Adenylate-forming enzymes

Stefan Schmelz, James Henderson Naismith

Research output: Contribution to journalArticlepeer-review

Abstract

Thioesters, amides, and esters are common chemical building blocks in a wide array of natural products. The formation of these bonds can be catalyzed in a variety of ways. For chemists, the use of an activating group is a common strategy and adenylate enzymes are exemplars of this approach. Adenylating enzymes activate the otherwise unreactive carboxylic acid by transforming the normal hydroxyl leaving group into adenosine monophosphate. Recently there have been a number of studies of such enzymes and in this review we suggest a new classification scheme. The review highlights the diversity in enzyme fold, active site architecture, and metal coordination that has evolved to catalyze this particular reaction.

Original languageEnglish
Pages (from-to)666-671
Number of pages6
JournalCurrent Opinion in Structural Biology
Volume19
Issue number6
DOIs
Publication statusPublished - Dec 2009

Keywords

  • TRANSFER-RNA-SYNTHETASE
  • SITE-DIRECTED MUTAGENESIS
  • PROTEIN LIGASE DLTA
  • CRYSTAL-STRUCTURE
  • ESCHERICHIA-COLI
  • COENZYME-A
  • STRUCTURAL BASIS
  • BACILLUS-CEREUS
  • ACTIVE-SITE
  • ACTIVATION

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  • BBSRC BBS/B/14426: SPORT

    Naismith, J. (PI)

    BBSRC

    18/10/0430/04/12

    Project: Standard

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