PLK2
Serine/threonine-protein kinase PLK2
Also known as: PLK2_HUMAN, SNK
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NYY3
- Gene
- PLK2
- Ensembl
- ENSG00000145632
- Chromosome
- 5
- Canonical length
- 685 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Mitochondria,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a member of the polo family of serine/threonine protein kinases that have a role in normal cell division. This gene is most abundantly expressed in testis, spleen and fetal tissues, and its expression is inducible by serum, suggesting that it may also play an important role in cells undergoing rapid cell division. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]
Canonical amino-acid sequenceUniProt
685 residues, UniProt reviewed canonical sequence.
>Q9NYY3|PLK2
1 MELLRTITYQ PAASTKMCEQ ALGKGCGADS KKKRPPQPPE ESQPPQSQAQ VPPAAPHHHH
61 HHSHSGPEIS RIIVDPTTGK RYCRGKVLGK GGFAKCYEMT DLTNNKVYAA KIIPHSRVAK
121 PHQREKIDKE IELHRILHHK HVVQFYHYFE DKENIYILLE YCSRRSMAHI LKARKVLTEP
181 EVRYYLRQIV SGLKYLHEQE ILHRDLKLGN FFINEAMELK VGDFGLAARL EPLEHRRRTI
241 CGTPNYLSPE VLNKQGHGCE SDIWALGCVM YTMLLGRPPF ETTNLKETYR CIREARYTMP
301 SSLLAPAKHL IASMLSKNPE DRPSLDDIIR HDFFLQGFTP DRLSSSCCHT VPDFHLSSPA
361 KNFFKKAAAA LFGGKKDKAR YIDTHNRVSK EDEDIYKLRH DLKKTSITQQ PSKHRTDEEL
421 QPPTTTVARS GTPAVENKQQ IGDAIRMIVR GTLGSCSSSS ECLEDSTMGS VADTVARVLR
481 GCLENMPEAD CIPKEQLSTS FQWVTKWVDY SNKYGFGYQL SDHTVGVLFN NGAHMSLLPD
541 KKTVHYYAEL GQCSVFPATD APEQFISQVT VLKYFSHYME ENLMDGGDLP SVTDIRRPRL
601 YLLQWLKSDK ALMMLFNDGT FQVNFYHDHT KIIICSQNEE YLLTYINEDR ISTTFRLTTL
661 LMSGCSSELK NRMEYALNML LQRCNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLK2 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)
- 0.35
- Highest tissue expression
- 84 nTPM
Expression across tissuesHPA
Tissue
- spleen: 84 nTPM
- basal ganglia: 53 nTPM
- heart muscle: 51 nTPM
- skin: 48 nTPM
- placenta: 45 nTPM
- salivary gland: 41 nTPM
Single-cell type
- extravillous trophoblasts: 390 nCPM
- epididymal basal cells: 263 nCPM
- breast myoepithelial cells: 247 nCPM
- endometrial secretory cells: 205 nCPM
- endometrial luminal cells: 166 nCPM
- breast secretory cells: 164 nCPM
Immune cell
- NK-cell: 9.1 nTPM
- basophil: 2.2 nTPM
- myeloid DC: 2.2 nTPM
- eosinophil: 1.9 nTPM
- neutrophil: 1.5 nTPM
- plasmacytoid DC: 1.5 nTPM
Brain region
- hippocampal formation: 90 nTPM
- basal ganglia: 70 nTPM
- cerebral cortex: 67 nTPM
- amygdala: 48 nTPM
- white matter: 30 nTPM
- choroid plexus: 29 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PLK2.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 65 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.18
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.01
- DepMap mean gene effect
- -0.03
- 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
- DNA damage response, signal transduction by p53 class mediator
- G1/S transition of mitotic cell cycle
- long-term synaptic depression
- long-term synaptic potentiation
- memory
- mitotic spindle organization
- negative regulation of angiogenesis
- negative regulation of apoptotic process
- negative regulation of apoptotic process in bone marrow cell
- negative regulation of cellular senescence
- negative regulation of inflammatory response to antigenic stimulus
- positive regulation of autophagy
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of cell migration involved in sprouting angiogenesis
- positive regulation of protein catabolic process
- protein phosphorylation
- Rap protein signal transduction
- Ras protein signal transduction
- regulation of centriole replication
- regulation of synaptic plasticity
Molecular functions
- ATP binding
- ATP-dependent protein binding
- protein serine kinase activity
- protein serine/threonine kinase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PLK2 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 PLK2 as an antibody target. Whether an autoantibody or antibody against PLK2 could matter depends on whether native PLK2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLK2 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 PLK2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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