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- Table of Contents
Facts about Spastin.
Severing activity is not dependent on tubulin acetylation or detyrosination (PubMed:26875866). Microtubule severing promotes reorganization of cellular microtubule arrays and the release of microtubules from the centrosome following nucleation.
Human | |
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Gene Name: | SPAST |
Uniprot: | Q9UBP0 |
Entrez: | 6683 |
Belongs to: |
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AAA ATPase family |
ADPSPSpastic paraplegia 4 protein; FSP2EC 3.6.4.3; KIAA1083EC 3.6.1.3; spastic paraplegia 4 (autosomal dominant; spastin); spastin; SPG4
Mass (kDA):
67.197 kDA
Human | |
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Location: | 2p22.3 |
Sequence: | 2; NC_000002.12 (32063551..32157637) |
Expressed in brain, heart, kidney, liver, lung, pancreas, placenta and skeletal muscle. The short isoforms may predominate in brain and spinal cord.
Membrane; Peripheral membrane protein. Endoplasmic reticulum. Midbody. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, cytoskeleton. Cytoplasm, perinuclear region. Nucleus. Cytoplasm, cytoskeleton, spindle. Cytoplasm. Forms an intramembrane hairpin-like structure in the membrane (PubMed:20200447). Localization to the centrosome is independent of microtubules (PubMed:15891913). Localizes to the midbody of dividing cells, and this requires CHMP1B (PubMed:18997780). Enriched in the distal axons and branches of postmitotic neurons (PubMed:15269182).; [Isoform 1]: End
PMID: 10610178 by Hazan J., et al. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.
PMID: 11809724 by Errico A., et al. Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics.