Analysis of the movements of helices in EF-hands

Proteins. 2012 Nov;80(11):2592-600. doi: 10.1002/prot.24143. Epub 2012 Jul 31.

Abstract

We have developed a method to place an EF-lobe in a coordinate system that recognizes the similarity of its two EF-hand domains as well as their relationship by a pseudo-two fold axis, z. The x-axis connects the center of mass, calculated from α-carbons of helices E1 and F1, with the center of mass of E2 and F2. The resulting coordinate system is intrinsic to each EF-lobe and requires no comparison with other EF-lobes. It has provided an intuitive and informative way to compare EF-lobes and especially those changes associated with calcium and/or target binding. We analyzed the EF-lobes of calmodulin and of other subfamilies with four EF-hands. We have rationalized a complex pattern of changes of conformation associated with calcium coordination and effector binding as observed in different subfamilies of EF-hand proteins.

MeSH terms

  • Animals
  • Calcium / metabolism
  • Calmodulin / chemistry*
  • Calmodulin / metabolism
  • Databases, Protein
  • EF Hand Motifs*
  • Humans
  • Models, Molecular
  • Myosin Light Chains / chemistry*
  • Myosin Light Chains / metabolism
  • Protein Structure, Tertiary
  • Troponin C / chemistry*
  • Troponin C / metabolism

Substances

  • Calmodulin
  • Myosin Light Chains
  • Troponin C
  • Calcium