Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | ubiquitin specific peptidase 1 | Starlite/ChEMBL | No references |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium ulcerans | divalent cation-transport integral membrane protein | 0.0045 | 0.1282 | 0.0164 |
Mycobacterium ulcerans | manganese transport protein MntH | 0.0117 | 0.3987 | 1 |
Mycobacterium leprae | DIVALENT CATION-TRANSPORT INTEGRAL MEMBRANE PROTEIN MNTH (BRAMP) (MRAMP) | 0.0072 | 0.2316 | 1 |
Mycobacterium ulcerans | divalent cation-transport integral membrane protein | 0.0045 | 0.1282 | 0.0164 |
Trypanosoma brucei | hypothetical protein, conserved | 0.0043 | 0.1237 | 0.5 |
Brugia malayi | beta-lactamase family protein | 0.0043 | 0.1237 | 0.3104 |
Echinococcus granulosus | divalent metal transporter DMT1B | 0.0117 | 0.3987 | 1 |
Brugia malayi | NRAMP-like transporter K11G12.4 | 0.0117 | 0.3987 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0117 | 0.3987 | 1 |
Plasmodium vivax | metal transporter, putative | 0.0117 | 0.3987 | 1 |
Plasmodium falciparum | transporter, putative | 0.0117 | 0.3987 | 0.5 |
Trichomonas vaginalis | penicillin-binding protein, putative | 0.0043 | 0.1237 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0043 | 0.1237 | 0.3104 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0043 | 0.1237 | 0.5 |
Trichomonas vaginalis | penicillin-binding protein, putative | 0.0043 | 0.1237 | 0.5 |
Brugia malayi | beta-lactamase | 0.0043 | 0.1237 | 0.3104 |
Schistosoma mansoni | divalent metal transporter DMT1B | 0.0117 | 0.3987 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0043 | 0.1237 | 0.3104 |
Brugia malayi | Hypothetical 52.5 kDa protein ZK945.1 in chromosome II, putative | 0.0043 | 0.1237 | 0.3104 |
Brugia malayi | beta-lactamase family protein | 0.0043 | 0.1237 | 0.3104 |
Leishmania major | hypothetical protein, conserved | 0.0043 | 0.1237 | 0.5 |
Loa Loa (eye worm) | beta-LACTamase domain containing family member | 0.0043 | 0.1237 | 0.3104 |
Loa Loa (eye worm) | hypothetical protein | 0.0043 | 0.1237 | 0.3104 |
Trichomonas vaginalis | D-aminoacylase, putative | 0.0043 | 0.1237 | 0.5 |
Toxoplasma gondii | divalent metal transporter, putative | 0.0117 | 0.3987 | 1 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0043 | 0.1237 | 0.5 |
Onchocerca volvulus | Protein Malvolio homolog | 0.0117 | 0.3987 | 1 |
Trichomonas vaginalis | D-aminoacylase, putative | 0.0043 | 0.1237 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0043 | 0.1237 | 0.3104 |
Onchocerca volvulus | 0.0043 | 0.1237 | 0.3104 | |
Loa Loa (eye worm) | beta-lactamase | 0.0043 | 0.1237 | 0.3104 |
Onchocerca volvulus | 0.0043 | 0.1237 | 0.3104 | |
Echinococcus multilocularis | divalent metal transporter DMT1B | 0.0117 | 0.3987 | 1 |
Schistosoma mansoni | family S12 unassigned peptidase (S12 family) | 0.0043 | 0.1237 | 0.3104 |
Loa Loa (eye worm) | hypothetical protein | 0.0043 | 0.1237 | 0.3104 |
Trichomonas vaginalis | esterase, putative | 0.0043 | 0.1237 | 0.5 |
Onchocerca volvulus | 0.0043 | 0.1237 | 0.3104 | |
Echinococcus granulosus | beta LACTamase domain containing family member | 0.0043 | 0.1237 | 0.3104 |
Schistosoma mansoni | divalent metal transporter DMT1B | 0.0117 | 0.3987 | 1 |
Schistosoma mansoni | family S12 unassigned peptidase (S12 family) | 0.0043 | 0.1237 | 0.3104 |
Loa Loa (eye worm) | hypothetical protein | 0.0043 | 0.1237 | 0.3104 |
Mycobacterium leprae | possible membrane transport protein | 0.0045 | 0.1282 | 0.0417 |
Loa Loa (eye worm) | hypothetical protein | 0.0117 | 0.3987 | 1 |
Echinococcus multilocularis | beta LACTamase domain containing family member | 0.0043 | 0.1237 | 0.3104 |
Trichomonas vaginalis | D-aminoacylase, putative | 0.0043 | 0.1237 | 0.5 |
Mycobacterium tuberculosis | Divalent cation-transport integral membrane protein MntH (BRAMP) (MRAMP) | 0.0072 | 0.2316 | 0.1231 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | 1 uM | PubChem BioAssay. Inhibitors of USP1/UAF1: Primary Screen. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 31.6228 um | PUBCHEM_BIOASSAY: qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins. (Class of assay: confirmatory) [Related pubchem assays: 1011 (Confirmation Concentration-Response Assay for Inhibitors of the Schistosoma mansoni Redox Cascade ), 448 (Schistosoma Mansoni Peroxiredoxins (Prx2) and thioredoxin glutathione reductase (TGR) coupled assay)] | ChEMBL. | No reference |
Potency (functional) | = 39.8107 um | PUBCHEM_BIOASSAY: qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (without detergent). (Class of assay: confirmatory) [Related pubchem assays: 2158 (Confirmation qHTS Assay for Inhibitors of Cruzain), 2249 (Probe Development Summary of Promiscuous Inhibitors (Artifacts) of Cruzain), 2161 (qHTS Assay for Inhibitors of Papain: Counterscreen for Cruzain Assay), 1478 (qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (with detergent))] | ChEMBL. | No reference |
Potency (functional) | 63.0957 uM | PUBCHEM_BIOASSAY: HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488962] | ChEMBL. | No reference |
Potency (functional) | 100 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of Polymerase Iota. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588623] | ChEMBL. | No reference |
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.