SDPhound, a Mutual Information-Based Method to Investigate Specificity-Determining Positions

Considerable importance in molecular biophysics is attached to influencing by mutagenesis the specific properties of a protein family. The working hypothesis is that mutating residues at few selected positions can affect specificity. Statistical analysis of homologue sequences can identify putative...

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Main Authors: Riccardo Nifosí, Valentina Tozzini, Pietro Amat, Sara Bonella, Walter Rocchia
Format: Article
Language:English
Published: MDPI AG 2009-05-01
Series:Algorithms
Subjects:
Online Access:http://www.mdpi.com/1999-4893/2/2/764/
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spelling doaj-c319eff984ce4bf78f5ee8c2509eee8c2020-11-25T01:56:12ZengMDPI AGAlgorithms1999-48932009-05-012276478910.3390/a2020764SDPhound, a Mutual Information-Based Method to Investigate Specificity-Determining PositionsRiccardo NifosíValentina TozziniPietro AmatSara BonellaWalter RocchiaConsiderable importance in molecular biophysics is attached to influencing by mutagenesis the specific properties of a protein family. The working hypothesis is that mutating residues at few selected positions can affect specificity. Statistical analysis of homologue sequences can identify putative specificity determining positions (SDPs) and help to shed some light on the peculiarities underlying their functional role. In this work, we present an approach to identify such positions inspired by state of the art mutual information-based SDP prediction methods. The algorithm based on this approach provides a systematic procedure to point at the relevant physical characteristics of putative SPDs and can investigate the effects of correlated mutations. The method is tested on two standard benchmarks in the field and further validated in the context of a biologically interesting problem: the multimerization of the Intrinsically Fluorescent Proteins (IFP). http://www.mdpi.com/1999-4893/2/2/764/specificity determining positionsintrinsically fluorescent proteinsmutual information
collection DOAJ
language English
format Article
sources DOAJ
author Riccardo Nifosí
Valentina Tozzini
Pietro Amat
Sara Bonella
Walter Rocchia
spellingShingle Riccardo Nifosí
Valentina Tozzini
Pietro Amat
Sara Bonella
Walter Rocchia
SDPhound, a Mutual Information-Based Method to Investigate Specificity-Determining Positions
Algorithms
specificity determining positions
intrinsically fluorescent proteins
mutual information
author_facet Riccardo Nifosí
Valentina Tozzini
Pietro Amat
Sara Bonella
Walter Rocchia
author_sort Riccardo Nifosí
title SDPhound, a Mutual Information-Based Method to Investigate Specificity-Determining Positions
title_short SDPhound, a Mutual Information-Based Method to Investigate Specificity-Determining Positions
title_full SDPhound, a Mutual Information-Based Method to Investigate Specificity-Determining Positions
title_fullStr SDPhound, a Mutual Information-Based Method to Investigate Specificity-Determining Positions
title_full_unstemmed SDPhound, a Mutual Information-Based Method to Investigate Specificity-Determining Positions
title_sort sdphound, a mutual information-based method to investigate specificity-determining positions
publisher MDPI AG
series Algorithms
issn 1999-4893
publishDate 2009-05-01
description Considerable importance in molecular biophysics is attached to influencing by mutagenesis the specific properties of a protein family. The working hypothesis is that mutating residues at few selected positions can affect specificity. Statistical analysis of homologue sequences can identify putative specificity determining positions (SDPs) and help to shed some light on the peculiarities underlying their functional role. In this work, we present an approach to identify such positions inspired by state of the art mutual information-based SDP prediction methods. The algorithm based on this approach provides a systematic procedure to point at the relevant physical characteristics of putative SPDs and can investigate the effects of correlated mutations. The method is tested on two standard benchmarks in the field and further validated in the context of a biologically interesting problem: the multimerization of the Intrinsically Fluorescent Proteins (IFP).
topic specificity determining positions
intrinsically fluorescent proteins
mutual information
url http://www.mdpi.com/1999-4893/2/2/764/
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AT valentinatozzini sdphoundamutualinformationbasedmethodtoinvestigatespecificitydeterminingpositions
AT pietroamat sdphoundamutualinformationbasedmethodtoinvestigatespecificitydeterminingpositions
AT sarabonella sdphoundamutualinformationbasedmethodtoinvestigatespecificitydeterminingpositions
AT walterrocchia sdphoundamutualinformationbasedmethodtoinvestigatespecificitydeterminingpositions
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