Nonproteinogenic Amino Acid Building Blocks for Nonribosomal Peptide and Hybrid Polyketide Scaffolds |
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Authors: | Prof. Christopher T. Walsh Dr. Robert V. O'Brien Prof. Chaitan Khosla |
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Affiliation: | 1. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115 (USA);2. Department of Chemistry, Stanford University, Stanford, CA 94305‐5025 (USA);3. Chemical Engineering, Stanford University, Stanford, CA 94305‐5025 (USA);4. Biochemistry, Stanford University, Stanford, CA 94305‐5025 (USA) |
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Abstract: | Freestanding nonproteinogenic amino acids have long been recognized for their antimetabolite properties and tendency to be uncovered to reactive functionalities by the catalytic action of target enzymes. By installing them regiospecifically into biogenic peptides and proteins, it may be possible to usher a new era at the interface between small molecule and large molecule medicinal chemistry. Site‐selective protein functionalization offers uniquely attractive strategies for posttranslational modification of proteins. Last, but not least, many of the amino acids not selected by nature for protein incorporation offer rich architectural possibilities in the context of ribosomally derived polypeptides. This Review summarizes the biosynthetic routes to and metabolic logic for the major classes of the noncanonical amino acid building blocks that end up in both nonribosomal peptide frameworks and in hybrid nonribosomal peptide‐polyketide scaffolds. |
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Keywords: | biosynthesis nonproteinogenic amino acids nonribosomal peptides polyketides |
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