Literature DB >> 17646295

Dead-end elimination with backbone flexibility.

Ivelin Georgiev1, Bruce R Donald.   

Abstract

MOTIVATION: Dead-End Elimination (DEE) is a powerful algorithm capable of reducing the search space for structure-based protein design by a combinatorial factor. By using a fixed backbone template, a rotamer library, and a potential energy function, DEE identifies and prunes rotamer choices that are provably not part of the Global Minimum Energy Conformation (GMEC), effectively eliminating the majority of the conformations that must be subsequently enumerated to obtain the GMEC. Since a fixed-backbone model biases the algorithm predictions against protein sequences for which even small backbone movements may result in a significantly enhanced stability, the incorporation of backbone flexibility can improve the accuracy of the design predictions. If explicit backbone flexibility is incorporated into the model, however, the traditional DEE criteria can no longer guarantee that the flexible-backbone GMEC, the lowest-energy conformation when the backbone is allowed to flex, will not be pruned.
RESULTS: We derive a novel DEE pruning criterion, flexible-backbone DEE (BD), that is provably accurate with backbone flexibility, guaranteeing that no rotamers belonging to the flexible-backbone GMEC are pruned; we also present further enhancements to BD for improved pruning efficiency. The results from applying our novel algorithms to redesign the beta1 domain of protein G and to switch the substrate specificity of the NRPS enzyme GrsA-PheA are then compared against the results from previous fixed-backbone DEE algorithms. We confirm experimentally that traditional-DEE is indeed not provably-accurate with backbone flexibility and that BD is capable of generating conformations with significantly lower energies, thus confirming the feasibility of our novel algorithms. AVAILABILITY: Contact authors for source code.

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Year:  2007        PMID: 17646295     DOI: 10.1093/bioinformatics/btm197

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  36 in total

1.  A Bayesian approach for determining protein side-chain rotamer conformations using unassigned NOE data.

Authors:  Jianyang Zeng; Kyle E Roberts; Pei Zhou; Bruce Randall Donald
Journal:  J Comput Biol       Date:  2011-10-04       Impact factor: 1.479

2.  Predicting resistance mutations using protein design algorithms.

Authors:  Kathleen M Frey; Ivelin Georgiev; Bruce R Donald; Amy C Anderson
Journal:  Proc Natl Acad Sci U S A       Date:  2010-07-19       Impact factor: 11.205

3.  Discovery of entry inhibitors for HIV-1 via a new de novo protein design framework.

Authors:  M L Bellows; M S Taylor; P A Cole; L Shen; R F Siliciano; H K Fung; C A Floudas
Journal:  Biophys J       Date:  2010-11-17       Impact factor: 4.033

4.  BWM*: A Novel, Provable, Ensemble-based Dynamic Programming Algorithm for Sparse Approximations of Computational Protein Design.

Authors:  Jonathan D Jou; Swati Jain; Ivelin S Georgiev; Bruce R Donald
Journal:  J Comput Biol       Date:  2016-01-08       Impact factor: 1.479

5.  Computational structure-based redesign of enzyme activity.

Authors:  Cheng-Yu Chen; Ivelin Georgiev; Amy C Anderson; Bruce R Donald
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-19       Impact factor: 11.205

Review 6.  Engineering the acyltransferase substrate specificity of assembly line polyketide synthases.

Authors:  Briana J Dunn; Chaitan Khosla
Journal:  J R Soc Interface       Date:  2013-05-29       Impact factor: 4.118

7.  OPUS-Rota: a fast and accurate method for side-chain modeling.

Authors:  Mingyang Lu; Athanasios D Dousis; Jianpeng Ma
Journal:  Protein Sci       Date:  2008-06-12       Impact factor: 6.725

Review 8.  Computer-aided design of functional protein interactions.

Authors:  Daniel J Mandell; Tanja Kortemme
Journal:  Nat Chem Biol       Date:  2009-11       Impact factor: 15.040

9.  OSPREY: protein design with ensembles, flexibility, and provable algorithms.

Authors:  Pablo Gainza; Kyle E Roberts; Ivelin Georgiev; Ryan H Lilien; Daniel A Keedy; Cheng-Yu Chen; Faisal Reza; Amy C Anderson; David C Richardson; Jane S Richardson; Bruce R Donald
Journal:  Methods Enzymol       Date:  2013       Impact factor: 1.600

10.  Explicit orientation dependence in empirical potentials and its significance to side-chain modeling.

Authors:  Jianpeng Ma
Journal:  Acc Chem Res       Date:  2009-08-18       Impact factor: 22.384

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