Neisseria gonorrhoeae carbonic anhydrase inhibition

Enzymes. 2024:55:243-281. doi: 10.1016/bs.enz.2024.05.008. Epub 2024 Jun 6.

Abstract

Carbonic anhydrases (CAs) are ubiquitous enzymes that are found in all kingdoms of life. Though different classes of CAs vary in their roles and structures, their primary function is to catalyze the reaction between carbon dioxide and water to produce bicarbonate and a proton. Neisseria gonorrhoeae encodes for three distinct CAs (NgCAs) from three different families: an α-, a β-, and a γ-isoform. This chapter details the differences between the three NgCAs, summarizing their subcellular locations, roles, essentiality, structures, and enzyme kinetics. These bacterial enzymes have the potential to be drug targets; thus, previous studies have investigated the inhibition of NgCAs-primarily the α-isoform. Therefore, the classes of inhibitors that have been shown to bind to the NgCAs will be discussed as well. These classes include traditional CA inhibitors, such as sulfonamides, phenols, and coumarins, as well as non-traditional inhibitors including anions and thiocarbamates.

Keywords: Antibiotics; Bacterial carbonic anhydrases; Carbonic anhydrase inhibitors; Neisseria gonorrhoeae; Structure-activity relationship.

Publication types

  • Review

MeSH terms

  • Bacterial Proteins / antagonists & inhibitors
  • Bacterial Proteins / metabolism
  • Carbonic Anhydrase Inhibitors* / pharmacology
  • Carbonic Anhydrases* / metabolism
  • Humans
  • Neisseria gonorrhoeae* / drug effects
  • Neisseria gonorrhoeae* / enzymology

Substances

  • Carbonic Anhydrase Inhibitors
  • Carbonic Anhydrases
  • Bacterial Proteins