Sandbox Reserved 1068: Difference between revisions
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'''Isochorismate pyruvate lyase (IPL)''' | '''Isochorismate pyruvate lyase (IPL)''' | ||
Isochorismate is converted to salicylate and pyruvate through abstraction of the C2 hydrogen followed by protonation of C9 atom and the breakage of the C3-O7 bond. Histidine residue (His334) was proposed to act as a base, abstracting the C2 proton of isochorismate through a second order elimination mechanism. However, recent studies have shown that this residue lies more than 13 A away from C2 atom and no other water molecules appear close enough to the C2 atom to act as a base. IPL reaction has been proposed to proceed through an intramolecular pericyclic mechanisms, involving a concerted hydrogen transfer from C2 to C9 and breakage of the C3-O7 bond. | Isochorismate is converted to salicylate and pyruvate through abstraction of the C2 hydrogen followed by protonation of C9 atom and the breakage of the C3-O7 bond (Zwahlen 2006)<ref name="8a"/>. Histidine residue (His334) was proposed to act as a base, abstracting the C2 proton of isochorismate through a second order elimination mechanism(Zwahlen 2006)<ref name="8a"/>. However, recent studies have shown that this residue lies more than 13 A away from C2 atom and no other water molecules appear close enough to the C2 atom to act as a base(Zwahlen 2006)<ref name="8a"/>. IPL reaction has been proposed to proceed through an intramolecular pericyclic mechanisms, involving a concerted hydrogen transfer from C2 to C9 and breakage of the C3-O7 bond(Zwahlen 2006)<ref name="8a"/>. | ||
[[Image:IPL2.png|500 px|center|thumb|Figure 3: Isochorismate pyruvate activity <ref name= "8a"/>.]] | [[Image:IPL2.png|500 px|center|thumb|Figure 3: Isochorismate pyruvate activity <ref name= "8a"/>.]] | ||