Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | methionyl aminopeptidase 2 | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | nmda type glutamate receptor | 0.0116 | 1 | 1 |
Giardia lamblia | Methionine aminopeptidase | 0.011 | 0.9096 | 0.5 |
Trypanosoma brucei | methionine aminopeptidase 2, putative | 0.011 | 0.9096 | 1 |
Schistosoma mansoni | methionyl aminopeptidase 2 (M24 family) | 0.011 | 0.9096 | 1 |
Brugia malayi | initiation factor 2-associated protein. | 0.011 | 0.9096 | 1 |
Echinococcus granulosus | nmda type glutamate receptor | 0.0076 | 0.4255 | 0.1769 |
Plasmodium vivax | methionine aminopeptidase 2, putative | 0.011 | 0.9096 | 1 |
Mycobacterium tuberculosis | Methionine aminopeptidase MapB (map) (peptidase M) | 0.0048 | 0.0146 | 0.5 |
Mycobacterium ulcerans | methionine aminopeptidase MapB | 0.0048 | 0.0146 | 0.5 |
Echinococcus multilocularis | methionyl aminopeptidase 1 (M24 family) | 0.0048 | 0.0146 | 0.0146 |
Mycobacterium ulcerans | methionine aminopeptidase | 0.0048 | 0.0146 | 0.5 |
Trichomonas vaginalis | Clan MG, familly M24, aminopeptidase P-like metallopeptidase | 0.011 | 0.9096 | 0.5 |
Wolbachia endosymbiont of Brugia malayi | methionine aminopeptidase | 0.0048 | 0.0146 | 0.5 |
Trypanosoma cruzi | metallo-peptidase, Clan MG, Family M24 | 0.011 | 0.9096 | 1 |
Trichomonas vaginalis | Clan MG, familly M24, aminopeptidase P-like metallopeptidase | 0.011 | 0.9096 | 0.5 |
Echinococcus multilocularis | methionyl aminopeptidase 2 | 0.011 | 0.9096 | 0.9096 |
Toxoplasma gondii | methionine aminopeptidase 2, putative | 0.011 | 0.9096 | 1 |
Chlamydia trachomatis | methionine aminopeptidase | 0.0048 | 0.0146 | 0.5 |
Trichomonas vaginalis | Clan MG, familly M24, aminopeptidase P-like metallopeptidase | 0.011 | 0.9096 | 0.5 |
Plasmodium falciparum | methionine aminopeptidase 1b, putative | 0.0067 | 0.302 | 0.3211 |
Echinococcus granulosus | methionyl aminopeptidase 2 | 0.011 | 0.9096 | 0.8705 |
Plasmodium falciparum | methionine aminopeptidase 2 | 0.011 | 0.9096 | 1 |
Mycobacterium leprae | PROBABLE METHIONINE AMINOPEPTIDASE MAPA (MAP) (PEPTIDASE M) (MetAP) | 0.0048 | 0.0146 | 0.5 |
Plasmodium vivax | methionine aminopeptidase 1b, putative | 0.0067 | 0.302 | 0.3211 |
Echinococcus granulosus | glutamate receptor NMDA | 0.0069 | 0.3289 | 0.0386 |
Trypanosoma cruzi | metallo-peptidase, Clan MG, Family M24 | 0.011 | 0.9096 | 1 |
Echinococcus multilocularis | nmda type glutamate receptor | 0.0076 | 0.4255 | 0.4255 |
Trichomonas vaginalis | Clan MG, familly M24, aminopeptidase P-like metallopeptidase | 0.011 | 0.9096 | 0.5 |
Loa Loa (eye worm) | initiation factor 2-associated protein | 0.011 | 0.9096 | 1 |
Schistosoma mansoni | glutamate receptor NMDA | 0.0089 | 0.6138 | 0.6695 |
Mycobacterium leprae | PROBABLE METHIONINE AMINOPEPTIDASE MAPB (MAP) (PEPTIDASE M) | 0.0048 | 0.0146 | 0.5 |
Entamoeba histolytica | methionine aminopeptidase, putative | 0.011 | 0.9096 | 0.5 |
Treponema pallidum | methionine aminopeptidase (map) | 0.0048 | 0.0146 | 0.5 |
Onchocerca volvulus | Methionine aminopeptidase 2 homolog | 0.011 | 0.9096 | 0.5 |
Echinococcus multilocularis | methionyl aminopeptidase 1 (M24 family) | 0.0067 | 0.302 | 0.302 |
Toxoplasma gondii | methionine aminopeptidase | 0.0067 | 0.302 | 0.3211 |
Trypanosoma brucei | metallo-peptidase, Clan MG, Family M24 | 0.011 | 0.9096 | 1 |
Mycobacterium tuberculosis | Methionine aminopeptidase MapA (map) (peptidase M) (MetAP) | 0.0048 | 0.0146 | 0.5 |
Leishmania major | methionine aminopeptidase 2, putative | 0.011 | 0.9096 | 1 |
Echinococcus multilocularis | glutamate receptor NMDA | 0.0069 | 0.3289 | 0.3289 |
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.