Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium tuberculosis | Methionine aminopeptidase MapB (map) (peptidase M) | 0.0117 | 0 | 0.5 |
Mycobacterium leprae | PROBABLE METHIONINE AMINOPEPTIDASE MAPA (MAP) (PEPTIDASE M) (MetAP) | 0.0117 | 0 | 0.5 |
Leishmania major | methionine aminopeptidase, putative,metallo-peptidase, Clan MG, Family M24 | 0.0184 | 0.4106 | 0.5 |
Mycobacterium leprae | PROBABLE METHIONINE AMINOPEPTIDASE MAPB (MAP) (PEPTIDASE M) | 0.0117 | 0 | 0.5 |
Toxoplasma gondii | methionine aminopeptidase | 0.0184 | 0.4106 | 1 |
Brugia malayi | Methionine aminopeptidase protein type I | 0.0184 | 0.4106 | 0.5 |
Plasmodium falciparum | methionine aminopeptidase 1b, putative | 0.0184 | 0.4106 | 1 |
Chlamydia trachomatis | methionine aminopeptidase | 0.0117 | 0 | 0.5 |
Mycobacterium ulcerans | methionine aminopeptidase MapB | 0.0117 | 0 | 0.5 |
Echinococcus multilocularis | microtubule associated protein 2 | 0.0281 | 1 | 1 |
Treponema pallidum | methionine aminopeptidase (map) | 0.0117 | 0 | 0.5 |
Trypanosoma cruzi | metallo- peptidase, Clan MG, Family M24 | 0.0184 | 0.4106 | 0.5 |
Wolbachia endosymbiont of Brugia malayi | methionine aminopeptidase | 0.0117 | 0 | 0.5 |
Plasmodium vivax | methionine aminopeptidase 1b, putative | 0.0184 | 0.4106 | 1 |
Mycobacterium tuberculosis | Methionine aminopeptidase MapA (map) (peptidase M) (MetAP) | 0.0117 | 0 | 0.5 |
Mycobacterium ulcerans | methionine aminopeptidase | 0.0117 | 0 | 0.5 |
Loa Loa (eye worm) | methionine aminopeptidase type I | 0.0184 | 0.4106 | 0.5 |
Trypanosoma cruzi | metallo- peptidase, Clan MG, Family M24 | 0.0184 | 0.4106 | 0.5 |
Trypanosoma brucei | metallo- peptidase, Clan MG, Family M24 | 0.0184 | 0.4106 | 0.5 |
Trypanosoma brucei | methionine aminopeptidase, type I, putative | 0.0184 | 0.4106 | 0.5 |
Echinococcus multilocularis | methionyl aminopeptidase 1 (M24 family) | 0.0184 | 0.4106 | 0.4106 |
Trypanosoma brucei | methionine aminopeptidase, putative | 0.0184 | 0.4106 | 0.5 |
Schistosoma mansoni | microtubule-associated protein tau | 0.0281 | 1 | 1 |
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.