pI: 10.3731 |
Length (AA): 531 |
MW (Da): 60962 |
Paralog Number:
1
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 |
---|---|---|---|---|---|---|---|---|---|
6 | 76 | 2j7j (A) | 13 | 85 | 7.00 | 0.00045 | 0 | 0.23701 | -0.88 |
122 | 518 | 4ljy (A) | 256 | 586 | 32.00 | 0 | 1 | 0.699146 | 1.29 |
129 | 335 | 3bor (A) | 38 | 221 | 39.00 | 0.0000000000055 | 1 | 0.713331 | -0.53 |
142 | 330 | 1wrb (A) | 202 | 379 | 39.00 | 0 | 1 | 0.809432 | -0.63 |
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:
Ortholog group members (OG5_128047)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G16840 | P-loop containing nucleoside triphosphate hydrolases superfamily protein |
Babesia bovis | BBOV_IV001200 | DEAD/DEAH box helicase, putative |
Brugia malayi | Bm1_54000 | DEAD/DEAH box helicase family protein |
Candida albicans | CaO19.3540 | ATP-dependent RNA helicase |
Candida albicans | CaO19.11024 | ATP-dependent RNA helicase |
Caenorhabditis elegans | CELE_F55F8.2 | Protein F55F8.2, isoform B |
Cryptosporidium hominis | Chro.80030 | DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 24 |
Cryptosporidium parvum | cgd8_190 | Mak5 pre-mRNA splicing RNA SFII helicase |
Dictyostelium discoideum | DDB_G0281841 | DEAD/DEAH box helicase |
Drosophila melanogaster | Dmel_CG9143 | CG9143 gene product from transcript CG9143-RA |
Echinococcus granulosus | EgrG_000086400 | DEAD box ATP dependent RNA helicase 13 |
Entamoeba histolytica | EHI_145050 | DEAD/DEAH box helicase, putative |
Echinococcus multilocularis | EmuJ_000086400 | DEAD box ATP dependent RNA helicase 13 |
Giardia lamblia | GL50803_13220 | ATP-dependent RNA helicase |
Homo sapiens | ENSG00000089737 | DEAD (Asp-Glu-Ala-Asp) box helicase 24 |
Leishmania braziliensis | LbrM.35.4640 | ATP-dependent RNA helicase-like protein |
Leishmania donovani | LdBPK_364620.1 | ATP-dependent DEAD/H RNA helicase, putative |
Leishmania infantum | LinJ.36.4620 | ATP-dependent RNA helicase-like protein |
Leishmania major | LmjF.36.4400 | ATP-dependent RNA helicase-like protein |
Leishmania mexicana | LmxM.36.4400 | ATP-dependent RNA helicase-like protein |
Loa Loa (eye worm) | LOAG_16125 | hypothetical protein |
Loa Loa (eye worm) | LOAG_10144 | hypothetical protein |
Mus musculus | ensembl-mmu:ENSMUSG00000041645 | DEAD (Asp-Glu-Ala-Asp) box polypeptide 24 |
Neospora caninum | NCLIV_036150 | hypothetical protein |
Oryza sativa | 4336370 | Os04g0510400 |
Plasmodium berghei | PBANKA_1309000 | ATP-dependent RNA helicase MAK5, putative |
Plasmodium falciparum | PF3D7_1445200 | ATP-dependent RNA helicase MAK5, putative |
Plasmodium knowlesi | PKNH_1237100 | ATP-dependent RNA helicase MAK5, putative |
Plasmodium vivax | PVX_118230 | RNA helicase, putative |
Plasmodium vivax | PVX_198290 | unspecified product |
Plasmodium yoelii | PY07373 | ATP-dependent RNA helicase |
Saccharomyces cerevisiae | YBR142W | Mak5p |
Schistosoma japonicum | Sjp_0081920 | ko:K01509 adenosinetriphosphatase [EC3.6.1.3], putative |
Schistosoma mansoni | Smp_131360 | DEAD box ATP-dependent RNA helicase |
Schmidtea mediterranea | mk4.000337.09 | ATP-dependent RNA helicase DDX24 |
Schmidtea mediterranea | mk4.000337.08 | ATP-dependent RNA helicase DDX24 |
Trypanosoma brucei gambiense | Tbg972.10.11950 | ATP-dependent DEAD/H RNA helicase, putative,ATP- dependent RNA helicase, putative |
Trypanosoma brucei | Tb927.10.9780 | ATP-dependent DEAD/H RNA helicase, putative |
Trypanosoma congolense | TcIL3000_10_8570 | ATP-dependent DEAD/H RNA helicase, putative |
Trypanosoma cruzi | TcCLB.504147.150 | ATP-dependent DEAD/H RNA helicase, putative |
Toxoplasma gondii | TGME49_270620 | DEAD/DEAH box helicase domain-containing protein |
Theileria parva | TP01_0146 | ATP-dependent RNA helicase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.9780 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.9780 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.9780 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.9780 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F55F8.2 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_F55F8.2 | Caenorhabditis elegans | slow growth | wormbase |
YBR142W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_1309000 | Plasmodium berghei | Essential | plasmo |
TGME49_270620 | Toxoplasma gondii | Probably essential | sidik |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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 |
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.