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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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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 |
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. |
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