8TWN
Crystal structure of nitrile synthase AetD with substrate bound
Summary for 8TWN
| Entry DOI | 10.2210/pdb8twn/pdb |
| Descriptor | AetD, (2S)-2-azanyl-3-[5,7-bis(bromanyl)-1H-indol-3-yl]propanoic acid, D-MALATE, ... (4 entities in total) |
| Functional Keywords | nitrile synthase, non-heme iron enzyme, diiron enzyme, oxidoreductase |
| Biological source | Aetokthonos hydrillicola |
| Total number of polymer chains | 1 |
| Total formula weight | 31136.83 |
| Authors | Ye, N.,Drennan, C.L. (deposition date: 2023-08-21, release date: 2024-08-28, Last modification date: 2024-12-18) |
| Primary citation | Adak, S.,Ye, N.,Calderone, L.A.,Duan, M.,Lubeck, W.,Schafer, R.J.B.,Lukowski, A.L.,Houk, K.N.,Pandelia, M.E.,Drennan, C.L.,Moore, B.S. A single diiron enzyme catalyses the oxidative rearrangement of tryptophan to indole nitrile. Nat.Chem., 16:1989-1998, 2024 Cited by PubMed Abstract: Nitriles are uncommon in nature and are typically constructed from oximes through the oxidative decarboxylation of amino acid substrates or from the derivatization of carboxylic acids. Here we report a third nitrile biosynthesis strategy featuring the cyanobacterial nitrile synthase AetD. During the biosynthesis of the eagle-killing neurotoxin, aetokthonotoxin, AetD transforms the 2-aminopropionate portion of 5,7-dibromo-L-tryptophan to a nitrile. Employing a combination of structural, biochemical and biophysical techniques, we characterized AetD as a non-haem diiron enzyme that belongs to the emerging haem-oxygenase-like dimetal oxidase superfamily. High-resolution crystal structures of AetD together with the identification of catalytically relevant products provide mechanistic insights into how AetD affords this unique transformation, which we propose proceeds via an aziridine intermediate. Our work presents a unique template for nitrile biogenesis and portrays a substrate binding and metallocofactor assembly mechanism that may be shared among other haem-oxygenase-like dimetal oxidase enzymes. PubMed: 39285206DOI: 10.1038/s41557-024-01603-z PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.08 Å) |
Structure validation
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