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TargetSerine/threonine-protein kinase PAK 2
LigandBDBM50112347
Substrate/Competitorn/a
Meas. Tech.Z'-LYTEBiochemical Assay
IC50 12.8±0.0 nM
Citation Licciulli, SMaksimoska, JZhou, CTroutman, SKota, SLiu, QDuron, SCampbell, DChernoff, JField, JMarmorstein, RKissil, JL FRAX597, a small molecule inhibitor of the p21-activated kinases, inhibits tumorigenesis of neurofibromatosis type 2 (NF2)-associated Schwannomas. J Biol Chem288:29105-14 (2013) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Serine/threonine-protein kinase PAK 2
Name:Serine/threonine-protein kinase PAK 2
Synonyms:PAK2 | PAK2_HUMAN | Serine/threonine-protein kinase PAK 1/PAK 2/PAK 3 | Serine/threonine-protein kinase PAK 2 | Serine/threonine-protein kinase PAK 2 (PAK2) | p21-Activated kinase 2 (PAK2)
Type:Enzyme
Mol. Mass.:58037.40
Organism:Homo sapiens (Human)
Description:Q13177
Residue:524
Sequence:
MSDNGELEDKPPAPPVRMSSTIFSTGGKDPLSANHSLKPLPSVPEEKKPRHKIISIFSGT
EKGSKKKEKERPEISPPSDFEHTIHVGFDAVTGEFTGMPEQWARLLQTSNITKLEQKKNP
QAVLDVLKFYDSNTVKQKYLSFTPPEKDGFPSGTPALNAKGTEAPAVVTEEEDDDEETAP
PVIAPRPDHTKSIYTRSVIDPVPAPVGDSHVDGAAKSLDKQKKKTKMTDEEIMEKLRTIV
SIGDPKKKYTRYEKIGQGASGTVFTATDVALGQEVAIKQINLQKQPKKELIINEILVMKE
LKNPNIVNFLDSYLVGDELFVVMEYLAGGSLTDVVTETCMDEAQIAAVCRECLQALEFLH
ANQVIHRDIKSDNVLLGMEGSVKLTDFGFCAQITPEQSKRSTMVGTPYWMAPEVVTRKAY
GPKVDIWSLGIMAIEMVEGEPPYLNENPLRALYLIATNGTPELQNPEKLSPIFRDFLNRC
LEMDVEKRGSAKELLQHPFLKLAKPLSSLTPLIMAAKEAMKSNR
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50112347
n/a
NameBDBM50112347
Synonyms:CHEMBL3609327 | FRAX597
TypeSmall organic molecule
Emp. Form.C29H28ClN7OS
Mol. Mass.558.097
SMILESCCn1c2nc(Nc3ccc(cc3)N3CCN(C)CC3)ncc2cc(-c2ccc(cc2Cl)-c2cncs2)c1=O
Structure
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