A Covalent Succinylcysteine-like Intermediate in the Enzyme-Catalyzed Transformation of Maleate to Fumarate by Maleate Isomerase

Maleate isomerase (MI), a member of the Asp/Glu racemase superfamily, catalyzes cis−trans isomerization of the C2−C3 double bond in maleate to yield fumarate. Mutational studies, in conjunction with the structure of the C194A mutant of Nocardia farcinica MI cocrystallized with maleate, have revealed...

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Veröffentlicht in:Journal of the American Chemical Society 2010-08, Vol.132 (33), p.11455-11457
Hauptverfasser: Fisch, Florian, Fleites, Carlos Martinez, Delenne, Marie, Baudendistel, Nina, Hauer, Bernhard, Turkenburg, Johan P., Hart, Sam, Bruce, Neil C., Grogan, Gideon
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Sprache:eng
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Zusammenfassung:Maleate isomerase (MI), a member of the Asp/Glu racemase superfamily, catalyzes cis−trans isomerization of the C2−C3 double bond in maleate to yield fumarate. Mutational studies, in conjunction with the structure of the C194A mutant of Nocardia farcinica MI cocrystallized with maleate, have revealed an unprecedented mode of catalysis for the superfamily in which the isomerization reaction is initiated by nucleophilic attack of cysteine at the double bond, yielding a covalent succinylcysteine-like intermediate.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja1053576