Evidence map›Paper›PMID 30240202›Full record

ArticleJournal of chemical theory and computation2018

Template-Guided Protein Structure Prediction and Refinement Using Optimized Folding Landscape Force Fields.

Mingchen Chen, Xingcheng Lin, Wei Lu, Nicholas P Schafer, José N Onuchic, Peter G Wolynes

Abstract read
In one paragraph

Article in Journal of chemical theory and computation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Molecular dissection studies ofFrontiers in microbiology · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Forging tools for refining predicted protein structures.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Mingchen ChenCenter for Theoretical Biological Physics, Rice University , Houston , Texas 77030 , United States.ORCID http://orcid.org/0000-0003-3916-7871
Xingcheng LinCenter for Theoretical Biological Physics, Rice University , Houston , Texas 77030 , United States.ORCID http://orcid.org/0000-0002-9378-6174
Wei LuCenter for Theoretical Biological Physics, Rice University , Houston , Texas 77030 , United States.
Nicholas P SchaferCenter for Theoretical Biological Physics, Rice University , Houston , Texas 77030 , United States.
José N OnuchicCenter for Theoretical Biological Physics, Rice University , Houston , Texas 77030 , United States.ORCID http://orcid.org/0000-0002-9448-0388
Peter G WolynesCenter for Theoretical Biological Physics, Rice University , Houston , Texas 77030 , United States.ORCID http://orcid.org/0000-0001-7975-9287

Funding

CONCEPTUAL ASPECTS OF THE PROTEIN FOLDING PROBLEMR01GM044557 · NIGMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI WOLYNES, PETER GUY · 1990 to 2018
$4.2M
NIGMS NIH HHS R01 GM044557
6 · The paper itself

Abstract

When good structural templates can be identified, template-based modeling is the most reliable way to predict the tertiary structure of proteins. In this study, we combine template-based modeling with a realistic coarse-grained force field, AWSEM, that has been optimized using the principles of energy landscape theory. The Associative memory, Water mediated, Structure and Energy Model (AWSEM) is a coarse-grained force field having both transferable tertiary interactions and knowledge-based local-in-sequence interaction terms. We incorporate template information into AWSEM by introducing soft collective biases to the template structures, resulting in a model that we call AWSEM-Template. Structure prediction tests on eight targets, four of which are in the low sequence identity "twilight zone" of homology modeling, show that AWSEM-Template can achieve high-resolution structure prediction. Our results also confirm that using a combination of AWSEM and a template-guided potential leads to more accurate prediction of protein structures than simply using a template-guided potential alone. Free energy profile analyses demonstrate that the soft collective biases to the template effectively increase funneling toward native-like structures while still allowing significant flexibility so as to allow for correction of discrepancies between the target structure and the template. A further stage of refinement using all-atom molecular dynamics augmented with soft collective biases to the structures predicted by AWSEM-Template leads to a further improvement of both backbone and side-chain accuracy by maintaining sufficient flexibility but at the same time discouraging unproductive unfolding events often seen in unrestrained all-atom refinement simulations. The all-atom refinement simulations also reduce patches of frustration of the initial predictions. Some of the backbones found among the structures produced during the initial coarse-grained prediction step already have CE-RMSD values of less than 3 Å with 90% or more of the residues aligned to the experimentally solved structure for all targets. All-atom structures generated during the following all-atom refinement simulations, which started from coarse-grained structures that were chosen without reference to any knowledge about the native structure, have CE-RMSD values of less than 2.5 Å with 90% or more of the residues aligned for 6 out of 8 targets. Clustering low energy structures generated during the initial coarse-grained annealing picks out reliably structures that are within 1 Å of the best sampled structures in 5 out of 8 cases. After the all-atom refinement, structures that are within 1 Å of the best sampled structures can be selected using a simple algorithm based on energetic features alone in 7 out of 8 cases.

Indexed as

Models, MolecularProtein ConformationProtein FoldingProteinsProteins

Identifiers

PMID30240202
PMCPMC6713208

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.