Recombinant Human ERAB protein
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Recombinant Human ERAB protein is a Human Full Length protein, expressed in Baculovirus infected Sf9 cells, with >95%, suitable for SDS-PAGE, WB.
View Alternative Names
ERAB, HADH2, MRPP2, SCHAD, SDR5C1, XH98G2, HSD17B10, 3-hydroxyacyl-CoA dehydrogenase type-2, 17-beta-estradiol 17-dehydrogenase, 2-methyl-3-hydroxybutyryl-CoA dehydrogenase, 3-alpha-(17-beta)-hydroxysteroid dehydrogenase (NAD(+)), 3-hydroxy-2-methylbutyryl-CoA dehydrogenase, 3-hydroxyacyl-CoA dehydrogenase type II, 3alpha(or 20beta)-hydroxysteroid dehydrogenase, 7-alpha-hydroxysteroid dehydrogenase, Endoplasmic reticulum-associated amyloid beta-peptide-binding protein, Mitochondrial ribonuclease P protein 2, Short chain dehydrogenase/reductase family 5C member 1, Short-chain type dehydrogenase/reductase XH98G2, Type II HADH, MHBD, Mitochondrial RNase P protein 2
- SDS-PAGE
Unknown
SDS-PAGE - Recombinant Human ERAB protein (AB85241)
SDS-PAGE showing ab85241 at approximately 51kDa.
Reactivity data
Sequence info
Properties and storage information
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The function of this enzyme extends beyond its metabolic activities. ERAB is part of the mitochondrial enzyme complex responsible for fatty acid oxidation and energy production. This places it centrally in cellular energy homeostasis. Additionally ERAB participates in the metabolism of neurosteroids which impacts brain function. Through its interactions ERAB influences signaling pathways by modulating local steroid concentrations in the nervous system affecting cellular communication and response.
Pathways
ERAB associates with key biochemical pathways including the beta-oxidation of fatty acids and the steroid hormone metabolism pathway. It interacts with acetyl-CoA acyltransferase 2 (ACAA2) within these metabolic pathways facilitating the conversion of substrates vital for energy production and steroid synthesis. This involvement underpins the enzyme’s significance in maintaining metabolic equilibrium through its catalytic activities on essential biological molecules.
Specifications
Form
Liquid
Additional notes
Affinity purified.
General info
Function
Mitochondrial dehydrogenase involved in pathways of fatty acid, branched-chain amino acid and steroid metabolism (PubMed : 10600649, PubMed : 12917011, PubMed : 18996107, PubMed : 19706438, PubMed : 20077426, PubMed : 25925575, PubMed : 26950678, PubMed : 28888424, PubMed : 9553139). Acts as (S)-3-hydroxyacyl-CoA dehydrogenase in mitochondrial fatty acid beta-oxidation, a major degradation pathway of fatty acids. Catalyzes the third step in the beta-oxidation cycle, namely the reversible conversion of (S)-3-hydroxyacyl-CoA to 3-ketoacyl-CoA. Preferentially accepts straight medium- and short-chain acyl-CoA substrates with highest efficiency for (3S)-hydroxybutanoyl-CoA (PubMed : 10600649, PubMed : 12917011, PubMed : 25925575, PubMed : 26950678, PubMed : 9553139). Acts as 3-hydroxy-2-methylbutyryl-CoA dehydrogenase in branched-chain amino acid catabolic pathway. Catalyzes the oxidation of 3-hydroxy-2-methylbutanoyl-CoA into 2-methyl-3-oxobutanoyl-CoA, a step in isoleucine degradation pathway (PubMed : 18996107, PubMed : 19706438, PubMed : 20077426). Has hydroxysteroid dehydrogenase activity toward steroid hormones and bile acids. Catalyzes the oxidation of 3alpha-, 17beta-, 20beta- and 21-hydroxysteroids and 7alpha- and 7beta-hydroxy bile acids (PubMed : 10600649, PubMed : 12917011). Oxidizes allopregnanolone/brexanolone at the 3alpha-hydroxyl group, which is known to be critical for the activation of gamma-aminobutyric acid receptors (GABAARs) chloride channel (PubMed : 19706438, PubMed : 28888424). Has phospholipase C-like activity toward cardiolipin and its oxidized species. Likely oxidizes the 2'-hydroxyl in the head group of cardiolipin to form a ketone intermediate that undergoes nucleophilic attack by water and fragments into diacylglycerol, dihydroxyacetone and orthophosphate. Has higher affinity for cardiolipin with oxidized fatty acids and may degrade these species during the oxidative stress response to protect cells from apoptosis (PubMed : 26338420). By interacting with intracellular amyloid-beta, it may contribute to the neuronal dysfunction associated with Alzheimer disease (AD) (PubMed : 9338779). Essential for structural and functional integrity of mitochondria (PubMed : 20077426).. In addition to mitochondrial dehydrogenase activity, moonlights as a component of mitochondrial ribonuclease P, a complex that cleaves tRNA molecules in their 5'-ends (PubMed : 18984158, PubMed : 24549042, PubMed : 25925575, PubMed : 26950678, PubMed : 28888424). Together with TRMT10C/MRPP1, forms a subcomplex of the mitochondrial ribonuclease P, named MRPP1-MRPP2 subcomplex, which displays functions that are independent of the ribonuclease P activity (PubMed : 23042678, PubMed : 29040705). The MRPP1-MRPP2 subcomplex catalyzes the formation of N(1)-methylguanine and N(1)-methyladenine at position 9 (m1G9 and m1A9, respectively) in tRNAs; HSD17B10/MRPP2 acting as a non-catalytic subunit (PubMed : 23042678, PubMed : 25925575, PubMed : 28888424). The MRPP1-MRPP2 subcomplex also acts as a tRNA maturation platform : following 5'-end cleavage by the mitochondrial ribonuclease P complex, the MRPP1-MRPP2 subcomplex enhances the efficiency of 3'-processing catalyzed by ELAC2, retains the tRNA product after ELAC2 processing and presents the nascent tRNA to the mitochondrial CCA tRNA nucleotidyltransferase TRNT1 enzyme (PubMed : 29040705). Associates with mitochondrial DNA complexes at the nucleoids to initiate RNA processing and ribosome assembly.
Sequence similarities
Belongs to the short-chain dehydrogenases/reductases (SDR) family.
Subcellular localisation
Mitochondrion
Target data
Product promise
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