Lipase: Difference between revisions

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The carbonyl reforms with the glycerol backbone segment acting as the leaving group (Reaction 2).   
The carbonyl reforms with the glycerol backbone segment acting as the leaving group (Reaction 2).   


[[Image:M0218.stg02.gif|center|]]
[[Image:M0218.stg02r.gif|center|]]
A water molecule then donates a proton to the histidine, creating a reactive hydroxyl anion. The hydroxyl anion can then attack the carbonyl carbon of the lipid, forming another negatively charged tetrahedral intermediate which is stabilized in the oxyanion hole (Reaction 3).   
A water molecule then donates a proton to the histidine, creating a reactive hydroxyl anion. The hydroxyl anion can then attack the carbonyl carbon of the lipid, forming another negatively charged tetrahedral intermediate which is stabilized in the oxyanion hole (Reaction 3).   


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David Canner, Joel L. Sussman, Eran Hodis, Alexander Berchansky, Michal Harel, Stephanie Schell, Natalie Ziegler, Quinn R. Murray, Katelyn Clark, Leben Tadesse, Eric Martz