Abstract

Lysine Lipoylation is a protective and conserved Post Translational Modification (PTM) in proteomics research like prokaryotes and eukaryotes. It is connected with many biological processes and closely linked with many metabolic diseases. To develop a perfect and accurate classification model for identifying lipoylation sites at the protein level, the computational methods and several other factors play a key role in this purpose. Usually, most of the techniques and different traditional experimental models have a very high cost. They are time-consuming; so, it is required to construct a predictor model to extract lysine lipoylation sites. This study proposes a model that could predict lysine lipoylation sites with the help of a classification method known as Artificial Neural Network (ANN). The ANN algorithm deals with the noise problem and imbalance classification in lipoylation sites dataset samples. As the result shows in ten-fold cross-validation, a brilliant performance is achieved through the predictor model with an accuracy of 99.88%, and also achieved 0.9976 as the highest value of MCC. So, the predictor model is a very useful and helpful tool for lipoylation sites prediction. Some of the residues around lysine lipoylation sites play a vital part in prediction, as demonstrated during feature analysis. The wonderful results reported through the evaluation and prediction of this model can provide an informative and relative explanation for lipoylation and its molecular mechanisms.

Highlights

  • Lipoylation is one of the most meaningful elements in biology

  • (1) Which metrics are best for our prediction model quality? (2) What are the test methods that should use for score metrics?

  • 3.3.1 Self-Model Consistency Testing The proposed Computational model is applied for predicted and actual classification, and the results show the values of true positive (TP), false positive (FP), false negative (FN) and true negative (TN)

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Summary

Introduction

Lipoylation is one of the most meaningful elements in biology. It is a unique and highly protective lysine Post Translational Modification (PTM) present in eukaryotes and prokaryotes’. Lysine lipoylation sites are known to be the most impressive modification processions that can become visible in most enzymes that are relevant and present in most organisms, including mammals and bacteria [7,8,9,10]. Lysine lipoylation sites play a significant role in protein communications and metabolic pathways [1]. It is catalyzed by the lipoate-activating enzyme (LAE). A method has been observed to develop our predictor model known as Chou’s 5 step rule; that is, for the prediction of lysine lipoylation sites

Proposed System and Methodology
Standardised Dataset
Formulation of Samples
Calculation of SVV as Site Vicinity Vector
Feature Predictor
Discussion and Results
Predictor Model Validation Process
Comparison Analysis of Our Proposed Method with Other Feature Methods
Conclusion
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