Abstract
Motivation: The coiled coil is a ubiquitous α-helical protein structure domain that directs and facilitates protein-protein interactions in a wide variety of biological processes. At the protein-sequence level, coiled coils are quite straightforward and readily recognized via the conspicuous heptad repeats of hydrophobic and polar residues. However, structurally they are more complicated, existing in a range of oligomer states and topologies. Here, we address the issue of predicting coiled-coil oligomeric state from protein sequence. Results: The predominant coiled-coil oligomer states in Nature are parallel dimers and trimers. Here, we improve and retrain the first-published algorithm, SCORER, that distinguishes these states, and test it against the current standard, MultiCoil. The SCORER algorithm has been revised in two key respects: first, the statistical basis for SCORER is improved markedly. Second, the training set for SCORER has been expanded and updated to include only structurally validated coiled coils. The result is a much-improved oligomer state predictor that outperforms MultiCoil, particularly in assigning oligomer state to short coiled coils, and those that are diverse from the training set. © The Author 2011. Published by Oxford University Press. All rights reserved.
Cite
CITATION STYLE
Armstrong, C. T., Vincent, T. L., Green, P. J., & Woolfson, D. N. (2011). SCORER 2.0: An algorithm for distinguishing parallel dimeric and trimeric coiled-coil sequences. Bioinformatics, 27(14), 1908–1914. https://doi.org/10.1093/bioinformatics/btr299
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.