Maqsood Hayat

Discrimination of acidic and alkaline enzyme using Chou's pseudo amino acid composition in conjunction with probabilistic neural network model.

Enzyme catalysis is one of the most essential and striking processes among of all the complex processes that have evolved in living organisms. Enzymes are biological catalysts, which play a significant role in industrial applications as well as in medical areas, due to profound specificity, selectivity and catalytic efficiency. Refining catalytic efficiency of enzymes has become the most challenging job of enzyme engineering, into acidic and alkaline. Discrimination of acidic and alkaline enzymes through experimental approaches is difficult, sometimes impossible due to lack of established structures. Therefore, it is highly desirable to develop a computational model for discriminating acidic and alkaline enzymes from primary sequences. In this study, we have developed a robust, accurate and high throughput computational model using two discrete sample representation methods Pseudo amino acid composition (PseAAC) and split amino acid composition. Various classification algorithms including probabilistic neural network (PNN), K-nearest neighbor, decision tree, multi-layer perceptron and support vector machine are applied to predict acidic and alkaline with high accuracy. 10-fold cross validation test and several statistical measures namely, accuracy, F-measure, and area under ROC are used to evaluate the performance of the proposed model. The performance of the model is examined using two benchmark datasets to demonstrate the effectiveness of the model. The empirical results show that the performance of PNN in conjunction with PseAAC is quite promising compared to existing approaches in the literature so for. It has achieved 96.3% accuracy on dataset1 and 99.2% on dataset2. It is ascertained that the proposed model might be useful for basic research and drug related application areas.

Classification of membrane protein types using Voting Feature Interval in combination with Chou׳s Pseudo Amino Acid Composition

Membrane protein is a major constituent of cell, performing numerous crucial functions in the cell. These functions are mostly concerned with membrane proteins types. Initially, membrane proteins types are classified through traditional methods and reasonable results were obtained using these methods. However, due to large exploration of protein sequences in databases, it is very difficult or sometimes impossible to classify through conventional methods, because it is laborious and wasting of time. Therefore, a new powerful discriminating model is indispensable for classification of membrane proteins types with high precision. In this work, a quite promising classification model is developed having effective discriminating power of membrane proteins types. In our classification model, silent features of protein sequences are extracted via Pseudo Amino Acid Composition. Five classification algorithms were utilized. Among these classification algorithms Voting Feature Interval has obtained outstanding performance in all the three datasets. The accuracy of proposed model is 93.9% on dataset S1, 89.33% on S2 and 86.9% on dataset S3, respectively, applying 10-fold cross validation test. The success rates revealed that our proposed model has obtained the utmost outcomes than other existing models in literatures so far and will be played a substantial role in the fields of drug design and pharmaceutical industry.

Identification of Heat Shock Protein families and J-protein types by incorporating Dipeptide Composition into Chou's general PseAAC

Heat Shock Proteins (HSPs) are the substantial ingredients for cell growth and viability, which are found in all living organisms. HSPs manage the process of folding and unfolding of proteins, the quality of newly synthesized proteins and protecting cellular homeostatic processes from environmental stress. On the basis of functionality, HSPs are categorized into six major families namely: (i) HSP20 or sHSP (ii) HSP40 or J-proteins types (iii) HSP60 or GroEL/ES (iv) HSP70 (v) HSP90 and (vi) HSP100. Identification of HSPs family and sub-family through conventional approaches is expensive and laborious. It is therefore, highly desired to establish an automatic, robust and accurate computational method for prediction of HSPs quickly and reliably. Regard, a computational model is developed for the prediction of HSPs family. In this model, protein sequences are formulated using three discrete methods namely: Split Amino Acid Composition, Pseudo Amino Acid Composition, and Dipeptide Composition. Several learning algorithms are utilized to choice the best one for high throughput computational model. Leave one out test is applied to assess the performance of the proposed model. The empirical results showed that support vector machine achieved quite promising results using Dipeptide Composition feature space. The predicted outcomes of proposed model are 90.7% accuracy for HSPs dataset and 97.04% accuracy for J-protein types, which are higher than existing methods in the literature so far.

Unb-DPC: Identify mycobacterial membrane protein types by incorporating un-biased dipeptide composition into Chou's general PseAAC

This study investigates an efficient and accurate computational method for predicating mycobacterial membrane protein. Mycobacterium is a pathogenic bacterium which is the causative agent of tuberculosis and leprosy. The existing feature encoding algorithms for protein sequence representation such as composition and translation, and split amino acid composition cannot suitably express the mycobacterium membrane protein and their types due to biasness among different types. Therefore, in this study a novel un-biased dipeptide composition (Unb-DPC) method is proposed. The proposed encoding scheme has two advantages, first it avoid the biasness among the different mycobacterium membrane protein and their types. Secondly, the method is fast and preserves protein sequence structure information. The experimental results yield SVM based classification accurately of 97.1% for membrane protein types and 95.0% for discriminating mycobacterium membrane and non-membrane proteins by using jackknife cross validation test. The results exhibit that proposed model achieved significant predictive performance compared to the existing algorithms and will lead to develop a powerful tool for anti-mycobacterium drugs.

Discriminating protein structure classes by incorporating Pseudo Average Chemical Shift to Chou's general PseAAC and Support Vector Machine

Proteins control all biological functions in living species. Protein structure is comprised of four major classes including all-α class, all-β class, α+β, and α/β. Each class performs different function according to their nature. Owing to the large exploration of protein sequences in the databanks, the identification of protein structure classes is difficult through conventional methods with respect to cost and time. Looking at the importance of protein structure classes, it is thus highly desirable to develop a computational model for discriminating protein structure classes with high accuracy. For this purpose, we propose a silco method by incorporating Pseudo Average Chemical Shift and Support Vector Machine. Two feature extraction schemes namely Pseudo Amino Acid Composition and Pseudo Average Chemical Shift are used to explore valuable information from protein sequences. The performance of the proposed model is assessed using four benchmark datasets 25PDB, 1189, 640 and 399 employing jackknife test. The success rates of the proposed model are 84.2%, 85.0%, 86.4%, and 89.2%, respectively on the four datasets. The empirical results reveal that the performance of our proposed model compared to existing models is promising in the literature so far and might be useful for future research.

Prediction of protein structure classes using hybrid space of multi-profile Bayes and bi-gram probability feature spaces

Proteins are the executants of biological functions in living organisms. Comprehension of protein structure is a challenging problem in the era of proteomics, computational biology, and bioinformatics because of its pivotal role in protein folding patterns. Owing to the large exploration of protein sequences in protein databanks and intricacy of protein structures, experimental and theoretical methods are insufficient for prediction of protein structure classes. Therefore, it is highly desirable to develop an accurate, reliable, and high throughput computational model to predict protein structure classes correctly from polygenetic sequences. In this regard, we propose a promising model employing hybrid descriptor space in conjunction with optimized evidence-theoretic K-nearest neighbor algorithm. Hybrid space is the composition of two descriptor spaces including Multi-profile Bayes and bi-gram probability. In order to enhance the generalization power of the classifier, we have selected high discriminative descriptors from the hybrid space using particle swarm optimization, a well-known evolutionary feature selection technique. Performance evaluation of the proposed model is performed using the jackknife test on three low similarity benchmark datasets including 25PDB, 1189, and 640. The success rates of the proposed model are 87.0%, 86.6%, and 88.4%, respectively on the three benchmark datasets. The comparative analysis exhibits that our proposed model has yielded promising results compared to the existing methods in the literature. In addition, our proposed prediction system might be helpful in future research particularly in cases where the major focus of research is on low similarity datasets.

iMem-2LSAAC: A two-level model for discrimination of membrane proteins and their types by extending the notion of SAAC into chou's pseudo amino acid composition

Membrane proteins execute significant roles in cellular processes of living organisms, ranging from cell signaling to cell adhesion. As a major part of a cell, the identification of membrane proteins and their functional types become a challenging job in the field of bioinformatics and proteomics from last few decades. Traditional experimental procedures are slightly applicable due to lack of recognized structures, enormous time and space. In this regard, the demand for fast, accurate and intelligent computational method is increased day by day. In this paper, a two-tier intelligent automated predictor has been developed called iMem-2LSAAC, which classifies protein sequence as membrane or non-membrane in first-tier (phase1) and in case of membrane the second-tier (phase2) identifies functional types of membrane protein. Quantitative attributes were extracted from protein sequences by applying three discrete features extraction schemes namely amino acid composition, pseudo amino acid composition and split amino acid composition (SAAC). Various learning algorithms were investigated by using jackknife test to select the best one for predictor. Experimental results exhibited that the highest predictive outcomes were yielded by SVM in conjunction with SAAC feature space on all examined datasets. The true classification rate of iMem-2LSAAC predictor is significantly higher than that of other state-of- the- art methods so far in the literature. Finally, it is expected that the proposed predictor will provide a solid framework for the development of pharmaceutical drug discovery and might be useful for researchers and academia.

Identification of DNA binding proteins using evolutionary profiles position specific scoring matrix

DNA-binding plays a crucial role in different genomics processes including identification of specific nucleotides, regulation of transcription and regulation of gene expression. Various conventional methods have been used for identification of DNA-binding proteins. However, due to large explosion of protein sequences in databases, it is intricate or sometimes impossible to identify DNA-binding proteins. Therefore, it is intensively desired to establish an automated model for identification of DNA binding proteins. In this model, numerical attributes are extracted through Dipeptide composition, Split Amino Acid Composition, and position specific scoring matrix (PSSM). In order to overcome the issue of biasness and reduce true error, oversampling technique SMOTE was applied to balance the datasets. Several classification learners including K-nearest neighbor, Probability Neural Network, Support vector machine (SVM) and Random forest are utilized. Two benchmark datasets and jackknife test are applied to assess the performance of classification algorithms. Among various classification algorithms, SVM achieved the highest success rates in conjunction with PSSM feature space, which are 92.3% accuracy on dataset1 and 88.5% on dataset2. The empirical results revealed that our proposed model obtained the highest results so far in the literatures. It is anticipated that our proposed model might be useful and provides a substance for research and academia community.

iTIS-PseKNC

Translation is an essential genetic process for understanding the mechanism of gene expression. Due to the large number of protein sequences generated in the post-genomic era, conventional methods are unable to identify Translation Initiation Site (TIS) in human genes timely and accurately. It is thus highly desirable to develop an automatic and accurate computational model for identification of TIS. Considerable improvements have been achieved in developing computational models; however, development of accurate and reliable automated systems for TIS identification in human genes is still a challenging task. In this connection, we propose iTIS-PseKNC, a novel protocol for identification of TIS. Three protein sequence representation methods including dinucleotide composition, pseudo-dinucleotide composition and Trinucleotide composition have been used in order to extract numerical descriptors. Support Vector Machine (SVM), K-nearest neighbor and Probabilistic Neural Network are assessed for their performance using the constructed descriptors. The proposed model iTIS-PseKNC has achieved 99.40% accuracy using jackknife test. The experimental results validated the superior performance of iTIS-PseKNC over the existing methods reported in the literature. It is highly anticipated that the iTIS-PseKNC predictor will be useful for basic research studies.

Sequence based predictor for discrimination of enhancer and their types by applying general form of Chou's trinucleotide composition

BACKGROUND AND OBJECTIVES Enhancers are pivotal DNA elements, which are widely used in eukaryotes for activation of transcription genes. On the basis of enhancer strength, they are further classified into two groups; strong enhancers and weak enhancers. Due to high availability of huge amount of DNA sequences, it is needed to develop fast, reliable and robust intelligent computational method, which not only identify enhancers but also determines their strength. Considerable progress has been achieved in this regard; however, timely and precisely identification of enhancers is still a challenging task. METHODS Two-level intelligent computational model for identification of enhancers and their subgroups is proposed. Two different feature extraction techniques including di-nucleotide composition and tri-nucleotide composition were adopted for extraction of numerical descriptors. Four classification methods including probabilistic neural network, support vector machine, k-nearest neighbor and random forest were utilized for classification. RESULTS The proposed method yielded 77.25% of accuracy for dataset S1 contains enhancers and non-enhancers, whereas 64.70% of accuracy for dataset S2 comprises of strong enhancer and weak enhancer sequences using jackknife cross-validation test. CONCLUSION The predictive results validated that the proposed method is better than that of existing approaches so far reported in the literature. It is thus highly observed that the developed method will be useful and expedient for basic research and academia.