Glutamine-specific N-terminal amidase, a component of the N-end rule pathway

Mol Cell. 2009 Jun 26;34(6):686-95. doi: 10.1016/j.molcel.2009.04.032.


Deamidation of N-terminal Gln by Nt(Q)-amidase, an N-terminal amidohydrolase, is a part of the N-end rule pathway of protein degradation. We detected the activity of Nt(Q)-amidase, termed Ntaq1, in mouse tissues, purified Ntaq1 from bovine brains, identified its gene, and began analyzing this enzyme. Ntaq1 is highly conserved among animals, plants, and some fungi, but its sequence is dissimilar to sequences of other amidases. An earlier mutant in the Drosophila Cg8253 gene that we show here to encode Nt(Q)-amidase has defective long-term memory. Other studies identified protein ligands of the uncharacterized human C8orf32 protein that we show here to be the Ntaq1 Nt(Q)-amidase. Remarkably, "high-throughput" studies have recently solved the crystal structure of C8orf32 (Ntaq1). Our site-directed mutagenesis of Ntaq1 and its crystal structure indicate that the active site and catalytic mechanism of Nt(Q)-amidase are similar to those of transglutaminases.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidohydrolases / chemistry
  • Amidohydrolases / genetics
  • Amidohydrolases / isolation & purification
  • Amidohydrolases / physiology*
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Cattle
  • Cloning, Molecular
  • Conserved Sequence
  • Crystallography, X-Ray
  • Escherichia coli / genetics
  • Glutamine / chemistry*
  • Glutamine / metabolism
  • Half-Life
  • Mice
  • Models, Molecular
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • NIH 3T3 Cells
  • Protein Structure, Tertiary
  • Saccharomyces cerevisiae / genetics
  • Substrate Specificity


  • Glutamine
  • Amidohydrolases
  • Ntaq1 protein, mouse