Abstract

S-palmitoylation, the covalent attachment of 16-carbon palmitic acids to a cysteine residue via a thioester linkage, is an important reversible lipid modification that plays a regulatory role in a variety of physiological and biological processes. As the number of experimentally identified S-palmitoylated peptides increases, it is imperative to investigate substrate motifs to facilitate the study of protein S-palmitoylation. Based on 710 non-homologous S-palmitoylation sites obtained from published databases and the literature, we carried out a bioinformatics investigation of S-palmitoylation sites based on amino acid composition. Two Sample Logo indicates that positively charged and polar amino acids surrounding S-palmitoylated sites may be associated with the substrate site specificity of protein S-palmitoylation. Additionally, maximal dependence decomposition (MDD) was applied to explore the motif signatures of S-palmitoylation sites by categorizing a large-scale dataset into subgroups with statistically significant conservation of amino acids. Single features such as amino acid composition (AAC), amino acid pair composition (AAPC), position specific scoring matrix (PSSM), position weight matrix (PWM), amino acid substitution matrix (BLOSUM62), and accessible surface area (ASA) were considered, along with the effectiveness of incorporating MDD-identified substrate motifs into a two-layered prediction model. Evaluation by five-fold cross-validation showed that a hybrid of AAC and PSSM performs best at discriminating between S-palmitoylation and non-S-palmitoylation sites, according to the support vector machine (SVM). The two-layered SVM model integrating MDD-identified substrate motifs performed well, with a sensitivity of 0.79, specificity of 0.80, accuracy of 0.80, and Matthews Correlation Coefficient (MCC) value of 0.45. Using an independent testing dataset (613 S-palmitoylated and 5412 non-S-palmitoylated sites) obtained from the literature, we demonstrated that the two-layered SVM model could outperform other prediction tools, yielding a balanced sensitivity and specificity of 0.690 and 0.694, respectively. This two-layered SVM model has been implemented as a web-based system (MDD-Palm), which is now freely available at http://csb.cse.yzu.edu.tw/MDDPalm/.

Highlights

  • S-palmitoylation is an important reversible lipid modification of proteins that involves the covalent attachment of 16-carbon palmitic acid to a cysteine residue via thioester linkage [1,2,3,4,5]

  • Cysteine was placed in the middle of the fragment sequences, and positions of the flanking amino acids ranged from −10 to +10

  • We proposed a bioinformatics method for the characterization and identification of S-palmitoylation sites with substrate site specificity

Read more

Summary

Introduction

S-palmitoylation ( known as S-acylation) is an important reversible lipid modification of proteins that involves the covalent attachment of 16-carbon palmitic acid to a cysteine residue via thioester linkage [1,2,3,4,5]. S-palmitoylation plays a significant role in regulating protein trafficking and protein-protein interaction by modifying the target cysteine residues on proteins [6,7,8]. Protein S-palmitoylation plays a regulatory role in various diseases including Huntington’s disease [10], type 1 diabetes with ZDHHC17 [11], and amyloidosis, alopecia, and osteoporosis with ZDHHC13 [12]. Previous studies have reported that there are no consensus motifs for S-palmitoylation substrate sites [2,3,4,15]. Designing an effective method to explore the potential substrate motifs of protein S-palmitoylation sites is an urgent demand in bioinformatics

Objectives
Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.