pI: 5.9263 |
Length (AA): 580 |
MW (Da): 67082 |
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 4 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 |
---|---|---|---|---|---|---|---|---|---|
40 | 161 | 3ljc (A) | 117 | 238 | 9.00 | 0.89 | 0 | 0.378145 | -0.97 |
191 | 568 | 5vqa (A) | 45 | 422 | 34.00 | 0 | 1 | 0.802524 | 0.93 |
242 | 543 | 4xgu (A) | 102 | 410 | 41.00 | 0 | 1 | 0.87609 | 0.17 |
245 | 567 | 5vqa (A) | 107 | 421 | 48.00 | 0 | 1 | 0.990297 | -0.11 |
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 | Male gametocyte. | Yeoh LM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | Gametocyte, 22 hs Schizont. | Otto TD |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | Ookinete. | Otto TD |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | Erthyrocytic stages, Female gametocyte. | Yeoh LM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 0-20% percentile | 4 hs Ring, 16 hs Trophozoite. | Otto TD |
Otto TD | A comprehensive evaluation of rodent malaria parasite genomes and gene expression. |
Yeoh LM | Comparative transcriptomics of female and male gametocytes in Plasmodium berghei and the evolution of sex in alveolates. |
Ortholog group members (OG5_128995)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G24710 | P-loop containing nucleoside triphosphate hydrolases superfamily protein |
Brugia malayi | Bm1_18485 | ATPase, AAA family protein |
Caenorhabditis elegans | CELE_F10B5.5 | Protein PCH-2 |
Cryptosporidium hominis | Chro.60073 | thyroid receptor interacting protein 13 (TRIP-13) |
Cryptosporidium hominis | Chro.60074 | protein-related binding protein |
Cryptosporidium parvum | cgd6_550 | Pch2p like AAA ATpase |
Dictyostelium discoideum | DDB_G0279111 | AAA ATPase domain-containing protein |
Drosophila melanogaster | Dmel_CG31453 | CG31453 gene product from transcript CG31453-RB |
Echinococcus granulosus | EgrG_000823600 | pachytene checkpoint protein 2 |
Echinococcus multilocularis | EmuJ_000823600 | pachytene checkpoint protein 2 |
Giardia lamblia | GL50803_8524 | Transitional endoplasmic reticulum ATPase |
Homo sapiens | ENSG00000071539 | thyroid hormone receptor interactor 13 |
Leishmania braziliensis | LbrM.28.1960 | ATPase-like protein |
Leishmania donovani | LdBPK_281910.1 | ATPase-like protein |
Leishmania infantum | LinJ.28.1910 | ATPase-like protein |
Leishmania major | LmjF.28.1790 | ATPase-like protein |
Leishmania mexicana | LmxM.28.1790 | ATPase-like protein |
Loa Loa (eye worm) | LOAG_11130 | hypothetical protein |
Mus musculus | ENSMUSG00000021569 | thyroid hormone receptor interactor 13 |
Neospora caninum | NCLIV_040990 | Cell division cycle protein, related |
Oryza sativa | 4336167 | Os04g0479000 |
Plasmodium berghei | PBANKA_0909500 | AAA family ATPase, putative |
Plasmodium falciparum | PF3D7_1139500 | AAA family ATPase, putative, unspecified product |
Plasmodium knowlesi | PKNH_0937400 | AAA family ATPase, putative |
Plasmodium vivax | PVX_092575 | AAA family ATPase, putative |
Plasmodium yoelii | PY02067 | ATPase, AAA family, putative |
Saccharomyces cerevisiae | YBR186W | Pch2p |
Schistosoma japonicum | Sjp_0028260 | ko:K01516 nucleoside-triphosphatase [EC3.6.1.15], putative |
Schistosoma mansoni | Smp_171260 | thyroid hormone receptor interactor |
Schmidtea mediterranea | mk4.000527.02 | Pachytene checkpoint protein 2 homolog |
Trypanosoma brucei gambiense | Tbg972.11.10240 | ATPase-like protein, putative |
Trypanosoma brucei | Tb927.11.9160 | ATPase-like protein, putative |
Trypanosoma congolense | TcIL3000.11.9520 | ATPase-like protein, putative |
Trypanosoma cruzi | TcCLB.510901.90 | ATPase protein, putative |
Toxoplasma gondii | TGME49_288520 | ATPase, AAA family protein |
Trichomonas vaginalis | TVAG_077100 | spermatogenesis associated factor, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.01.0900 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb11.01.0900 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb11.01.0900 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb11.01.0900 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F10B5.5 | Caenorhabditis elegans | embryonic lethal | wormbase |
PBANKA_0909500 this record | Plasmodium berghei | Dispensable | plasmo |
TGME49_288520 | Toxoplasma gondii | Probably non-essential | sidik |
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 |
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 |
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.