Q9NPH5

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession NOX4_HUMAN; Q9NPH5;
Entrez ID 50507
GenBank Protein ID NM_001143836.2; NM_001143837.1; NM_001291926.1; NM_001291927.1; NM_001300995.1; NM_016931.4; XM_011542857.2;
GenBank Nucleotide ID NP_001137308.1; NP_001137309.1; NP_001278855.1; NP_001278856.1; NP_001287924.1; NP_058627.1; XP_011541159.1;
Protein Name NADPH oxidase 4 (EC 1.6.3.-) (Kidney oxidase-1) (KOX-1) (Kidney superoxide-producing NADPH oxidase) (Renal NAD(P)H-oxidase)
Gene Name NOX4; RENOX
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionConstitutive NADPH oxidase which generates superoxide intracellularly upon formation of a complex with CYBA/p22phox. Regulates signaling cascades probably through phosphatases inhibition. May function as an oxygen sensor regulating the KCNK3/TASK-1 potassium channel and HIF1A activity. May regulate insulin signaling cascade. May play a role in apoptosis, bone resorption and lipolysaccharide-mediated activation of NFKB. May produce superoxide in the nucleus and play a role in regulating gene expression upon cell stimulation. Isoform 3 is not functional. Isoform 5 and isoform 6 display reduced activity.;Isoform 4: Involved in redox signaling in vascular cells. Constitutively and NADPH-dependently generates reactive oxygen species (ROS). Modulates the nuclear activation of ERK1/2 and the ELK1 transcription factor, and is capable of inducing nuclear DNA damage. Displays an increased activity relative to isoform 1.
Sequence
(Fasta)
MAVSWRSWLA NEGVKHLCLF IWLSMNVLLF WKTFLLYNQG PEYHYLHQML GLGLCLSRAS 60
ASVLNLNCSL ILLPMCRTLL AYLRGSQKVP SRRTRRLLDK SRTFHITCGV TICIFSGVHV 120
AAHLVNALNF SVNYSEDFVE LNAARYRDED PRKLLFTTVP GLTGVCMVVV LFLMITASTY 180
AIRVSNYDIF WYTHNLFFVF YMLLTLHVSG GLLKYQTNLD THPPGCISLN RTSSQNISLP 240
EYFSEHFHEP FPEGFSKPAE FTQHKFVKIC MEEPRFQANF PQTWLWISGP LCLYCAERLY 300
RYIRSNKPVT IISVMSHPSD VMEIRMVKEN FKARPGQYIT LHCPSVSALE NHPFTLTMCP 360
TETKATFGVH LKIVGDWTER FRDLLLPPSS QDSEILPFIQ SRNYPKLYID GPFGSPFEES 420
LNYEVSLCVA GGIGVTPFAS ILNTLLDDWK PYKLRRLYFI WVCRDIQSFR WFADLLCMLH 480
NKFWQENRPD YVNIQLYLSQ TDGIQKIIGE KYHALNSRLF IGRPRWKLLF DEIAKYNRGK 540
TVGVFCCGPN SLSKTLHKLS NQNNSYGTRF EYNKESFS 579

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1Tyrosine PhosphorylationHeart failureDY56627525436
[Reference]: Mechanistically, we found that direct phosphorylation of tyrosine 566 on NOX4 was critical for this FYN-mediated negative regulation.?

※ Disease Cross-ref Annotation

DatabaseAnnotation
CTD (Curated)
(count: 7)
(view all)
MESH:D056486 ; Chemical and Drug Induced Liver Injury
MESH:D003110 ; Colonic Neoplasms
MESH:D006333 ; Heart Failure
MESH:D006973 ; Hypertension
MESH:D007676 ; Kidney Failure, Chronic
MESH:D008106 ; Liver Cirrhosis, Experimental
GWASdb
(count: 32)
(view all)
rs3897708; Antineutrophil cytoplasmic antibody-associated vasculitis; vasculitis
rs3897708; Smoking initiation; nicotine dependence
rs1847138; Narcolepsy; narcolepsy
rs7944576; Prostate cancer; prostate cancer
rs10830264; Cholesterol; arteriosclerosis|coronary artery disease|lipid metabolism disorder
rs10830265; Obesity-related traits; obesity

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 1)
491       WQENRPDYVNIQLYL     dbPAF