Journal article
The Roc-COR tandem domain of leucine-rich repeat kinase 2 forms dimers and exhibits conventional Ras-like GTPase properties
RD Mills, LY Liang, DSS Lio, YF Mok, TD Mulhern, G Cao, M Griffin, VB Kenche, JG Culvenor, HC Cheng
Journal of Neurochemistry | WILEY | Published : 2018
DOI: 10.1111/jnc.14566
Abstract
Abstract: The Parkinson's disease (PD)-causative leucine-rich repeat kinase 2 (LRRK2) belongs to the Roco family of G-proteins comprising a Ras-of-complex (Roc) domain followed by a C-terminal of Roc (COR) domain in tandem (called Roc-COR domain). Two prokaryotic Roc-COR domains have been characterized as ‘G proteins activated by guanine nucleotide-dependent dimerization’ (GADs), which require dimerization for activation of their GTPase activity and bind guanine nucleotides with relatively low affinities. Additionally, LRRK2 Roc domain in isolation binds guanine nucleotides with relatively low affinities. As such, LRRK2 GTPase domain was predicted to be a GAD. Herein, we describe the design ..
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