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histone H3 associated protein kinase

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Target id: 2028

Nomenclature: histone H3 associated protein kinase

Abbreviated Name: Haspin

Family: Haspin family

Contents:

Gene and Protein Information Click here for help
Species TM AA Chromosomal Location Gene Symbol Gene Name Reference
Human - 798 17p13.2 HASPIN histone H3 associated protein kinase
Mouse - 754 11 45.25 cM Haspin histone H3 associated protein kinase
Previous and Unofficial Names Click here for help
Germ cell-specific gene 2 protein | Haploid germ cell-specific nuclear protein kinase | haspin | Serine/threonine-protein kinase haspin | germ cell associated 2 (haspin) | germ cell-specific gene 2 | GSG2 | germ cell associated 2, haspin | Gsg2
Database Links Click here for help
Alphafold Q8TF76 (Hs), Q9Z0R0 (Mm)
BRENDA 2.7.11.1
ChEMBL Target CHEMBL1075163 (Hs)
Ensembl Gene ENSG00000177602 (Hs), ENSMUSG00000050107 (Mm)
Entrez Gene 83903 (Hs), 14841 (Mm)
Human Protein Atlas ENSG00000177602 (Hs)
KEGG Enzyme 2.7.11.1
KEGG Gene hsa:83903 (Hs), mmu:14841 (Mm)
OMIM 609240 (Hs)
Pharos Q8TF76 (Hs)
RefSeq Nucleotide NM_031965 (Hs), NM_010353 (Mm)
RefSeq Protein NP_114171 (Hs), NP_034483 (Mm)
UniProtKB Q8TF76 (Hs), Q9Z0R0 (Mm)
Wikipedia HASPIN (Hs)
Selected 3D Structures Click here for help
Image of receptor 3D structure from RCSB PDB
Description:  Crystal structure of haspin kinase
PDB Id:  2WB8
Resolution:  2.15Å
Species:  Human
References:  4
Image of receptor 3D structure from RCSB PDB
Description:  Crystal Structure of Human Haspin with an Imidazo-pyridazine ligand
PDB Id:  3F2N
Resolution:  1.8Å
Species:  Human
References: 
Enzyme Reaction Click here for help
EC Number: 2.7.11.1

Download all structure-activity data for this target as a CSV file go icon to follow link

Inhibitors
Key to terms and symbols View all chemical structures Click column headers to sort
Ligand Sp. Action Value Parameter Reference
SGI-1776 Small molecule or natural product Click here for species-specific activity table Hs Inhibition 7.5 pIC50 2
⤷ pIC50 7.5 (IC50 3.4x10-8 M) [2]
EMD Millipore KinaseProfilerTM screen/Reaction Biology Kinase HotspotSM screen Click here for help
A screen profiling 158 kinase inhibitors (Calbiochem Protein Kinase Inhibitor Library I and II, catalogue numbers 539744 and 539745) for their inhibitory activity at 1µM and 10µM against 234 human recombinant kinases using the EMD Millipore KinaseProfilerTM service.

A screen profiling the inhibitory activity of 178 commercially available kinase inhibitors at 0.5µM against a panel of 300 recombinant protein kinases using the Reaction Biology Corporation Kinase HotspotSM platform.

http://www.millipore.com/techpublications/tech1/pf3036
http://www.reactionbiology.com/webapps/main/pages/kinase.aspx

Reference: 1,3
Key to terms and symbols Click column headers to sort
Target used in screen: Haspin/Haspin
Ligand Sp. Type Action % Activity remaining at 0.5µM % Activity remaining at 1µM % Activity remaining at 10µM
PKR inhibitor Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 5.7 3.0 1.0
staurosporine Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 6.9 1.0 2.5
PKR inhibitor, negative control Small molecule or natural product Hs Inhibitor Inhibition 8.7 12.0 1.0
K-252a Small molecule or natural product Hs Inhibitor Inhibition 10.2 8.0 5.0
SB 218078 Small molecule or natural product Hs Inhibitor Inhibition 18.5 50.0 22.0
JAK3 inhibitor VI Small molecule or natural product Hs Inhibitor Inhibition 22.5 9.0 1.0
Cdc2-like kinase inhibitor Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 25.0 17.0 4.0
Gö 6976 Small molecule or natural product Ligand has a PDB structure Hs Inhibitor Inhibition 27.2 11.0 8.0
JNK inhibitor V Small molecule or natural product Hs Inhibitor Inhibition 31.0 36.0 -2.0
indirubin derivative E804 Small molecule or natural product Hs Inhibitor Inhibition 32.8 13.0 11.0
Displaying the top 10 most potent ligands  View all ligands in screen »

References

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1. Anastassiadis T, Deacon SW, Devarajan K, Ma H, Peterson JR. (2011) Comprehensive assay of kinase catalytic activity reveals features of kinase inhibitor selectivity. Nat Biotechnol, 29 (11): 1039-45. [PMID:22037377]

2. Drygin D, Haddach M, Pierre F, Ryckman DM. (2012) Potential use of selective and nonselective Pim kinase inhibitors for cancer therapy. J Med Chem, 55 (19): 8199-208. [PMID:22924342]

3. Gao Y, Davies SP, Augustin M, Woodward A, Patel UA, Kovelman R, Harvey KJ. (2013) A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery. Biochem J, 451 (2): 313-28. [PMID:23398362]

4. Villa F, Capasso P, Tortorici M, Forneris F, de Marco A, Mattevi A, Musacchio A. (2009) Crystal structure of the catalytic domain of Haspin, an atypical kinase implicated in chromatin organization. Proc Natl Acad Sci USA, 106 (48): 20204-9. [PMID:19918049]

How to cite this page

Haspin family: histone H3 associated protein kinase. Last modified on 23/05/2017. Accessed on 25/04/2025. IUPHAR/BPS Guide to PHARMACOLOGY, https://www.guidetomalariapharmacology.org/GRAC/ObjectDisplayForward?objectId=2028.