SVM based prediction of RNA-binding proteins using binding residues and evolutionary information
✍ Scribed by Manish Kumar; M. Michael Gromiha; Gajendra P. S. Raghava
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 231 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0952-3499
- DOI
- 10.1002/jmr.1061
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
RNA‐binding proteins (RBPs) play crucial role in transcription and gene‐regulation. This paper describes a support vector machine (SVM) based method for discriminating and classifying RNA‐binding and non‐binding proteins using sequence features. With the threshold of 30% interacting residues, RNA‐binding amino acid prediction method PPRINT achieved the Matthews correlation coefficient (MCC) of 0.32. BLAST and PSI‐BLAST identified RBPs with the coverage of 32.63 and 33.16%, respectively, at the e‐value of 1e‐4. The SVM models developed with amino acid, dipeptide and four‐part amino acid compositions showed the MCC of 0.60, 0.46, and 0.53, respectively. This is the first study in which evolutionary information in form of position specific scoring matrix (PSSM) profile has been successfully used for predicting RBPs. We achieved the maximum MCC of 0.62 using SVM model based on PSSM called PSSM‐400. Finally, we developed different hybrid approaches and achieved maximum MCC of 0.66. We also developed a method for predicting three subclasses of RNA binding proteins (e.g., rRNA, tRNA, mRNA binding proteins). The performance of the method was also evaluated on an independent dataset of 69 RBPs and 100 non‐RBPs (NBPs). An additional benchmarking was also performed using gene ontology (GO) based annotation. Based on the hybrid approach a web‐server RNApred has been developed for predicting RNA binding proteins from amino acid sequences (http://www.imtech.res.in/raghava/rnapred/). Copyright © 2010 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract The identification of RNA‐binding residues in proteins is important in several areas such as protein function, posttranscriptional regulation and drug design. We have developed PRBR (Prediction of RNA Binding Residues), a novel method for identifying RNA‐binding residues from amino acid
## Abstract The rapid accumulation of gene sequences, many of which are hypothetical proteins with unknown function, has stimulated the development of accurate computational tools for protein function prediction with evolution/structure‐based approaches showing considerable promise. In this article
The contribution of lysine and arginine residues to the formation of yeast ribonucleoprotein complex 5S RNA. protein YL3 has been investigated by determining the effects on complex formation of modification with chemical reagents specific for either lysine or arginine. Treatment of protein YL3 with