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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.
7 dopamine D5 receptor (D(5)R) interacts with sorting nexin 1 (SNX1), a protein involved in receptor r
9 on of vesicle protein sorting 35 (VPS35) and sorting nexin 1 (SNX1), as well as decreased mannose 6 p
13 t the putative mammalian retromer components sorting nexins 1 and 2 (Snx1 and Snx2) result in embryon
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
23 g endosomal signaling compartment containing Sorting Nexin 16 and a reduction in late endosomes conta
28 ified a novel intracellular adaptor protein, sorting nexin 17 (SNX17), that binds specifically to the
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
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
48 s regulated by the psychostimulant-sensitive sorting nexin 27 (SNX27) protein through a class I (-X-S
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
54 entification of the OTULIN interactor SNX27 (sorting nexin 27), an adaptor of the endosomal retromer
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
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(
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
71 inity purification (TAP), we herein identify sorting nexin 6 (SNX6) as a BACE1-associated protein.
73 ein signaling complex composed of eukaryotic sorting nexin 9 (SNX9) and neuronal Wiskott-Aldrich synd
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
86 e temporal ordering of three proteins-actin, sorting nexin 9, and clathrin-in the endocytic pathway.
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
93 17) is a member of the family of cytoplasmic sorting nexin adaptor proteins that regulate endosomal t
96 In mammals, it is composed of a dimer of sorting nexins and of the core retromer consisting of va
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
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
113 sability, due to truncating mutations in the sorting nexin gene SNX14, encoding a ubiquitously expres
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
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
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.
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
136 hox-homology (PX) domain-containing proteins sorting nexin (SNX) 17, SNX27, and SNX31 have emerged re
139 that participates in cargo recognition and a sorting nexin (SNX) dimer that binds to endosomal membra
146 Retromer (VPS26/VPS35/VPS29) binds multiple sorting nexin (SNX) proteins on endosomal membranes, but
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-
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
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.
165 vidence, however, as to whether a homologous sorting nexin, SNX2, is truly a component of the retrome
167 rize the interaction between L2 and a second sorting nexin, SNX27, which is also part of the retromer
169 We further showed that the cargo-selective sorting nexin Snx3 is required for Neo1 trafficking and
172 he VPS26 and VPS35 subunits of retromer, the sorting nexin SNX3, and a recycling signal from the diva
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.
186 ing family of proteins known collectively as sorting nexins, some of which have been shown to be invo
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
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