Protein structure optimization by side-chain positioning via beta-complex
- Title
- Protein structure optimization by side-chain positioning via beta-complex
- Author
- 김덕수
- Keywords
- Protein structure optimization; Protein design; Rotamer; Voronoi diagram; Quasi-triangulation; Beta-complex; Integer linear programming; Optimal; Heuristic; BetaSCP; SCWRL; RASP
- Issue Date
- 2013-09
- Publisher
- Springer Science + Business Media
- Citation
- Journal of global optimization, 2013, 57(1), p.217-250
- Abstract
- A molecular structure determines a molecular function(s) and a correct understanding of molecular structure is important for biotechnology. The computational prediction of molecular structure is a frequent requirement for important biomolecular applications such as a homology modeling, a docking simulation, a protein design, etc. where the optimization of molecular structure is fundamental. One of the core problems in the optimization of protein structure is the optimization of side-chains called the side-chain positioning problem. The side-chain positioning problem, assuming the rigidity of backbone and a rotamer library, attempts to optimally assign a rotamer to each residue so that the potential energy of protein is minimized in its entirety. The optimal solution approach using (mixed) integer linear programming, with the dead-end elimination technique, suffers even for moderate-sized proteins because the side-chain positioning problem is NP-hard. On the other hand, popular heuristic approaches focusing on speed produce solutions of low quality. This paper presents an efficient algorithm, called the BetaSCP, for the side-chain positioning problem based on the beta-complex which is a derivative geometric construct of the Voronoi diagram. Placing a higher priority on solution quality, the BetaSCP algorithm produces a solution very close to the optima within a reasonable computation time. The effectiveness and efficiency of the BetaSCP are experimentally shown via a benchmark test against well-known algorithms using twenty test models selected from Protein Data Bank.
- URI
- https://link.springer.com/article/10.1007%2Fs10898-012-9886-3http://hdl.handle.net/20.500.11754/50661
- ISSN
- 0925-5001
- DOI
- 10.1007/s10898-012-9886-3
- Appears in Collections:
- COLLEGE OF ENGINEERING[S](공과대학) > MECHANICAL ENGINEERING(기계공학부) > Articles
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