8qpo
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E. coli NfsB with the unnatural amino acid p-nitrophenylalanine at position 124.
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Structural highlights
FunctionNFSB_ECOLI Reduction of a variety of nitroaromatic compounds using NADH (and to lesser extent NADPH) as source of reducing equivalents; two electrons are transferred. Capable of reducing nitrofurazone, quinones and the anti-tumor agent CB1954 (5-(aziridin-1-yl)-2,4-dinitrobenzamide). The reduction of CB1954 results in the generation of cytotoxic species.[1] References
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This page was last modified 08:16, 14 August 2024.