CIPDB: A biological structure databank for studying cation and '7C interactions
文献类型: 外文期刊
第一作者: Yang, Jing-Fang
作者: Yang, Jing-Fang;Wang, Fan;Wang, Meng-Yao;Wang, Di;Hao, Ge-Fei;Yang, Guang-Fu;Yang, Jing-Fang;Wang, Fan;Wang, Meng-Yao;Wang, Di;Hao, Ge-Fei;Yang, Guang-Fu;Yang, Jing-Fang;Zhou, Zhong-Shi;Hao, Ge-Fei;Li, Qing X.;Yang, Guang-Fu
作者机构:
关键词: cation -p; noncovalent interaction; dataset; biological; function; structure; drug; pesticide
期刊名称:DRUG DISCOVERY TODAY ( 影响因子:7.4; 五年影响因子:8.1 )
ISSN: 1359-6446
年卷期: 2023 年 28 卷 5 期
页码:
收录情况: SCI
摘要: As major forces for modulating protein folding and molecular recognition, cation and 7C interactions are extensively identified in protein structures. They are even more competitive than hydrogen bonds in molecular recognition, thus, are vital in numerous biological pro-cesses. In this review, we introduce the methods for the identification and quantification of cation and 7C interac-tions, provide insights into the characteristics of cation and 7C interactions in the natural state, and reveal their biological function together with our developed database (Cation and 7C Interaction in Protein Data Bank; CIPDB; http://chemyang.ccnu.edu.cn/ccb/database/CIPDB). This review lays the foundation for the in-depth study of cation and rc interactions and will guide the use of molecular design for drug discovery.
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