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TargetGeranylgeranyl pyrophosphate synthase
LigandBDBM543954
Substrate/Competitorn/a
Meas. Tech.In Vitro hGGPPS Inhibition Assay
IC50<100±n/a nM
Citation Tsantrizos, YSSebag, M Substituted bicyclic pyrimidine-based compounds and compositions and uses thereof US Patent US11279719 Publication Date 3/22/2022
More Info.:Get all data from this article,  Assay Method
 
Geranylgeranyl pyrophosphate synthase
Name:Geranylgeranyl pyrophosphate synthase
Synonyms:Dimethylallyltranstransferase | Farnesyltranstransferase | GGPP synthetase | GGPPS_HUMAN | GGPPSase | GGPS1 | Geranylgeranyl Diphosphate Synthase (GGPPS) | Geranylgeranyl diphosphate synthase | Geranylgeranyl pyrophosphate synthetase | Geranyltranstransferase
Type:Homooctamer; transferase
Mol. Mass.:34867.94
Organism:Homo sapiens (Human)
Description:Recombinant human GGPPS was cloned and expressed in E. coli.
Residue:300
Sequence:
MEKTQETVQRILLEPYKYLLQLPGKQVRTKLSQAFNHWLKVPEDKLQIIIEVTEMLHNAS
LLIDDIEDNSKLRRGFPVAHSIYGIPSVINSANYVYFLGLEKVLTLDHPDAVKLFTRQLL
ELHQGQGLDIYWRDNYTCPTEEEYKAMVLQKTGGLFGLAVGLMQLFSDYKEDLKPLLNTL
GLFFQIRDDYANLHSKEYSENKSFCEDLTEGKFSFPTIHAIWSRPESTQVQNILRQRTEN
IDIKKYCVHYLEDVGSFEYTRNTLKELEAKAYKQIDARGGNPELVALVKHLSKMFKEENE
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  Blast E-value cutoff:
BDBM543954
n/a
NameBDBM543954
Synonyms:US11279719, Example Literature Compound 1 (mixture of E/Z isomers) Positive control
TypeSmall organic molecule
Emp. Form.C16H29N3O6P2
Mol. Mass.421.3655
SMILES[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]-[#6]-n1cc(-[#6]-[#6](P([#8])([#8])=O)P([#8])([#8])=O)nn1 |w:9.8|
Structure
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