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Molecular dynamics simulations to understand LRKK2 mutations in Parkinson
- 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.
- Subjects :
- 0301 basic medicine
Kinase
Chemistry
General Chemical Engineering
General Chemistry
GTPase
Condensed Matter Physics
LRRK2
Molecular biology
nervous system diseases
Domain (software engineering)
Cell biology
03 medical and health sciences
Molecular dynamics
030104 developmental biology
Modeling and Simulation
Helix
Mutation testing
General Materials Science
Protein kinase A
Information Systems
Subjects
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