pI: 8.777 |
Length (AA): 291 |
MW (Da): 33425 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 0
Targets have been classified into druggability groups (DG) according to their druggability score in network driven prioritizations. DGs range from 1 to 5; the higher the group number, the higher the chance of the target to be druggable
Modbase 3D models:
There are 8 models calculated for this protein. More info on
these models, including the
models themselves is available at:
Modbase
Target Beg | Target End | Template | Template Beg | Template End | Identity | Evalue | Model Score | MPQS | zDope |
---|---|---|---|---|---|---|---|---|---|
13 | 58 | 3flv (A) | 6 | 88 | 30.00 | 0 | 0.96 | -0.119324 | -1.93 |
65 | 140 | 4k29 (A) | 2 | 67 | 47.00 | 0.13 | 0.66 | 0.539768 | 0.37 |
80 | 282 | 4u19 (A) | 107 | 348 | 43.00 | 0 | 1 | 0.978194 | 0.19 |
80 | 291 | 3pea (A) | 5 | 252 | 23.00 | 0.000078 | 1 | 0.869122 | -0.01 |
80 | 291 | 1ef8 (A) | 6 | 255 | 25.00 | 0.32 | 1 | 0.885122 | 0.33 |
81 | 291 | 2fw2 (A) | 5 | 257 | 31.00 | 0 | 1 | 0.857686 | 0.11 |
84 | 285 | 1hnu (A) | 15 | 270 | 24.00 | 0 | 0.59 | 0.677758 | 0.59 |
85 | 286 | 3hrx (A) | 7 | 243 | 32.00 | 0.000000000043 | 0.92 | 0.799758 | 0.86 |
Help me make sense of these data.
A more detailed description of these scores is available at the Modbase Model Evaluation Help Pages, and in the papers referenced therein.
PDB Structures:
Ortholog group members (OG5_129422)
Species | Accession | Gene Product |
---|---|---|
Brugia malayi | Bm1_17680 | enoyl-CoA hydratase/isomerase family protein |
Candida albicans | CaO19.13801 | one of two potential enoyl-CoA hydratase/isomerase genes similar to S. cerevisiae ECI1 (YLR284C) and DCI1 (YOR180C) peroxisomal |
Candida albicans | CaO19.13803 | one of two potential enoyl-CoA hydratase/isomerase genes similar to S. cerevisiae ECI1 (YLR284C) and DCI1 (YOR180C) peroxisomal |
Candida albicans | CaO19.6445 | one of two potential enoyl-CoA hydratase/isomerase genes similar to S. cerevisiae ECI1 (YLR284C) and DCI1 (YOR180C) peroxisomal |
Candida albicans | CaO19.6443 | one of two potential enoyl-CoA hydratase/isomerase genes similar to S. cerevisiae ECI1 (YLR284C) and DCI1 (YOR180C) peroxisomal |
Caenorhabditis elegans | CELE_R06F6.9 | Protein ECH-4 |
Drosophila melanogaster | Dmel_CG13890 | CG13890 gene product from transcript CG13890-RA |
Echinococcus granulosus | EgrG_000068800 | enoyl coenzyme A hydratase |
Echinococcus multilocularis | EmuJ_000068800 | enoyl coenzyme A hydratase |
Homo sapiens | ENSG00000198721 | enoyl-CoA delta isomerase 2 |
Loa Loa (eye worm) | LOAG_10599 | hypothetical protein |
Mus musculus | ENSMUSG00000021416 | enoyl-Coenzyme A delta isomerase 3 |
Mus musculus | ENSMUSG00000021417 | enoyl-Coenzyme A delta isomerase 2 |
Mycobacterium ulcerans | MUL_0359 | enoyl-CoA hydratase |
Mycobacterium ulcerans | MUL_2995 | enoyl-CoA hydratase, EchA8_6 |
Saccharomyces cerevisiae | YLR284C | dodecenoyl-CoA isomerase |
Saccharomyces cerevisiae | YOR180C | putative dodecenoyl-CoA isomerase DCI1 |
Schistosoma mansoni | Smp_078280 | enoyl-CoA hydratase-related |
Schmidtea mediterranea | mk4.002105.02 | Enoyl-CoA delta isomerase 2, mitochondrial |
Schmidtea mediterranea | mk4.002805.04 | Enoyl-CoA delta isomerase 2, mitochondrial |
Schmidtea mediterranea | mk4.008477.00 | Enoyl-CoA hydratase-related |
In TDR Targets, information about phenotypes that are caused by drugs, or by genetic manipulation of cells (e.g. gene knockouts or knockdowns) is manually curated from the literature. These descriptions help to describe the potential of the target for drug development. If no information is available for this gene or if the information is incomplete, this may mean that i) the papers containing this information either appeared after the curation effort for this organism was carried out or they were inadvertently missed by curators; or that ii) the curation effort for this organism has not yet started.
In any case, if you have information about papers containing relevant validation data for this target, please contact us.