pI: 10.2502 |
Length (AA): 302 |
MW (Da): 32684 |
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 8 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 |
---|---|---|---|---|---|---|---|---|---|
94 | 214 | 1x4b (A) | 3 | 115 | 25.00 | 0 | 1 | 0.52 | 0.53 |
124 | 244 | 1fxl (A) | 37 | 155 | 23.00 | 0 | 1 | 0.72 | -0.22 |
128 | 238 | 1cvj (A) | 13 | 123 | 28.00 | 0 | 1 | 0.76 | -0.36 |
128 | 202 | 1rk8 (A) | 75 | 149 | 21.00 | 0 | 1 | 0.75 | -2.04 |
57 | 214 | 2kn4 (A) | 6 | 158 | 21.00 | 0 | 1 | 0.783879 | -0.07 |
127 | 188 | 4a8x (A) | 162 | 224 | 29.00 | 0.99 | 1 | 0.724298 | -1.5 |
128 | 199 | 1p27 (B) | 75 | 146 | 25.00 | 0.076 | 1 | 0.785411 | -2.08 |
156 | 203 | 2dgw (A) | 323 | 368 | 48.00 | 0.012 | 0.91 | 0.68994 | -0.11 |
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 60-80% percentile | VEG Tachyzoite, ME49 Tachyzoite, ME49 merozoite, ME49 Oocyst, ME49 Bradyzoite. | Gregory Hehl AB Fritz HM Sibley/Greg |
Hehl AB | Asexual expansion of Toxoplasma gondii merozoites is distinct from tachyzoites and entails expression of non-overlapping gene families to attach, invade, and replicate within feline enterocytes. |
Gregory | ToxoDB |
Sibley/Greg | ToxoDB |
Fritz HM | Transcriptomic analysis of toxoplasma development reveals many novel functions and structures specific to sporozoites and oocysts. |
Ortholog group members (OG5_129161)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G04500 | RNA recognition motif-containing protein |
Babesia bovis | BBOV_II004860 | RNA recognition motif (RRM)-containing protein |
Brugia malayi | Bm1_40380 | RNA recognition motif. |
Candida albicans | CaO19.444 | RRM-containing orf similar to S. pombe SPAC22E12.02 |
Candida albicans | CaO19.8074 | RRM-containing orf similar to S. pombe SPAC22E12.02 |
Caenorhabditis elegans | CELE_Y54H5A.3 | Protein TAG-262 |
Cryptosporidium hominis | Chro.10128 | RNA recognition motif |
Cryptosporidium parvum | cgd1_1070 | RRM domain protein |
Dictyostelium discoideum | DDB_G0277875 | ssRNA-binding protein |
Drosophila melanogaster | Dmel_CG2931 | CG2931 gene product from transcript CG2931-RA |
Echinococcus granulosus | EgrG_000727000 | RNA binding protein 42 |
Entamoeba histolytica | EHI_194440 | RNA recognition motif domain containing protein |
Echinococcus multilocularis | EmuJ_000727000 | RNA binding protein 42 |
Homo sapiens | ENSG00000126254 | RNA binding motif protein 42 |
Loa Loa (eye worm) | LOAG_04208 | RNA recognition domain-containing protein |
Mus musculus | ENSMUSG00000036733 | RNA binding motif protein 42 |
Neospora caninum | NCLIV_021850 | RNA recognition motif-containing protein, putative |
Oryza sativa | 4346363 | Os08g0567200 |
Plasmodium berghei | PBANKA_1136300 | RNA-binding protein, putative |
Plasmodium falciparum | PF3D7_1360100 | RNA-binding protein, putative |
Plasmodium knowlesi | PKNH_1111200 | RNA-binding protein, putative |
Plasmodium vivax | PVX_114975 | RNA-binding protein, putative |
Plasmodium yoelii | PY00947 | RNA recognition motif, putative |
Toxoplasma gondii | TGME49_203080 | RNA recognition motif-containing protein |
Theileria parva | TP02_0264 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_004040 | rrm-containing protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_Y54H5A.3 | Caenorhabditis elegans | sterile | wormbase |
TGME49_203080 this record | Toxoplasma gondii | Probably essential | sidik |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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.