Results 1 to 10 of about 92,949 (326)

Targeting acetyl-CoA carboxylase 1 for cancer therapy [PDF]

open access: yesFrontiers in Pharmacology, 2023
Metabolic adaptation is an emerging hallmark of tumors. De novo fatty acid synthesis is an important metabolic process to produce metabolic intermediates for energy storage, biosynthesis of membrane lipids and generation of signaling molecules.
Yong Yu   +5 more
doaj   +3 more sources

Acetyl-CoA carboxylase 1 is a suppressor of the adipocyte thermogenic program [PDF]

open access: yesCell Reports, 2023
Summary: Disruption of adipocyte de novo lipogenesis (DNL) by deletion of fatty acid synthase (FASN) in mice induces browning in inguinal white adipose tissue (iWAT). However, adipocyte FASN knockout (KO) increases acetyl-coenzyme A (CoA) and malonyl-CoA
Adilson Guilherme   +18 more
doaj   +3 more sources

Chemical Genetics of Acetyl-CoA Carboxylases [PDF]

open access: yesMolecules, 2013
Chemical genetic studies on acetyl-CoA carboxylases (ACCs), rate-limiting enzymes in long chain fatty acid biosynthesis, have greatly advanced the understanding of their biochemistry and molecular biology and promoted the use of ACCs as targets for ...
Xuyu Zu   +9 more
doaj   +7 more sources

Increasing the Ascomycin Yield by Relieving the Inhibition of Acetyl/Propionyl-CoA Carboxylase by the Signal Transduction Protein GlnB

open access: goldFrontiers in Microbiology, 2021
Ascomycin (FK520) is a multifunctional antibiotic produced by Streptomyces hygroscopicus var. ascomyceticus. In this study, we demonstrated that the inactivation of GlnB, a signal transduction protein belonging to the PII family, can increase the ...
Pan Wang   +20 more
doaj   +2 more sources

The dynamic organization of fungal acetyl-CoA carboxylase [PDF]

open access: yesNature Communications, 2016
Acetyl-CoA carboxylases are central regulatory hubs of fatty acid metabolism and are important targets for drug development in obesity and cancer. Here, the authors demonstrate that the regulation of these highly dynamic enzymes in fungi is governed by a
Moritz Hunkeler   +4 more
doaj   +2 more sources

Filament structures unveil the dynamic organization of human acetyl-CoA carboxylase. [PDF]

open access: yesSci Adv
Human acetyl-CoA carboxylases (ACCs) catalyze the carboxylation of acetyl-CoA, which is the rate-limiting step in fatty acid synthesis. The molecular mechanism underlying the dynamic organization of ACCs is largely unknown.
Zhou F   +5 more
europepmc   +2 more sources

Docking of acetyl-CoA carboxylase to the plastid envelope membrane attenuates fatty acid production in plants

open access: yesNature Communications, 2020
In plants, light-dependent activation fatty acid synthesis (FAS) is mediated in part by acetyl-CoA carboxylase (ACCase). Here the authors identify a family of genes encoding carboxyltransferase interactors that attenuate FAS in the light by docking ...
Yajin Ye   +7 more
doaj   +2 more sources

Acetyl-CoA carboxylase obstructs CD8<sup>+</sup> T cell lipid utilization in the tumor microenvironment. [PDF]

open access: yesCell Metab
SUMMARY The solid tumor microenvironment (TME) imprints a compromised metabolic state in tumor-infiltrating T cells (TILs), hallmarked by the inability to maintain effective energy synthesis for antitumor function and survival.
Hunt EG   +13 more
europepmc   +2 more sources

Purification of Native Acetyl CoA Carboxylase From Mammalian Cells [PDF]

open access: yesBio-Protocol
Fatty acid (FA) biosynthesis is a crucial cellular process that converts nutrients into metabolic intermediates necessary for membrane biosynthesis, energy storage, and the production of signaling molecules. Acetyl-CoA carboxylase (ACACA) plays a pivotal
Yaxue Sun   +3 more
doaj   +2 more sources

Acetyl-CoA-Carboxylase 1-mediated de novo fatty acid synthesis sustains Lgr5+ intestinal stem cell function

open access: yesNature Communications, 2022
Here the authors report that inhibition of de novo fatty acid synthesis by deleting the enzyme Acetyl-CoA-Carboxylase 1 in the intestinal epithelium results in the loss of crypt structures and a specific decline in Lgr5+ intestinal epithelial stem cells.
Shuting Li   +14 more
doaj   +2 more sources

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