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

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

4 propriate UNC-104 activity randomized axonal protein sorting.

5 ous cellular functions such as signaling and protein sorting.

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

7 ent with its previously reported function in protein sorting.

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

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

10 th a particular focus on pathways regulating protein sorting.

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

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

13 four ESCRT complexes in multivesicular body protein sorting.

14 for degradation by ubiquitination-dependent protein sorting.

15 be important for the function of the GGAs in protein sorting.

16 lecular mechanisms governing plasma membrane protein sorting.

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

18 hip between raft association and subcellular protein sorting.

19 omain formation as a mechanism for endosomal protein sorting.

20 r these proteins in membrane trafficking and protein sorting.

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

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

23 11 belong to the sortilin family of vacuolar protein sorting-10 (Vps10) domain-containing proteins.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 hinery that is normally involved in vacuolar protein sorting and multivesicular body (MVB) biogenesis

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

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

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

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

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

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

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

74 Lipid and protein sorting and trafficking in intracellular pathway

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

76 63-linked chains control ribosome function, protein sorting and trafficking, and endocytosis of memb

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

78 ntracellular vesicular trafficking, that is, protein sorting and vesicle docking and fusion.

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

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

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

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

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

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

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

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

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

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

89 bind ubiquitylated proteins during vacuolar protein sorting, and probably many other biological proc

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

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

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

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

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

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

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

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

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

99 Models for protein sorting at multivesicular bodies in the endocyti

100 scuss the implications of this mechanism for protein sorting at the exit sites of the Golgi and endop

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

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

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

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

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

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

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

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

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

110 Protein sorting between eukaryotic compartments requires

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 Pase Ypt7p, the homotypic fusion and vacuole protein sorting complex (HOPS)-VpsC Rab effector complex

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

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

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

130 -1, BLOC-2, and homotypic fusion and vacuole protein sorting complex subunits; clathrin; and phosphat

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

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

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

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

135 Endosomal protein sorting controls the localization of many physio

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

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

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

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

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

141 1 and Vps4p and exhibits synthetic vacuolar protein sorting defects when combined with mutations in

142 This resulted in vacuole protein sorting defects, vacuolar fragmentation, and the

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

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

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

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

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

148 n-protein contacts with the class E vacuolar protein sorting factors, Tsg101 and AIP1/ALIX.

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

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

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

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

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

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

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

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

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

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

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

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

161 odes a homolog of the class C yeast vacuolar protein sorting gene, Vps33, that contains a Sec1-like d

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

191 Cullen studies protein sorting in the endosomal network.

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

193 ly as a Rab11 binding protein that regulates protein sorting in tubular endosomes.

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

195 roteins involved in endocytosis and vacuolar protein sorting including Hrs, Vps27p, Stam1, and Eps15

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

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

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

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

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

201 ry should stimulate work on the mechanism of protein sorting into vesicles and the role of vesicles i

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

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

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

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

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

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

208 ecessarily be a sole determinant in membrane protein sorting, its properties can markedly modulate th

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

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

211 odel integral protein to begin investigating protein-sorting mechanisms.

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

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

214 dc1(Ts) suppressors as class E vps (vacuolar protein sorting) mutants and shows that these, as well a

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

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

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

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

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

220 TGN to the PVC but had no effect on vacuolar protein sorting or cycling of Vps10p.

221 pon the functioning of the cellular vacuolar protein sorting pathway and reveal yet another facet of

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

223 ganelles composing the conventional lysosome protein sorting pathway.

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

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

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

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

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

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

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

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

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

233 e most, if not all, previously characterized protein sorting pathways, the information that identifie

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

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

236 the cytosolic tail (C-tail) of the vacuolar protein sorting receptor, Vps10p, is also efficiently tr

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

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

239 Distinct types of protein sorting receptors that recognize carbohydrate an

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

241 Protein sorting represents a potential point of regulati

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

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

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

245 contains putative transmembrane regions and protein-sorting signals.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

261 together, these data indicate that membrane protein sorting to the INM is an active process involvin

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

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

264 I) 3-kinase in Saccharomyces cerevisiae, for protein sorting to the vacuole in yeast has exemplified

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

266 uch as amylase, thereby supporting a role in protein sorting to the zymogen granule.

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

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

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

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

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

272 show that ESCRT-I and other class E vacuolar protein sorting (VPS) factors are linked by a complex se

273 P-1/ALIX, both of which are class E vacuolar protein sorting (VPS) factors, normally required for the

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

275 Deletion of class E vacuolar protein sorting (VPS) genes, which encode proteins that

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

277 require components of the cellular vacuolar protein sorting (VPS) machinery for efficient viral rele

278 Tsg101, a component of the class E vacuolar protein sorting (VPS) machinery, is required for the bud

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

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

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

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

283 tions in both HIV-1 budding and the vacuolar protein sorting (VPS) pathway, where it binds ubiquityla

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

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

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

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

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

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

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

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

292 veloped viruses exploit the class E vacuolar protein-sorting (VPS) pathway to bud from cells, and use

293 ) and SNX2, homologues of the yeast vacuolar protein-sorting (Vps)5p, contain a phospholipid-binding

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.