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TargetRAC-alpha serine/threonine-protein kinase [1-123]
LigandBDBM50304371
Substrate/Competitorn/a
Meas. Tech.SPR Competitive Binding Assay
Ki>50000±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:
BDBM50304371
n/a
NameBDBM50304371
Synonyms:CHEMBL611216 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfamoyl)phenyl)-2-(2-(2-methoxyethoxy)ethoxy)acetamide | US9320734, 103
TypeSmall organic molecule
Emp. Form.C15H20N4O6S2
Mol. Mass.416.472
SMILESCOCCOCCOCC(=O)Nc1ccc(cc1)S(=O)(=O)Nc1nncs1
Structure
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