Evidence map›Paper›PMID 19887634›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Constructing the equilibrium ensemble of folding pathways from short off-equilibrium simulations.

Frank Noé, Christof Schütte, Eric Vanden-Eijnden, Lothar Reich, Thomas R Weikl

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 324 papers.

0numbers the graph read from it
0cells of the map it votes in
324citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

324 citing papers in PubMed.

  1. Article
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  7. Dynamic mechanism for subtype selectivity of endocannabinoids.The Journal of biological chemistry · 2026
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  8. Conformational Dynamics of NaJournal of chemical information and modeling · 2026
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  9. Article
  10. De novo Folding Mechanisms of Lasso Peptides.bioRxiv : the preprint server for biology · 2026
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Topological Analysis Reveals Multiple Pathways in Molecular Dynamics.Journal of chemical theory and computation · 2025
    Article
  17. A Cryptic Binding Pocket Regulates the Metal-Dependent Activity of Cas9.bioRxiv : the preprint server for biology · 2025
    Article
  18. Article
  19. Article
  20. Synthesis and Characterization of Photoswitchable Covalent Ligands for the βAngewandte Chemie (International ed. in English) · 2025
    Article

264 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Frank NoéDeutsche Forschungsgemeinschaft Research Center Matheon, Freie Universität Berlin, Arnimallee 6, 14195 Berlin, Germany. frank.noe@fu-berlin.de
Christof Schütte
Eric Vanden-Eijnden
Lothar Reich
Thomas R Weikl

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Characterizing the equilibrium ensemble of folding pathways, including their relative probability, is one of the major challenges in protein folding theory today. Although this information is in principle accessible via all-atom molecular dynamics simulations, it is difficult to compute in practice because protein folding is a rare event and the affordable simulation length is typically not sufficient to observe an appreciable number of folding events, unless very simplified protein models are used. Here we present an approach that allows for the reconstruction of the full ensemble of folding pathways from simulations that are much shorter than the folding time. This approach can be applied to all-atom protein simulations in explicit solvent. It does not use a predefined reaction coordinate but is based on partitioning the state space into small conformational states and constructing a Markov model between them. A theory is presented that allows for the extraction of the full ensemble of transition pathways from the unfolded to the folded configurations. The approach is applied to the folding of a PinWW domain in explicit solvent where the folding time is two orders of magnitude larger than the length of individual simulations. The results are in good agreement with kinetic experimental data and give detailed insights about the nature of the folding process which is shown to be surprisingly complex and parallel. The analysis reveals the existence of misfolded trap states outside the network of efficient folding intermediates that significantly reduce the folding speed.

Indexed as

Models, ChemicalProtein FoldingComputational BiologyComputer SimulationProtein ConformationProteinsProteins

Identifiers

PMID19887634
PMCPMC2772816

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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.