pI: 6.6061 |
Length (AA): 563 |
MW (Da): 64791 |
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:
There is 1 model calculated for this protein. More info on
this model, including the
model itself is available at:
Modbase
Target Beg | Target End | Template | Template Beg | Template End | Identity | Evalue | Model Score | MPQS | zDope |
---|---|---|---|---|---|---|---|---|---|
21 | 104 | 5dxh (A) | 422 | 527 | 29.00 | 0.81 | 0.18 | 0.456901 | -0.16 |
Help me make sense of these data.
A more detailed description of these scores is available at the Modbase Model Evaluation Help Pages, and in the papers referenced therein.
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_131728)
Species | Accession | Gene Product |
---|---|---|
Drosophila melanogaster | Dmel_CG17669 | CG17669 gene product from transcript CG17669-RA |
Echinococcus granulosus | EgrG_000087700 | wd40 repeat |
Echinococcus multilocularis | EmuJ_000087700 | wd40 repeat |
Homo sapiens | ENSG00000167646 | dynein, axonemal, assembly factor 3 |
Leishmania braziliensis | LbrM.27.0700 | hypothetical protein, conserved |
Leishmania infantum | LinJ.27.2600 | hypothetical protein, conserved |
Leishmania major | LmjF.27.0590 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.27.0590 | hypothetical protein, conserved |
Mus musculus | ENSMUSG00000055809 | dynein, axonemal assembly factor 3 |
Neospora caninum | NCLIV_035550 | GH22156, related |
Schistosoma japonicum | Sjp_0205480 | similar to UPF0470 protein CG17669, putative |
Schistosoma japonicum | Sjp_0315750 | expressed protein |
Schistosoma mansoni | Smp_168710 | hypothetical protein |
Trypanosoma brucei gambiense | Tbg972.11.1280 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.11.1210 | Domain of unknown function (DUF4470)/Domain of unknown function (DUF4471), putative |
Trypanosoma congolense | TcIL3000.11.1160 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.510799.9 | Domain of unknown function (DUF4470)/Domain of unknown function (DUF4471), putative |
Trypanosoma cruzi | TcCLB.511445.90 | Domain of unknown function (DUF4470)/Domain of unknown function (DUF4471), putative |
Toxoplasma gondii | TGME49_271315 | hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.47.0028 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb11.47.0028 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb11.47.0028 this record | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb11.47.0028 this record | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
TGME49_271315 | Toxoplasma gondii | Probably non-essential | sidik |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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 |
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) | increased (PATO:0000470) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | increased cell proliferation (significant 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.
1 literature reference was collected for this gene.