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Molecular dynamics simulations to understand LRKK2 mutations in Parkinson

Authors :
Yunbao Guo
Song-Bai Xu
Hai-Yan Liu
Jing Chen
Xing-Dong Zhang
Source :
Molecular Simulation. 42:64-70
Publication Year :
2015
Publisher :
Informa UK Limited, 2015.

Abstract

Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of Parkinson's disease (PD). LRRK2 contains a Ras of complex proteins (ROC) domain that may acts as a GTPase to regulate its protein kinase activity. Here, we performed 10 ns molecular dynamics simulations on LRRK2 Apo, complex with GDP and mutations (R1441C, R1441G and R1441H). Our results strongly suggest that the formations of helix in L1 and its pliable plays a major role in the LRRK2 functions.

Details

ISSN :
10290435 and 08927022
Volume :
42
Database :
OpenAIRE
Journal :
Molecular Simulation
Accession number :
edsair.doi...........61bbe78908dd69b52786393c9698a5fa
Full Text :
https://doi.org/10.1080/08927022.2015.1008471