Magnesium binding to the bacterial chemotaxis protein CheY results in large conformational changes involving its functional surface

J Mol Biol. 1994 May 13;238(4):489-95. doi: 10.1006/jmbi.1994.1308.

Abstract

The three-dimensional crystal structure of the bacterial chemotaxis protein CheY with the essential Mg2+ cation bound to the active site reveals large conformational changes caused by the metal binding. Displacements of up to 10 A are observed in several residues at the N terminus of alpha-helix 4 and in the preceding loop. One turn of this helix unwinds, and an Asn residue that was located inside the helix becomes the new N-cap. This supports the important role that N or C-cap residues play in alpha-helix stability. In addition the preceding beta-strand becomes elongated and a new beta-turn appears. The final effect is a significant modification of the surface relief of the protein in a region previously indicated, by genetic analysis, to be essential for CheY function. It is suggested that binding of a divalent cation to CheY could play a significant part in CheY activation and consequently in signal transduction in prokaryotes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins*
  • Binding Sites
  • Chemotaxis*
  • Computer Graphics
  • Hydrogen Bonding
  • Lysine / chemistry
  • Magnesium / metabolism*
  • Membrane Proteins / chemistry*
  • Membrane Proteins / metabolism
  • Methyl-Accepting Chemotaxis Proteins
  • Models, Molecular
  • Protein Conformation
  • Protein Kinases / chemistry*
  • Protein Kinases / metabolism
  • Protein Structure, Secondary

Substances

  • Bacterial Proteins
  • Membrane Proteins
  • Methyl-Accepting Chemotaxis Proteins
  • Protein Kinases
  • Magnesium
  • Lysine