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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 DOI10.2210/pdb8dle/pdb
Descriptor8-amino-7-oxononanoate synthase, Acyl carrier protein, PYRIDOXAL-5'-PHOSPHATE, ... (7 entities in total)
Functional Keywordsbiof, aons, crosslinking, acp, complex, plp, transferase
Biological sourceEscherichia coli
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Total number of polymer chains2
Total formula weight52574.77
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 citationChen, 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: 38176024
DOI: 10.1021/jacs.3c10181
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

238895

數據於2025-07-16公開中

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