Detailed view for LinJ.28.1970

Basic information

TDR Targets ID: 437318
Leishmania infantum, C-terminal motor kinesin, putative
Source Database / ID: 

pI: 8.3695 | Length (AA): 965 | MW (Da): 103564 | Paralog Number: 1

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

Druggability Group : DG

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

Gene Ontology

Mouse over links to read term descriptions.
GO:0008017   microtubule binding  
GO:0005524   ATP binding  
GO:0003777   microtubule motor activity  
GO:0007018   microtubule-based 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
201 376 2iak (A) 20 210 7.00 0 0.05 0.322583 -1.2
579 955 1cz7 (A) 322 672 31.00 0.027 1 0.657674 0.07
642 952 5wdh (A) 346 662 46.00 0 1 0.76128 -0.69
652 951 5wde (A) 489 766 43.00 0 1 0.824881 -0.94

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_126975)

Species Accession Gene Product
Arabidopsis thaliana AT4G27180   kinesin 2
Arabidopsis thaliana AT4G21270   kinesin-like motor protein heavy chain
Arabidopsis thaliana AT4G05190   kinesin 5
Arabidopsis thaliana AT1G72250   Di-glucose binding protein with Kinesin motor domain
Arabidopsis thaliana AT5G54670   kinesin 3
Arabidopsis thaliana AT2G22610   Di-glucose binding protein with Kinesin motor domain
Brugia malayi Bm1_12505   Kinesin-like protein klp-3
Candida albicans CaO19.11581   C terminus of kinesin motor domain protein
Candida albicans CaO19.564   N terminus of kinesin motor domain protein
Candida albicans CaO19.4100   C terminus of kinesin motor domain protein
Caenorhabditis elegans CELE_T09A5.2   Protein KLP-3, isoform C
Caenorhabditis elegans CELE_W02B12.7   Protein KLP-17
Cryptosporidium hominis Chro.30298   kinesin-related protein K2
Cryptosporidium parvum cgd3_2590   kinesin-related protein K2
Dictyostelium discoideum DDB_G0267396   kinesin family member 2
Drosophila melanogaster Dmel_CG7831   non-claret disjunctional
Entamoeba histolytica EHI_119530   kinesin, putative
Echinococcus multilocularis EmuJ_000585600   kinesin family member c
Echinococcus multilocularis EmuJ_001123400   kinesin protein KIFC3
Giardia lamblia GL50803_8886   Kinesin-14
Homo sapiens ENSG00000237649   kinesin family member C1
Homo sapiens ENSG00000140859   kinesin family member C3
Leishmania braziliensis LbrM.28.2020   C-terminal motor kinesin, putative
Leishmania braziliensis LbrM.19.0570   C-terminal motor kinesin, putative
Leishmania donovani LdBPK_190250.1   C-terminal motor kinesin, putative
Leishmania donovani LdBPK_281970.1   C-terminal motor kinesin, putative
Leishmania infantum LinJ.19.0250   C-terminal motor kinesin, putative
Leishmania infantum LinJ.28.1970   C-terminal motor kinesin, putative
Leishmania major LmjF.19.0260   C-terminal motor kinesin, putative
Leishmania major LmjF.28.1850   C-terminal motor kinesin, putative
Leishmania mexicana LmxM.19.0260   C-terminal motor kinesin, putative
Leishmania mexicana LmxM.28.1850   C-terminal motor kinesin, putative
Mus musculus ENSMUSG00000024301   kinesin family member C5B
Mus musculus ENSMUSG00000079553   kinesin family member C1
Mus musculus ENSMUSG00000031788   kinesin family member C3
Oryza sativa 4342193   Os07g0105700
Oryza sativa 4334882   Os03g0862200
Oryza sativa 4337093   Os04g0629700
Oryza sativa 4352796   Os12g0616000
Oryza sativa 4331382   Os03g0114000
Saccharomyces cerevisiae YPR141C   Kar3p
Schmidtea mediterranea mk4.000314.08  
Schmidtea mediterranea mk4.000786.13  
Trypanosoma brucei gambiense Tbg972.11.10180   C-terminal motor kinesin, putative
Trypanosoma brucei gambiense Tbg972.10.18070   C-terminal motor kinesin, putative
Trypanosoma brucei Tb927.11.9110   C-terminal motor kinesin, putative
Trypanosoma brucei Tb11.v5.0625   C-terminal motor kinesin, putative
Trypanosoma brucei Tb927.10.14890   C-terminal motor kinesin, putative
Trypanosoma congolense TcIL3000.11.9460   C-terminal motor kinesin, putative
Trypanosoma cruzi TcCLB.510901.50   C-terminal motor kinesin, putative
Trypanosoma cruzi TcCLB.506211.114   C-terminal motor kinesin, putative

Essentiality

LinJ.28.1970 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.10.14890 Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb927.10.14890 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.10.14890 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.10.14890 Trypanosoma brucei no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms alsford
Tb11.01.0850 Trypanosoma brucei significant gain of fitness in bloodstream forms (3 days) alsford
Tb11.01.0850 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (6 days) alsford
Tb11.01.0850 Trypanosoma brucei significant loss of fitness in procyclic forms alsford
Tb11.01.0850 Trypanosoma brucei no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms alsford
CELE_T09A5.2 Caenorhabditis elegans embryonic arrest wormbase
CELE_T09A5.2 Caenorhabditis elegans embryonic lethal wormbase
Show/Hide essentiality data references
  • 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
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • 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.
  • 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
  • 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.
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • 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

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 kinesin family member C1 Compounds References
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

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 LinJ.28.1970 (Leishmania infantum), C-terminal motor kinesin, putative
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