs.

114 Cytosolic proteins containing SH2 and SH3 domains, such

115 a strategy for analyzing axonal transport of cytosolic proteins (CPs) using photoactivatable GFP-PAGF

116 Bacteria possess cytosolic proteins (Csp3s) capable of binding large quan

117 known about the quality control of misfolded cytosolic proteins (CytoQC).

118 easome inhibition enhanced activation of the cytosolic protein damage sensor HSF1, elevated levels of

119 ydomonas reinhardtii, we discovered that the cytosolic protein degradation machinery is concentrated

120 that distinct autophagic mechanisms control cytosolic protein delivery to late endosomes and identif

121 cytosol (yHsp60c) inhibits degradation of a cytosolic protein DeltaMTS-Aco1 tagged with the degron S

122 -10) cm(2) s(-1)) but increased with time as cytosolic protein density, which was initially high, dec

123 It enables a subset of cytosolic proteins devoid of signal peptide sequences, a

124 The cytosolic protein dGIPC interacts with Gyc76C and facili

125 ave indicated that mammalian cells contain a cytosolic protein disaggregation machinery comprised of

126 homolog, is a mitochondrial protein, and the cytosolic protein Dld3.

127 SEC61 also serves as a translation site for cytosolic protein-encoding mRNAs remains unknown.

128 sociated with alpha-synuclein (alpha-syn), a cytosolic protein enriched in presynaptic terminals.

129 is work, we investigated the function of the cytosolic protein EspG(5), which is essential for ESX-5-

130 Bassoon and Piccolo are active zone specific cytosolic proteins essential for active zone assembly in

131 ultisite membrane-anchored proteins, but not cytosolic proteins, even when enzymes are in excess.

132 tes, about one-third of the Escherichia coli cytosolic proteins exhibit cotranslational folding, with

133 euticals, as well as membrane-associated and cytosolic proteins expressed in mammalian cells.

134 rt system requires three proteins: the small cytosolic proteins FeoA and FeoC and a large cytoplasmic

135 bes resulted in selective degradation of the cytosolic protein FKBP12.

136 termine whether there is evidence of altered cytosolic protein folding by assessing whether amyloid d

137 fy new mechanisms for selection of misfolded cytosolic proteins for degradation via defining function

138 ng a genetic screen, we identified two novel cytosolic proteins, Fra1 and Fra2, that are part of a co

139 drophobic indices of the peptide segments of cytosolic proteins from N to C termini.

140 Using the cytosolic protein galectin-3 (gal3) as a marker of membr

141 that zGrad can inactivate transmembrane and cytosolic proteins globally, locally and temporally with

142 We report a 52 kDa cytosolic protein, GOSPEL, which physiologically binds G

143 l degradation of slGFP that is released from cytosolic protein handling centers.

144 et nuclear proteins and, to a lesser extent, cytosolic proteins, hardly anything is known about the S

145 tants to establish that the levels of ZTL, a cytosolic protein, help govern the abundance and distrib

146 raded to avoid aggregation and disruption of cytosolic protein homeostasis.

147 A pull-down assay using cytosolic proteins identified that Ku70 and Ku80 are the

148 tes by Nogo-A exposure, identifying CRMP2, a cytosolic protein implicated in axon growth inhibition b

149 ith a short cytoplasmic domain can recruit a cytosolic protein in a phospholipid and Ca(2+)-specific

150 loid-related protein 14 (MRP14), an abundant cytosolic protein in myeloid cells, acts as an endogenou

151 our application of STICS to freely diffusing cytosolic protein in small cells extends the utility of

152 Recently, we found that cytosolic proteins in axons of mouse cultured neurons ar

153 ations, including membrane, cytoskeletal and cytosolic proteins in fixed and living cells.

154 nisms that contribute to the distribution of cytosolic proteins in growing nerve cells.

155 a selective mechanism for the degradation of cytosolic proteins in lysosomes that contributes to cell

156 gy (CMA), a selective form of degradation of cytosolic proteins in lysosomes, contributes to maintena

157 A), a selective mechanism for degradation of cytosolic proteins in lysosomes, contributes to the remo

158 tes the degradation of a selective subset of cytosolic proteins in lysosomes.

159 conditions through selective degradation of cytosolic proteins in lysosomes.

160 dification, we assessed the carbonylation of cytosolic proteins in phagocytic neutrophils.

161 Transport of membrane and cytosolic proteins in primary cilia is thought to depend

162 al locations of transport routes for various cytosolic proteins in the 250-nm-wide shaft of live prim

163 the external medium requires the addition of cytosolic proteins including coatomer protein complex I

164 Cytosolic proteins including the ESCRT machineries are k

165 selected peptide-bound glutamine residues of cytosolic proteins (including actin and tubulin), while

166 d by a variety of receptor interactions with cytosolic proteins, including those that may be previous

167 osis inhibitory molecule (FAIM) is a soluble cytosolic protein inhibitor of programmed cell death and

168 Ric-8A) is a highly evolutionarily conserved cytosolic protein initially identified in Caenorhabditis

169 ively implicate the luminal location of host cytosolic proteins inside secreted exosomes, we provide

170 propose a model in which active transport of cytosolic proteins into both nuclear and ciliary compart

171 el where Hsc70 activity dynamically clusters cytosolic proteins into cargo complexes, allowing transp

172 h mitochondrial enlargement and transport of cytosolic proteins into mitochondria.

173 t leads to enhanced turnover of non-critical cytosolic proteins into sources of energy or clearance o

174 ays for proteasomal degradation of misfolded cytosolic proteins involve functional interplay between

175 Alpha-synuclein (alphaS) is a cytosolic protein involved in the etiology of Parkinson'

176 alpha-Synuclein (alpha-Syn) is an abundant cytosolic protein involved in the release of neurotransm

177 or proteins 5 (CRMP5) belongs to a family of cytosolic proteins involved in axon guidance and neurite

178 m the ER membrane not only YOD1 and p97, two cytosolic proteins involved in the extraction of ER tran

179 Our findings show that a cytosolic protein is necessary for transit of selective

180 nd its "constitutive" interactions with some cytosolic proteins, it nevertheless is a prerequisite bo

181 Nrf2 activity is controlled, in part, by the cytosolic protein Keap1, but the nature of this pathway

182 NOD2 receptor and the cytosolic protein kinase RIPK2 regulate NF-kappaB and MA

183 The RAF proteins are cytosolic protein kinases that regulate cell responses t

184 Dimeric tubulin, an abundant water-soluble cytosolic protein known primarily for its role in the cy

185 s for transfer between cells of membrane and cytosolic proteins, lipids, and RNA.

186 Unlike classical calpains, CAPN5 is a non-cytosolic protein localized to the nucleus and extra-nuc

187 implicate the periplasmic protein LptA, the cytosolic protein LptB, and the IM proteins LptC, LptF,

188 Here, we show that aminoglycosides cause cytosolic protein misfolding and that chaperonin GroEL/G

189 early adaptation of cellular compartments to cytosolic protein misfolding are less clear.

190 Liver fatty acid binding protein (L-FABP), a cytosolic protein most abundant in liver, is associated

191 r (vasopressin type 2 receptor; V(2)R) and a cytosolic protein (Na(+)/H(+) exchanger regulatory facto

192 serine and threonine residues of nuclear and cytosolic proteins (O-GlcNAc) is a posttranslational mod

193 Here, we show that MIG12, a 22 kDa cytosolic protein of previously unknown function, binds

194 Alpha-synuclein (alphaSyn) is a small cytosolic protein of unknown function, which is highly e

195 d except HspB7 suppressed the aggregation of cytosolic proteins of HEK293 cells.

196 neral homeostatic process for degradation of cytosolic proteins or organelles, has been reported to m

197 hat this regulation does not require soluble cytosolic proteins or small molecules such as ATP.

198 to the accumulation of damaged or aggregated cytosolic proteins, or membranes, and rely on autophagy

199 A mutation, L166P, in the cytosolic protein, PARK7/DJ-1, causes protein misfolding

200 Thus, many cytosolic proteins proceed through a prolonged "fragile

201 Here we show that, in yeast, cytosolic proteins prone to aggregation are imported int

202 The cytosolic proteins protein kinase Ctheta (PKCtheta), Bcl

203 ntify SBP-AR and associated ligand-sensitive cytosolic proteins/protein complexes linked to AR activa

204 nappreciated regulatory pathway coordinating cytosolic protein quality control and mTORC1 signaling.

205 eover, mitochondrial proteostasis depends on cytosolic protein quality control mechanisms during cris

206 In conclusion, our results suggest that a cytosolic protein quality control pathway monitors foldi

207 e that ubiquitin chain editing is key to the cytosolic protein quality control under stress condition

208 his protein family, ZFP36L3 is a "full-time" cytosolic protein, rather than a nucleocytoplasmic shutt

209 no spurious signal even with highly abundant cytosolic proteins readily accessible to the bud neck (i

210 Two cytosolic proteins, Rei1 and Jjj1, are required, but the

211 However, it is not known how cytosolic proteins released from traumatized brain tissu

212 GMD is a cytosolic protein required for the first step of fucose

213 Degradation of these damaged cytosolic proteins requires the ubiquitin-proteasome pat

214 The mechanisms by which cytosolic proteins reversibly bind the membrane and indu

215 Myeloid-related proteins (MRPs) 8 and 14 are cytosolic proteins secreted from myeloid cells as proinf

216 The cytosolic protein Sharpin is a component of the linear u

217 n of these degradative compartments requires cytosolic proteins, some of which are autophagy specific

218 In conclusion, CRBP-I is a cytosolic protein specifically expressed in preadipocyte

219 intracellular inclusion pathology formed by cytosolic proteins such as Tau, alpha-synuclein and TDP-

220 Several large fragments of typical cytosolic proteins, such as GAPDH, triosephosphate isome

221 ajority of the identified proteins were host cytosolic proteins, suggesting that S. aureus was rapidl

222 osterically through binding to a site on the cytosolic protein surface, which is different from the e

223 ylation and thus affecting the status of the cytosolic protein synthesis apparatus.

224 Stromule induction by ABA was dependent on cytosolic protein synthesis, but not plastid protein syn

225 of nascent chain length for Escherichia coli cytosolic proteins synthesized on both arrested and cont

226 found that in cultured axons, populations of cytosolic proteins tagged to photoactivatable GFP (PAGFP

227 While all cytosolic proteins tested primarily utilize the IFT path

228 lexin, also known as synaphin, is a neuronal cytosolic protein that acts as a major regulator of syna

229 GpsB is a cytosolic protein that affects cell wall synthesis by bi

230 Here, we describe ALIX, a cytosolic protein that associates with MVB by interactin

231 We visualized complexin (cplx), a cytosolic protein that binds assembled SNARE complexes,

232 quitinated proteins and that it is a soluble cytosolic protein that can be induced by interferons and

233 AnxA2 is a cytosolic protein that can bind PI(4,5)P2 and other acid

234 sicle-trafficking proteins, and for DHAR1, a cytosolic protein that facilitates the scavenging of rea

235 FL1 appears to be an example of a eukaryotic cytosolic protein that has been coopted for a function i

236 ors of Cholinesterase A (Ric-8A) is a 60-kDa cytosolic protein that has chaperone and guanine nucleot

237 y acid-binding protein (L-Fabp), an abundant cytosolic protein that modulates fatty acid (FA) metabol

238 RH domain-interacting protein (SHARPIN) is a cytosolic protein that plays a key role in activation of

239 clear prelamin A recognition factor-like), a cytosolic protein that plays a role in the cytosolic iro

240 Rhesus TRIM5alpha (TRIM5alpha(rh)) is a cytosolic protein that potently restricts HIV-1 at an ea

241 TRIM5alpha(rh) is a cytosolic protein that potently restricts HIV-1 before r

242 TRIM21 is a ubiquitously expressed cytosolic protein that recognizes the Fc region of Abs.

243 t, an integral membrane protein but rather a cytosolic protein that tightly associates with cellular

244 OXO1beta [NOXO1 (Nox organizer 1) beta] is a cytosolic protein that, in conjunction with NOXA1 (Nox a

245 on chromatography, we identified hundreds of cytosolic proteins that appeared to exist as components

246 exins, found in most eukaryotic species, are cytosolic proteins that are able to bind negatively-char

247 embrane proteins, cytoskeletal proteins, and cytosolic proteins that are strongly associated with the

248 Profilins are abundant cytosolic proteins that are universally expressed in euk

249 Complexins I and II are highly related cytosolic proteins that bind tightly to the assembled SN

250 somes containing kidney-derived membrane and cytosolic proteins that can be used to probe the proteom

251 he interleukin-1 (IL-1) family cytokines are cytosolic proteins that exhibit inflammatory activity up

252 of 30 yeast strains with single deletions of cytosolic proteins that have known or hypothesized chape

253 liary subunits KCTD8, -12, -12b, and -16 are cytosolic proteins that influence agonist potency and G-

254 UBX-containing protein, UBXD4, as one of the cytosolic proteins that interact directly with the alpha

255 the basis for NO inhibition and to identify cytosolic proteins that may be involved, using inducible

256 of the neurofilament transport kinetics with cytosolic proteins that move at faster rates.

257 rotein 5 (CRMP5) belongs to a family of five cytosolic proteins that play a major role in nervous sys

258 Arrestins are cytosolic proteins that regulate G-protein-coupled recep

259 proteomic approaches, we identified numerous cytosolic proteins that show specific losses in solubili

260 RGPs are plant-specific cytosolic proteins that tend to associate with the endom

261 7) are an evolutionarily conserved family of cytosolic proteins that transiently assembles into helic

262 In cytosolic proteins the cation-pi box provides a suitable

263 It is both a secreted and cytosolic protein, the latter regulating precursor cell

264 For about 20% of all cytosolic proteins this delay in folding can exceed the

265 Orai with the carboxy terminus of Stim as a cytosolic protein to activate the Orai channel without i

266 e demonstrate light-induced recruitment of a cytosolic protein to individual centromeres, kinetochore

267 Thus, p62 brings cytosolic proteins to autolysosomes where they are proce

268 ed specific ribosomal and bulk ubiquitinated cytosolic proteins to autolysosomes where they were prot

269 , our results suggest that routing misfolded cytosolic proteins to ER may be an effective strategy fo

270 agy (CMA), a process that delivers selective cytosolic proteins to lysosomes for degradation, with pr

271 -mediated autophagy involved in transport of cytosolic proteins to the lysosome for degradation.

272 To address this issue, we have targeted cytosolic proteins to the mitochondrion, a poly(A) speci

273 autophagy-like process that delivers soluble cytosolic proteins to the vesicles of late endosomes/mul

274 idic clusters, which interact with PACS-1, a cytosolic protein, to mediate retrograde transport from

275 r bound of about 7 to 16% on the fraction of cytosolic protein translation carried out by ribosomes a

276 stress via a uniquely selective reduction of cytosolic protein translation.

277 Candidates included cytoskeletal regulators, cytosolic protein transporters, exocytosis and endocytos

278 axonal transport via motor-driven vesicles, cytosolic proteins travel in slow axonal transport via m

279 ane adapter protein PAG1, which recruits the cytosolic protein tyrosine kinase Csk to the plasma memb

280 inducible F(V)2E dimerization domain and the cytosolic protein tyrosine kinase domain of the insulin

281 ollows: BCR, Lyn, Fyn, Csk, PAG1, and Syk, a cytosolic protein tyrosine kinase that is activated as a

282 gle DHCH1 and FTL genes encoding exclusively cytosolic proteins, unlike other organisms where isoform

283 Attachment of CL1 to the cytosolic protein Ura3p destabilizes Ura3p, targeting it

284 regulation involves assembly of an ISC on a cytosolic protein using Fecyt and a sulfur species gener

285 The UPR-Cyto response is induced by the cytosolic protein, VHL-L158P, and is characterized by a

286 c) availability, and lead to modification of cytosolic proteins via O-linked attachment of the monosa

287 Soluble cytosolic proteins vital to axonal and presynaptic funct

288 Efflux time courses of endogenous cytosolic proteins were obtained from rabbit psoas muscl

289 urred during evolution, whenever ancestrally cytosolic proteins were recruited to the secretory pathw

290 While a number of cytosolic proteins were shared, others were unique to ea

291 IDE is a ubiquitously expressed cytosolic protein, where monomeric Ub is also present.

292 l TDP-43 increased the levels of nuclear and cytosolic protein, whereas Parkin co-expression mediated

293 ding to tyrosine-phosphorylated receptors or cytosolic proteins, which leads to the formation of larg

294 ha- and gamma-adaptin-binding protein p34, a cytosolic protein with a Rab-like GTPase domain, was sho

295 Doc2B is a cytosolic protein with binding sites for Munc13 and Tcte

296 Here, we show that synapsin-a cytosolic protein with known roles in SV mobilization an

297 Armadillo repeat containing 5 (ARMC5) is a cytosolic protein with no enzymatic activities.

298 Using fluorescent protein fusion to cytosolic proteins with known redox-active cysteines, we

299 with only protein disulfide isomerase or all cytosolic proteins with only PA700, the 19S regulatory p

300 tion of double-membraned vesicles containing cytosolic protein within mitochondria.