DocumentCode
3375886
Title
Prediction of protein phosphorylation sites by support vector machines
Author
Ishino, Tomoki ; Nishikawa, Ikuko ; Tohsato, Yukako ; Fukuchi, Satoshi ; Nishikawa, Kiisa
Author_Institution
Coll. of Inf. Sci. & Eng., Ritsumeikan Univ., Kusatsu, Japan
fYear
2013
fDate
16-18 Dec. 2013
Firstpage
817
Lastpage
821
Abstract
Protein phosphorylation is one of the most important post-translational modifications, and revealing its mechanism is an important research topic. In this paper, phosphorylation sites in human proteins are predicted by support vector machine (SVM). First, two types of SVMs are constructed, each for phosphorylation sites in domain and in intrinsically disordered region (IDR). In domain, wide range of information of amino acid sequence is found effective, while it is not effective in IDR. As phosphorylation is abundant in IDR, the second part of the study focuses on the prediction of phosphorylation sites in IDR, especially, the phosphorylation sites with any known function. Then, it is found that the evolutionary conservation of each site is different in IDR, and multiple ortholog sequences which contain the conservation information is effective for the prediction compared with single sequence information.
Keywords
biochemistry; bioinformatics; molecular biophysics; proteins; support vector machines; SVM; amino acid sequence; conservation information; human proteins; intrinsic disordered region; multiple ortholog sequences; post-translational modifications; protein phosphorylation sites; single sequence information; support vector machines; Accuracy; Amino acids; Databases; Educational institutions; Protein engineering; Proteins; Support vector machines; intrinsically disordered region; protein phosphorylation; suppot vector machine;
fLanguage
English
Publisher
ieee
Conference_Titel
Biomedical Engineering and Informatics (BMEI), 2013 6th International Conference on
Conference_Location
Hangzhou
Print_ISBN
978-1-4799-2760-9
Type
conf
DOI
10.1109/BMEI.2013.6747053
Filename
6747053
Link To Document