Missense mutation of SPAST protein (I344K) results in loss of ATPase activity and prolonged the half-life, implicated in autosomal dominant hereditary spastic paraplegia

The spastin protein (SPAST) contains an ATPase with diverse cellular activities (AAA) domain and regulates microtubule dynamics. Missense mutations of the SPAST gene are frequently detected in patients with hereditary spastic paraplegias (HSPs) and represent the main reason of loss of SPAST function...

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Veröffentlicht in:Biochimica et biophysica acta. Molecular basis of disease 2018-10, Vol.1864 (10), p.3221-3233
Hauptverfasser: Lim, Jung Hwa, Kang, Hyun Mi, Jung, Hong-Ryul, Kim, Dae-Soo, Noh, Kyung Hee, Chang, Tae Kyung, Kim, Byoung Joon, Sung, Duk Hyun, Cho, Hyun-Soo, Chung, Kyung-Sook, Kim, Nam-Soon, Jung, Cho-Rok
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Sprache:eng
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