8SCD

Crystal structure of sulfonamide resistance enzyme Sul3 in complex with reaction intermediate

Summary for 8SCD

• Entry DOI: 10.2210/pdb8scd/pdb
• Related: 7S2I 7S2J 7S2K 7S2L 7S2M 7TQ1
• Descriptor: Sulfonamide resistance enzyme Sul3, 2-amino-6-methylidene-6,7-dihydropteridin-4(3H)-one, 4-AMINOBENZOIC ACID, ... (8 entities in total)
• Functional Keywords: tim barrel, alpha beta protein, antibiotic resistance, sulfonamides, structural genomics, csgid, center for structural genomics of infectious diseases, csbid, center for structural biology of infectious diseases, niaid, national institute of allergy and infectious diseases, transferase
• Biological source: uncultured bacterium
• Total number of polymer chains: 1
• Total formula weight: 29751.38

Authors

Stogios, P.J.,Venkatesan, M.,Michalska, K.,Mesa, N.,Di Leo, R.,Savchenko, A.,Joachimiak, A.,Satchell, K.J.F.,Center for Structural Biology of Infectious Diseases (CSBID),Center for Structural Genomics of Infectious Diseases (CSGID) (deposition date: 2023-04-05, release date: 2023-05-03, Last modification date: 2024-05-22)

Primary citation

Venkatesan, M.,Fruci, M.,Verellen, L.A.,Skarina, T.,Mesa, N.,Flick, R.,Pham, C.,Mahadevan, R.,Stogios, P.J.,Savchenko, A.
Molecular mechanism of plasmid-borne resistance to sulfonamide antibiotics.
Nat Commun, 14:4031-4031, 2023

PubMed Abstract: The sulfonamides (sulfas) are the oldest class of antibacterial drugs and inhibit the bacterial dihydropteroate synthase (DHPS, encoded by folP), through chemical mimicry of its co-substrate p-aminobenzoic acid (pABA). Resistance to sulfa drugs is mediated either by mutations in folP or acquisition of sul genes, which code for sulfa-insensitive, divergent DHPS enzymes. While the molecular basis of resistance through folP mutations is well understood, the mechanisms mediating sul-based resistance have not been investigated in detail. Here, we determine crystal structures of the most common Sul enzyme types (Sul1, Sul2 and Sul3) in multiple ligand-bound states, revealing a substantial reorganization of their pABA-interaction region relative to the corresponding region of DHPS. We use biochemical and biophysical assays, mutational analysis, and in trans complementation of E. coli ΔfolP to show that a Phe-Gly sequence enables the Sul enzymes to discriminate against sulfas while retaining pABA binding and is necessary for broad resistance to sulfonamides. Experimental evolution of E. coli results in a strain harboring a sulfa-resistant DHPS variant that carries a Phe-Gly insertion in its active site, recapitulating this molecular mechanism. We also show that Sul enzymes possess increased active site conformational dynamics relative to DHPS, which could contribute to substrate discrimination. Our results reveal the molecular foundation for Sul-mediated drug resistance and facilitate the potential development of new sulfas less prone to resistance.

PubMed: 37419898
DOI: 10.1038/s41467-023-39778-7

Experimental method

X-RAY DIFFRACTION (2.06 Å)