8OF7
Cyc15 Diels Alderase
Summary for 8OF7
Entry DOI | 10.2210/pdb8of7/pdb |
Descriptor | Rhs family protein, IMIDAZOLE, DI(HYDROXYETHYL)ETHER, ... (8 entities in total) |
Functional Keywords | diels alderase, cyclase, dimer, ligase |
Biological source | Streptomyces sp. NL15-2K |
Total number of polymer chains | 2 |
Total formula weight | 35680.01 |
Authors | Back, C.R.,Barringer, R.W.L.,Zorn, K.,Manzo-Ruiz, M.,Race, P.R. (deposition date: 2023-03-14, release date: 2023-06-21, Last modification date: 2024-06-19) |
Primary citation | Zorn, K.,Back, C.R.,Barringer, R.,Chadimova, V.,Manzo-Ruiz, M.,Mbatha, S.Z.,Mobarec, J.C.,Williams, S.E.,van der Kamp, M.W.,Race, P.R.,Willis, C.L.,Hayes, M.A. Interrogation of an Enzyme Library Reveals the Catalytic Plasticity of Naturally Evolved [4+2] Cyclases. Chembiochem, 24:e202300382-e202300382, 2023 Cited by PubMed Abstract: Stereoselective carbon-carbon bond forming reactions are quintessential transformations in organic synthesis. One example is the Diels-Alder reaction, a [4+2] cycloaddition between a conjugated diene and a dienophile to form cyclohexenes. The development of biocatalysts for this reaction is paramount for unlocking sustainable routes to a plethora of important molecules. To obtain a comprehensive understanding of naturally evolved [4+2] cyclases, and to identify hitherto uncharacterised biocatalysts for this reaction, we constructed a library comprising forty-five enzymes with reported or predicted [4+2] cycloaddition activity. Thirty-one library members were successfully produced in recombinant form. In vitro assays employing a synthetic substrate incorporating a diene and a dienophile revealed broad-ranging cycloaddition activity amongst these polypeptides. The hypothetical protein Cyc15 was found to catalyse an intramolecular cycloaddition to generate a novel spirotetronate. The crystal structure of this enzyme, along with docking studies, establishes the basis for stereoselectivity in Cyc15, as compared to other spirotetronate cyclases. PubMed: 37305956DOI: 10.1002/cbic.202300382 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.66 Å) |
Structure validation
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