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| Parameter | Value |
|---|---|
| Gene | CLK3 |
| Protein Name | CLK3_HUMAN |
| Organism | Homo sapiens (Human) |
| Alternative name(s) | Dual specificity protein kinase CLK3 (EC 2.7.12.1) (CDC-like kinase 3) |
| Protein Family | Protein kinase superfamily |
| NCBI Gene ID | 1198 |
| UniProt ID | P49761 |
| Enzyme Class | 2.7.12.1 |
| Molecular Weight | 73515 |
| Protein Length | 638 |
| Protein Domain | InterPro | Pfam |
| 3D Structure |
PDBe |
PDBj |
RCSB PDB |
DrugPort
ModBase | SwissModel |
| Gene Expression | Gene Expression Atlas |
| Function and Disease | OMIM |
| Protein-protein Interaction Database | STRING | IntAct | MINT |
| Kinase Database | Phospho.ELM | PhosphoSite | NetworKIN |
| Catalytic Activity (UniProt annotation) | ATP + a protein = ADP + a phosphoprotein. |
| Localization | Isoform 1: Nucleus. Cytoplasm; Isoform 2: Nucleus speckle. Note=Co-localizes with serine- and arginine-rich (SR) proteins in the nuclear speckles. |
| Function (UniProt annotation) | Dual specificity kinase acting on both serine/threonine and tyrosine-containing substrates. Phosphorylates serine- and arginine-rich (SR) proteins of the spliceosomal complex. May be a constituent of a network of regulatory mechanisms that enable SR proteins to control RNA splicing and can cause redistribution of SR proteins from speckles to a diffuse nucleoplasmic distribution. Phosphorylates SRSF1 and SRSF3. Regulates the alternative splicing of tissue factor (F3) pre-mRNA in endothelial cells. |
| Gene Ontology | GO:0001669; GO:0003723; GO:0004674; GO:0004712; GO:0004713; GO:0005524; GO:0005634; GO:0005654; GO:0006468; GO:0016020; GO:0016607; GO:0042802; GO:0043484; GO:0045111; GO:0046777 |
| Gene Name | Organism | P-Site | Sequence(+/-7) | Conservation | Disorder | Curator Assessment | Reliability | Evidence Class | Evidence Logic | PubMed | Phospho-ELM | PhosphoSite-Plus |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CHEK1 (O14757) | Homo sapiens | S157 | HHCKRYRSPEPDPYL | 0.999 | 0.5707 | - | - | - | - | - | - |
|
Reactome Pathways
No KEGG pathways found
No NCI Nature pathways found