VRK1
Serine/threonine-protein kinase VRK1
Also known as: VRK1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99986
- Gene
- VRK1
- Ensembl
- ENSG00000100749
- Chromosome
- 14
- Canonical length
- 396 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene encodes a member of the vaccinia-related kinase (VRK) family of serine/threonine protein kinases. This gene is widely expressed in human tissues and has increased expression in actively dividing cells, such as those in testis, thymus, fetal liver, and carcinomas. Its protein localizes to the nucleus and has been shown to promote the stability and nuclear accumulation of a transcriptionally active p53 molecule and, in vitro, to phosphorylate Thr18 of p53 and reduce p53 ubiquitination. This gene, therefore, may regulate cell proliferation. This protein also phosphorylates histone, casein, and the transcription factors ATF2 (activating transcription factor 2) and c-JUN. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
396 residues, UniProt reviewed canonical sequence.
>Q99986|VRK1
1 MPRVKAAQAG RQSSAKRHLA EQFAVGEIIT DMAKKEWKVG LPIGQGGFGC IYLADMNSSE
61 SVGSDAPCVV KVEPSDNGPL FTELKFYQRA AKPEQIQKWI RTRKLKYLGV PKYWGSGLHD
121 KNGKSYRFMI MDRFGSDLQK IYEANAKRFS RKTVLQLSLR ILDILEYIHE HEYVHGDIKA
181 SNLLLNYKNP DQVYLVDYGL AYRYCPEGVH KEYKEDPKRC HDGTIEFTSI DAHNGVAPSR
241 RGDLEILGYC MIQWLTGHLP WEDNLKDPKY VRDSKIRYRE NIASLMDKCF PEKNKPGEIA
301 KYMETVKLLD YTEKPLYENL RDILLQGLKA IGSKDDGKLD LSVVENGGLK AKTITKKRKK
361 EIEESKEPGV EDTEWSNTQT EEAIQTRSRT RKRVQKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against VRK1 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)
- 0.32
- Highest tissue expression
- 48 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 48 nTPM
- thymus: 33 nTPM
- tonsil: 26 nTPM
- testis: 26 nTPM
- lymph node: 25 nTPM
- appendix: 12 nTPM
Single-cell type
- parietal cells: 354 nCPM
- oocytes: 345 nCPM
- neutrophil progenitors: 331 nCPM
- early primary spermatocytes: 282 nCPM
- erythrocyte progenitors: 268 nCPM
- monocyte progenitors: 177 nCPM
Immune cell
- NK-cell: 46 nTPM
- basophil: 43 nTPM
- T-reg: 35 nTPM
- naive B-cell: 33 nTPM
- memory B-cell: 31 nTPM
- MAIT T-cell: 29 nTPM
Brain region
- basal ganglia: 12 nTPM
- white matter: 12 nTPM
- thalamus: 10 nTPM
- cerebellum: 9.8 nTPM
- cerebral cortex: 9.8 nTPM
- midbrain: 9.3 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about VRK1.
Disease | AllUniProt
Conditions VRK1 is implicated in, by any mechanism.
- Pontocerebellar hypoplasia 1A (PCH1A) MIM:607596
- Neuronopathy, distal hereditary motor, autosomal recessive 10 (HMNR10) MIM:620542
Disease | GeneticClinVar
96 pathogenic / likely-pathogenic of 607 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Pontocerebellar hypoplasia type 1A
- Neuronopathy, distal hereditary motor, autosomal recessive 10
- Inborn genetic diseases
- Congenital pontocerebellar hypoplasia type 1
- Pontoneocerebellar hypoplasia
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)
- 0.63
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.17
- DepMap mean gene effect
- -0.47
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- Cajal body organization
- cell division
- chromatin remodeling
- DNA damage response
- Golgi disassembly
- mitotic nuclear membrane disassembly
- neuron projection development
- positive regulation of protein localization to chromatin
- protein autophosphorylation
- protein phosphorylation
- regulation of neuron migration
- signal transduction
Molecular functions
- ATP binding
- histone binding
- histone H3S10 kinase activity
- histone H3T3 kinase activity
- kinase activity
- nucleosomal DNA binding
- protein kinase activity
- protein kinase binding
- protein serine kinase activity
- protein serine/threonine kinase activity
- histone H2AX kinase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of VRK1 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 VRK1 as an antibody target. Whether an autoantibody or antibody against VRK1 could matter depends on whether native VRK1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
VRK1 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 VRK1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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