pI: 10.6175 |
Length (AA): 455 |
MW (Da): 50435 |
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 5 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 |
---|---|---|---|---|---|---|---|---|---|
150 | 349 | 1fje (B) | 3 | 173 | 29.00 | 0.0000026 | 1 | 0.52 | 0.97 |
272 | 330 | 1x4e (A) | 8 | 64 | 28.00 | 0.00000038 | 0.72 | 0.57 | -1.34 |
162 | 362 | 4n0t (A) | 42 | 211 | 26.00 | 0.13 | 1 | 0.468258 | 0.33 |
267 | 344 | 3ucg (A) | 169 | 244 | 33.00 | 0 | 1 | 0.722529 | -1.7 |
271 | 330 | 2mzr (A) | 162 | 217 | 43.00 | 0.00091 | 0.97 | 0.623368 | -0.45 |
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 |
---|---|---|---|
Mid 40-60% percentile | metacyclic. | Fernandes MC |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | amastigotes. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_128354)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G46840 | RNA recognition motif-containing protein |
Babesia bovis | BBOV_III009290 | RNA recognition motif domain containing protein |
Brugia malayi | Bm1_37250 | RNA recognition motif. |
Candida albicans | CaO19.8429 | nucleolar protein |
Candida albicans | CaO19.809 | nucleolar protein |
Caenorhabditis elegans | CELE_F11A10.7 | Protein F11A10.7 |
Cryptosporidium hominis | Chro.30395 | hypothetical protein |
Cryptosporidium parvum | cgd3_3500 | Nop12p nucleolar protein, RRM domain |
Dictyostelium discoideum | DDB_G0289941 | hypothetical protein |
Drosophila melanogaster | Dmel_CG12288 | CG12288 gene product from transcript CG12288-RA |
Echinococcus granulosus | EgrG_000762400 | RNA binding protein 34 |
Entamoeba histolytica | EHI_137710 | RNA recognition motif domain containing protein |
Echinococcus multilocularis | EmuJ_000762400 | RNA binding protein 34 |
Homo sapiens | ENSG00000188739 | RNA binding motif protein 34 |
Leishmania braziliensis | LbrM.34.2480 | RNA binding protein, putative |
Leishmania donovani | LdBPK_352590.1 | Double RNA binding domain protein 9 |
Leishmania infantum | LinJ.35.2590 | RNA binding protein, putative |
Leishmania major | LmjF.35.2550 | RNA binding protein, putative |
Leishmania mexicana | LmxM.34.2550 | RNA binding protein, putative |
Loa Loa (eye worm) | LOAG_04878 | RNA recognition domain-containing protein |
Mus musculus | ENSMUSG00000033931 | RNA binding motif protein 34 |
Neospora caninum | NCLIV_028890 | hypothetical protein |
Oryza sativa | 4334825 | Os03g0854300 |
Plasmodium berghei | PBANKA_0504200 | RNA-binding protein 34, putative |
Plasmodium falciparum | PF3D7_1020000 | RNA-binding protein 34, putative |
Plasmodium knowlesi | PKNH_0604200 | RNA-binding protein 34, putative |
Plasmodium vivax | PVX_001865 | RNA-binding protein, putative |
Plasmodium yoelii | PY00605 | KED |
Saccharomyces cerevisiae | YOL041C | Nop12p |
Schistosoma japonicum | Sjp_0024100 | RNA-binding protein 34, putative |
Schistosoma mansoni | Smp_130190 | RNA binding protein |
Schmidtea mediterranea | mk4.000024.16 | RNA-binding protein 34 |
Trypanosoma brucei gambiense | Tbg972.9.8260 | RNA-binding protein, putative,DRBD9 |
Trypanosoma brucei | Tb927.9.13280 | Double RNA binding domain protein 9 |
Trypanosoma congolense | TcIL3000_9_5600 | Double RNA binding domain protein 9 |
Trypanosoma cruzi | TcCLB.510657.160 | Double RNA binding domain protein 9 |
Trypanosoma cruzi | TcCLB.510747.80 | Double RNA binding domain protein 9 |
Toxoplasma gondii | TGME49_283882 | hypothetical protein |
Theileria parva | TP04_0838 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_108440 | ribonucleoprotein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.4120 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.4120 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.4120 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb09.211.4120 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F11A10.7 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_F11A10.7 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_F11A10.7 | Caenorhabditis elegans | sterile | wormbase |
TGME49_283882 | Toxoplasma gondii | Probably essential | sidik |
TGME49_283882 | Toxoplasma gondii | Essentiality uncertain | sidik |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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.
Type | Source | Notes |
---|---|---|
soluble recombinant protein | Structural Genomics for Pathogenic Protozoa (SGPP) | Lmaj00499; Recombinant protein: full-length; Source: L major; hypothetical protein, conserved ; |