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9KHP

The crystal structure of XhnM1 with SAH

Summary for 9KHP
Entry DOI10.2210/pdb9khp/pdb
DescriptorClass I SAM-dependent methyltransferase, S-ADENOSYL-L-HOMOCYSTEINE, CYSTEINE, ... (7 entities in total)
Functional Keywordsmethyl group, transferase, xinhaicarxin bg
Biological sourceStreptomyces xinghaiensis
Total number of polymer chains1
Total formula weight30540.26
Authors
Wu, L.,Tang, G.L. (deposition date: 2024-11-11, release date: 2025-08-20, Last modification date: 2025-12-03)
Primary citationNie, Q.Y.,Fang, S.Q.,Wu, L.,Gao, R.Q.,Hu, Y.,Ding, D.,Pan, H.X.,Pei, Z.F.,He, J.B.,Zhou, Q.,Chen, Z.H.,Hou, X.F.,Zhao, X.Q.,Tang, G.L.
Targeted Discovery and Characterization of Type-II PKS-NRPS Hybrid DNA-Alkylating Antibiotics.
Angew.Chem.Int.Ed.Engl., 64:e202512820-e202512820, 2025
Cited by
PubMed Abstract: DNA alkylating natural products usually exhibit diverse bioactivity and serve as a crucial source of drug leads. Here, we employed genome mining guided by HTH-42 superfamily resistance gene to precisely discover a new class of DNA-alkylating antibiotics, xinghaicarcins, from Streptomyces xinghaiensis. They possess an intricate spiro-epoxide-bearing spiroketal heptacyclic scaffold fused with a pipecolic acid, assembled by a type II polyketide synthase-nonribosomal peptide synthetase hybrid system. An aminotransferase XhnB1 and a methyltransferase XhnM are identified to catalyze the formation of N-methylated pipecolic acid building block, leading to the completion of the polyketide-peptide backbone. The identification of XhnM facilitated stereochemical determination of six chiral centers in xinghaicarcins by co-crystallization. Notably, xinghaicarcins exhibit potent antibacterial activity against drug-resistant pathogens and cytotoxicity against multiple cancer cell lines. Additionally, the HTH-42 superfamily resistant protein, XhnU2, was characterized to mitigate xinghaicarcin-induced genotoxicity. This work provides comprehensive insights into structure, biosynthesis, bioactivity, and self-resistance mechanisms of xinghaicarcins, expanding diversity of DNA alkylating natural products.
PubMed: 40761108
DOI: 10.1002/anie.202512820
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.73006100024 Å)
Structure validation

246031

数据于2025-12-10公开中

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