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TargetRAC-alpha serine/threonine-protein kinase [1-123]
LigandBDBM50338943
Substrate/Competitorn/a
Meas. Tech.SPR Competitive Binding Assay
Kd 109000±n/a nM
Citation Mahadevan, DMeuillet, EJMash, Jr., EAGokhale, VMPowis, GZhang, S Small molecule inhibitors of the pleckstrin homology domain and methods for using same US Patent US9320734 Publication Date 4/26/2016
More Info.:Get all data from this article,  Assay Method
 
RAC-alpha serine/threonine-protein kinase [1-123]
Name:RAC-alpha serine/threonine-protein kinase [1-123]
Synonyms:AKT1 | AKT1_HUMAN | PKB | RAC | RAC-alpha serine/threonine-protein kinase (Akt)
Type:Enzyme
Mol. Mass.:14664.42
Organism:Homo sapiens (Human)
Description:PLECKSTRIN HOMOLOGY DOMAIN RESIDUES 1-123 (PH Domain)
Residue:123
Sequence:
MSDVAIVKEGWLHKRGEYIKTWRPRYFLLKNDGTFIGYKERPQDVDQREAPLNNFSVAQC
QLMKTERPRPNTFIIRCLQWTTVIERTFHVETPEEREEWTTAIQTVADGLKKQEEEEMDF
RSG
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  Blast E-value cutoff:
BDBM50338943
n/a
NameBDBM50338943
Synonyms:CHEMBL1685043 | Ethyl 5-(4-Decanamidophenylsulfonamido)-1,3,4-thiadiazole-2-carboxylate | US9320734, 123E
TypeSmall organic molecule
Emp. Form.C21H30N4O5S2
Mol. Mass.482.617
SMILESCCCCCCCCCC(=O)Nc1ccc(cc1)S(=O)(=O)Nc1nnc(s1)C(=O)OCC
Structure
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