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Key Documents

A6986

Sigma-Aldrich

Acetyl-CoA Carboxylase 1 human

recombinant, expressed in Sf9 cells

Synonyme(s) :

ACAC, ACACA, ACC, ACC1, ACCA, acetyl-CoA carboxylase alpha

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About This Item

Numéro de classification (Commission des enzymes):
Code UNSPSC :
12352204
Nomenclature NACRES :
NA.26

Produit recombinant

expressed in Sf9 cells

Niveau de qualité

Forme

liquid

Activité spécifique

≥20 units/μg protein

Numéro d'accès NCBI

Maladie(s) pertinente(s)

cancer

Conditions d'expédition

dry ice

Température de stockage

−70°C

Informations sur le gène

human ... ACACA(31)

Description générale

Acetyl-CoA Carboxylase 1 (ACACA) is mapped to human chromosome 17q12. It is majorly expressed in liver and adipose tissue. ACACA has biotin carboxylase (BC), biotin carboxyl carrier protein (BCCP) and carboxyl transferase (CT) domains and an additional interaction domain. (BT) A central domain region (CD) connects the BC and CT domains. ACACA is a key regulator of energy balance. The ACACA catalysis is the rate-limiting step in the synthesis of malonyl-CoA and regulation of free fatty acid oxidation. Elevated levels of ACACA contributes to obesity and tumor progression.
Formulation: Solution in Tris-HCl (pH 8), NaCl, Glycerol

Application

Useful for the study of enzyme kinetics, screening inhibitors, and selectivity profiling.

Actions biochimiques/physiologiques

Acetyl-CoA Carboxylase (ACC) regulates the metabolism of fatty acids. This enzyme catalzes the formation of Malonyl CoA through the irreversible carboxylation of acetyl CoA. There are two main isoforms of Acetyl-CoA carboxylase expressed in mammals, Acetyl-CoA carboxylase 1 (ACACA) and Acetyl-CoA carboxylase 2 (ACACB). ACACA has broad tissue distribution but is enriched in tissues critical for fatty acid sythesis such as adipose tissue. ACACB is enriched in tissues such as skeletal muscle and heart that are critical for fatty acid oxidation.

The Acetyl-CoA Carboxylase enzymes are activated by citrate, glutamate, and dicarboxylic acids and negatively regulated by long and short chain fatty acyl CoAs. Acetyl-CoA Carboxylase 1 is essential for breast cancer and prostrate cancer cell survival. Because of thier roles in fatty acid metabolism and oxidation, ACACA and ACACB are therapeutic targets for treating obesity and metabolic syndrome disorders.

Propriétés physiques

α transcript variant 1, C-terminal histidine-tagged 270 kDa protein containing amino acids 1-2383 (end)

Définition de l'unité

One unit will cause the conversion of 1 picomole of ATP to ADP per minute at pH 7.4 at 30 °C

Notes préparatoires

Thaw on ice. Upon first thaw, briefly spin tube containing enzyme to recover full content of the tube. Aliquot enzyme into single use aliquots. Store remaining undiluted enzyme in aliquots at -70°C. Note: Enzyme is very sensitive to freeze/thaw cycles.

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Structural basis for regulation of human acetyl-CoA carboxylase
Hunkeler M, et al.
Nature, 558, 470-474 (2018)
Regulation of acetyl CoA carboxylase and carnitine palmitoyl transferase-1 in rat adipocytes
Zang Y, et al.
Obesity Research, 13(9), 1530-1539 (2005)
Kalyan K Sadhu et al.
Journal of the American Chemical Society, 134(49), 20013-20016 (2012-11-29)
The photoreduction of azide-based immolative linker by Ru(II) conjugates to uncage rhodamine was achieved using different oligomeric protein templates. The generality of the approach was validated with three sets of ligand having varying affinity to their target (biotin, desthiobiotin and
Morgan D Fullerton et al.
Nature medicine, 19(12), 1649-1654 (2013-11-05)
The obesity epidemic has led to an increased incidence of nonalcoholic fatty liver disease (NAFLD) and type 2 diabetes. AMP-activated protein kinase (Ampk) regulates energy homeostasis and is activated by cellular stress, hormones and the widely prescribed type 2 diabetes
Graeme J Gowans et al.
Cell metabolism, 18(4), 556-566 (2013-10-08)
While allosteric activation of AMPK is triggered only by AMP, binding of both ADP and AMP has been reported to promote phosphorylation and inhibit dephosphorylation at Thr172. Because cellular concentrations of ADP and ATP are higher than AMP, it has

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