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TargetTyrosine-protein kinase BTK [393-659]
LigandBDBM287414
Substrate/Competitorn/a
Meas. Tech.Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET)
pH6.5±n/a
Temperature298.15±n/a K
IC50<100±n/a nM
Commentsextracted
Citation Bonafoux, DDavis, HMFrank, KEFriedman, MMHerold, JMHoemann, MZHuntley, ROsuma, ASheppard, GSomal, GKVan Camp, JVan Epps, SAVasudevan, AWallace, GAWang, LWang, LWang, ZWilson, NSXu, X Primary carboxamides as BTK inhibitors US Patent US9567339 Publication Date 2/14/2017
More Info.:Get all data from this article,  Assay Method
 
Tyrosine-protein kinase BTK [393-659]
Name:Tyrosine-protein kinase BTK [393-659]
Synonyms:AGMX1 | ATK | BPK | BTK | BTK_HUMAN | Tyrosine-protein kinase BTK
Type:Enzyme Catalytic Domain
Mol. Mass.:31165.48
Organism:Homo sapiens (Human)
Description:aa 393-659
Residue:267
Sequence:
GSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEFIEEAKVMMNL
SHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMCKDVCEAMEYL
ESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVRWSPPEVLMYS
KFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLASEKVYTIMYS
CWHEKADERPTFKILLSNILDVMDEES
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  Blast E-value cutoff:
BDBM287414
n/a
NameBDBM287414
Synonyms:US9567339, Example E.9.13
TypeSmall organic molecule
Emp. Form.C26H30N6O3
Mol. Mass.474.5548
SMILESCN(C1CN(C1)C(=O)C=C)c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(CN2CCOCC2)cn1
Structure
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