Detailed view for Sjp_0303940

Basic information

TDR Targets ID: 968073
Schistosoma japonicum, ko:K09602 ubiquitin thioesterase protein OTUB1, putative
Source Database / ID:  Wormbase Parasite  

pI: 4.3222 | Length (AA): 299 | MW (Da): 33929 | Paralog Number: 0

Signal peptide: N | GPI Anchor: | Predicted trans-membrane segments: 0

Druggability Group : DG

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

PF10275   Peptidase C65 Otubain

Gene Ontology

Mouse over links to read term descriptions.
GO:0016579   protein deubiquitination  
GO:0016787   hydrolase activity  

Metabolic Pathways

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

Structural information

Modbase 3D models:

No model available for this protein in Modbase.

PDB Structures:

No structure availble in the PDB for this protein

Expression

No expression data available for this gene

Orthologs

Ortholog group members (OG5_128982)

Species Accession Gene Product
Arabidopsis thaliana AT1G28120   ubiquitin thioesterase otubain-like protein
Caenorhabditis elegans CELE_C25D7.8   Protein OTUB-1
Drosophila melanogaster Dmel_CG4968   CG4968 gene product from transcript CG4968-RA
Echinococcus granulosus EgrG_000540000   Ubiquitin thioesterase otubain protein
Echinococcus multilocularis EmuJ_000540000   Ubiquitin thioesterase otubain protein
Homo sapiens ENSG00000167770   OTU deubiquitinase, ubiquitin aldehyde binding 1
Homo sapiens ENSG00000089723   OTU deubiquitinase, ubiquitin aldehyde binding 2
Leishmania braziliensis LbrM.17.1540   otubain, putative,otubain cysteine peptidase, Clan CA, family C65, putative
Leishmania donovani LdBPK_171520.1   otubain cysteine peptidase, Clan CA, family C65, putative
Leishmania infantum LinJ.17.1520   otubain, putative,otubain cysteine peptidase, Clan CA, family C65, putative
Leishmania major LmjF.17.1400   otubain, putative,otubain cysteine peptidase, Clan CA, family C65, putative
Leishmania mexicana LmxM.17.1400   otubain, putative,otubain cysteine peptidase, Clan CA, family C65, putative
Loa Loa (eye worm) LOAG_04168   hypothetical protein
Mus musculus ENSMUSG00000024767   OTU domain, ubiquitin aldehyde binding 1
Mus musculus ENSMUSG00000021203   OTU domain, ubiquitin aldehyde binding 2
Neospora caninum NCLIV_026530   ubiquitin thiolesterase protein, putative
Oryza sativa 4346169   Os08g0537800
Schistosoma japonicum Sjp_0303940   ko:K09602 ubiquitin thioesterase protein OTUB1, putative
Schistosoma mansoni Smp_097810.2   otubain-1 (C65 family)
Schmidtea mediterranea mk4.008804.00  
Schmidtea mediterranea mk4.020692.00   Ubiquitin thioesterase otubain-like
Trypanosoma brucei gambiense Tbg972.5.3790   otubain, putative,otubain cysteine peptidase, Clan CA, family C65, putative
Trypanosoma brucei Tb927.5.2700   otubain cysteine peptidase, Clan CA, family C65, putative
Trypanosoma congolense TcIL3000_5_2790   otubain cysteine peptidase, Clan CA, family C65, putative
Trypanosoma cruzi TcCLB.507047.110   otubain cysteine peptidase, Clan CA, family C65, putative
Trypanosoma cruzi TcCLB.509179.150   otubain cysteine peptidase, Clan CA, family C65, putative
Toxoplasma gondii TGME49_260510   ubiquitin thioesterase otubain-like family protein

Essentiality

Sjp_0303940 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.5.2700 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (3 days) alsford
Tb927.5.2700 Trypanosoma brucei significant gain of fitness in bloodstream forms (6 days) alsford
Tb927.5.2700 Trypanosoma brucei significant gain of fitness in procyclic forms alsford
Tb927.5.2700 Trypanosoma brucei significant gain of fitness in differentiation of procyclic to bloodstream forms alsford
TGME49_260510 Toxoplasma gondii Probably non-essential sidik
Show/Hide essentiality data references
  • 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
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • 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
  • 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.
  • 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
  • neb C. elegans RNAi phenotypes Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs

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
Leishmania major otubain, putative,otubain cysteine peptidase, Clan CA, family C65, putative 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

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Gene identifier Sjp_0303940 (Schistosoma japonicum), ko:K09602 ubiquitin thioesterase protein OTUB1, putative
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