Generalized dead-end elimination algorithms make large-scale protein side-chain structure prediction tractable: implications for protein design and structural genomics

J Mol Biol. 2001 Mar 16;307(1):429-45. doi: 10.1006/jmbi.2000.4424.

Abstract

The dead-end elimination (DEE) theorems are powerful tools for the combinatorial optimization of protein side-chain placement in protein design and homology modeling. In order to reach their full potential, the theorems must be extended to handle very hard problems. We present a suite of new algorithms within the DEE paradigm that significantly extend its range of convergence and reduce run time. As a demonstration, we show that a total protein design problem of 10(115) combinations, a hydrophobic core design problem of 10(244) combinations, and a side-chain placement problem of 10(1044) combinations are solved in less than two weeks, a day and a half, and an hour of CPU time, respectively. This extends the range of the method by approximately 53, 144 and 851 log-units, respectively, using modest computational resources. Small to average-sized protein domains can now be designed automatically, and side-chain placement calculations can be solved for nearly all sizes of proteins and protein complexes in the growing field of structural genomics.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Algorithms*
  • Amino Acid Sequence
  • DNA-Binding Proteins*
  • Fibronectins / chemistry
  • Fibronectins / genetics
  • Genome
  • Humans
  • Immunoglobulin Fab Fragments / chemistry
  • Immunoglobulin Fab Fragments / genetics
  • Models, Chemical
  • Protein Conformation*
  • Protein Engineering
  • Protein Folding
  • Repressor Proteins / chemistry
  • Repressor Proteins / genetics
  • Sequence Homology, Amino Acid
  • Viral Proteins
  • Viral Regulatory and Accessory Proteins
  • X-Ray Diffraction

Substances

  • DNA-Binding Proteins
  • Fibronectins
  • Immunoglobulin Fab Fragments
  • Repressor Proteins
  • Viral Proteins
  • Viral Regulatory and Accessory Proteins
  • phage repressor proteins