Proteins · 2026
Structural Analysis and Inhibitor Modeling of Bacterioferritin From Brucella abortus.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Liu Lijun, Harmon Elizabeth K, Craig Justin K, Yao Huili, Battaile Kevin P, Johnson David K, Subramanian Sandhya, Van Voorhis Wesley C, Rivera Mario, Lovell Scott
Аннотация
Iron homeostasis in various pathogenic bacteria is regulated by bacterioferritins (Bfr) which function to store Fe3+ and release Fe2+ as needed for metabolic processes. The Bfr structure consists of 18 kDa subunits in which dimer pairs bind a heme molecule and are assembled into a highly symmetrical 24-meric spherical structure with an internal core diameter of approximately 80 Å. Release of iron is facilitated by the binding of a 7 kDa [2Fe-2S] ferredoxin (Bfd) to specific sites on the surface of Bfr which transfers electrons to the core thereby reducing the stored Fe3+ to Fe2+ for mobilization. The crystal structures of Bfr from Brucella abortus (Ba) in the apo and iron bound forms are presented and compared with those from Acinetobacter baumannii (Ab) and Pseudomonas aeruginosa (Pa). Additionally, models of the Bfr:Bfd complexes for Ba and Ab are provided and compared with the Pa complex. Finally, compounds known to target the Bfr:Bfd interaction in Pa were docked to the Ba and Ab structures which provided insight regarding the potential binding mode and inhibitory mechanism.