Phylogenetic and in silico structural analysis of the Parkinson disease‐related kinase PINK1
Identifieur interne : 000190 ( Main/Exploration ); précédent : 000189; suivant : 000191Phylogenetic and in silico structural analysis of the Parkinson disease‐related kinase PINK1
Auteurs : Fernando Cardona [Espagne] ; Jose Vicente Sánchez-Mut [Espagne] ; Hernán Dopazo [Espagne] ; Jordi Pérez-Tur [Espagne]Source :
- Human Mutation [ 1059-7794 ] ; 2011-04.
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Abstract
Parkinson disease (PD) is the second most common neurodegenerative disorder and is characterized by the loss of dopaminergic neurons in the substantia nigra. Mutations in PINK1 were shown to cause recessive familial PD, and today are proposed to be associated with the disease via mitochondrial dysfunction and oxidative damage. The PINK1 gene comprises eight exons, which encode a ubiquitously expressed 581 amino acid protein that contains an N‐terminal mitochondrial targeting domain and a serine/threonine protein kinase. To better understand the relationship between PINK1 and PD we have first analyzed the evolutionary history of the gene showing its late emergence in evolution. In addition, we have modeled the three‐dimensional structure of PINK1 and found some evidences that help to explain the effect of some PD‐related mutations in this protein's function. Hum Mutat 32:369–378, 2011. © 2011 Wiley‐Liss, Inc.
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DOI: 10.1002/humu.21444
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Mutations in PINK1 were shown to cause recessive familial PD, and today are proposed to be associated with the disease via mitochondrial dysfunction and oxidative damage. The PINK1 gene comprises eight exons, which encode a ubiquitously expressed 581 amino acid protein that contains an N‐terminal mitochondrial targeting domain and a serine/threonine protein kinase. To better understand the relationship between PINK1 and PD we have first analyzed the evolutionary history of the gene showing its late emergence in evolution. In addition, we have modeled the three‐dimensional structure of PINK1 and found some evidences that help to explain the effect of some PD‐related mutations in this protein's function. Hum Mutat 32:369–378, 2011. © 2011 Wiley‐Liss, Inc.</div></front></TEI><affiliations><list><country><li>Espagne</li></country><region><li>Catalogne</li></region><settlement><li>Barcelone</li></settlement></list><tree><country name="Espagne"><noRegion><name sortKey="Cardona, Fernando" sort="Cardona, Fernando" uniqKey="Cardona F" first="Fernando" last="Cardona">Fernando Cardona</name></noRegion><name sortKey="Cardona, Fernando" sort="Cardona, Fernando" uniqKey="Cardona F" first="Fernando" last="Cardona">Fernando Cardona</name><name sortKey="Dopazo, Hernan" sort="Dopazo, Hernan" uniqKey="Dopazo H" first="Hernán" last="Dopazo">Hernán Dopazo</name><name sortKey="Perez Ur, Jordi" sort="Perez Ur, Jordi" uniqKey="Perez Ur J" first="Jordi" last="Pérez-Tur">Jordi Pérez-Tur</name><name sortKey="Perez Ur, Jordi" sort="Perez Ur, Jordi" uniqKey="Perez Ur J" first="Jordi" last="Pérez-Tur">Jordi Pérez-Tur</name><name sortKey="Sanchez Ut, Jose Vicente" sort="Sanchez Ut, Jose Vicente" uniqKey="Sanchez Ut J" first="Jose Vicente" last="Sánchez-Mut">Jose Vicente Sánchez-Mut</name><name sortKey="Sanchez Ut, Jose Vicente" sort="Sanchez Ut, Jose Vicente" uniqKey="Sanchez Ut J" first="Jose Vicente" last="Sánchez-Mut">Jose Vicente Sánchez-Mut</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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