pI: 11.1318 |
Length (AA): 192 |
MW (Da): 22436 |
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 |
---|---|---|---|---|---|---|---|---|---|
7 | 184 | 4kzy (J) | 8 | 185 | 82.00 | 0 | 1 | 1.83868 | 0 |
26 | 158 | 5wxm (A) | 28 | 160 | 25.00 | 0 | 1 | 1.10001 | -0.78 |
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:
Ortholog group members (OG5_126983)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G39850 | 40S ribosomal protein S9-2 |
Arabidopsis thaliana | AT5G15200 | 40S ribosomal protein S9-1 |
Babesia bovis | BBOV_II002670 | 40S ribosomal subunit protein S9, putative |
Brugia malayi | Bm1_15065 | 40S ribosomal protein S9 |
Candida albicans | CaO19.8459 | potential cytosolic ribosomal protein similar to S. cerevisiae RPS9B (YBR189W) and RPS9A (YPL081W) small subunit protein S9 (E. |
Caenorhabditis elegans | CELE_F40F8.10 | Protein RPS-9 |
Cryptosporidium hominis | Chro.80213 | 40S ribosomal subunit protein S9 |
Cryptosporidium parvum | cgd8_1840 | 40S ribosomal subunit protein S9, putative |
Dictyostelium discoideum | DDB_G0289877 | 40S ribosomal protein S9 |
Drosophila melanogaster | Dmel_CG3395 | Ribosomal protein S9 |
Echinococcus granulosus | EgrG_000430500 | 40S ribosomal protein S9 |
Entamoeba histolytica | EHI_179000 | 40S ribosomal protein S9 |
Entamoeba histolytica | EHI_125780 | 40S ribosomal protein S9 |
Entamoeba histolytica | EHI_152610 | 40S ribosomal protein S9 |
Entamoeba histolytica | EHI_152080 | 40S ribosomal protein S9 |
Echinococcus multilocularis | EmuJ_000430500 | 40S ribosomal protein S9 |
Giardia lamblia | GL50803_4547 | Ribosomal protein S9 |
Homo sapiens | ENSG00000170889 | ribosomal protein S9 |
Leishmania braziliensis | LbrM.35.1380 | 40S ribosomal protein S9, putative |
Leishmania braziliensis | LbrM.07.0750 | 40S ribosomal protein S9, putative |
Leishmania donovani | LdBPK_361310.1 | 40S ribosomal protein S9, putative |
Leishmania infantum | LinJ.36.1310 | 40S ribosomal protein S9, putative |
Leishmania infantum | LinJ.07.0760 | 40S ribosomal protein S9, putative |
Leishmania major | LmjF.36.1250 | 40S ribosomal protein S9, putative |
Leishmania major | LmjF.07.0680 | 40S ribosomal protein S9, putative |
Leishmania mexicana | LmxM.36.1250 | 40S ribosomal protein S9, putative |
Loa Loa (eye worm) | LOAG_12353 | 40S ribosomal protein S9 |
Mus musculus | ENSMUSG00000006333 | ribosomal protein S9 |
Neospora caninum | NCLIV_064440 | hypothetical protein |
Oryza sativa | 9268088 | Os11g0602501 |
Oryza sativa | 4350869 | Os11g0602600 |
Oryza sativa | 4331662 | Os03g0154700 |
Plasmodium berghei | PBANKA_1234800 | 40S ribosomal protein S9, putative |
Plasmodium falciparum | PF3D7_0520000 | 40S ribosomal protein S9, putative |
Plasmodium knowlesi | PKNH_1013100 | 40S ribosomal protein S9, putative |
Plasmodium vivax | PVX_080245 | 40S ribosomal protein S9, putative |
Plasmodium yoelii | PY02191 | ribosomal protein S4, putative |
Saccharomyces cerevisiae | YBR189W | ribosomal 40S subunit protein S9B |
Saccharomyces cerevisiae | YPL081W | ribosomal 40S subunit protein S9A |
Schistosoma japonicum | Sjp_0304980 | ko:K02997 small subunit ribosomal protein S9e, putative |
Schistosoma mansoni | Smp_180000 | 40S ribosomal protein S9 |
Schmidtea mediterranea | mk4.000094.07 | 40S ribosomal protein S9 |
Trypanosoma brucei gambiense | Tbg972.8.670 | 40S ribosomal protein S9, putative |
Trypanosoma brucei gambiense | Tbg972.10.6820 | 40S ribosomal protein S9, putative |
Trypanosoma brucei | Tb927.10.5610 | 40S ribosomal protein S9, putative |
Trypanosoma brucei | Tb927.8.1110 | 40S ribosomal protein S9, putative |
Trypanosoma congolense | TcIL3000_8_730 | 40S ribosomal protein S9, putative |
Trypanosoma cruzi | TcCLB.506401.120 | 40S ribosomal protein S9, putative |
Trypanosoma cruzi | TcCLB.508543.30 | 40S ribosomal protein S9, putative |
Trypanosoma cruzi | TcCLB.504163.30 | 40S ribosomal protein S9, putative |
Toxoplasma gondii | TGME49_248480 | ribosomal protein RPS9 |
Theileria parva | TP04_0309 | 40S ribosomal protein S9, putative |
Trichomonas vaginalis | TVAG_259540 | 40S ribosomal protein S9, putative |
Trichomonas vaginalis | TVAG_204300 | 40S ribosomal protein S9, putative |
Trichomonas vaginalis | TVAG_204310 | 30S 40S ribosomal protein, putative |
Trichomonas vaginalis | TVAG_173990 | 30S 40S ribosomal protein, putative |
Trichomonas vaginalis | TVAG_010560 | 30S 40S ribosomal protein, putative |
Trichomonas vaginalis | TVAG_495360 | 30S 40S ribosomal protein, putative |
Trichomonas vaginalis | TVAG_041350 | 30S 40S ribosomal protein, putative |
Trichomonas vaginalis | TVAG_474000 | 30S ribosomal protein S4p, putative |
Trichomonas vaginalis | TVAG_139990 | 30S ribosomal protein S4p, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.8.1110 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.8.1110 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.8.1110 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.8.1110 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
Tb927.10.5610 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.5610 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.5610 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.10.5610 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F40F8.10 | Caenorhabditis elegans | adult lethal | wormbase |
CELE_F40F8.10 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_F40F8.10 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_F40F8.10 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_F40F8.10 | Caenorhabditis elegans | slow growth | wormbase |
CELE_F40F8.10 | Caenorhabditis elegans | sterile | wormbase |
TGME49_248480 | 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 |
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 |
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 |
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.