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MCCC2 encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. Additionally we are shipping Methylcrotonoyl-CoA Carboxylase 2 (Beta) Antibodies (69) and Methylcrotonoyl-CoA Carboxylase 2 (Beta) Kits (1) and many more products for this protein.
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This study reports data mainly obtained from the Portuguese newborn screening program collected over a ten-year period. Analysis of the MCCC1 (show MCCC1 Proteins) and MCCC2 genes yielded 26 previously unreported mutations and a variant of clinically unknown significance.
Novel mutation in MCCC2 gene was identified in Chinese population.
Mutation in 3-methylcrotonyl CoA carboxylase 2 gene is associated with 3-methylcrotonyl-CoA carboxylase deficiency.
study reports eight different mutant alleles of MCCC1 (show MCCC1 Proteins) or MCCC2 including six novel mutations in Korean patients with 3-methylcrotonyl-CoA carboxylase (MCC (show MCC Proteins)) deficiency
identified two novel MCCA (show MCCC1 Proteins) and four novel MCCB (show MCCC1 Proteins) mutant alleles from five MCC (show MCC Proteins)-deficient patients
factors other than the genotype at the MCCA (show MCCC1 Proteins) and MCCB (show MCCC1 Proteins) loci have a major influence on the phenotype of MCC (show MCC Proteins) deficiency
The Kd value of soraphen A for the BC domains of human ACC1 and ACC2 is 1 nM. This high binding affinity is mainly due to the extensive interactions between soraphen A and the human biotin carboxylase domain
Molecular analyses revealed novel mutations in one of the causative genes, MCCA (show MCCC1 Proteins) or MCCB (show MCCC1 Proteins), in all five of the MCC (show MCC Proteins) deficiency patients
Studies indicate that mutations in either 3-methylcrotonyl CoA carboxylase MCCA (show MCCC1 Proteins) (At1g03090) or MCCB (At4g34030) block mitochondrial Leu catabolism, as inferred from the increased accumulation of Leu.
This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism.
methylcrotonoyl-CoA carboxylase beta chain, mitochondrial
, methylcrotonoyl-Coenzyme A carboxylase 2 (beta)
, methylcrotonoyl-CoA carboxylase 2 (beta)
, methylcrotonoyl-CoA carboxylase beta chain, mitochondrial-like
, 3-methylcrotonyl-CoA carboxylase 2
, 3-methylcrotonyl-CoA carboxylase non-biotin-containing subunit
, 3-methylcrotonyl-CoA:carbon dioxide ligase subunit beta
, MCCase subunit beta
, biotin carboxylase
, non-biotin containing subunit of 3-methylcrotonyl-CoA carboxylase