KCNMB3
Calcium-activated potassium channel subunit beta-3
Also known as: KCMB3_HUMAN, KCNMB2, KCNMBL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NPA1
- Gene
- KCNMB3
- Ensembl
- ENSG00000171121
- Chromosome
- 3
- Canonical length
- 279 aa
- Protein class
- FDA approved drug targets, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoplasm,Mitochondria
OverviewNCBI Gene
MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit and the modulatory beta subunit. The protein encoded by this gene is an auxiliary beta subunit which may partially inactivate or slightly decrease the activation time of MaxiK alpha subunit currents. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 22. [provided by RefSeq, Jul 2009]
Canonical amino-acid sequenceUniProt
279 residues, UniProt reviewed canonical sequence.
>Q9NPA1|KCNMB3
1 MDFSPSSELG FHFVAFILLT RHRTAFPASG KKRETDYSDG DPLDVHKRLP SSAGEDRAVM
61 LGFAMMGFSV LMFFLLGTTI LKPFMLSIQR EESTCTAIHT DIMDDWLDCA FTCGVHCHGQ
121 GKYPCLQVFV NLSHPGQKAL LHYNEEAVQI NPKCFYTPKC HQDRNDLLNS ALDIKEFFDH
181 KNGTPFSCFY SPASQSEDVI LIKKYDQMAI FHCLFWPSLT LLGGALIVGM VRLTQHLSLL
241 CEKYSTVVRD EVGGKVPYIE QHQFKLCIMR RSKGRAEKSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KCNMB3 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
- 2
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 8.4 nTPM
Expression across tissuesHPA
Tissue
- spleen: 8.4 nTPM
- cerebellum: 7.8 nTPM
- cerebral cortex: 6.7 nTPM
- liver: 6.3 nTPM
- pancreas: 6.1 nTPM
- hippocampal formation: 5.6 nTPM
Single-cell type
- podocytes: 31 nCPM
- late spermatids: 27 nCPM
- cardiomyocytes: 19 nCPM
- epicardial cells: 18 nCPM
- renal collecting duct intercalated cells: 18 nCPM
- renal collecting duct principal cells: 16 nCPM
Immune cell
- memory B-cell: 1.2 nTPM
- NK-cell: 1.1 nTPM
- basophil: 0.8 nTPM
- naive B-cell: 0.7 nTPM
- neutrophil: 0.6 nTPM
- gdT-cell: 0.4 nTPM
Brain region
- medulla oblongata: 4.6 nTPM
- cerebral cortex: 4.4 nTPM
- basal ganglia: 4.2 nTPM
- pons: 4.2 nTPM
- thalamus: 4.2 nTPM
- choroid plexus: 4.1 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)
- 1.87
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.84
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% 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
InteractionsUniProt · HPA
Protein binding partners of KCNMB3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KCNMB3 as an antibody target. Whether an autoantibody or antibody against KCNMB3 could matter depends on whether native KCNMB3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KCNMB3 is annotated at the cell surface, where native KCNMB3 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 KCNMB3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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