pI: 7.7435 |
Length (AA): 555 |
MW (Da): 62025 |
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 2 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 |
---|---|---|---|---|---|---|---|---|---|
175 | 473 | 1vhn (A) | 6 | 268 | 27.00 | 0 | 1 | 0.731139 | -0.24 |
178 | 454 | 1vhn (A) | 9 | 247 | 34.00 | 0 | 1 | 0.629199 | 0.52 |
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_127309)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G38890 | tRNA-dihydrouridine(47) synthase [NAD(P)(+)]-like |
Brugia malayi | Bm1_16415 | dihydrouridine synthase domain containing protein |
Candida albicans | CaO19.9138 | potential tRNA dihydrouridine synthase similar to S. cerevisiae DUS3 (YLR401C) |
Candida albicans | CaO19.1565 | potential tRNA dihydrouridine synthase similar to S. cerevisiae DUS3 (YLR401C) |
Caenorhabditis elegans | CELE_Y37E11B.5 | Protein Y37E11B.5 |
Cryptosporidium hominis | Chro.50134 | hypothetical protein |
Cryptosporidium parvum | cgd5_2440 | Ylr401cp-like protein with 2 CCCH domains plus Dus1p tRNA dihydrouridine synthase Tim barrel |
Chlamydia trachomatis | CT_644 | tRNA-dihydrouridine synthase |
Dictyostelium discoideum | DDB_G0292686 | CCCH-type zinc finger-containing protein |
Drosophila melanogaster | Dmel_CG10463 | CG10463 gene product from transcript CG10463-RA |
Escherichia coli | b3260 | tRNA-dihydrouridine synthase B |
Entamoeba histolytica | EHI_140340 | hypothetical protein, conserved |
Giardia lamblia | GL50803_3565 | Dihydrouridine synthase, putative |
Homo sapiens | ENSG00000141994 | dihydrouridine synthase 3-like (S. cerevisiae) |
Leishmania braziliensis | LbrM.17.0330 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_170400.1 | dihydrouridine synthase (Dus), putative |
Leishmania infantum | LinJ.17.0400 | hypothetical protein, conserved |
Leishmania major | LmjF.17.0350 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.17.0350 | hypothetical protein, conserved |
Mycobacterium leprae | ML2186 | POSSIBLE TRANSCRIPTIONAL REGULATORY PROTEIN |
Mus musculus | ENSMUSG00000007603 | dihydrouridine synthase 3-like (S. cerevisiae) |
Mycobacterium tuberculosis | Rv0823c | Possible transcriptional regulatory protein |
Mycobacterium ulcerans | MUL_0444 | transcriptional regulator |
Neospora caninum | NCLIV_045330 | Dihydrouridine synthase, related |
Oryza sativa | 4334955 | Os04g0117600 |
Onchocerca volvulus | OVOC9137 |
|
Saccharomyces cerevisiae | YLR401C | Dus3p |
Schmidtea mediterranea | mk4.000116.07 | tRNA-dihydrouridine(47) synthase |
Trypanosoma brucei gambiense | Tbg972.7.7460 | tRNA-dihydrouridine synthase 3, putative |
Trypanosoma brucei | Tb927.7.6450 | tRNA-dihydrouridine synthase 3, putative |
Trypanosoma congolense | TcIL3000_7_5350 | tRNA-dihydrouridine synthase 3, putative |
Trypanosoma cruzi | TcCLB.510053.70 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.511321.20 | hypothetical protein, conserved |
Toxoplasma gondii | TGME49_228080 | dihydrouridine synthase (dus) protein |
Treponema pallidum | TP0980 | histidine phosphokinase/phophatase (ntrB) |
Trichomonas vaginalis | TVAG_243820 | tRNA-dihydrouridine synthase, putative |
Wolbachia endosymbiont of Brugia malayi | Wbm0462 | tRNA-dihydrouridine synthase |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
mtu839 | Mycobacterium tuberculosis | non-essential | nmpdr |
Tb927.7.6450 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.7.6450 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.7.6450 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.7.6450 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b3260 | Escherichia coli | non-essential | goodall |
TGME49_228080 | Toxoplasma gondii | Probably non-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.