Evidence map›Paper›PMID 19445713›Full record

ArticleBMC bioinformatics2009

How to find simple and accurate rules for viral protease cleavage specificities.

Thorsteinn Rögnvaldsson, Terence A Etchells, Liwen You, Daniel Garwicz, Ian Jarman, Paulo J G Lisboa

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Article in BMC bioinformatics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Thorsteinn RögnvaldssonEmbedded and Intelligent Systems, Halmstad University, Halmstad, Sweden. denni@ide.hh.se
Terence A Etchells
Liwen You
Daniel Garwicz
Ian Jarman
Paulo J G Lisboa

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProteases of human pathogens are becoming increasingly important drug targets, hence it is necessary to understand their substrate specificity and to interpret this knowledge in practically useful ways. New methods are being developed that produce large amounts of cleavage information for individual proteases and some have been applied to extract cleavage rules from data. However, the hitherto proposed methods for extracting rules have been neither easy to understand nor very accurate. To be practically useful, cleavage rules should be accurate, compact, and expressed in an easily understandable way.

resultsA new method is presented for producing cleavage rules for viral proteases with seemingly complex cleavage profiles. The method is based on orthogonal search-based rule extraction (OSRE) combined with spectral clustering. It is demonstrated on substrate data sets for human immunodeficiency virus type 1 (HIV-1) protease and hepatitis C (HCV) NS3/4A protease, showing excellent prediction performance for both HIV-1 cleavage and HCV NS3/4A cleavage, agreeing with observed HCV genotype differences. New cleavage rules (consensus sequences) are suggested for HIV-1 and HCV NS3/4A cleavages. The practical usability of the method is also demonstrated by using it to predict the location of an internal cleavage site in the HCV NS3 protease and to correct the location of a previously reported internal cleavage site in the HCV NS3 protease. The method is fast to converge and yields accurate rules, on par with previous results for HIV-1 protease and better than previous state-of-the-art for HCV NS3/4A protease. Moreover, the rules are fewer and simpler than previously obtained with rule extraction methods.

conclusionA rule extraction methodology by searching for multivariate low-order predicates yields results that significantly outperform existing rule bases on out-of-sample data, but are more transparent to expert users. The approach yields rules that are easy to use and useful for interpreting experimental data.

Indexed as

Data Interpretation, StatisticalAmino Acid SequenceCatalytic DomainCluster AnalysisComputer SimulationDatabases, ProteinDEAD-box RNA HelicasesHIV ProteaseHumansNucleoside-TriphosphatasePeptide HydrolasesProtease InhibitorsProteomicsReproducibility of ResultsROC CurveSerine EndopeptidasesDEAD-box RNA HelicasesHIV ProteaseNS3 protein, hepatitis C virusNucleoside-Triphosphatasep16 protease, Human immunodeficiency virus 1Peptide HydrolasesProtease InhibitorsSerine EndopeptidasesViral Nonstructural ProteinsViral ProteasesViral Proteins

Identifiers

PMID19445713
PMCPMC2698905

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.