Detailed view for TVAG_013050

Basic information

TDR Targets ID: 836678
Trichomonas vaginalis, spliceosomal protein sap, putative
Source Database / ID: 

pI: 5.0859 | Length (AA): 1142 | MW (Da): 127955 | 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

PF03178   CPSF A subunit region
PF10433   Mono-functional DNA-alkylating methyl methanesulfonate N-term

Gene Ontology

Mouse over links to read term descriptions.
GO:0005634   nucleus  
GO:0005515   protein binding  
GO:0003676   nucleic acid binding  

Metabolic Pathways

Spliceosome (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_128558)

Species Accession Gene Product
Arabidopsis thaliana AT3G55220   spliceosome-associated protein 130B
Arabidopsis thaliana AT3G55200   spliceosomal associated protein 130A
Babesia bovis BBOV_II004270   splicing factor 3b, subunit 3, 130kD, putative
Brugia malayi Bm1_19455   splicing factor 3B subunit 3
Candida albicans CaO19.12846   similar to U2 snRNP complex splicing factor SF3b subunit SAP130 and to S. cerevisiae RSE1 (YML049C)
Candida albicans CaO19.5391   similar to U2 snRNP complex splicing factor SF3b subunit SAP130 and to S. cerevisiae RSE1 (YML049C)
Caenorhabditis elegans CELE_K02F2.3   Protein TEG-4
Cryptosporidium hominis Chro.80487   CG13900 gene product
Cryptosporidium parvum cgd8_4240   possible spliceosome factor
Dictyostelium discoideum DDB_G0282569   CPSF domain-containing protein
Drosophila melanogaster Dmel_CG13900   CG13900 gene product from transcript CG13900-RA
Echinococcus granulosus EgrG_000633300   splicing factor 3b subunit 3
Entamoeba histolytica EHI_144720   CPSF A subunit region protein, putative
Echinococcus multilocularis EmuJ_000633300   splicing factor 3b subunit 3
Homo sapiens ENSG00000189091   splicing factor 3b, subunit 3, 130kDa
Loa Loa (eye worm) LOAG_03297   hypothetical protein
Mus musculus ENSMUSG00000033732   splicing factor 3b, subunit 3
Neospora caninum NCLIV_031340   Splicing factor 3B subunit 3, putative
Oryza sativa 4328237   Os02g0137400
Onchocerca volvulus OVOC11814  
Plasmodium berghei PBANKA_1449400   splicing factor 3B subunit 3, putative
Plasmodium falciparum PF3D7_1234800   splicing factor 3B subunit 3, putative
Plasmodium knowlesi PKNH_1454200   splicing factor 3B subunit 3, putative
Plasmodium vivax PVX_100690   splicing factor 3B subunit 3, putative
Plasmodium yoelii PY03514   Drosophila melanogaster CG13900 gene product
Saccharomyces cerevisiae YML049C   Rse1p
Schistosoma japonicum Sjp_0025810   Splicing factor 3B subunit 3, putative
Schmidtea mediterranea mk4.018922.00   Splicing factor 3B subunit 3
Schmidtea mediterranea mk4.043164.00   Splicing factor 3B subunit 3
Schmidtea mediterranea mk4.039880.00   Splicing factor 3B subunit 3
Schmidtea mediterranea mk4.005874.00   Splicing factor 3B subunit 3
Schmidtea mediterranea mk4.039880.01   Splicing factor 3B subunit 3
Toxoplasma gondii TGME49_230960   splicing factor 3b, subunit 3, putative
Theileria parva TP04_0182   hypothetical protein
Trichomonas vaginalis TVAG_013050   spliceosomal protein sap, putative

Essentiality

TVAG_013050 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
CELE_K02F2.3 Caenorhabditis elegans embryonic lethal wormbase
CELE_K02F2.3 Caenorhabditis elegans larval arrest wormbase
CELE_K02F2.3 Caenorhabditis elegans sterile wormbase
YML049C Saccharomyces cerevisiae inviable yeastgenome
PBANKA_1449400 Plasmodium berghei Essential plasmo
TGME49_230960 Toxoplasma gondii Probably 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
  • 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.
  • 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
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • 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
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database

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 splicing factor 3b, subunit 3, 130kDa 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
0.0096 1 1
0.0028 0.806 0.5

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 TVAG_013050 (Trichomonas vaginalis), spliceosomal protein sap, putative
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