Discovery of a Non-Peptidic Inhibitor of West Nile Virus NS3 Protease by High-Throughput Docking 英文参考文献.docVIP

下载本文档

7
0
约4.44万字
约 9页
2017-05-11 发布于上海
举报
版权申诉

Discovery of a Non-Peptidic Inhibitor of West Nile Virus NS3 Protease by High-Throughput Docking 英文参考文献.doc

1、本文档共9页，可阅读全部内容。
2、原创力文档（book118）网站文档一经付费（服务费），不意味着购买了该文档的版权，仅供个人/单位学习、研究之用，不得用于商业用途，未经授权，严禁复制、发行、汇编、翻译或者网络传播等，侵权必究。
3、本站所有内容均由合作方或网友上传，本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺！文档内容仅供研究参考，付费前请自行鉴别。如您付费，意味着您自己接受本站规则且自行承担风险，本站不退款、不进行额外附加服务；查看《如何避免下载的几个坑》。如果您已付费下载过本站文档，您可以点击这里二次下载。
4、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等，请点击“版权申诉”（推荐），也可以打举报电话：400-050-0827(电话支持时间：9:00-18:30)。
5、该文档为VIP文档，如果想要下载，成为VIP会员后，下载免费。
6、成为VIP后，下载本文档将扣除1次下载权益。下载后，不支持退款、换文档。如有疑问请联系我们。
7、成为VIP后，您将拥有八大权益，权益包括：VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
8、VIP文档为合作方或网友上传，每下载1次，网站将根据用户上传文档的质量评分、类型等，对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档

Discovery of a Non-Peptidic Inhibitor of West Nile Virus NS3 Protease by High-Throughput Docking 英文参考文献

DiscoveryofaNon-PeptidicInhibitorofWestNileVirus NS3ProteasebyHigh-ThroughputDocking DariuszEkonomiuk1,Xun-ChengSu2,KiyoshiOzawa2,ChristopheBodenreider3,SiewPhengLim3, ZhengYin3,ThomasH.Keller3,DavidBeer3,ViralPatel3,GottfriedOtting2,AmedeoCaflisch1 ,Danzhi Huang1* 1DepartmentofBiochemistry,UniversityofZu¨rich,Zu¨rich,Switzerland,2ResearchSchoolofChemistry,TheAustralianNationalUniversity,Canberra,Australia,3Novartis InstituteforTropicalDiseases,Chromos,Singapore Abstract Background: The non-structural 3 protease (NS3pro) is an essential flaviviral enzyme and therefore one of the most promisingtargetsfordrugdevelopmentagainstWestNilevirus(WNV)anddengueinfections. Methodology:Inthiswork,asmall-moleculeinhibitoroftheWNVNS3prohasbeenidentifiedbyautomaticfragment-based dockingofabout12000compoundsandtestingbynuclearmagneticresonance(NMR)spectroscopyofonly22molecules. Specific binding of the inhibitor into the active site of NS3pro and its binding mode are confirmed by 15N-HSQC NMR spectra.Theinhibitoryactivityisfurthervalidatedbyanenzymaticassayandatryptophanfluorescencequenchingassay. Conclusion: The inhibitor [4-(carbamimidoylsulfanylmethyl)-2,5-dimethylphenyl]-methylsulfanylmethanimidamide has a goodratioofbindingaffinityversusmolecularweight(ligandefficiencyof0.33kcal/molpernon-hydrogenatom),andthus hasgoodpotentialasleadcompoundforfurtherdevelopmenttocombatWestNilevirusinfections. Citation:EkonomiukD,SuX-C,OzawaK,BodenreiderC,LimSP,etal.(2009)DiscoveryofaNon-PeptidicInhibitorofWestNileVirusNS3ProteasebyHigh- ThroughputDocking.PLoSNeglTropDis3(1):e356.doi:10.1371/journal.pntd.0000356 Editor:DianeJoseph-McCarthy,WyethResearch,UnitedStatesofAmerica ReceivedSeptember11,2008;AcceptedDecember14,2008;PublishedJanuary13,2009 Copyright: ?2009Ekonomiuketal.Thisisanopen-accessarticledistributedunderthetermsoftheCreativeCommonsAttributionLicense,whichpermits unrestricteduse,distribution,andreproductioninanymedium,providedtheoriginalauthorandsourcearecredited. Funding:Theautho