pI: 7.12 |
Length (AA): 405 |
MW (Da): 46405 |
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 7 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 |
---|---|---|---|---|---|---|---|---|---|
1 | 405 | 2eyq (A) | 545 | 955 | 18.00 | 0 | 1 | 1.07 | -0.07 |
28 | 231 | 1vec (A) | 83 | 286 | 55.00 | 0 | 1 | 1.39 | -2.48 |
30 | 405 | 1s2m (A) | 46 | 420 | 73.00 | 0 | 1 | 1.97 | -2.25 |
1 | 405 | 2eyq (A) | 545 | 955 | 19.00 | 0 | 1 | 1.1266 | 0.5 |
31 | 405 | 1s2m (A) | 47 | 420 | 74.00 | 0 | 1 | 1.90083 | -1.53 |
31 | 234 | 2oxc (A) | 63 | 266 | 38.00 | 0 | 1 | 1.1449 | -1.69 |
31 | 234 | 1fuu (A) | 22 | 223 | 40.00 | 0 | 1 | 1.1664 | -1.88 |
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 | amastigotes, metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_127804)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G45810 | DEAD-box ATP-dependent RNA helicase 6 |
Arabidopsis thaliana | AT3G61240 | DEAD-box ATP-dependent RNA helicase 12 |
Arabidopsis thaliana | AT4G00660 | DEAD-box ATP-dependent RNA helicase 8 |
Babesia bovis | BBOV_II006480 | ATP-dependent RNA helicase, putative |
Brugia malayi | Bm1_30200 | germline helicase protein 1 |
Candida albicans | CaO19.6197 | RNA helicase of DEAD box family |
Candida albicans | CaO19.13577 | RNA helicase of DEAD box family |
Caenorhabditis elegans | CELE_C07H6.5 | Protein CGH-1 |
Cryptosporidium hominis | Chro.80211 | ATP-dependent RNA helicase |
Cryptosporidium parvum | cgd8_1820 | ATP-dependent RNA helicase, putative |
Dictyostelium discoideum | DDB_G0291804 | DEAD/DEAH box helicase |
Drosophila melanogaster | Dmel_CG4916 | maternal expression at 31B |
Echinococcus granulosus | EgrG_001180000 | ATP dependent RNA helicase me31b |
Echinococcus granulosus | EgrG_000123700 | ATP dependent RNA helicase DDX6 |
Echinococcus granulosus | EgrG_001179800 | e3 ubiquitin protein ligase RFWD3 |
Echinococcus multilocularis | EmuJ_000123700 | ATP dependent RNA helicase DDX6 |
Echinococcus multilocularis | EmuJ_001180000 | ATP dependent RNA helicase me31b |
Echinococcus multilocularis | EmuJ_001179800 | e3 ubiquitin protein ligase RFWD3 |
Giardia lamblia | GL50803_2098 | ATP-dependent RNA helicase p54, putative |
Homo sapiens | ENSG00000110367 | DEAD (Asp-Glu-Ala-Asp) box helicase 6 |
Leishmania donovani | LdBPK_350370.1 | ATP-dependent DEAD-box RNA helicase, putative |
Leishmania infantum | LinJ.35.0370 | ATP-dependent DEAD-box RNA helicase, putative |
Leishmania major | LmjF.35.0370 | ATP-dependent DEAD-box RNA helicase, putative |
Leishmania mexicana | LmxM.34.0370 | ATP-dependent DEAD-box RNA helicase, putative |
Loa Loa (eye worm) | LOAG_02698 | ATP-dependent RNA helicase DHH1 |
Mus musculus | ENSMUSG00000032097 | DEAD (Asp-Glu-Ala-Asp) box polypeptide 6 |
Neospora caninum | NCLIV_056360 | Eukaryotic initiation factor, related |
Oryza sativa | 4349053 | Os10g0503700 |
Oryza sativa | 4336501 | Os04g0533000 |
Oryza sativa | 4330120 | Os02g0641800 |
Plasmodium berghei | PBANKA_1217700 | ATP-dependent RNA helicase DDX6 |
Plasmodium falciparum | PF3D7_0320800 | ATP-dependent RNA helicase DDX6 |
Plasmodium knowlesi | PKNH_0820000 | ATP-dependent RNA helicase DDX6, putative |
Plasmodium vivax | PVX_095195 | ATP-dependent RNA helicase DDX6, putative |
Plasmodium yoelii | PY01870 | ATP-dependent RNA Helicase |
Saccharomyces cerevisiae | YDL160C | DExD/H-box ATP-dependent RNA helicase DHH1 |
Schistosoma japonicum | Sjp_0311860 | RING finger and WD repeat domain-containing protein 3, putative |
Schistosoma japonicum | Sjp_0043670 | ko:K08849 mixed lineage kinase domain-like, putative |
Schistosoma japonicum | Sjp_0036950 | ko:K01509 adenosinetriphosphatase [EC3.6.1.3], putative |
Schistosoma mansoni | Smp_173970 | DEAD box ATP-dependent RNA helicase |
Schmidtea mediterranea | mk4.018587.01 | Probable ATP-dependent RNA helicase DDX6 |
Schmidtea mediterranea | mk4.005911.00 | Probable ATP-dependent RNA helicase DDX6 |
Schmidtea mediterranea | mk4.000222.07 | Probable ATP-dependent RNA helicase DDX6 |
Schmidtea mediterranea | mk4.002614.04 | Probable ATP-dependent RNA helicase DDX6 |
Schmidtea mediterranea | mk4.007746.03 | ATP-dependent RNA helicase cgh-1 |
Schmidtea mediterranea | mk4.021485.01 | Probable ATP-dependent RNA helicase DDX6 |
Schmidtea mediterranea | mk4.020079.00 | Probable ATP-dependent RNA helicase DDX6 |
Trypanosoma brucei gambiense | Tbg972.10.4980 | hypothetical protein, conserved,ATP-dependent DEAD-box RNA helicase, putative |
Trypanosoma brucei | Tb927.10.3990 | DHH1 |
Trypanosoma congolense | TcIL3000_10_3320 | ATP-dependent DEAD-box RNA helicase, putative |
Trypanosoma cruzi | TcCLB.506959.30 | ATP-dependent DEAD/H RNA helicase, putative |
Toxoplasma gondii | TGME49_313010 | DEAD (Asp-Glu-Ala-Asp) box polypeptide DDX6 |
Theileria parva | TP02_0613 | ATP-dependent RNA helicase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.3990 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.3990 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.3990 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.10.3990 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_C07H6.5 | Caenorhabditis elegans | adult lethal | wormbase |
CELE_C07H6.5 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_C07H6.5 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_C07H6.5 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_C07H6.5 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_1217700 | Plasmodium berghei | Dispensable | plasmo |
TGME49_313010 | Toxoplasma gondii | Essentiality uncertain | sidik |
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 |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
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.