Skip to main navigation Skip to search Skip to main content

Structural Studies of Modular Nonribosomal Peptide Synthetases

  • SUNY Buffalo

Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

7 Scopus citations

Abstract

The non-ribosomal peptide synthetases (NRPSs) are a family of modular enzymes involved in the production of peptide natural products. Not restricted by the constraints of ribosomal peptide and protein production, the NRPSs are able to incorporate unusual amino acids and other suitable building blocks into the final product. The NRPSs operate with an assembly line strategy in which peptide intermediates are covalently tethered to a peptidyl carrier protein and transported to different catalytic domains for the multiple steps in the biosynthesis. Often the carrier and catalytic domains are joined into a single large multidomain protein. This chapter serves to introduce the NRPS enzymes, using the nocardicin NRPS system as an example that highlights many common features to NRPS biochemistry. We then describe recent advances in the structural biology of NRPSs focusing on large multidomain structures that have been determined.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages17-46
Number of pages30
DOIs
StatePublished - 2023

Publication series

NameMethods in Molecular Biology
Volume2670
ISSN (Print)1064-3745
ISSN (Electronic)1940-6029

Keywords

  • Conformational changes
  • Modular enzymes
  • Natural products
  • Non-ribosomal Peptide Synthetase
  • NRPS
  • Protein–protein interactions
  • Secondary metabolites
  • Structural biology

Fingerprint

Dive into the research topics of 'Structural Studies of Modular Nonribosomal Peptide Synthetases'. Together they form a unique fingerprint.

Cite this