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TargetFocal adhesion kinase 1 [410-689]
LigandBDBM418860
Substrate/Competitorn/a
Meas. Tech.In Vitro Activity Assay
IC50<0.595±n/a nM
Citation Luzzio, MJFreeman-Cook, KDBhattacharya, SKHayward, MMHulford, CAAutry, CLZhao, XXiao, JNelson, KL Sulfonyl amide derivatives for the treatment of abnormal cell growth US Patent US10450297 Publication Date 10/22/2019
More Info.:Get all data from this article,  Assay Method
 
Focal adhesion kinase 1 [410-689]
Name:Focal adhesion kinase 1 [410-689]
Synonyms:FAK | FAK1 | FAK1_HUMAN | Focal adhesion kinase 1 (FAK) (aa 410-689) | PTK2
Type:Enzyme Catalytic Domain
Mol. Mass.:32163.33
Organism:Homo sapiens (Human)
Description:aa 410-689
Residue:280
Sequence:
PSTRDYEIQRERIELGRCIGEGQFGDVHQGIYMSPENPALAVAIKTCKNCTSDSVREKFL
QEALTMRQFDHPHIVKLIGVITENPVWIIMELCTLGELRSFLQVRKYSLDLASLILYAYQ
LSTALAYLESKRFVHRDIAARNVLVSSNDCVKLGDFGLSRYMEDSTYYKASKGKLPIKWM
APESINFRRFTSASDVWMFGVCMWEILMHGVKPFQGVKNNDVIGRIENGERLPMPPNCPP
TLYSLMTKCWAYDPSRRPRFTELKAQLSTILEEEKAQQEE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM418860
n/a
NameBDBM418860
Synonyms:2-chloro-4-({4-[({3- [methyl(methylsulfonyl)amino]pyrazin-2- yl}methyl)amino]-5- (trifluoromethyl)pyrimidin-2- yl}amino)benzamide (360) | US10450297, Example 360
TypeSmall organic molecule
Emp. Form.C19H18ClF3N8O3S
Mol. Mass.530.911
SMILESCN(c1nccnc1CNc1nc(Nc2ccc(C(N)=O)c(Cl)c2)ncc1C(F)(F)F)S(C)(=O)=O
Structure
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