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Substrate binding to ProTQQQ caused allosteric tightening associated with affinity of many SC(1-246) variants, in keeping with zymogen activation through profession of the specificity pocket. Traditional changes at jobs 1 and 2 had been well accepted, with Val1-Val2, Ile1-Ala2, and Leu1-Val2 variants displaying ProTQQQ affinity and activation effectiveness much like wild-type SC(1-246). Weaker binding variants typically had paid down activation rat

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