Detailed view for LOAG_05314

Basic information

TDR Targets ID: 943187
Loa Loa (eye worm), Pex2/Pex12 amino terminal region family protein
Source Database / ID:  KEGG  

pI: 10.1229 | Length (AA): 317 | MW (Da): 37368 | Paralog Number: 0

Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 3

Druggability Group : DG1

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

PF04757   Pex2 / Pex12 amino terminal region

Gene Ontology

Mouse over links to read term descriptions.
GO:0006625   protein targeting to peroxisome  
GO:0008022   protein C-terminus binding  
GO:0005779   integral to peroxisomal membrane  
GO:0008270   zinc ion binding  

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
49 104 1xdz (A) 29 85 34.00 0.38 0.07 0.371456 1.36
266 313 2ckl (A) 13 60 15.00 0.0059 0.09 0.32062 -0.26
266 313 4s3o (C) 13 60 10.00 0.015 0.04 0.28862 -0.49

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_129605)

Species Accession Gene Product
Arabidopsis thaliana AT3G04460   Peroxisome biogenesis protein 12
Brugia malayi Bm1_09280   Pex2 / Pex12 amino terminal region family protein
Candida albicans CaO19.2009   similar to P. pastoris Peroxin-12 and to S. cerevisiae PEX12 (YMR026C) peroxisomal import complex protein
Candida albicans CaO19.9560   similar to P. pastoris Peroxin-12 and to S. cerevisiae PEX12 (YMR026C) peroxisomal import complex protein
Caenorhabditis elegans CELE_F08B12.2   Protein PRX-12
Dictyostelium discoideum DDB_G0285523   RING zinc finger-containing protein
Drosophila melanogaster Dmel_CG3639   Peroxin 12
Homo sapiens ENSG00000108733   peroxisomal biogenesis factor 12
Leishmania braziliensis LbrM.19.1470   peroxisome assembly protein, putative
Leishmania donovani LdBPK_191240.1   peroxisome assembly protein, putative
Leishmania infantum LinJ.19.1240   peroxisome assembly protein, putative
Leishmania major LmjF.19.1250   peroxisome assembly protein, putative
Leishmania mexicana LmxM.19.1250   peroxisome assembly protein, putative
Loa Loa (eye worm) LOAG_05314   Pex2/Pex12 amino terminal region family protein
Mus musculus ENSMUSG00000018733   peroxisomal biogenesis factor 12
Oryza sativa 4348849   Os10g0467200
Saccharomyces cerevisiae YMR026C   ubiquitin-protein ligase peroxin 12
Schmidtea mediterranea mk4.001698.02   Putative peroxisome assembly protein 12
Trypanosoma brucei gambiense Tbg972.10.19440   peroxisome assembly protein, putative
Trypanosoma brucei Tb927.10.15850   Peroxisome biogenesis factor 12
Trypanosoma congolense TcIL3000_10_13660   peroxisome assembly protein, putative
Trypanosoma cruzi TcCLB.503809.20   peroxin 12, putative
Trypanosoma cruzi TcCLB.503641.19   peroxin 12, putative

Essentiality

LOAG_05314 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.10.15850 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (3 days) alsford
Tb927.10.15850 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.10.15850 Trypanosoma brucei significant gain of fitness in procyclic forms alsford
Tb927.10.15850 Trypanosoma brucei no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms alsford
CELE_F08B12.2 Caenorhabditis elegans embryonic lethal wormbase
CELE_F08B12.2 Caenorhabditis elegans larval arrest wormbase
CELE_F08B12.2 Caenorhabditis elegans slow growth wormbase
Show/Hide essentiality data references
  • 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
  • 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
  • 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.
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • 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.

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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Gene identifier LOAG_05314 (Loa Loa (eye worm)), Pex2/Pex12 amino terminal region family protein
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