Evaluation of the structural models of the human reference proteome: AlphaFold2 versus ESMFold

The human reference proteome is routinely modelled with predictive tools such as AlphaFold2. We recently released a database in which, for each human protein, the AlphaFold2 model is paired with its ESMFold counterpart. The two predictive methods take advantage of different procedures and it is interesting to compare them in relation to their quality, particularly when an experimental protein structure is not available. Here, we select three state-of-the-art quality assessment methods and we adopt them to compare 42,942 pairs of models. This procedure helps to find the most reliable models for human proteins, particularly for the set of proteins for which structure prediction methods give dissimilar results. We obtain that when predicted structures are similar, AlphaFold2 models consistently receive higher scores than the ESMFold counterparts. When predicted structures differ, the ESMFold model is the best choice for 49 % of the proteins according to a consensus of the three QA tools.

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Publication Details

Journal
Current Research in Structural Biology
Published
2025-05-22
DOI
https://doi.org/10.1016/j.crstbi.2025.100167
Citations
4
Primary Topic
Advanced Proteomics Techniques and Applications
Type
article
Field-Weighted Citation Impact
3.03
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article

Evaluation of the structural models of the human reference proteome: AlphaFold2 versus ESMFold

Pier Luigi Martelli, Rita Casadio, Castrense Savojardo, Matteo Manfredi
4 citations
Current Research in Structural Biology
Advanced Proteomics Techniques and Applications
3.03
article

Evaluation of the structural models of the human reference proteome: AlphaFold2 versus ESMFold

Pier Luigi Martelli, Rita Casadio, Castrense Savojardo, Matteo Manfredi
article en
4 citations

Abstract

The human reference proteome is routinely modelled with predictive tools such as AlphaFold2. We recently released a database in which, for each human protein, the AlphaFold2 model is paired with its ESMFold counterpart. The two predictive methods take advantage of different procedures and it is interesting to compare them in relation to their quality, particularly when an experimental protein structure is not available. Here, we select three state-of-the-art quality assessment methods and we adopt them to compare 42,942 pairs of models. This procedure helps to find the most reliable models for human proteins, particularly for the set of proteins for which structure prediction methods give dissimilar results. We obtain that when predicted structures are similar, AlphaFold2 models consistently receive higher scores than the ESMFold counterparts. When predicted structures differ, the ESMFold model is the best choice for 49 % of the proteins according to a consensus of the three QA tools.

Current Research in Structural BiologyVol. 9
Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies (IT), University of Bologna (IT)
Zero hunger
Openalex Percentile: Top 9%
Advanced Proteomics Techniques and Applications
3.03
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