ライフサイエンスコーパス: protein sorting

1 r complex HOPS (homotypic fusion and vacuole protein sorting).

2 omain formation as a mechanism for endosomal protein sorting.

3 r these proteins in membrane trafficking and protein sorting.

4 is a model for the study of metal-regulated protein sorting.

5 early endosome processing and ubiquitinated protein sorting.

6 uitous clathrin adaptor AP-1A in basolateral protein sorting.

7 ansfer and lipid A synthesis and possibly by protein sorting.

8 propriate UNC-104 activity randomized axonal protein sorting.

9 d level of specificity in ubiquitin-mediated protein sorting.

10 ent with its previously reported function in protein sorting.

11 known function of the class C Vps complex in protein sorting.

12 rminus is vital for both voltage sensing and protein sorting.

13 th a particular focus on pathways regulating protein sorting.

14 a function of the BLOC-1 complex in membrane protein sorting.

15 disease-related defects in the regulation of protein sorting.

16 four ESCRT complexes in multivesicular body protein sorting.

17 domain proteins may be effectors of PI3P for protein sorting.

18 ous cellular functions such as signaling and protein sorting.

19 hip between raft association and subcellular protein sorting.

20 Members of the vacuolar protein sorting 10 (Vps10) family of receptors (includin

21 11 belong to the sortilin family of vacuolar protein sorting-10 (Vps10) domain-containing proteins.

22 Sorcs1 belongs to the Vacuolar protein sorting-10 (Vps10) gene family.

23 -nucleotide insertion in the vps11 (vacuolar protein sorting 11) gene.

24 nucleotide insertion in the vps11 (vacuolar protein sorting 11) gene.

25 that all six HOPS subunits (Vps11 [vacuolar protein sorting 11]/CG32350, Vps18/Dor, Vps16A, Vps33A/C

26 amino acid substitutions in Vps13 (vacuolar protein sorting 13), a large universally conserved eukar

27 warblers to identify a single gene-vacuolar protein sorting 13A (VPS13A)-that is associated with dis

28 eterozygous truncating mutations in vacuolar protein sorting 13C (VPS13C).

29 -coil domain of the ESCRT-I subunit vacuolar protein sorting 23 (Vps23).

30 viously described ESCRT-I subunits (vacuolar protein sorting 23, -28, and -37), suggesting a distinct

31 20/VPS25 (ELL-associated protein 20/vacuolar protein sorting 25) and the Bro1 proteins HD-PTP (His do

32 the arrestin-like structure of the vacuolar protein sorting 26A (VPS26A) retromer subunit.

33 the protein-trafficking regulators vacuolar protein sorting 33A protein (VPS33A) or cappuccino prote

34 Vacuolar protein sorting 34 (Vps34) complexes, the class III PtdI

35 Vacuolar protein sorting 34 (VPS34) contributes to the regulation

36 class III phosphoinositide 3-kinase vacuolar protein sorting 34 (Vps34) plays a central role in modul

37 The class III PI3K Vacuolar protein sorting 34 (Vps34) plays a role in both canonica

38 wn of the autophagy-specific genes, vacuolar protein sorting 34 (VPS34), and autophagy-related protei

39 sphatidylinositol (PtdIns) 3-kinase vacuolar protein sorting 34 (Vps34), in podocytes results in aber

40 beclin 1 is a core component of the vacuolar protein sorting 34 (Vps34)/class III phosphatidylinosito

41 Vacuolar protein-sorting 34 (Vps34), the catalytic subunit in the

42 ion of PI3KC3-C1 consisting of VPS (vacuolar protein sorting) 34, VPS15, BECN1 (Beclin 1), and ATG (a

43 bulation and membrane association of vesicle protein sorting 35 (VPS35) and sorting nexin 1 (SNX1), a

44 The vacuolar protein sorting 35 (VPS35) is a major component of the r

45 of one of its major components, the vacuolar protein sorting 35 (VPS35), has been reported in Alzheim

46 Mutations in the vacuolar protein sorting 35 homolog (VPS35) gene at the PARK17 lo

47 P-2 adaptor protein), RAB5A, VPS35 (vacuolar protein sorting 35 homolog), and M6PR (mannose 6-phospha

48 Mutations in the vacuolar protein sorting 35 ortholog (VPS35) gene represent a cau

49 he retromer core component FgVps35 (Vacuolar Protein Sorting 35) in the cytoplasm as fast-moving punc

50 uncharacterized factors, including vacuolar protein sorting 37 homolog A (VPS37A), transmembrane pro

51 The ESCRT disassembly factor vacuolar protein sorting 4 (VPS4) follows CHMP4B to this site, an

52 inclusion in microvesicles, whereas vacuolar protein sorting 4 (VPS4) mediates scission of microvesic

53 is was blocked by dominant-negative vacuolar protein sorting 4 (Vps4), indicating that the Wnt pathwa

54 lopment, we identified an allele of Vacuolar protein sorting 4 (Vps4), which encodes an AAA ATPase th

55 The vacuolar protein sorting 4 AAA-ATPase (Vps4) recycles endosomal s

56 ase activity of SKD1 (also known as Vacuolar Protein Sorting 4 or VPS4), a critical component require

57 ort) components ESCRT-III and VPS4 (vacuolar protein sorting 4).

58 als, the AAA ATPase Vps4p/SKD1 (for Vacuolar protein sorting 4/SUPPRESSOR OF K(+) TRANSPORT GROWTH DE

59 EGFR signaling by repressing Vps4b (vacuolar protein-sorting 4 homolog B), encoding a protein implica

60 ve (DN) form of a key ESCRT ATPase, vacuolar protein sorting-4 (Vps4DN) in HCMV replication.

61 nsport is likely to be regulated by vacuolar protein sorting 74 (Vps74p), a peripheral Golgi protein

62 The vacuolar protein sorting 75 (Vps75) histone chaperone participate

63 also requires a histone chaperone, vacuolar protein sorting 75 (Vps75), as well as the major chapero

64 g protein C, fast type [MYBPC2] and vacuolar protein sorting 8 [VPS8], 2 families, 4.2%) or in anothe

65 dition of HOPS (homotypic fusion and vacuole protein sorting), a Ypt7p (Rab)-effector complex with a

66 e findings demonstrate that Erv26p acts as a protein sorting adaptor for a variety of Type II transme

67 These lipid "rafts" are implicated in protein sorting and are attractive candidates as platfor

68 This review discusses the mechanisms of protein sorting and compartmentalization in photorecepto

69 I) is essential for exocytosis, endocytosis, protein sorting and cytokinesis.

70 sport of cationic transmitters as well as in protein sorting and degradation.

71 specific mechanisms in terms of biogenesis, protein sorting and fate, which are far from completely

72 CA512 RESP18HD being a condensing factor for protein sorting and granulogenesis early in the secretor

73 TIP47 (PAT) family of proteins implicated in protein sorting and lipid droplet biogenesis.

74 d biological membranes, although its role in protein sorting and membrane function still remains uncl

75 (AP-1) complex, implicated in intracellular protein sorting and packaging.

76 titative live cell imaging method to analyze protein sorting and post-Golgi vesicular trafficking.

77 dium falciparum and used by the parasite for protein sorting and protein export.

78 To understand protein sorting and quality control in the secretory pat

79 ctyostelium, we demonstrate that WASH drives protein sorting and recycling from macropinosomes and is

80 d the shp1Delta mutation, implicated in both protein sorting and regulation of the Glc7p protein phos

81 ons block VPS4 recruitment, impair endosomal protein sorting and relieve dominant-negative VPS4 inhib

82 neration of functionally distinct membranes, protein sorting and the development of polarized differe

83 Lipid and protein sorting and trafficking in intracellular pathway

84 l cells are known, but when and how directed protein sorting and trafficking occur to initiate cell s

85 idence that aberrant regulation of endosomal protein sorting and trafficking secondary to a dysfuncti

86 Recent evidence has implicated defective protein sorting and trafficking secondary to deficiencie

87 63-linked chains control ribosome function, protein sorting and trafficking, and endocytosis of memb

88 n core complex which regulates intracellular protein sorting and trafficking.

89 ion in apical, but not basolateral, membrane protein sorting and transport.

90 e budding is essential for processes such as protein sorting and transport.

91 RT-II complex performs a central role in MVB protein sorting and vesicle formation, as it is recruite

92 lattice, thereby allowing multiple rounds of protein sorting and vesicle formation.

93 uction but rather plays an essential role in protein sorting and/or trafficking.

94 e Vps-C complexes HOPS (homotypic fusion and protein sorting) and CORVET (class C core vacuole/endoso

95 r complex HOPS (homotypic fusion and vacuole protein sorting), and four SNAREs.

96 ex termed HOPS (homotypic fusion and vacuole protein sorting), and soluble N-ethylmaleimide-sensitive

97 ESCRT-I/MVB12 subunits, Crag, a regulator of protein sorting, and bacterial pore-forming proteins mig

98 omplexes: AP-3, homotypic fusion and vacuole protein sorting, and BLOC-1, -2, and -3.

99 regulation of innate immunity, inflammation, protein sorting, and chromatin remodeling.

100 protein implicated in endocytosis, endosomal protein sorting, and cytoskeletal organization.

101 ctions in enveloped virus budding, endosomal protein sorting, and many other cellular processes.

102 athway and plays key roles in glycosylation, protein sorting, and secretion in plants.

103 Early endosomes (EEs) mediate protein sorting, and their cytoskeleton-dependent motili

104 Our study establishes mitochondrial protein sorting as an intervention point for ATP synthas

105 nally, we show that CHX17 and CHX20 affected protein sorting as measured by carboxypeptidase Y secret

106 equences of Arn1p were required for vacuolar protein sorting, as mutation of ubiquitinatable lysine r

107 s persicae associates with the host Vacuolar Protein Sorting Associated Protein52 (VPS52).

108 other retromer components SNX-3 and vacuolar protein sorting-associated protein 35 (VPS-35) did not a

109 usceptibility protein domains and a vacuolar protein sorting-associated protein 9 with a coupling of

110 ons for signaling at cell-cell junctions and protein sorting at intracellular contact points between

111 Models for protein sorting at multivesicular bodies in the endocyti

112 dundant, cargo-specific, or not required for protein sorting at the multivesicular body.

113 Class E vps mutations, which impair protein sorting at the MVB, also decrease activation by

114 tween Drs2p and the AP-1 clathrin adaptor in protein sorting at the TGN and early endosomes of Saccha

115 Our results suggest a model of protein sorting at the TGN that involves a peripheral, p

116 in response to nutrient availability governs protein sorting at the TGN, likely by regulating sterol

117 These results establish a role for active protein sorting at the trans-Golgi en route to the plasm

118 component of a non-clathrin coat involved in protein sorting at the trans-Golgi network (TGN).

119 e GA altered the functional organization and protein sorting at the trans-Golgi network.

120 -beta4-mu4-sigma4) AP-4 complex, involved in protein sorting at the trans-Golgi network.

121 ESCRT complex assembly/disassembly cycle in protein sorting at the yeast late endosome.

122 Protein sorting between eukaryotic compartments requires

123 f plasma membrane proteins and receptors and protein sorting between the trans-Golgi network (TGN) an

124 tor proteins implicated in clathrin-mediated protein sorting between the trans-Golgi network and endo

125 in mouse erythroblasts, nor at the membrane protein-sorting boundary in human erythroblasts, which d

126 how the ZBP1-RNA complex achieves asymmetric protein sorting by localizing beta-actin mRNA.

127 sruption of endosome-lysosome fusion but not protein sorting by the MVB.

128 rough interactions with the class C vacuolar protein sorting (C-Vps) tethering complex and endosomal

129 mbrane fusion is essential for intracellular protein sorting, cell growth, hormone secretion, and neu

130 or transport) genes grouped by their vacuole protein sorting Class E mutant phenotypes.

131 tosis/actin dynamics (SLA1, SLA2, and END3), protein sorting (class E vps), and vesicle-vacuole fusio

132 We show that the homotypic fusion and protein-sorting/class C vacuole protein-sorting (HOPS/cl

133 partner for the homotypic fusion and vacuole protein sorting complex (a master regulator of vacuole f

134 is enhanced by homotypic fusion and vacuole protein sorting complex (HOPS) and Sec17p/Sec18p, the va

135 8) and its effector homotypic fusion/vacuole protein sorting complex (HOPS) to (phago)lysosome membra

136 hering complex, homotypic fusion and vacuole protein sorting complex (HOPS), and phosphoinositides, w

137 ddition of pure homotypic fusion and vacuole protein sorting complex (HOPS), which bears the vacuolar

138 fector complex, homotypic fusion and vacuole protein sorting complex (HOPS).

139 d the hexameric homotypic fusion and vacuole protein sorting complex (HOPS).

140 Sec18p, and the homotypic fusion and vacuole protein sorting complex (HOPS).

141 -1, BLOC-2, and homotypic fusion and vacuole protein sorting complex subunits; clathrin; and phosphat

142 g complex HOPS (homotypic fusion and vacuole protein sorting complex), whereas the C-terminal SNARE m

143 complex, HOPS (HOmotypic fusion and vacuolar Protein Sorting complex).

144 vacuolar HOPS (homotypic fusion and vacuole protein sorting) complex in the yeast Saccharomyces cere

145 r4-Not complex, V-type ATPases, and vacuolar protein-sorting complexes as well as genes with unknown

146 Endosomal protein sorting controls the localization of many physio

147 e remodeling events that accompany endosomal protein sorting, cytokinesis, and enveloped RNA virus bu

148 rom the early endosomes (EE) requires active protein sorting decoded by a number of protein coats.

149 ular multiplication, CteG induced a vacuolar protein sorting defect when expressed in Saccharomyces c

150 The mammalian homologue of yeast vacuolar protein sorting defective 34 (mVps34) has been implicate

151 This effect was accompanied by protein sorting defects at multivesicular endosomes that

152 The delayed onset of matrix protein sorting defects may account for the relatively w

153 1 and Vps4p and exhibits synthetic vacuolar protein sorting defects when combined with mutations in

154 uired for transport (ESCRT), which regulates protein sorting during endosomal trafficking, this assoc

155 y was undertaken to explore whether aberrant protein sorting, during enucleation, creates these membr

156 ve emerged as important players in endosomal protein sorting, dynamics and motility.

157 little is known regarding the mechanisms of protein sorting/entry into olfactory cilia.

158 Endosomes function as a hub for multiple protein-sorting events, including retrograde transport t

159 propose that the principle of membrane-based protein sorting extends to monotopic membrane proteins,

160 r a synthetic yeast prion, we identified two protein-sorting factors of the Hook family, termed Btn2

161 c concentrations of molecular chaperones and protein-sorting factors.

162 thers have observed in class C VPS (vacuolar protein sorting) family mutants and morphants, and we re

163 nent of the cellular machinery that controls protein sorting from endosomes to lysosomes and speciali

164 RT complexes form the main machinery driving protein sorting from endosomes to lysosomes.

165 hree complexes, termed BLOC-1 to -3, mediate protein sorting from the early endosome to lysosomes and

166 he thylakoid-transfer signal is required for protein sorting from the stroma to thylakoids, mainly vi

167 We propose that CTL1 regulates protein sorting from the TGN to the PM through its funct

168 asolateral plasma membrane domains depend on protein sorting from the trans-Golgi network (TGN) and v

169 e, two essential steps in vacuolar/lysosomal protein sorting from yeast to humans.

170 ed for protein complex formation and for the protein-sorting function of Bro1.

171 Mutation of the class C vacuolar protein sorting gene vps18 results in hepatomegaly assoc

172 mutants disrupted established VPS (vacuolar protein sorting) genes, The sixth, LTE1, is a Low Temper

173 While aberrant endosomal protein sorting has been linked to several neurodegenera

174 The homotypic fusion and vacuole protein sorting (HOPS) complex links these two processes

175 Homotypic fusion and vacuole protein sorting (HOPS) complex members were identified a

176 a member of the homotypic fusion and vacuole protein sorting (HOPS) complex that delivers biosyntheti

177 the GTPase Rab7 and the homotypic fusion and protein sorting (HOPS) complex, but adaptor proteins tha

178 ntrolled by the homotypic fusion and vacuole protein sorting (HOPS) complex, rescued the neurotransmi

179 somal tethering homotypic fusion and vacuole protein sorting (HOPS) complex, was recently identified

180 bunit tethering homotypic fusion and vacuole protein sorting (HOPS) complex, which is essential for t

181 subunit of the homotypic fusion and vacuole protein sorting (HOPS) complex, which plays a key role i

182 lass C components of the homotypic vesicular protein sorting (HOPS) complex.

183 tegrated by the homotypic fusion and vacuole protein sorting (HOPS) complex.

184 hering (CORVET) and the homotypic fusion and protein sorting (HOPS) complexes, which have essential f

185 Homotypic fusion and vacuole protein sorting (HOPS) is a tethering complex required f

186 he multisubunit homotypic fusion and vacuole protein sorting (HOPS) membrane-tethering complex is req

187 ther, the Vps-C/homotypic fusion and vacuole protein sorting (HOPS) subunit Vps41, and a SNARE, Vam3.

188 uolar/lysosomal homotypic fusion and vacuole protein sorting (HOPS) tethering complex combines both a

189 ependent on the homotypic fusion and vacuole protein sorting (HOPS) tethering complex.

190 ane fusion, and homotypic fusion and vacuole protein sorting (HOPS), that serve as adaptors which tet

191 of their known roles in homotypic fusion and protein sorting (HOPS)-mediated vesicle tethering, are r

192 lipids, and the homotypic fusion and vacuole protein sorting (HOPS)/class C Vps complex, an effector

193 it of the yeast homotypic fusion and vacuole protein-sorting (HOPS) complex, bound to two individual

194 coding a subunit of the homotypic fusion and protein-sorting (HOPS) complex-as a critical determinant

195 the class C Vps/homotypic fusion and vacuole protein-sorting (HOPS) complex.

196 members of the homotypic fusion and vacuole protein-sorting (HOPS) multisubunit tethering complex, w

197 c fusion and protein-sorting/class C vacuole protein-sorting (HOPS/class C Vps) complex can tether lo

198 Endosomes are the major protein-sorting hubs of the endocytic pathway.

199 Targeting TIM23-dependent protein sorting improves an array of phenotypes associat

200 that COP9-associated CSN5 regulates exosomal protein sorting in both a deubiquitinating activity-depe

201 discoveries that have revealed insight into protein sorting in cells.

202 n complexes are important mediators of cargo protein sorting in clathrin-coated vesicles.

203 e current model of polarized plasma membrane protein sorting in epithelial cells has been largely gen

204 nd mechanisms that regulate polarized apical protein sorting in hepatocytes, the major epithelial cel

205 trameric adaptor protein 1 (AP-1) complex in protein sorting in intracellular compartments is not yet

206 to provide insights into raft formation and protein sorting in model lipid membranes.

207 ptor protein (AP) complex family involved in protein sorting in the endomembrane system of eukaryotic

208 Cullen studies protein sorting in the endosomal network.

209 dressing fundamental questions, ranging from protein sorting in the photoreceptor cilium to photorece

210 inery that mediates membrane trafficking and protein sorting in yeast.

211 M complex HOPS (homotypic fusion and vacuole protein sorting) increases the fusion of membranes beari

212 The Legionella pneumophila effector vacuolar protein sorting inhibitor protein D (VipD) localizes to

213 daptor protein (AP) complexes, which mediate protein sorting into endosomal vesicles.

214 embranes requires host functions involved in protein sorting into late endosomal multivesicular bodie

215 from vacuole/lysosomal compartments and for protein sorting into multivesicular bodies.

216 wo-step kinetic and affinity-based model for protein sorting into the sequence-dependent recycling pa

217 role of the yeast Nedd4 homologue, Rsp5, in protein sorting into vesicles that bud into the multives

218 Actin-binding protein sorting is critical for the self-organization of

219 Stn2 and favor a model according to which SV protein sorting is guarded by both cargo-specific mechan

220 We conclude that aberrant protein sorting is one mechanistic basis for protein def

221 An outstanding question in protein sorting is why polarized epithelial cells expres

222 protein to a specific destination (known as protein sorting) is a crucial event that is intrinsicall

223 nsporter-like 1 (CTL1) as a new regulator of protein sorting may enable researchers to understand not

224 plast proteins engage one of four additional protein sorting mechanisms that direct targeting to the

225 ed in these studies regulates cargo-specific protein sorting mediated by the epithelial cell specific

226 a C-terminal region containing intracellular protein sorting motifs.

227 hat there are probably multiple pathways for protein sorting/MVB vesicle formation in human cells and

228 inds two isoforms of the retromer-associated protein sorting nexin 3 (SNX3), including a novel isofor

229 ring RNA screens, we find that the endosomal protein sorting nexin 5 (SNX5)(3,4) is essential for vir

230 ave identified a novel intracellular adaptor protein, sorting nexin 17 (SNX17), that binds specifical

231 ave identified a unique rodent intracellular protein, sorting nexin 27 (SNX27), which regulates the t

232 The Phox-homology (PX) domain-containing proteins sorting nexin (SNX) 17, SNX27, and SNX31 have e

233 the ESCRT proteins of the cellular vacuolar protein sorting pathway for efficient egress from the ce

234 ganelles composing the conventional lysosome protein sorting pathway.

235 or, a known cargo of the multivesicular body protein sorting pathway.

236 y virus type 1 (HIV-1) exploits the vacuolar protein-sorting pathway by engaging Tsg101 and ALIX thro

237 demonstrate that the polarization of the EMV protein-sorting pathway can occur in morphologically non

238 biquitin-proteasome pathway and the vacuolar protein-sorting pathway of cells.

239 to evade phagocytic killing via a dedicated protein-sorting pathway termed type III secretion.

240 d levels of EMV cargoes (i) polarize the EMV protein-sorting pathway, (ii) generate a nascent posteri

241 ttling it into the multivesicular body (MVB) protein-sorting pathway.

242 (TGN) to the vacuolar lumen via the vacuolar protein-sorting pathway.

243 e targets as part of the multivesicular-body protein-sorting pathway.

244 n and release that is controlled by vacuolar protein sorting protein 33b (VPS33B).

245 is a homologue of the yeast class C vacuolar protein sorting protein Vps33p that is involved in the b

246 date the great diversity in secretory cargo, protein sorting receptors are required in a number of in

247 incorporation into COPII transport vesicles, protein sorting receptors release bound cargo in pre-Gol

248 Distinct types of protein sorting receptors that recognize carbohydrate an

249 er of the ARF family of membrane budding and protein sorting regulators.

250 Protein sorting represents a potential point of regulati

251 il, containing the G-protein recognition and protein sorting sequences, exhibited a high mobility, in

252 We demonstrate interaction of the protein sorting signal Ubiquitin with the Vps9-CUE, a Ub

253 Multiple new prokaryotic C-terminal protein-sorting signals were found that reprise the trip

254 contains putative transmembrane regions and protein-sorting signals.

255 Rabs and coiled transport factors to enable protein sorting specificity, could be applicable to vesi

256 m a coat-like complex, with AP-5 involved in protein sorting, SPG15 facilitating the docking of the c

257 the most distal stop and hence the ultimate protein-sorting station for distinct apical and basolate

258 ram-negative equivalent of the LPXTG/sortase protein-sorting system of Gram-positive bacteria.

259 d the class C Vps/HOPS (HOmotypic fusion and Protein Sorting) tether follow this model as their inter

260 AREs, the HOPS (homotypic fusion and vacuole protein sorting) tethering and SNARE-assembly complex, a

261 it of the HOPS (homotypic fusion and vacuole protein sorting) tethering complex, all of which are req

262 ring) and HOPS (homotypic fusion and vacuole protein sorting) tethering complexes require their organ

263 plex) and HOPS (homotypic fusion and vacuole protein sorting)-tethering complex to elicit neuroprotec

264 tethering complex HOPS (homotypic fusion and protein sorting); the small GTPases Rab2, Rab7, and its

265 urvive under cell wall stress and for proper protein sorting through the carboxypeptidase Y pathway.

266 tetramer that is involved in signal-mediated protein sorting to endosomal-lysosomal organelles.

267 In addition, a new mechanism for protein sorting to exosomes, involving an endogenous lec

268 ese organelles and reduces amyloid precursor protein sorting to intraluminal vesicles.

269 that (1) AP-3, BLOC-1, and BLOC-3 facilitate protein sorting to lysosomes to support ultimate secreti

270 indings in relation to the current model for protein sorting to storage vacuoles are discussed.

271 ue, Reczek et al. identify a new pathway for protein sorting to the lysosome.

272 quired for at least two different processes: protein sorting to the vacuole and sporulation.

273 that enolase deficiency also prevents normal protein sorting to the vacuole, exacerbating the fusion

274 s-Golgi network (TGN), but the mechanism for protein sorting to this regulated secretory pathway (RSP

275 ignaling and the assembly of polyubiquinated proteins sorting to sequestosomes and proteasomes.

276 provides a platform for receptor signaling, protein sorting, transport, and endocytosis, whose regul

277 erved protein complex composed of a vacuolar protein sorting trimer (Vps 26/29/35) that participates

278 -enriched endosomal membranes and a vacuolar protein sorting (Vps) 26/29/35 trimer that participates

279 We validated the role of a set of vacuolar protein sorting (VPS) genes during infection, VPS51 to V

280 ires the recruitment of the class E vacuolar protein sorting (VPS) machinery by short, virally encode

281 ished a compilation of the 41 yeast vacuolar protein sorting (vps) mutant groups and described a larg

282 t in controlling dissociation using vacuolar protein sorting (vps) mutants that accumulate proteins i

283 ed protein complexes in the class E vacuolar protein sorting (VPS) pathway required for the sorting o

284 transport-1) complex protein in the vacuolar protein sorting (vps) pathway, to the plasma membrane du

285 The vacuolar protein sorting (Vps) protein Vps27 is a component of ES

286 een shown that ESCRT-I contains the vacuolar protein sorting (Vps) proteins Vps23, Vps28, and Vps37.

287 is increasing evidence that certain Vacuolar protein sorting (Vps) proteins, factors that mediate ves

288 of the core retromer consisting of vacuolar protein sorting (VPS)26, VPS29, and VPS35.

289 The link is formed by the vacuolar protein sorting (Vps)28 C-terminus (ESCRT-I) binding wit

290 mammalian cells, the class III PI3K vacuolar protein sorting (Vps)34 is thought to play a critical ro

291 that produced membrane trafficking [vacuole protein sorting (VPS)] defects in yeast.

292 ociating proteins also required for vacuolar protein-sorting (VPS) in yeast.

293 transporter VPS13, humans have four vacuolar protein-sorting (VPS) protein 13 isoforms.

294 ursor protein (APP) mediated by the vacuolar protein sorting (Vps10) family of receptors plays a deci

295 bset of the mutations implicated in vacuolar protein sorting, vps34Delta, vps15Delta, vps45Delta, and

296 /vacuoles in a homotypic fusion- and vacuole protein sorting/Vps41-dependent manner.

297 uncated peripherin/rds (Xper38)-GFP chimeric protein sorting was followed by immunofluorescence micro

298 Stn2) in mice compromises the fidelity of SV protein sorting, whereas the apparent speed of SV retrie

299 r, the endosome represents a dynamic site of protein sorting with a majority of proteins destined for

300 a key role in regulating various aspects of protein sorting within the cell.