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               <dc:title>On the use of direct-coupling analysis with a reduced alphabet of amino acids combined with super-secondary structure motifs for protein fold prediction</dc:title>
               <dc:creator>Anton, Bernat</dc:creator>
               <dc:creator>Besalú, Mireia</dc:creator>
               <dc:creator>Fornés Crespo, Oriol, 1983-</dc:creator>
               <dc:creator>Bonet Martínez, Jaume, 1982-</dc:creator>
               <dc:creator>Molina, Alexis</dc:creator>
               <dc:creator>Molina Fernández, Rubén</dc:creator>
               <dc:creator>Cuevas, Gemma de las</dc:creator>
               <dc:creator>Fernández Fuentes, Narcís</dc:creator>
               <dc:creator>Oliva Miguel, Baldomero</dc:creator>
               <dc:description>Direct-coupling analysis (DCA) for studying the coevolution of residues in proteins has been widely used to predict the three-dimensional structure of a protein from its sequence. We present RADI/raDIMod, a variation of the original DCA algorithm that groups chemically equivalent residues combined with super-secondary structure motifs to model protein structures. Interestingly, the simplification produced by grouping amino acids into only two groups (polar and non-polar) is still representative of the physicochemical nature that characterizes the protein structure and it is in line with the role of hydrophobic forces in protein-folding funneling. As a result of a compressed alphabet, the number of sequences required for the multiple sequence alignment is reduced. The number of long-range contacts predicted is limited; therefore, our approach requires the use of neighboring sequence-positions. We use the prediction of secondary structure and motifs of super-secondary structures to predict local contacts. We use RADI and raDIMod, a fragment-based protein structure modelling, achieving near native conformations when the number of super-secondary motifs covers &amp;gt;30-50% of the sequence. Interestingly, although different contacts are predicted with different alphabets, they produce similar structures.</dc:description>
               <dc:description>Spanish Ministry of Economy MINECO [BIO2014-57518-R, BIO2017-83591-R (FEDER, UE), BIO2017-85329-R (FEDER, UE)]; Generalitat de Catalunya [SGR17-1020].</dc:description>
               <dc:date>2021-10-26T05:58:10Z</dc:date>
               <dc:date>2021-10-26T05:58:10Z</dc:date>
               <dc:date>2021</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>NAR Genom Bioinform. 2021;3(2):lqab027</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/ES/1PE/BIO2014-57518-R</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/ES/2PE/BIO2017-85329-R</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/ES/2PE/BIO2017-83591-R</dc:relation>
               <dc:rights>© The Author(s) 2021. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Oxford University Press</dc:publisher>
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