Detailed view for Smp_146670

Basic information

TDR Targets ID: 287397
Schistosoma mansoni, acylaminoacyl-peptidase (S09 family)

Source Database / ID:  GeneDB

pI: 6.8464 | Length (AA): 1269 | MW (Da): 143706 | 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

PF00326   Prolyl oligopeptidase family
PF02735   Ku70/Ku80 beta-barrel domain
PF03730   Ku70/Ku80 C-terminal arm
PF03731   Ku70/Ku80 N-terminal alpha/beta domain

Gene Ontology

Mouse over links to read term descriptions.
GO:0043564   Ku70:Ku80 complex  
GO:0005958   DNA-dependent protein kinase complex  
GO:0005634   nucleus  
GO:0042162   telomeric DNA binding  
GO:0008236   serine-type peptidase activity  
GO:0005488   binding  
GO:0004003   ATP-dependent DNA helicase activity  
GO:0003684   damaged DNA binding  
GO:0003677   DNA binding  
GO:0006508   proteolysis  
GO:0006303   double-strand break repair via nonhomologous end joining  
GO:0000723   telomere maintenance  

Metabolic Pathways

This gene is not mapped to any metabolic pathway in KEGG.

Structural information

Modbase 3D models:

There are 7 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
60 640 5l8s (A) 1 604 18.00 0 1 0.535641 0.27
374 629 3pfb (A) 1 244 16.00 0 0.93 0.373034 -0.6
388 486 5ao9 (A) 41 131 31.00 0.82 0.42 0.196814 0.24
555 628 3doh (A) 315 389 14.00 0.79 0.02 0.0361136 0.69
663 1268 1jeq (A) 35 609 35.00 0 1 0.733341 0.75
1224 1269 2kvu (A) 19 63 20.00 0 1 0.414549 -1.22
1228 1268 2rno (A) 9 48 28.00 0.66 0.98 0.462109 -1.07

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_129086)

Species Accession Gene Product
Arabidopsis thaliana AT1G16970   ATP-dependent DNA helicase 2 subunit KU70
Brugia malayi Bm1_41430   ATP-dependent DNA helicase II, 70 kDa subunit
Candida albicans CaO19.3491   one of two closely related genes similar to S. cerevisiae YKU70 (YMR284W) Ku70-like DNA binding protein subunit involved in nonh
Candida albicans CaO19.1135   one of two closely related genes similar to S. cerevisiae YKU70 (YMR284W) Ku70-like DNA binding protein subunit involved in nonh
Candida albicans CaO19.8728   one of two closely related genes similar to S. cerevisiae YKU70 (YMR284W) Ku70-like DNA binding protein subunit involved in nonh
Caenorhabditis elegans CELE_Y47D3A.4   Protein CKU-70
Dictyostelium discoideum DDB_G0286069   ATP-dependent DNA helicase
Drosophila melanogaster Dmel_CG5247   Inverted repeat-binding protein
Echinococcus granulosus EgrG_000843250   x ray repair cross complementing protein 6
Echinococcus multilocularis EmuJ_000843250   x ray repair cross complementing protein 6
Homo sapiens ENSG00000196419   X-ray repair complementing defective repair in Chinese hamster cells 6
Leishmania braziliensis LbrM.29.1130   KU70 protein, putative
Leishmania donovani LdBPK_291140.1   KU70 protein, putative
Leishmania infantum LinJ.29.1140   KU70 protein, putative
Leishmania major LmjF.29.1050   KU70 protein, putative
Leishmania mexicana LmxM.08_29.1050   KU70 protein, putative
Loa Loa (eye worm) LOAG_01147   hypothetical protein
Mus musculus ENSMUSG00000022471   X-ray repair complementing defective repair in Chinese hamster cells 6
Neospora caninum NCLIV_064150   ATP-dependent DNA helicase II, 70 kDa subunit, putative
Oryza sativa 4342584   Os07g0184900
Saccharomyces cerevisiae YMR284W   Yku70p
Schistosoma japonicum Sjp_0065680   ko:K01303 acylaminoacyl-peptidase [EC3.4.19.1], putative
Schistosoma japonicum Sjp_0047080   hypothetical protein
Schistosoma japonicum Sjp_0065690   ATP-dependent DNA helicase 2 subunit 1, putative
Schistosoma mansoni Smp_146670   acylaminoacyl-peptidase (S09 family)
Schmidtea mediterranea mk4.001927.02   Acylaminoacyl-peptidase
Trypanosoma brucei gambiense Tbg972.3.5630   KU70 protein, putative
Trypanosoma brucei Tb927.3.5030   KU70 protein
Trypanosoma congolense TcIL3000_0_22830   KU70 protein
Trypanosoma cruzi TcCLB.503643.10   KU70 protein, putative
Trypanosoma cruzi TcCLB.504121.10   KU70 protein, putative
Toxoplasma gondii TGME49_248160   hypothetical protein

Essentiality

Smp_146670 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.3.5030 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (3 days) alsford
Tb927.3.5030 Trypanosoma brucei significant gain of fitness in bloodstream forms (6 days) alsford
Tb927.3.5030 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.3.5030 Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
TGME49_248160 Toxoplasma gondii Essentiality uncertain sidik
Show/Hide essentiality data references
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • 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.
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • 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.
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • 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
  • 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.
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924

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 Smp_146670 (Schistosoma mansoni), acylaminoacyl-peptidase (S09 family)
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