Template:Heidelberg/improved part

ß-Lactamase_E102F

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Circularization Construct
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The ß-lactamase_E102F was the outstanding candidate of our deep learning software based mutation screen, which could even grow at 19.2 mg/ml without affection by the antibiotic. This results in a improvement of at least 100 % in comparison to the wildtype ß-lactamase. This remarkable gain of activity proves, that our software is not only able to recognize protein classes, but also to generate new function.
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