Abstract
Fluorescent proteins are ubiquitous as a visualization tool in biological research and efforts to improve their experimentally useful properties are of practical interest. Owing to a diversity of existing methods, such as photophysical characterization and protein structural studies, there is substantial literature about residues and secondary structures that can be altered to modulate spectroscopic properties. Yet, an efficient strategy for identifying such sites and predicting the impact of mutagenesis remains elusive.
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