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Sandbox 156
From Proteopedia
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| + | In the first step of the reaction, Histidine-156 abstracts a proton from the 3-hydroxyl of chloramphenicol, causing a nucleophilic attack from the deprotonated oxygen onto the thioester bond of the acetyl-CoA. The 3-acetylchloramphenicol intermediate then rearranges, non-enzymatically, to a 1-acetylchloramphenicol intermediate. CAT III then causes another acetylation of the now regenerated 3-hydroxyl and 1,3-diacetylchloramphenicol is produced. | ||
Revision as of 04:22, 21 March 2010
| Please do NOT make changes to this Sandbox until after April 23, 2010. Sandboxes 151-200 are reserved until then for use by the Chemistry 307 class at UNBC taught by Prof. Andrea Gorrell. |
