Source:http://linkedlifedata.com/resource/pubmed/id/17504761
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
34
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pubmed:dateCreated |
2007-8-20
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pubmed:abstractText |
Mutations in the DJ-1 protein are present in patients suffering from familial Parkinson disease. Here we use computational methods and biological assays to investigate the relationship between DJ-1 missense mutations and the protein oligomeric state. Molecular dynamics calculations suggest that: (i) the structure of DJ-1 wild type (WT) in aqueous solution, in both oxidized and reduced forms, is similar to the crystal structure of the reduced form; (ii) the Parkinson disease-causing M26I variant is structurally similar to the WT, consistent with the experimental evidence showing the protein is a dimer as WT; (iii) R98Q is structurally similar to the WT, consistent with the fact that this is a physiological variant; and (iv) the L166P monomer rapidly evolves toward a conformation significantly different from WT, suggesting a change in its ability to oligomerize. Our combined computational and experimental approach is next used to identify a mutant (R28A) that, in contrast to L166P, destabilizes the dimer subunit-subunit interface without significantly changing secondary structure elements.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Alanine,
http://linkedlifedata.com/resource/pubmed/chemical/Cross-Linking Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides...,
http://linkedlifedata.com/resource/pubmed/chemical/Oncogene Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PARK7 protein, human
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
24
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pubmed:volume |
282
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
24905-14
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pubmed:meshHeading |
pubmed-meshheading:17504761-Alanine,
pubmed-meshheading:17504761-Cell Line,
pubmed-meshheading:17504761-Cross-Linking Reagents,
pubmed-meshheading:17504761-Crystallography, X-Ray,
pubmed-meshheading:17504761-Dimerization,
pubmed-meshheading:17504761-Humans,
pubmed-meshheading:17504761-Intracellular Signaling Peptides and Proteins,
pubmed-meshheading:17504761-Models, Molecular,
pubmed-meshheading:17504761-Molecular Conformation,
pubmed-meshheading:17504761-Mutation,
pubmed-meshheading:17504761-Mutation, Missense,
pubmed-meshheading:17504761-Oncogene Proteins,
pubmed-meshheading:17504761-Parkinson Disease,
pubmed-meshheading:17504761-Protein Conformation,
pubmed-meshheading:17504761-Protein Structure, Secondary,
pubmed-meshheading:17504761-Software,
pubmed-meshheading:17504761-Time Factors
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pubmed:year |
2007
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pubmed:articleTitle |
On the oligomeric state of DJ-1 protein and its mutants associated with Parkinson Disease. A combined computational and in vitro study.
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pubmed:affiliation |
International School for Advanced Studies, INFM DEMOCRITOS, SISSA Unit, Italian Institute of Technology, Via Beirut 2-4, 34014 Trieste, Italy.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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