pI: 8.0354 |
Length (AA): 761 |
MW (Da): 85617 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: | Predicted trans-membrane segments: 2
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 |
---|---|---|---|
Mid 40-60% 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_128373)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G62240 | RING/U-box domain-containing protein |
Arabidopsis thaliana | AT2G47090 | zinc ion binding/nucleic acid binding |
Brugia malayi | Bm1_01350 | RE33889p |
Candida albicans | CaO19.10953 | potential zinc ring finger protein similar to S. cerevisiae YDR266C |
Candida albicans | CaO19.3449 | potential zinc ring finger protein similar to S. cerevisiae YDR266C |
Caenorhabditis elegans | CELE_C52E12.1 | Protein C52E12.1 |
Dictyostelium discoideum | DDB_G0275581 | hypothetical protein |
Drosophila melanogaster | Dmel_CG11414 | CG11414 gene product from transcript CG11414-RA |
Entamoeba histolytica | EHI_020100 | hypothetical protein |
Giardia lamblia | GL50803_4343 | Zinc finger domain |
Homo sapiens | ENSG00000167962 | zinc finger protein 598 |
Leishmania braziliensis | LbrM.30.1350 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_301290.1 | Zinc finger, C3HC4 type (RING finger), putative |
Leishmania infantum | LinJ.30.1290 | hypothetical protein, conserved |
Leishmania major | LmjF.30.1230 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.29.1230 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_15469 | hypothetical protein |
Mus musculus | ENSMUSG00000041130 | zinc finger protein 598 |
Oryza sativa | 4327105 | Os01g0251200 |
Oryza sativa | 4338285 | Os05g0279400 |
Onchocerca volvulus | OVOC10144 | Zinc finger protein 598 homolog |
Saccharomyces cerevisiae | YDR266C | Hel2p |
Trypanosoma brucei gambiense | Tbg972.6.2480 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.6.2710 | hypothetical protein, conserved |
Trypanosoma congolense | TcIL3000_6_2160 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.509059.20 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_326460 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_388390 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_403790 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_045380 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_118120 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_021850 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.6.2710 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.6.2710 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.6.2710 this record | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.6.2710 this record | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
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 |
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 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 6 days). | 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 procyclic forms . | 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 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.
1 literature reference was collected for this gene.