ATP12A
Potassium-transporting ATPase alpha chain 2
Also known as: AT12A_HUMAN, ATP1AL1, H-K-ATPase, HK
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P54707
- Gene
- ATP12A
- Ensembl
- ENSG00000075673
- Chromosome
- 13
- Canonical length
- 1039 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Plasma membrane,Actin filaments,Cytosol
OverviewNCBI Gene
The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This gene encodes a catalytic subunit of the ouabain-sensitive H+/K+ -ATPase that catalyzes the hydrolysis of ATP coupled with the exchange of H(+) and K(+) ions across the plasma membrane. It is also responsible for potassium absorption in various tissues. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]
Canonical amino-acid sequenceUniProt
1039 residues, UniProt reviewed canonical sequence.
>P54707|ATP12A
1 MHQKTPEIYS VELSGTKDIV KTDKGDGKEK YRGLKNNCLE LKKKNHKEEF QKELHLDDHK
61 LSNRELEEKY GTDIIMGLSS TRAAELLARD GPNSLTPPKQ TPEIVKFLKQ MVGGFSILLW
121 VGAFLCWIAY GIQYSSDKSA SLNNVYLGCV LGLVVILTGI FAYYQEAKST NIMSSFNKMI
181 PQQALVIRDS EKKTIPSEQL VVGDIVEVKG GDQIPADIRV LSSQGCRVDN SSLTGESEPQ
241 PRSSEFTHEN PLETKNICFY STTCLEGTVT GMVINTGDRT IIGHIASLAS GVGNEKTPIA
301 IEIEHFVHIV AGVAVSIGIL FFIIAVSLKY QVLDSIIFLI GIIVANVPEG LLATVTVTLS
361 LTAKRMAKKN CLVKNLEAVE TLGSTSIICS DKTGTLTQNR MTVAHLWFDN QIFVADTSED
421 HSNQVFDQSS RTWASLSKII TLCNRAEFKP GQENVPIMKK AVIGDASETA LLKFSEVILG
481 DVMEIRKRNR KVAEIPFNST NKFQLSIHEM DDPHGKRFLM VMKGAPERIL EKCSTIMING
541 EEHPLDKSTA KTFHTAYMEL GGLGERVLGF CHLYLPADEF PETYSFDIDA MNFPTSNLCF
601 VGLLSMIDPP RSTVPDAVTK CRSAGIKVIM VTGDHPITAK AIAKSVGIIS ANSETVEDIA
661 HRLNIAVEQV NKRDAKAAVV TGMELKDMSS EQLDEILANY QEIVFARTSP QQKLIIVEGC
721 QRQDAVVAVT GDGVNDSPAL KKADIGIAMG IAGSDAAKNA ADMVLLDDNF ASIVTGVEEG
781 RLIFDNLKKT IAYSLTKNIA ELCPFLIYII VGLPLPIGTI TILFIDLGTD IIPSIALAYE
841 KAESDIMNRK PRHKNKDRLV NQPLAVYSYL HIGLMQALGA FLVYFTVYAQ EGFLPRTLIN
901 LRVEWEKDYV NDLKDSYGQE WTRYQREYLE WTGYTAFFVG ILVQQIADLI IRKTRRNSIF
961 QQGLFRNKVI WVGITSQIII GLILSYGLGS VTALSFTMLR AQYWFVAVPH AILIWVYDEV
1021 RKLFIRLYPG SWWDKNMYYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ATP12A 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
- 10
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 14 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 14 nTPM
- esophagus: 11 nTPM
- skin: 5.8 nTPM
- placenta: 5.2 nTPM
- kidney: 5 nTPM
- rectum: 1.9 nTPM
Single-cell type
- respiratory secretory cells: 185 nCPM
- respiratory deuterosomal cells: 145 nCPM
- respiratory basal cells: 30 nCPM
- renal connecting tubule cells: 27 nCPM
- esophageal apical cells: 26 nCPM
- submucosal glandular cells: 12 nCPM
Immune cell
- T-reg: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 0.5 nTPM
- white matter: 0.4 nTPM
- hippocampal formation: 0.3 nTPM
- medulla oblongata: 0.2 nTPM
- midbrain: 0.2 nTPM
- basal ganglia: 0.1 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)
- 0.82
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.83
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intracellular potassium ion homeostasis
- intracellular sodium ion homeostasis
- potassium ion import across plasma membrane
- proton transmembrane transport
- regulation of pH
- sodium ion export across plasma membrane
Molecular functions
- ATP binding
- ATP hydrolysis activity
- metal ion binding
- P-type potassium:proton transporter activity
- P-type sodium:potassium-exchanging transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- P-type ATPase
- Cation-transporting P-type ATPase, N-terminal
- P-type ATPase subfamily IIC, subunit alpha
- Cation-transporting P-type ATPase, C-terminal
- P-type ATPase, A domain superfamily
- P-type ATPase, phosphorylation site
- HAD superfamily
- P-type ATPase, transmembrane domain superfamily
- P-type ATPase, cytoplasmic domain N
- HAD-like superfamily
- P-type ATPase, haloacid dehalogenase domain
- Cation transport ATPase (P-type)
- P-type ATPase, A domain
- P-type ATPase actuator domain
- Cation transporting ATPase, C-terminus
- Cation transporter/ATPase, N-terminus
- haloacid dehalogenase-like hydrolase
- P-type ATPase, cytoplasmic domain N
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ATP12A as an antibody target. Whether an autoantibody or antibody against ATP12A could matter depends on whether native ATP12A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ATP12A is annotated at the cell surface, where native ATP12A 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 ATP12A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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