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44YL

crystal structure of CyaI in complex with the substrate marinacarbolines E

Summary for 44YL
Entry DOI10.2210/pdb44yl/pdb
DescriptorNocardicin N-oxygenase, 1-ethanoyl-9-methyl-~{N}-(2-phenylethyl)pyrido[3,4-b]indole-3-carboxamide, PROTOPORPHYRIN IX CONTAINING FE, ... (5 entities in total)
Functional Keywordscytochrome p450, imidazolidin formation, alkaloid cyanogramide, oxidoreductase
Biological sourceActinoalloteichus caeruleus DSM 43889
Total number of polymer chains2
Total formula weight91234.37
Authors
Zhang, L.P.,Zhu, Y.G.,Zhou, J.H.,Zhang, C.S. (deposition date: 2026-08-18, release date: 2026-09-16)
Primary citationZhu, Y.,Wang, Y.,Zhang, L.,Fang, C.,Yong, Y.,Chen, R.,Zhou, J.,Zhang, Q.,Wang, B.,Zhang, C.
A Cytochrome P450 Enzyme-Catalyzed Acetyl Migration in Cyanogramide Biosynthesis.
Angew.Chem.Int.Ed.Engl., :e7360177-e7360177, 2026
Cited by
PubMed Abstract: Cyanogramide (1) is a unique spirooxindole alkaloid derived from a marine actinomycete and is characterized by its distinct spirocyclic pyrrolo[1,2-c]imidazolidin-4-one scaffold. Although we have successfully elucidated the biosynthetic pathway of 1, the mechanism underlying the formation of the characteristic imidazolidin-4-one remains unclear. In this study, we demonstrate that the cytochrome P450 monooxygenase CyaI catalyzes an oxidation reaction through a zwitterionic intermediate and facilitates a subsequent unusual C→N acetyl migration, which triggers a spontaneous intramolecular cyclization to forge the imidazolidin-4-one ring during 1 biosynthesis. In addition, CyaI is identified as a bifunctional enzyme that also catalyzes N-demethylation. High-resolution crystallography and mutagenesis studies determine Thr245 as a crucial catalytic residue that modulates the balance between imidazolidine-4-one synthesis and demethylation. This work not only expands the catalytic repertoire of P450 enzymes but also opens the way for the development of multifunctional biocatalysts in the synthesis of complex natural products.
PubMed: 42638169
DOI: 10.1002/anie.7360177
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5 Å)
Structure validation

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PDB entries from 2026-09-16

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