pI: 6.8342 |
Length (AA): 225 |
MW (Da): 26466 |
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 |
---|---|---|---|---|---|---|---|---|---|
125 | 182 | 1wi2 (A) | 42 | 99 | 17.00 | 0.000067 | 0.04 | 0.44 | -0.28 |
5 | 70 | 3whj (A) | 30 | 92 | 33.00 | 0.074 | 0.45 | 0.612433 | -1.01 |
110 | 222 | 4o06 (A) | 115 | 220 | 26.00 | 0.0000019 | 0.78 | 0.675422 | 0.37 |
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 | intra-erythrocytic - 0 hs, intra-erythrocytic - 8 hs, intra-erythrocytic - 16 hs, intra-erythrocytic - 24 hs, intra-erythrocytic - 32 hs, sporozoite, early ring, early trophozoite, late trophozoite. | Otto TD PlasmoDB |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intra-erythrocytic - 48 hs, early schizont, late ring, late schizont, Oocyst, Ring, Sporozoite. | Otto TD PlasmoDB Zanghi G |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 40 hs, Male Gametocyte. | Otto TD Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 0-20% percentile | Female Gametocyte. | Lasonder E |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
Otto TD | New insights into the blood-stage transcriptome of Plasmodium falciparum using RNA-Seq. |
Lasonder E | Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes. Molecular insight into sex-specific processes and translational repression. |
PlasmoDB | Data on upregulation of P. falciparum genes in different life cycle stages, combined from several microarray experiments available in PlasmoDB |
Ortholog group members (OG5_128010)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G57950 | 26S proteasome non-ATPase regulatory subunit 9 |
Babesia bovis | BBOV_II004550 | conserved hypothetical protein |
Brugia malayi | Bm1_11015 | Probable 26S proteasome non-ATPase regulatory subunit 9 |
Brugia malayi | Bm1_10245 | Probable 26S proteasome non-ATPase regulatory subunit 9 |
Brugia malayi | Bm1_23495 | Probable 26S proteasome non-ATPase regulatory subunit 9 |
Candida albicans | CaO19.9837 | similar to human proteosomal modulator subunit p27 |
Candida albicans | CaO19.1014 | similar to human proteosomal modulator subunit p27 |
Candida albicans | CaO19.2301 | similar to human proteosomal modulator subunit p27 |
Cryptosporidium hominis | Chro.50142 | proteasome (prosome, macropain) 26S subunit, non-ATPase, 9 |
Cryptosporidium parvum | cgd5_2360 | p27 like 26S proteasomal subunit with a PDZ domain |
Dictyostelium discoideum | DDB_G0275753 | 26S proteasome non-ATPase regulatory subunit 9 |
Drosophila melanogaster | Dmel_CG9588 | CG9588 gene product from transcript CG9588-RA |
Echinococcus granulosus | EgrG_000982600 | 26S proteasome non ATPase regulatory subunit |
Entamoeba histolytica | EHI_074770 | proteasome regulatory subunit, putative |
Echinococcus multilocularis | EmuJ_000982600 | 26S proteasome non ATPase regulatory subunit |
Giardia lamblia | GL50803_6647 | Hypothetical protein |
Homo sapiens | ENSG00000110801 | proteasome (prosome, macropain) 26S subunit, non-ATPase, 9 |
Leishmania braziliensis | LbrM.16.0290 | proteasome 26S non-ATPase subunit 9, putative |
Leishmania donovani | LdBPK_160300.1 | proteasome 26S non-ATPase subunit 9, putative |
Leishmania infantum | LinJ.16.0300 | proteasome 26S non-ATPase subunit 9, putative |
Leishmania major | LmjF.16.0290 | proteasome 26S non-ATPase subunit 9, putative |
Leishmania mexicana | LmxM.16.0290 | proteasome 26S non-ATPase subunit 9, putative |
Loa Loa (eye worm) | LOAG_04601 | hypothetical protein |
Mus musculus | ENSMUSG00000029440 | proteasome (prosome, macropain) 26S subunit, non-ATPase, 9 |
Neospora caninum | NCLIV_047130 | hypothetical protein |
Oryza sativa | 4347083 | Os09g0420600 |
Plasmodium berghei | PBANKA_0807400 | 26S proteasome non-ATPase regulatory subunit 9, putative |
Plasmodium falciparum | PF3D7_0317800 | 26S proteasome non-ATPase regulatory subunit 9, putative |
Plasmodium knowlesi | PKNH_0824000 | 26S proteasome non-ATPase regulatory subunit 9, putative |
Plasmodium vivax | PVX_095340 | 26S proteasome regulatory subunit p27, putative |
Plasmodium yoelii | PY02649 | PDZ domain, putative |
Saccharomyces cerevisiae | YIL007C | Nas2p |
Schistosoma japonicum | Sjp_0311100 | ko:K06693 26S proteasome non-ATPase regulatory subunit 9, putative |
Schistosoma japonicum | Sjp_0301990 | expressed protein |
Schistosoma mansoni | Smp_181380 | 26S proteasome non-ATPase regulatory subunit |
Schmidtea mediterranea | mk4.000039.02 | Probable 26S proteasome non-ATPase regulatory subunit 9 |
Trypanosoma brucei gambiense | Tbg972.8.5740 | proteasome 26S non-ATPase subunit 9, putative |
Trypanosoma brucei | Tb927.8.5740 | proteasome 26S non-ATPase subunit 9, putative |
Trypanosoma congolense | TcIL3000_8_5530 | proteasome 26S non-ATPase subunit 9, putative |
Trypanosoma cruzi | TcCLB.503473.4 | proteasome 26S non-ATPase subunit 9, putative |
Trypanosoma cruzi | TcCLB.503851.54 | proteasome 26S non-ATPase subunit 9, putative |
Trypanosoma cruzi | TcCLB.506743.150 | proteasome 26S non-ATPase subunit 9, putative |
Toxoplasma gondii | TGME49_225580 | proteasome (prosome, macropain) 26S subunit, non-ATPase, 9, putative |
Theileria parva | TP02_0299 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_468020 | 26S proteasome non-ATPase regulatory subunit, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.8.5740 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.8.5740 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.8.5740 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.8.5740 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
TGME49_225580 | Toxoplasma gondii | Probably essential | sidik |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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.
15 literature references were collected for this gene.