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Understanding E3 ligase and target substrate interactions are important for cell biology and therapeutic development. However, experimental identification of E3 target relationships is not an easy task due to the labor-intensive nature of the experiments. In this article, a sequence-based E3-target prediction model is proposed for the first time. The proposed framework utilizes composition of k-spaced amino acid pairs (CKSAAP) to learn the relationship between E3 ligases and their target protein. A class separable latent space encoding scheme is also devised that provides a compressed representation of feature space. A thorough ablation study is performed to identify an optimal gap size for CKSAAP and the number of latent variables that can represent the E3-target relationship successfully. The proposed scheme is evaluated on an independent dataset for a variety of standard quantitative measures. In particular, it achieves an average accuracy of $70.63%$ on an independent dataset. The source code and datasets used in the study are available at the authors GitHub page (https://github.com/psychemistz/E3targetPred).
The knowledge of potentially druggable binding sites on proteins is an important preliminary step towards the discovery of novel drugs. The computational prediction of such areas can be boosted by following the recent major advances in the deep learn
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The branching fraction for the decay $K^{-} to pi^{0} e bar u$ is measured using in-flight decays detected with {bf ISTRA+} setup working at the 25 GeV negative secondary beam of the U-70 PS:linebreak $Br_{K_{e3}}= (5.124 pm 0.009 (stat) pm 0.029(no