Clathrin coat assembly protein AP180 is a protein that in humans is encoded by the SNAP91gene.[1][2][3][4]
References
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↑Yao PJ, O'Herron TM, Coleman PD (Dec 2002). "Immunohistochemical characterization of clathrin assembly protein AP180 and synaptophysin in human brain". Neurobiology of Aging. 24 (1): 173–8. doi:10.1016/S0197-4580(02)00055-6. PMID12493563.
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Slepnev VI, Ochoa GC, Butler MH, De Camilli P (June 2000). "Tandem arrangement of the clathrin and AP-2 binding domains in amphiphysin 1 and disruption of clathrin coat function by amphiphysin fragments comprising these sites". The Journal of Biological Chemistry. 275 (23): 17583–9. doi:10.1074/jbc.M910430199. PMID10748223.
Han SJ, Lee JH, Hong SH, Park SD, Kim CG, Song MD, Park TK, Kim CG (January 2002). "AP180 binds to the C-terminal SH2 domain of phospholipase C-gamma1 and inhibits its enzymatic activity". Biochemical and Biophysical Research Communications. 290 (1): 35–41. doi:10.1006/bbrc.2001.6154. PMID11779129.
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Hussain NK, Yamabhai M, Bhakar AL, Metzler M, Ferguson SS, Hayden MR, McPherson PS, Kay BK (August 2003). "A role for epsin N-terminal homology/AP180 N-terminal homology (ENTH/ANTH) domains in tubulin binding". The Journal of Biological Chemistry. 278 (31): 28823–30. doi:10.1074/jbc.M300995200. PMID12750376.
Morgan JR, Prasad K, Jin S, Augustine GJ, Lafer EM (August 2003). "Eps15 homology domain-NPF motif interactions regulate clathrin coat assembly during synaptic vesicle recycling". The Journal of Biological Chemistry. 278 (35): 33583–92. doi:10.1074/jbc.M304346200. PMID12807910.
Ballif BA, Villén J, Beausoleil SA, Schwartz D, Gygi SP (November 2004). "Phosphoproteomic analysis of the developing mouse brain". Molecular & Cellular Proteomics. 3 (11): 1093–101. doi:10.1074/mcp.M400085-MCP200. PMID15345747.
Zhan X, Desiderio DM (December 2004). "The human pituitary nitroproteome: detection of nitrotyrosyl-proteins with two-dimensional Western blotting, and amino acid sequence determination with mass spectrometry". Biochemical and Biophysical Research Communications. 325 (4): 1180–6. doi:10.1016/j.bbrc.2004.10.169. PMID15555551.