Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/nature06482.pdf
Reference34 articles.
1. Hazan, J. et al. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nature Genet. 23, 296–303 (1999)
2. Frickey, T. & Lupas, A. N. Phylogenetic analysis of AAA proteins. J. Struct. Biol. 146, 2–10 (2004)
3. Roll-Mecak, A. & Vale, R. D. The Drosophila homologue of the hereditary spastic paraplegia protein, spastin, severs and disassembles microtubules. Curr. Biol. 15, 650–655 (2005)
4. Evans, K. J., Gomes, E. R., Reisenweber, S. M., Gundersen, G. G. & Lauring, B. P. Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing. J. Cell Biol. 168, 599–606 (2005)
5. Salinas, S. et al. Human spastin has multiple microtubule-related functions. J. Neurochem. 95, 1411–1420 (2005)
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