pI: 8.6175 |
Length (AA): 472 |
MW (Da): 52523 |
Paralog Number:
2
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 |
---|---|---|---|---|---|---|---|---|---|
4 | 56 | 2dh8 (A) | 11 | 63 | 13.00 | 0.25 | 0.07 | 0.165588 | 0.57 |
297 | 375 | 4qu7 (A) | 401 | 479 | 52.00 | 0 | 1 | 0.962573 | -1.83 |
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_129021)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G66010 | RNA recognition motif-containing protein |
Brugia malayi | Bm1_32715 | RNA recognition motif. |
Brugia malayi | Bm1_12005 | RNA binding protein |
Brugia malayi | Bm1_48255 | Heterogeneous nuclear ribonucleoprotein H' |
Caenorhabditis elegans | CELE_Y73B6BL.33 | Protein HRPF-2 |
Drosophila melanogaster | Dmel_CG6946 | glorund |
Echinococcus granulosus | EgrG_000083900 | heterogeneous nuclear ribonucleoprotein |
Echinococcus multilocularis | EmuJ_000083900 | heterogeneous nuclear ribonucleoprotein |
Homo sapiens | ENSG00000126945 | heterogeneous nuclear ribonucleoprotein H2 (H') |
Homo sapiens | ENSG00000169813 | heterogeneous nuclear ribonucleoprotein F |
Homo sapiens | ENSG00000169045 | heterogeneous nuclear ribonucleoprotein H1 (H) |
Loa Loa (eye worm) | LOAG_07344 | RNA binding protein |
Loa Loa (eye worm) | LOAG_12543 | hypothetical protein |
Loa Loa (eye worm) | LOAG_11458 | hypothetical protein |
Loa Loa (eye worm) | LOAG_11457 | hypothetical protein |
Loa Loa (eye worm) | LOAG_00436 | heterogeneous nuclear ribonucleoprotein H |
Mus musculus | ENSMUSG00000007850 | heterogeneous nuclear ribonucleoprotein H1 |
Mus musculus | ENSMUSG00000042079 | heterogeneous nuclear ribonucleoprotein F |
Mus musculus | ENSMUSG00000045427 | heterogeneous nuclear ribonucleoprotein H2 |
Neospora caninum | NCLIV_050590 | GL11864, related |
Neospora caninum | NCLIV_001680 | RRM domain-containing protein, putative |
Onchocerca volvulus | OVOC9534 |
|
Onchocerca volvulus | OVOC3029 |
|
Plasmodium berghei | PBANKA_0508400 | RNA-binding protein, putative |
Plasmodium falciparum | PF3D7_1024200 | RNA-binding protein, putative |
Plasmodium knowlesi | PKNH_0608700 | RNA-binding protein, putative |
Plasmodium vivax | PVX_111500 | RNA-binding protein, putative |
Schistosoma japonicum | Sjp_0023270 | Heterogeneous nuclear ribonucleoprotein F, putative |
Schistosoma mansoni | Smp_179270.1 | heterogeneous nuclear ribonucleoprotein |
Schistosoma mansoni | Smp_179270.2 | heterogeneous nuclear ribonucleoprotein |
Schistosoma mansoni | Smp_179270.3 | heterogeneous nuclear ribonucleoprotein |
Schmidtea mediterranea | mk4.011751.02 | G-rich sequence factor 1 |
Schmidtea mediterranea | mk4.000502.07 | |
Trypanosoma brucei gambiense | Tbg.972.2.2100 | heterogeneous nuclear ribonucleoprotein H/F, putative |
Trypanosoma brucei | Tb927.2.3880 | heterogeneous nuclear ribonucleoproteins F/H homologue |
Trypanosoma congolense | TcIL3000_0_16520 | heterogeneous nuclear ribonucleoprotein H/F, putative |
Trypanosoma cruzi | TcCLB.504157.10 | heterogeneous nuclear ribonucleoprotein H/F, putative |
Trypanosoma cruzi | TcCLB.511109.130 | heterogeneous nuclear ribonucleoprotein H/F, putative |
Toxoplasma gondii | TGME49_236540 | RNA recognition motif-containing protein |
Toxoplasma gondii | TGME49_294812 | RNA recognition motif-containing protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.2.3880 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.2.3880 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.2.3880 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.2.3880 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_Y73B6BL.33 | Caenorhabditis elegans | embryonic lethal | wormbase |
PBANKA_0508400 | Plasmodium berghei | Essential | plasmo |
TGME49_294812 | Toxoplasma gondii | Probably essential | sidik |
TGME49_236540 | Toxoplasma gondii | Probably essential | sidik |
TGME49_294812 | Toxoplasma gondii | Probably non-essential | sidik |
TGME49_236540 | Toxoplasma gondii | Probably non-essential | sidik |
TGME49_294812 | Toxoplasma gondii | Essentiality uncertain | sidik |
TGME49_236540 | Toxoplasma gondii | Essentiality uncertain | sidik |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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 |
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.