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Deep learning techniques have significantly impacted protein structure prediction and protein design
Open accessAbstract
Protein structure prediction and design can be regarded as two inverse processes governed by the same folding principle. Although progress remained stagnant over the past two decades, the recent application of deep neural networks to spatial constraint prediction and end-to-end model training has significantly improved the accuracy of protein structure prediction, largely solving the problem at the fold level for single-domain proteins. The field of protein design has also witnessed dramatic improvement, where noticeable examples have shown that information stored in neural-network models can be used to advance functional protein design. Thus, incorporation of deep learning techniques into different steps of protein folding and design approaches represents an exciting future direction and should continue to have a transformative impact on both fields.
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“Despite recent progress10–14, existing methods fall far short of atomic accuracy, especially when no homologous structure is available.”
From Highly accurate protein structure prediction with AlphaFold (2021) · cites this paper as [14]
Experimental — accuracy not yet measuredIn the citing paper
“Deep learning has also been already exploited in structural modeling and design60,194−196 and analysis191 and linking these to function.197”
From AlphaFold, Artificial Intelligence (AI), and Allostery (2022) · cites this paper as [195]
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Cites
LeCun, Y., Bengio, Y., & Hinton, G. (2015) · Nature · doi:10.1038/nature14539 · Cited by 84,126
Comparative Protein Modelling by Satisfaction of Spatial Restraints
Šali, A., & Blundell, T. L. (1993) · Journal of Molecular Biology · doi:10.1006/jmbi.1993.1626 · Cited by 12,977
I-TASSER: a unified platform for automated protein structure and function prediction
Roy, A., Küçükural, A., & Zhang, Y. (2010) · Nature Protocols · doi:10.1038/nprot.2010.5 · Cited by 6,212
Self-citationImproved protein structure prediction using potentials from deep learning
Senior, A. W., Evans, R., Jumper, J., Kirkpatrick, J., Sifre, L., Green, T., Qin, C., Žídek, A., Nelson, A. W. R., Bridgland, A., et al. (2020) · Nature · doi:10.1038/s41586-019-1923-7 · Cited by 3,378
Protein homology detection by HMM–HMM comparison
Söding, J. (2004) · Bioinformatics · doi:10.1093/bioinformatics/bti125 · Cited by 2,459
Scoring function for automated assessment of protein structure template quality
Zhang, Y., & Skolnick, J. (2004) · Proteins: Structure, Function, and Bioinformatics · doi:10.1002/prot.20264 · Cited by 2,392
Self-citationProtein Structure Prediction Using Rosetta
Rohl, C. A., Strauss, C. E. M., Misura, K. M. S., & Baker, D. A. (2004) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(04)83004-0 · Cited by 1,754
Design of a Novel Globular Protein Fold with Atomic-Level Accuracy
Kuhlman, B. A., Dantas, G. A., Ireton, G. C., Varani, G., Stoddard, B. L., & Baker, D. A. (2003) · Science · doi:10.1126/science.1089427 · Cited by 1,666
The Rosetta All-Atom Energy Function for Macromolecular Modeling and Design
Alford, R. F., Leaver-Fay, A., Jeliazkov, J. R., O’Meara, M. J., DiMaio, F. P., Park, H., Shapovalov, M. V., Renfrew, P. D., Mulligan, V. K., Kappel, K., et al. (2017) · Journal of Chemical Theory and Computation · doi:10.1021/acs.jctc.7b00125 · Cited by 1,532
Morcos, F., Pagnani, A., Lunt, B., Bertolino, A., Marks, D. S., Sander, C., Zecchina, R., Onuchic, J. N., Hwa, T., & Weigt, M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1111471108 · Cited by 1,434
Research works printed but not linked: 3
- Li, 2020, Protein 3D structure prediction by Zhang human group in CASP14, 14th Community Wide Experiment on the Critical Assessment of Techniques for Protein Structure Prediction
- Jumper, 2020, High accuracy protein structure prediction using deep learning, 14th Community Wide Experiment on the Critical Assessment of Techniques for Protein Structure Prediction
- Grishin, 2020, 3D assessment, 14th Community Wide Experiment on the Critical Assessment of Techniques for Protein Structure Prediction
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Zhou, X., Zheng, W. H., Li, Y., Pearce, R., Zhang, C., Bell, E. W., Zhang, G., & Zhang, Y. (2022) · Nature Protocols · doi:10.1038/s41596-022-00728-0 · Cited by 538
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AlphaFold, Artificial Intelligence (AI), and Allostery
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Game changers in science and technology - now and beyond
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Self-citationGe, S., Sun, S., Xu, H., Cheng, Q. S., & Ren, Z. (2025) · Briefings in Bioinformatics · doi:10.1093/bib/bbaf136 · Cited by 97
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Sun, Q., Wang, H., Xie, J., Wang, L., Mu, J., Li, J., Ren, Y., & Lai, L. (2025) · Chemical Reviews · doi:10.1021/acs.chemrev.4c00969 · Cited by 72
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Self-citationAppadurai, R., Koneru, J. K., Bonomi, M., Robustelli, P., & Srivastava, A. K. (2023) · Journal of Chemical Theory and Computation · doi:10.1021/acs.jctc.3c00224 · Cited by 57
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Misiura, M., Shroff, R., Thyer, R., & Kolomeisky, A. B. (2022) · Proteins: Structure, Function, and Bioinformatics · doi:10.1002/prot.26311 · Cited by 51
Luu, R. K., Wysokowski, M., & Buehler, M. J. (2023) · Applied Physics Letters · doi:10.1063/5.0155890 · Cited by 50
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Buscajoni, L., Martinetz, M. C., Berkemeyer, M., & Brocard, C. (2022) · Biotechnology Advances · doi:10.1016/j.biotechadv.2022.108050 · Cited by 52
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Defresne, M., Barbe, S., & Schiex, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111741 · Cited by 48
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Pearce, R., Li, Y., Omenn, G. S., & Zhang, Y. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010539 · Cited by 48
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Wuyun, Q., Chen, Y., Shen, Y., Cao, Y., Hu, G., Cui, W., Gao, J., & Zheng, W. H. (2024) · Molecules · doi:10.3390/molecules29040832 · Cited by 48
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Du, H., Jiang, D., Gao, J., Zhang, X., Jiang, L., Zeng, Y., Wu, Z., Shen, C., Xu, L., Cao, D., et al. (2022) · Research · doi:10.34133/2022/9873564 · Cited by 23
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Nallasamy, V., & Seshiah, M. (2022) · Neural Computing and Applications · doi:10.1007/s00521-022-07868-0 · Cited by 2
Drogalin, A., Monteiro, L. S., Alves, M. J., & Castro, T. G. (2023) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2023.2209184 · Cited by 2
Zheng, W. H., Wuyun, Q., & Zhang, Y. (2024) · Clinical and Translational Medicine · doi:10.1002/ctm2.1689 · Cited by 2
Self-citationBangash, S. H., Ibrahim, M., Ali, A., Wei, C., Hussain, A., Riaz, M., Rehman, M. F. U., Ahmed, F., Al‐Salahi, R. A., & Tang, W. (2025) · RSC Advances · doi:10.1039/d5ra00505a · Cited by 2
Quintana, F. M., Kong, Z., He, L., & Chen, B. Y. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.22.456843 · Cited by 2
ALPHAFOLD: DERİN ÖĞRENME VE SİNİR AĞLARI YOLUYLA PROTEİN KATLAMASINDA DEVRİM YARATMAK
Tekin, B., & Gurbanov, R. (2023) · İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi · doi:10.55071/ticaretfbd.1323165 · Cited by 2
Metadata
- Authors
- Pearce, R., & Zhang, Y.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Zhang, Yang
- Venue
- Current Opinion in Structural Biology
- Publisher
- Elsevier BV
- Published
- 2021-06
- Volume
- 68
- Pages
- 194-207
- ISSN
- 0959-440X (ISSN-L)
- PMC
- PMC8222070
- OpenAlex
- W3132448805
- Cited by
- 127
- References
- 66
- Citations by year
- 2026: 8 · 2025: 29 · 2024: 21 · 2023: 29 · 2022: 29 · 2021: 11
- FWCI
- 2.36
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (am, 268 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Current Opinion in Structural Biology (acceptedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation (DBI2030790, IIS1901191, MTM2025426)
- National Institute of General Medical Sciences (GM136422, S10OD026825)
- National Institute of Allergy and Infectious Diseases (AI134678)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Enzyme Structure and Function
- Keywords
- protein structure prediction, protein design, deep learning, deep neural network, protein folding, single-domain proteins
- MeSH terms
- Deep Learning, Proteins, Neural Networks, Computer, Protein Folding
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