Syntaxin 3
Template:PBB Syntaxin 3, also known as STX3, is a human gene.[1]
The protein encoded by this gene is a member of the syntaxin family of cellular receptors for transport vesicles which participate in exocytosis in neutrophils.[2] STX3 has an important role in the growth of neurites and serves as a direct target for omega-6 arachidonic acid.[3] Interestingly a N-terminal cleavage product of STX3 interacts very strong with RanBP5 and may act in nuclear signaling and cell polarity. The helices might play an important role in this aspect. STX3 is the only syntaxin which can lack the transmembran domain. An alternatively spliced Syntaxin 1 (STX1B) which lacks the transmembrane domain localizes to the cell nucleus.[4]
References
- ^ "Entrez Gene: STX3 syntaxin 3".
- ^ Martín-Martín B, Nabokina SM, Lazo PA, Mollinedo F (1999). "Co-expression of several human syntaxin genes in neutrophils and differentiating HL-60 cells: variant isoforms and detection of syntaxin 1". J. Leukoc. Biol. 65 (3): 397–406. PMID 10080545.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ Darios F, Davletov B (2006). "Omega-3 and omega-6 fatty acids stimulate cell membrane expansion by acting on syntaxin 3". Nature. 440 (7085): 813–7. doi:10.1038/nature04598. PMID 16598260.
{{cite journal}}: Unknown parameter|month=ignored (help) - ^ Pereira S, Massacrier A, Roll P, Vérine A, Etienne-Grimaldi MC, Poitelon Y, Robaglia-Schlupp A, Jamali S, Roeckel-Trevisiol N, Royer B, Pontarotti P, Lévêque C, Seagar M, Lévy N, Cau P, Szepetowski P (2008). "Nuclear localization of a novel human syntaxin 1B isoform". Gene. doi:10.1016/j.gene.2008.07.010. PMID 18691641.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link)
Further reading
 | This article on a gene on human chromosome 11 is a stub. You can help Wikipedia by expanding it. |