pI: 10.7868 |
Length (AA): 119 |
MW (Da): 13679 |
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 is 1 model calculated for this protein. More info on
this model, including the
model itself is available at:
Modbase
Target Beg | Target End | Template | Template Beg | Template End | Identity | Evalue | Model Score | MPQS | zDope |
---|---|---|---|---|---|---|---|---|---|
1 | 100 | 1914 (A) | 2001 | 3003 | 58.00 | 0 | 1 | 1.41304 | -0.51 |
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_129782)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G43640 | signal recognition particle subunit SRP14 |
Caenorhabditis elegans | CELE_F25G6.8 | Protein F25G6.8 |
Caenorhabditis elegans | CELE_F25G6.9 | Protein F25G6.9 |
Dictyostelium discoideum | DDB_G0272590 | signal recognition particle 14 kDa subunit |
Dictyostelium discoideum | DDB_G0273977 | signal recognition particle 14 kDa subunit |
Drosophila melanogaster | Dmel_CG5417 | Signal recognition particle protein 14 |
Echinococcus granulosus | EgrG_000665200 | signal recognition particle 14 kda protein |
Entamoeba histolytica | EHI_194075 | signal recognition particle 14 domain containing protein |
Echinococcus multilocularis | EmuJ_000665200 | signal recognition particle 14 kda protein |
Homo sapiens | ENSG00000140319 | signal recognition particle 14kDa (homologous Alu RNA binding protein) |
Loa Loa (eye worm) | LOAG_11231 | hypothetical protein |
Mus musculus | 102642637 | signal recognition particle 14 kDa protein-like |
Mus musculus | ENSMUSG00000009549 | signal recognition particle 14 |
Oryza sativa | 4337050 | Os04g0623700 |
Onchocerca volvulus | OVOC12000 | Signal recognition particle 14 kDa protein homolog |
Plasmodium berghei | PBANKA_0602200 | signal recognition particle subunit SRP14, putative |
Plasmodium falciparum | PF3D7_1203200 | signal recognition particle subunit SRP14 |
Plasmodium knowlesi | PKNH_1303100 | signal recognition particle subunit SRP14, putative |
Plasmodium vivax | PVX_084205 | signal recognition particle subunit SRP14, putative |
Plasmodium yoelii | PY05285 | hypothetical protein |
Toxoplasma gondii | TGME49_256050 | signal recognition particle 14kd protein |
Theileria parva | TP03_0473 | signal recognition particle, putative |
Trichomonas vaginalis | TVAG_260070 | signal recognition particle 14 kD protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_F25G6.9 | Caenorhabditis elegans | embryonic lethal | wormbase |
TGME49_256050 | Toxoplasma gondii | Essentiality uncertain | sidik |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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 |
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 |
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.