8ZN0
The Crystal Structure of an Atypical N-methyltransferasea PaOMT9 in P. amurense
This is a non-PDB format compatible entry.
Summary for 8ZN0
| Entry DOI | 10.2210/pdb8zn0/pdb |
| Descriptor | PaOMT9, S-ADENOSYLMETHIONINE, (1~{S})-1-[(4-hydroxyphenyl)methyl]-6-methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol, ... (4 entities in total) |
| Functional Keywords | n-methyltransferasea paomt9, transferase |
| Biological source | Phellodendron amurense |
| Total number of polymer chains | 2 |
| Total formula weight | 81507.96 |
| Authors | |
| Primary citation | Xu, Z.,Tian, Y.,Wang, J.,Ma, Y.,Li, Q.,Zhou, Y.,Zhang, W.,Liu, T.,Kong, L.,Wang, Y.,Xie, Z.,An, Z.,Zheng, B.,Zhang, Y.,Cao, C.,Liu, C.,Tian, L.,Fan, C.,Liu, J.,Yao, H.,Song, J.,Duan, B.,Liu, H.,Gao, R.,Sun, W.,Chen, S. Convergent evolution of berberine biosynthesis. Sci Adv, 10:eads3596-eads3596, 2024 Cited by PubMed Abstract: Berberine is an effective antimicrobial and antidiabetic alkaloid, primarily extracted from divergent botanical lineages, specifically (Ranunculales, early-diverging eudicot) and (Sapindales, core eudicot). In comparison with its known pathway in species, its biosynthesis in species remains elusive. Using chromosome-level genome assembly, coexpression matrix, and biochemical assays, we identified six key steps in berberine biosynthesis from , including methylation, hydroxylation, and berberine bridge formation. Notably, we discovered a specific class of -methyltransferases (NOMT) responsible for -methylation. Structural analysis and mutagenesis of PaNOMT9 revealed its unique substrate-binding conformation. In addition, unlike the classical FAD-dependent berberine bridge formation in Ranunculales, uses a NAD(P)H-dependent monooxygenase (PaCYP71BG29) for berberine bridge formation, originating from the neofunctionalization of tryptamine 5-hydroxylase. Together, these findings reveal the convergence of berberine biosynthesis between and and signify the role of the convergent evolution in plant specialized metabolisms. PubMed: 39612339DOI: 10.1126/sciadv.ads3596 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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