Detailed view for Tb927.5.1230

Basic information

TDR Targets ID: 14314
Trypanosoma brucei, hypothetical protein, conserved
Source Database / ID:  TriTrypDB  GeneDB

pI: 10.0197 | Length (AA): 483 | MW (Da): 58564 | Paralog Number: 0

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

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

PF13868   Trichohyalin-plectin-homology domain

Gene Ontology

Mouse over links to read term descriptions.
GO:0060271   GO:cilium assembly  

GO:0003341   GO:cilium movement  

Metabolic Pathways

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

Structural information

Modbase 3D models:

There are 4 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
5 333 5h7c (A) 56 398 25.00 0.014 0.92 0.913359 -0.22
95 312 5cwq (A) 4 226 29.00 0.023 0.72 0.698546 -0.17
233 351 5j0l (A) 4 130 29.00 0.095 0.69 0.652577 -1.89
282 460 4f61 (I) 44 209 34.00 0.0092 0.07 0.3498 1.06

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

Upregulation Percent Ranking Stage Dataset
Lower 20-40% percentile Procyclic, Bloodstream Form. Siegel TN
Show/Hide expression data references
  • Siegel TN Genome-wide analysis of mRNA abundance in two life-cycle stages of Trypanosoma brucei and identification of splicing and polyadenylation sites.

Orthologs

Ortholog group members (OG5_129329)

Species Accession Gene Product
Drosophila melanogaster Dmel_CG17230   CG17230 gene product from transcript CG17230-RA
Echinococcus granulosus EgrG_000178600   trichoplein keratin filament binding protein
Echinococcus multilocularis EmuJ_000178600   trichoplein keratin filament binding protein
Giardia lamblia GL50803_16013   Spindle pole protein, putative
Homo sapiens ENSG00000139437   trichoplein, keratin filament binding
Homo sapiens ENSG00000172361   cilia and flagella associated protein 53
Leishmania braziliensis LbrM.23.1690   hypothetical protein, conserved
Leishmania donovani LdBPK_231850.1   Tumour suppressor, Mitostatin, putative
Leishmania infantum LinJ.23.1850   hypothetical protein, conserved
Leishmania major LmjF.23.1450   hypothetical protein, conserved
Leishmania mexicana LmxM.23.1450   hypothetical protein, conserved
Mus musculus ENSMUSG00000035394   cilia and flagella associated protein 53
Mus musculus ENSMUSG00000002486   trichoplein, keratin filament binding
Neospora caninum NCLIV_034180   hypothetical protein, conserved
Schistosoma japonicum Sjp_0015500   expressed protein
Schistosoma japonicum Sjp_0015520   Trichoplein keratin filament-binding protein, putative
Schistosoma japonicum Sjp_0206900   expressed protein
Schistosoma mansoni Smp_180580   meiosis-specific nuclear structural protein 1
Schistosoma mansoni Smp_174880   FOG precursor
Schmidtea mediterranea mk4.001488.00  
Trypanosoma brucei gambiense Tbg972.5.1700   T. brucei spp.-specific protein
Trypanosoma brucei Tb927.5.1230   hypothetical protein, conserved
Trypanosoma congolense TcIL3000_5_1170   hypothetical protein, conserved
Trypanosoma cruzi TcCLB.509767.150   hypothetical protein, conserved
Trypanosoma cruzi TcCLB.509601.150   hypothetical protein, conserved
Toxoplasma gondii TGME49_273468   hypothetical protein
Trichomonas vaginalis TVAG_436250   coiled-coil domain-containing protein, putative
Trichomonas vaginalis TVAG_023280   coiled-coil domain-containing protein, putative

Essentiality

Tb927.5.1230 has direct evidence of essentiality
Gene/Ortholog Organism Phenotype Source Study
Tb927.5.1230 this record Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb927.5.1230 this record Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.5.1230 this record Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.5.1230 this record Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
TGME49_273468 Toxoplasma gondii Probably non-essential sidik
TGME49_273468 Toxoplasma gondii Essentiality uncertain sidik
Show/Hide essentiality data references
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • 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.
  • 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
  • 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
  • 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.
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930

Phenotypes and Validation (curated)

Annotated phenotypes:

Affected Entity Phenotypic quality Occurs in Occurs at Evidence Observed in Drugs/Inhibitors
cell proliferation (GO:0008283) decreased (PATO:0000468) bloodstream stage trypomastigotes (PLO:0027) inferred from RNAi experiment (ECO:0000019) No drug identifiers listed for this gene.
Annotator: fernan@iib.unsam.edu.ar. Comment: decreased cell proliferation (significant loss of fitness) in bloodstream forms (stage 6 days). References: 21363968
cell proliferation (GO:0008283) normal (PATO:0000461) procyclic (PLO:0034) inferred from RNAi experiment (ECO:0000019) No drug identifiers listed for this gene.
Annotator: fernan@iib.unsam.edu.ar. Comment: normal cell proliferation (no significant loss or gain of fitness) in procyclic forms . References: 21363968
cell proliferation (GO:0008283) decreased (PATO:0000468) procyclic (PLO:0034) inferred from RNAi experiment (ECO:0000019) No drug identifiers listed for this gene.
Annotator: fernan@iib.unsam.edu.ar. Comment: decreased cell proliferation (significant loss of fitness) in differentiation of procyclic to bloodstream forms . References: 21363968

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

1 literature reference was collected for this gene.

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Gene identifier Tb927.5.1230 (Trypanosoma brucei), hypothetical protein, conserved
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