pI: 8.1029 |
Length (AA): 906 |
MW (Da): 106856 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: N | 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 are 2 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 |
---|---|---|---|---|---|---|---|---|---|
50 | 904 | 5xwp (A) | 48 | 921 | 24.00 | 0.00016 | 1 | 0.921709 | 1.48 |
134 | 312 | 4uos (A) | 5 | 179 | 30.00 | 0.18 | 0.97 | 0.604572 | -1.24 |
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 | Female gametocyte. | Yeoh LM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | Male gametocyte. | Yeoh LM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | Gametocyte, 22 hs Schizont, Erthyrocytic stages. | Otto TD Yeoh LM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 0-20% percentile | Ookinete, 4 hs Ring, 16 hs Trophozoite. | Otto TD |
Yeoh LM | Comparative transcriptomics of female and male gametocytes in Plasmodium berghei and the evolution of sex in alveolates. |
Otto TD | A comprehensive evaluation of rodent malaria parasite genomes and gene expression. |
Ortholog group members (OG5_129277)
Species | Accession | Gene Product |
---|---|---|
Dictyostelium discoideum | DDB_G0287291 | actin binding protein D |
Drosophila melanogaster | Dmel_CG6059 | CG6059 gene product from transcript CG6059-RA |
Drosophila melanogaster | Dmel_CG5882 | CG5882 gene product from transcript CG5882-RA |
Drosophila melanogaster | Dmel_CG40446 | Occludin-Related Y |
Echinococcus granulosus | EgrG_000954700 | coiled coil domain containing protein 147 |
Echinococcus multilocularis | EmuJ_000954700 | coiled coil domain containing protein 147 |
Giardia lamblia | GL50803_3409 | Coiled-coil protein |
Homo sapiens | ENSG00000120051 | cilia and flagella associated protein 58 |
Leishmania braziliensis | LbrM.35.5270 | hypothetical protein, conserved |
Leishmania braziliensis | LbrM.03.0310 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_030300.1 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_365250.1 | hypothetical protein, conserved |
Leishmania infantum | LinJ.36.5250 | hypothetical protein, conserved |
Leishmania infantum | LinJ.03.0300 | hypothetical protein, conserved |
Leishmania major | LmjF.36.5020 | hypothetical protein, conserved |
Leishmania major | LmjF.03.0320 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.03.0320 | hypothetical protein, conserved |
Mus musculus | ENSMUSG00000046585 | cilia and flagella associated protein 58 |
Neospora caninum | NCLIV_023900 | hypothetical protein |
Plasmodium berghei | PBANKA_1125300 | conserved Plasmodium protein, unknown function |
Plasmodium falciparum | PF3D7_0626500 | conserved Plasmodium protein, unknown function |
Plasmodium knowlesi | PKNH_1123300 | conserved Plasmodium protein, unknown function |
Plasmodium vivax | PVX_114430 | hypothetical protein, conserved |
Plasmodium yoelii | PY07530 | hypothetical protein |
Schistosoma japonicum | Sjp_0111790 | IPR010978,tRNA-binding arm,domain-containing |
Schistosoma japonicum | Sjp_0045650 | Conserved hypothetical protein |
Schistosoma mansoni | Smp_156370 | hypothetical protein |
Schmidtea mediterranea | mk4.002732.02 | |
Trypanosoma brucei gambiense | Tbg972.10.4180 | hypothetical protein, conserved |
Trypanosoma brucei gambiense | Tbg972.11.12210 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.10.3310 | Component of motile flagella 76b |
Trypanosoma brucei | Tb927.11.10900 | Component of motile flagella 9 |
Trypanosoma congolense | TcIL3000.11.11580 | MENG |
Trypanosoma congolense | TcIL3000_10_2750 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.510941.20 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.508179.30 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.510423.70 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.510425.10 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.509825.20 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_470210 | RAB6-interacting protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.01.2670 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.2670 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.2670 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb11.01.2670 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
Tb927.10.3310 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.3310 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.3310 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.3310 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_1125300 this record | Plasmodium berghei | Dispensable | plasmo |
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 |
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 |
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 |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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.