Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | intermediate filament protein | 0.0028 | 0.0563 | 0.0646 |
Brugia malayi | Latrophilin receptor protein 2 | 0.0015 | 0.0015 | 0.0017 |
Trypanosoma cruzi | ISWI complex protein | 0.0032 | 0.0722 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0028 | 0.0563 | 0.0646 |
Echinococcus multilocularis | fetal alzheimer antigen, falz | 0.0047 | 0.1371 | 0.2894 |
Schistosoma mansoni | hypothetical protein | 0.0032 | 0.0722 | 0.1412 |
Brugia malayi | Bromodomain containing protein | 0.0155 | 0.6072 | 0.6974 |
Trypanosoma cruzi | ISWI complex protein | 0.0032 | 0.0722 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0084 | 0.3001 | 0.3447 |
Schistosoma mansoni | methyl-cpg binding protein mbd | 0.0035 | 0.0879 | 0.1726 |
Echinococcus granulosus | bromodomain adjacent to zinc finger domain | 0.0123 | 0.4701 | 1 |
Echinococcus granulosus | zinc finger protein | 0.004 | 0.1105 | 0.2327 |
Onchocerca volvulus | 0.0031 | 0.0693 | 0.0137 | |
Schistosoma mansoni | lamin | 0.0028 | 0.0563 | 0.1095 |
Loa Loa (eye worm) | hypothetical protein | 0.0015 | 0.0015 | 0.0017 |
Echinococcus granulosus | lamin | 0.0028 | 0.0563 | 0.117 |
Schistosoma mansoni | hypothetical protein | 0.0033 | 0.0785 | 0.1539 |
Echinococcus multilocularis | zinc finger protein | 0.004 | 0.1105 | 0.2327 |
Brugia malayi | PHD-finger family protein | 0.0051 | 0.1583 | 0.1818 |
Schistosoma mansoni | intermediate filament proteins | 0.0028 | 0.0563 | 0.1095 |
Schistosoma mansoni | histone-lysine n-methyltransferase suv9 | 0.0031 | 0.0693 | 0.1354 |
Loa Loa (eye worm) | hypothetical protein | 0.0033 | 0.0785 | 0.0902 |
Echinococcus multilocularis | methyl CpG binding domain protein 2 | 0.0035 | 0.0879 | 0.1844 |
Trichomonas vaginalis | set domain proteins, putative | 0.0245 | 1 | 0.5 |
Toxoplasma gondii | histone lysine methyltransferase SET/SUV39 | 0.0031 | 0.0693 | 0.5 |
Echinococcus multilocularis | histone lysine methyltransferase setb histone lysine methyltransferase eggless | 0.0066 | 0.2221 | 0.4708 |
Echinococcus granulosus | methyl CpG binding domain protein 2 | 0.0035 | 0.0879 | 0.1844 |
Echinococcus multilocularis | lamin dm0 | 0.0028 | 0.0563 | 0.117 |
Loa Loa (eye worm) | hypothetical protein | 0.0048 | 0.1449 | 0.1664 |
Echinococcus granulosus | fetal alzheimer antigen falz | 0.0047 | 0.1371 | 0.2894 |
Echinococcus granulosus | intermediate filament protein | 0.0028 | 0.0563 | 0.117 |
Echinococcus multilocularis | bromodomain adjacent to zinc finger domain | 0.0123 | 0.4701 | 1 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.0048 | 0.1449 | 0.1664 |
Loa Loa (eye worm) | hypothetical protein | 0.0079 | 0.2789 | 0.3203 |
Loa Loa (eye worm) | PHD-finger family protein | 0.0043 | 0.12 | 0.1378 |
Loa Loa (eye worm) | pre-SET domain-containing protein family protein | 0.0216 | 0.8707 | 1 |
Brugia malayi | intermediate filament protein | 0.0028 | 0.0563 | 0.0646 |
Echinococcus multilocularis | bromodomain adjacent to zinc finger domain | 0.0074 | 0.2571 | 0.5455 |
Loa Loa (eye worm) | latrophilin receptor protein 2 | 0.0015 | 0.0015 | 0.0017 |
Schistosoma mansoni | bromodomain containing protein | 0.0131 | 0.5022 | 1 |
Echinococcus multilocularis | histone lysine N methyltransferase SETMAR | 0.0031 | 0.0693 | 0.1447 |
Echinococcus granulosus | 5'partial|histone lysine N methyltransferase SETDB2 | 0.003 | 0.0643 | 0.1342 |
Plasmodium vivax | SET domain protein, putative | 0.0031 | 0.0693 | 0.5 |
Brugia malayi | Intermediate filament tail domain containing protein | 0.0028 | 0.0563 | 0.0646 |
Schistosoma mansoni | histone-lysine n-methyltransferase setb1 | 0.0031 | 0.0693 | 0.1354 |
Schistosoma mansoni | histone-lysine n-methyltransferase setb1 | 0.0066 | 0.2221 | 0.4406 |
Schistosoma mansoni | histone-lysine n-methyltransferase setb1 | 0.0066 | 0.2221 | 0.4406 |
Schistosoma mansoni | zinc finger protein | 0.004 | 0.1105 | 0.2178 |
Brugia malayi | Bromodomain containing protein | 0.0079 | 0.2783 | 0.3196 |
Loa Loa (eye worm) | bromodomain containing protein | 0.0036 | 0.0934 | 0.1072 |
Schistosoma mansoni | zinc finger protein | 0.0032 | 0.0722 | 0.1412 |
Loa Loa (eye worm) | hypothetical protein | 0.0146 | 0.5689 | 0.6533 |
Loa Loa (eye worm) | hypothetical protein | 0.0066 | 0.2221 | 0.2551 |
Schistosoma mansoni | methyl-cpg binding protein mbd | 0.0035 | 0.0879 | 0.1726 |
Schistosoma mansoni | acetyl-CoA C-acetyltransferase | 0.0047 | 0.1371 | 0.2709 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.0048 | 0.1449 | 0.1664 |
Echinococcus multilocularis | lamin | 0.0028 | 0.0563 | 0.117 |
Brugia malayi | Pre-SET motif family protein | 0.0031 | 0.0693 | 0.0795 |
Schistosoma mansoni | lamin | 0.0028 | 0.0563 | 0.1095 |
Schistosoma mansoni | hypothetical protein | 0.0043 | 0.12 | 0.2367 |
Leishmania major | hypothetical protein, conserved | 0.0032 | 0.0722 | 0.5 |
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.0048 | 0.1449 | 0.1664 |
Trypanosoma brucei | ISWI complex protein | 0.0032 | 0.0722 | 0.5 |
Echinococcus granulosus | bromodomain adjacent to zinc finger domain | 0.0074 | 0.2571 | 0.5455 |
Echinococcus granulosus | histone lysine methyltransferase setb | 0.0066 | 0.2221 | 0.4708 |
Echinococcus multilocularis | musashi | 0.0028 | 0.0563 | 0.117 |
Brugia malayi | latrophilin 2 splice variant baaae | 0.0033 | 0.0785 | 0.0902 |
Echinococcus granulosus | lamin dm0 | 0.0028 | 0.0563 | 0.117 |
Brugia malayi | calcium-independent alpha-latrotoxin receptor 2, putative | 0.0015 | 0.0015 | 0.0017 |
Loa Loa (eye worm) | intermediate filament tail domain-containing protein | 0.0028 | 0.0563 | 0.0646 |
Loa Loa (eye worm) | hypothetical protein | 0.0088 | 0.3173 | 0.3644 |
Brugia malayi | Pre-SET motif family protein | 0.0216 | 0.8707 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0027 | 0.0541 | 0.0621 |
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.