pI: 8.4061 |
Length (AA): 377 |
MW (Da): 42232 |
Paralog Number:
1
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 3
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 |
---|---|---|---|---|---|---|---|---|---|
178 | 371 | 4by7 (G) | 1 | 169 | 23.00 | 0 | 1 | 0.578189 | 0.89 |
178 | 373 | 2c35 (B) | 1 | 171 | 20.00 | 0 | 0.97 | 0.616494 | 0.53 |
178 | 377 | 3ayh (B) | 1 | 203 | 35.00 | 0 | 1 | 0.760404 | 0.5 |
200 | 301 | 4by7 (G) | 19 | 125 | 31.00 | 0.00000001 | 0.73 | 0.456457 | 1.27 |
288 | 370 | 1ve5 (C) | 59 | 182 | 37.00 | 0.99 | 0.13 | 0.275059 | 1.58 |
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 | ME49 Tachyzoite, ME49 Oocyst. | Gregory Fritz HM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | VEG Tachyzoite, ME49 merozoite, ME49 Bradyzoite. | Gregory Hehl AB Sibley/Greg |
Sibley/Greg | ToxoDB |
Fritz HM | Transcriptomic analysis of toxoplasma development reveals many novel functions and structures specific to sporozoites and oocysts. |
Gregory | ToxoDB |
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. |
Ortholog group members (OG5_127589)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G06790 | RNA polymerase Rpb7 N-terminal domain-containing protein |
Babesia bovis | BBOV_III006170 | conserved hypothetical protein |
Brugia malayi | Bm1_54365 | RNA polymerase Rpb7, N-terminal domain containing protein |
Candida albicans | CaO19.8073 | RNA polymerase 3 subunit |
Candida albicans | CaO19.443 | RNA polymerase 3 subunit |
Caenorhabditis elegans | CELE_ZK856.10 | Protein RPC-25 |
Cryptosporidium hominis | Chro.10225 | hypothetical protein |
Cryptosporidium parvum | cgd1_1960 | RPB7 subunit of the RNA polymerase III, OB fold |
Dictyostelium discoideum | DDB_G0273425 | RNA polymerase III subunit |
Dictyostelium discoideum | DDB_G0273523 | RNA polymerase III subunit |
Drosophila melanogaster | Dmel_CG7339 | CG7339 gene product from transcript CG7339-RB |
Echinococcus granulosus | EgrG_000678100 | DNA directed RNA polymerase III subunit |
Entamoeba histolytica | EHI_050830 | DNA-directed RNA polymerase III subunit, putative |
Echinococcus multilocularis | EmuJ_000678100 | DNA directed RNA polymerase III subunit |
Giardia lamblia | GL50803_3974 | DNA-directed RNA polymerase III subunit 22.9 kDa polypeptide |
Homo sapiens | ENSG00000100413 | polymerase (RNA) III (DNA directed) polypeptide H (22.9kD) |
Leishmania braziliensis | LbrM.09.1120 | DNA-directed RNA polymerase III subunit, putative |
Leishmania donovani | LdBPK_091120.1 | DNA-directed RNA polymerase III subunit, putative |
Leishmania infantum | LinJ.09.1120 | DNA-directed RNA polymerase III subunit, putative |
Leishmania major | LmjF.09.1060 | DNA-directed RNA polymerase III subunit, putative |
Leishmania mexicana | LmxM.09.1060 | DNA-directed RNA polymerase III subunit, putative |
Loa Loa (eye worm) | LOAG_05614 | RNA polymerase Rpb7 domain-containing protein |
Mus musculus | ENSMUSG00000022476 | polymerase (RNA) III (DNA directed) polypeptide H |
Neospora caninum | NCLIV_043800 | hypothetical protein |
Oryza sativa | 4343220 | Os07g0477000 |
Oryza sativa | 9266139 | Os08g0290900 |
Onchocerca volvulus | OVOC13497 |
|
Plasmodium berghei | PBANKA_0942200 | DNA-directed RNA polymerase III subunit RPC8, putative |
Plasmodium falciparum | PF3D7_1104700 | DNA-directed RNA polymerase III subunit RPC8, putative |
Plasmodium knowlesi | PKNH_0902300 | DNA-directed RNA polymerase III subunit RPC8, putative |
Plasmodium vivax | PVX_090915 | RNA polymerase Rpb7, N-terminal domain containing protein |
Plasmodium yoelii | PY02385 | RNA polymerase Rpb7, N-terminal domain, putative |
Saccharomyces cerevisiae | YKL144C | DNA-directed RNA polymerase III subunit RPC25 |
Schistosoma japonicum | Sjp_0212400 | ko:K03022 DNA-directed RNA polymerase III subunit C25, putative |
Schistosoma mansoni | Smp_174370 | DNA-directed rna polymerase III 25 kD polypeptide |
Schmidtea mediterranea | mk4.000039.00 | DNA-directed RNA polymerase III subunit RPC8 |
Trypanosoma brucei gambiense | Tbg972.11.14780 | RNA polymerase subunit, putative |
Trypanosoma brucei | Tb927.11.13240 | RNA polymerase subunit, putative |
Trypanosoma congolense | TcIL3000.11.13600 | RNA polymerase subunit, putative |
Trypanosoma cruzi | TcCLB.510359.320 | DNA-directed RNA polymerase III subunit, putative |
Trypanosoma cruzi | TcCLB.503819.20 | DNA-directed RNA polymerase III subunit, putative |
Toxoplasma gondii | TGME49_292300 | DNA-directed RNA polymerase III RPC8 |
Toxoplasma gondii | TGME49_292310 | RNA polymerase Rpb7, N-terminal domain-containing protein |
Theileria parva | TP02_0345 | hypothetical protein |
Trichomonas vaginalis | TVAG_200150 | DNA-directed RNA polymerase II, III, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.01.4820 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.4820 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.4820 | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb11.01.4820 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_ZK856.10 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_ZK856.10 | Caenorhabditis elegans | slow growth | wormbase |
CELE_ZK856.10 | Caenorhabditis elegans | sterile | wormbase |
YKL144C | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_292300 | Toxoplasma gondii | Essentiality uncertain | sidik |
TGME49_292310 this record | Toxoplasma gondii | Essentiality uncertain | sidik |
TGME49_292300 | Toxoplasma gondii | Probably essential | sidik |
TGME49_292310 this record | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
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.