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Target not currently curated in GtoImmuPdb
Target id: 2090
Nomenclature: mitogen-activated protein kinase 15
Abbreviated Name: ERK7
Family: Erk7 subfamily
Gene and Protein Information | ||||||
Species | TM | AA | Chromosomal Location | Gene Symbol | Gene Name | Reference |
Human | - | 544 | 8q24.3 | MAPK15 | mitogen-activated protein kinase 15 | |
Mouse | - | 549 | 15 D3 | Mapk15 | mitogen-activated protein kinase 15 | |
Rat | - | 547 | 7q34 | Mapk15 | mitogen-activated protein kinase 15 |
Previous and Unofficial Names |
ERK8 | extracellular signal regulated kinase 8 | extracellular signal-regulated kinase 7 | MAP kinase 15 |
Database Links | |
Alphafold | Q8TD08 (Hs), Q80Y86 (Mm), Q9Z2A6 (Rn) |
BRENDA | 2.7.11.24 |
ChEMBL Target | CHEMBL5198 (Hs) |
Ensembl Gene | ENSG00000181085 (Hs), ENSMUSG00000063704 (Mm), ENSRNOG00000009336 (Rn) |
Entrez Gene | 225689 (Hs), 332110 (Mm), 286997 (Rn) |
Human Protein Atlas | ENSG00000181085 (Hs) |
KEGG Enzyme | 2.7.11.24 |
KEGG Gene | hsa:225689 (Hs), mmu:332110 (Mm), rno:286997 (Rn) |
Pharos | Q8TD08 (Hs) |
RefSeq Nucleotide | NM_139021 (Hs), NM_177922 (Mm), NM_173331 (Rn) |
RefSeq Protein | NP_620590 (Hs), NP_808590 (Mm), NP_775453 (Rn) |
UniProtKB | Q8TD08 (Hs), Q80Y86 (Mm), Q9Z2A6 (Rn) |
Wikipedia | MAPK15 (Hs) |
Enzyme Reaction | ||||
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Download all structure-activity data for this target as a CSV file
Inhibitors | |||||||||||||||||||||||||||||||||||||||||||||||||||
Key to terms and symbols | View all chemical structures | Click column headers to sort | |||||||||||||||||||||||||||||||||||||||||||||||||
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DiscoveRx KINOMEscan® screen | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
A screen of 72 inhibitors against 456 human kinases. Quantitative data were derived using DiscoveRx KINOMEscan® platform. http://www.discoverx.com/services/drug-discovery-development-services/kinase-profiling/kinomescan Reference: 1,3 |
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Key to terms and symbols | Click column headers to sort | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Target used in screen: ERK8 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Displaying the top 10 most potent ligands View all ligands in screen » |
Immuno Process Associations | ||
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1. Davis MI, Hunt JP, Herrgard S, Ciceri P, Wodicka LM, Pallares G, Hocker M, Treiber DK, Zarrinkar PP. (2011) Comprehensive analysis of kinase inhibitor selectivity. Nat Biotechnol, 29 (11): 1046-51. [PMID:22037378]
2. Heathcote DA, Patel H, Kroll SH, Hazel P, Periyasamy M, Alikian M, Kanneganti SK, Jogalekar AS, Scheiper B, Barbazanges M et al.. (2010) A novel pyrazolo[1,5-a]pyrimidine is a potent inhibitor of cyclin-dependent protein kinases 1, 2, and 9, which demonstrates antitumor effects in human tumor xenografts following oral administration. J Med Chem, 53 (24): 8508-22. [PMID:21080703]
3. Wodicka LM, Ciceri P, Davis MI, Hunt JP, Floyd M, Salerno S, Hua XH, Ford JM, Armstrong RC, Zarrinkar PP et al.. (2010) Activation state-dependent binding of small molecule kinase inhibitors: structural insights from biochemistry. Chem Biol, 17 (11): 1241-9. [PMID:21095574]
Erk7 subfamily: mitogen-activated protein kinase 15. Last modified on 18/02/2015. Accessed on 20/09/2024. IUPHAR/BPS Guide to PHARMACOLOGY, https://www.guidetoimmunopharmacology.org/GRAC/ObjectDisplayForward?objectId=2090.