8OVH
Crystal structure of O-acetyl-L-homoserine sulfhydrolase from Saccharomyces cerevisiae in complex with Pyridoxal-5'-phosphate
Summary for 8OVH
Entry DOI | 10.2210/pdb8ovh/pdb |
Descriptor | Homocysteine/cysteine synthase, PYRIDOXAL-5'-PHOSPHATE, DI(HYDROXYETHYL)ETHER, ... (4 entities in total) |
Functional Keywords | homocysteine/cysteine synthase, o-acetyl-l-homoserine lyase, lyase |
Biological source | Saccharomyces cerevisiae (baker's yeast) |
Total number of polymer chains | 4 |
Total formula weight | 205004.24 |
Authors | Saleem-Batcha, R.,Andexer, J.N.,Mohr, M. (deposition date: 2023-04-26, release date: 2023-06-21, Last modification date: 2024-09-25) |
Primary citation | Mohr, M.K.F.,Saleem-Batcha, R.,Cornelissen, N.V.,Andexer, J.N. Enzymatic Synthesis of l-Methionine Analogues and Application in a Methyltransferase Catalysed Alkylation Cascade. Chemistry, 29:e202301503-e202301503, 2023 Cited by PubMed Abstract: Chemical modification of small molecules is a key step for the development of pharmaceuticals. S-adenosyl-l-methionine (SAM) analogues are used by methyltransferases (MTs) to transfer alkyl, allyl and benzyl moieties chemo-, stereo- and regioselectively onto nucleophilic substrates, enabling an enzymatic way for specific derivatisation of a wide range of molecules. l-Methionine analogues are required for the synthesis of SAM analogues. Most of these are not commercially available. In nature, O-acetyl-l-homoserine sulfhydrolases (OAHS) catalyse the synthesis of l-methionine from O-acetyl-l-homoserine or l-homocysteine, and methyl mercaptan. Here, we investigated the substrate scope of ScOAHS from Saccharomyces cerevisiae for the production of l-methionine analogues from l-homocysteine and organic thiols. The promiscuous enzyme was used to synthesise nine different l-methionine analogues with modifications on the thioether residue up to a conversion of 75 %. ScOAHS was combined with an established MT dependent three-enzyme alkylation cascade, allowing transfer of in total seven moieties onto two MT substrates. For ethylation, conversion was nearly doubled with the new four-enzyme cascade, indicating a beneficial effect of the in situ production of l-methionine analogues with ScOAHS. PubMed: 37235813DOI: 10.1002/chem.202301503 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.171 Å) |
Structure validation
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