Structural basis of keto acid utilization in nonribosomal depsipeptide synthesis.
Diego A AlonzoClarisse Chiche-LapierreMichael J TarryJimin WangT Martin SchmeingPublished in: Nature chemical biology (2020)
Nonribosomal depsipeptides are natural products composed of amino and hydroxy acid residues. The hydroxy acid residues often derive from α-keto acids, reduced by ketoreductase domains in the depsipeptide synthetases. Biochemistry and structures reveal the mechanism of discrimination for α-keto acids and a remarkable architecture: flanking intact adenylation and ketoreductase domains are sequences separated by >1,100 residues that form a split 'pseudoAsub' domain, structurally important for the depsipeptide module's synthetic cycle.