Homo sapiens Protein: VRK1
Summary
InnateDB Protein IDBP-19299.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol VRK1
Protein Name vaccinia related kinase 1
Synonyms PCH1; PCH1A;
Species Homo sapiens
Ensembl Protein ENSP00000216639
InnateDB Gene IDBG-19297 (VRK1)
Protein Structure
UniProt Annotation
Function Serine/threonine kinase involved in Golgi disassembly during the cell cycle: following phosphorylation by PLK3 during mitosis, required to induce Golgi fragmentation. Acts by mediating phosphorylation of downstream target protein. Phosphorylates 'Thr- 18' of p53/TP53 and may thereby prevent the interaction between p53/TP53 and MDM2. Phosphorylates casein and histone H3. Phosphorylates BANF1: disrupts its ability to bind DNA, reduces its binding to LEM domain-containing proteins and causes its relocalization from the nucleus to the cytoplasm. Phosphorylates ATF2 which activates its transcriptional activity. {ECO:0000269PubMed:10951572, ECO:0000269PubMed:14645249, ECO:0000269PubMed:15105425, ECO:0000269PubMed:16495336, ECO:0000269PubMed:18617507, ECO:0000269PubMed:19103756}.
Subcellular Localization Cytoplasm. Nucleus. Cytoplasm, cytoskeleton, spindle {ECO:0000250}. Note=Dispersed throughout the cell but not located on mitotic spindle or chromatids during mitosis.
Disease Associations Pontocerebellar hypoplasia 1A (PCH1A) [MIM:607596]: A disorder characterized by an abnormally small cerebellum and brainstem, central and peripheral motor dysfunction from birth, gliosis and spinal cord anterior horn cells degeneration resembling infantile spinal muscular atrophy. Additional features include muscle hypotonia, congenital contractures and respiratory insufficiency that is evident at birth. {ECO:0000269PubMed:19646678}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Widely expressed. Highly expressed in fetal liver, testis and thymus. {ECO:0000269PubMed:9344656}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 19 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 19 [view]
Protein-Protein 18 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 1 [view]
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004672 protein kinase activity
GO:0004674 protein serine/threonine kinase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016772 transferase activity, transferring phosphorus-containing groups
GO:0031493 nucleosomal histone binding
GO:0035175 histone kinase activity (H3-S10 specific)
GO:0072354 histone kinase activity (H3-T3 specific)
Biological Process
GO:0000278 mitotic cell cycle
GO:0006468 protein phosphorylation
GO:0007067 mitotic nuclear division
GO:0007077 mitotic nuclear envelope disassembly
GO:0007084 mitotic nuclear envelope reassembly
GO:0043987 histone H3-S10 phosphorylation
GO:0046777 protein autophosphorylation
GO:0072355 histone H3-T3 phosphorylation
GO:0090166 Golgi disassembly
Cellular Component
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005795 Golgi stack
GO:0005819 spindle
GO:0005829 cytosol
Protein Structure and Domains
PDB ID
InterPro IPR000719 Protein kinase domain
IPR001245 Serine-threonine/tyrosine-protein kinase catalytic domain
IPR002290 Serine/threonine/dual specificity protein kinase, catalytic domain
IPR011009 Protein kinase-like domain
PFAM PF00069
PF07714
PRINTS PR00109
PIRSF
SMART SM00220
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q99986
PhosphoSite PhosphoSite-Q99986
TrEMBL
UniProt Splice Variant
Entrez Gene 7443
UniGene Hs.622262
RefSeq NP_003375
HUGO HGNC:12718
OMIM 602168
CCDS CCDS9947
HPRD 03701
IMGT
EMBL AB000449 BC103761 BC112075 BC113510
GenPept AAI03762 AAI12076 AAI13511 BAA19108