Detailed view for LOAG_04336

Basic information

TDR Targets ID: 951409
Loa Loa (eye worm), eukaryotic translation initiation factor 4E type 3
Source Database / ID:  KEGG  

pI: 6.1309 | Length (AA): 246 | MW (Da): 28350 | Paralog Number: 0

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

PF01652   Eukaryotic initiation factor 4E

Gene Ontology

Mouse over links to read term descriptions.
GO:0005737   cytoplasm  
GO:0003743   translation initiation factor activity  
GO:0003723   RNA binding  
GO:0006413   translational initiation  

Metabolic Pathways

RNA transport (KEGG)
mTOR signaling pathway (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
25 228 1ap8 (A) 9 201 32.00 0 1 1.08047 0.46
55 237 2jgb (A) 45 231 58.00 0 1 1.571 -1.63
94 228 4ue8 (A) 96 233 37.00 0 1 1.14038 -1.49

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_129419)

Species Accession Gene Product
Arabidopsis thaliana AT5G18110   translation initiation factor NCBP
Brugia malayi Bm1_32915   Eukaryotic translation initiation factor 4E type 3, putative
Caenorhabditis elegans CELE_C05D9.5   Protein IFE-4
Dictyostelium discoideum DDB_G0284841   hypothetical protein
Dictyostelium discoideum DDB_G0291820   hypothetical protein
Drosophila melanogaster Dmel_CG33100   eIF4E-Homologous Protein
Giardia lamblia GL50803_7990   Translation elongation factor
Homo sapiens ENSG00000135930   eukaryotic translation initiation factor 4E family member 2
Loa Loa (eye worm) LOAG_04336   eukaryotic translation initiation factor 4E type 3
Mus musculus ENSMUSG00000026254   eukaryotic translation initiation factor 4E member 2
Neospora caninum NCLIV_057910   hypothetical protein
Oryza sativa 4332327   Os03g0262400
Schmidtea mediterranea mk4.000548.03   4EHP
Trypanosoma brucei gambiense Tbg972.10.19680   eukaryotic translation initiation factor 4e, putative
Trypanosoma brucei Tb927.10.16070   Eukaryotic translation initiation factor 4E-2
Trypanosoma congolense TcIL3000_0_03820   Eukaryotic translation initiation factor 4E-2
Toxoplasma gondii TGME49_315150   eukaryotic initiation factor-4E, putative
Trichomonas vaginalis TVAG_450940   eukaryotic translation initiation factor 4E, putative

Essentiality

LOAG_04336 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.10.16070 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (3 days) alsford
Tb927.10.16070 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.10.16070 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.10.16070 Trypanosoma brucei no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms alsford
CELE_C05D9.5 Caenorhabditis elegans embryonic lethal wormbase
TGME49_315150 Toxoplasma gondii Essentiality uncertain sidik
Show/Hide essentiality data references
  • 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
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • 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.
  • 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
  • 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
  • neb C. elegans RNAi phenotypes Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs
  • 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
Non orthologous druggable targets
By sequence similarity to non orthologous druggable targets
Species Target Length Identity Alignment span Linked Drugs Reference
Oryctolagus cuniculus Eukaryotic translation initiation factor 4E 217 aa 28.1% 178 aa Compounds References
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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Gene identifier LOAG_04336 (Loa Loa (eye worm)), eukaryotic translation initiation factor 4E type 3
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