pI: 6.2793 |
Length (AA): 437 |
MW (Da): 46883 |
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 6 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 |
---|---|---|---|---|---|---|---|---|---|
18 | 337 | 1erj (A) | 336 | 709 | 18.00 | 0 | 1 | 0.85 | 0.47 |
106 | 336 | 2iwa (A) | 27 | 258 | 8.00 | 0 | 0.57 | 0.42 | -0.14 |
147 | 323 | 3ow8 (A) | 44 | 209 | 27.00 | 0.0016 | 1 | 0.566534 | 0.62 |
147 | 278 | 3sfz (A) | 1067 | 1194 | 28.00 | 0.34 | 0.85 | 0.418559 | 0.82 |
237 | 317 | 1jmx (B) | 264 | 349 | 11.00 | 0 | 0.14 | 0.242855 | -0.19 |
250 | 314 | 5bpw (A) | 8 | 72 | 18.00 | 0 | 0.48 | 0.306241 | 0.47 |
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 60-80% percentile | ME49 Tachyzoite, ME49 Oocyst, ME49 Bradyzoite. | Gregory Fritz HM Sibley/Greg |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | VEG Tachyzoite, ME49 merozoite. | Gregory Hehl AB |
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 |
Sibley/Greg | ToxoDB |
Fritz HM | Transcriptomic analysis of toxoplasma development reveals many novel functions and structures specific to sporozoites and oocysts. |
Ortholog group members (OG5_128201)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G66240 | transducin/WD40 domain-containing protein |
Arabidopsis thaliana | AT5G14530 | transducin/WD40 domain-containing protein |
Babesia bovis | BBOV_IV008010 | conserved hypothetical protein |
Brugia malayi | Bm1_48420 | Hypothetical 37.1 kDa Trp-Asp repeats containing protein in RAM2-ATP7intergenic region |
Candida albicans | CaO19.10306 | WD40 repeat protein similar to S. cerevisiae SWD2 (YKL018W) subunit of the COMPASS histone methyltransferase |
Candida albicans | CaO19.2790 | WD40 repeat protein similar to S. cerevisiae SWD2 (YKL018W) subunit of the COMPASS histone methyltransferase |
Caenorhabditis elegans | CELE_C33H5.7 | Protein SWD-2.2 |
Cryptosporidium hominis | Chro.80455 | RIKEN cDNA 9430077D24 gene |
Cryptosporidium parvum | cgd8_3960 | RIKEN cDNA 9430077D24 gene, putative |
Dictyostelium discoideum | DDB_G0278945 | hypothetical protein |
Drosophila melanogaster | Dmel_CG17293 | CG17293 gene product from transcript CG17293-RA |
Echinococcus granulosus | EgrG_000067200 | WD repeat containing protein 82 |
Entamoeba histolytica | EHI_140490 | WD domain containing protein |
Echinococcus multilocularis | EmuJ_000067200 | WD repeat containing protein 82 |
Homo sapiens | ENSG00000164091 | WD repeat domain 82 |
Loa Loa (eye worm) | LOAG_01806 | hypothetical protein |
Loa Loa (eye worm) | LOAG_11002 | hypothetical protein |
Mus musculus | ENSMUSG00000020257 | WD repeat domain containing 82 |
Neospora caninum | NCLIV_056640 | WD-40 repeat-containing protein, putative |
Oryza sativa | 4339488 | Os05g0543300 |
Oryza sativa | 4343770 | Os07g0589400 |
Onchocerca volvulus | OVOC1043 |
|
Plasmodium berghei | PBANKA_1457100 | WD repeat-containing protein 82, putative |
Plasmodium falciparum | PF3D7_1243800 | WD repeat-containing protein 82, putative |
Plasmodium knowlesi | PKNH_1463100 | WD repeat-containing protein 82, putative |
Plasmodium vivax | PVX_101090 | hypothetical protein, conserved |
Plasmodium yoelii | PY01212 | Drosophila melanogaster GH09638p |
Saccharomyces cerevisiae | YKL018W | Swd2p |
Schistosoma japonicum | Sjp_0075180 | WD repeat-containing protein 82, putative |
Schistosoma mansoni | Smp_151180 | hypothetical protein |
Schmidtea mediterranea | mk4.003216.03 | |
Schmidtea mediterranea | mk4.002286.02 | Wdr82-2 |
Schmidtea mediterranea | mk4.002286.03 | |
Toxoplasma gondii | TGME49_313350 | hypothetical protein |
Theileria parva | TP01_0986 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_016940 | COMPASS component SWD2, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_C33H5.7 | Caenorhabditis elegans | adult lethal | wormbase |
CELE_C33H5.7 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_C33H5.7 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_C33H5.7 | Caenorhabditis elegans | sterile | wormbase |
YKL018W | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_313350 this record | Toxoplasma gondii | Probably non-essential | sidik |
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 |
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.