TY - GEN
T1 - Protein Subcellular and Secreted Localization Prediction Using Deep Learning
AU - Zidoum, Hamza
AU - Magdy, Mennatollah
N1 - Publisher Copyright:
© 2018 IEEE.
PY - 2018/6/5
Y1 - 2018/6/5
N2 - Predicting the protein structure and discovering its function according to its location in the cell is crucial for understanding the cellular translocation process and has direct applications in drug discovery. Computational prediction of protein localization is alternative to the time consuming experimental counterpart approach. We use deep learning approach to enhance the prediction accuracy while reducing the time in predicting uncharacterized protein sequence localization site. Our approach is based on general biological features of the protein sequence, and compartment specific features to which we added the physico-chemical sequence features. We collected the protein sequences from UniProt1/SWISS-PROT, then we collected the features for each protein. We consider five locations in the dataset, namely cytoplasm (CP), inner membrane (IM), outer membrane (OM), periplasm (PE) and secreted (SEC). We choose the protein sequences to be at least 100 amino-Acid-length and a maximum length of 1000 amino acids. Each location contains 500 protein sequences. We propose a deep learning prediction method for bacteria taxonomy that combines a one-versus-one and one-versus all models along with feature selec-Tion using linear SVM ranking, and deep auto-encoders to initialize the weights. The method achieves overall accuracy of 97.81% using 10-fold cross-validation on our data. Our approach outperforms the current state of the art computational methods in protein subcellular localization on the selected dataset.
AB - Predicting the protein structure and discovering its function according to its location in the cell is crucial for understanding the cellular translocation process and has direct applications in drug discovery. Computational prediction of protein localization is alternative to the time consuming experimental counterpart approach. We use deep learning approach to enhance the prediction accuracy while reducing the time in predicting uncharacterized protein sequence localization site. Our approach is based on general biological features of the protein sequence, and compartment specific features to which we added the physico-chemical sequence features. We collected the protein sequences from UniProt1/SWISS-PROT, then we collected the features for each protein. We consider five locations in the dataset, namely cytoplasm (CP), inner membrane (IM), outer membrane (OM), periplasm (PE) and secreted (SEC). We choose the protein sequences to be at least 100 amino-Acid-length and a maximum length of 1000 amino acids. Each location contains 500 protein sequences. We propose a deep learning prediction method for bacteria taxonomy that combines a one-versus-one and one-versus all models along with feature selec-Tion using linear SVM ranking, and deep auto-encoders to initialize the weights. The method achieves overall accuracy of 97.81% using 10-fold cross-validation on our data. Our approach outperforms the current state of the art computational methods in protein subcellular localization on the selected dataset.
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U2 - 10.1109/ICCSE1.2018.8374220
DO - 10.1109/ICCSE1.2018.8374220
M3 - Conference contribution
AN - SCOPUS:85049371576
T3 - 2018 International Conference on Computing Sciences and Engineering, ICCSE 2018 - Proceedings
SP - 1
EP - 6
BT - 2018 International Conference on Computing Sciences and Engineering, ICCSE 2018 - Proceedings
A2 - Raafat, Hazem
A2 - Abd-El-Barr, Mostafa
A2 - Sarfraz, Muhammad
A2 - Manuel, Paul
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2nd International Conference on Computing Sciences and Engineering, ICCSE 2018
Y2 - 11 March 2018 through 13 March 2018
ER -