The multiple facets of acetyl-CoA metabolism: Energetics, biosynthesis, regulation, acylation and inborn errors
Y Wang, H Yang, C Geerts, A Furtos, P Waters… - Molecular Genetics and …, 2023 - Elsevier
Abstract Acetyl-coenzyme A (Ac-CoA) is a core metabolite with essential roles throughout
cell physiology. These functions can be classified into energetics, biosynthesis, regulation …
cell physiology. These functions can be classified into energetics, biosynthesis, regulation …
Acetyl-CoA and the regulation of metabolism: mechanisms and consequences
L Shi, BP Tu - Current opinion in cell biology, 2015 - Elsevier
Acetyl-CoA represents a key node in metabolism due to its intersection with many metabolic
pathways and transformations. Emerging evidence reveals that cells monitor the levels of …
pathways and transformations. Emerging evidence reveals that cells monitor the levels of …
Molecular biology of acetyl-CoA metabolism
We have characterized the expression of potential acetyl-CoA-generating genes (acetyl-
CoA synthetase, pyruvate decarboxylase, acetaldehyde dehydrogenase, plastidic pyruvate …
CoA synthetase, pyruvate decarboxylase, acetaldehyde dehydrogenase, plastidic pyruvate …
Hereditary and acquired diseases of acyl-coenzyme A metabolism
GA Mitchell, N Gauthier, A Lesimple, SP Wang… - Molecular genetics and …, 2008 - Elsevier
Coenzyme A (CoA) sequestration, toxicity or redistribution (CASTOR) is predicted to occur in
many hereditary and acquired conditions in which the degradation of organic acyl esters of …
many hereditary and acquired conditions in which the degradation of organic acyl esters of …
Inborn errors of mitochondrial acyl-coenzyme a metabolism: Acyl-CoA biology meets the clinic
H Yang, C Zhao, MC Tang, Y Wang, SP Wang… - Molecular Genetics and …, 2019 - Elsevier
The last decade saw major advances in understanding the metabolism of Coenzyme A
(CoA) thioesters (acyl-CoAs) and related inborn errors (CoA metabolic diseases, CAMDs) …
(CoA) thioesters (acyl-CoAs) and related inborn errors (CoA metabolic diseases, CAMDs) …
Aberrant protein acylation is a common observation in inborn errors of acyl-CoA metabolism
O Pougovkina, H Te Brinke, RJA Wanders… - Journal of inherited …, 2014 - Springer
Inherited disorders of acyl-CoA metabolism, such as defects in amino acid metabolism and
fatty acid oxidation can present with severe clinical symptoms either neonatally or later in …
fatty acid oxidation can present with severe clinical symptoms either neonatally or later in …
Coenzyme A and its derivatives: renaissance of a textbook classic
FL Theodoulou, OCM Sibon… - Biochemical Society …, 2014 - portlandpress.com
In 1945, Fritz Lipmann discovered a heat-stable cofactor required for many enzyme-
catalysed acetylation reactions. He later determined the structure for this acetylation …
catalysed acetylation reactions. He later determined the structure for this acetylation …
[HTML][HTML] Acetyl coenzyme A: a central metabolite and second messenger
Acetyl-coenzyme A (acetyl-CoA) is a central metabolic intermediate. The abundance of
acetyl-CoA in distinct subcellular compartments reflects the general energetic state of the …
acetyl-CoA in distinct subcellular compartments reflects the general energetic state of the …
Regulation of mammalian acetyl-coenzyme A carboxylase
KH Kim - Annual review of nutrition, 1997 - annualreviews.org
▪ Abstract Long-chain fatty acids are involved in all aspects of cellular structure and function.
For controlling amounts of fatty acids, cells are endowed with two acetyl-coenzyme A …
For controlling amounts of fatty acids, cells are endowed with two acetyl-coenzyme A …
Mutant mice lacking acetyl-CoA carboxylase 1 are embryonically lethal
L Abu-Elheiga, MM Matzuk, P Kordari… - Proceedings of the …, 2005 - National Acad Sciences
Acetyl-CoA carboxylases (ACC1 and ACC2) catalyze the carboxylation of acetyl-CoA to form
malonyl-CoA, an intermediate metabolite that plays a pivotal role in the regulation of fatty …
malonyl-CoA, an intermediate metabolite that plays a pivotal role in the regulation of fatty …
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