pI: 10.2254 |
Length (AA): 803 |
MW (Da): 89691 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
2 | 566 | 2eyq (A) | 564 | 1144 | 15.00 | 0 | 1 | 0.76 | 0.21 |
20 | 225 | 1vec (A) | 83 | 287 | 35.00 | 0 | 1 | 0.94 | -2.53 |
24 | 229 | 3ber (A) | 26 | 230 | 39.00 | 0 | 1 | 0.848238 | -1.33 |
24 | 227 | 2oxc (A) | 64 | 266 | 36.00 | 0 | 1 | 0.823747 | -1.41 |
24 | 621 | 2zj2 (A) | 3 | 636 | 15.00 | 0 | 1 | 0.788407 | 0.46 |
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 | amastigotes, metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_128298)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G77030 | putative DEAD-box ATP-dependent RNA helicase 29 |
Babesia bovis | BBOV_I003430 | DEAD/DEAH box helicase and helicase conserved C-terminal domain containing protein |
Brugia malayi | Bm1_41715 | DEAD/DEAH box helicase family protein |
Candida albicans | CaO19.5991 | likely DEAD box ATP-dependent RNA helicase similar to S. cerevisiae DBP10 (YDL031W) nucleolar protein involved in rRNA processin |
Candida albicans | CaO19.13412 | likely DEAD box ATP-dependent RNA helicase similar to S. cerevisiae DBP10 (YDL031W) nucleolar protein involved in rRNA processin |
Caenorhabditis elegans | CELE_Y94H6A.5 | Protein Y94H6A.5, isoform B |
Cryptosporidium hominis | Chro.30274 | hypothetical protein |
Cryptosporidium parvum | cgd3_2330 | hypothetical protein |
Dictyostelium discoideum | DDB_G0292992 | hypothetical protein |
Drosophila melanogaster | Dmel_CG32344 | CG32344 gene product from transcript CG32344-RA |
Echinococcus granulosus | EgrG_000122300 | ATP dependent RNA helicase DDX54 |
Entamoeba histolytica | EHI_069410 | DEAD/DEAH box helicase, putative |
Echinococcus multilocularis | EmuJ_000122300 | ATP dependent RNA helicase DDX54 |
Giardia lamblia | GL50803_90950 | ATP-dependent RNA helicase |
Homo sapiens | ENSG00000123064 | DEAD (Asp-Glu-Ala-Asp) box polypeptide 54 |
Leishmania braziliensis | LbrM.20.1540 | ATP-dependent RNA helicase, putative |
Leishmania donovani | LdBPK_341800.1 | ATP-dependent RNA helicase, putative |
Leishmania infantum | LinJ.34.1800 | ATP-dependent RNA helicase, putative |
Leishmania major | LmjF.34.2050 | ATP-dependent RNA helicase, putative |
Leishmania mexicana | LmxM.33.2050 | ATP-dependent RNA helicase, putative |
Loa Loa (eye worm) | LOAG_08896 | DEAD/DEAH box helicase |
Mus musculus | ENSMUSG00000029599 | DEAD (Asp-Glu-Ala-Asp) box polypeptide 54 |
Neospora caninum | NCLIV_003170 | ATP-dependent RNA helicase, putative |
Oryza sativa | 4345577 | Os08g0416100 |
Onchocerca volvulus | OVOC1554 |
|
Plasmodium berghei | PBANKA_0703700 | ATP-dependent RNA helicase DBP10, putative |
Plasmodium falciparum | PF3D7_0827000 | ATP-dependent RNA helicase DBP10, putative |
Plasmodium knowlesi | PKNH_1321100 | ATP-dependent RNA helicase DBP10, putative |
Plasmodium vivax | PVX_089015 | ATP-dependent RNA helicase DBP10, putative |
Plasmodium yoelii | PY03587 | similar ATP-dependent RNA Helicase |
Saccharomyces cerevisiae | YDL031W | Dbp10p |
Schistosoma japonicum | Sjp_0043800 | ko:K01529 DEAD (Asp-Glu-Ala-Asp) box polypeptide 54 [EC:3.6.1.-], putative |
Schistosoma japonicum | Sjp_0122990 | ko:K01529 ATP-dependent RNA-helicase [EC:3.6.1.-], putative |
Schistosoma mansoni | Smp_020200 | DEAD box ATP-dependent RNA helicase |
Schmidtea mediterranea | mk4.003274.01 | ATP-dependent RNA helicase DDX54 |
Trypanosoma brucei gambiense | Tbg972.4.2580 | ATP-dependent DEAD/H RNA helicase, putative |
Trypanosoma brucei | Tb927.4.2630 | ATP-dependent DEAD/H RNA helicase, putative |
Trypanosoma congolense | TcIL3000_4_2520 | ATP-dependent DEAD/H RNA helicase, putative |
Trypanosoma congolense | TcIL3000_0_44840 | ATP-dependent DEAD/H RNA helicase, putative |
Trypanosoma cruzi | TcCLB.506635.20 | ATP-dependent RNA helicase, putative |
Trypanosoma cruzi | TcCLB.508027.70 | ATP-dependent RNA helicase, putative |
Toxoplasma gondii | TGME49_208540 | DEAD/DEAH box helicase domain-containing protein |
Theileria parva | TP03_0195 | ATP-dependent RNA helicase, putative |
Trichomonas vaginalis | TVAG_109450 | DEAD box ATP-dependent RNA helicase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.4.2630 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.4.2630 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.4.2630 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.4.2630 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_Y94H6A.5 | Caenorhabditis elegans | slow growth | wormbase |
YDL031W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0703700 | Plasmodium berghei | Slow | plasmo |
TGME49_208540 | Toxoplasma gondii | Probably essential | sidik |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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 |
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 |
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 |
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 |
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.