Literature DB >> 19136552

Masking residues using context-specific evolutionary conservation significantly improves short linear motif discovery.

Norman E Davey1, Denis C Shields, Richard J Edwards.   

Abstract

MOTIVATION: Short linear motifs (SLiMs) are important mediators of protein-protein interactions. Their short and degenerate nature presents a challenge for computational discovery. We sought to improve SLiM discovery by incorporating evolutionary information, since SLiMs are more conserved than surrounding residues.
RESULTS: We have developed a new method that assesses the evolutionary signal of a residue in its sequence and structural context. Under-conserved residues are masked out prior to SLiM discovery, allowing incorporation into the existing statistical model employed by SLiMFinder. The method shows considerable robustness in terms of both the conservation score used for individual residues and the size of the sequence neighbourhood. Optimal parameters significantly improve return of known functional motifs from benchmarking data, raising the return of significant validated SLiMs from typical human interaction datasets from 20% to 60%, while retaining the high level of stringency needed for application to real biological data. The success of this regime indicates that it could be of general benefit to computational annotation and prediction of protein function at the sequence level. AVAILABILITY: All data and tools in this article are available at http://bioware.ucd.ie/~slimdisc/slimfinder/conmasking/.

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Year:  2009        PMID: 19136552     DOI: 10.1093/bioinformatics/btn664

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  32 in total

1.  Natural variability of minimotifs in 1092 people indicates that minimotifs are targets of evolution.

Authors:  Kenneth F Lyon; Christy L Strong; Steve G Schooler; Richard J Young; Nervik Roy; Brittany Ozar; Mark Bachmeier; Sanguthevar Rajasekaran; Martin R Schiller
Journal:  Nucleic Acids Res       Date:  2015-06-11       Impact factor: 16.971

Review 2.  Human Protein Reference Database and Human Proteinpedia as resources for phosphoproteome analysis.

Authors:  Renu Goel; H C Harsha; Akhilesh Pandey; T S Keshava Prasad
Journal:  Mol Biosyst       Date:  2011-12-08

3.  PSSMSearch: a server for modeling, visualization, proteome-wide discovery and annotation of protein motif specificity determinants.

Authors:  Izabella Krystkowiak; Jean Manguy; Norman E Davey
Journal:  Nucleic Acids Res       Date:  2018-07-02       Impact factor: 16.971

4.  Novel peptide-mediated interactions derived from high-resolution 3-dimensional structures.

Authors:  Amelie Stein; Patrick Aloy
Journal:  PLoS Comput Biol       Date:  2010-05-20       Impact factor: 4.475

5.  seeMotif: exploring and visualizing sequence motifs in 3D structures.

Authors:  Darby Tien-Hao Chang; Ting-Ying Chien; Chien-Yu Chen
Journal:  Nucleic Acids Res       Date:  2009-05-28       Impact factor: 16.971

6.  Evidence for the concerted evolution between short linear protein motifs and their flanking regions.

Authors:  Claudia Chica; Francesca Diella; Toby J Gibson
Journal:  PLoS One       Date:  2009-07-08       Impact factor: 3.240

7.  A structure filter for the Eukaryotic Linear Motif Resource.

Authors:  Allegra Via; Cathryn M Gould; Christine Gemünd; Toby J Gibson; Manuela Helmer-Citterich
Journal:  BMC Bioinformatics       Date:  2009-10-24       Impact factor: 3.169

8.  SLiMFinder: a web server to find novel, significantly over-represented, short protein motifs.

Authors:  Norman E Davey; Niall J Haslam; Denis C Shields; Richard J Edwards
Journal:  Nucleic Acids Res       Date:  2010-05-23       Impact factor: 16.971

9.  Estimation and efficient computation of the true probability of recurrence of short linear protein sequence motifs in unrelated proteins.

Authors:  Norman E Davey; Richard J Edwards; Denis C Shields
Journal:  BMC Bioinformatics       Date:  2010-01-07       Impact factor: 3.169

10.  IUPred3: prediction of protein disorder enhanced with unambiguous experimental annotation and visualization of evolutionary conservation.

Authors:  Gábor Erdős; Mátyás Pajkos; Zsuzsanna Dosztányi
Journal:  Nucleic Acids Res       Date:  2021-07-02       Impact factor: 16.971

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