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Constraint-based assembly of tertiary protein structures from secondary structure elements

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

A challenge in computational protein folding is to assemble secondary structure elements - helices and strands - into well-packed tertiary structures. Particularly difficult is the formation of β-sheets from strands, because they involve large conformational searches at the same time as precise packing and hydrogen bonding. Here we describe a method, called Geocore-2, that (1) grows chains one monomer or secondary structure at a time, then (2) disconnects the loops and performs a fast rigid-body docking step to achieve canonical packings, then (3) in the case of intrasheet strand packing, adjusts the side-chain rotamers; and finally (4) reattaches loops. Computational efficiency is enhanced by using a branch-and-bound search in which pruning rules aim to achieve a hydrophobic core and satisfactory hydrogen bonding patterns. We show that the pruning rules reduce computational time by 103- to 105-fold, and that this strategy is computationally practical at least for molecules up to about 100 amino acids long.

Original languageEnglish
Pages (from-to)1935-1946
Number of pages12
JournalProtein Science
Volume9
Issue number10
StatePublished - 2000

Keywords

  • Conformational search
  • Protein folding
  • Structure prediction
  • Tertiary structure assembly

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