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Computational Identification of MoRFs in Protein Sequences Using Hierarchical Application of Bayes Rule

MOTIVATION: Intrinsically disordered regions of proteins play an essential role in the regulation of various biological processes. Key to their regulatory function is often the binding to globular protein domains via sequence elements known as molecular recognition features (MoRFs). Development of c...

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Detalles Bibliográficos
Autores principales: Malhis, Nawar, Wong, Eric T. C., Nassar, Roy, Gsponer, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627796/
https://www.ncbi.nlm.nih.gov/pubmed/26517836
http://dx.doi.org/10.1371/journal.pone.0141603
Descripción
Sumario:MOTIVATION: Intrinsically disordered regions of proteins play an essential role in the regulation of various biological processes. Key to their regulatory function is often the binding to globular protein domains via sequence elements known as molecular recognition features (MoRFs). Development of computational tools for the identification of candidate MoRF locations in amino acid sequences is an important task and an area of growing interest. Given the relative sparseness of MoRFs in protein sequences, the accuracy of the available MoRF predictors is often inadequate for practical usage, which leaves a significant need and room for improvement. In this work, we introduce MoRF(CHiBi_Web), which predicts MoRF locations in protein sequences with higher accuracy compared to current MoRF predictors. METHODS: Three distinct and largely independent property scores are computed with component predictors and then combined to generate the final MoRF propensity scores. The first score reflects the likelihood of sequence windows to harbour MoRFs and is based on amino acid composition and sequence similarity information. It is generated by MoRF(CHiBi) using small windows of up to 40 residues in size. The second score identifies long stretches of protein disorder and is generated by ESpritz with the DisProt option. Lastly, the third score reflects residue conservation and is assembled from PSSM files generated by PSI-BLAST. These propensity scores are processed and then hierarchically combined using Bayes rule to generate the final MoRF(CHiBi_Web) predictions. RESULTS: MoRF(CHiBi_Web) was tested on three datasets. Results show that MoRF(CHiBi_Web) outperforms previously developed predictors by generating less than half the false positive rate for the same true positive rate at practical threshold values. This level of accuracy paired with its relatively high processing speed makes MoRF(CHiBi_Web) a practical tool for MoRF prediction. AVAILABILITY: http://morf.chibi.ubc.ca:8080/morf/.