Heterochiral coupling in non-ribosomal peptide macrolactamization
Heterochiral coupling is favoured in abiotic peptide bond formation, whereas biotic peptide bond formation is dominated by homochiral coupling. Here, we report that heterochiral coupling is a rather general paradigm in the head-to-tail macrolactamization of non-ribosomal peptide biosynthesis. The canonical cis-acting offloading cyclases, such as type I
openaire
Macrocyclizing-thioesterases in bacterial non-ribosomal peptide biosynthesis. [PDF]
Matsuda K.
europepmc +1 more source
Scalable Total Synthesis, IP3R Inhibitory Activity of Desmethylxestospongin B, and Effect on Mitochondrial Function and Cancer Cell Survival. [PDF]
Podunavac M +8 more
europepmc +1 more source
Isolation, total synthesis and structure determination of antifungal macrocyclic depsipeptide, tetraselide. [PDF]
Nakahara H +9 more
europepmc +1 more source
Multistep Cascade Catalyzed by a Single-Chiral Lewis Acid: Efficient Asymmetric Synthesis of Macrocyclic Chiral Dilactones and Dilactams. [PDF]
Wang BL, Yu JQ, Zhang Q, Wang XW.
europepmc +1 more source
Rapid Peptide Cyclization Inspired by the Modular Logic of Nonribosomal Peptide Synthetases. [PDF]
Ding Y +12 more
europepmc +1 more source
Stereoselective Synthesis and Antiproliferative Activity of Nemamide Analogs. [PDF]
Yu R +6 more
europepmc +1 more source
Chemoenzymatic synthesis of macrocyclic peptides and polyketides via thioesterase-catalyzed macrocyclization. [PDF]
Qiao S, Cheng Z, Li F.
europepmc +1 more source
Non-ribosomal peptide cyclase-directed chemoenzymatic synthesis of lariat lipopeptides. [PDF]
Kobayashi M +11 more
europepmc +1 more source
Synergy of Prediction Rule and Total Synthesis in Solving the Stereochemical Puzzle of Valactamides. [PDF]
Zhang T, Feng J, Oikawa H, Guo Y, Ye T.
europepmc +1 more source

