Literature DB >> 26365322

Functional profiling of adenylation domains in nonribosomal peptide synthetases by competitive activity-based protein profiling.

Shota Kasai1, Sho Konno1, Fumihiro Ishikawa1, Hideaki Kakeya1.   

Abstract

We describe competitive activity-based protein profiling (ABPP) to accelerate the functional prediction and assessment of adenylation (A) domains in nonribosomal peptide synthetases (NRPSs) in proteomic environments. Using a library of sulfamoyloxy-linked aminoacyl-AMP analogs, the competitive ABPP technique offers a simple and rapid assay system for adenylating enzymes and provides insight into enzyme substrate candidates and enzyme active-site architecture.

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Year:  2015        PMID: 26365322     DOI: 10.1039/c5cc04953a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Activity-based protein profiling of a surfactin-producing nonribosomal peptide synthetase in Bacillus subtilis.

Authors:  Fumihiro Ishikawa; Rina Ohnishi; Chiharu Uchida; Genzoh Tanabe
Journal:  STAR Protoc       Date:  2022-06-13

Review 2.  Trapping interactions between catalytic domains and carrier proteins of modular biosynthetic enzymes with chemical probes.

Authors:  Andrew M Gulick; Courtney C Aldrich
Journal:  Nat Prod Rep       Date:  2018-11-14       Impact factor: 13.423

  2 in total

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