2004Journal of the American Chemical SocietyRequires access

Mirror “Base-off” Conformation of Coenzyme B 12 in Human Adenosyltransferase and Its Downstream Target, Methylmalonyl-CoA Mutase

Mamoru Yamanishi, Tetyana Labunska, Ruma V. Banerjee

Open publisher page 50 citations

Abstract

Human adenosyltransferase synthesizes coenzyme B12, for the target mitochondrial B12 enzyme, methylmalonyl-CoA mutase. It binds B12 in the "base-off" conformation in both the Co2+ and Co3+ oxidation states as revealed by UV-visible and EPR spectroscopy although it lacks the signature DXHXXG motif found in other B12 proteins that bind the cofactor in this conformation. The "base-off" conformation, which is rare at physiological pH, mirrors that in the target enzyme, methylmalonyl-CoA mutase, which utilizes the product, AdoCbl. However, the coordination environment for cobalt in the two proteins is distinct, which is reflected in an approximately 40-fold difference in their affinity for the cofactor.

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What this paper is about

Human adenosyltransferase synthesizes coenzyme B12, for the target mitochondrial B12 enzyme, methylmalonyl-CoA mutase. It binds B12 in the "base-off" conformation in both the Co2+ and Co3+ oxidation states as revealed by UV-visible and EPR spectroscopy although it lacks the signature DXHXXG motif found in other B12 proteins that bind the cofactor in this conformation. The "base-off" conformation, which is rare at physiological pH, mirrors that in the target enzyme, methylmalonyl-CoA mutase, which utilizes the product, AdoCbl. However, the coordination environment for cobalt in the two proteins is distinct, which is reflected in an approximately 40-fold difference in their affinity for the cofactor.

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Available abstract

Human adenosyltransferase synthesizes coenzyme B12, for the target mitochondrial B12 enzyme, methylmalonyl-CoA mutase. It binds B12 in the "base-off" conformation in both the Co2+ and Co3+ oxidation states as revealed by UV-visible and EPR spectroscopy although it lacks the signature DXHXXG motif found in other B12 proteins that bind the cofactor in this conformation. The "base-off" conformation, which is rare at physiological pH, mirrors that in the target enzyme, methylmalonyl-CoA mutase, which utilizes the product, AdoCbl. However, the coordination environment for cobalt in the two proteins is distinct, which is reflected in an approximately 40-fold difference in their affinity for the cofactor.

Key concepts: Mutase, Chemistry, Adenosylcobalamin, Cofactor, Stereochemistry, Enzyme, Biochemistry

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Mirror “Base-off” Conformation of Coenzyme B 12 in Human Adenosyltransferase and Its Downstream Target, Methylmalonyl-CoA Mutase — Research Paper | ScholarLens