Target
Cyclin-dependent kinase 2
Ligand
BDBM150752
Substrate
n/a
Meas. Tech.
Protein Kinase Assay
pH
7.5±n/a
Temperature
303.15±n/a K
Kd
2.83e+4± 3e+3 nM
Comments
extracted
Citation
 Hamdi, ALesnard, ASuzanne, PRobert, TMiteva, MAPellerano, MDidier, BFicko-Blean, ELobstein, AHibert, MRault, SMorris, MCColas, P Tampering with cell division by using small-molecule inhibitors of CDK-CKS protein interactions. Chembiochem 16:432-9 (2015) [PubMed]  Article 
Target
Name:
Cyclin-dependent kinase 2
Synonyms:
CDK2 | CDK2-Kinase | CDK2_HUMAN | CDKN2 | Cell division protein kinase 2 | Cyclin-dependent kinase 2 (CDK2) | Protein cereblon/Cyclin-dependent kinase 2 | p33 protein kinase
Type:
Enzyme Subunit
Mol. Mass.:
33938.17
Organism:
Homo sapiens (Human)
Description:
P24941
Residue:
298
Sequence:
MENFQKVEKIGEGTYGVVYKARNKLTGEVVALKKIRLDTETEGVPSTAIREISLLKELNHPNIVKLLDVIHTENKLYLVFEFLHQDLKKFMDASALTGIPLPLIKSYLFQLLQGLAFCHSHRVLHRDLKPQNLLINTEGAIKLADFGLARAFGVPVRTYTHEVVTLWYRAPEILLGCKYYSTAVDIWSLGCIFAEMVTRRALFPGDSEIDQLFRIFRTLGTPDEVVWPGVTSMPDYKPSFPKWARQDFSKVVPPLDEDGRSLLSQMLHYDPNKRISAKAALAHPFFQDVTKPVPHLRL
  
Inhibitor
Name:
BDBM150752
Synonyms:
4-hydrazino-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidine (A)
Type:
Small organic molecule
Emp. Form.:
C10H12N4S
Mol. Mass.:
220.294
SMILES:
NNc1ncnc2sc3CCCCc3c12
Structure:
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