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cyclin dependent kinase 15

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Target not currently curated in GtoImmuPdb

Target id: 1968

Nomenclature: cyclin dependent kinase 15

Abbreviated Name: CDK15

Family: TAIRE subfamily

Contents:

Gene and Protein Information Click here for help
Species TM AA Chromosomal Location Gene Symbol Gene Name Reference
Human - 435 2q33.1 CDK15 cyclin dependent kinase 15
Mouse - 433 1 C1.3 Cdk15 cyclin dependent kinase 15
Rat - 437 9q31 Cdk15 cyclin-dependent kinase 15
Previous and Unofficial Names Click here for help
ALS2CR7 | PFTAIRE protein kinase 2 | PFTAIRE2 | Cell division protein kinase 15 | frizzled family receptor 7 | cyclin-dependent kinase 15
Database Links Click here for help
Alphafold Q96Q40 (Hs), Q3V3A1 (Mm)
BRENDA 2.7.11.22
ChEMBL Target CHEMBL5856 (Hs)
Ensembl Gene ENSG00000138395 (Hs), ENSMUSG00000026023 (Mm), ENSRNOG00000022899 (Rn)
Entrez Gene 65061 (Hs), 271697 (Mm), 301440 (Rn)
Human Protein Atlas ENSG00000138395 (Hs)
KEGG Enzyme 2.7.11.22
KEGG Gene hsa:65061 (Hs), mmu:271697 (Mm), rno:301440 (Rn)
Pharos Q96Q40 (Hs)
RefSeq Nucleotide NM_001261435 (Hs), NM_001033373 (Mm), XM_237191 (Rn)
RefSeq Protein NP_631897 (Hs), NP_001028545 (Mm), XP_237191 (Rn)
UniProtKB Q96Q40 (Hs), Q3V3A1 (Mm)
Wikipedia CDK15 (Hs)
Enzyme Reaction Click here for help
EC Number: 2.7.11.22
DiscoveRx KINOMEscan® screen Click here for help
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
Key to terms and symbols Click column headers to sort
Target used in screen: PFTAIRE2
Ligand Sp. Type Action Value Parameter
R547 Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 8.1 pKd
foretinib Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 7.5 pKd
AT-7519 Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 7.2 pKd
AST-487 Small molecule or natural product Hs Inhibitor Inhibition 7.1 pKd
staurosporine Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 6.6 pKd
alvocidib Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 6.5 pKd
PHA-665752 Small molecule or natural product Hs Inhibitor Inhibition 6.3 pKd
BMS-387032 Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 6.1 pKd
lestaurtinib Small molecule or natural product Ligand has a PDB structure Immunopharmacology Ligand Hs Inhibitor Inhibition 5.9 pKd
bosutinib Small molecule or natural product Approved drug Ligand has a PDB structure Immunopharmacology Ligand Hs Inhibitor Inhibition 5.8 pKd
Displaying the top 10 most potent ligands  View all ligands in screen »

References

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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. 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]

How to cite this page

TAIRE subfamily: cyclin dependent kinase 15. Last modified on 20/03/2013. Accessed on 24/01/2025. IUPHAR/BPS Guide to PHARMACOLOGY, https://www.guidetoimmunopharmacology.org/GRAC/ObjectDisplayForward?objectId=1968.