The Gene or DNA sequence in every cell does not control genetic properties on its own; Rather, this is done through the translation of DNA into protein and subsequent formation of a certain 3D structure. The biological function of a protein is tightly connected to its specific 3D structure. Prediction of the protein secondary structure is a crucial intermediate step towards elucidating its 3D structure and function. Traditional experimental methods for prediction of protein structure are expensive and time-consuming. Nevertheless, the average accuracy of the suggested solutions has hardly reached beyond 80%. The possible underlying reasons are the ambiguous sequence-structure relation, noise in input protein data, class imbalance, and the high dimensionality of the encoding schemes. Furthermore, we utilize a compound string dissimilarity measure to directly interpret protein sequence content and avoid information loss. In order to improve accuracy, we employ two different classifiers including support vector machine and fuzzy nearest neighbor and collectively aggregate the classification outcomes to infer the final protein structures. We conduct comprehensive experiments to compare our model with the current state-of-the-art approaches. The experimental results demonstrate that given a set of input sequences, our multi-component framework can accurately predict the protein structure. Nevertheless, the effectiveness of our unified model can be further enhanced through framework configuration.
Keywords: Ensemble prediction machine; Fuzzy k-nearest neighbor; Protein secondary structure prediction; Support vector machine.
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