Abstract

We present an approach that integrates protein structure analysis and text mining for protein functional site prediction, called LEAP-FS (Literature Enhanced Automated Prediction of Functional Sites). The structure analysis was carried out using Dynamics Perturbation Analysis (DPA), which predicts functional sites at control points where interactions greatly perturb protein vibrations. The text mining extracts mentions of residues in the literature, and predicts that residues mentioned are functionally important. We assessed the significance of each of these methods by analyzing their performance in finding known functional sites (specifically, small-molecule binding sites and catalytic sites) in about 100,000 publicly available protein structures. The DPA predictions recapitulated many of the functional site annotations and preferentially recovered binding sites annotated as biologically relevant vs. those annotated as potentially spurious. The text-based predictions were also substantially supported by the functional site annotations: compared to other residues, residues mentioned in text were roughly six times more likely to be found in a functional site. The overlap of predictions with annotations improved when the text-based and structure-based methods agreed. Our analysis also yielded new high-quality predictions of many functional site residues that were not catalogued in the curated data sources we inspected. We conclude that both DPA and text mining independently provide valuable high-throughput protein functional site predictions, and that integrating the two methods using LEAP-FS further improves the quality of these predictions.

Highlights

  • There are more than 75,000 experimentally determined structures in the Protein Data Bank

  • Allosteric sites, where molecular interactions can remotely control the behavior of the active site, represent a potentially large, untapped source of alternative sites for drug design [5]

  • The first is a structure-based method known as Dynamics Perturbation Analysis (DPA) that predicts functional sites by considering the dynamics of physical interactions [9]

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Summary

Introduction

There are more than 75,000 experimentally determined structures in the Protein Data Bank (www.pdb.org [1]). After obtaining an atomic structure of a potential target, the first key step in structure-based drug design is to identify functional sites that might directly mediate drug interactions [3]. Drug leads are unsuccessful when they inadequately block the active site, as often happens. To overcome this limitation, drug developers have begun targeting alternative sites where interactions can remotely disable protein activity; for example, a recently discovered inhibitor of HIV protease blocks a site that controls access to the active site [4]. Allosteric sites, where molecular interactions can remotely control the behavior of the active site, represent a potentially large, untapped source of alternative sites for drug design [5]

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