pI: 6.5924 |
Length (AA): 657 |
MW (Da): 73228 |
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 |
---|---|---|---|---|---|---|---|---|---|
29 | 570 | 2eyq (A) | 392 | 923 | 16.00 | 0 | 1 | 0.785762 | 1.21 |
196 | 429 | 5gvr (A) | 169 | 402 | 59.00 | 0 | 1 | 1.19496 | -2.07 |
240 | 653 | 1a1v (A) | 191 | 563 | 17.00 | 0 | 0.72 | 0.495937 | 1.28 |
433 | 593 | 2p6n (A) | 406 | 566 | 75.00 | 0 | 1 | 1.25645 | -1.81 |
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 Oocyst. | Fritz HM |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | VEG Tachyzoite, ME49 Tachyzoite, ME49 merozoite, ME49 Bradyzoite. | Gregory Hehl AB Sibley/Greg |
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. |
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_129688)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G51280 | putative DEAD-box ATP-dependent RNA helicase 35 |
Arabidopsis thaliana | AT4G33370 | putative DEAD-box ATP-dependent RNA helicase 43 |
Brugia malayi | Bm1_49040 | DEAD |
Caenorhabditis elegans | CELE_H27M09.1 | Protein SACY-1 |
Cryptosporidium hominis | Chro.70507 | RNA helicase-1 |
Cryptosporidium parvum | cgd7_4600 | abstrakt protein SF II helicase + Znknuckle C2HC (PA) |
Dictyostelium discoideum | DDB_G0287361 | DEAD box protein abstrakt |
Drosophila melanogaster | Dmel_CG14637 | abstrakt |
Echinococcus granulosus | EgrG_000941700 | ATP dependent RNA helicase abstrakt |
Echinococcus granulosus | EgrG_000941800 | ATP dependent RNA helicase abstrakt |
Echinococcus multilocularis | EmuJ_000941800 | ATP dependent RNA helicase abstrakt |
Echinococcus multilocularis | EmuJ_000941700 | ATP dependent RNA helicase abstrakt |
Homo sapiens | ENSG00000183258 | DEAD (Asp-Glu-Ala-Asp) box polypeptide 41 |
Loa Loa (eye worm) | LOAG_07898 | ATP-dependent RNA helicase DDX41 |
Mus musculus | ENSMUSG00000021494 | DEAD (Asp-Glu-Ala-Asp) box polypeptide 41 |
Neospora caninum | NCLIV_043620 | hypothetical protein |
Oryza sativa | 4341945 | Os06g0697200 |
Oryza sativa | 4328308 | Os02g0150100 |
Plasmodium berghei | PBANKA_1242500 | ATP-dependent RNA helicase DDX41, putative |
Plasmodium falciparum | PF3D7_0527900 | ATP-dependent RNA helicase DDX41, putative |
Plasmodium knowlesi | PKNH_1004800 | ATP-dependent RNA helicase DDX41, putative |
Plasmodium vivax | PVX_079855 | RNA helicase-1, putative |
Plasmodium yoelii | PY01284 | RNA helicase-1 |
Schistosoma japonicum | Sjp_0118940 | Probable ATP-dependent RNA helicase DDX41, putative |
Schistosoma japonicum | Sjp_0081620 | ko:K01529 DEAD (Asp-Glu-Ala-Asp) box polypeptide 41 [EC:3.6.1.-], putative |
Schistosoma japonicum | Sjp_0132060 | ko:K01529 abstrakt [EC:3.6.1.-], putative |
Schistosoma mansoni | Smp_172030 | DEAD box ATP-dependent RNA helicase |
Schmidtea mediterranea | mk4.001812.02 | Probable ATP-dependent RNA helicase DDX41 |
Schmidtea mediterranea | mk4.000001.38 | Probable ATP-dependent RNA helicase DDX41 |
Toxoplasma gondii | TGME49_210360 | DEAD (Asp-Glu-Ala-Asp) box polypeptide 41 family protein |
Theileria parva | TP02_0316 | RNA helicase-1, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_H27M09.1 | Caenorhabditis elegans | adult lethal | wormbase |
CELE_H27M09.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_H27M09.1 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_H27M09.1 | Caenorhabditis elegans | slow growth | wormbase |
PBANKA_1242500 | Plasmodium berghei | Essential | plasmo |
TGME49_210360 this record | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
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.