- SNAG1
Sorting nexin associated golgi protein 1, also known as SNAG1, is a human
gene .cite web | title = Entrez Gene: SNAG1 sorting nexin associated golgi protein 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=112574| accessdate = ]PBB_Summary
section_title =
summary_text = 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. The specific function of this protein has not been determined.cite web | title = Entrez Gene: SNAG1 sorting nexin associated golgi protein 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=112574| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Seet LF, Hong W |title=The Phox (PX) domain proteins and membrane traffic. |journal=Biochim. Biophys. Acta |volume=1761 |issue= 8 |pages= 878-96 |year= 2006 |pmid= 16782399 |doi= 10.1016/j.bbalip.2006.04.011
*cite journal | author=Worby CA, Dixon JE |title=Sorting out the cellular functions of sorting nexins. |journal=Nat. Rev. Mol. Cell Biol. |volume=3 |issue= 12 |pages= 919-31 |year= 2003 |pmid= 12461558 |doi= 10.1038/nrm974
*cite journal | author=Xu Y, Seet LF, Hanson B, Hong W |title=The Phox homology (PX) domain, a new player in phosphoinositide signalling. |journal=Biochem. J. |volume=360 |issue= Pt 3 |pages= 513-30 |year= 2002 |pmid= 11736640 |doi=
*cite journal | author=Thornhill PB, Cohn JB, Drury G, "et al." |title=A proteomic screen reveals novel Fas ligand interacting proteins within nervous system Schwann cells. |journal=FEBS Lett. |volume=581 |issue= 23 |pages= 4455-62 |year= 2008 |pmid= 17761170 |doi= 10.1016/j.febslet.2007.08.025
*cite journal | author=Ozyildirim AM, Wistow GJ, Gao J, "et al." |title=The lacrimal gland transcriptome is an unusually rich source of rare and poorly characterized gene transcripts. |journal=Invest. Ophthalmol. Vis. Sci. |volume=46 |issue= 5 |pages= 1572-80 |year= 2005 |pmid= 15851553 |doi= 10.1167/iovs.04-1380
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Schulze WX, Mann M |title=A novel proteomic screen for peptide-protein interactions. |journal=J. Biol. Chem. |volume=279 |issue= 11 |pages= 10756-64 |year= 2004 |pmid= 14679214 |doi= 10.1074/jbc.M309909200
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Teasdale RD, Loci D, Houghton F, "et al." |title=A large family of endosome-localized proteins related to sorting nexin 1. |journal=Biochem. J. |volume=358 |issue= Pt 1 |pages= 7-16 |year= 2001 |pmid= 11485546 |doi=PBB_Controls
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