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TargetInterlukin-2-inducible tyrosine kinase (Itk)
LigandBDBM213213
Substrate/Competitorn/a
Meas. Tech.LanthaScreen Kinase Binding Assay
IC50 1.3e+3±0 nM
Citation Harling JDDeakin AMCampos SGrimley RChaudry LNye CPolyakova OBessant CMBarton NSomers DBarrett JGraves RHHanns LKerr WJSolari 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
More Info.:Get all data from this article,  Assay Method
 
Interlukin-2-inducible tyrosine kinase (Itk)
Name:Interlukin-2-inducible tyrosine kinase (Itk)
Synonyms:n/a
Type:Enzyme
Mol. Mass.:30027.99
Organism:Homo sapiens (Human)
Description:Human Itk truncation (357-620 aa) with Y512E mutation
Residue:264
Sequence:
VIDPSELTFVQEIGSGQFGLVHLGYWLNKDKVAIKTIREGAMSEEDFIEEAEVMMKLSHP
KLVQLYGVCLEQAPICLVFEFMEHGCLSDYLRTQRGLFAAETLLGMCLDVCEGMAYLEEA
CVIHRDLAARNCLVGENQVIKVSDFGMTRFVLDDQETSSTGTKFPVKWASPEVFSFSRYS
SKSDVWSFGVLMWEVFSEGKIPYENRSNSEVVEDISTGFRLYKPRLASTHVYQIMNHCWK
ERPEDRPAFSRLLRQLAEIAESGL
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  Blast E-value cutoff:
BDBM213213
n/a
NameBDBM213213
Synonyms:N-(2-{[4-(4-Morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]amino}ethyl)-2-propenamide (2)
TypeSmall organic molecule
Emp. Form.C20H24N8O2S
Mol. Mass.440.522
SMILESC=CC(=O)NCCNc1nc(CN2CCOCC2)cc(Nc2nc3cccnc3s2)n1
Structure
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