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May 31, 2013Angewandte Chemie International Edition410 citationsOpen Access

Nonproteinogenic Amino Acid Building Blocks for Nonribosomal Peptide and Hybrid Polyketide Scaffolds

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CWChristopher T. WalshRORobert V. O’BrienCKChaitan Khosla

Key Points

  • The aim is to explore how nonproteinogenic amino acids can be utilized for enhancing medicinal chemistry through structural modifications.
  • Reviewing biosynthetic pathways of nonproteinogenic amino acids
  • Discussing their incorporation into biogenic peptides
  • Analyzing metabolic logic behind their functions in peptide frameworks
  • Nonproteinogenic amino acids can enhance the functionality of biogenic peptides in medicinal applications.
  • Unique architectures from these amino acids provide new opportunities for drug design.
  • Site-selective functionalization offers innovative strategies for modifying proteins effectively.

Abstract

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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Cite This Study

Walsh et al. (2013) studied this question.

synapsesocial.com/papers/69dcc17e7873f5f05b133b22https://doi.org/10.1002/anie.201208344
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