Ontology highlight
ABSTRACT:
SUBMITTER: van Veen S
PROVIDER: S-EPMC4033846 | biostudies-literature | 2014
REPOSITORIES: biostudies-literature
van Veen Sarah S Sørensen Danny M DM Holemans Tine T Holen Henrik W HW Palmgren Michael G MG Vangheluwe Peter P
Frontiers in molecular neuroscience 20140527
Mutations in ATP13A2 lead to Kufor-Rakeb syndrome, a parkinsonism with dementia. ATP13A2 belongs to the P-type transport ATPases, a large family of primary active transporters that exert vital cellular functions. However, the cellular function and transported substrate of ATP13A2 remain unknown. To discuss the role of ATP13A2 in neurodegeneration, we first provide a short description of the architecture and transport mechanism of P-type transport ATPases. Then, we briefly highlight key P-type AT ...[more]