3. The molecules below both inhibit proline racemase. Explain why these molecules would be potent inhibitors of this enzyme. What catalytic strategy do these molecules take advantage of? COO H Pyrrole-2-carboxylate C00 4-1-Pyrroline-2-carboxylate

EBK A SMALL SCALE APPROACH TO ORGANIC L
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Chapter32A: Preparation Of Benzoin By Thiamine Catalysis
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3. The molecules below both inhibit proline racemase. Explain why these molecules would be potent inhibitors of this
enzyme. What catalytic strategy do these molecules take advantage of?
Pyrrole-2-carboxylate
C0O
H
4-1-Pyrroline-2-carboxylate
Transcribed Image Text:3. The molecules below both inhibit proline racemase. Explain why these molecules would be potent inhibitors of this enzyme. What catalytic strategy do these molecules take advantage of? Pyrrole-2-carboxylate C0O H 4-1-Pyrroline-2-carboxylate
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