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ACS Chemical Biology|April 7, 2015
Substrate-Controlled Stereochemistry in Natural Product BiosynthesisWei Ding, Yongzhen Li, Qi ZhangAngewandte Chemie (International Ed. in English)|July 4, 2015
Substrate-Tuned Catalysis of the Radical S-Adenosyl-L-Methionine Enzyme NosL Involved in Nosiheptide BiosynthesisXinjian Ji, Yongzhen Li, Wei Ding, et al.Frontiers in Chemistry|July 23, 2016
Catalytic Promiscuity of the Radical S-adenosyl-L-methionine Enzyme NosLWei Ding, Xinjian Ji, Yongzhen Li, et al.Angewandte Chemie (International Ed. in English)|February 3, 2016
Mechanistic Insights into the Radical S-adenosyl-l-methionine Enzyme NosL From a Substrate Analogue and the Shunt ProductsXinjian Ji, Yongzhen Li, Youli Jia, et al.Angewandte Chemie (International Ed. in English)|August 31, 2016
Expanding Radical SAM Chemistry by Using Radical Addition Reactions and SAM AnaloguesXinjian Ji, Yongzhen Li, Liqi Xie, et al.Chemical Communications (Cambridge, England)|July 4, 2017
A mechanistic study of the non-oxidative decarboxylation catalyzed by the radical S-adenosyl-l-methionine enzyme BlsE involved in blasticidin S biosynthesisLei Liu, Xinjian Ji, Yongzhen Li, et al.Proceedings of the National Academy of Sciences of the United States of America|March 17, 2016
Biosynthetic investigation of phomopsins reveals a widespread pathway for ribosomal natural products in AscomycetesWei Ding, Wan-Qiu Liu, Youli Jia, et al.Journal of the American Chemical Society|April 28, 2016
Characterization of a C3 Deoxygenation Pathway Reveals a Key Branch Point in Aminoglycoside BiosynthesisMeinan Lv, Xinjian Ji, Junfeng Zhao, et al.Angewandte Chemie (International Ed. in English)|January 24, 2017
The Catalytic Mechanism of the Class C Radical S-Adenosylmethionine Methyltransferase NosNWei Ding, Yongzhen Li, Junfeng Zhao, et al.RSC Chemical Biology|February 9, 2024
Discovery and engineering of ribosomally synthesized and post-translationally modified peptide (RiPP) natural productsHe Li, Wei Ding, Qi ZhangPageof 1,411