- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
BioMed Research International
Volume 2013 (2013), Article ID 109549, 9 pages
Position-Specific Analysis and Prediction of Protein Pupylation Sites Based on Multiple Features
1College of Computer Science and Information Technology, Northeast Normal University, 2555 Jingyue Street, Changchun 130117, China
2Key Laboratory of Intelligent Information Processing of Jilin Universities, Northeast Normal University, Changchun 130117, China
Received 25 April 2013; Revised 20 July 2013; Accepted 20 July 2013
Academic Editor: Bilal Alatas
Copyright © 2013 Xiaowei Zhao et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Pupylation is one of the most important posttranslational modifications of proteins; accurate identification of pupylation sites will facilitate the understanding of the molecular mechanism of pupylation. Besides the conventional experimental approaches, computational prediction of pupylation sites is much desirable for their convenience and fast speed. In this study, we developed a novel predictor to predict the pupylation sites. First, the maximum relevance minimum redundancy (mRMR) and incremental feature selection methods were made on five kinds of features to select the optimal feature set. Then the prediction model was built based on the optimal feature set with the assistant of the support vector machine algorithm. As a result, the overall jackknife success rate by the new predictor on a newly constructed benchmark dataset was 0.764, and the Mathews correlation coefficient was 0.522, indicating a good prediction. Feature analysis showed that all features types contributed to the prediction of protein pupylation sites. Further site-specific features analysis revealed that the features of sites surrounding the central lysine contributed more to the determination of pupylation sites than the other sites.
As the firstly identified posttranslational small protein modifier in prokaryotes, prokaryotic ubiquitin-like protein (Pup) in Mycobacterium tuberculosis (Mtb) is an important signal for the selective degradation of proteins . Pup attaches to substrate lysine via isopeptide bonds in a manner reminiscent of ubiquitin (Ub) and ubiquitin-like modifier (Ubl) conjugation to proteins in eukaryotes . Although pupylation and ubiquitylation have functional similarity, the enzymology of pupylation and ubiquitylation is different . Generally, there are three-steo reaction and three kinds of enzymes participating in the eukaryotic ubiquitylation process, including ubiquitin-activating enzymes, ubiquitin-conjugating enzymes, and ubiquitin ligases [4, 5], but only two-step reaction and two enzymes are participating in the prokaryotic pupylation process. Firstly, the Pup-GGQ C-terminal is deamidated to -GGE by deamidase of Pup , and then the proteasome accessory factor A (PafA) attaches the deamidated Pup to specific lysine residues of substrates .
Since identification of protein pupylation sites are of fundamental importance to understand the molecular mechanism of pupylation in biological systems, much interest has focused on this field, and large-scale proteomics technology has been applied to identify pupylation proteins and pupylation sites [8–10]. However, the experimental determination of exact modified sites of pupylated substrates is labor-intensive and time-consuming, especially for large-scale data sets. In this regard, the computation approaches which could effectively and accurately predict the pupylation sites is urgently needed. Liu et al. had constructed the first online predictor, GPS-PUP, for the prediction of the pupylation sites . In their method, 127 experimentally identified pupylation sites in 109 prokaryotic proteins had been utilized as the training dataset, with an accuracy of 0.789 and a MCC of 0.286.
In this study, a new predictor was developed to predict pupylation sites based on amino acid sequence features. Firstly, five kinds of features, which describe each amino acid of pupylation site and its surrounding ones, were extracted from each protein sequence, including physicochemical/biochemical properties of amino acids, Position-Specific Scoring Matrices (PSSM) which contain evolution information of amino acids, structural disorder of amino acids, second structure, and solvent accessibility. Secondly, the maximum relevance minimum redundancy (mRMR) and incremental feature selection methods were made on five kinds of features to find the optimal feature set. Finally, the predictor model was built based on the optimal feature set with the assistance of the support vector machine algorithm. For the new constructed pupylation sites dataset, the accuracy of the proposed predictor was 0.764 on the training dataset, and the MCC was 0.522. Compared with GPS-PUP, our predictor has the following features: (1) a larger benchmark dataset was used; (2) our study showed how much important the roles these features played in the prediction. Our feature analysis shows that evolutionary information and physicochemical/biochemical properties played important role in the recognition of pupylation sites, and sites 7, 10, and 11 contributed the most to the determination of pupylation sites. (A web server for predicting pupylation sites was developed and is available at http://22.214.171.124:8080/PrePup/).
2. Materials and Methods
The pupylated proteins used in this study were extracted from PupDB . Protein sequences with less than 50 amino acids were excluded because they may be just fragments [12, 13]. Protein sequences including nonstandard amino acids, such as “B,” “J,” “O,” “U,” “X,” and “Z,” were excluded as well. As a result, there were 182 pupylated proteins with 215 known pupylation sites. After a homology-reducing screening procedure by using CD-HIT [14, 15] to remove those proteins that had 40% sequence identity to any other, we finally got 153 pupylated proteins with 183 positive sites, which constructed the nonredundant training dataset in this study (see Supporting Information Text S1 available online at http://dx.doi.org/10.1155/2013/109549).
Subsequently, similar to the development of other PTM site predictors [16, 17], the sliding window strategy was utilized to extract positive and negative samples. After a preliminary evaluation, the optimal window size was 21 in this paper, with 10 residues located upstream and 10 residues located downstream the pupylation sites in the protein sequence. In order to ensure the peptides (sequence fragments) with a unified length, a nonexisting residue coded by “-” was used to fill the corresponding position. Peptides with pupylation lysine as the middle residue were positive samples, and the remaining peptides with nonpupylation lysine as the middle residue were negative samples. Since the numbers of pupylation lysine sites and the nonpupylation lysine sites were highly imbalanced, we randomly selected three times negative samples (non-pupylated lysine fragments) to match the positive ones (pupylated lysine fragments) in the training dataset.
2.2. Feature Construction
2.2.1. Amino Acid Factors
Amino Acid Index (AAIndex) [18, 19] database is a collection of numerical indices that stand for various physicochemical and biochemical properties of amino acids. Atchley et al.  did multivariable statistical analyses on AAIndex and produced five multidimensional and highly interpretable numeric patters of attributes: codon diversity, covariation reflecting polarity, molecular volume, secondary structure, and electrostatic charge. These five numerical pattern scores (called “amino acid factors”) have been used to successfully solve many biology problems [21–24]. Here, we also used these five amino acid factors to encode each amino acid of a given protein.
2.2.2. PSSM Conservation Scores
Evolutionary conservation always indicates important biology function, and posttranslational modifications are prone to occur in the conservation protein segments. In this study, we used Position Specific Iterated BLAST  (PSI-BLAST) to quantify the sequence conservation with Position-Specific Scoring Matrix (PSSM) which has been demonstrated to be effective for the identification of many posttranslational modification sites [26–30]. PSSM depicts the conservation of each amino acid in the sequence by a 20D numerical vector, each dimension of which measures the likelihood that the amino acid mutates to 20 different amino acids. The PSSM matrix for each of the proteins is generated by the “blastpgp” program of the PSI-BLAST package with three iterations of searching at cutoff -value of 0.0001 for inclusion of sequences in subsequent iterations. And the alignment database is UniRef 100 (Release: 15.9).
2.2.3. Structural Disorder Score
Intrinsic disorder regions  are often rich in binding sites which are important loci for various protein posttranslational modifications such as methylation and phosphorylation . Thus, we used the structural disorder feature of residue in the sequence to encode the peptides. VSL2 , which can accurately predict both long and short disordered regions in proteins, was utilized to calculate disorder score that represented the disorder status of each residue in a given protein sequence.
2.2.4. Secondary Structure
Protein structures play important roles in protein functioning and the posttranslational modification of specific residues may be influenced by the secondary structure of the relevant residues. Thus, we also used protein secondary structure to encode each peptide. In investigating secondary structures surrounding pupylation sites, PSIPRED  was utilized to predict the secondary structure from a given protein sequence. PSIPRED applied two feed-forward neural networks to predict the secondary structure using the results from PSI-BLAST. The result data of PSIPRED was encoded in terms of “C” for coil, “H” for helix, and “E” for strand. In order to transform these terms into numeric vectors, a 3D binary vector was used: coil (C) was encoded as “001,” helix (H) was encoded as “010,” and strand (E) was encoded as “100.”
2.2.5. Solvent Accessibility
It has been found that the posttranslational modifications of specific residues may be affected by the solvent accessibility . Therefore, the solvent accessibility was also considered to encode each peptide. The SSPro program in the SCRATCH software package  was utilized to calculate the ASA value, which classified solvent accessibility of each amino acid as “buried” or “exposed,” encoded with “10” and “01,” respectively.
2.2.6. The Feature Space
Since the middle residues of the peptides were always the same and shared the common amino acid factors, these middle residues were thus encoded by 20 features of PSSM conservation scores, 1 feature of disorder score, 3 features of secondary structure, and 2 features of solvent accessibility, totally 26 features. Other residues were represented by 5 features of amino acid factors, 20 features of PSSM conservation scores, 1 feature of disorder score, 3 features of secondary structure, and 2 features of solvent accessibility, totally 31 features. Overall, each peptide consisting of 21 amino acid residues was represented by 20 × 31 + 26 = 646 features.
2.3. Model Constructing
After the encoding of each peptide in the training dataset, we firstly used maximum relevance, minimum redundancy [37, 38] to prioritize the 646 features according to their importance. Then, based on the order of the sorted features, we obtained 646 feature sets. For each feature set, a prediction model was built with the nearest neighbor algorithm and evaluated by the jackknife cross-validation. The incremental feature selection method was then used to find the optimal feature set corresponding to the best prediction performance. Finally, the optimal feature set was input into support vector machine classifier to establish the final prediction model.
2.4. Prediction Algorithms
In this study, nearest neighbor algorithm (NNA) was used to find the optimal feature subset. NNA predicts an unknown sample to share the common class as its nearest neighbor. For details on this algorithm, readers are advised to refer to .
Support vector machine (SVM) is a popular machine learning algorithm mainly used in dealing with binary classification problem. In this paper, LIBSVM package  with radial basis kernels (RBF) is used, where the kernel width parameter represents how the samples are transformed to a high-dimensional space. Grid search strategy based on 5-fold cross-validation is utilized to find the optimal parameters and , so that a total number of 256 grids are evaluated.
2.5. Performance Assessment
The jackknife cross-validation test is adopted here [41, 42], since the outcome obtained by it is always unique for a given benchmark dataset, and has been widely used to examine the performance of various predictors [41, 43–45]. In the jackknife cross-validation process, the proteins are singled out from the dataset one by one as a testing protein, and the classifier is trained by the remaining proteins.
In order to evaluate the predictor proposed in this study, four measurements are used: sensitivity (Sn), specificity (Sp), accuracy (Ac) and Matthews correlation coefficient (MCC). For the definition of these four measurements, readers are advised to refer to . In addition, the receiver operating characteristic (ROC) curves and the area under the curve (AUC) value are also carried out.
3. Results and Discussion
3.1. The Ordered Features by mRMR
By running the mRMR software, we obtained two ranked feature lists (see Supporting Information Text S2): (1) the MaxRel feature list that contained all the 646 features ordered by their relevance to the class of samples, (2) the mRMR feature list that contained all the 646 features ordered by the maximum relevance and minimum redundancy criteria. Within these two lists, a smaller index of a feature meant that it was more important in discriminating pupylation sites from nonpupylation sites. The mRMR feature list was used in the following IFS procedure for the selection of the optimal feature set.
3.2. IFS Result and the Optimal Feature Set
By adding the ordered features one by one, we constructed 646 feature sets. For each feature set, the predictor was built using the nearest neighbor algorithm and evaluated by the jackknife cross-validation. The IFS results can be seen in Supporting Information Text S3. Figure 1 showed the IFS curve plotted based on the data in Supporting Information Text S2, and the curve reached its peak with the MCC of 0.337 and the number of features was 113. So, these 113 features (see Supporting Information Text S4) were regarded as the optimal feature set of our predictor. The predictive sensitivity, specificity, and accuracy based on these 113 features were 0.541, 0.792, and 0.709, respectively.
3.3. Biological Feature Analysis of the Optimal Feature Set
As described in Section 2, there were five kinds of features: amino acid factors, PSSM conservation scores, structural disorder scores, secondary structure, and solvent accessibility. The number of each type of features in the optimal feature set was investigated and shown in Figure 2(a). In the 113 optimal features, there were 81 features of PSSM conservation score, 16 features of amino acid factor, 1 feature of disorder, 10 features of solvent accessibility, and 5 features of secondary structure, indicating that all types of features played some roles in the determination of pupylation sites, and PSSM conservation score may play an irreplaceable role in pupylation sites prediction. The number of each site of features in the optimal feature set was shown in Figure 2(b). In can be clearly seen from Figure 2(b) that sites 7, 10, and 11 influenced mostly the determination of pupylation, and sites 14, 20, and 21 have a relatively small effect on pupylation, and sites 1–6, 8, 9, 12, 13, and 15–19 have the smallest effect on pupylation. The site-specific distribution of the 113 optimal features revealed that the residues at the left side of the pupylation site were more important for pupylation prediction than the other sites.
3.4. Biological Feature Analysis of the PSSM Conservation Score
As previously mentioned, there were 81 features of PSSM conservation score, which had the greatest proportion of the 113 optimal features. Therefore, we investigated the number of each type of PSSM features in the optimal feature set (see Figure 3(a)) and found that the conservation against mutations to different amino acids has different effect on the determination of pupylation sites. Mutations to amino acids R, T, E, and H have a larger influence on pupylation than mutations to other amino acids. The first feature in the mRMR feature list (Supporting Information Text S4) was the conservation status against residue K, which meant that the conservation of lysine was very important for predicting of pupylation sites. We also investigated the number of each site of PSSM features in the optimal feature set. It can be seen from Figure 3(b) that the conservation of lysine site (AA11) played the most important role in the determination of pupylation sites, and the conservation status of the sites 7, 10, 14, and 20 also played relatively more roles than the other sites. Particularly, the amino acid at site 6 has been shown to be imperfectly conserved and in most case was a D residue. There were seven PSSM features in the top 10 features of the optimal feature set: the conservation status against residue K at site 11, the conservation status against residue E at site 10, the conservation status against residue E at site 7, the conservation status against residue S at site 10, the conservation status against residue V at site 19, the conservation status against residue K at site 8, and the conservation status against residue E at site 14. This may suggest that conservation influenced more the pupylation sites prediction.
3.5. Biological Feature Analysis of the Amino Acid Factor
Figure 4 showed the feature- and site-specific distribution of the amino acid factor features in the optimal feature set. It can be seen from Figure 4(a) that the codon diversity, electrostatic charge, and molecular volume were almost equally important features in the determination of pupylation sites. The polarity and secondary structure amino acid factor features have a small influence on pupylation sites prediction. In Figure 4(b), residues at sites 6, 7, and 10 have the most important effect in the determination of pupylation sites, and the other sites 1-2, 4-5, 9, 13-14, 17, and 20-21 were almost equally important. Among these sites, sites 6 and 7 were located in the upstream of the pupylation sites. The electrostatic charge of site 20 had an index of 6 in the optimal feature set, indicating that it was an important feature for the prediction of pupylation sites.
3.6. Biological Feature Analysis of the Solvent Accessibility
The number of each type of and the number of each site of solvent accessibility features in the optimal feature set has been investigated. It can be clearly seen from Figure 5(a) that the number of two types of solvent accessibility (buried and exposed) was equal. That is to say, both types of solvent accessibility features had equal impact on the determination of pupylation sites. Moreover, as can be seen from Figure 5(b), residues at sites 7 and 11 played the most important roles in the determination of pupylation sites than the other sites. There were 2 solvent accessibility features in the top 10 features: the solvent accessibility feature of site 11 had an index of 3, and the solvent accessibility feature of site 21 had an index of 4.
3.7. Biological Feature Analysis of the Disorder Score
In the optimal feature set, there was only 1 disorder feature. A reasonable explanation was that the nearby residue’s disorder statue had an important influence on pupylation modification process. This disorder feature of site 10 had an index of 72.
3.8. Biological Feature Analysis of the Secondary Structure
The feature- and site-specific distribution of the secondary structure features in the optimal feature set was shown in Figure 6. The number of the three types of 5 secondary structure features (helix, coil, and strand) in the optimal feature set was investigated and shown in Figure 6(a), from which we can see that all types of secondary structure features affected the pupylation sites prediction. Moreover, in Figure 6(b), residues at the sites 5, 11, 15, 19, and 20 have relatively more impact on the determination of pupylation sites.
3.9. Comparisons with Other Methods
When the 113 optimal features were input into the NNA classifier, the predictive sensitivity, specificity, accuracy, and MCC were 0.541, 0.792, 0.709, and 0.337, respectively. We also put the 113 optimal features into a SVM classifier, and the predictive sensitivity, specificity, accuracy, and MCC were 0.522, 0.938, 0.764, and 0.522, respectively. The ROC curve of the SVM classifier was given in Figure 7, and the AUC value was 0.791. Overall, the SVM-based method was better than the NNA-based method for pupylation sites prediction, and we adopted this model as our final prediction model.
We have demonstrated that the proposed method could achieve a promising prediction performance for pupylation sites prediction. To objectively evaluate our proposed predictor, we further compared the proposed predictor with GPS-PUP . Liu et al. searched PubMed with the keywords of “pupylation” and “prokaryotic ubiquitin” and collected 127 experimentally identified pupylation sites in 109 prokaryotic proteins. Since we did not know the ratio of positive to negative samples in their training dataset, we established a prediction model based on a training dataset in which the negative samples were three times the positive ones and only reported the sensitivity of the prediction model. The sensitivity of our method was 0.739, and the sensitivity of GPS-PUP was 0.448 when the threshold was medium. That is to say, the sensitivity of our proposed method was better than that of GPS-PUP.
3.10. Direction for Experimental Validation
By means of the mRMR feature selection method, an optimal feature set including 113 features was selected. We analyzed the feature- and site-specific distribution of each kind of features in the optimal feature set. As a result, we found that evolutionary information and physicochemical/biochemical properties played an important role in the recognition of pupylation sites. Sites 7, 10, and 11 contributed the most to the determination of pupylation sites. Particularly, the residues located in the upstream of the pupylation sites may play an important role in pupylation modification process. The selected features at different sites could provide some useful clues for understanding the mechanism of pupylation process and guide experimental validation.
In this study, a wide range of features had been combined to predict pupylation sites, including physicochemical/biochemical properties of amino acids, Position-Specific Scoring Matrices (PSSM) which contain evolution information of amino acids, structural disorder of amino acids, second structure, and solvent accessibility. Unlike other reports, we not only improved the prediction performance, but also analyzed how much important the roles these features played in the prediction. With the selected optimal feature set, our predictor reached a sensitivity of 0.522, a specificity of 0.937, and an accuracy of 0.764. Although the results obtained here were very promising, further investigation was needed to further clarify the mechanism of pupylation process.
This research is partially supported by the Science Foundation for Young Teachers of Northeast Normal University (Grant no. 12QNJJ005) and the Natural Science Foundation of JiLin Province (Grant nos. 20101506 and 20110104).
- R. A. Festa, F. McAllister, M. J. Pearce et al., “Prokayrotic ubiquitin-like protein (Pup) proteome of Mycobacterium tuberculosis,” PLoS ONE, vol. 5, no. 1, Article ID e8589, 2010.
- K. H. Darwin, “Prokaryotic ubiquitin-like protein (Pup), proteasomes and pathogenesis,” Nature Reviews Microbiology, vol. 7, no. 7, pp. 485–491, 2009.
- C.-W. Tung, “PupDB: a database of pupylated proteins,” BMC Bioinformatics, vol. 13, no. 1, article 40, 2012.
- R. L. Welchman, C. Gordon, and R. J. Mayer, “Ubiquitin and ubiquitin-like proteins as multifunctional signals,” Nature Reviews Molecular Cell Biology, vol. 6, no. 8, pp. 599–609, 2005.
- A. Hershko and A. Ciechanover, “The ubiquitin system,” Annual Review of Biochemistry, vol. 67, pp. 425–479, 1998.
- F. Striebel, F. Imkamp, M. Sutter, M. Steiner, A. Mamedov, and E. Weber-Ban, “Bacterial ubiquitin-like modifier Pup is deamidated and conjugated to substrates by distinct but homologous enzymes,” Nature Structural and Molecular Biology, vol. 16, no. 6, pp. 647–651, 2009.
- E. Guth, M. Thommen, and E. Weber-Ban, “Mycobacterial ubiquitin-like protein ligase PafA follows a two-step reaction pathway with a phosphorylated Pup intermediate,” Journal of Biological Chemistry, vol. 286, no. 6, pp. 4412–4419, 2011.
- F. A. Cerda-Maira, F. McAllister, N. J. Bode, K. E. Burns, S. P. Gygi, and K. H. Darwin, “Reconstitution of the Mycobacterium tuberculosis pupylation pathway in Escherichia coli,” EMBO Reports, vol. 12, no. 8, pp. 863–870, 2011.
- C. Poulsen, Y. Akhter, A. H.-W. Jeon et al., “Proteome-wide identification of mycobacterial pupylation targets,” Molecular systems biology, vol. 6, p. 386, 2010.
- J. Watrous, K. Burns, W.-T. Liu et al., “Expansion of the mycobacterial “pUPylome”,” Molecular BioSystems, vol. 6, no. 2, pp. 376–385, 2010.
- Z. Liu, Q. Ma, J. Cao, X. Gao, J. Ren, and Y. Xue, “GPS-PUP: computational prediction of pupylation sites in prokaryotic proteins,” Molecular BioSystems, vol. 7, no. 10, pp. 2737–2740, 2011.
- K.-C. Chou and H.-B. Shen, “Hum-PLoc: a novel ensemble classifier for predicting human protein subcellular localization,” Biochemical and Biophysical Research Communications, vol. 347, no. 1, pp. 150–157, 2006.
- K.-C. Chou and H.-B. Shen, “Large-scale plant protein subcellular location prediction,” Journal of Cellular Biochemistry, vol. 100, no. 3, pp. 665–678, 2007.
- Y. Huang, B. Niu, Y. Gao, L. Fu, and W. Li, “CD-HIT Suite: a web server for clustering and comparing biological sequences,” Bioinformatics, vol. 26, no. 5, Article ID btq003, pp. 680–682, 2010.
- W. Li and A. Godzik, “Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences,” Bioinformatics, vol. 22, no. 13, pp. 1658–1659, 2006.
- L.-L. Hu, Z. Li, K. Wang et al., “Prediction and analysis of protein methylarginine and methyllysine based on Multisequence features,” Biopolymers, vol. 95, no. 11, pp. 763–771, 2011.
- X. Zhao, X. Li, Z. Ma, and M. Yin, “Prediction of lysine ubiquitylation with ensemble classifier and feature selection,” International Journal of Molecular Sciences, vol. 12, no. 12, pp. 8347–8361, 2011.
- S. Kawashima and M. Kanehisa, “AAindex: amino acid index database,” Nucleic Acids Research, vol. 28, no. 1, p. 374, 2000.
- S. Kawashima, P. Pokarowski, M. Pokarowska, A. Kolinski, T. Katayama, and M. Kanehisa, “AAindex: amino acid index database, progress report 2008,” Nucleic Acids Research, vol. 36, no. 1, pp. D202–D205, 2008.
- W. R. Atchley, J. Zhao, A. D. Fernandes, and T. Drüke, “Solving the protein sequence metric problem,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 18, pp. 6395–6400, 2005.
- A. Torkamani and N. J. Schork, “Accurate prediction of deleterious protein kinase polymorphisms,” Bioinformatics, vol. 23, no. 21, pp. 2918–2925, 2007.
- N. D. Rubinstein, I. Mayrose, and T. Pupko, “A machine-learning approach for predicting B-cell epitopes,” Molecular Immunology, vol. 46, no. 5, pp. 840–847, 2009.
- L. Marsella, F. Sirocco, A. Trovato, F. Seno, and S. C. E. Tosatto, “REPETITA: detection and discrimination of the periodicity of protein solenoid repeats by discrete Fourier transform,” Bioinformatics, vol. 25, no. 12, pp. i289–i295, 2009.
- T. Huang, P. Wang, Z. Ye et al., “Prediction of deleterious non-synonymous SNPs based on protein interaction network and hybrid properties,” PLoS ONE, vol. 5, no. 7, Article ID e11900, 2010.
- S. F. Altschul, T. L. Madden, A. A. Schäffer et al., “Gapped BLAST and PSI-BLAST: a new generation of protein database search programs,” Nucleic Acids Research, vol. 25, no. 17, pp. 3389–3402, 1997.
- C.-W. Tung and S.-Y. Ho, “Computational identification of ubiquitylation sites from protein sequences,” BMC Bioinformatics, vol. 9, article 310, 2008.
- P. Radivojac, V. Vacic, C. Haynes et al., “Identification, analysis, and prediction of protein ubiquitination sites,” Proteins, vol. 78, no. 2, pp. 365–380, 2010.
- C. L. Sun, Z. Z. Shi, X. B. Zhou, L. N. Chen, and X. M. Zhao, “Prediction of s-glutathionylation sites based on protein sequences,” PLoS ONE, vol. 8, no. 2, Article ID e55512, 2013.
- B. Q. Li, L. L. Hu, L. Chen, K. Y. Feng, Y. D. Cai, and K. C. Chou, “Prediction of protein domain with mRMR feature selection and analysis,” PLoS ONE, vol. 7, Article ID e39308, 2012.
- L.-L. Hu, S.-B. Wan, S. Niu et al., “Prediction and analysis of protein palmitoylation sites,” Biochimie, vol. 93, no. 3, pp. 489–496, 2011.
- B. He, K. Wang, Y. Liu, B. Xue, V. N. Uversky, and A. K. Dunker, “Predicting intrinsic disorder in proteins: an overview,” Cell Research, vol. 19, no. 8, pp. 929–949, 2009.
- R. B. Russell and T. J. Gibson, “A careful disorderliness in the proteome: sites for interaction and targets for future therapies,” FEBS Letters, vol. 582, no. 8, pp. 1271–1275, 2008.
- K. Peng, P. Radivojac, S. Vucetic, A. K. Dunker, and Z. Obradovic, “Length-dependent prediction of protein in intrinsic disorder,” BMC Bioinformatics, vol. 7, article 208, 2006.
- L. J. McGuffin, K. Bryson, and D. T. Jones, “The PSIPRED protein structure prediction server,” Bioinformatics, vol. 16, no. 4, pp. 404–405, 2000.
- C. N. I. Pang, A. Hayen, and M. R. Wilkins, “Surface accessibility of protein post-translational modifications,” Journal of Proteome Research, vol. 6, no. 5, pp. 1833–1845, 2007.
- J. Cheng, A. Z. Randall, M. J. Sweredoski, and P. Baldi, “SCRATCH: a protein structure and structural feature prediction server,” Nucleic Acids Research, vol. 33, no. 2, pp. W72–W76, 2005.
- H. Peng, F. Long, and C. Ding, “Feature selection based on mutual information: criteria of max-dependency, max-relevance, and min-redundancy,” IEEE Transactions on Pattern Analysis and Machine Intelligence, vol. 27, no. 8, pp. 1226–1238, 2005.
- C. Ding and H. Peng, “Minimum redundancy feature selection from microarray gene expression data,” Journal of Bioinformatics and Computational Biology, vol. 3, no. 2, pp. 185–205, 2005.
- Z. Qian, Y.-D. Cai, and Y. Li, “A novel computational method to predict transcription factor DNA binding preference,” Biochemical and Biophysical Research Communications, vol. 348, no. 3, pp. 1034–1037, 2006.
- C.-C. Chang and C.-J. Lin, “LIBSVM: a Library for support vector machines,” ACM Transactions on Intelligent Systems and Technology, vol. 2, no. 3, article 27, 2011.
- K.-C. Chou and C.-T. Zhang, “Prediction of protein structural classes,” Critical Reviews in Biochemistry and Molecular Biology, vol. 30, no. 4, pp. 275–349, 1995.
- K.-C. Chou and H.-B. Shen, “Cell-PLoc: a package of Web servers for predicting subcellular localization of proteins in various organisms,” Nature Protocols, vol. 3, no. 2, pp. 153–162, 2008.
- K.-C. Chou and H.-B. Shen, “Recent progress in protein subcellular location prediction,” Analytical Biochemistry, vol. 370, no. 1, pp. 1–16, 2007.
- X. Zheng, T. Liu, and J. Wang, “A complexity-based method for predicting protein subcellular location,” Amino Acids, vol. 37, no. 2, pp. 427–433, 2009.
- H.-B. Shen and K.-C. Chou, “Predicting protein subnuclear location with optimized evidence-theoretic K-nearest classifier and pseudo amino acid composition,” Biochemical and Biophysical Research Communications, vol. 337, no. 3, pp. 752–756, 2005.