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Prediction of protein tertiary structure using PROFESY, a novel method based on fragment assembly and conformational space annealing

Authors
Lee, JKim, SYJoo, KKim, ILee, J
Issue Date
1-Sep-2004
Publisher
WILEY
Keywords
protein folding; tertiary structure prediction; ab initio prediction; fragment assembly; global optimization
Citation
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, v.56, no.4, pp.704 - 714
Journal Title
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
Volume
56
Number
4
Start Page
704
End Page
714
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/19966
DOI
10.1002/prot.20150
ISSN
0887-3585
Abstract
A novel method for ab initio prediction of protein tertiary structures, PROFESY (PROFile Enumerating SYstem.), is proposed. This method utilizes the secondary structure prediction information of a query sequence and the fragment assembly procedure based on global optimization. Fifteen-residue-long fragment libraries are constructed using the secondary structure prediction method PREDICT, and fragments in these libraries are assembled to generate full-length chains of a query protein. Tertiary structures of 50 to 100 conformations are obtained by minimizing an energy function for proteins, using the conformational space annealing method that enables one to sample diverse low-lying local minima of the energy. We apply PROFESY for benchmark tests to proteins with known structures to demonstrate its feasibility. In addition, we participated in CASP5 and applied PROFESY to four new-fold targets for blind prediction. The results are quite promising, despite the fact that PROFESY was in its early stages of development. In particular, PROFESY successfully provided us the best model-one structure for the target T0161. (C) 2004 Wiley-Liss, Inc.
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College of Natural Sciences (Department of Bioinformatics & Life Science)
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