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Identification of metal ion binding sites based on amino acid sequences

The identification of metal ion binding sites is important for protein function annotation and the design of new drug molecules. This study presents an effective method of analyzing and identifying the binding residues of metal ions based solely on sequence information. Ten metal ions were extracted...

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Detalles Bibliográficos
Autores principales: Cao, Xiaoyong, Hu, Xiuzhen, Zhang, Xiaojin, Gao, Sujuan, Ding, Changjiang, Feng, Yonge, Bao, Weihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576659/
https://www.ncbi.nlm.nih.gov/pubmed/28854211
http://dx.doi.org/10.1371/journal.pone.0183756
Descripción
Sumario:The identification of metal ion binding sites is important for protein function annotation and the design of new drug molecules. This study presents an effective method of analyzing and identifying the binding residues of metal ions based solely on sequence information. Ten metal ions were extracted from the BioLip database: Zn(2+), Cu(2+), Fe(2+), Fe(3+), Ca(2+), Mg(2+), Mn(2+), Na(+), K(+) and Co(2+). The analysis showed that Zn(2+), Cu(2+), Fe(2+), Fe(3+), and Co(2+) were sensitive to the conservation of amino acids at binding sites, and promising results can be achieved using the Position Weight Scoring Matrix algorithm, with an accuracy of over 79.9% and a Matthews correlation coefficient of over 0.6. The binding sites of other metals can also be accurately identified using the Support Vector Machine algorithm with multifeature parameters as input. In addition, we found that Ca(2+) was insensitive to hydrophobicity and hydrophilicity information and Mn(2+) was insensitive to polarization charge information. An online server was constructed based on the framework of the proposed method and is freely available at http://60.31.198.140:8081/metal/HomePage/HomePage.html.