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Sorting nexin 18

sorting nexin 18, SNX18
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members, but contains a SH3 domain. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] (from NCBI)
Top mentioned proteins: sorting nexin 9, Rab11, beta 2-adrenoceptor, SNX33, Dynamin I
Papers on sorting nexin 18
Viral bimolecular fluorescence complementation: a novel tool to study intracellular vesicular trafficking pathways.
Dikeakos et al., London, Canada. In Plos One, 2014
Using the F2A cleavage site from the foot and mouth disease virus we generated a viral BiFC expression vector capable of concurrent expression of Nef and host cellular proteins; PACS-1, MHC-I and SNX18.
Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease.
Shub et al., In J Clin Invest, 2014
Using surface biotinylation and dual immunofluorescence staining in MYO5B-KD cells expressing mutant forms of MYO5B, we observed that early microvillus inclusions were positive for the sorting marker SNX18 and derived from apical membrane internalization.
FIP5 phosphorylation during mitosis regulates apical trafficking and lumenogenesis.
Prekeris et al., Aurora, United States. In Embo Rep, 2014
The interaction of FIP5 with SNX18, which is required for the formation of apical endocytic carriers, is inhibited by GSK-3 phosphorylation at FIP5-T276.
SNX18 tubulates recycling endosomes for autophagosome biogenesis.
Simonsen et al., Oslo, Norway. In Autophagy, 2013
Indeed, the PX-BAR protein SNX18 was identified as a positive regulator of autophagosome formation using an image-based siRNA screen.
Membrane remodeling by the PX-BAR protein SNX18 promotes autophagosome formation.
Simonsen et al., Oslo, Norway. In J Cell Biol, 2013
The PX-BAR protein SNX18 was identified as a positive regulator of autophagosome formation, and its Drosophila melanogaster homologue SH3PX1 was found to be required for efficient autophagosome formation in the larval fat body.
SNX9, SNX18 and SNX33 are required for progression through and completion of mitosis.
Chircop et al., Sydney, Australia. In J Cell Sci, 2012
Here, we report that the sorting nexin 9 (SNX9) subfamily members - SNX9, SNX18 and SNX33 - are required for progression and completion of mitosis.
Interaction between FIP5 and SNX18 regulates epithelial lumen formation.
Prekeris et al., Aurora, United States. In J Cell Biol, 2011
FIP5-SNX18 complex plays a pivotal role in the polarized transport of apical proteins during apical lumen initiation in epithelial cells.
Expression of sorting nexin 18 (SNX18) is dynamically regulated in developing spinal motor neurons.
Yamamoto et al., Sapporo, Japan. In J Histochem Cytochem, 2011
Here the authors found that SNX18, which belongs to the Src-homology-3-PX-Bin/Amphiphysin/Rvs domain-containing SNX subfamily, was specifically expressed in differentiating motor neurons in the chick and mouse embryonic spinal cord.
The E3 ubiquitin ligase Itch regulates sorting nexin 9 through an unconventional substrate recognition domain.
Lévy et al., Lausanne, Switzerland. In Febs J, 2010
SNX18, a second member of the SNX family containing an SH3 domain, was also found to bind to Itch.
SNX18 shares a redundant role with SNX9 and modulates endocytic trafficking at the plasma membrane.
Chang et al., Seoul, South Korea. In J Cell Sci, 2010
functions in multiple pathways of endocytosis at the plasma membrane
The SNX-PX-BAR family in macropinocytosis: the regulation of macropinosome formation by SNX-PX-BAR proteins.
Teasdale et al., Brisbane, Australia. In Plos One, 2009
macropinosomes), SNX18 (88.2+/-8 macropinosomes), SNX33 (65.25+/-6.95
SNX18 is an SNX9 paralog that acts as a membrane tubulator in AP-1-positive endosomal trafficking.
Carlsson et al., Umeå, Sweden. In J Cell Sci, 2008
The results indicate that SNX9-family members make up discrete membrane-scission units together with dynamin, and suggest that SNX18 mediates budding of carriers for AP-1-positive endosomal trafficking.
A proteomic screen reveals novel Fas ligand interacting proteins within nervous system Schwann cells.
Desbarats et al., Montréal, Canada. In Febs Lett, 2007
We identified two novel FasL interacting proteins, sorting nexin 18 and adaptin beta, as well as two proteins previously identified as FasL interacting proteins in T cells, PACSIN2 and PACSIN3.
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