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Nine novel isovaleryl-CoA dehydrogenase mutations have been found in a Spanish cohort with isovaleric acidemia.
kinetics and ligand binding of isovaleryl-CoA dehydrogenase
A heterogeneous mutation spectrum in the IVD gene was identified in isovaleric acidemia patients in the United Arab Emirates.
A child with isovaleric acidemia was subsequently found to harbour a known missense mutation (c.A1199G [p.Y371C]) and a novel 4-bp duplication (c.1148_1151dupGCTA [p.Y355X]) in the IVD gene. The former may be a founder mutation in the Chinese population.
Replacement of the catalytic glutamate (show GRIN1 Antibodies) in either short-chain acyl-CoA dehydrogenase (SCAD (show Acads Antibodies)) or isovaleryl-CoA dehydrogenase (IVD)with glycine resulted in a several-fold reduction in affinity for substrate.
Mutations of isovaleryl-CoA dehydrogenase gene is associated with isovaleric acidemia
Data elucidates the pathway of plant Lys (show LYZ Antibodies) catabolism and demonstrate that both isovaleryl-CoA dehydrogenase and 2-hydroxyglutarate dehydrogenase (show L2HGDH Antibodies) act as electron donors to the ubiquinol pool via an ETF (show TEAD2 Antibodies)/ETFQO (show ETFDH Antibodies)-mediated route. [IVDH]
Accumulation of both homomethionine and 3-isovaleroyloxypropyl-glucosinolate cosegregates with the high branched chain amino acid phenotype in IVD mutants.
Isovaleryl-CoA dehydrogenase (IVD) is a mitochondrial matrix enzyme that catalyzes the third step in leucine catabolism. The genetic deficiency of IVD results in an accumulation of isovaleric acid, which is toxic to the central nervous system and leads to isovaleric acidemia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
, isovaleryl-CoA dehydrogenase, mitochondrial
, isovaleryl CoA dehydrogenase
, isovaleryl Coenzyme A dehydrogenase
, isovaleryl coenzyme A dehydrogenase