泛素连接酶
泛素
发病机制
疾病
功能(生物学)
遗传学
帕金森病
生物
计算生物学
医学
基因
免疫学
病理
作者
Suzanne J. Randle,Heike Laman
出处
期刊:Current Protein & Peptide Science
[Bentham Science]
日期:2017-05-08
卷期号:18 (7): 715-724
被引量:17
标识
DOI:10.2174/1389203717666160311121433
摘要
Fbxo7/PARK15 has well-defined roles, acting as part of a Skp1-Cul1-F box protein (SCF)- type E3 ubiquitin ligase and also having SCF-independent activities. Mutations within FBXO7 have been found to cause an early-onset Parkinson's disease, and these are found within or near to its functional domains, including its F-box domain (FBD), its proline rich region (PRR), and its ubiquitinlike domain (Ubl). We highlight recent advances in our understanding of Fbxo7 function in Parkinson's disease, with respect to these mutations and where they occur in the Fbxo7 protein. We hypothesize that many of Fbxo7 functions contribute to its role in PD pathogenesis.
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