CATH Classification
| Level | CATH Code | Description | 
|---|---|---|
 
	 | 
    3 | Alpha Beta | 
 
	 | 
    3.30 | 2-Layer Sandwich | 
 
	 | 
    3.30.200 | Phosphorylase Kinase; domain 1 | 
 
	 | 
    3.30.200.20 | Phosphorylase Kinase; domain 1 | 
Domain Context
CATH Clusters
| Superfamily | Phosphorylase Kinase; domain 1 | 
| Functional Family | Mitogen-activated protein kinase | 
Enzyme Information
| 2.7.11.24 | 
							 Mitogen-activated protein kinase. 
							based on mapping to UniProt P53779 		
							ATP + a protein = ADP + a phosphoprotein. 
							-!- Phosphorylation of specific tyrosine and threonine residues in the activation loop of this enzyme by EC 2.7.12.2 is necessary for enzyme activation. -!- Once activated, the enzyme phosphorylates target substrates on serine or threonine residues followed by a proline. -!- A distinguishing feature of all MAPKs is the conserved sequence Thr- Xaa-Tyr (TXY). -!- Mitogen-activated protein kinase (MAPK) signal transduction pathways are among the most widespread mechanisms of cellular regulation. -!- Mammalian MAPK pathways can be recruited by a wide variety of stimuli including hormones (e.g. insulin and growth hormone), mitogens (e.g. epidermal growth factor and platelet-derived growth factor), vasoactive peptides (e.g. angiotensin-II and endothelin), inflammatory cytokines of the tumor necrosis factor (TNF) family and environmental stresses such as osmotic shock, ionizing radiation and ischemeic injury. -!- Formerly EC 2.7.1.37. 
						 | 
					
UniProtKB Entries (1)
| P53779 | 
						 MK10_HUMAN 
						Homo sapiens 
						Mitogen-activated protein kinase 10 
					 | 
				
PDB Structure
| PDB | 4Y5H | 
| External Links | |
| Method | X-RAY DIFFRACTION | 
| Organism | |
| Primary Citation | 
					 Pyridopyrimidinone Derivatives as Potent and Selective c-Jun N-Terminal Kinase (JNK) Inhibitors. 
					    
					    Acs Med.Chem.Lett. 
					    
					 | 
			
