Detailed view for LOAG_13163

Basic information

TDR Targets ID: 942456
Loa Loa (eye worm), hypothetical protein
Source Database / ID:  KEGG  

pI: 7.2939 | Length (AA): 210 | MW (Da): 23096 | Paralog Number: 1

Signal peptide: N | GPI Anchor: N | 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

PF08324   PUL domain

Gene Ontology

Mouse over links to read term descriptions.
GO:0005488   binding  

Metabolic Pathways

This gene is not mapped to any metabolic pathway in 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
2 207 3ebb (A) 608 795 20.00 0 1 1.27635 -0.95
54 210 5cwp (A) 31 191 30.00 0.68 0.81 0.923819 -0.31
143 209 2ru4 (B) 133 198 17.00 0.61 0.51 0.586448 -0.66

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_128172)

Species Accession Gene Product
Arabidopsis thaliana AT3G18860   transducin family protein / WD-40 repeat family protein
Babesia bovis BBOV_II004810   WD domain, G-beta repeat containing protein
Brugia malayi Bm1_21170   WD domain containing protein
Candida albicans CaO19.12292   ubiquitin proteolysis
Candida albicans CaO19.4829   ubiquitin proteolysis
Caenorhabditis elegans CELE_C05C10.6   Protein UFD-3, isoform B
Caenorhabditis elegans CELE_C05C10.6a   Protein UFD-3, isoform C
Cryptosporidium hominis Chro.40262   At3g18860/MCB22_3
Cryptosporidium parvum cgd4_2320   At3g18860/MCB22_3
Dictyostelium discoideum DDB_G0291003   hypothetical protein
Drosophila melanogaster Dmel_CG5105   Phospholipase A2 activator protein
Echinococcus granulosus EgrG_000477800   phospholipase A 2 activating protein
Echinococcus multilocularis EmuJ_000477800   phospholipase A 2 activating protein
Homo sapiens ENSG00000137055   phospholipase A2-activating protein
Leishmania braziliensis LbrM.24.1970   hypothetical protein, conserved
Leishmania donovani LdBPK_241970.1   WD domain, G-beta repeat/PFU (PLAA family ubiquitin binding), putative
Leishmania infantum LinJ.24.1970   hypothetical protein, conserved
Leishmania major LmjF.24.1900   hypothetical protein, conserved
Leishmania mexicana LmxM.24.1900   hypothetical protein, conserved
Loa Loa (eye worm) LOAG_13163   hypothetical protein
Loa Loa (eye worm) LOAG_05630   WD domain-containing protein
Mus musculus 18786   phospholipase A2, activating protein
Neospora caninum NCLIV_040730   hypothetical protein
Oryza sativa 4342300   Os07g0123700
Plasmodium berghei PBANKA_1139400   polyubiquitin binding protein, putative
Plasmodium falciparum PF3D7_1363400   polyubiquitin binding protein, putative
Plasmodium knowlesi PKNH_1107900   polyubiquitin binding protein, putative
Plasmodium yoelii PY05801   Arabidopsis thaliana At3g18860/MCB22_3
Saccharomyces cerevisiae YKL213C   Doa1p
Schistosoma japonicum Sjp_0129740   Phospholipase A-2-activating protein, putative
Schistosoma mansoni Smp_017750   phospholipase A-2-activating protein
Schmidtea mediterranea mk4.001405.12  
Schmidtea mediterranea mk4.002121.09  
Schmidtea mediterranea mk4.001405.13   Phospholipase A-2-activating protein
Schmidtea mediterranea mk4.002121.10   Phospholipase A-2-activating protein
Trypanosoma brucei gambiense Tbg972.8.6390   hypothetical protein, conserved
Trypanosoma brucei Tb927.8.6330   WD domain, G-beta repeat/PFU (PLAA family ubiquitin binding), putative
Trypanosoma congolense TcIL3000_0_44870   PFU (PLAA family ubiquitin binding), putative
Trypanosoma cruzi TcCLB.503885.90   WD domain, G-beta repeat/PFU (PLAA family ubiquitin binding), putative
Trypanosoma cruzi TcCLB.511903.290   WD domain, G-beta repeat/PFU (PLAA family ubiquitin binding), putative
Toxoplasma gondii TGME49_288210   PUL domain-containing protein
Theileria parva TP02_0270   hypothetical protein
Trichomonas vaginalis TVAG_358850   phospholipase A-2-activating protein, putative
Trichomonas vaginalis TVAG_287800   phospholipase A-2-activating protein, putative

Essentiality

LOAG_13163 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.8.6330 Trypanosoma brucei significant gain of fitness in bloodstream forms (3 days) alsford
Tb927.8.6330 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (6 days) alsford
Tb927.8.6330 Trypanosoma brucei significant gain of fitness in procyclic forms alsford
Tb927.8.6330 Trypanosoma brucei significant gain of fitness in differentiation of procyclic to bloodstream forms alsford
CELE_C05C10.6 Caenorhabditis elegans embryonic lethal wormbase
CELE_C05C10.6 Caenorhabditis elegans slow growth wormbase
TGME49_288210 Toxoplasma gondii Probably essential sidik
Show/Hide essentiality data references
  • 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.
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • 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.
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • 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.
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection

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
Species Known druggable target Linked compounds Reference
Homo sapiens phospholipase A2-activating protein Compounds References
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

No user comments are available for this gene. Log in to add comments, or register.

Enter your comment

User ()
Gene identifier LOAG_13163 (Loa Loa (eye worm)), hypothetical protein
Title for this comment
Comment