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8OF7

Cyc15 Diels Alderase

Summary for 8OF7
Entry DOI10.2210/pdb8of7/pdb
DescriptorRhs family protein, IMIDAZOLE, DI(HYDROXYETHYL)ETHER, ... (8 entities in total)
Functional Keywordsdiels alderase, cyclase, dimer, ligase
Biological sourceStreptomyces sp. NL15-2K
Total number of polymer chains2
Total formula weight35680.01
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 citationZorn, 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: 37305956
DOI: 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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数据于2024-11-06公开中

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