pI: 11.0285 |
Length (AA): 260 |
MW (Da): 29766 |
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 3 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 |
---|---|---|---|---|---|---|---|---|---|
5 | 80 | 2nca (A) | 38 | 110 | 34.00 | 0.19 | 0.02 | 0.709008 | -1.19 |
7 | 167 | 4uos (A) | 20 | 173 | 25.00 | 0.062 | 0.86 | 1.05953 | -1.61 |
167 | 260 | 2mvf (A) | 168 | 261 | 72.00 | 0 | 1 | 1.16124 | 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 | metacyclic. | Fernandes MC |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | amastigotes. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_128061)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G06360 | ribosomal protein S8e family protein |
Babesia bovis | BBOV_III000260 | ribosomal protein Se8, putative |
Brugia malayi | Bm1_51110 | TGF beta-inducible nuclear protein 1 |
Candida albicans | CaO19.7424 | similar to S. cerevisiae NSA2 (YER126C) Nop7 Associated Protein 2 involved in ribosomal large subunit maturation |
Candida albicans | CaO19.7398 | similar to C terminus of S. cerevisiae NSA2 (YER126C) involved in ribosomal large subunit maturation |
Caenorhabditis elegans | CELE_W09C5.1 | Protein W09C5.1 |
Cryptosporidium hominis | Chro.30461 | RIKEN cDNA 5730427N09 gene |
Cryptosporidium parvum | cgd3_4100 | conserved protein, COG SSU ribosomal protein S8E |
Dictyostelium discoideum | DDB_G0290031 | hypothetical protein |
Drosophila melanogaster | Dmel_CG5277 | Intronic Protein 259 |
Echinococcus granulosus | EgrG_000478000 | TGF beta inducible nuclear protein 1 |
Entamoeba histolytica | EHI_099760 | hypothetical protein, conserved |
Echinococcus multilocularis | EmuJ_000478000 | TGF beta inducible nuclear protein 1 |
Giardia lamblia | GL50803_11755 | Hypothetical protein |
Homo sapiens | ENSG00000164346 | NSA2 ribosome biogenesis homolog (S. cerevisiae) |
Leishmania braziliensis | LbrM.35.6730 | 40S ribosomal protein S8, putative |
Leishmania donovani | LdBPK_366680.1 | 40S ribosomal protein S8, putative |
Leishmania infantum | LinJ.36.6680 | 40S ribosomal protein S8, putative |
Leishmania major | LmjF.36.6400 | 40S ribosomal protein S8, putative |
Leishmania mexicana | LmxM.36.6400 | 40S ribosomal protein S8, putative |
Loa Loa (eye worm) | LOAG_09193 | TGF beta-inducible nuclear protein 1 |
Mus musculus | ENSMUSG00000060739 | NSA2 ribosome biogenesis homolog (S. cerevisiae) |
Mus musculus | 101055813 | predicted gene, 29726 |
Mus musculus | 102642514 | ribosome biogenesis protein NSA2 homolog |
Neospora caninum | NCLIV_017790 | TGF-beta-inducible nuclear protein 1, putative |
Oryza sativa | 4344253 | Os07g0673100 |
Onchocerca volvulus | OVOC11911 | Ribosome biogenesis protein NSA2 homolog |
Plasmodium berghei | PBANKA_0805100 | ribosomal protein S8e, putative |
Plasmodium falciparum | PF3D7_0707900 | ribosomal protein S8e, putative |
Plasmodium knowlesi | PKNH_0106400 | ribosomal protein S8e, putative |
Plasmodium vivax | PVX_087920 | ribosomal protein S8e, putative |
Plasmodium yoelii | PY00137 | hairy cell leukemia protein 1 |
Saccharomyces cerevisiae | YER126C | Nsa2p |
Schistosoma japonicum | Sjp_0211090 | Ribosome biogenesis protein NSA2 homolog, putative |
Schistosoma japonicum | Sjp_0133960 | Ribosome biogenesis protein NSA2 homolog, putative |
Schistosoma mansoni | Smp_054120 | Ribosome biogenesis protein NSA2 homologue |
Schmidtea mediterranea | mk4.006414.02 | Ribosome biogenesis protein NSA2 homologue |
Trypanosoma brucei gambiense | Tbg972.10.9450 | 40S ribosomal protein S8, putative |
Trypanosoma brucei | Tb927.10.7710 | 40S ribosomal protein S8, putative |
Trypanosoma cruzi | TcCLB.506249.60 | 40S ribosomal protein S8, putative |
Trypanosoma cruzi | TcCLB.508231.200 | 40S ribosomal protein S8, putative |
Toxoplasma gondii | TGME49_242800 | ribosome biogenesis protein NSA2, putative |
Theileria parva | TP03_0821 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_192990 | TGF-beta-inducible nuclear protein, putative |
Trichomonas vaginalis | TVAG_247360 | TGF-beta-inducible nuclear protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.7710 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.7710 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.7710 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.10.7710 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_W09C5.1 | Caenorhabditis elegans | slow growth | wormbase |
YER126C | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0805100 | Plasmodium berghei | Slow | plasmo |
TGME49_242800 | Toxoplasma gondii | Probably essential | sidik |
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 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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 |
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.