| Autor: |
Kim, Ki‐Han, López‐Casillas, F., Bai, D. H., Luo, X., Pape, M. E. |
| Zdroj: |
The FASEB Journal; September 1989, Vol. 3 Issue: 11 p2250-2256, 7p |
| Abstrakt: |
Acetyl‐CoA carboxylase, the rate‐limiting enzyme in the biogenesis of long‐chain fatty acids, is regulated by phosphorylation and dephosphorylation. The major phosphorylation sites that affect carboxylase activity and the specific protein kinases responsible for phosphorylation of different sites have been identified. A form of acetyl‐CoA carboxylase that is independent of citrate for activity occurs in vivo. This active form of caboxylase becomes citrate‐dependent upon phosphorylation under conditions of reduced lipogenesis. Therefore, phosphorylation‐dephosphorylation of acetyl‐CoA carboxylase is the enzyme's primary short‐term regulatory mechanism; this control mechanism together with cellular metabolites such as CoA, citrate, and palmitoyl‐CoA serves to fine‐tune the synthesis of long‐chain fatty acids under different physiological conditions.— Kim, K.‐H.; López‐Casillas, F.; Bai, D. H.; Luo, X.; Pape, M. E. Physiological significance of covalent phosphorylation‐dephosphorylation of acetyl‐CoA carboxylase in the regulation of long‐chain fatty acids. FASEB J.3: 2250‐2256; 1989. |
| Databáze: |
Supplemental Index |
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