Target
Tyrosine-protein kinase FRK
Ligand
BDBM25617
Substrate
Substrate Peptide Tyr 01
Meas. Tech.
Z-LYTE Enzymatic Kinase Assay
pH
7.5±n/a
Temperature
295.15±n/a K
IC50
1300±n/a nM
Citation
 Tsai, JLee, JTWang, WZhang, JCho, HMamo, SBremer, RGillette, SKong, JHaass, NKSproesser, KLi, LSmalley, KSFong, DZhu, YLMarimuthu, ANguyen, HLam, BLiu, JCheung, IRice, JSuzuki, YLuu, CSettachatgul, CShellooe, RCantwell, JKim, SHSchlessinger, JZhang, KYWest, BLPowell, BHabets, GZhang, CIbrahim, PNHirth, PArtis, DRHerlyn, MBollag, G Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity. Proc Natl Acad Sci U S A 105:3041-6 (2008) [PubMed]  Article 
Target
Name:
Tyrosine-protein kinase FRK
Synonyms:
FRK | FRK_HUMAN | FYN-related kinase | Nuclear tyrosine protein kinase RAK | PTK5 | RAK | SRC | Tyrosine Kinase FRK
Type:
Tyrosine-protein kinase
Mol. Mass.:
58254.41
Organism:
Homo sapiens (Human)
Description:
P42685
Residue:
505
Sequence:
MSNICQRLWEYLEPYLPCLSTEADKSTVIENPGALCSPQSQRHGHYFVALFDYQARTAEDLSFRAGDKLQVLDTLHEGWWFARHLEKRRDGSSQQLQGYIPSNYVAEDRSLQAEPWFFGAIGRSDAEKQLLYSENKTGSFLIRESESQKGEFSLSVLDGAVVKHYRIKRLDEGGFFLTRRRIFSTLNEFVSHYTKTSDGLCVKLGKPCLKIQVPAPFDLSYKTVDQWEIDRNSIQLLKRLGSGQFGEVWEGLWNNTTPVAVKTLKPGSMDPNDFLREAQIMKNLRHPKLIQLYAVCTLEDPIYIITELMRHGSLQEYLQNDTGSKIHLTQQVDMAAQVASGMAYLESRNYIHRDLAARNVLVGEHNIYKVADFGLARVFKVDNEDIYESRHEIKLPVKWTAPEAIRSNKFSIKSDVWSFGILLYEIITYGKMPYSGMTGAQVIQMLAQNYRLPQPSNCPQQFYNIMLECWNAEPKERPTFETLRWKLEDYFETDSSYSDANNFIR
  
Inhibitor
Name:
BDBM25617
Synonyms:
N-[3-({5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl}carbonyl)-2,4-difluorophenyl]propane-1-sulfonamide | PLX4720
Type:
Small organic molecule
Emp. Form.:
C17H14ClF2N3O3S
Mol. Mass.:
413.826
SMILES:
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(Cl)cc23)c1F
Structure:
Search PDB for entries with ligand similarity:
Substrate
Name:
Substrate Peptide Tyr 01
Synonyms:
n/a
Type:
Peptide
Mol. Mass.:
358.43
Organism:
n/a
Description:
Z -LYTE biochemical assay kit (SelectScreen; Invitrogen).
Residue:
3
Sequence:
NA