Detailed view for TcCLB.507087.40

Basic information

TDR Targets ID: 36204
Trypanosoma cruzi, kinesin, putative

Source Database / ID:  TriTrypDB  GeneDB

pI: 6.5219 | Length (AA): 1339 | MW (Da): 150291 | Paralog Number: 1

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

PF00225   Kinesin motor domain
PF01067   Calpain large subunit, domain III

Gene Ontology

Mouse over links to read term descriptions.
GO:0005622   intracellular  
GO:0008017   microtubule binding  
GO:0005524   ATP binding  
GO:0005515   protein binding  
GO:0005488   binding  
GO:0004198   calcium-dependent cysteine-type endopeptidase activity  
GO:0003777   microtubule motor activity  
GO:0007018   microtubule-based movement  
GO:0006508   proteolysis  

Metabolic Pathways

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

Structural information

Modbase 3D models:

There are 13 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
10 342 1x88 (A) 20 363 37.00 0 1 0.66 -0.93
10 364 1goj (A) 9 354 37.00 0 1 0.74 -0.59
417 808 1wa5 (B) 139 506 16.00 0.000000000016 0.81 0.46 -0.64
511 791 2c1m (A) 227 482 16.00 0.00000000029 0.83 0.27 -0.38
10 334 5wde (A) 447 764 38.00 0 1 0.725718 -0.84
10 380 4frz (A) 891 1244 37.00 0 1 0.649072 -0.23
10 335 3x2t (A) 10 324 41.00 0 1 0.570465 0.02
10 245 2kin (A) 10 239 33.00 0 1 0.521551 -0.23
29 335 5x3e (A) 29 423 36.00 0 1 0.446276 -0.48
134 621 2qmr (C) 284 793 12.00 0 1 0.424751 0.42
258 363 2kin (B) 252 350 43.00 0 0.34 0.361464 0.74
472 627 4dba (A) 30 184 24.00 0.61 0.9 0.451505 -0.66
574 667 3l6y (E) 363 449 21.00 0 0.51 0.330502 -1.16

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

No expression data available for this gene

Orthologs

Ortholog group members (OG5_148471)

Species Accession Gene Product
Leishmania braziliensis LbrM.17.1220   kinesin, putative
Leishmania donovani LdBPK_171210.1   kinesin, putative
Leishmania infantum LinJ.17.1210   kinesin, putative
Leishmania major LmjF.17.1110   kinesin, putative
Leishmania mexicana LmxM.17.1110   kinesin, putative
Trypanosoma brucei gambiense Tbg972.5.3420   kinesin, putative
Trypanosoma brucei Tb927.5.2410   kinesin, putative
Trypanosoma congolense TcIL3000_5_2280   kinesin, putative
Trypanosoma cruzi TcCLB.507087.40   kinesin, putative
Trypanosoma cruzi TcCLB.511307.10   kinesin, putative

Essentiality

TcCLB.507087.40 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.5.2410 Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb927.5.2410 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.5.2410 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.5.2410 Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
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.
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • neb C. elegans RNAi phenotypes Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • 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
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • 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.
  • 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
  • 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

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): 0.3


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
0.0022 0.2562 1
0.0288 0.2604 0.8181
0.0023 0.2562 1
0.0288 0.2604 0.8181

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 TcCLB.507087.40 (Trypanosoma cruzi), kinesin, putative
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