XRRpred: accurate predictor of crystal structure quality from protein sequence

Abstract

Abstract Motivation X-ray crystallography was used to produce nearly 90% of protein structures. These efforts were supported by numerous sequence-based tools that accurately predict crystallizable proteins. However, protein structures vary widely in their quality, typically measured with resolution and R-free. This impacts the ability to use these structures for some applications including rational drug design and molecular docking and motivates development of methods that accurately predict structure quality from sequence. Results We introduce XRRpred, the first predictor of the resolution and R-free values from protein sequences. XRRpred relies on original sequence profiles, hand-crafted features, empirically selected and parametrized regressors and modern resampling techniques. Using an independent test dataset, we show that XRRpred provides accurate predictions of resolution and R-free. We demonstrate that XRRpred’s predictions correctly model relationship between the resolution and R-free and reproduce structure quality relations between structural classes of proteins. We also show that XRRpred significantly outperforms indirect alternative ways to predict the structure quality that include predictors of crystallization propensity and an alignment-based approach. XRRpred is available as a convenient webserver that allows batch predictions and offers informative visualization of the results. Availability and implementation http://biomine.cs.vcu.edu/servers/XRRPred/. Supplementary information Supplementary data are available at Bioinformatics online.