Biology:STXBP5
 Generic protein structure example |
Syntaxin-binding protein 5 is a protein that in humans is encoded by the STXBP5 gene. It is also known as tomosyn, after 友, "friend" in Japanese, for its role as a binding protein.[1][2][3]
Function
Syntaxin 1 is a component of the 7S and 20S SNARE complexes which are involved in docking and fusion of synaptic vesicles with the presynaptic plasma membrane. This gene encodes a syntaxin 1 binding protein. In rat, a similar protein dissociates syntaxin 1 from the Munc18/n-Sec1/rbSec1 complex to form a 10S complex, an intermediate which can be converted to the 7S SNARE complex. Thus this protein is thought to be involved in neurotransmitter release by stimulating SNARE complex formation. Alternatively spliced variants have been identified, but their biological validity has not been determined.[3]
Positional cloning suggested that tomosyn might inhibit neurotransmitter secretion in Caenorhabditis elegans neurons.][4] This hypothesis was tested and confirmed, showing that tomosyn specifically inhibits synaptic vesicle priming—the biochemical step immediately preceding vesicle fusion and neurotransmitter release.[5]
Structure
Two functional domains were originally identified, including one which binds to syntaxin, but recent crystallization of the yeast homolog Sro7 revealed that tomosyn likely has three functional domains: one WD40 domain and one syntaxin-binding domain, as previously recognized, but also another WD40 domain. The study also suggested that tomosyn's 'syntaxin binding domain' is not the reason tomosyn is inhibitory for neurotransmitter release, as originally proposed.[6] The Sro7-based structure is currently given on SWISS-MODEL, which includes the WD40 domains but not most of the coiled coil syntaxin-binding domain seen in the infobox.[7]
Interactions
STXBP5 has been shown to interact with STX4[8] and STX1A.[1][8]
References
- ↑ 1.0 1.1 "Tomosyn: a syntaxin-1-binding protein that forms a novel complex in the neurotransmitter release process". Neuron 20 (5): 905–15. Jun 1998. doi:10.1016/S0896-6273(00)80472-9. PMID 9620695.
- ↑ "Identification and characterization of human LLGL4 gene and mouse Llgl4 gene in silico". Int. J. Oncol. 24 (3): 737–42. Feb 2004. doi:10.3892/ijo.24.3.737. PMID 14767561.
- ↑ 3.0 3.1 "Entrez Gene: STXBP5 syntaxin binding protein 5 (tomosyn)". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=134957.
- ↑ "Using microarrays to facilitate positional cloning: identification of tomosyn as an inhibitor of neurosecretion". PLOS Genet. 1 (1): 6–16. July 2005. doi:10.1371/journal.pgen.0010002. PMID 16103915.
- ↑ "Tomosyn inhibits synaptic vesicle priming in Caenorhabditis elegans". PLOS Biol. 4 (8): e261. July 2006. doi:10.1371/journal.pbio.0040261. PMID 16895441.
- ↑ "Structure of the yeast polarity protein Sro7 reveals a SNARE regulatory mechanism". Nature 446 (7135): 567–71. March 2007. doi:10.1038/nature05635. PMID 17392788. Bibcode: 2007Natur.446..567H.
- ↑ "Q5T5C0". https://swissmodel.expasy.org/repository/uniprot/Q5T5C0.
- ↑ 8.0 8.1 "Tomosyn interacts with the t-SNAREs syntaxin4 and SNAP23 and plays a role in insulin-stimulated GLUT4 translocation". J. Biol. Chem. 278 (37): 35093–101. Sep 2003. doi:10.1074/jbc.M304261200. PMID 12832401.
Further reading
- "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell 127 (3): 635–48. 2006. doi:10.1016/j.cell.2006.09.026. PMID 17081983.
- "Tomosyn interacts with the t-SNAREs syntaxin4 and SNAP23 and plays a role in insulin-stimulated GLUT4 translocation". J. Biol. Chem. 278 (37): 35093–101. 2003. doi:10.1074/jbc.M304261200. PMID 12832401.
- "Three splicing variants of tomosyn and identification of their syntaxin-binding region". Biochem. Biophys. Res. Commun. 256 (1): 218–22. 1999. doi:10.1006/bbrc.1999.0300. PMID 10066450.
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