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pNitro-Tyr-PseAAC: Predict Nitrotyrosine Sites in Proteins by Incorporating Five Features into Chou’s General PseAAC

[ Vol. 24 , Issue. 34 ]

Author(s):

Ahmad W. Ghauri, Yaser D. Khan, Nouman Rasool, Sher A. Khan* and Kuo-Chen Chou   Pages 4034 - 4043 ( 10 )

Abstract:


Background: Closely related to causes of various diseases such as rheumatoid arthritis, septic shock, and coeliac disease; tyrosine nitration is considered as one of the most important post-translational modification in proteins. Inside a cell, protein modifications occur accurately by the action of sophisticated cellular machinery. Specific enzymes present in endoplasmic reticulum accomplish this task. The identification of potential tyrosine residues in a protein primary sequence, which can be nitrated, is a challenging task. </P><P> Methods: To counter the prevailing, laborious and time-consuming experimental approaches, a novel computational model is introduced in the present study. Based on data collected from experimentally verified tyrosine nitration sites feature vectors are formed. Later, an adaptive training algorithm is used to train a back propagation neural network for prediction purposes. To objectively measure the accuracy of the proposed model, rigorous verification and validation tests are carried out. </P><P> Results: Through verification and validation, a promising accuracy of 88%, a sensitivity of 85%, a specificity of 89.18% and Mathew’s Correlation Coefficient of 0.627 is achieved. </P><P> Conclusion: It is concluded that the proposed computational model provides the foundation for further investigation and be used for the identification of nitrotyrosine sites in proteins.

Keywords:

Nitrotyrosine, PseAAC, statistical moments, 5-step rule, prediction, rheumatoid arthritis.

Affiliation:

Department of Computer Science, School of Systems and Technology, Department of Life Sciences, School of Science, University of Management and Technology, Lahore, Department of Computer Science, School of Systems and Technology, Department of Life Sciences, School of Science, University of Management and Technology, Lahore, Dr Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, King Abdul Aziz University, Faculty of Computing and Information Technology in Rabigh, Jeddah, 21577, Gordon Life Science Institute, Boston, MA 02478, USA; 5Abdul Wali Khan University, Department of Computer Sciences, Mardan



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