Evidence map›Paper›PMID 41481844›Full record

ArticleJournal of chemical theory and computation2026

Efficient Sampling of Short Protein Trajectories with Conditional Diffusion Models.

Chuanye Xiong, Palanisamy Kandhan, Dongyang Chen, Zerui Ma, Eleanor D Smith, Peng Tao

Abstract read
In one paragraph

Article in Journal of chemical theory and computation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. AI-Physics-Experiment Trinity for Integrated Protein Dynamics Modeling.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. 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.

Chuanye XiongDepartment of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States.
Palanisamy KandhanDepartment of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States.ORCID 0000-0002-3088-0032
Dongyang ChenDepartment of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States.ORCID 0009-0000-2681-1379
Zerui MaDepartment of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States.ORCID 0009-0005-9846-6056
Eleanor D SmithDepartment of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States.
Peng TaoDepartment of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States.ORCID 0000-0002-2488-0239

Funding

Probing Hidden Conformational Space and Dynamical States of Circadian Clock Proteins through Rigid Residue Scan and Machine LearningR15GM122013 · NIGMS · SOUTHERN METHODIST UNIVERSITY · PI TAO, PENG · 2018 to 2023
$800k
NIGMS NIH HHS R15 GM122013
6 · The paper itself

Abstract

Understanding how protein structures dictate their diverse biological functions remains one of the central and enduring challenges in structural biology. The development of AlphaFold and ESMAtlas marks a significant advance in protein science, enabling the reliable prediction of protein structure directly from amino acid sequence. This advance in structure prediction underscores the need for complementary methods that can explore conformational space and enable efficient sampling of dynamic trajectories. Here, we present TSS-Pro, a conditional generative diffusion framework that enables efficient sampling of protein conformational trajectory space. TSS-Pro takes the initial frame as conditional input and generates protein conformational trajectories. It supports two sampling strategies: (1) consecutive sampling, where each trajectory segment is generated step by step by conditioning on the final frame of the previously generated segment, enabling temporally coherent propagation of structural transitions; (2) parallel sampling, where multiple trajectory branches are independently generated from initial conditions to enhance conformational diversity. We validate TSS-Pro on three representative systems of increasing complexity: alanine dipeptide, ubiquitin, and

Indexed as

CryptochromesDrosophila ProteinsMolecular Dynamics SimulationProteinsUbiquitinAnimalsDiffusionDipeptidesProtein ConformationThermodynamicsCryptochromesDipeptidesDrosophila ProteinsProteinsUbiquitin

Identifiers

PMID41481844
PMCPMC12861079

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.