Detailed view for Tb927.11.1710

Basic information

TDR Targets ID: 11764
Trypanosoma brucei, guide RNA-binding protein of 21 kDa

Source Database / ID:  TriTrypDB  GeneDB

pI: 9.9959 | Length (AA): 206 | MW (Da): 23253 | 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

PF09387   Mitochondrial RNA binding protein MRP

Gene Ontology

Mouse over links to read term descriptions.
GO:0016556   mRNA modification  
GO:0006355   regulation of transcription, DNA-dependent  
GO:0005739   mitochondrion  
GO:0003723   RNA binding  
GO:0003677   DNA binding  

Metabolic Pathways

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

Structural information

Modbase 3D models:

There is 1 model calculated for this protein. More info on this model, including the model itself is available at: Modbase

Target Beg Target End Template Template Beg Template End Identity Evalue Model Score MPQS zDope
28 173 2gia (B) 28 173 99.00 0 1 1.92004 -1.33

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:

  • 2GIA:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date
  • 2GID:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date
  • 2GJE:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date

Expression

Upregulation Percent Ranking Stage Dataset
Upper 80-100% 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_148774)

Species Accession Gene Product
Leishmania braziliensis LbrM.27.1200   mitochondrial RNA binding protein 1,gBP21, MRP1
Leishmania donovani LdBPK_270980.1   guide RNA-binding protein of 21 kDa
Leishmania infantum LinJ.27.0980   mitochondrial RNA binding protein 1,gBP21, MRP1
Leishmania major LmjF.27.1110   mitochondrial RNA binding protein 1,gBP21, MRP1
Leishmania mexicana LmxM.27.1110   mitochondrial RNA binding protein 1,gBP21, MRP1
Trypanosoma brucei gambiense Tbg972.11.1830   mitochondrial RNA binding protein 1,gBP21, putative,MRP1, putative
Trypanosoma brucei Tb927.11.1710   guide RNA-binding protein of 21 kDa
Trypanosoma congolense TcIL3000.11.1490   guide RNA-binding protein of 21 kDa
Trypanosoma cruzi TcCLB.506629.30   guide RNA-binding protein of 21 kDa
Trypanosoma cruzi TcCLB.509831.36   mitochondrial RNA binding protein 1

Essentiality

Tb927.11.1710 has direct evidence of essentiality
Gene/Ortholog Organism Phenotype Source Study
Tb11.55.0009 this record Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb11.55.0009 this record Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb11.55.0009 this record Trypanosoma brucei significant loss of fitness in procyclic forms alsford
Tb11.55.0009 this record Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
Show/Hide essentiality data references
  • 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
  • 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.
  • 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
  • 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
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • 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.

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) 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.

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 Tb927.11.1710 (Trypanosoma brucei), guide RNA-binding protein of 21 kDa
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