Methylmalonyl-CoA Mutase

Known as: Mutase, Methylmalonyl-CoA, Methylmalonyl-CoA Isomerase, Methylmalonyl CoA mutase 
An enzyme that catalyzes the conversion of methylmalonyl-CoA to succinyl-CoA by transfer of the carbonyl group. It requires a cobamide coenzyme. A… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1984-2017
012319842017

Papers overview

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2015
2015
Methylmalonic aciduria (MMA) is an autosomal recessive disorder of methylmalonate and cobalamin (cbl; vitamin B12) metabolism. It… (More)
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2015
2015
Isolated methylmalonic acidemia (MMA) is an autosomal recessive, inherited disorder that results from either a mut defect of the… (More)
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2012
2012
The mutation R403stop was found in an individual with mut(0) methylmalonic aciduria (MMA) which resulted from a single base… (More)
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2012
2012
We report the electrophilic Fukui function analysis based on density functional reactivity theory (DFRT) to demonstrate the… (More)
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2005
2005
Vitamin B12 deficiency causes decreased Methionine Synthase and L-Methylmalonyl-CoA Mutase activity and results in accumulation… (More)
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2000
2000
An excellent substrate of methylmalonyl-CoA mutase, methylmalonyl-carba-(dethia) coenzyme A (methylmalonyl-CH(2)-CoA), was… (More)
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1998
1998
BACKGROUND Methylmalonyl CoA mutase catalyses the interconversion of succinyl CoA and methylmalonyl CoA via a free radical… (More)
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Review
1990
Review
1990
Methylmalonyl CoA mutase deficiency (methylmalonic acidemia) has been a paradigm for biochemical and somatic cell genetic… (More)
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1988
1988
Methylmalonyl CoA mutase (MCM) catalyzes an essential step in the degradation of several branch-chain amino acids and odd-chain… (More)
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1984
1984
Methylmalonyl CoA mutase from Ascaris lumbricoides has been purified to homogeneity. The mutase is homogeneous as judged by… (More)
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