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Target
Tyrosine-protein kinase ITK/TSK [357-620,Y512E]
Ligand
BDBM213216
Substrate
n/a
Meas. Tech.
LanthaScreen Kinase Binding Assay
IC50
2.0e+3±0 nM
Citation
 Harling, JD; Deakin, AM; Campos, S; Grimley, R; Chaudry, L; Nye, C; Polyakova, O; Bessant, CM; Barton, N; Somers, D; Barrett, J; Graves, RH; Hanns, L; Kerr, WJ; Solari, R Discovery of novel irreversible inhibitors of interleukin (IL)-2-inducible tyrosine kinase (Itk) by targeting cysteine 442 in the ATP pocket. J Biol Chem 288:28195-206 (2013) [PubMed]  Article 
Target
Name:
Tyrosine-protein kinase ITK/TSK [357-620,Y512E]
Synonyms:
EMT | ITK | ITK_HUMAN | Interlukin-2-inducible tyrosine kinase (Itk) | LYK
Type:
Enzyme
Mol. Mass.:
30027.99
Organism:
Homo sapiens (Human)
Description:
Human Itk truncation (357-620 aa) with Y512E mutation
Residue:
264
Sequence:
VIDPSELTFVQEIGSGQFGLVHLGYWLNKDKVAIKTIREGAMSEEDFIEEAEVMMKLSHPKLVQLYGVCLEQAPICLVFEFMEHGCLSDYLRTQRGLFAAETLLGMCLDVCEGMAYLEEACVIHRDLAARNCLVGENQVIKVSDFGMTRFVLDDQETSSTGTKFPVKWASPEVFSFSRYSSKSDVWSFGVLMWEVFSEGKIPYENRSNSEVVEDISTGFRLYKPRLASTHVYQIMNHCWKERPEDRPAFSRLLRQLAEIAESGL
  
Inhibitor
Name:
BDBM213216
Synonyms:
N-(trans-4-{[4-(4-Morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]amino}cyclohexyl)-2-propenamide (5)
Type:
Small organic molecule
Emp. Form.:
C24H30N8O2S
Mol. Mass.:
494.612
SMILES:
C=CC(=O)N[C@H]1CC[C@@H](CC1)Nc1nc(CN2CCOCC2)cc(Nc2nc3cccnc3s2)n1 |r,wU:5.4,wD:8.11,(-13.52,-3.78,;-12.18,-4.55,;-10.85,-3.78,;-10.85,-2.24,;-9.51,-4.55,;-8.18,-3.78,;-8.18,-2.24,;-6.85,-1.47,;-5.51,-2.24,;-5.51,-3.78,;-6.85,-4.55,;-4.18,-1.47,;-4.18,.07,;-5.51,.84,;-5.51,2.38,;-6.85,3.15,;-6.85,4.69,;-5.51,5.46,;-5.51,7,;-6.85,7.77,;-8.18,7,;-8.18,5.46,;-4.18,3.15,;-2.85,2.38,;-1.51,3.15,;-.18,2.38,;1.23,3.01,;2.26,1.87,;3.8,1.87,;4.57,.53,;3.8,-.8,;2.26,-.8,;1.49,.53,;-.02,.85,;-2.85,.84,)|
Structure:
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