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Directed evolution of piperazic acid incorporation by a nonribosomal peptide synthetase**
Stephan, P., Langley, C., Winkler, D., Basquin, J., Caputi, L., O'Connor, S. E., & Kries, H. (2023). Directed evolution of piperazic acid incorporation by a nonribosomal peptide synthetase**. Angewandte Chemie International Edition, 62(35), e202304843 (6 pp.). https://doi.org/10.1002/anie.202304843
HaloTag engineering for enhanced fluorogenicity and kinetics with a styrylpyridium dye
Miró-Vinyals, C., Stein, A., Fischer, S., Ward, T. R., & Deliz Liang, A. (2021). HaloTag engineering for enhanced fluorogenicity and kinetics with a styrylpyridium dye. ChemBioChem, 22(24), 3398-3401. https://doi.org/10.1002/cbic.202100424
Evolved, selective erasers of distinct lysine acylations
Spinck, M., Neumann-Staubitz, P., Ecke, M., Gasper, R., & Neumann, H. (2020). Evolved, selective erasers of distinct lysine acylations. Angewandte Chemie International Edition, 59(27), 11142-11149. https://doi.org/10.1002/anie.202002899
Directed evolution of an artificial imine reductase
Hestericová, M., Heinisch, T., Alonso-Cotchico, L., Maréchal, J. D., Vidossich, P., & Ward, T. R. (2018). Directed evolution of an artificial imine reductase. Angewandte Chemie International Edition, 57(7), 1863-1868. https://doi.org/10.1002/anie.201711016
Unveiling the basis of alkaline stability of an evolved versatile peroxidase
Saez-Jimenez, V., Acebes, S., Garcia-Ruiz, E., Romero, A., Guallar, V., Alcalde, M., … Ruiz-Duenas, F. J. (2016). Unveiling the basis of alkaline stability of an evolved versatile peroxidase. Biochemical Journal, 473(13), 1917-1928. https://doi.org/10.1042/BCJ20160248
Generation of fluorogen-activating designed ankyrin repeat proteins (FADAs) as versatile sensor tools
Schütz, M., Batyuk, A., Klenk, C., Kummer, L., De Picciotto, S., Gülbakan, B., … Plückthun, A. (2016). Generation of fluorogen-activating designed ankyrin repeat proteins (FADAs) as versatile sensor tools. Journal of Molecular Biology, 428(6), 1272-1289. https://doi.org/10.1016/j.jmb.2016.01.017
A promiscuous de novo retro-aldolase catalyzes asymmetric Michael additions via Schiff base intermediates
Garrabou, X., Beck, T., & Hilvert, D. (2015). A promiscuous de novo retro-aldolase catalyzes asymmetric Michael additions via Schiff base intermediates. Angewandte Chemie International Edition, 54(19), 5609-5612. https://doi.org/10.1002/anie.201500217