7R1V

Crystal structure of E.coli BamA beta-barrel in complex with dynobactin A

Summary for 7R1V

• Entry DOI: 10.2210/pdb7r1v/pdb
• Related PRD ID: PRD_002404
• Descriptor: Outer membrane protein assembly factor BamA, Dynobactin A (3 entities in total)
• Functional Keywords: beta-barrel, outer membrane, protein insertion, protein folding, protein maturation, antibiotic, natural product, cyclized peptide, membrane protein
• Biological source: Escherichia coli O157:H7; More
• Total number of polymer chains: 2
• Total formula weight: 45116.86

Authors

Jakob, R.P.,Hiller, S.,Maier, T. (deposition date: 2022-02-03, release date: 2022-09-28, Last modification date: 2024-04-03)

Primary citation

Miller, R.D.,Iinishi, A.,Modaresi, S.M.,Yoo, B.K.,Curtis, T.D.,Lariviere, P.J.,Liang, L.,Son, S.,Nicolau, S.,Bargabos, R.,Morrissette, M.,Gates, M.F.,Pitt, N.,Jakob, R.P.,Rath, P.,Maier, T.,Malyutin, A.G.,Kaiser, J.T.,Niles, S.,Karavas, B.,Ghiglieri, M.,Bowman, S.E.J.,Rees, D.C.,Hiller, S.,Lewis, K.
Computational identification of a systemic antibiotic for gram-negative bacteria.
Nat Microbiol, 7:1661-1672, 2022

PubMed Abstract: Discovery of antibiotics acting against Gram-negative species is uniquely challenging due to their restrictive penetration barrier. BamA, which inserts proteins into the outer membrane, is an attractive target due to its surface location. Darobactins produced by Photorhabdus, a nematode gut microbiome symbiont, target BamA. We reasoned that a computational search for genes only distantly related to the darobactin operon may lead to novel compounds. Following this clue, we identified dynobactin A, a novel peptide antibiotic from Photorhabdus australis containing two unlinked rings. Dynobactin is structurally unrelated to darobactins, but also targets BamA. Based on a BamA-dynobactin co-crystal structure and a BAM-complex-dynobactin cryo-EM structure, we show that dynobactin binds to the BamA lateral gate, uniquely protruding into its β-barrel lumen. Dynobactin showed efficacy in a mouse systemic Escherichia coli infection. This study demonstrates the utility of computational approaches to antibiotic discovery and suggests that dynobactin is a promising lead for drug development.

PubMed: 36163500
DOI: 10.1038/s41564-022-01227-4

Experimental method

X-RAY DIFFRACTION (2.5 Å)