ENOX1
Ecto-NOX disulfide-thiol exchanger 1
Also known as: cCNOX, CNOX, ENOX1_HUMAN, FLJ10094, PIG38
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TC92
- Gene
- ENOX1
- Ensembl
- ENSG00000120658
- Chromosome
- 13
- Canonical length
- 643 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
The protein encoded by this gene is involved in plasma membrane electron transport pathways. The encoded protein has both a hydroquinone (NADH) oxidase activity and a protein disulfide-thiol interchange activity. The two activities cycle with a periodicity of 24 minutes, with one activity being at its peak when the other is at its lowest. [provided by RefSeq, Dec 2016]
Canonical amino-acid sequenceUniProt
643 residues, UniProt reviewed canonical sequence.
>Q8TC92|ENOX1
1 MVDAGGVENI TQLPQELPQM MAAAADGLGS IAIDTTQLNM SVTDPTAWAT AMNNLGMVPV
61 GLPGQQLVSD SICVPGFDPS LNMMTGITPI NPMIPGLGLV PPPPPTEVAV VKEIIHCKSC
121 TLFPQNPNLP PPSTRERPPG CKTVFVGGLP ENATEEIIQE VFEQCGDITA IRKSKKNFCH
181 IRFAEEFMVD KAIYLSGYRM RLGSSTDKKD SGRLHVDFAQ ARDDFYEWEC KQRMRAREER
241 HRRKLEEDRL RPPSPPAIMH YSEHEAALLA EKLKDDSKFS EAITVLLSWI ERGEVNRRSA
301 NQFYSMVQSA NSHVRRLMNE KATHEQEMEE AKENFKNALT GILTQFEQIV AVFNASTRQK
361 AWDHFSKAQR KNIDIWRKHS EELRNAQSEQ LMGIRREEEM EMSDDENCDS PTKKMRVDES
421 ALAAQAYALK EENDSLRWQL DAYRNEVELL KQEKEQLFRT EENLTKDQQL QFLQQTMQGM
481 QQQLLTIQEE LNNKKSELEQ AKEEQSHTQA LLKVLQEQLK GTKELVETNG HSHEDSNEIN
541 VLTVALVNQD RENNIEKRSQ GLKSEKEALL IGIISTFLHV HPFGANIEYL WSYMQQLDSK
601 ISANEIEMLL MRLPRMFKQE FTGVGATLEK RWKLCAFEGI KTTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ENOX1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.46
- Highest tissue expression
- 8.4 nTPM
Expression across tissuesHPA
Tissue
- testis: 8.4 nTPM
- skeletal muscle: 7.6 nTPM
- ovary: 6.2 nTPM
- cerebral cortex: 5.8 nTPM
- heart muscle: 4.3 nTPM
- placenta: 4.1 nTPM
Single-cell type
- oligodendrocytes: 793 nCPM
- retinal amacrine cells: 551 nCPM
- brain inhibitory neurons: 520 nCPM
- brain excitatory neurons: 471 nCPM
- medullary thymic epithelial cells: 420 nCPM
- late spermatids: 418 nCPM
Immune cell
- myeloid DC: 0.3 nTPM
- basophil: 0.2 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- white matter: 31 nTPM
- cerebral cortex: 29 nTPM
- pons: 24 nTPM
- medulla oblongata: 22 nTPM
- thalamus: 22 nTPM
- basal ganglia: 21 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.65
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.03
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ENOX1 as an antibody target. Whether an autoantibody or antibody against ENOX1 could matter depends on whether native ENOX1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ENOX1 is annotated at the cell surface, where native ENOX1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ENOX1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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