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1 somes that involves tethering to the ER by a sorting nexin.
2 ting, tubular carriers along with a range of sorting nexins.
3                                              Sorting nexin 1 (SNX1) and SNX2 are the mammalian homolo
4                                              Sorting nexin 1 (SNX1) and SNX2, homologues of the yeast
5                     Acute renal depletion of sorting nexin 1 (SNX1) in mice results in blunted natriu
6                                              Sorting nexin 1 (SNX1) is a protein that binds to the ep
7  dopamine D5 receptor (D(5)R) interacts with sorting nexin 1 (SNX1), a protein involved in receptor r
8      Here, we report that Hrs interacts with sorting nexin 1 (SNX1), a recently identified mammalian
9 on of vesicle protein sorting 35 (VPS35) and sorting nexin 1 (SNX1), as well as decreased mannose 6 p
10 we investigated whether PAR1 interacted with sorting nexin 1 (SNX1).
11 rotrophin receptors with retromer-associated sorting nexin 1.
12                                              Sorting nexins 1 (Snx1) and 2 (Snx2) are homologues of t
13 t the putative mammalian retromer components sorting nexins 1 and 2 (Snx1 and Snx2) result in embryon
14                                   A protein, sorting nexin-1 (SNX1), was identified in a human cell l
15 significant sequence homology with mammalian sorting nexin-1.
16 n c.212 + 1 G > T in the SNX10 gene encoding sorting nexin 10.
17  microtubule-dependent shuttle that requires sorting nexin 11 (Snx11).
18                       RGS-PX1 (also known as sorting nexin 13) is a member of both the regulator of G
19 rt the identification of causal mutations in Sorting Nexin 14 (SNX14) found in seven affected individ
20 -associated splice donor site variant in the sorting nexin 14 gene (SNX14) as a strong causative cand
21      Here, we identified mechanisms by which Sorting Nexin 16 (SNX16) controls neuronal endosomal mat
22 Nwk acts through a physical interaction with sorting nexin 16 (SNX16).
23 g endosomal signaling compartment containing Sorting Nexin 16 and a reduction in late endosomes conta
24                            Here we show that sorting nexin 17 (Snx 17) is part of the cellular sortin
25                  During endosomal recycling, Sorting Nexin 17 (SNX17) facilitates the transport of nu
26                                              Sorting nexin 17 (SNX17) functions as cargo receptor on
27                                              Sorting nexin 17 (SNX17) is a member of the family of cy
28 ified a novel intracellular adaptor protein, sorting nexin 17 (SNX17), that binds specifically to the
29 ein potentially involved in TCR transport is sorting nexin 17 (SNX17).
30 ies have demonstrated an interaction between sorting nexin 17 and the L2 capsid proteins from a varie
31  FERM-domain-containing proteins kindlin and sorting nexin 17 plays pivotal roles in integrin recycli
32 cycling pathway, in part by association with sorting nexin 17, to ensure that virus DNA bound to L2 i
33 llomavirus (HPV) L2 minor capsid protein and sorting nexins 17 and 27 (SNX17 and SNX27) during virus
34 romer.IMPORTANCE Previous studies identified sorting nexins 17 and 27, as well as the retromer comple
35 somal Commander assembly associates with the sorting nexin-17 (SNX17) cargo adaptor to regulate cell
36 d carboxy-terminal tail of the cargo adaptor sorting nexin-17 (SNX17) directly binds to the Retriever
37                      Commander organizes the sorting nexin-17 (SNX17)-dependent recycling of hundreds
38                   In this study, we identify sorting nexin 18 as a novel FIP5-interacting protein and
39 X domain of the novel D(1) R-binding partner sorting nexin 19 (SNX19) resulted in D(1) R partitioning
40 luding a class of exon 9-spliced isoforms of Sorting nexin-19 (SNX19(d9)) and an isoform of Arsenic m
41                                              Sorting Nexin 2 (SNX2), which is involved in trafficking
42                                              Sorting nexin 27 (SNX27) contains a PDZ domain that is p
43                            Here we show that sorting nexin 27 (SNX27) functions as an adaptor that co
44                 Mass spectrometry identified sorting nexin 27 (SNX27) in isolated endosomes as a PTHR
45                                              Sorting nexin 27 (SNX27) is a 62-kDa protein localized t
46                                              Sorting nexin 27 (SNX27) is a PDZ-containing protein kno
47                           Here, we show that sorting nexin 27 (SNX27) is required for efficient PDZ-d
48 s regulated by the psychostimulant-sensitive sorting nexin 27 (SNX27) protein through a class I (-X-S
49                                              Sorting nexin 27 (SNX27), a brain-enriched PDZ domain pr
50 fies one member of the sorting nexin family, Sorting Nexin 27 (SNX27), as a critical component in thi
51 oteins and the related PX-FERM family member sorting nexin 27 (SNX27), which is mediated in part by a
52 ified a unique rodent intracellular protein, sorting nexin 27 (SNX27), which regulates the traffickin
53                                          The sorting nexin 27 (SNX27)-retromer complex is a major reg
54 entification of the OTULIN interactor SNX27 (sorting nexin 27), an adaptor of the endosomal retromer
55 th protein kinase C alpha 1, syntenin-1, and sorting nexin 27.
56        The endosome-associated cargo adaptor sorting nexin-27 (SNX27) is linked to various neuropatho
57                            Here, we describe Sorting Nexin 3 (SNX3), a member of the recycling retrom
58  isoforms of the retromer-associated protein sorting nexin 3 (SNX3), including a novel isoform that b
59 mined interactions between components of the sorting nexin 3 (SNX3)-retromer sorting pathway using qu
60 ed to endosomes by the small GTPase Rab7 and sorting nexin 3.
61                                              Sorting nexin 4 (SNX4) is an evolutionary conserved orga
62  and have identified essential roles for the sorting nexin 4 (SNX4)-mediated, signal-independent path
63 egulation of vesicular trafficking regulator sorting nexin 5 (SNX5) expression, and PI3 kinase activa
64  screens, we find that the endosomal protein sorting nexin 5 (SNX5)(3,4) is essential for virus-induc
65 e discovery of a dynamic interaction between sorting nexin 5 (SNX5), a component of the mammalian ret
66 In this pathway, PIPKIgammai5 interacts with sorting nexin 5 (SNX5), a protein that binds PtdIns4,5P(
67 d regulation of intracellular traffic (e.g., sorting nexin 5 [SNX5], SNX6, and SNX9).
68 e retromer components identified in mammals, sorting nexin 5 and 1 (SNX5; SNX1) have recently been fo
69 reported that IncE binds specifically to the Sorting Nexin 5 Phox domain (SNX5-PX) and disrupts retro
70                               CHC22 binds to sorting nexin 5 through a coiled-coil domain present in
71 inity purification (TAP), we herein identify sorting nexin 6 (SNX6) as a BACE1-associated protein.
72      We demonstrate that GIT1 interacts with sorting nexin 6 (SNX6), a member of the SNX family that
73 ein signaling complex composed of eukaryotic sorting nexin 9 (SNX9) and neuronal Wiskott-Aldrich synd
74                            Here, we identify sorting nexin 9 (SNX9) as a new regulator of breast canc
75                      Under these conditions, sorting nexin 9 (Snx9) can be implicated as a specific a
76                                              Sorting nexin 9 (SNX9) functions in a complex with the G
77 chemical, and immunofluorescence approaches, sorting nexin 9 (SNX9) is identified as being required f
78 upon CD28 triggering, the BAR-domain protein sorting nexin 9 (SNX9) is recruited to CD28 clusters at
79 target cell's plasma membrane and recruiting sorting nexin 9 (SNX9), a central multifunctional endocy
80  inflammatory conditions, we discovered that sorting nexin 9 (SNX9), a protein that participates in e
81 hat is fused to an aminoterminal sequence of sorting nexin 9 (SNX9), which was previously shown to bi
82 derived vesicles in a manner that depends on sorting nexin 9 (SNX9).
83  several host proteins, including N-WASP and sorting nexin 9 (SNX9).
84 is, namely the sorting nexin protein SH3PX1 (sorting nexin 9).
85                                              Sorting nexin 9, an abundant dynamin partner, transientl
86 e temporal ordering of three proteins-actin, sorting nexin 9, and clathrin-in the endocytic pathway.
87 identified protein partner of dynamin, SNX9, sorting nexin 9.
88 g an initial proteomic screen, we identified sorting nexin-9 (SNX9) and dynamins, key components of c
89  knockout validation experiments, we uncover sorting nexin-9 (SNX9) as a mediator of T cell exhaustio
90 ic lysine beta-hydroxybutyrylation (Kbhb) of sorting nexin-9 (SNX9), a key regulator of MDV biogenesi
91 iven by phosphoinositide-3-kinase (PI3K) and sorting-nexin-9 (SNX9).
92                                  Unlike many sorting nexins, a SNX15 ortholog has not been identified
93 17) is a member of the family of cytoplasmic sorting nexin adaptor proteins that regulate endosomal t
94 an that observed for the knockdown of either sorting nexin alone.
95                                        These sorting nexins also associated with the long isoform of
96     In mammals, it is composed of a dimer of sorting nexins and of the core retromer consisting of va
97                                              Sorting nexins are a family of phox homology domain cont
98        Despite their hydrophilic nature, the sorting nexins are found partially associated with cellu
99 of cargo into transport carriers coated with sorting nexin BAR domain proteins (SNX-BARs).
100 nt of the retromer complex and the endosomal sorting nexin-BAR proteins into VROs.
101 e delivery of the co-opted retromer complex, sorting nexin-BAR proteins, and lipid enzymes into VROs
102 esses in collaboration with the retromer and sorting nexins, but its in vivo function has not been ex
103 ains are in many protein families, including sorting nexins, centaurins, and oligophrenins.
104                                 We find that sorting nexin CG1514 or Snazarus (Snz) associates with p
105 vacuole endosome dependent on the Snx4-Atg20 sorting nexin complex.
106 nt role and begins to shed light on how both sorting nexins contribute to retromer and retriever recr
107 eracting retromer complex, consisting of the sorting nexin dimer (SNX-BAR) and the trimeric cargo sel
108 lishing a precedent for a mechanism by which sorting nexins expand the repertoire of retromer-depende
109  studies have revealed that retromer-related Sorting Nexin family (SNX)-Bin/Amphiphysin/Rvs (BAR) pro
110 ive, this study identifies one member of the sorting nexin family, Sorting Nexin 27 (SNX27), as a cri
111 present the first mutations in the mammalian sorting nexin gene family and indicate that sorting nexi
112 af-6 mutants, we identified an allele of the sorting nexin gene snx-1.
113 sability, due to truncating mutations in the sorting nexin gene SNX14, encoding a ubiquitously expres
114 closure, we investigated the role of Snx3, a sorting nexin gene.
115 an endocytic recycling pathway requiring the sorting nexin Grd19/Snx3p, the pentameric retromer compl
116    As with Golgi proteins, this requires the sorting nexin Grd19p and components of the retromer coat
117 ssible implication for overexpression of the sorting nexin in tumor samples.
118  and differential functions of two groups of sorting nexins in phagosome maturation and reveal a sign
119 ur findings suggest a general role for yeast sorting nexins in protein retrieval, rather than degrada
120 ytosis and SH3PX1 has sequence similarity to sorting nexins in yeast, we propose that endophilin I an
121 rols the retrograde transport of CI-M6PR via sorting nexins, including the PI4P effector SNX6.
122                       We also show that both sorting nexins may interact with either of the recycling
123 ed, although the tissue distribution of each sorting nexin mRNA varies.
124              The FERM-like domain-containing sorting nexins of the SNX17/SNX27/SNX31 family have been
125        At the same time, retromer associated sorting nexin one (SNX-1) and its binding partner, J-dom
126 han degradation, and indicate that different sorting nexins operate in different classes of endosomes
127  sorting nexin gene family and indicate that sorting nexins perform essential functions in mammals.
128 y been implicated in endocytosis, namely the sorting nexin protein SH3PX1 (sorting nexin 9).
129                           Here, we show that sorting nexin protein Snx14, an ER-resident protein asso
130 PS35/VPS29 subunits) assembles with multiple sorting nexin proteins on membranes to mediate endosomal
131 ain undefined, and retromer engages multiple sorting nexin proteins to sort cargoes to different dest
132  infection but that double knockdown of both sorting nexins results in a striking reduction in infect
133 -dependent recycling tubules marked by actin/sorting nexin/retromer tubular (ASRT) microdomains.
134  The regulation of endosomal trafficking via sorting nexins reveals a previously unknown mechanism fo
135                                              Sorting nexin (SNX) 1 and SNX2 are mammalian orthologs o
136 hox-homology (PX) domain-containing proteins sorting nexin (SNX) 17, SNX27, and SNX31 have emerged re
137                                   Vps17 is a sorting nexin (SNX) and a component of the retromer, a p
138        The Retromer complex coordinates with sorting nexin (SNX) cargo adaptors including SNX27, and
139 that participates in cargo recognition and a sorting nexin (SNX) dimer that binds to endosomal membra
140          Mammalian retromer is composed of a sorting nexin (SNX) dimer that binds to phosphatidylinos
141                                    Two other sorting nexin (SNX) family members, namely SNX27 and SNX
142                                          The sorting nexin (SNX) family of proteins is characterized
143            There are 17 human members of the sorting nexin (SNX) family of proteins that contain Phox
144 e regulator of G protein signaling (RGS) and sorting nexin (SNX) protein families.
145  responses, we identified the members of the SORTING NEXIN (SNX) protein family.
146  Retromer (VPS26/VPS35/VPS29) binds multiple sorting nexin (SNX) proteins on endosomal membranes, but
147                                              Sorting nexin (SNX) proteins that normally function in e
148 s a Phox (PX) domain that resembles those in sorting nexin (SNX) proteins.
149 are sorted to different pathways, in part by sorting nexin (SNX) proteins.
150  sorting pathway in conjunction with various sorting nexin (SNX) proteins.
151 nsport, the targeting of the retromer-linked sorting nexin (SNX)-Bin, Amphiphysin, and Rvs (BAR) prot
152 5 trimer and a membrane-deforming subunit of sorting nexin (SNX)-Bin, Amphyphysin, and Rvs (BAR; SNX-
153                                              Sorting nexins (SNX) are a family of proteins containing
154                                              Sorting nexins (SNX) are a family of PX domain-containin
155                                              Sorting nexins (SNX) comprise a family of proteins with
156                                              Sorting nexins (SNX) orchestrate membrane trafficking an
157 mplexes contain specific combinations of the sorting nexins (SNX), SNX1, SNX2, SNX5, and SNX6.
158   We identify five (clathrin, dynamin1, AP2, sorting nexins [SNX] SNX27, and SNX1) that increase and
159 When expressed in COS7 cells, epitope-tagged sorting nexins SNX1, SNX1A, SNX2, and SNX4 coimmunopreci
160 ins, named Vps26, Vps29, and Vps35, plus the sorting nexin, SNX1.
161 ve identified a novel 342-amino acid residue sorting nexin, SNX15, and a 252-amino acid splice varian
162  recently discovered pathway, which includes sorting-nexin SNX17, Retriever, WASH, and CCC complexes.
163                      Herein we show that the sorting nexin SNX19 tethers endolysosomes to the endopla
164 omologous proteins, which were denoted human sorting nexins (SNX2, SNX3, and SNX4).
165 vidence, however, as to whether a homologous sorting nexin, SNX2, is truly a component of the retrome
166                  Retromer and its associated sorting nexin, SNX27, phenocopied each other in matrix d
167 rize the interaction between L2 and a second sorting nexin, SNX27, which is also part of the retromer
168                                    Like most sorting nexins, SNX27 possesses a functional PX domain t
169   We further showed that the cargo-selective sorting nexin Snx3 is required for Neo1 trafficking and
170                             We show that the sorting nexin SNX3 is transported with Rab5a vesicles an
171 bled with the non-Bin1/Amphiphysin/Rvs (BAR) sorting nexin SNX3 using cryo-electron tomography.
172 he VPS26 and VPS35 subunits of retromer, the sorting nexin SNX3, and a recycling signal from the diva
173 eins contains a cytosolic tail that binds to sorting nexin Snx3.
174 s identified a requirement for the conserved sorting nexin Snx4 in the autophagic turnover of proteas
175 via two independent pathways mediated by the sorting nexins Snx4/41/42 and the retromer complex, resp
176 ase (Drs2-Cdc50), an F-box protein (Rcy1), a sorting nexin (Snx4-Atg20), and the COPI coat complex.
177     We demonstrate that Snx4 cooperates with sorting nexins Snx41 and Snx42 to mediate proteasome tur
178 Snc1p from post-Golgi endosomes requires the sorting nexin Snx4p, to which Snc1p can be cross-linked.
179 he membrane tubulating BAR domain-containing sorting nexins SNX5 and SNX6.
180                                          The sorting nexin, SNX9, localizes to clathrin-coated pits w
181                                IncE binds to sorting nexins (SNXs) 5/6, components of the retromer, w
182                   We screened the Drosophila sorting nexins (SNXs) and discovered that one, SH3PX1, p
183                                              Sorting nexins (Snxs) are a recently discovered family o
184                                              Sorting nexins (SNXs) are regulators of endosomal sortin
185                                              Sorting nexins (SNXs) or phox homology (PX) domain conta
186 ing family of proteins known collectively as sorting nexins, some of which have been shown to be invo
187            The retromer complex, composed of sorting nexin subunits and a Vps26/Vps29/Vps35 trimer, m
188 GTP and requires the Vps5 and Vps17 retromer sorting nexin subunits.
189 demonstration of a large conserved family of sorting nexins that interact with a variety of receptor
190 NX-1, and SNX-6, three BAR domain-containing sorting nexins, that act in two parallel pathways to dri
191 sphorylation of DSH3PX1 by DAck targets this sorting nexin to a protein complex that includes Dock, a
192                  SNX27, however, is the only sorting nexin to contain a PDZ domain.
193                               The ability of sorting nexins to bind specific phospholipids as well as
194 ed by PtdIns(3)P, and executed through these sorting nexins to degrade apoptotic cells.
195                                    The yeast sorting nexins Vps5p and Vps17p form a dimer and are als
196 ly define the different domains of the yeast sorting nexins Vps5p and Vps17p, we have generated vario
197 sting findings with yeast orthologs of other sorting nexins, we propose that overexpression of SNX15

 
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