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Critical assessment of methods of protein structure prediction (CASP) - progress and new directions in Round XI

Moult, John and Fidelis, Krzysztof and Kryshtafovych, Andriy and Schwede, Torsten and Tramontano, Anna. (2016) Critical assessment of methods of protein structure prediction (CASP) - progress and new directions in Round XI. Proteins, 84 (1). pp. 4-14.

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Official URL: http://edoc.unibas.ch/43850/

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Abstract

Modeling of protein structure from amino acid sequence now plays a major role in structural biology. Here we report new developments and progress from the CASP11 community experiment, assessing the state of the art in structure modeling. Notable points include the following: (1) New methods for predicting three dimensional contacts resulted in a few spectacular template free models in this CASP, whereas models based on sequence homology to proteins with experimental structure continue to be the most accurate. (2) Refinement of initial protein models, primarily using molecular dynamics related approaches, has now advanced to the point where the best methods can consistently (though slightly) improve nearly all models. (3) The use of relatively sparse NMR constraints dramatically improves the accuracy of models, and another type of sparse data, chemical crosslinking, introduced in this CASP, also shows promise for producing better models. (4) A new emphasis on modeling protein complexes, in collaboration with CAPRI, has produced interesting results, but also shows the need for more focus on this area. (5) Methods for estimating the accuracy of models have advanced to the point where they are of considerable practical use. (6) A first assessment demonstrates that models can sometimes successfully address biological questions that motivate experimental structure determination. (7) There is continuing progress in accuracy of modeling regions of structure not directly available by comparative modeling, while there is marginal or no progress in some other areas. This article is protected by copyright. All rights reserved.
Faculties and Departments:05 Faculty of Science > Departement Biozentrum > Computational & Systems Biology > Bioinformatics (Schwede)
10 Zentrale universitäre Einrichtungen > SciCore
UniBasel Contributors:Schwede, Torsten
Item Type:Article, refereed
Publisher:Wiley-Liss
ISSN:0887-3585
Note:Publication type according to Uni Basel Research Database: Journal article
Identification Number:
Last Modified:05 Sep 2019 15:16
Deposited On:05 Jan 2017 07:59

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