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Assessment of model accuracy estimations in CASP12.
Kryshtafovych, Andriy; Monastyrskyy, Bohdan; Fidelis, Krzysztof; Schwede, Torsten; Tramontano, Anna.
Afiliação
  • Kryshtafovych A; Genome Center, University of California, Davis, California.
  • Monastyrskyy B; Genome Center, University of California, Davis, California.
  • Fidelis K; Genome Center, University of California, Davis, California.
  • Schwede T; Biozentrum, University of Basel, Basel, Switzerland.
  • Tramontano A; Computational Stuctural Biology Group, SIB Swiss Institute of Bioinformatics, Basel, Switzerland.
Proteins ; 86 Suppl 1: 345-360, 2018 03.
Article em En | MEDLINE | ID: mdl-28833563
The record high 42 model accuracy estimation methods were tested in CASP12. The paper presents results of the assessment of these methods in the whole-model and per-residue accuracy modes. Scores from four different model evaluation packages were used as the "ground truth" for assessing accuracy of methods' estimates. They include a rigid-body score-GDT_TS, and three local-structure based scores-LDDT, CAD and SphereGrinder. The ability of methods to identify best models from among several available, predict model's absolute accuracy score, distinguish between good and bad models, predict accuracy of the coordinate error self-estimates, and discriminate between reliable and unreliable regions in the models was assessed. Single-model methods advanced to the point where they are better than clustering methods in picking the best models from decoy sets. On the other hand, consensus methods, taking advantage of the availability of large number of models for the same target protein, are still better in distinguishing between good and bad models and predicting local accuracy of models. The best accuracy estimation methods were shown to perform better with respect to the frozen in time reference clustering method and the results of the best method in the corresponding class of methods from the previous CASP. Top performing single-model methods were shown to do better than all but three CASP12 tertiary structure predictors when evaluated as model selectors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Conformação Proteica / Proteínas / Modelos Moleculares / Biologia Computacional Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Conformação Proteica / Proteínas / Modelos Moleculares / Biologia Computacional Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article