Conformational selection turns on phenylalanine hydroxylase

J Biol Chem. 2018 Dec 21;293(51):19544-19545. doi: 10.1074/jbc.H118.006676.

Abstract

Phenylalanine hydroxylase catalyzes a critical step in the phenylalanine catabolic pathway, and impairment of the human enzyme is linked to phenylketonuria. Phenylalanine is also a positive allosteric regulator of the enzyme, and the allosteric binding site has been determined by crystallography. However, the allosteric activation mechanism remains unclear. Using large-scale simulations to explore how phenylalanine binds to the regulatory site, Ge et al. discovered gating motions of the protein that suggest a conformational selection mechanism.

Publication types

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

MeSH terms

  • Allosteric Regulation
  • Catalytic Domain
  • Humans
  • Molecular Dynamics Simulation*
  • Phenylalanine / metabolism
  • Phenylalanine Hydroxylase / chemistry*
  • Phenylalanine Hydroxylase / metabolism*

Substances

  • Phenylalanine
  • Phenylalanine Hydroxylase