pI: 5.7259 |
Length (AA): 479 |
MW (Da): 55311 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: | Predicted trans-membrane segments: 0
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
Modbase 3D models:
PDB Structures:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 80-100% percentile | Procyclic, Bloodstream Form. | Siegel TN |
Siegel TN | Genome-wide analysis of mRNA abundance in two life-cycle stages of Trypanosoma brucei and identification of splicing and polyadenylation sites. |
Ortholog group members (OG5_129983)
Species | Accession | Gene Product |
---|---|---|
Babesia bovis | BBOV_I001870 | conserved hypothetical protein |
Candida albicans | CaO19.4560 | implicated in secretion and nuclear segregation |
Candida albicans | CaO19.12029 | implicated in secretion and nuclear segregation |
Cryptosporidium hominis | Chro.20287 | similar to yeast nuclear segregation protein Bfr1 involved in mitosis and vesicular transport |
Cryptosporidium parvum | cgd2_2700 | Brf1p like coiled coil protein |
Dictyostelium discoideum | DDB_G0268236 | hypothetical protein |
Leishmania braziliensis | LbrM.32.0030 | hypothetical protein, conserved |
Leishmania braziliensis | LbrM.32.0060 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_320020.1 | nuclear segregation protein, putative |
Leishmania infantum | LinJ.32.0020 | hypothetical protein, conserved |
Leishmania major | LmjF.32.0020 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.31.0020 | hypothetical protein, conserved |
Neospora caninum | NCLIV_032430 | hypothetical protein, conserved |
Plasmodium berghei | PBANKA_1116800 | conserved Plasmodium protein, unknown function |
Plasmodium falciparum | PF3D7_0617200 | conserved Plasmodium protein, unknown function |
Plasmodium knowlesi | PKNH_1132800 | conserved Plasmodium protein, unknown function |
Plasmodium vivax | PVX_114000 | hypothetical protein, conserved |
Plasmodium yoelii | PY05078 | hypothetical protein |
Saccharomyces cerevisiae | YOR198C | Bfr1p |
Trypanosoma brucei gambiense | Tbg972.10.16530 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.10.14150 | nuclear segregation protein, putative |
Trypanosoma congolense | TcIL3000_10_12030 | nuclear segregation protein, putative |
Trypanosoma cruzi | TcCLB.506525.10 | nuclear segregation protein, putative |
Trypanosoma cruzi | TcCLB.511283.10 | nuclear segregation protein, putative |
Toxoplasma gondii | TGME49_232440 | Brf1p family coiled coil protein |
Theileria parva | TP03_0147 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_333110 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.14150 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.14150 this record | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.14150 this record | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.14150 this record | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_1116800 | Plasmodium berghei | Essential | plasmo |
TGME49_232440 | Toxoplasma gondii | Probably non-essential | sidik |
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 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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 |
Affected Entity | Phenotypic quality | Occurs in | Occurs at | Evidence | Observed in | Drugs/Inhibitors |
---|---|---|---|---|---|---|
cell proliferation (GO:0008283) | normal (PATO:0000461) | bloodstream stage trypomastigotes (PLO:0027) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | normal cell proliferation (no significant loss or gain of fitness) in bloodstream forms (stage 3 days). | References: | 21363968 | |
cell proliferation (GO:0008283) | decreased (PATO:0000468) | bloodstream stage trypomastigotes (PLO:0027) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | decreased cell proliferation (significant loss of fitness) in bloodstream forms (stage 6 days). | References: | 21363968 | |
cell proliferation (GO:0008283) | normal (PATO:0000461) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | normal cell proliferation (no significant loss or gain of fitness) in procyclic forms . | References: | 21363968 | |
cell proliferation (GO:0008283) | decreased (PATO:0000468) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | decreased cell proliferation (significant loss of fitness) in differentiation of procyclic to bloodstream forms . | References: | 21363968 |
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.
Druggability index (range: 0 to 1): 0.1
1 literature reference was collected for this gene.