Detailed view for OVOC3406

Basic information

TDR Targets ID: 988488
Onchocerca volvulus,
Source Database / ID:  Wormbase Parasite  

pI: 7.7319 | Length (AA): 388 | MW (Da): 45205 | Paralog Number: 1

Signal peptide: N | GPI Anchor: | Predicted trans-membrane segments: 0

Druggability Group : DG2

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

Pfam domains

PF00755  

Gene Ontology

Mouse over links to read term descriptions.
GO:0016746   transferase activity, transferring acyl groups  

Metabolic Pathways

Peroxisome (KEGG)

Structural information

Modbase 3D models:

There are 3 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
25 625 2deb (A) 34 652 22.00 0 1 1.25215 -0.77
35 632 1ndb (A) 30 625 33.00 0 1 1.4734 -1.23
135 239 2gd9 (A) 58 169 39.00 0.54 0.17 0.158339 2.05

Help me make sense of these data.

Target Beg: first modeled residue
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:

No structure availble in the PDB for this protein

Expression

No expression data available for this gene

Orthologs

Ortholog group members (OG5_129452)

Species Accession Gene Product
Candida albicans CaO19.4591   similar to peroxisomal and mitochondrial carnitine O-acetyltransferase
Candida albicans CaO19.12060   similar to peroxisomal and mitochondrial carnitine O-acetyltransferase
Caenorhabditis elegans CELE_B0395.3   Protein B0395.3
Drosophila melanogaster Dmel_CG5122   CG5122 gene product from transcript CG5122-RA
Drosophila melanogaster Dmel_CG1041   CG1041 gene product from transcript CG1041-RA
Drosophila melanogaster Dmel_CG5265   CG5265 gene product from transcript CG5265-RA
Homo sapiens ENSG00000095321   carnitine O-acetyltransferase
Mus musculus ensembl-mmu:ENSMUSG00000026853   carnitine acetyltransferase
Onchocerca volvulus OVOC3406  
Onchocerca volvulus OVOC3409  
Saccharomyces cerevisiae YML042W   carnitine O-acetyltransferase CAT2
Schmidtea mediterranea mk4.025144.00   Choline O-acetyltransferase
Schmidtea mediterranea mk4.014511.00   Choline O-acetyltransferase
Schmidtea mediterranea mk4.005732.00  
Schmidtea mediterranea mk4.004133.03  
Trypanosoma brucei gambiense Tbg972.11.2450   carnitine O-acetyltransferase, putative
Trypanosoma brucei Tb927.11.2230   carnitine O-acetyltransferase, putative
Trypanosoma cruzi TcCLB.511303.40   carnitine O-acetyltransferase, putative
Trypanosoma cruzi TcCLB.508355.40   choline/carnitine O-acetyltransferase, putative
Trypanosoma cruzi TcCLB.511763.19   hypothetical protein, conserved

Essentiality

OVOC3406 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb11.18.0006 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (3 days) alsford
Tb11.18.0006 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (6 days) alsford
Tb11.18.0006 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb11.18.0006 Trypanosoma brucei significant gain of fitness in differentiation of procyclic to bloodstream forms alsford
Show/Hide essentiality data references
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • goodall The Essential Genome of Escherichia coli K-12 (Transposon directed high-throughput mutagenesis) Goodall, Emily CA, et al. "The essential genome of Escherichia coli K-12." mBio 9.1 (2018): e02096-17.
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection
  • neb C. elegans RNAi phenotypes Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs
  • plasmo Functional Profiling of a Plasmodium Genome Reveals an Abundance of Essential Genes. Bushell, Ellen, et al. "Functional profiling of a Plasmodium genome reveals an abundance of essential genes." Cell 170.2 (2017): 260-272.
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • sidik A Genome-wide CRISPR Screen in Toxoplasma Identifies Essential Apicomplexan Genes. Sidik, Saima M., et al. "A genome-wide CRISPR screen in toxoplasma identifies essential apicomplexan genes." Cell 166.6 (2016): 1423-1435.

Phenotypes and Validation (curated)

We have no manually annotated phenotypes for this target. What does this mean? / Care to help?

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

No validation data for this target

Associated compounds / Druggability

Known modulators for this target

No chemical compounds associated to this gene

Predicted associations

By orthology with druggable targets
Non orthologous druggable targets
By sequence similarity to non orthologous druggable targets
No additional associated druggable targets
Obtained from network model
No druggable targets predicted through repurposing network model

Assayability

Assay information

No assay information for this target.

Reagent availability

No reagent availability information for this target.

Bibliographic References

No literature references available for this target.

If you have references for this gene, please enter them in a user comment (below) or Contact us.

User comments

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