ATP4B
Potassium-transporting ATPase subunit beta
Also known as: ATP4B_HUMAN, ATP6B
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P51164
- Gene
- ATP4B
- Ensembl
- ENSG00000186009
- Chromosome
- 13
- Canonical length
- 291 aa
- Protein class
- FDA approved drug targets, Metabolic proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
The protein encoded by this gene belongs to a family of P-type cation-transporting ATPases. The gastric H+, K+-ATPase is a heterodimer consisting of a high molecular weight catalytic alpha subunit and a smaller but heavily glycosylated beta subunit. This enzyme is a proton pump that catalyzes the hydrolysis of ATP coupled with the exchange of H(+) and K(+) ions across the plasma membrane. It is also responsible for gastric acid secretion. This gene encodes the beta subunit of the gastric H+, K+-ATPase. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
291 residues, UniProt reviewed canonical sequence.
>P51164|ATP4B
1 MAALQEKKTC GQRMEEFQRY CWNPDTGQML GRTLSRWVWI SLYYVAFYVV MTGLFALCLY
61 VLMQTVDPYT PDYQDQLRSP GVTLRPDVYG EKGLEIVYNV SDNRTWADLT QTLHAFLAGY
121 SPAAQEDSIN CTSEQYFFQE SFRAPNHTKF SCKFTADMLQ NCSGLADPNF GFEEGKPCFI
181 IKMNRIVKFL PSNGSAPRVD CAFLDQPREL GQPLQVKYYP PNGTFSLHYF PYYGKKAQPH
241 YSNPLVAAKL LNIPRNAEVA IVCKVMAEHV TFNNPHDPYE GKVEFKLKIE KLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ATP4B 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
- 1
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 1,002 nTPM
Expression across tissuesHPA
Tissue
- stomach: 1,002 nTPM
- choroid plexus: 6.8 nTPM
- fallopian tube: 3.1 nTPM
- hypothalamus: 0.9 nTPM
- hippocampal formation: 0.6 nTPM
- amygdala: 0.4 nTPM
Single-cell type
- parietal cells: 7,052 nCPM
- gastric chief cells: 141 nCPM
- mucous neck cells: 16 nCPM
- fallopian tube ciliated cells: 13 nCPM
- epididymal efferent duct ciliated cells: 11 nCPM
- ependymal cells: 9.3 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 7.9 nTPM
- medulla oblongata: 1.4 nTPM
- midbrain: 1.3 nTPM
- spinal cord: 1.2 nTPM
- hippocampal formation: 0.6 nTPM
- hypothalamus: 0.6 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)
- 1.05
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.17
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell adhesion
- intracellular potassium ion homeostasis
- intracellular sodium ion homeostasis
- pH reduction
- potassium ion import across plasma membrane
- potassium ion transmembrane transport
- response to lipopolysaccharide
- sodium ion export across plasma membrane
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ATP4B as an antibody target. Whether an autoantibody or antibody against ATP4B could matter depends on whether native ATP4B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ATP4B is annotated at the cell surface, where native ATP4B 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 ATP4B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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