pI: 8.8387 |
Length (AA): 442 |
MW (Da): 47752 |
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 |
---|---|---|---|---|---|---|---|---|---|
2 | 436 | 4clq (A) | 7 | 361 | 29.00 | 0 | 1 | 1.06696 | 0.45 |
2 | 434 | 3pqv (A) | 6 | 356 | 30.00 | 0 | 1 | 1.11504 | 0.16 |
2 | 326 | 4clq (A) | 7 | 287 | 36.00 | 0 | 1 | 1.03159 | 0.06 |
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 | VEG Tachyzoite, ME49 merozoite. | Gregory Hehl AB |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | ME49 Tachyzoite, ME49 Oocyst, ME49 Bradyzoite. | Gregory Fritz HM Sibley/Greg |
Sibley/Greg | ToxoDB |
Fritz HM | Transcriptomic analysis of toxoplasma development reveals many novel functions and structures specific to sporozoites and oocysts. |
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. |
Gregory | ToxoDB |
Ortholog group members (OG5_127812)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G22100 | RNA 3'-terminal phosphate cyclase-like protein |
Babesia bovis | BBOV_IV007230 | RNA 3'-terminal phosphate cyclase, putative |
Brugia malayi | Bm1_10025 | Probable RNA 3'-terminal phosphate cyclase-like protein |
Candida albicans | CaO19.9442 | RNA 3'-terminal phosphate cyclase similar to S. cerevisiae RCL1 involved in rRNA processing |
Candida albicans | CaO19.1886 | RNA 3'-terminal phosphate cyclase similar to S. cerevisiae RCL1 involved in rRNA processing |
Caenorhabditis elegans | CELE_ZK1127.5 | Protein ZK1127.5 |
Cryptosporidium hominis | Chro.80423 | RNA 3-Terminal Phosphate Cyclase-like protein |
Cryptosporidium parvum | cgd8_3660 | RNA 3-Terminal Phosphate Cyclase-like protein |
Dictyostelium discoideum | DDB_G0282803 | RNA 3'-terminal phosphate cyclase family protein |
Drosophila melanogaster | Dmel_CG11130 | CG11130 gene product from transcript CG11130-RA |
Echinococcus granulosus | EgrG_000646400 | RNA 3' terminal phosphate cyclase protein |
Entamoeba histolytica | EHI_115370 | RNA 3-terminal phosphate cyclase, putative |
Echinococcus multilocularis | EmuJ_000646400 | RNA 3' terminal phosphate cyclase protein |
Giardia lamblia | GL50803_6590 | RNA 3-terminal phosphate cyclase-like protein |
Homo sapiens | ENSG00000120158 | RNA terminal phosphate cyclase-like 1 |
Leishmania braziliensis | LbrM.34.1610 | RNA 3-terminal phosphate cyclase, putative |
Leishmania donovani | LdBPK_351700.1 | RNA re-capping enzyme, cytoplasmic, putative |
Leishmania infantum | LinJ.35.1700 | RNA 3-terminal phosphate cyclase, putative |
Leishmania major | LmjF.35.1700 | RNA 3-terminal phosphate cyclase, putative |
Leishmania mexicana | LmxM.34.1700 | RNA 3-terminal phosphate cyclase, putative |
Loa Loa (eye worm) | LOAG_02169 | hypothetical protein |
Mus musculus | ENSMUSG00000024785 | RNA terminal phosphate cyclase-like 1 |
Neospora caninum | NCLIV_032370 | rna 3 terminal phosphate cyclase, putative |
Oryza sativa | 4334688 | Os03g0833700 |
Plasmodium berghei | PBANKA_1334200 | RNA 3'-terminal phosphate cyclase-like protein, putative |
Plasmodium falciparum | PF3D7_1471000 | RNA 3'-terminal phosphate cyclase-like protein, putative |
Plasmodium knowlesi | PKNH_1210000 | RNA 3'-terminal phosphate cyclase-like protein, putative |
Plasmodium vivax | PVX_116920 | RNA 3'-terminal phosphate cyclase-like protein, putative |
Plasmodium yoelii | PY05891 | probable RNA 3'-terminal phosphate cyclase-like protein |
Saccharomyces cerevisiae | YOL010W | Rcl1p |
Schistosoma japonicum | Sjp_0015290 | ko:K01974 RNA-3'-phosphate cyclase [EC6.5.1.4], putative |
Schistosoma mansoni | Smp_102450 | rna 3' terminal phosphate cyclase |
Schmidtea mediterranea | mk4.000449.00 | Putative rna 3' terminal phosphate cyclase |
Trypanosoma brucei gambiense | Tbg972.9.9050 | RNA 3-terminal phosphate cyclase-like protein, putative |
Trypanosoma brucei | Tb927.9.14410 | RNA re-capping enzyme, cytoplasmic |
Trypanosoma congolense | TcIL3000_9_6200 | RNA re-capping enzyme, cytoplasmic, putative |
Trypanosoma cruzi | TcCLB.510761.30 | RNA re-capping enzyme, cytoplasmic, putative |
Toxoplasma gondii | TGME49_232390 | 18S rRNA biogenesis protein RCL1 protein |
Theileria parva | TP03_0231 | RNA 3'-terminal phosphate cyclase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.4870 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.4870 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.4870 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb09.211.4870 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_ZK1127.5 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_ZK1127.5 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_ZK1127.5 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_ZK1127.5 | Caenorhabditis elegans | slow growth | wormbase |
CELE_ZK1127.5 | Caenorhabditis elegans | sterile | wormbase |
YOL010W | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_232390 this record | 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.
Target | Type | Source | Notes |
---|---|---|---|
TGME49_232390 | cloned gene | BRENDA | A gene with this EC number or name or sequence has been cloned from Toxoplasma gondii ( 1 ) |