Structure and stability of an immunoglobulin superfamily domain from twitchin, a muscle protein of the nematode Caenorhabditis elegans

J Mol Biol. 1996 Dec 6;264(3):624-39. doi: 10.1006/jmbi.1996.0665.

Abstract

The NMR solution structure of an immunoglobulin superfamily module of twitchin (Ig 18') has been determined and the kinetic and equilibrium folding behaviour characterised. Thirty molecular coordinates were calculated using a hybrid distance geometry-simulated annealing protocol based on 1207 distance and 48 dihedral restraints. The atomic rms distributions about the mean coordinate for the ensemble of structures is 0.55( +/- 0.09) A for backbone atoms and 1.10( +/- 0.08) A for all heavy atoms. The protein has a topology very similar to that of telokin and the titin Ig domains and thus it falls into the I set of the immunoglobulin superfamily. The close agreement between the predicted and observed structures of Ig 18' demonstrates clearly that the I set profile can be applied in the structure prediction of immunoglobulin-like domains of diverse modular proteins. Folding studies reveal that the protein has relatively low thermodynamic stability, deltaG(H2O)U-F = 4.0 kcal mol(-1) at physiological pH. Unfolding studies suggest that the protein has considerable kinetic stability, the half life of the unfolding is greater than 40 minutes in the absence of denaturant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Caenorhabditis elegans / chemistry*
  • Caenorhabditis elegans Proteins*
  • Calmodulin-Binding Proteins / chemistry*
  • Helminth Proteins / chemistry*
  • Immunoglobulins / chemistry*
  • Magnetic Resonance Spectroscopy
  • Molecular Sequence Data
  • Muscle Proteins / chemistry*
  • Myosin-Light-Chain Kinase
  • Peptide Fragments
  • Peptides
  • Protein Denaturation
  • Protein Folding
  • Protein Structure, Secondary
  • Protein Structure, Tertiary*
  • Sequence Alignment

Substances

  • Caenorhabditis elegans Proteins
  • Calmodulin-Binding Proteins
  • Helminth Proteins
  • Immunoglobulins
  • Muscle Proteins
  • Peptide Fragments
  • Peptides
  • unc-22 protein, C elegans
  • telokin
  • Myosin-Light-Chain Kinase

Associated data

  • PDB/1WIT
  • PDB/1WIU