Table 3.
The specific protein families of targets that TMFS predicted for the top five most promiscuous drugs.
Molecule | Families Targeted |
---|---|
DB02197 | Protein kinases (catalytic subunit), HSP90 (N-terminal domain), MutT- like, Matrix metalloproteinases (catalytic domain), Higher-molecular- weight phosphotyrosine protein phosphatases, Motor proteins, Phosphoribulokinase/pantothenate kinase, Tyrosine-dependent oxidoreductases, Aldo-keto reductases (NADP), Galectin (animal S- lectin), Transthyretin (prealbumin) |
DB03869 | Protein kinases (catalytic subunit), HSP90 (N-terminal domain), Aldo- keto reductases (NADP), NAD-binding domain of HMG-CoA reductase, ITPase (HAM1), G proteins, Carbonic anhydrase, Eukaryotic proteases, PDEase, Nuclear receptor ligand-binding domain |
DB02010 | Protein kinases (catalytic subunit), Higher-molecular-weight phosphotyrosine protein phosphatases, G proteins, Aldo-keto reductases (NADP), Eukaryotic proteases, GRIP domain, 5′(3′)- deoxyribonucleotidase (dNT-2), DPP6 N-terminal domain-like, BadF/BadG/BcrA/BcrD-like, SH2-domain |
DB00686 | Protein kinases (catalytic subunit), HSP90 (N-terminal domain), Higher- molecular-weight phosphotyrosine protein phosphatases, G proteins, Phosphoribulokinase/pantothenate kinase, Eukaryotic proteases, Nuclear receptor ligand-binding domain, Cofactor-dependent phosphoglycerate mutase, Fatty acid binding protein-like, Cyclin |
DB04700 | Protein kinases (catalytic subunit), HSP90 (N-terminal domain), Carbonic anhydrase, Nuclear receptor ligand-binding domain, Purine and uridine phosphorylases, Terpene synthases, Transducin (alpha subunit), Glutathione S-transferase (C-terminal domain), Methionine aminopeptidase |