2017
DOI: 10.1002/prot.25373
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Protein structure model refinement in CASP12 using short and long molecular dynamics simulations in implicit solvent

Abstract: Protein structure prediction has matured over years, particularly those which use structure templates for building a model. It can build a model with correct overall conformation in cases where appropriate templates are available. Models with the correct topology can be practically useful for limited purposes that need residue-level accuracy, but further improvement of the models can allow the models to be used in tasks that need detailed structures, such as molecular replacement in X-ray crystallography or st… Show more

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Cited by 12 publications
(10 citation statements)
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“…In CASP8, 70% of the participants in an evaluation of protein structure refinement failed to improve agreement with experimental data compared to initial models [4]. In the last decade, access to more computational power led to an increase of the use of physics-based methods such as molecular dynamics (MD) simulations and force fields in protein structure prediction [5][6][7][8][9]. Whereas physics-based methods initially had very limited success in CASP, performance has improved in recent assessments.…”
Section: Introductionmentioning
confidence: 99%
“…In CASP8, 70% of the participants in an evaluation of protein structure refinement failed to improve agreement with experimental data compared to initial models [4]. In the last decade, access to more computational power led to an increase of the use of physics-based methods such as molecular dynamics (MD) simulations and force fields in protein structure prediction [5][6][7][8][9]. Whereas physics-based methods initially had very limited success in CASP, performance has improved in recent assessments.…”
Section: Introductionmentioning
confidence: 99%
“…based on repeated molecular dynamics simulations, 38,39 at this time the approach is computationally too expensive to be implemented as a public server.…”
Section: Discussionmentioning
confidence: 99%
“…This is a MD-based refinement method our group used in CASP13. Based on our group's CASP12 refinement protocol 64 , in this protocol we used the CHARMM22 force field with the FACTS 53 implicit solvent model in CHARMM 54 . Initially, the refinement target structure is put through minimization with all heavy atoms fixed, before being put through minimization with tapering harmonic restraints on all heavy atoms.…”
Section: Md-based Refinement From Casp13 (Casp13-kiharalab)mentioning
confidence: 99%