Detailed view for LinJ.35.5330

Basic information

TDR Targets ID: 440506
Leishmania infantum, protein kinase, putative
Source Database / ID: 

pI: 9.8652 | Length (AA): 392 | MW (Da): 44183 | Paralog Number: 0

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

PF00069   Protein kinase domain

Gene Ontology

Mouse over links to read term descriptions.
GO:0005524   ATP binding  
GO:0004672   protein kinase activity  
GO:0006468   protein amino acid phosphorylation  

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
1 290 3niz (A) 20 307 37.00 0 1 1.193 -0.5
1 291 4bgq (A) 10 301 42.00 0 1 1.07855 0.07
1 290 3o0g (A) 1 289 38.00 0 1 1.1641 -0.63
3 371 4cfh (A) 15 455 21.00 0 1 1.04313 1.09

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_131024)

Species Accession Gene Product
Giardia lamblia GL50803_14004   Long-flagella protein, kinase, CMGC RCK
Homo sapiens ENSG00000080823   MOK protein kinase
Leishmania braziliensis LbrM.34.4950   protein kinase, putative
Leishmania donovani LdBPK_355330.1   protein kinase, putative
Leishmania infantum LinJ.35.5330   protein kinase, putative
Leishmania major LmjF.35.5010   protein kinase, putative
Mus musculus ENSMUSG00000056458   MOK protein kinase
Schmidtea mediterranea mk4.001235.06  
Schmidtea mediterranea mk4.001235.05  
Trypanosoma brucei gambiense Tbg972.9.5250   protein kinase, putative
Trypanosoma brucei Tb927.9.9320   MAPK/MAK/MRK overlapping kinase, putative
Trypanosoma congolense TcIL3000_9_3400   protein kinase, putative
Trypanosoma cruzi TcCLB.506885.120   MAPK/MAK/MRK overlapping kinase, putative
Trichomonas vaginalis TVAG_328960   CMGC family protein kinase
Trichomonas vaginalis TVAG_144010   CMGC family protein kinase
Trichomonas vaginalis TVAG_272410   CMGC family protein kinase
Trichomonas vaginalis TVAG_057050   CMGC family protein kinase

Essentiality

LinJ.35.5330 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb09.211.0960 Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb09.211.0960 Trypanosoma brucei significant gain of fitness in bloodstream forms (6 days) alsford
Tb09.211.0960 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb09.211.0960 Trypanosoma brucei significant gain of fitness in differentiation of procyclic to bloodstream forms alsford
Show/Hide essentiality data references
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • 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.
  • 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
  • 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
  • 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
  • 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
  • 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)

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
Non orthologous druggable targets
By sequence similarity to non orthologous druggable targets
Species Target Length Identity Alignment span Linked Drugs Reference
Patiria pectinifera Cdc2 300 aa 37.1% 294 aa Compounds References
Zea mays Casein kinase II alpha 332 aa 30.9% 307 aa Compounds References
Schizosaccharomyces pombe 972h- Casein kinase II subunit alpha 332 aa 30.9% 301 aa Compounds References
Homo sapiens Cyclin-dependent kinase 1/cyclin B1 297 aa 37.5% 304 aa Compounds References
Rattus norvegicus Cell division protein kinase 5 292 aa 40.0% 295 aa Compounds References
Plasmodium falciparum (isolate 3D7) Cell division control protein 2 homolog 288 aa 37.5% 296 aa Compounds References
Oryctolagus cuniculus Cyclin-dependent kinase 4 189 aa 39.6% 169 aa Compounds References
Bos taurus cAMP-dependent protein kinase alpha-catalytic subunit 351 aa 25.2% 282 aa Compounds References
Rattus norvegicus Mitogen-activated protein kinase 1 358 aa 34.1% 296 aa Compounds References
Rattus norvegicus MAP kinase p38 alpha 360 aa 32.6% 301 aa Compounds References
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.35.5330 (Leishmania infantum), protein kinase, putative
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