Loops are often vital for protein function, however, their irregular structures make them difficult to model accurately. Current loop modelling algorithms can mostly be divided into two categories: knowledge-based, where databases of fragments are searched to find suitable conformations and ab initio, where conformations are generated computationally. Existing knowledge-based methods only use fragments that are the same length as the target, even though loops of slightly different lengths may adopt similar conformations. Here, we present a novel method, Sphinx, which combines ab initio techniques with the potential extra structural information contained within loops of a different length to improve structure prediction.We show that Sphinx is able to generate high-accuracy predictions and decoy sets enriched with near-native loop conformations, performing better than the ab initio algorithm on which it is based. In addition, it is able to provide predictions for every target, unlike some knowledge-based methods. Sphinx can be used successfully for the difficult problem of antibody H3 prediction, outperforming RosettaAntibody, one of the leading H3-specific ab initio methods, both in accuracy and speed.Sphinx is available at http://opig.stats.ox.ac.uk/webapps/sphinx.deane@stats.ox.ac.uk.Supplemen... data are available at Bioinformatics online.
Knowledge Bases
,Computational Biology
,Antibodies
,Animals
,Software
,Protein Conformation
,research-article
,Research Support, Non-U.S. Gov't
,Algorithms
,Models, Molecular
,Journal Article