Versatility of ARD1/NAA10-mediated protein lysine acetylation

Exp Mol Med. 2018 Jul 27;50(7):1-13. doi: 10.1038/s12276-018-0100-7.

Abstract

Post-translational modifications (PTMs) are chemical alterations that occur in proteins that play critical roles in various cellular functions. Lysine acetylation is an important PTM in eukaryotes, and it is catalyzed by lysine acetyltransferases (KATs). KATs transfer acetyl-coenzyme A to the internal lysine residue of substrate proteins. Arrest defective 1 (ARD1) is a member of the KAT family. Since the identification of its KAT activity 15 years ago, many studies have revealed that diverse cellular proteins are acetylated by ARD1. ARD1-mediated lysine acetylation is a key switch that regulates the enzymatic activities and biological functions of proteins and influences cell biology from development to pathology. In this review, we summarize protein lysine acetylation mediated by ARD1 and describe the biological meanings of this modification.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acetylation
  • Animals
  • Humans
  • Lysine / metabolism
  • N-Terminal Acetyltransferase A / metabolism*
  • N-Terminal Acetyltransferase E / metabolism*
  • Protein Processing, Post-Translational*

Substances

  • N-Terminal Acetyltransferase A
  • NAA10 protein, human
  • N-Terminal Acetyltransferase E
  • Lysine