Biology:STX17
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Revision as of 06:26, 25 May 2022 by imported>John Marlo (change)
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Syntaxin 17 is a protein that in humans is encoded by the STX17 gene.[1] In horses a duplication in intron 6 causes progressive graying.[2]
See also
References
Further reading
- "The hairpin-type tail-anchored SNARE syntaxin 17 targets to autophagosomes for fusion with endosomes/lysosomes". Cell 151 (6): 1256–69. 2012. doi:10.1016/j.cell.2012.11.001. PMID 23217709.
- "Genome-wide association study in alopecia areata implicates both innate and adaptive immunity". Nature 466 (7302): 113–7. 2010. doi:10.1038/nature09114. PMID 20596022. Bibcode: 2010Natur.466..113P.
- "Syntaxin 17 cycles between the ER and ERGIC and is required to maintain the architecture of ERGIC and Golgi". Biol. Cell 103 (7): 333–50. 2011. doi:10.1042/BC20110006. PMID 21545355.
- "Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma". Melanoma Res. 19 (2): 80–6. 2009. doi:10.1097/CMR.0b013e328322fc45. PMID 19209086.
- "Three novel proteins of the syntaxin/SNAP-25 family". J. Biol. Chem. 273 (51): 34171–9. 1998. doi:10.1074/jbc.273.51.34171. PMID 9852078.
- "Protein interactions regulating vesicle transport between the endoplasmic reticulum and Golgi apparatus in mammalian cells". Cell 89 (1): 149–58. 1997. doi:10.1016/s0092-8674(00)80191-9. PMID 9094723.
- "Syntaxin 17 is abundant in steroidogenic cells and implicated in smooth endoplasmic reticulum membrane dynamics". Mol. Biol. Cell 11 (8): 2719–31. 2000. doi:10.1091/mbc.11.8.2719. PMID 10930465.
External links
- Overview of all the structural information available in the PDB for UniProt: P56962 (Human Syntaxin-17 (STX17)) at the PDBe-KB.
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