Spastin, chordate
Short name | Spastin_chordate |
family relationships |
Description
References
1.The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia. Ciccarelli FD, Proukakis C, Patel H, Cross H, Azam S, Patton MA, Bork P, Crosby AH. Genomics 81, 437-41, (2003). View articlePMID: 12676568
2.Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics. Errico A, Ballabio A, Rugarli EI. Hum. Mol. Genet. 11, 153-63, (2002). View articlePMID: 11809724
3.Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing. Evans KJ, Gomes ER, Reisenweber SM, Gundersen GG, Lauring BP. J. Cell Biol. 168, 599-606, (2005). View articlePMID: 15716377
Further reading
4. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Hazan J, Fonknechten N, Mavel D, Paternotte C, Samson D, Artiguenave F, Davoine CS, Cruaud C, Durr A, Wincker P, Brottier P, Cattolico L, Barbe V, Burgunder JM, Prud'homme JF, Brice A, Fontaine B, Heilig B, Weissenbach J. Nat. Genet. 23, 296-303, (1999). View articlePMID: 10610178
GO terms
biological process
- None
molecular function
cellular component
- None
Cross References
ENZYME
Contributing Member Database Entry
- PIRSF:PIRSF037338