Academic Journals Database
Disseminating quality controlled scientific knowledge

Sparse estimation for structural variability

ADD TO MY LIST
 
Author(s): Hosur Raghavendra | Singh Rohit | Berger Bonnie

Journal: Algorithms for Molecular Biology
ISSN 1748-7188

Volume: 6;
Issue: 1;
Start page: 12;
Date: 2011;
Original page

ABSTRACT
Abstract Background Proteins are dynamic molecules that exhibit a wide range of motions; often these conformational changes are important for protein function. Determining biologically relevant conformational changes, or true variability, efficiently is challenging due to the noise present in structure data. Results In this paper we present a novel approach to elucidate conformational variability in structures solved using X-ray crystallography. We first infer an ensemble to represent the experimental data and then formulate the identification of truly variable members of the ensemble (as opposed to those that vary only due to noise) as a sparse estimation problem. Our results indicate that the algorithm is able to accurately distinguish genuine conformational changes from variability due to noise. We validate our predictions for structures in the Protein Data Bank by comparing with NMR experiments, as well as on synthetic data. In addition to improved performance over existing methods, the algorithm is robust to the levels of noise present in real data. In the case of Human Ubiquitin-conjugating enzyme Ubc9, variability identified by the algorithm corresponds to functionally important residues implicated by mutagenesis experiments. Our algorithm is also general enough to be integrated into state-of-the-art software tools for structure-inference.
Save time & money - Smart Internet Solutions      Why do you need a reservation system?