Detailed view for LOAG_08245

Basic information

TDR Targets ID: 950140
Loa Loa (eye worm), proteasome subunit alpha type 2

Source Database / ID:  KEGG  

pI: 5.6632 | Length (AA): 235 | MW (Da): 25877 | 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

PF00227   Proteasome subunit
PF10584   Proteasome subunit A N-terminal signature

Gene Ontology

Mouse over links to read term descriptions.
GO:0019773   proteasome core complex, alpha-subunit complex  
GO:0005839   proteasome core complex  
GO:0004298   threonine endopeptidase activity  
GO:0004175   endopeptidase activity  
GO:0051603   proteolysis involved in cellular protein catabolic process  
GO:0006511   ubiquitin-dependent protein catabolic process  

Metabolic Pathways

Proteasome (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
4 235 1ryp (B) 2 250 57.00 0 1 1.61843 -0.69
7 178 1ryp (G) 7 177 40.00 0 1 1.22011 -0.36
7 235 5le5 (A) 5 232 68.00 0 1 1.82567 -1.09

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_127791)

Species Accession Gene Product
Arabidopsis thaliana AT1G16470   20S proteasome subunit PAB1
Arabidopsis thaliana AT1G79210   proteasome subunit alpha type-2-B
Babesia bovis BBOV_III000310   proteasome A-type and B-type family protein
Brugia malayi Bm1_21080   proteasome subunit alpha type 2
Candida albicans CaO19.7335   multicatalytic endopeptidase
Caenorhabditis elegans CELE_D1054.2   Protein PAS-2
Cryptosporidium hominis Chro.70408   proteasome subunit alpha type 2 (20S proteasome alpha subunit B) (20S proteasome subunit alpha-2)
Cryptosporidium parvum cgd7_3660   proteasome subunit alpha2, protease of the acylase family and NTN hydrolase fold
Dictyostelium discoideum DDB_G0292122   20S proteasome subunit alpha-2
Drosophila melanogaster Dmel_CG5266   Proteasome alpha2 subunit
Echinococcus granulosus EgrG_001120300   proteasome subunit alpha type 2
Entamoeba histolytica EHI_052140   proteasome subunit alpha type 2-A, putative
Echinococcus multilocularis EmuJ_001120300   proteasome subunit alpha type 2
Giardia lamblia GL50803_11434   20S proteasome alpha subunit 2
Homo sapiens ENSG00000106588   proteasome (prosome, macropain) subunit, alpha type, 2
Leishmania braziliensis LbrM.21.2010   proteasome alpha 2 subunit, putative
Leishmania donovani LdBPK_212070.1   proteasome alpha 2 subunit, putative
Leishmania infantum LinJ.21.2070   proteasome alpha 2 subunit, putative
Leishmania major LmjF.21.1700   proteasome alpha 2 subunit, putative
Leishmania mexicana LmxM.21.1700   proteasome alpha 2 subunit, putative
Loa Loa (eye worm) LOAG_08245   proteasome subunit alpha type 2
Mus musculus ensembl-mmu:ENSMUSG00000015671   proteasome (prosome, macropain) subunit, alpha type 2
Neospora caninum NCLIV_013780   hypothetical protein
Oryza sativa 4333000   Os03g0387100
Oryza sativa 4330075   Os02g0634900
Plasmodium berghei PBANKA_0107100   proteasome subunit alpha type-2, putative
Plasmodium falciparum PF3D7_0608500   proteasome subunit alpha type-2, putative
Plasmodium knowlesi PKNH_1141700   proteasome subunit alpha type-2, putative
Plasmodium vivax PVX_113585   proteasome subunit alpha type-2, putative
Plasmodium yoelii PY03034   proteasome subunit alpha type 2
Saccharomyces cerevisiae YML092C   proteasome core particle subunit alpha 2
Schistosoma japonicum Sjp_0204140   ko:K02726 20S proteasome subunit alpha 2, putative
Schistosoma mansoni Smp_067890   proteasome subunit alpha 2 (T01 family)
Trypanosoma brucei gambiense Tbg972.10.200   proteasome alpha 2 subunit, putative
Trypanosoma brucei Tb927.10.290   proteasome alpha 2 subunit, putative
Trypanosoma congolense TcIL3000_10_150   proteasome alpha 2 subunit, putative
Trypanosoma cruzi TcCLB.504069.10   proteasome alpha 2 subunit, putative
Trypanosoma cruzi TcCLB.416883.18   proteasome alpha 2 subunit, putative
Toxoplasma gondii TGME49_287210   proteasome subunit alpha2, protease of the acylase family and NTN hydrolase fold, putative
Theileria parva TP03_0809   proteasome subunit alpha type 2, putative
Trichomonas vaginalis TVAG_103780   Family T1, proteasome alpha subunit, threonine peptidase

Essentiality

LOAG_08245 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.10.290 Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb927.10.290 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.10.290 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.10.290 Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
CELE_D1054.2 Caenorhabditis elegans embryonic lethal wormbase
CELE_D1054.2 Caenorhabditis elegans larval lethal wormbase
YML092C Saccharomyces cerevisiae inviable yeastgenome
TGME49_287210 Toxoplasma gondii Probably essential sidik
Show/Hide essentiality data references
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • 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.
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • 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
  • neb C. elegans RNAi phenotypes Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs
  • 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.
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan

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 proteasome (prosome, macropain) subunit, alpha type, 2 Compounds References
By sequence similarity to non orthologous druggable targets
No additional associated druggable targets

Obtained from network model

Ranking Plot


Putative Drugs List


Compound Raw Global Species
0.0262 0.3498 0.3803
0.0146 0.3484 0.5109
0.0126 0.3687 0.3839
0.0146 0.3484 0.5109
0.0118 0.3484 0.5109
0.0275 0.3479 0.3465
0.0129 0.3683 0.3861
0.0146 0.3484 0.5109
0.0271 0.3485 0.3485
0.0146 0.3498 0.5124
0.0141 0.3473 0.5097
0.0253 0.3498 0.3695
0.0146 0.3498 0.5124
0.0243 0.3498 0.4207
0.0146 0.3484 0.5109
0.0121 0.2889 0.2889
0.0134 0.3484 0.5109
0.0268 0.3615 0.4044

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_08245 (Loa Loa (eye worm)), proteasome subunit alpha type 2
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