5zok
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Crystal structure of human SMAD1-MAN1 complex.
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Structural highlights
DiseaseMAN1_HUMAN Isolated osteopoikilosis;Buschke-Ollendorff syndrome;12q14 microdeletion syndrome;Melorheostosis with osteopoikilosis. The disease is caused by mutations affecting the gene represented in this entry. FunctionMAN1_HUMAN Can function as a specific repressor of TGF-beta, activin, and BMP signaling through its interaction with the R-SMAD proteins. Antagonizes TGF-beta-induced cell proliferation arrest.[1] [2] References
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This page was last modified 10:28, 27 March 2024.