Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10871707 | FEBS Letters | 2012 | 9 Pages |
Abstract
⺠Catalytic promiscuity can potentially play an important role in enzyme evolution. ⺠We theoretically probed the highly promiscuous arylsulfatase from P. aeruginosa. ⺠The enzyme tightens all transition states, particularly for the native reaction. ⺠An active site lysine with depressed pKa appears to be a “specificity switch”. ⺠The molecular basis for the promiscuity appears to be purely electrostatic.
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Authors
Jinghui Luo, Bert van Loo, Shina C.L. Kamerlin,