Detailed view for LbrM.26.1990

Basic information

TDR Targets ID: 428523
Leishmania braziliensis, SUMO1/Ulp2, putative,cysteine peptidase, Clan CA, family C48, putative

Source Database / ID: 

pI: 8.8282 | Length (AA): 1391 | MW (Da): 151183 | Paralog Number: 0

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

Pfam domains

PF02902   Ulp1 protease family, C-terminal catalytic domain

Gene Ontology

Mouse over links to read term descriptions.
GO:0008234   cysteine-type peptidase activity  
GO:0006508   proteolysis  

Metabolic Pathways

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

Structural information

Modbase 3D models:

No model available for this protein in Modbase.

PDB Structures:

No structure availble in the PDB for this protein

Expression

No expression data available for this gene

Orthologs

Ortholog group members (OG5_140391)

Species Accession Gene Product
Leishmania braziliensis LbrM.26.1990   SUMO1/Ulp2, putative,cysteine peptidase, Clan CA, family C48, putative
Leishmania donovani LdBPK_262070.1   SUMO1/Ulp2, putative
Leishmania infantum LinJ.26.2070   SUMO1/Ulp2, putative,cysteine peptidase, Clan CA, family C48, putative
Leishmania major LmjF.26.2070   SUMO1/Ulp2, putative,cysteine peptidase, Clan CA, family C48, putative
Leishmania mexicana LmxM.26.2070   SUMO1/Ulp2, putative,cysteine peptidase, Clan CA, family C48, putative
Trypanosoma brucei gambiense Tbg972.9.890   SUMO1/Ulp2, putative,cysteine peptidase, Clan CA, family C48, putative
Trypanosoma brucei Tb927.9.2220   SUMO1/Ulp2, putative
Trypanosoma congolense TcIL3000_0_10410   SUMO1/Ulp2, putative
Trypanosoma congolense TcIL3000_0_59400   SUMO1/Ulp2, putative
Trypanosoma cruzi TcCLB.505193.40   cysteine peptidase, Clan CA, family C48, putative
Trypanosoma cruzi TcCLB.503407.20   SUMO1/Ulp2, putative

Essentiality

LbrM.26.1990 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb09.160.0970 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (3 days) alsford
Tb09.160.0970 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb09.160.0970 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb09.160.0970 Trypanosoma brucei no significant loss or gain 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
  • 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.
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • 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.
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • 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.
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924

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 log in using your TDR Targets username and password and send them to us using the corresponding form in this page (only visible to registered users) or 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
Leishmania major SUMO1/Ulp2, putative,cysteine peptidase, Clan CA, family C48, putative 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.

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User comments

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Gene identifier LbrM.26.1990 (Leishmania braziliensis), SUMO1/Ulp2, putative,cysteine peptidase, Clan CA, family C48, putative
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