Biology:SYT11

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A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Synaptotagmin-11 is a protein that in humans is encoded by the SYT11 gene.[1][2]

Interactions

SYT11 has been shown to interact with Parkin (ligase).[3]

References

  1. ↑ "Genomic analysis of synaptotagmin genes". Genomics 77 (1–2): 43–9. September 2001. doi:10.1006/geno.2001.6619. PMID 11543631. 
  2. ↑ "Entrez Gene: SYT11 synaptotagmin XI". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=23208. 
  3. ↑ "The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI". Human Molecular Genetics 12 (20): 2587–97. October 2003. doi:10.1093/hmg/ddg269. PMID 12925569. 

Further reading

  • "Prediction of the coding sequences of unidentified human genes. II. The coding sequences of 40 new genes (KIAA0041-KIAA0080) deduced by analysis of cDNA clones from human cell line KG-1". DNA Research 1 (5): 223–9. 1995. doi:10.1093/dnares/1.5.223. PMID 7584044. 
  • "SYNCRIP, a cytoplasmic counterpart of heterogeneous nuclear ribonucleoprotein R, interacts with ubiquitous synaptotagmin isoforms". The Journal of Biological Chemistry 275 (13): 9823–31. March 2000. doi:10.1074/jbc.275.13.9823. PMID 10734137. 
  • "The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI". Human Molecular Genetics 12 (20): 2587–97. October 2003. doi:10.1093/hmg/ddg269. PMID 12925569. 
  • "Screening for mutations in synaptotagmin XI in Parkinson's disease". Journal of Neural Transmission. Supplementum. Journal of Neural Transmission. Supplementa 68 (68): 21–8. 2004. doi:10.1007/978-3-7091-0579-5_3. ISBN 978-3-211-21114-4. PMID 15354386. 
  • "Towards a proteome-scale map of the human protein-protein interaction network". Nature 437 (7062): 1173–8. October 2005. doi:10.1038/nature04209. PMID 16189514. Bibcode: 2005Natur.437.1173R. 
  • "Synaptotagmin XI as a candidate gene for susceptibility to schizophrenia". American Journal of Medical Genetics Part B 144B (3): 332–40. April 2007. doi:10.1002/ajmg.b.30465. PMID 17192956. 





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