PLK1
Serine/threonine-protein kinase PLK1
Also known as: PLK, PLK1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P53350
- Gene
- PLK1
- Ensembl
- ENSG00000166851
- Chromosome
- 16
- Canonical length
- 603 aa
- Protein class
- Cancer-related genes, Disease related genes, Enzymes, Potential drug targets, Predicted intracellular proteins
OverviewNCBI Gene
The Ser/Thr protein kinase encoded by this gene belongs to the CDC5/Polo subfamily. It is highly expressed during mitosis and elevated levels are found in many different types of cancer. Depletion of this protein in cancer cells dramatically inhibited cell proliferation and induced apoptosis; hence, it is a target for cancer therapy. [provided by RefSeq, Sep 2015]
Canonical amino-acid sequenceUniProt
603 residues, UniProt reviewed canonical sequence.
>P53350|PLK1
1 MSAAVTAGKL ARAPADPGKA GVPGVAAPGA PAAAPPAKEI PEVLVDPRSR RRYVRGRFLG
61 KGGFAKCFEI SDADTKEVFA GKIVPKSLLL KPHQREKMSM EISIHRSLAH QHVVGFHGFF
121 EDNDFVFVVL ELCRRRSLLE LHKRRKALTE PEARYYLRQI VLGCQYLHRN RVIHRDLKLG
181 NLFLNEDLEV KIGDFGLATK VEYDGERKKT LCGTPNYIAP EVLSKKGHSF EVDVWSIGCI
241 MYTLLVGKPP FETSCLKETY LRIKKNEYSI PKHINPVAAS LIQKMLQTDP TARPTINELL
301 NDEFFTSGYI PARLPITCLT IPPRFSIAPS SLDPSNRKPL TVLNKGLENP LPERPREKEE
361 PVVRETGEVV DCHLSDMLQQ LHSVNASKPS ERGLVRQEEA EDPACIPIFW VSKWVDYSDK
421 YGLGYQLCDN SVGVLFNDST RLILYNDGDS LQYIERDGTE SYLTVSSHPN SLMKKITLLK
481 YFRNYMSEHL LKAGANITPR EGDELARLPY LRTWFRTRSA IILHLSNGSV QINFFQDHTK
541 LILCPLMAAV TYIDEKRDFR TYRLSLLEEY GCCKELASRL RYARTMVDKL LSSRSASNRL
601 KASLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLK1 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)
- 0.31
- Highest tissue expression
- 41 nTPM
Expression across tissuesHPA
Tissue
- thymus: 41 nTPM
- testis: 32 nTPM
- bone marrow: 30 nTPM
- tonsil: 28 nTPM
- lymph node: 26 nTPM
- esophagus: 14 nTPM
Single-cell type
- late primary spermatocytes: 180 nCPM
- early spermatids: 111 nCPM
- monocyte progenitors: 108 nCPM
- extravillous trophoblasts: 59 nCPM
- enteric transient amplifying cells: 55 nCPM
- migrating cytotrophoblasts: 51 nCPM
Immune cell
- T-reg: 5.7 nTPM
- total PBMC: 1.4 nTPM
- memory B-cell: 1.1 nTPM
- NK-cell: 0.9 nTPM
- memory CD4 T-cell: 0.8 nTPM
- neutrophil: 0.5 nTPM
Brain region
- white matter: 1.8 nTPM
- cerebral cortex: 1.7 nTPM
- thalamus: 1.3 nTPM
- cerebellum: 1.2 nTPM
- medulla oblongata: 1 nTPM
- amygdala: 0.9 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)
- 0.31
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 2.52
- DepMap mean gene effect
- -2.69
- DepMap dependency class
- pan
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- astral microtubule organization
- centrosome cycle
- double-strand break repair
- double-strand break repair via alternative nonhomologous end joining
- establishment of protein localization
- female meiosis chromosome segregation
- G2/M transition of mitotic cell cycle
- Golgi inheritance
- homologous chromosome segregation
- metaphase/anaphase transition of mitotic cell cycle
- microtubule bundle formation
- mitotic cell cycle
- mitotic chromosome condensation
- mitotic cleavage furrow formation
- mitotic cytokinesis
- mitotic G2 DNA damage checkpoint signaling
- mitotic nuclear membrane disassembly
- mitotic sister chromatid segregation
- mitotic spindle assembly checkpoint signaling
- mitotic spindle organization
- negative regulation of apoptotic process
- negative regulation of double-strand break repair via homologous recombination
- negative regulation of transcription by RNA polymerase II
- positive regulation of mitotic metaphase/anaphase transition
- positive regulation of proteasomal ubiquitin-dependent protein catabolic process
- positive regulation of protein localization to nucleus
- positive regulation of ubiquitin-dependent protein catabolic process
- protein localization to chromatin
- protein phosphorylation
- regulation of anaphase-promoting complex-dependent catabolic process
- regulation of cell cycle
- regulation of cytokinesis
- regulation of mitotic cell cycle
- regulation of mitotic cell cycle phase transition
- regulation of mitotic metaphase/anaphase transition
- regulation of mitotic spindle assembly
- sister chromatid cohesion
- synaptonemal complex disassembly
- positive regulation of mitotic nuclear envelope disassembly
- regulation of protein localization to cell cortex
Molecular functions
- anaphase-promoting complex binding
- ATP binding
- identical protein binding
- magnesium ion binding
- microtubule binding
- protein kinase activity
- protein kinase binding
- protein serine kinase activity
- protein serine/threonine kinase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein kinase domain
- POLO box domain
- Serine/threonine-protein kinase, active site
- Protein kinase-like domain superfamily
- Protein kinase, ATP binding site
- Second polo-box domain
- First polo-box domain
- POLO box domain superfamily
- Protein kinase domain
- POLO box duplicated region
- Polo-like kinase 1, catalytic domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PLK1 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 PLK1 as an antibody target. Whether an autoantibody or antibody against PLK1 could matter depends on whether native PLK1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLK1 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 PLK1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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