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  Automatic prediction of protein 3D Structures by probabilistic multi-template homology modeling.

Meier, A., & Söding, J. (2015). Automatic prediction of protein 3D Structures by probabilistic multi-template homology modeling. PLoS Computational Biology, 11(10): e1004343. doi:10.1371/journal.pcbi.1004343.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0027-1418-D Version Permalink: http://hdl.handle.net/11858/00-001M-0000-002A-1CA7-4
Genre: Journal Article

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 Creators:
Meier, A., Author
Söding, J.1, Author              
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1Research Group of Computational Biology, MPI for Biophysical Chemistry, Max Planck Society, ou_1933286              

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 Abstract: Homology modeling predicts the 3D structure of a query protein based on the sequence alignment with one or more template proteins of known structure. Its great importance for biological research is owed to its speed, simplicity, reliability and wide applicability, covering more than half of the residues in protein sequence space. Although multiple templates have been shown to generally increase model quality over single templates, the information from multiple templates has so far been combined using empirically motivated, heuristic approaches. We present here a rigorous statistical framework for multi-template homology modeling. First, we find that the query proteins' atomic distance restraints can be accurately described by two-component Gaussian mixtures. This insight allowed us to apply the standard laws of probability theory to combine restraints from multiple templates. Second, we derive theoretically optimal weights to correct for the redundancy among related templates. Third, a heuristic template selection strategy is proposed. We improve the average GDT-ha model quality score by 11% over single template modeling and by 6.5% over a conventional multi-template approach on a set of 1000 query proteins. Robustness with respect to wrong constraints is likewise improved. We have integrated our multi-template modeling approach with the popular MODELLER homology modeling software in our free HHpred server http://toolkit.tuebingen.mpg.de/hhpred and also offer open source software for running MODELLER with the new restraints at https://bitbucket.org/soedinglab/hh-suite.

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Language(s): eng - English
 Dates: 2015-10-23
 Publication Status: Published online
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 Rev. Method: Peer
 Identifiers: DOI: 10.1371/journal.pcbi.1004343
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Title: PLoS Computational Biology
Source Genre: Journal
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Pages: 20 Volume / Issue: 11 (10) Sequence Number: e1004343 Start / End Page: - Identifier: -