Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | geminin, DNA replication inhibitor | Starlite/ChEMBL | No references |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Brugia malayi | Hypothetical 65.5 kDa Trp-Asp repeats containing protein F02E8.5 inchromosome X | geminin, DNA replication inhibitor | 209 aa | 176 aa | 27.8 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | brahma associated protein | 0.0142 | 0.5896 | 1 |
Mycobacterium leprae | PROBABLE ATP-DEPENDENT CLP PROTEASE PROTEOLYTIC SUBUNIT 2 CLPP2 (ENDOPEPTIDASE CLP 2) | 0.0079 | 0.1772 | 1 |
Treponema pallidum | ATP-dependent Clp protease proteolytic subunit | 0.0079 | 0.1772 | 0.5 |
Plasmodium falciparum | SWIB/MDM2 domain-containing protein | 0.0142 | 0.5896 | 1 |
Echinococcus granulosus | Upstream activation factor subunit UAF30 | 0.0142 | 0.5896 | 0.5896 |
Schistosoma mansoni | hypothetical protein | 0.0142 | 0.5896 | 0.5012 |
Echinococcus multilocularis | ATP dependent Clp protease proteolytic subunit | 0.0079 | 0.1772 | 0.1772 |
Plasmodium vivax | hypothetical protein, conserved | 0.0142 | 0.5896 | 1 |
Echinococcus multilocularis | SWI:SNF matrix associated | 0.0142 | 0.5896 | 0.5896 |
Chlamydia trachomatis | DNA topoisomerase I | 0.0142 | 0.5896 | 1 |
Echinococcus granulosus | ATP dependent Clp protease proteolytic subunit | 0.0079 | 0.1772 | 0.1772 |
Mycobacterium ulcerans | ATP-dependent Clp protease proteolytic subunit | 0.0079 | 0.1772 | 0.5 |
Echinococcus multilocularis | SWI:SNF matrix associated | 0.0142 | 0.5896 | 0.5896 |
Brugia malayi | brahma associated protein 60 kDa | 0.0142 | 0.5896 | 1 |
Brugia malayi | brahma associated protein 60 kDa | 0.0142 | 0.5896 | 1 |
Plasmodium falciparum | SWIB/MDM2 domain-containing protein | 0.0142 | 0.5896 | 1 |
Chlamydia trachomatis | SWIB complex protein | 0.0142 | 0.5896 | 1 |
Brugia malayi | SWIB/MDM2 domain containing protein | 0.0142 | 0.5896 | 1 |
Loa Loa (eye worm) | SWIB/MDM2 domain-containing protein | 0.0142 | 0.5896 | 1 |
Echinococcus granulosus | SWI:SNF matrix associated | 0.0142 | 0.5896 | 0.5896 |
Toxoplasma gondii | SWIB/MDM2 domain-containing protein | 0.0142 | 0.5896 | 1 |
Plasmodium vivax | SWIB/MDM2 domain-containing protein, putative | 0.0142 | 0.5896 | 1 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0142 | 0.5896 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0142 | 0.5896 | 0.5012 |
Onchocerca volvulus | 0.0142 | 0.5896 | 0.5 | |
Echinococcus multilocularis | Upstream activation factor subunit UAF30 | 0.0142 | 0.5896 | 0.5896 |
Schistosoma mansoni | hypothetical protein | 0.0142 | 0.5896 | 0.5012 |
Wolbachia endosymbiont of Brugia malayi | ATP-dependent Clp protease proteolytic subunit | 0.0079 | 0.1772 | 0.5 |
Echinococcus multilocularis | SWI:SNF matrix associated | 0.0142 | 0.5896 | 0.5896 |
Toxoplasma gondii | DNA topoisomerase domain-containing protein | 0.0142 | 0.5896 | 1 |
Mycobacterium ulcerans | ATP-dependent Clp protease proteolytic subunit | 0.0079 | 0.1772 | 0.5 |
Schistosoma mansoni | brg-1 associated factor | 0.0142 | 0.5896 | 0.5012 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | 0.0291 uM | PubChem BioAssay. A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 25.1189 um | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II). (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 29.0929 uM | PUBCHEM_BIOASSAY: qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID493107, AID493125] | ChEMBL. | No reference |
Potency (functional) | = 35.4813 um | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of 12-hLO (12-human lipoxygenase). (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 39.8107 uM | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504404] | 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.