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Tracking the redox reaction of the iron enzyme ribonucleotide reductase using continuous SerialED and SFX
Serial femtosecond crystallography (SFX) and continuous serial electron diffraction (c-SerialED) both enable high-resolution structure determination from protein microcrystals with minimal radiation damage, making it ideal for studying redox-active metalloenzymes. Here, c-SerialED and SFX were used
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