8TJO
Crosslinked 6-deoxyerythronolide B synthase (DEBS) Module 1 in complex with antibody fragment 1B2: Crosslinked Intra-State 1
Summary for 8TJO
Entry DOI | 10.2210/pdb8tjo/pdb |
EMDB information | 41305 41306 41307 |
Descriptor | EryAI,6-deoxyerythronolide-B synthase EryA3, modules 5 and 6, Antibody Fragment 1B2, Heavy Chain, Antibody Fragment 1B2, Light Chain (3 entities in total) |
Functional Keywords | polyketide synthase, antibody, biosynthetic protein-immune system complex, biosynthetic protein/immune system |
Biological source | Saccharopolyspora erythraea More |
Total number of polymer chains | 6 |
Total formula weight | 482109.32 |
Authors | Cogan, D.P.,Soohoo, A.M.,Chen, M.,Brodsky, K.L.,Liu, Y.,Khosla, C. (deposition date: 2023-07-23, release date: 2024-07-24, Last modification date: 2024-09-04) |
Primary citation | Cogan, D.P.,Soohoo, A.M.,Chen, M.,Liu, Y.,Brodsky, K.L.,Khosla, C. Structural basis for intermodular communication in assembly-line polyketide biosynthesis. Nat.Chem.Biol., 2024 Cited by PubMed Abstract: Assembly-line polyketide synthases (PKSs) are modular multi-enzyme systems with considerable potential for genetic reprogramming. Understanding how they selectively transport biosynthetic intermediates along a defined sequence of active sites could be harnessed to rationally alter PKS product structures. To investigate functional interactions between PKS catalytic and substrate acyl carrier protein (ACP) domains, we employed a bifunctional reagent to crosslink transient domain-domain interfaces of a prototypical assembly line, the 6-deoxyerythronolide B synthase, and resolved their structures by single-particle cryogenic electron microscopy (cryo-EM). Together with statistical per-particle image analysis of cryo-EM data, we uncovered interactions between ketosynthase (KS) and ACP domains that discriminate between intra-modular and inter-modular communication while reinforcing the relevance of conformational asymmetry during the catalytic cycle. Our findings provide a foundation for the structure-based design of hybrid PKSs comprising biosynthetic modules from different naturally occurring assembly lines. PubMed: 39179672DOI: 10.1038/s41589-024-01709-y PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.61 Å) |
Structure validation
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