8ALL
NMR structure of holo-acp
Summary for 8ALL
Entry DOI | 10.2210/pdb8all/pdb |
NMR Information | BMRB: 34744 |
Descriptor | Hybrid non ribosomal peptide synthetase-polyketide synthase, 4'-PHOSPHOPANTETHEINE (2 entities in total) |
Functional Keywords | acyl carrier protein, transferase |
Biological source | Streptomyces virginiae |
Total number of polymer chains | 1 |
Total formula weight | 9296.41 |
Authors | Collin, S.,Weissman, K.J.,Chagot, B.,Gruez, A. (deposition date: 2022-08-01, release date: 2023-03-22, Last modification date: 2023-03-29) |
Primary citation | Collin, S.,Cox, R.J.,Paris, C.,Jacob, C.,Chagot, B.,Weissman, K.J.,Gruez, A. Decrypting the programming of beta-methylation in virginiamycin M biosynthesis. Nat Commun, 14:1327-1327, 2023 Cited by PubMed Abstract: During biosynthesis by multi-modular trans-AT polyketide synthases, polyketide structural space can be expanded by conversion of initially-formed electrophilic β-ketones into β-alkyl groups. These multi-step transformations are catalysed by 3-hydroxy-3-methylgluratryl synthase cassettes of enzymes. While mechanistic aspects of these reactions have been delineated, little information is available concerning how the cassettes select the specific polyketide intermediate(s) to target. Here we use integrative structural biology to identify the basis for substrate choice in module 5 of the virginiamycin M trans-AT polyketide synthase. Additionally, we show in vitro that module 7, at minimum, is a potential additional site for β-methylation. Indeed, analysis by HPLC-MS coupled with isotopic labelling and pathway inactivation identifies a metabolite bearing a second β-methyl at the expected position. Collectively, our results demonstrate that several control mechanisms acting in concert underpin β-branching programming. Furthermore, variations in this control - whether natural or by design - open up avenues for diversifying polyketide structures towards high-value derivatives. PubMed: 36899003DOI: 10.1038/s41467-023-36974-3 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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