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. 2019 Apr 5;6(Pt 3):401–411. doi: 10.1107/S2052252519002926

Figure 5.

Figure 5

Mutation of Asn373 enhances the ability of FhuE to utilize ferrioxamine B. (a) A solid agar growth assay showing the enhanced ability of the N373A mutant to support growth using ferrioxamine B as an iron source relative to the growth observed in the presence of FhuE. (b) Structural modelling of the N373A mutant with ferrioxamine B docked into the substrate-binding pocket. The removal of the asparagine side chain opens the substrate-binding channel of FhuE to better accommodate ferrioxamine B. (c) The position of Asn373 (blue sticks) relative to coprogen (left) and ferrioxamine B (right). In the crystal structure, Asn373 forms a hydrogen bond to a carbonyl group from the coprogen diketopiperazine ring. This group is not present in ferrioxamine B.