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논문 기본 정보

자료유형
학술저널
저자정보
Cao, Guang Ping (Division of Applied Life Science [BK21 Program], Systems and Synthetic Agrobiotech Center [SSAC], Plant Molecular Biology and Biotechnology Research Center [PMBBRC], Research Institute) Thangapandian, Sundarapandian (Division of Applied Life Science [BK21 Program], Systems and Synthetic Agrobiotech Center [SSAC], Plant Molecular Biology and Biotechnology Research Center [PMBBRC], Rese) John, Shalini (Division of Applied Life Science [BK21 Program], Systems and Synthetic Agrobiotech Center [SSAC], Plant Molecular Biology and Biotechnology Research Center [PMBBRC], Research Institute o) Lee, Keun-Woo (Division of Applied Life Science [BK21 Program], Systems and Synthetic Agrobiotech Center [SSAC], Plant Molecular Biology and Biotechnology Research Center [PMBBRC], Research Institute o)
저널정보
한국생물정보시스템생물학회 Interdisciplinary Bio Central Interdisciplinary Bio Central 제4권 제1호
발행연도
2012.1
수록면
21 - 27 (7page)

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Introduction: Histone deacetylases (HDAC) are a class of enzymes that remove acetyl groups from ${\varepsilon}$-N-acetyl lysine amino acids of histone proteins. Their action is opposite to that of histone acetyltransferase that adds acetyl groups to these lysines. Only few HDAC inhibitors are approved and used as anti-cancer therapeutics. Thus, discovery of new and potential HDAC inhibitors are necessary in the effective treatment of cancer. Materials and Methods: This study proposed a method using support vector machine (SVM) to classify HDAC8 inhibitors and non-inhibitors in early-phase virtual compound filtering and screening. The 100 experimentally known HDAC8 inhibitors including 52 inhibitors and 48 non-inhibitors were used in this study. A set of molecular descriptors was calculated for all compounds in the dataset using ADRIANA. Code of Molecular Networks. Different kernel functions available from SVM Tools of free support vector machine software and training and test sets of varying size were used in model generation and validation. Results and Conclusion: The best model obtained using kernel functions has shown 75% of accuracy on test set prediction. The other models have also displayed good prediction over the test set compounds. The results of this study can be used as simple and effective filters in the drug discovery process.

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