<scp>CASP16</scp> Protein Monomer Structure Prediction Assessment

The assessment of monomer targets in the Critical Assessment of Structure Prediction Round 16 (CASP16) underscores that the problem of single-domain protein fold prediction is nearly solved-no target folds were incorrectly predicted across all Evaluation Units. However, challenges remain in accurately modeling truncated sequences, irregular secondary structures, and interaction-induced conformational changes. The release of AlphaFold3 (AF3) during CASP16, and its effective integration by many groups, demonstrated its superiority over AlphaFold2 (AF2), particularly in confidence estimation and model selection. Additional improvements in multiple sequence alignments (MSAs) and fragment-based prediction, that is, selecting the optimal fragment of the full sequence for modeling, also contributed to enhanced prediction accuracy. The top three groups-all from the Yang lab-consistently outperformed others across CASP16 monomer targets, reflecting their robust modeling pipelines and successful adoption of AF3. CASP16 also introduced three new challenges: Phase 0, in which stoichiometry was withheld; Phase 2, which supplied ~8000 MassiveFold models per target to test model selection strategies; and Model 6, which limited predictors to using MSAs provided by the organizers. While we evaluated group performance in these additional challenges, the insights gained were limited due to low participation and caveats in the design of experiments. We suggest improvements for the organization of these challenges and encourage broader engagement from the prediction community. The progress in monomer modeling from CASP15 to CASP16 was subtle, but more groups in CASP16 were able to outperform ColabFold, reflecting the community's improved ability in optimizing AF2 and the growing adoption of AF3. We anticipate that the recent release of the AF3 source code will stimulate future progress through user-driven optimization and innovations in model architecture. Finally, model ranking remains a persistent weakness across most groups, highlighting a critical area for future development.

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Publication Details

Journal
Proteins Structure Function and Bioinformatics
Published
2025-08-17
DOI
https://doi.org/10.1002/prot.70031
Citations
8
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
6.45

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article

CASP16 Protein Monomer Structure Prediction Assessment

R. Dustin Schaeffer, Qian Cong, Rongqing Yuan, Andriy Kryshtafovych et al.
8 citations
Proteins Structure Function and Bioinformatics
Protein Structure and Dynamics
6.45
article

CASP16 Protein Monomer Structure Prediction Assessment

R. Dustin Schaeffer, Qian Cong, Rongqing Yuan, Andriy Kryshtafovych, Jing Zhang, Jian Zhou, Nick V. Grishin
article en
8 citations

Abstract

The assessment of monomer targets in the Critical Assessment of Structure Prediction Round 16 (CASP16) underscores that the problem of single-domain protein fold prediction is nearly solved-no target folds were incorrectly predicted across all Evaluation Units. However, challenges remain in accurately modeling truncated sequences, irregular secondary structures, and interaction-induced conformational changes. The release of AlphaFold3 (AF3) during CASP16, and its effective integration by many groups, demonstrated its superiority over AlphaFold2 (AF2), particularly in confidence estimation and model selection. Additional improvements in multiple sequence alignments (MSAs) and fragment-based prediction, that is, selecting the optimal fragment of the full sequence for modeling, also contributed to enhanced prediction accuracy. The top three groups-all from the Yang lab-consistently outperformed others across CASP16 monomer targets, reflecting their robust modeling pipelines and successful adoption of AF3. CASP16 also introduced three new challenges: Phase 0, in which stoichiometry was withheld; Phase 2, which supplied ~8000 MassiveFold models per target to test model selection strategies; and Model 6, which limited predictors to using MSAs provided by the organizers. While we evaluated group performance in these additional challenges, the insights gained were limited due to low participation and caveats in the design of experiments. We suggest improvements for the organization of these challenges and encourage broader engagement from the prediction community. The progress in monomer modeling from CASP15 to CASP16 was subtle, but more groups in CASP16 were able to outperform ColabFold, reflecting the community's improved ability in optimizing AF2 and the growing adoption of AF3. We anticipate that the recent release of the AF3 source code will stimulate future progress through user-driven optimization and innovations in model architecture. Finally, model ranking remains a persistent weakness across most groups, highlighting a critical area for future development.

Proteins Structure Function and BioinformaticsVol. 94(1)
Southwestern Medical Center (US), University of California, Davis (US), The University of Texas Southwestern Medical Center (US)
National Science Foundation, Cancer Prevention and Research Institute of Texas, University of Texas Southwestern Medical Center, National Institute of General Medical Sciences, National Institute of Allergy and Infectious Diseases, Division of Biological Infrastructure
Industry, innovation and infrastructure
Openalex Percentile: Top 3%
Protein Structure and Dynamics
6.45
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