protein
| binding the heme moiety of soluble guanylate cyclase forming a metal-nitrosyl adduct that is activated to catalyze the conversion of GTP to LGMP |
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RPA1, repressor of NOS3 associated with the development of coronary artery |
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calmodulin |
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PRKCZ binds and phosphorylates MAPK7, thereby decreasing NOS3 protein stability and contributing to early events of atherosclerosis |
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controls the expression of the angiogenesis inhibitor thrombospondin 2 |
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JNK2 is a physiological kinase responsible for NOS3-Ser(116) phosphorylation and regulates NO production |
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GIT1 plays an important role in NOS3 function, in both normal and abnormal pathophysiologic states |
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GIT1 might regulate NOS3 activity in sinusoidal endothelial cells |
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activation of NOS3 promotes SRC-dependent CAV1-Tyr-14 phosphorylation and NOS3/CAV1 binding, that is, NOS3 feedback inhibition |
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VEGFA-mediated NOS3 phosphorylation on Ser1177 regulates angioblast and embryonic endothelial cells (EEC) division, which underlies the formation of blood vessels and vascular networks |
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UBIAD1 is a nonmitochondrial COQ10-forming enzyme with specific cardiovascular protective function via the modulation of NOS3 activity |
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HRAS mediates VEGFA-induced activation of endothelial nitric-oxide synthase (NOS3) and migratory response of human endothelial cells |
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neuronal NOS1 and endothelial NOS3 are constitutive calcium-dependent forms of the enzyme that regulate neural and vascular function respectively |
Variant & Polymorphism
SNP
, other
| G894T not likely to be involved in atherosclerosis |
|
E298D variant in hypertension in pregnancy and in lower age at end stage renal disease in PKD1 |
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Glu 298 ASP in fabry disease with severe phenotype |
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SNP increasing the risk of limb deficiency defects in the presence of maternal smoking |
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G894T associated to embryonic spina bifida |
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intron 4-VNTR and T-786C mutation enhance the inflammatory process in patients with chronic coronary artery disease |
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polymorphism 894G>T associated with increased CAD risk |
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subjects carrying the rs753482-C genotype express a novel stable truncated form of NOS3 with altered enzymatic activity that influences endothelial function, and associated with altered vascular function |
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