Richard Russell Wenwen Wang, 1, * Aihua Mei, 1, * Hang Qian, 1, * Dongfeng Li, 1 Hao Xu, 1 Jishun Chen, 1 Handong Yang, 1 Xinwen Min, 1 Chunlei Li, 1 Li Cheng, 1 Jun Chen 1, 2 1 Sinopharm Dongfeng General Hospital, Hubei University of Medicine, Hubei Key Laboratory of Wudang Local Chinese Medicine Research (Hubei University of Medicine), Shiyan, Peoples Republic of China
2014), the FAK-paxillin pathway (Chang et al
Docking analysis revealed a binding energy of 9.4 kcal/mol (Figure 1B), which corresponds to an estimated inhibition constant (Ki) of approximately 0.13 M, indicating a highly potent inhibitory effect
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Elongation to the D- O -Leu-D-Ala-L- O -Val-L-Val chain is presumably followed by transfer to the hydroxy group of a serine of the thioesterase (TE) domain, while a second tetradepsipeptide builds up on the adjacent PCP of CesB
