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EC Number Reaction Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.117[N-(6-aminohexanoyl)]n + H2O = [N-(6-aminohexanoyl)]n-x + [N-(6-aminohexanoyl)]x - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.117[N-(6-aminohexanoyl)]n + H2O = [N-(6-aminohexanoyl)]n-x + [N-(6-aminohexanoyl)]x NylB active site with a tyrosine residue Tyr170, cleavage mechanism of the Ald amide bond in acylation of NylB is as a two-step reaction, various intermediate states, catalytic mechanism, hybrid QM/MM dynamics in combination with free-energy sampling simulations, detailed overview -, 730264
Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.117[N-(6-aminohexanoyl)]n + H2O = [N-(6-aminohexanoyl)]n-x + [N-(6-aminohexanoyl)]x the Tyr170 residue points the NH group towards the proton-acceptor site of an artificial amide bond, reaction mechanism, overview -, 734851
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