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Target not currently curated in GtoImmuPdb
Target id: 2079
Nomenclature: mitogen-activated protein kinase kinase kinase 4
Abbreviated Name: MEKK4
Family: STE11 family
Gene and Protein Information | ||||||
Species | TM | AA | Chromosomal Location | Gene Symbol | Gene Name | Reference |
Human | - | 1608 | 6q26 | MAP3K4 | mitogen-activated protein kinase kinase kinase 4 | |
Mouse | - | 1597 | 17 A1 | Map3k4 | mitogen-activated protein kinase kinase kinase 4 | |
Rat | - | 1387 | 1 q11 | Map3k4 | mitogen activated protein kinase kinase kinase 4 |
Previous and Unofficial Names |
MAP three kinase 1 | MAPK/ERK kinase kinase 4 | MAPKKK4 | MTK1 | RP17 | Tas |
Database Links | |
Alphafold | Q9Y6R4 (Hs), O08648 (Mm) |
BRENDA | 2.7.11.25 |
ChEMBL Target | CHEMBL4853 (Hs) |
Ensembl Gene | ENSG00000085511 (Hs), ENSMUSG00000014426 (Mm), ENSRNOG00000017419 (Rn) |
Entrez Gene | 4216 (Hs), 26407 (Mm), 308106 (Rn) |
Human Protein Atlas | ENSG00000085511 (Hs) |
KEGG Enzyme | 2.7.11.25 |
KEGG Gene | hsa:4216 (Hs), mmu:26407 (Mm), rno:308106 (Rn) |
OMIM | 602425 (Hs) |
Pharos | Q9Y6R4 (Hs) |
RefSeq Nucleotide | NM_005922 (Hs), NM_011948 (Mm), NM_001107456 (Rn) |
RefSeq Protein | NP_005913 (Hs), NP_036078 (Mm), NP_001100926 (Rn) |
UniProtKB | Q9Y6R4 (Hs), O08648 (Mm) |
Wikipedia | MAP3K4 (Hs) |
Enzyme Reaction | ||||
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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: 1-2 |
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Key to terms and symbols | Click column headers to sort | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Target used in screen: MAP3K4 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Displaying the top 10 most potent ligands View all ligands in screen » |
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. 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]
STE11 family: mitogen-activated protein kinase kinase kinase 4. Last modified on 18/08/2014. Accessed on 08/12/2024. IUPHAR/BPS Guide to PHARMACOLOGY, https://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=2079.