6LYI
Crystal structure of a N-methyltransferase CkTbS from Camellia assamica var. kucha
Summary for 6LYI
Entry DOI | 10.2210/pdb6lyi/pdb |
Descriptor | N-methyltransferase CkTbS (2 entities in total) |
Functional Keywords | cktbs, n-methyltransferase, tea, transferase |
Biological source | Camellia sinensis var. assamica |
Total number of polymer chains | 2 |
Total formula weight | 82888.46 |
Authors | Wang, Y.,Zhang, Z.M. (deposition date: 2020-02-14, release date: 2020-03-04, Last modification date: 2023-11-29) |
Primary citation | Zhang, Y.H.,Li, Y.F.,Wang, Y.,Tan, L.,Cao, Z.Q.,Xie, C.,Xie, G.,Gong, H.B.,Sun, W.Y.,Ouyang, S.H.,Duan, W.J.,Lu, X.,Ding, K.,Kurihara, H.,Hu, D.,Zhang, Z.M.,Abe, I.,He, R.R. Identification and characterization of N9-methyltransferase involved in converting caffeine into non-stimulatory theacrine in tea. Nat Commun, 11:1473-1473, 2020 Cited by PubMed Abstract: Caffeine is a major component of xanthine alkaloids and commonly consumed in many popular beverages. Due to its occasional side effects, reduction of caffeine in a natural way is of great importance and economic significance. Recent studies reveal that caffeine can be converted into non-stimulatory theacrine in the rare tea plant Camellia assamica var. kucha (Kucha), which involves oxidation at the C8 and methylation at the N9 positions of caffeine. However, the underlying molecular mechanism remains unclear. Here, we identify the theacrine synthase CkTcS from Kucha, which possesses novel N9-methyltransferase activity using 1,3,7-trimethyluric acid but not caffeine as a substrate, confirming that C8 oxidation takes place prior to N9-methylation. The crystal structure of the CkTcS complex reveals the key residues that are required for the N9-methylation, providing insights into how caffeine N-methyltransferases in tea plants have evolved to catalyze regioselective N-methylation through fine tuning of their active sites. These results may guide the future development of decaffeinated drinks. PubMed: 32193380DOI: 10.1038/s41467-020-15324-7 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.49 Å) |
Structure validation
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