8Y9E
Versatile Aromatic Prenyltransferase auraA for Imidazole-Containing Diketopiperazines
Summary for 8Y9E
Entry DOI | 10.2210/pdb8y9e/pdb |
EMDB information | 39075 |
Descriptor | Versatile Aromatic Prenyltransferase auraA (1 entity in total) |
Functional Keywords | prenyltransferase, imidazole-containing diketopiperazines, transferase |
Biological source | Penicillium |
Total number of polymer chains | 4 |
Total formula weight | 195902.26 |
Authors | |
Primary citation | Wang, W.,Wang, P.,Ma, C.,Li, K.,Wang, Z.,Liu, Y.,Wang, L.,Zhang, G.,Che, Q.,Zhu, T.,Zhang, Y.,Li, D. Characterization and structural analysis of a versatile aromatic prenyltransferase for imidazole-containing diketopiperazines. Nat Commun, 16:144-144, 2025 Cited by PubMed Abstract: Prenylation modifications of natural products play essential roles in chemical diversity and bioactivities, but imidazole modification prenyltransferases are not well investigated. Here, we discover a dimethylallyl tryptophan synthase family prenyltransferase, AuraA, that catalyzes the rare dimethylallylation on the imidazole moiety in the biosynthesis of aurantiamine. Biochemical assays validate that AuraA could accept both cyclo-(L-Val-L-His) and cyclo-(L-Val-DH-His) as substrates, while the prenylation modes are completely different, yielding C2-regular and C5-reverse products, respectively. Cryo-electron microscopy analysis of AuraA and its two ternary complex structures reveal two distinct modes for receptor binding, demonstrating a tolerance for altered orientations of highly similar receptors. The mutation experiments further demonstrate the promiscuity of AuraA towards imidazole-C-dimethylallylation. In this work, we also characterize a case of AuraA mutant-catalyzed dimethylallylation of imidazole moiety, offering available structural insights into the utilization and engineering of dimethylallyl tryptophan synthase family prenyltransferases. PubMed: 39747040DOI: 10.1038/s41467-024-55537-8 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.95 Å) |
Structure validation
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