Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | lysine (K)-specific demethylase 1A | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0083 | 0.8489 | 0.8651 |
Onchocerca volvulus | 0.0034 | 0.2225 | 0.0235 | |
Plasmodium falciparum | lysine-specific histone demethylase 1, putative | 0.0017 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0024 | 0.0901 | 0.0918 |
Echinococcus multilocularis | adenylate cyclase 9 | 0.0034 | 0.2225 | 0.262 |
Loa Loa (eye worm) | hypothetical protein | 0.0034 | 0.2225 | 0.2267 |
Onchocerca volvulus | 0.009 | 0.9391 | 0.9235 | |
Schistosoma mansoni | Lysine-specific histone demethylase 1 | 0.0083 | 0.8489 | 1 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.0022 | 0.0643 | 0.0656 |
Brugia malayi | amine oxidase, flavin-containing family protein | 0.0024 | 0.0901 | 0.096 |
Plasmodium vivax | protoporphyrinogen oxidase, putative | 0.0017 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0083 | 0.8489 | 0.8651 |
Mycobacterium leprae | PROBABLE PROTOPORPHYRINOGEN OXIDASE HEMY (PROTOPORPHYRINOGEN-IX OXIDASE) (PROTOPORPHYRINOGENASE) (PPO) | 0.0017 | 0 | 0.5 |
Trypanosoma cruzi | UDP-galactopyranose mutase | 0.0017 | 0 | 0.5 |
Trypanosoma cruzi | UDP-galactopyranose mutase | 0.0017 | 0 | 0.5 |
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.0022 | 0.0643 | 0.0685 |
Plasmodium vivax | hypothetical protein, conserved | 0.0017 | 0 | 0.5 |
Mycobacterium ulcerans | monoamine oxidase | 0.0017 | 0 | 0.5 |
Leishmania major | UDP-galactopyranose mutase | 0.0017 | 0 | 0.5 |
Mycobacterium ulcerans | flavin-containing monoamine oxidase AofH | 0.0017 | 0 | 0.5 |
Plasmodium vivax | hypothetical protein, conserved | 0.0017 | 0 | 0.5 |
Echinococcus granulosus | adenylate cyclase 9 | 0.0034 | 0.2225 | 0.262 |
Loa Loa (eye worm) | hypothetical protein | 0.009 | 0.9391 | 0.9569 |
Mycobacterium ulcerans | protoporphyrinogen oxidase | 0.0017 | 0 | 0.5 |
Brugia malayi | SWIRM domain containing protein | 0.009 | 0.9391 | 1 |
Mycobacterium tuberculosis | Possible oxidoreductase | 0.0017 | 0 | 0.5 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.0022 | 0.0643 | 0.0685 |
Plasmodium falciparum | conserved Plasmodium protein, unknown function | 0.0017 | 0 | 0.5 |
Mycobacterium ulcerans | flavin-containing monoamine oxidase AofH | 0.0017 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0093 | 0.9813 | 1 |
Plasmodium falciparum | protoporphyrinogen oxidase | 0.0017 | 0 | 0.5 |
Echinococcus multilocularis | lysine specific histone demethylase 1A | 0.0083 | 0.8489 | 1 |
Mycobacterium ulcerans | dehydrogenase | 0.0017 | 0 | 0.5 |
Plasmodium vivax | lysine-specific histone demethylase 1, putative | 0.0017 | 0 | 0.5 |
Chlamydia trachomatis | protoporphyrinogen oxidase | 0.0017 | 0 | 0.5 |
Toxoplasma gondii | histone lysine-specific demethylase | 0.0017 | 0 | 0.5 |
Echinococcus granulosus | lysine specific histone demethylase 1A | 0.0083 | 0.8489 | 1 |
Loa Loa (eye worm) | adenylyl cyclase 3 | 0.0034 | 0.2225 | 0.2267 |
Brugia malayi | Adenylyl cyclase protein | 0.0034 | 0.2225 | 0.2369 |
Onchocerca volvulus | Adenylate cyclase type 2 homolog | 0.0034 | 0.2225 | 0.0235 |
Toxoplasma gondii | histone lysine-specific demethylase LSD1/BHC110/KDMA1A | 0.0017 | 0 | 0.5 |
Mycobacterium ulcerans | oxidoreductase | 0.0017 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0022 | 0.0643 | 0.0656 |
Mycobacterium tuberculosis | Conserved hypothetical protein | 0.0017 | 0 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 11.19 uM | Inhibition of recombinant LSD1 (157 to 852) (unknown origin) transfected in Escherichia coli BL21(DE) by fluorescence assay | ChEMBL. | 25610955 |
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.