FLAD1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | FLAD1 , FAD1, FADS, PP591, flavin adenine dinucleotide synthetase 1, LSMFLAD | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 610595 MGI: 2443030 HomoloGene: 115598 GeneCards: FLAD1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Flavin adenine dinucleotide synthetase 1 is a protein that in humans is encoded by the FLAD1 gene. [5]
This gene encodes the enzyme that catalyzes adenylation of flavin mononucleotide (FMN) to form flavin adenine dinucleotide (FAD) coenzyme. Alternatively spliced transcript variants encoding distinct isoforms have been observed.
Glutaryl-CoA dehydrogenase (GCDH) is an enzyme encoded by the GCDH gene on chromosome 19. The protein belongs to the acyl-CoA dehydrogenase family (ACD). It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and carbon dioxide in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants.
In enzymology, a phosphopantothenate—cysteine ligase also known as phosphopantothenoylcysteine synthetase (PPCS) is an enzyme that catalyzes the chemical reaction which constitutes the second of five steps involved in the conversion of pantothenate to Coenzyme A. The reaction is:
Dimethylaniline monooxygenase [N-oxide-forming] 4 is an enzyme that in humans is encoded by the FMO4 gene.
D-aspartate oxidase is an enzyme that is encoded by the DDO gene.
Glutamine-dependent NAD(+) synthetase is an enzyme that in humans is encoded by the NADSYN1 gene.
L-2-hydroxyglutarate dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the L2HGDH gene, also known as C14orf160, on chromosome 14.
Bile acyl-CoA synthetase is an enzyme that in humans is encoded by the SLC27A5 gene.
Probable histidyl-tRNA synthetase, mitochondrial is an enzyme that in humans is encoded by the HARS2 gene.
Globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 is an enzyme that in humans is encoded by the GBGT1 gene.
GDP-L-fucose synthetase is an enzyme that in humans is encoded by the TSTA3 gene.
Zinc finger and BTB domain containing 11 is a protein that in humans is encoded by the ZBTB11 gene.
Inositol monophosphatase 3 also known as inositol monophosphatase domain-containing protein 1 (IMPAD1) is an enzyme that in humans is encoded by the IMPAD1 gene.
Calcium/calmodulin-dependent protein kinase ID is a protein in humans that is encoded by the CAMK1D gene on chromosome 10.
Forkhead box B1 is a protein that in humans is encoded by the FOXB1 gene.
Acyl-CoA synthetase short-chain family member 3 is a protein that in humans is encoded by the ACSS3 gene.
Forkhead box Q1 is a protein that in humans is encoded by the FOXQ1 gene.
LanC like 1 is a protein that in humans is encoded by the LANCL1 gene.
Solute carrier family 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene.
Forkhead box S1 is a protein that in humans is encoded by the FOXS1 gene.
Acyl-CoA synthetase medium chain family member 2A is a protein that in humans is encoded by the ACSM2A gene.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.