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- W4299865485 abstract "An exactly solvable model based on the topology of a protein native state is applied to identify bottlenecks and key-sites for the folding of HIV-1 Protease. The predicted sites are found to correlate well with clinical data on resistance to FDA-approved drugs. It has been observed that the effects of drug therapy are to induce multiple mutations on the protease. The sites where such mutations occur correlate well with those involved in folding bottlenecks identified through the deterministic procedure proposed in this study. The high statistical significance of the observed correlations suggests that the approach may be promisingly used in conjunction with traditional techniques to identify candidate locations for drug attacks." @default.
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- W4299865485 date "2002-09-13" @default.
- W4299865485 modified "2023-10-18" @default.
- W4299865485 title "Crucial stages of protein folding through a solvable model: predicting target sites for enzyme-inhibiting drugs" @default.
- W4299865485 doi "https://doi.org/10.48550/arxiv.cond-mat/0209325" @default.
- W4299865485 hasPublicationYear "2002" @default.
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