8DLE
Crosslinked Crystal Structure of the 8-amino-7-oxonanoate synthase, BioF, and Benzene Sulfonyl Fluoride-crypto Acyl Carrier Protein, BSF-ACP
Summary for 8DLE
Entry DOI | 10.2210/pdb8dle/pdb |
Descriptor | 8-amino-7-oxononanoate synthase, Acyl carrier protein, PYRIDOXAL-5'-PHOSPHATE, ... (7 entities in total) |
Functional Keywords | biof, aons, crosslinking, acp, complex, plp, transferase |
Biological source | Escherichia coli More |
Total number of polymer chains | 2 |
Total formula weight | 52574.77 |
Authors | Chen, A.,Davis, T.D.,Louie, G.V.,Bowman, M.E.,Noel, J.P.,Burkart, M.D. (deposition date: 2022-07-07, release date: 2023-07-12, Last modification date: 2024-07-24) |
Primary citation | Chen, A.,Re, R.N.,Davis, T.D.,Tran, K.,Moriuchi, Y.W.,Wu, S.,La Clair, J.J.,Louie, G.V.,Bowman, M.E.,Clarke, D.J.,Mackay, C.L.,Campopiano, D.J.,Noel, J.P.,Burkart, M.D. Visualizing the Interface of Biotin and Fatty Acid Biosynthesis through SuFEx Probes. J.Am.Chem.Soc., 146:1388-1395, 2024 Cited by PubMed Abstract: Site-specific covalent conjugation offers a powerful tool to identify and understand protein-protein interactions. In this study, we discover that sulfur fluoride exchange (SuFEx) warheads effectively crosslink the acyl carrier protein (AcpP) with its partner BioF, a key pyridoxal 5'-phosphate (PLP)-dependent enzyme in the early steps of biotin biosynthesis by targeting a tyrosine residue proximal to the active site. We identify the site of crosslink by MS/MS analysis of the peptide originating from both partners. We further evaluate the BioF-AcpP interface through protein crystallography and mutational studies. Among the AcpP-interacting BioF surface residues, three critical arginine residues appear to be involved in AcpP recognition so that pimeloyl-AcpP can serve as the acyl donor for PLP-mediated catalysis. These findings validate an evolutionary gain-of-function for BioF, allowing the organism to build biotin directly from fatty acid biosynthesis through surface modifications selective for salt bridge formation with acidic AcpP residues. PubMed: 38176024DOI: 10.1021/jacs.3c10181 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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