How to guarantee optimal stability for most representative structures in the Protein Data Bank

Proteins. 2001 Aug 1;44(2):79-96. doi: 10.1002/prot.1075.


We proposed recently an optimization method to derive energy parameters for simplified models of protein folding. The method is based on the maximization of the thermodynamic average of the overlap between protein native structures and a Boltzmann ensemble of alternative structures. Such a condition enforces protein models whose ground states are most similar to the corresponding native states. We present here an extensive testing of the method for a simple residue-residue contact energy function and for alternative structures generated by threading. The optimized energy function guarantees high stability and a well-correlated energy landscape to most representative structures in the PDB database. Failures in the recognition of the native structure can be attributed to the neglect of interactions between different chains in oligomeric proteins or with cofactors. When these are taken into account, only very few X-ray structures are not recognized. Most of them are short inhibitors or fragments and one is a structure that presents serious inconsistencies. Finally, we discuss the reasons that make NMR structures more difficult to recognizeCopyright 2001 Wiley-Liss, Inc.

Publication types

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

MeSH terms

  • Computational Biology / methods*
  • Databases, Factual*
  • Disulfides / chemistry
  • Models, Chemical
  • Nuclear Magnetic Resonance, Biomolecular
  • Protein Conformation
  • Protein Folding*
  • Proteins / chemistry*
  • Thermodynamics*


  • Disulfides
  • Proteins