Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | acetyl-CoA carboxylase alpha | Starlite/ChEMBL | References |
Homo sapiens | acetyl-CoA carboxylase beta | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | SWI:SNF matrix associated | 0.0107 | 0.3725 | 0.2402 |
Chlamydia trachomatis | DNA topoisomerase I | 0.0107 | 0.3725 | 1 |
Schistosoma mansoni | acetyl-CoA carboxylase | 0.0203 | 1 | 1 |
Mycobacterium tuberculosis | Probable pyruvate carboxylase Pca (pyruvic carboxylase) | 0.0077 | 0.1741 | 0.5 |
Trypanosoma brucei | 3-methylcrotonyl-CoA carboxylase alpha subunit, putative | 0.0077 | 0.1741 | 0.1741 |
Brugia malayi | Carboxyl transferase domain containing protein | 0.0196 | 0.9533 | 1 |
Wolbachia endosymbiont of Brugia malayi | Acetyl/propionyl-CoA carboxylase, alpha subunit | 0.0077 | 0.1741 | 0.5 |
Mycobacterium ulcerans | acetyl-/propionyl-coenzyme a carboxylase alpha chain AccA1 | 0.0077 | 0.1741 | 0.5 |
Mycobacterium ulcerans | acetyl-/propionyl-coenzyme a carboxylase alpha chain, AccA2 | 0.0077 | 0.1741 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0107 | 0.3725 | 0.2402 |
Plasmodium falciparum | biotin carboxylase subunit of acetyl CoA carboxylase, putative | 0.0147 | 0.6314 | 1 |
Mycobacterium leprae | Probable bifunctional protein acetyl-/propionyl-coenzyme A carboxylase, alpha chain AccA3 (BccP) | 0.0077 | 0.1741 | 0.5 |
Loa Loa (eye worm) | carboxyl transferase domain-containing protein | 0.0196 | 0.9533 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0107 | 0.3725 | 0.2402 |
Echinococcus multilocularis | SWI:SNF matrix associated | 0.0107 | 0.3725 | 0.2402 |
Trypanosoma brucei | 3-methylcrotonyl-CoA carboxylase alpha subunit, putative | 0.0077 | 0.1741 | 0.1741 |
Toxoplasma gondii | DNA topoisomerase domain-containing protein | 0.0107 | 0.3725 | 0.2402 |
Plasmodium vivax | biotin carboxylase subunit of acetyl CoA carboxylase, putative | 0.0147 | 0.6314 | 1 |
Mycobacterium ulcerans | bifunctional protein acetyl-/propionyl-coenzyme a carboxylase (alpha chain) AccA3 | 0.0077 | 0.1741 | 0.5 |
Echinococcus multilocularis | acetyl coenzyme A carboxylase 1 | 0.0203 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0107 | 0.3725 | 0.2402 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0107 | 0.3725 | 0.5 |
Chlamydia trachomatis | SWIB complex protein | 0.0107 | 0.3725 | 1 |
Toxoplasma gondii | acetyl-CoA carboxylase ACC1 | 0.0203 | 1 | 1 |
Echinococcus granulosus | Upstream activation factor subunit UAF30 | 0.0107 | 0.3725 | 0.2402 |
Toxoplasma gondii | acetyl-coA carboxylase ACC2 | 0.0203 | 1 | 1 |
Schistosoma mansoni | brg-1 associated factor | 0.0107 | 0.3725 | 0.2402 |
Mycobacterium ulcerans | pyruvate carboxylase | 0.0077 | 0.1741 | 0.5 |
Echinococcus granulosus | SWI:SNF matrix associated | 0.0107 | 0.3725 | 0.2402 |
Onchocerca volvulus | 0.0107 | 0.3725 | 0.5 | |
Echinococcus multilocularis | Upstream activation factor subunit UAF30 | 0.0107 | 0.3725 | 0.2402 |
Mycobacterium tuberculosis | Probable acetyl-/propionyl-coenzyme A carboxylase alpha chain (alpha subunit) AccA2: biotin carboxylase + biotin carboxyl carrie | 0.0077 | 0.1741 | 0.5 |
Trypanosoma cruzi | acetyl-CoA carboxylase | 0.0126 | 0.4918 | 1 |
Toxoplasma gondii | SWIB/MDM2 domain-containing protein | 0.0107 | 0.3725 | 0.2402 |
Leishmania major | acetyl-CoA carboxylase, putative | 0.0203 | 1 | 1 |
Trypanosoma brucei | acetyl-CoA carboxylase | 0.0203 | 1 | 1 |
Echinococcus multilocularis | SWI:SNF matrix associated | 0.0107 | 0.3725 | 0.2402 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 0.014 uM | Inhibition of human recombinant ACC2 | ChEMBL. | 16973360 |
IC50 (binding) | = 0.014 uM | Inhibition of human recombinant ACC2 | ChEMBL. | 16973360 |
IC50 (binding) | = 0.066 uM | Inhibition of human recombinant ACC1 | ChEMBL. | 16973360 |
IC50 (binding) | = 0.066 uM | Inhibition of human recombinant ACC1 | ChEMBL. | 16973360 |
Ratio IC50 (binding) | = 5 | Selectivity for human ACC2 over human ACC1 | ChEMBL. | 16973360 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
1 literature reference was collected for this gene.