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- W2057712462 abstract "Due to their key roles in a number of biological processes, protein–protein interactions are attractive and important targets, typically involving areas greater than 6 nm2. The disruption of such interactions remains a challenging feat but, in recent years, there has been considerable progress in the design of proteomimetics: molecules that mimic the structure and function of extended regions of protein surfaces. In particular, porphyrins, calixarenes, α-helical mimetics and small molecules have successfully modulated significant protein–protein interactions, including those involved in cancer and HIV." @default.
- W2057712462 created "2016-06-24" @default.
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- W2057712462 date "2005-12-01" @default.
- W2057712462 modified "2023-10-17" @default.
- W2057712462 title "Protein surface recognition and proteomimetics: mimics of protein surface structure and function" @default.
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- W2057712462 doi "https://doi.org/10.1016/j.cbpa.2005.10.006" @default.
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