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- W73247923 abstract "As part of our efforts toward developing catalytic five helix bundle proteins, we have modified the de novo designed helical peptide, Leu 6, previously developed in our laboratories [1]. The original peptide sequence (Fig. 1) has been shown to aggregate into four and five helix bundles that can be covalently cross-linked through homocysteines incorporated in the sequence. By attaching different cyclic hexapeptides to the N-terminus of the individual peptide strands that make up the bundle, we hope to introduce a catalytic site upon bundle formation. Modifying Leu 6 with different cyclic hexapeptides would allow a library of selfassembled molecules to be created. Five different cyclic peptides have been prepared and ligated to Leu 6 through a thioether bond." @default.
- W73247923 created "2016-06-24" @default.
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- W73247923 date "2006-05-16" @default.
- W73247923 modified "2023-09-26" @default.
- W73247923 title "Synthetic steps toward de novo designed catalytic five helix bundle proteins" @default.
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- W73247923 doi "https://doi.org/10.1007/0-306-46881-6_196" @default.
- W73247923 hasPublicationYear "2006" @default.
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