Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/24240
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 18074/20272 (89%)
造訪人次 : 4152082      線上人數 : 6257
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/24240


    標題: Predicting Ligand-Receptor Interactions of Promiscuous Proteins by PhE/SVM: The Nuclear Receptor PXR
    作者: Yu-Hsuan Shih (施昱瑄)
    Ci-Nong Chen
    Max K. Leong
    日期: 2011
    上傳時間: 2011-06-23 14:57:27 (UTC+8)
    摘要: The nuclear receptor pregnane X receptor (PXR) plays a critical role in Phase I or II metabolism and excretion because it can increase induction levels of metabolismm enzymes upon activation by a wide range of endogenous and xenobiotic molecules. In this study, an in silico model was developed to predict the activation of hPXR using the newly invented pharmacophore ensemble/support vector machine (PhE/SVM) scheme, which can fully take into a account the promiscuous nature of hPXR, namely flexible protein conformation and multiple ligand orientatiotionsns. The predictions are in good experimental observations and the calculated results are consistent with the published hPXR-ligand co-complex structure. Furthermore, , the derived model not only showed highly statistical significance but completely met with various validation criteria. Therefore, this accurate PhE/SVM model can be utilized for predicting the activation of hPXR to facilitate drug discovery and drug development.
    關聯: 2011年台俄有機、藥物與生物化學交流暨藥物化學研討會,起迄日:2011/04/06~2011/04/05,地點:溪頭台大實驗林
    顯示於類別:[藥理學院] 2011年台俄有機、藥物與生物化學交流暨藥物化學研討會

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    pp-24.pdf62KbAdobe PDF391檢視/開啟


    在CNU IR中所有的資料項目都受到原著作權保護.

    TAIR相關文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋