Detailed view for TcCLB.509099.30

Basic information

TDR Targets ID: 38115
Trypanosoma cruzi, paraflagellar rod protein 5, putative
Source Database / ID:  TriTrypDB  GeneDB

pI: 6.0115 | Length (AA): 741 | MW (Da): 85860 | Paralog Number: 0

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

Druggability Group : DG4

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

PF00018   SH3 domain
PF05149   Paraflagellar rod protein

Gene Ontology

Mouse over links to read term descriptions.
GO:0031514   motile secondary cilium  
GO:0009434   microtubule-based flagellum  
GO:0005516   calmodulin binding  
GO:0005515   protein binding  

Metabolic Pathways

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

Structural information

Modbase 3D models:

There are 10 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
680 737 1zlm (A) 13 69 46.00 0.000054 1 0.73 -1.62
103 349 5j1i (A) 1148 1368 28.00 0.66 0.4 0.327033 0.67
265 492 5j1g (A) 1007 1231 15.00 0 0.63 0.441792 -0.79
409 616 4tql (A) 21 236 22.00 0.064 0.94 0.468402 -0.43
671 739 1udl (A) 23 91 35.00 0 1 0.425217 -0.38
680 739 3i5r (A) 4 79 32.00 0 0.98 0.210072 -1.08
682 736 2jte (A) 7 62 40.00 0 1 0.522324 -0.93
688 734 4wci (A) 8 54 49.00 0.00066 0.93 0.684128 -0.47
708 741 1gri (A) 184 217 38.00 0.41 0.15 0.288884 0.75
710 740 2cub (A) 45 75 32.00 0.065 0.04 0.226835 0.62

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
Upper 60-80% percentile epimastigote, metacyclic. Smircich P
Show/Hide expression data references
  • Smircich P Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi.

Orthologs

Ortholog group members (OG5_146951)

Species Accession Gene Product
Leishmania braziliensis LbrM.27.1990   paraflagellar rod protein-like protein
Leishmania donovani LdBPK_271750.1   paraflagellar rod protein 5, putative
Leishmania infantum LinJ.27.1750   paraflagellar rod protein-like protein
Leishmania major LmjF.27.1850   paraflagellar rod protein-like protein
Leishmania mexicana LmxM.27.1850   paraflagellar rod protein-like protein
Trypanosoma brucei gambiense Tbg.972.2.2410   paraflagellar rod protein, putative
Trypanosoma brucei Tb11.v5.0777   paraflagellar rod protein, putative
Trypanosoma brucei Tb927.2.4330   paraflagellar rod protein 5, putative
Trypanosoma congolense TcIL3000_2_740   paraflagellar rod protein 5, putative
Trypanosoma cruzi TcCLB.509099.30   paraflagellar rod protein 5, putative

Essentiality

TcCLB.509099.30 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.2.4330 Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb927.2.4330 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.2.4330 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.2.4330 Trypanosoma brucei no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms alsford
Show/Hide essentiality data references
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection
  • 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
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • 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.
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • 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.

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

Druggability index (range: 0 to 1): 0.1

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

Ranking Plot

Putative Drugs List

Compound Raw Global Species
0.00394418 0.278418 0
0.0065 0.3464 1
0.0322685 0.273741 0
0.0059 0.3 0.3608
0.0039 0.2713 0.7415
0.0137 0.2846 0
0.0027 0.3179 1
0.0061 1 0.5
0.0029 0.4037 0.3726
0.0027 0.3179 1
0.0378 0.315 0.315
0.0137 0.3036 1
0.0282 0.283 1
0.0039 0.2713 0.7415
0.0065 0.3464 1
0.0336199 0.276589 0
0.0048 0.281 1
0.0075 0.2576 0.5
0.0064 0.3347 1
0.0048 0.3625 1
0.0068 0.2794 0.2794
0.0351989 0.270507 0
0.0029 0.4037 0.3726
0.00394418 0.278418 0
0.0282 0.283 1

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.

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Gene identifier TcCLB.509099.30 (Trypanosoma cruzi), paraflagellar rod protein 5, putative
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