Pork and human cDNAs encoding glutaryl-CoA dehydrogenase.
Specific glutaryl-CoA dehydrogenating activity is deficient in cultured fibroblasts from glutaric aciduria patients.
Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli.
Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the Amish.
Glutaric aciduria type I in the Arab and Jewish communities in Israel.
The human glutaryl-CoA dehydrogenase gene: report of intronic sequences and of 13 novel mutations causing glutaric aciduria type I.
Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutations.
The function of Arg-94 in the oxidation and decarboxylation of glutaryl-CoA by human glutaryl-CoA dehydrogenase.
Complete sequencing and characterization of 21,243 full-length human cDNAs.
Severe phenotype despite high residual glutaryl-CoA dehydrogenase activity: a novel mutation in a Turkish patient with glutaric aciduria type I.
The DNA sequence and biology of human chromosome 19.
Crystal structures of human glutaryl-CoA dehydrogenase with and without an alternate substrate: structural bases of dehydrogenation and decarboxylation reactions.
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Kinetic mechanism of glutaryl-CoA dehydrogenase.
The effect of a Glu370Asp mutation in glutaryl-CoA dehydrogenase on proton transfer to the dienolate intermediate.
Disease-causing missense mutations affect enzymatic activity, stability and oligomerization of glutaryl-CoA dehydrogenase (GCDH).
Initial characterization of the human central proteome.
Functional characterization of rat glutaryl-CoA dehydrogenase and its comparison with straight-chain acyl-CoA dehydrogenase.
An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
Molecular analysis of Cypriot patients with Glutaric aciduria type I: identification of two novel mutations.
Human METTL20 is a mitochondrial lysine methyltransferase that targets the β subunit of electron transfer flavoprotein (ETFβ) and modulates its activity.
N-terminome analysis of the human mitochondrial proteome.
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
Lysine catabolism reprograms tumour immunity through histone crotonylation.
Gene Ontology annotation through association of InterPro records with GO terms
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
glutaryl-CoA + FAD => crotonyl-CoA + FADH2 + CO2
Glutaryl-CoA dehydrogenase, mitochondrial
Glutaryl-CoA dehydrogenase, mitochondrial
Glutaryl-CoA dehydrogenase, mitochondrial
OpenScientist review of GCDH fatty-acid oxidation process scope
Role of mitochondrial acyl-CoA dehydrogenases in the metabolism of dicarboxylic fatty acids.
Odd-Chain Dicarboxylic Acid Feeding Produces a Glutaric Aciduria Type 1-Like Metabolic Signature in Mice.