Detailed view for OVOC10712
Basic information
Onchocerca volvulus,
Source Database / ID: Wormbase Parasite
pI: 8.1611 |
Length (AA): 1261 |
MW (Da): 145799 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: | 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
Network
Pfam domains
Gene Ontology
Metabolic Pathways
Structural information
Modbase 3D models:
There is 1 model calculated for this protein. More info on
this model, including the
model itself is available at:
Modbase
| Target Beg | Target End | Template | Template Beg | Template End | Identity | Evalue | Model Score | MPQS | zDope |
|---|---|---|---|---|---|---|---|---|---|
| 241 | 378 | 5cwp (A) | 2 | 143 | 17.00 | 0.22 | 0.01 | 0.508105 | -0.53 |
Help me make sense of these data.
Target End: last modeled residue
Template: template structure used for modelling (PDB accession and chain)
Template Beg: first template residue in target-template alignment
Template End: last template residue in target-template alignment
Identity: sequence identity
Evalue: E value for target-template hit
Model Score: GA341 score (>0.7 for reliable model)
MPQS: ModPipe Quality Score (>1.1 for reliable model)
zDope: zDope Score (negative for reliable model)
A more detailed description of these scores is available at the Modbase Model Evaluation Help Pages, and in the papers referenced therein.
PDB Structures:
Expression
Orthologs
Ortholog group members (OG5_138705)
| Species | Accession | Gene Product |
|---|---|---|
| Brugia malayi | Bm1_44105 | hypothetical protein |
| Homo sapiens | ENSG00000120159 | caspase activity and apoptosis inhibitor 1 |
| Loa Loa (eye worm) | LOAG_14943 | hypothetical protein |
| Loa Loa (eye worm) | LOAG_11336 | hypothetical protein |
| Mus musculus | ensembl-mmu:ENSMUSG00000028578 | caspase activity and apoptosis inhibitor 1 |
| Onchocerca volvulus | OVOC10712 |
|
Essentiality
Phenotypes and Validation (curated)
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.
Annotated validation
Associated compounds / Druggability
Known modulators for this target
Predicted associations
By orthology with druggable targets
By sequence similarity to non orthologous druggable targets
| Species | Target | Length | Identity | Alignment span | Linked Drugs | Reference |
|---|---|---|---|---|---|---|
| Oryctolagus cuniculus | Cyclin-dependent kinase 4 | 189 aa | 28.7% | 164 aa | Compounds | References |
| Gallus gallus | Tyrosine-protein kinase SRC | 533 aa | 27.4% | 435 aa | Compounds | References |
| Plasmodium falciparum (isolate 3D7) | Cell division control protein 2 homolog | 288 aa | 28.3% | 237 aa | Compounds | References |
| Rattus norvegicus | Tyrosine-protein kinase Lyn | 512 aa | 25.6% | 418 aa | Compounds | References |
| Rattus norvegicus | Tyrosine-protein kinase SRC | 536 aa | 27.1% | 435 aa | Compounds | References |
| Rattus norvegicus | Cell division protein kinase 5 | 292 aa | 26.2% | 244 aa | Compounds | References |
Obtained from network model
Assayability
Assay information
Reagent availability
Bibliographic References