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Protein Page:
VRK1 (human)
p Phosphorylation
a Acetylation
m Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
u Ubiquitination
s Sumoylation
n Neddylation
gl O-GlcNAc
ga O-GalNAc
h Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage

Overview
VRK1 Serine/threonine kinase that phosphorylates Thr-18 of p53/TP53 and may thereby prevent the interaction between p53/TP53 and MDM2. Defects in VRK1 are the cause of pontocerebellar hypoplasia type 1 (PCH1); also called pontocerebellar hypoplasia with infantile spinal muscular atrophy or pontocerebellar hypoplasia with anterior horn cell disease. PCH1 is characterized by an abnormally small cerebellum and brainstem, central and peripheral motor dysfunction from birth, gliosis and anterior horn cell degeneration resembling infantile spinal muscular atrophy (SMA). Belongs to the protein kinase superfamily. CK1 Ser/Thr protein kinase family. VRK subfamily. Note: This description may include information from UniProtKB.
Protein type: Kinase, protein; Protein kinase, CK1; Protein kinase, Ser/Thr (non-receptor); EC 2.7.11.1; CK1 group; VRK family
Cellular Component: nucleoplasm; Golgi stack; cytoplasm; nucleolus; spindle; nucleus; cytosol
Molecular Function: protein serine/threonine kinase activity; protein binding; ATP binding
Biological Process: mitosis; mitotic nuclear envelope reassembly; protein amino acid autophosphorylation; mitotic nuclear envelope disassembly; mitotic cell cycle; protein amino acid phosphorylation
Reference #:  Q99986 (UniProtKB)
Alt. Names/Synonyms: MGC117401; MGC138280; MGC142070; PCH1; Serine/threonine-protein kinase VRK1; vaccinia related kinase 1; vaccinia virus B1R-related kinase 1; Vaccinia-related kinase 1; VRK1
Gene Symbols: VRK1
Molecular weight: 45,476 Da
Basal Isoelectric point: 9.02  Predict pI for various phosphorylation states
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
Select Structure to View Below

VRK1

Protein Structure Not Found.


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Sites Implicated In
cytoskeletal reorganization: S342‑p

Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 K16-u AGRQSSAkRHLAEQF
0 1 K112-u LKYLGVPkYWGSGLH
0 2 T153-p AKRFSRKtVLQLsLR
0 2 S158-p RKtVLQLsLRILDIL
0 3 K188-u SNLLLNYkNPDQVYL
0 3 K301-u NKPGEIAkYMETVKL
0 2 K329-u DILLQGLkAIGSKDD
2 2 S342-p DDGKLDLsVVENGGL
3 0 T355-p GLKAKTItKKRKKEI
0 2 S376-p GVEDTEWsNtQtEEA
0 17 T378-p EDTEWsNtQtEEAIQ
0 8 T380-p TEWsNtQtEEAIQTR
0 1 - gap
  mouse

 
K16 AGRPGPAKRRLAEQF
K112 LKYLGVPKYWGSGLH
T153 AKRFSRKTVLQLSLR
S158 RKTVLQLSLRILDIL
K188 SNLLLSHKNPDQVYL
K301 NKPGEIAKYMESVKL
K329 DILLQGLKAIGSKDD
S342 DDGKLDFSAVENGSV
S355-p SVKTRPAsKKRKKEA
S376 AVEDMECSDTQVQEA
T378 EDMECSDTQVQEAAQ
V380 MECSDTQVQEAAQTR
S411-p AGCSSSDsSRRQQHL
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