Gene interactions and pathways from curated databases and text-mining

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CYBA — NOX1

Pathways - manually collected, often from reviews:

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Huang et al., J Biol Chem 1999 : Activation of phagocyte NADPH oxidase requires interaction between p47(phox) and p22(phox)
Xiao et al., Am J Physiol Cell Physiol 2002 (Cardiomegaly...) : We found that ARVM express gp91(phox), p22(phox) , p67(phox), and p47(phox), four major components of NAD ( P ) H oxidase, and that alpha ( 1 ) -AR stimulated ERK1/2 activation was blocked by four structurally unrelated inhibitors of NAD ( P ) H oxidase [ diphenyleneiodonium, phenylarsine oxide, 4- ( 2-aminoethyl ) benzenesulfonyl fluoride, and cadmium ]
San José et al., Hypertension 2004 (Hypertension) : We thus investigated the relationships between the -930A/G polymorphism and p22phox expression and NADPH oxidase mediated superoxide production in phagocytic cells from 70 patients with essential hypertension and 70 normotensive controls
Kawahara et al., J Biol Chem 2005 : Similarly, p22phox ( P156Q ), a mutation that disrupts Src homology 3 binding by the PRR, potently inhibited reactive oxygen production from Nox1 and Nox2 but not from Nox4 and Nox5
Modlinger et al., Hypertension 2006 (Hypertension) : An increase in p22phox is required for increased renal NADPH oxidase activity, expression of Nox proteins and oxidative stress, and contributes < or =50 % to hypertension during an Ang II slow-pressor response
Nobuhisa et al., Biochem J 2006 : Activation of the superoxide producing phagocyte NADPH oxidase , crucial for host defence, requires an SH3 ( Src homology 3 ) -domain mediated interaction of the regulatory protein p47phox with p22phox , a subunit of the oxidase catalytic core flavocytochrome b558
Miyano et al., J Biol Chem 2006 : We also demonstrate that Nox1 activation requires membrane recruitment of Noxa1, which is normally mediated via Noxa1 binding to Noxo1, a protein tethered to the Nox1 partner p22(phox) : the Noxa1-Noxo1 and Noxo1-p22(phox) interactions are both essential for Nox1 activity
Haurani et al., Hypertension 2008 : Cotransfection with human Nox4 and human p22-phox plasmids combined with Ang II reduced endogenous Nox4 mRNA levels ( 37+/-5 % of control ; P < 0.05 ), whereas it had no significant effect on Nox1 or Nox2 ... Cotransfection with human Nox4 and human p22-phox plasmids combined with Ang II reduced endogenous Nox4 mRNA levels ( 37+/-5 % of control ; P < 0.05 ), whereas it had no significant effect on Nox1 or Nox2
Tian et al., Am J Physiol Regul Integr Comp Physiol 2008 (Disease Models, Animal...) : By day 35 in the high-Na S rats, mRNA expression of renal cortical gp91phox, p22phox , p47phox, and p67phox NADPH subunits in S rats increased markedly, and treatment of high-Na S rats with the NADPH oxidase inhibitor apocynin resulted in significant decreases in mRNA expression of these NADPH oxidase subunits
Lewis et al., J Biol Chem 2010 : Phosphorylation of p22phox on threonine 147 enhances NADPH oxidase activity by promoting p47phox binding ... We also explored the mechanism by which p22(phox) phosphorylation affects NADPH oxidase activity
Block et al., Am J Pathol 2010 (Anoxia...) : We have previously demonstrated that in VHL-deficient cells, p22(phox) dependent Nox1 and Nox4 oxidases maintain hypoxia inducible factor-2alpha ( HIF-2alpha ) protein expression through an Akt dependent translational pathway
Dutta et al., PloS one 2010 : NOX1 , an NADPH oxidase homologue that is most abundantly expressed in colon epithelial cells, requires the regulatory subunits NOXO1 ( NOX organizing protein 1 ) and NOXA1 ( NOX activating protein 1 ), as well as the flavocytochrome component p22(phox) for maximal activity
Sardina et al., Cell Death Differ 2010 : p22phox dependent NADPH oxidase activity is required for megakaryocytic differentiation ... RNA interference experiments have shown that a p22(phox) dependent NADPH oxidase activity is responsible for ROS production
Edderkaoui et al., J Biol Chem 2011 (Pancreatic Neoplasms) : Up-regulation of p22(phox) by the growth factors results in increased Nox4-p22(phox) complex formation and activation of NADPH oxidase
Zhao et al., Chin Med J (Engl) 2013 : AcorA significantly inhibited high glucose induced activation of NADPH oxidase , a ROS generating enzyme, by increasing phosphorylation of p47(phox) and enhancing interaction between p22(phox) and p47(phox)
Sumimoto et al., J Biol Chem 1996 : Specific interaction of the N-terminal Src homology 3 domain of p47phox with p22phox is required for activation of the NADPH oxidase
Marshall et al., Am J Respir Cell Mol Biol 1996 (Anoxia) : Together these observations demonstrate that the unique cytochrome b-245 containing NADPH-oxidase is present in pulmonary artery smooth muscle and that an NADPH-oxidase or NADH-oxidoreductase complex is activated to release superoxide by hypoxic conditions