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Exploring the kinase-inhibitor fragment interaction space facilitates the discovery of kinase inhibitor overcoming resistance by mutations

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成果类型:
期刊论文
作者:
Wang, Zhi-Zheng;Wang, Ming-Shu;Wang, Fan;Shi, Xing-Xing;Huang, Wei;...
通讯作者:
Wei Huang<&wdkj&>Ge-Fei Hao<&wdkj&>Guang-Fu Yang
作者机构:
[Wang, Zhi-Zheng] Cent China Normal Univ CCNU, Coll Chem, Wuhan, Peoples R China.
[Hao, Ge-Fei] Guizhou Univ, Key Lab Green Pesticide & Agr Bioengn, Guiyang, Peoples R China.
[Yang, Guang-Fu; Wang, Ming-Shu; Shi, Xing-Xing; Huang, Wei; Wang, Fan] CCNU, Coll Chem, Wuhan, Peoples R China.
[Hao, Ge-Fei] CCNU, Key Lab Pesticide & Chem Biol, Bioinformat, Wuhan, Peoples R China.
通讯机构:
[Wei Huang; Ge-Fei Hao; Guang-Fu Yang] K
Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, International Joint Research Center for Intelligent Biosensor Technology and Health, College of Chemistry, Central China Normal University , Wuhan, 430079 , P. R. China
语种:
英文
关键词:
fragment-based drug discovery;drug resistance;web platform;fragment growing;TRK inhibitor
期刊:
BRIEFINGS IN BIOINFORMATICS
ISSN:
1467-5463
年:
2022
卷:
23
期:
4
基金类别:
National Key Research and Development Program of China (2021YFD1700102), the National Natural Science Foundation of China (32125033), and the Key Research and Development Program of Hubei Province, China (2020BCB042). Program of Introducing Talents of Discipline to Universities of China (111 Program, D20023) and the Key Research and Development Program of Hubei Province, China (2020BCB042).
机构署名:
本校为第一机构
院系归属:
化学学院
摘要:
Protein kinases play crucial roles in many cellular signaling processes, making them become important targets for drug discovery. But drug resistance mediated by mutation puts a barrier to the therapeutic effect of kinase inhibitors. Fragment-based drug discovery has been successfully applied to overcome such resistance. However, the complicate kinase-inhibitor fragment interaction and fragment-to-lead process seriously limit the efficiency of kinase inhibitor discovery against resistance caused by mutation. Here, we constructed a comprehensive web platform KinaFrag for the fragment-based kina...

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