pI: 10.74 |
Length (AA): 59 |
MW (Da): 6592 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 1
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:
PDB Structures:
Ortholog group members (OG5_130196)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G27350 | ribosome associated membrane protein RAMP4 |
Arabidopsis thaliana | AT1G27330 | ribosome associated membrane protein RAMP4 |
Brugia malayi | Bm1_00455 | RAMP4-2 |
Caenorhabditis elegans | CELE_T09A12.5 | Protein T09A12.5 |
Caenorhabditis elegans | CELE_F59F4.2 | Protein F59F4.2 |
Cryptosporidium parvum | cgd2_140 | conserved hypothetical protein |
Dictyostelium discoideum | DDB_G0275381 | hypothetical protein |
Drosophila melanogaster | Dmel_CG32276 | CG32276 gene product from transcript CG32276-RB |
Echinococcus granulosus | EgrG_000414500 | ribosome associated membrane protein 4 |
Echinococcus multilocularis | EmuJ_000414500 | ribosome associated membrane protein 4 |
Homo sapiens | ENSG00000120742 | stress-associated endoplasmic reticulum protein 1 |
Homo sapiens | ENSG00000151778 | stress-associated endoplasmic reticulum protein family member 2 |
Loa Loa (eye worm) | LOAG_00998 | hypothetical protein |
Mus musculus | ENSMUSG00000052584 | stress-associated endoplasmic reticulum protein family member 2 |
Mus musculus | ENSMUSG00000027808 | stress-associated endoplasmic reticulum protein 1 |
Neospora caninum | NCLIV_068620 | Ribosome associated membrane domain-containing protein, putative |
Oryza sativa | 4350985 | Os11g0637400 |
Oryza sativa | 4343733 | Os07g0583000 |
Oryza sativa | 4352336 | Os12g0514100 |
Onchocerca volvulus | OVOC2392 |
|
Plasmodium berghei | PBANKA_0315800 | ribosome associated membrane protein RAMP4, putative |
Plasmodium falciparum | PF3D7_0219400 | ribosome associated membrane protein RAMP4, putative, unspecified product |
Plasmodium knowlesi | PKNH_0401500 | ribosome associated membrane protein RAMP4, putative |
Plasmodium vivax | PVX_002585 | ribosome associated membrane protein RAMP4, putative |
Plasmodium yoelii | PY04494 | Arabidopsis thaliana F17L21.12-related |
Schistosoma japonicum | Sjp_0308650 | IPR010580,Ribosome associated membrane RAMP4,domain-containing |
Schistosoma mansoni | Smp_089570 | stress associated endoplasmic reticulum protein (serp1/ramp4) |
Schmidtea mediterranea | mk4.044350.00 | Putative stress associated endoplasmic reticulum protein |
Schmidtea mediterranea | mk4.015384.01 | Putative stress associated endoplasmic reticulum protein |
Toxoplasma gondii | TGME49_276940 | ribosome associated membrane protein RAMP4, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
PBANKA_0315800 | Plasmodium berghei | Dispensable | plasmo |
TGME49_276940 | Toxoplasma gondii | Probably non-essential | sidik |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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 |
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 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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.