Detailed view for LbrM.22.0750

Basic information

TDR Targets ID: 431048
Leishmania braziliensis, protein kinase, putative,serine/threonine protein kinase sos2, putative
Source Database / ID: 

pI: 7.3826 | Length (AA): 426 | MW (Da): 47099 | Paralog Number: 0

Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 2

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 5 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
3 359 5ezv (A) 12 398 21.00 0 1 1.19541 0.09
3 345 4cfh (A) 12 408 30.00 0 1 1.26526 0.16
4 270 4d28 (A) 8 270 44.00 0 1 1.19341 -0.38
5 268 3dfa (A) 5 266 33.00 0 1 1.15541 -0.8
6 273 2rku (A) 52 314 33.00 0 1 1.16334 -0.67

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_148620)

Species Accession Gene Product
Leishmania braziliensis LbrM.22.0750   protein kinase, putative,serine/threonine protein kinase sos2, putative
Leishmania donovani LdBPK_220630.1   protein kinase, putative
Leishmania infantum LinJ.22.0630   protein kinase, putative,serine/threonine protein kinase sos2, putative
Leishmania major LmjF.22.0810   protein kinase, putative,serine/threonine protein kinase sos2, putative
Leishmania mexicana LmxM.22.0810   protein kinase, putative,serine/threonine protein kinase sos2, putative
Trypanosoma brucei gambiense Tbg972.7.3150   protein kinase, putative
Trypanosoma brucei Tb927.7.2750   calcium/calmodulin-dependent protein kinase, putative
Trypanosoma congolense TcIL3000_7_2070   protein kinase, putative
Trypanosoma cruzi TcCLB.510525.10   calcium/calmodulin-dependent protein kinase, putative
Trypanosoma cruzi TcCLB.511817.80   calcium/calmodulin-dependent protein kinase, putative

Essentiality

LbrM.22.0750 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.7.2750 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (3 days) alsford
Tb927.7.2750 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.7.2750 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.7.2750 Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
Show/Hide essentiality data references
  • 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
  • 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.
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • 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.

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
Rattus norvegicus Serine/threonine-protein kinase pim-3 326 aa 28.5% 274 aa Compounds References
Rattus norvegicus Glycogen synthase kinase-3 beta 420 aa 27.1% 377 aa Compounds References
Oryctolagus cuniculus Cyclin-dependent kinase 4 189 aa 34.8% 161 aa Compounds References
Bos taurus Glycogen synthase kinase-3 beta splice variant X1 419 aa 26.1% 383 aa Compounds References
Rattus norvegicus Cell division protein kinase 5 292 aa 29.7% 296 aa Compounds References
Homo sapiens Cyclin-dependent kinase 1/cyclin B1 297 aa 33.9% 254 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 LbrM.22.0750 (Leishmania braziliensis), protein kinase, putative,serine/threonine protein kinase sos2, putative
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