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• W2042006175 endingPage "R12" @default.
• W2042006175 startingPage "R1" @default.
• W2042006175 abstract "The endothelial nitric oxide synthase (eNOS), the expression of which is regulated by a range of transcriptional and posttranscriptional mechanisms, generates nitric oxide (NO) in response to a number of stimuli. The physiologically most important determinants for the continuous generation of NO and thus the regulation of local blood flow are fluid shear stress and pulsatile stretch. Although eNOS activity is coupled to changes in endothelial cell Ca 2+ levels, an increase in Ca 2+ alone is not sufficient to affect enzyme activity because the binding of calmodulin (CaM) and the flow of electrons from the reductase to the oxygenase domain of the enzyme is dependent on protein phosphorylation and dephosphorylation. Two amino acids seem to be particularly important in regulating eNOS activity and these are a serine residue in the reductase domain (Ser 1177 ) and a threonine residue (Thr 495 ) located within the CaM-binding domain. Simultaneous alterations in the phosphorylation of Ser 1177 and Thr 495 in response to a variety of stimuli are regulated by a number of kinases and phosphatases that continuously associate with and dissociate from the eNOS signaling complex. eNOS associated proteins, such as caveolin, heat shock protein 90, eNOS interacting protein, and possibly also motor proteins provide the scaffold for the formation of the protein complex as well as its intracellular localization." @default.
• W2042006175 created "2016-06-24" @default.
• W2042006175 creator A5050471583 @default.
• W2042006175 creator A5091173895 @default.
• W2042006175 date "2003-01-01" @default.
• W2042006175 modified "2023-10-11" @default.
• W2042006175 title "Molecular mechanisms involved in the regulation of the endothelial nitric oxide synthase" @default.
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