Constructing a Foundational Platform Driven by Japan's K Supercomputer for Next‐Generation Drug Design. Issue 11 (17th July 2014)
- Record Type:
- Journal Article
- Title:
- Constructing a Foundational Platform Driven by Japan's K Supercomputer for Next‐Generation Drug Design. Issue 11 (17th July 2014)
- Main Title:
- Constructing a Foundational Platform Driven by Japan's K Supercomputer for Next‐Generation Drug Design
- Authors:
- Brown, J. B.
Nakatsui, Masahiko
Okuno, Yasushi - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The cost of pharmaceutical R&amp;D has risen enormously, both worldwide and in Japan. However, Japan faces a particularly difficult situation in that its population is aging rapidly, and the cost of pharmaceutical R&amp;D affects not only the industry but the entire medical system as well. To attempt to reduce costs, the newly launched K supercomputer is available for big data drug discovery and structural simulation‐based drug discovery. We have implemented both primary (direct) and secondary (infrastructure, data processing) methods for the two types of drug discovery, custom tailored to maximally use the 88 128 compute nodes/CPUs of K, and evaluated the implementations. We present two types of results. In the first, we executed the virtual screening of nearly 19 billion compound‐protein interactions, and calculated the accuracy of predictions against publicly available experimental data. In the second investigation, we implemented a very computationally intensive binding free energy algorithm, and found that comparison of our binding free energies was considerably accurate when validated against another type of publicly available experimental data. The common feature of both result types is the scale at which computations were executed. The frameworks presented in this article provide prospectives and applications that, while tuned to the computing resources available in Japan, are equally applicable<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The cost of pharmaceutical R&amp;D has risen enormously, both worldwide and in Japan. However, Japan faces a particularly difficult situation in that its population is aging rapidly, and the cost of pharmaceutical R&amp;D affects not only the industry but the entire medical system as well. To attempt to reduce costs, the newly launched K supercomputer is available for big data drug discovery and structural simulation‐based drug discovery. We have implemented both primary (direct) and secondary (infrastructure, data processing) methods for the two types of drug discovery, custom tailored to maximally use the 88 128 compute nodes/CPUs of K, and evaluated the implementations. We present two types of results. In the first, we executed the virtual screening of nearly 19 billion compound‐protein interactions, and calculated the accuracy of predictions against publicly available experimental data. In the second investigation, we implemented a very computationally intensive binding free energy algorithm, and found that comparison of our binding free energies was considerably accurate when validated against another type of publicly available experimental data. The common feature of both result types is the scale at which computations were executed. The frameworks presented in this article provide prospectives and applications that, while tuned to the computing resources available in Japan, are equally applicable to any equivalent large‐scale infrastructure provided elsewhere.</p> </abstract> … (more)
- Is Part Of:
- Molecular informatics. Volume 33:Issue 11/12(2014)
- Journal:
- Molecular informatics
- Issue:
- Volume 33:Issue 11/12(2014)
- Issue Display:
- Volume 33, Issue 11/12 (2014)
- Year:
- 2014
- Volume:
- 33
- Issue:
- 11/12
- Issue Sort Value:
- 2014-0033-NaN-0000
- Page Start:
- 732
- Page End:
- 741
- Publication Date:
- 2014-07-17
- Subjects:
- Cheminformatics -- Periodicals
QSAR (Biochemistry) -- Periodicals
Structure-activity relationships (Biochemistry) -- Periodicals
Drugs -- Structure-activity relationships -- Periodicals
615.19 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1868-1751 ↗
http://www3.interscience.wiley.com/journal/123236613/home ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/minf.201400067 ↗
- Languages:
- English
- ISSNs:
- 1868-1743
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817750
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3663.xml