A Novel Framework for Ab Initio Coarse Protein Structure Prediction. (20th June 2018)
- Record Type:
- Journal Article
- Title:
- A Novel Framework for Ab Initio Coarse Protein Structure Prediction. (20th June 2018)
- Main Title:
- A Novel Framework for Ab Initio Coarse Protein Structure Prediction
- Authors:
- Dubey, Sandhya Parasnath
Balaji, S.
Kini, N. Gopalakrishna
Sathish Kumar, M. - Other Names:
- Deleage Gilbert Academic Editor.
- Abstract:
- Abstract : Hydrophobic-Polar model is a simplified representation of Protein Structure Prediction (PSP) problem. However, even with the HP model, the PSP problem remains NP-complete. This work proposes a systematic and problem specific design for operators of the evolutionary program which hybrids with local search hill climbing, to efficiently explore the search space of PSP and thereby obtain an optimum conformation. The proposed algorithm achieves this by incorporating the following novel features: (i) new initialization method which generates only valid individuals with (rather than random) better fitness values; (ii) use of probability-based selection operators that limit the local convergence; (iii) use of secondary structure based mutation operator that makes the structure more closely to the laboratory determined structure; and (iv) incorporating all the above-mentioned features developed a complete two-tier framework. The developed framework builds the protein conformation on the square and triangular lattice. The test has been performed using benchmark sequences, and a comparative evaluation is done with various state-of-the-art algorithms. Moreover, in addition to hypothetical test sequences, we have tested protein sequences deposited in protein database repository. It has been observed that the proposed framework has shown superior performance regarding accuracy (fitness value) and speed (number of generations needed to attain the final conformation). TheAbstract : Hydrophobic-Polar model is a simplified representation of Protein Structure Prediction (PSP) problem. However, even with the HP model, the PSP problem remains NP-complete. This work proposes a systematic and problem specific design for operators of the evolutionary program which hybrids with local search hill climbing, to efficiently explore the search space of PSP and thereby obtain an optimum conformation. The proposed algorithm achieves this by incorporating the following novel features: (i) new initialization method which generates only valid individuals with (rather than random) better fitness values; (ii) use of probability-based selection operators that limit the local convergence; (iii) use of secondary structure based mutation operator that makes the structure more closely to the laboratory determined structure; and (iv) incorporating all the above-mentioned features developed a complete two-tier framework. The developed framework builds the protein conformation on the square and triangular lattice. The test has been performed using benchmark sequences, and a comparative evaluation is done with various state-of-the-art algorithms. Moreover, in addition to hypothetical test sequences, we have tested protein sequences deposited in protein database repository. It has been observed that the proposed framework has shown superior performance regarding accuracy (fitness value) and speed (number of generations needed to attain the final conformation). The concepts used to enhance the performance are generic and can be used with any other population-based search algorithm such as genetic algorithm, ant colony optimization, and immune algorithm. … (more)
- Is Part Of:
- Advances in bioinformatics. Volume 2018(2018)
- Journal:
- Advances in bioinformatics
- Issue:
- Volume 2018(2018)
- Issue Display:
- Volume 2018, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 2018
- Issue:
- 2018
- Issue Sort Value:
- 2018-2018-2018-0000
- Page Start:
- Page End:
- Publication Date:
- 2018-06-20
- Subjects:
- Bioinformatics -- Periodicals
Bioinformatics
Computational Biology -- Periodicals
Periodicals
570.285 - Journal URLs:
- http://bibpurl.oclc.org/web/52720 ↗
https://www.hindawi.com/journals/abi/ ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/984/ ↗ - DOI:
- 10.1155/2018/7607384 ↗
- Languages:
- English
- ISSNs:
- 1687-8027
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 10256.xml