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Influenza A virus polymerase: an attractive target for next-generation anti-influenza therapeutics

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DRUG DISCOVERY TODAY
卷 23, 期 3, 页码 503-518

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ELSEVIER SCI LTD
DOI: 10.1016/j.drudis.2018.01.028

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资金

  1. National Natural Science Foundation of China (NSFC) [81773574, 81273354, 81573347]
  2. Key Project of NSFC for International Cooperation [81420108027, 30910103908]
  3. Young Scholars Program of Shandong University (YSPSDU) [2016WLJH32]
  4. Science and Technology Development Project of Shandong Province [2014GSF118175]
  5. Major Project of Science and Technology of Shandong Province [2015ZDJS04001]
  6. Key Research and Development Project of Shandong Province [2017CXGC1401]

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The influenza RNA-dependent RNA polymerase (RdRP) is conserved among different types of influenza virus, playing an important part in transcription and replication. In this regard, influenza RdRP is an attractive target for novel anti-influenza drug discovery. Herein, we will introduce the structural and functional information of influenza polymerase; and an overview of inhibitors targeting the PA endonuclease and PB2 cap-binding site is provided, along with the approaches utilized for identification of these inhibitors. The protein-protein interactions (PPIs) of the three polymerase subunits: PA, PB1 and PB2, are described based on the published crystal structures, and inhibitors targeting the PA-PB1 interaction are introduced briefly.

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