Abstract

BackgroundOne of the most evident achievements of bioinformatics is the development of methods that transfer biological knowledge from characterised proteins to uncharacterised sequences. This mode of protein function assignment is mostly based on the detection of sequence similarity and the premise that functional properties are conserved during evolution. Most automatic approaches developed to date rely on the identification of clusters of homologous proteins and the mapping of new proteins onto these clusters, which are expected to share functional characteristics.ResultsHere, we inverse the logic of this process, by considering the mapping of sequences directly to a functional classification instead of mapping functions to a sequence clustering. In this mode, the starting point is a database of labelled proteins according to a functional classification scheme, and the subsequent use of sequence similarity allows defining the membership of new proteins to these functional classes. In this framework, we define the Correspondence Indicators as measures of relationship between sequence and function and further formulate two Bayesian approaches to estimate the probability for a sequence of unknown function to belong to a functional class. This approach allows the parametrisation of different sequence search strategies and provides a direct measure of annotation error rates. We validate this approach with a database of enzymes labelled by their corresponding four-digit EC numbers and analyse specific cases.ConclusionThe performance of this method is significantly higher than the simple strategy consisting in transferring the annotation from the highest scoring BLAST match and is expected to find applications in automated functional annotation pipelines.

Highlights

  • One of the most evident achievements of bioinformatics is the development of methods that transfer biological knowledge from characterised proteins to uncharacterised sequences

  • Defining correspondence indicators Given a functional classification, annotating a new protein consists in establishing to which functional class or classes it belongs

  • To approach the problem we defined a Correspondence Indicator (CI) between the new protein and each of the functional classes, and second, formulated a classification scheme based on these indicators

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Summary

Introduction

One of the most evident achievements of bioinformatics is the development of methods that transfer biological knowledge from characterised proteins to uncharacterised sequences. This mode of protein function assignment is mostly based on the detection of sequence similarity and the premise that functional properties are conserved during evolution. The gap between the growth rate of biological sequence databases and the capability to characterise experimentally the roles and functions associated with these new sequences is constantly increasing [1]. This results in an accumulation of raw data that can lead to an increase in (page number not for citation purposes). These rely on the combination of the annotations of more than one homologue [10,11,12,13] or, for example, on semantic analyses of annotation lines [14]

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