ArticleJournal of chemical information and modeling2026
Which Metrics Best Capture Protein Structural Changes in Molecular Dynamics Simulations? Evaluating Score Combinations and Force-Field Effects.
Article in Journal of chemical information and modeling, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
The scores RMSD, TM-score, GDT, lDDT, SphereGrinder, CAD, QCS, FlexE, and MolProbity provide an automated, comprehensive assessment of conformational changes and structural quality of proteins and thus represent a promising tool for routine use in molecular dynamics (MD) simulations, particularly in high-throughput settings. However, it remains unclear to what extent these scores provide redundant information and which scores are most informative for capturing conformational changes. Based on MD simulations of 268 diverse proteins, we demonstrate that the investigated scores are highly correlated and that one global score (or QCS), one local score, and FlexE capture almost 90% of the variance across all scores. Since MD randomness partially explains FlexE's variability, we argue that a combination of one global and one local score is sufficient for most practical applications. We also investigate the influence of simulation setups and find that the choice of the force field can significantly affect scoring results. In particular, the setup using the Amber ff19sb force field yields systematically different scores than all CHARMM36m-based setups, emphasizing the importance of methodological choices when designing MD experiments and interpreting their results.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.