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Protein fold recognition

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Summary

An important, yet seemingly unattainable, goal in structural molecular biology is to be able to predict the native three-dimensional structure of a protein entirely from its amino acid sequence. Prediction methods based on rigorous energy calculations have not yet been successful, and best results have been obtained from homology modelling and statistical secondary structure prediction. Homology modelling is limited to cases where significant sequence similarity is shared between a protein of known structure and the unknown. Secondary structure prediction methods are not only unreliable, but also do not offer any obvious route to the full tertiary structure. Recently, methods have been developed whereby entire protein folds are recognized from sequence, even where little or no sequence similarity is shared between the proteins under consideration. In this paper we review the current methods, including our own, and in particular offer a historical background to their development. In addition, we also discuss the future of these methods and outline the developments under investigation in our laboratory.

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Authors and Affiliations

  1. Biomolecular Structure and Modelling Unit, Department of Biochemistry and Molecular Biology, University College, WC1E 6BT, London, U.K.

    David Jones & Janet Thornton

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  1. David Jones
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  2. Janet Thornton
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Jones, D., Thornton, J. Protein fold recognition. J Computer-Aided Mol Des 7, 439–456 (1993). https://doi.org/10.1007/BF02337560

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  • DOI: https://doi.org/10.1007/BF02337560

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