Literature DB >> 31376733

Evaluation of the scale-consistent UNRES force field in template-free prediction of protein structures in the CASP13 experiment.

Emilia A Lubecka1, Agnieszka S Karczyńska2, Agnieszka G Lipska2, Adam K Sieradzan2, Karolina Ziȩba2, Celina Sikorska2, Urszula Uciechowska2, Sergey A Samsonov2, Paweł Krupa3, Magdalena A Mozolewska4, Łukasz Golon2, Artur Giełdoń2, Cezary Czaplewski2, Rafał Ślusarz2, Magdalena Ślusarz2, Silvia N Crivelli5, Adam Liwo6.   

Abstract

The recent NEWCT-9P version of the coarse-grained UNRES force field for proteins, with scale-consistent formulas for the local and correlation terms, has been tested in the CASP13 experiment of the blind-prediction of protein structure, in the ab initio, contact-assisted, and data-assisted modes. Significant improvement of the performance has been observed with respect to the CASP11 and CASP12 experiments (by over 10 GDT_TS units for the ab initio mode predictions and by over 15 GDT_TS units for the contact-assisted prediction, respectively), which is a result of introducing scale-consistent terms and improved handling of contact-distance restraints. As in previous CASP exercises, UNRES ranked higher in the free modeling category than in the general category that included template based modeling targets. Use of distance restraints from the predicted contacts, albeit many of them were wrong, resulted in the increase of GDT_TS by over 8 units on average and introducing sparse restraints from small-angle X-ray/neutron scattering and chemical cross-link-mass-spectrometry experiments, and ambiguous restraints from nuclear magnetic resonance experiments has also improved the predictions by 8.6, 9.7, and 10.7 GDT_TS units on average, respectively.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Free and data-assisted modeling; Multiscale modeling; Replica-exchange molecular dynamics; UNRES force field; protein structure prediction

Mesh:

Substances:

Year:  2019        PMID: 31376733     DOI: 10.1016/j.jmgm.2019.07.013

Source DB:  PubMed          Journal:  J Mol Graph Model        ISSN: 1093-3263            Impact factor:   2.518


  4 in total

1.  Modeling the Structure, Dynamics, and Transformations of Proteins with the UNRES Force Field.

Authors:  Adam K Sieradzan; Cezary Czaplewski; Paweł Krupa; Magdalena A Mozolewska; Agnieszka S Karczyńska; Agnieszka G Lipska; Emilia A Lubecka; Ewa Gołaś; Tomasz Wirecki; Mariusz Makowski; Stanisław Ołdziej; Adam Liwo
Journal:  Methods Mol Biol       Date:  2022

2.  Improved Consensus-Fragment Selection in Template-Assisted Prediction of Protein Structures with the UNRES Force Field in CASP13.

Authors:  Agnieszka S Karczyńska; Karolina Ziȩba; Urszula Uciechowska; Magdalena A Mozolewska; Paweł Krupa; Emilia A Lubecka; Agnieszka G Lipska; Celina Sikorska; Sergey A Samsonov; Adam K Sieradzan; Artur Giełdoń; Adam Liwo; Rafał Ślusarz; Magdalena Ślusarz; Jooyoung Lee; Keehyoung Joo; Cezary Czaplewski
Journal:  J Chem Inf Model       Date:  2020-02-11       Impact factor: 4.956

3.  Residue-Level Contact Reveals Modular Domain Interactions of PICK1 Are Driven by Both Electrostatic and Hydrophobic Forces.

Authors:  Amy O Stevens; Yi He
Journal:  Front Mol Biosci       Date:  2021-01-27

4.  Theory and Practice of Coarse-Grained Molecular Dynamics of Biologically Important Systems.

Authors:  Adam Liwo; Cezary Czaplewski; Adam K Sieradzan; Agnieszka G Lipska; Sergey A Samsonov; Rajesh K Murarka
Journal:  Biomolecules       Date:  2021-09-11
  4 in total

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