TASSER: an automated method for the prediction of protein tertiary structures in CASP6

Proteins. 2005:61 Suppl 7:91-98. doi: 10.1002/prot.20724.

Abstract

The recently developed TASSER (Threading/ASSembly/Refinement) method is applied to predict the tertiary structures of all CASP6 targets. TASSER is a hierarchical approach that consists of template identification by the threading program PROSPECTOR_3, followed by tertiary structure assembly via rearranging continuous template fragments. Assembly occurs using parallel hyperbolic Monte Carlo sampling under the guide of an optimized, reduced force field that includes knowledge-based statistical potentials and spatial restraints extracted from threading alignments. Models are automatically selected from the Monte Carlo trajectories in the low-temperature replicas using the clustering program SPICKER. For all 90 CASP targets/domains, PROSPECTOR_3 generates initial alignments with an average root-mean-square deviation (RMSD) to native of 8.4 A with 79% coverage. After TASSER reassembly, the average RMSD decreases to 5.4 A over the same aligned residues; the overall cumulative TM-score increases from 39.44 to 52.53. Despite significant improvements over the PROSPECTOR_3 template alignment observed in all target categories, the overall quality of the final models is essentially dictated by the quality of threading templates: The average TM-scores of TASSER models in the three categories are, respectively, 0.79 [comparative modeling (CM), 43 targets/domains], 0.47 [fold recognition (FR), 37 targets/domains], and 0.30 [new fold (NF), 10 targets/domains]. This highlights the need to develop novel (or improved) approaches to identify very distant targets as well as better NF algorithms.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Algorithms
  • Automation
  • Computational Biology / methods*
  • Computer Simulation
  • Computers
  • Data Interpretation, Statistical
  • Databases, Protein
  • Models, Molecular
  • Monte Carlo Method
  • Protein Folding
  • Protein Structure, Secondary
  • Protein Structure, Tertiary*
  • Proteomics / methods*
  • Reproducibility of Results
  • Sequence Alignment
  • Software