STK17A
Serine/threonine-protein kinase 17A
Also known as: DRAK1, ST17A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UEE5
- Gene
- STK17A
- Ensembl
- ENSG00000164543
- Chromosome
- 7
- Canonical length
- 414 aa
- Protein class
- Enzymes, Plasma proteins, Predicted membrane proteins
- Subcellular location
- Nuclear speckles,Plasma membrane
OverviewNCBI Gene
This gene is a member of the DAP kinase-related apoptosis-inducing protein kinase family and encodes an autophosphorylated nuclear protein with a protein kinase domain. The protein has apoptosis-inducing activity. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
414 residues, UniProt reviewed canonical sequence.
>Q9UEE5|STK17A
1 MIPLEKPGSG GSSPGATSGS GRAGRGLSGP CRPPPPPQAR GLLTEIRAVV RTEPFQDGYS
61 LCPGRELGRG KFAVVRKCIK KDSGKEFAAK FMRKRRKGQD CRMEIIHEIA VLELAQDNPW
121 VINLHEVYET ASEMILVLEY AAGGEIFDQC VADREEAFKE KDVQRLMRQI LEGVHFLHTR
181 DVVHLDLKPQ NILLTSESPL GDIKIVDFGL SRILKNSEEL REIMGTPEYV APEILSYDPI
241 SMATDMWSIG VLTYVMLTGI SPFLGNDKQE TFLNISQMNL SYSEEEFDVL SESAVDFIRT
301 LLVKKPEDRA TAEECLKHPW LTQSSIQEPS FRMEKALEEA NALQEGHSVP EINSDTDKSE
361 TKESIVTEEL IVVTSYTLGQ CRQSEKEKME QKAISKRFKF EEPLLQEIPG EFIYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against STK17A 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 14 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 14 nTPM
- tonsil: 13 nTPM
- thymus: 8.4 nTPM
- appendix: 7.5 nTPM
- blood vessel: 7.5 nTPM
- spleen: 6.9 nTPM
Single-cell type
- neutrophils: 531 nCPM
- t-cells: 479 nCPM
- nk-cells: 460 nCPM
- b-cells: 458 nCPM
- alveolar cells type 1: 390 nCPM
- pancreatic duct cells: 385 nCPM
Immune cell
- NK-cell: 4.9 nTPM
- memory CD8 T-cell: 3.2 nTPM
- naive CD4 T-cell: 3.1 nTPM
- naive CD8 T-cell: 3 nTPM
- eosinophil: 2.7 nTPM
- memory B-cell: 2.4 nTPM
Brain region
- cerebellum: 14 nTPM
- midbrain: 9.2 nTPM
- hypothalamus: 8.9 nTPM
- basal ganglia: 8.7 nTPM
- choroid plexus: 8.5 nTPM
- cerebral cortex: 8.3 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)
- 0.61
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 0.47
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic process
- intracellular signal transduction
- positive regulation of apoptotic process
- positive regulation of fibroblast apoptotic process
- protein phosphorylation
- regulation of reactive oxygen species metabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein kinase domain
- Serine/threonine-protein kinase, active site
- Protein kinase-like domain superfamily
- Protein kinase, ATP binding site
- Protein kinase domain
- Serine/threonine-protein kinase 17A, catalytic domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads STK17A as an antibody target. Whether an autoantibody or antibody against STK17A could matter depends on whether native STK17A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
STK17A is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label STK17A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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