pI: 9.7443 |
Length (AA): 407 |
MW (Da): 46160 |
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 |
---|---|---|---|---|---|---|---|---|---|
1 | 125 | 4p6z (S) | 8 | 136 | 22.00 | 0 | 1 | 0.650425 | -0.78 |
1 | 406 | 4p6z (M) | 9 | 421 | 42.00 | 0 | 1 | 1.47474 | 0.05 |
1 | 406 | 2jkr (M) | 8 | 434 | 43.00 | 0 | 1 | 1.42884 | 0.23 |
70 | 112 | 2wl8 (A) | 222 | 264 | 33.00 | 0 | 0.9 | 0.535951 | -0.33 |
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:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | Trophozoite, Rahman HM-1 IMSS Trophozoite. | Hon CC |
Hon CC | Transcriptomics of virulent and avirulent strains |
Ortholog group members (OG5_128447)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G46630 | clathrin adaptor complexes medium subunit family protein |
Brugia malayi | Bm1_38960 | Dumpy : shorter than wild-type protein 23 |
Candida albicans | CaO19.2194 | similar to S. cerevisiae APM4 (YOL062C) medium subunit of the clathrin-associated protein AP-2 complex |
Candida albicans | CaO19.9740 | similar to S. cerevisiae APM4 (YOL062C) medium subunit of the clathrin-associated protein AP-2 complex |
Caenorhabditis elegans | CELE_R160.1 | Protein DPY-23, isoform A |
Dictyostelium discoideum | DDB_G0277139 | clathrin-adaptor medium chain AP-2 |
Drosophila melanogaster | Dmel_CG7057 | Adaptor Protein complex 2, mu subunit |
Echinococcus granulosus | EgrG_000440900 | AP 2 complex subunit mu 1 |
Entamoeba histolytica | EHI_135430 | Clathrin coat assembly protein, putative |
Entamoeba histolytica | EHI_124560 | AP-2 complex subunit mu, putative |
Echinococcus multilocularis | EmuJ_000440900 | AP 2 complex subunit mu 1 |
Giardia lamblia | GL50803_8917 | Mu adaptin |
Homo sapiens | ENSG00000161203 | adaptor-related protein complex 2, mu 1 subunit |
Leishmania braziliensis | LbrM.35.3250 | clathrin coat assembly protein-like protein |
Leishmania donovani | LdBPK_363180.1 | clathrin coat assembly protein-like protein |
Leishmania infantum | LinJ.36.3180 | clathrin coat assembly protein-like protein |
Leishmania major | LmjF.36.3030 | clathrin coat assembly protein-like protein |
Leishmania mexicana | LmxM.36.3030 | clathrin coat assembly protein-like protein |
Loa Loa (eye worm) | LOAG_02601 | shorter than wild-type protein 23 |
Mus musculus | ENSMUSG00000022841 | adaptor-related protein complex 2, mu 1 subunit |
Neospora caninum | NCLIV_031310 | clathrin coat assembly protein AP50, putative |
Oryza sativa | 4330379 | Os02g0690700 |
Saccharomyces cerevisiae | YOL062C | Apm4p |
Schistosoma japonicum | Sjp_0041760 | AP-2 complex subunit mu-1, putative |
Schistosoma japonicum | Sjp_0041720 | Ubiquitin-like modifier-activating enzyme 6, putative |
Schistosoma japonicum | Sjp_0041730 | AP-2 complex subunit mu-1, putative |
Schistosoma japonicum | Sjp_0088960 | Ubiquitin-like modifier-activating enzyme 6, putative |
Schistosoma japonicum | Sjp_0306750 | Ubiquitin-like modifier-activating enzyme 6, putative |
Schistosoma japonicum | Sjp_0105920 | AP-2 complex subunit mu-1-B, putative |
Schistosoma mansoni | Smp_026540.2 | clathrin coat associated protein ap-50 |
Schistosoma mansoni | Smp_026540.1 | clathrin coat associated protein ap-50 |
Schmidtea mediterranea | mk4.003048.02 | AP-2 complex subunit mu |
Schmidtea mediterranea | mk4.025010.01 | Putative clathrin coat associated protein ap-50 |
Schmidtea mediterranea | mk4.003048.01 | Putative clathrin coat associated protein ap-50 |
Schmidtea mediterranea | mk4.003048.03 | AP-2 complex subunit mu |
Schmidtea mediterranea | mk4.026123.01 | |
Trypanosoma cruzi | TcCLB.510105.30 | clathrin coat assembly protein, putative |
Trypanosoma cruzi | TcCLB.509715.20 | clathrin coat assembly protein, putative |
Toxoplasma gondii | TGME49_230920 | adaptor complexes medium subunit family protein |
Trichomonas vaginalis | TVAG_453580 | clathrin coat assembly protein, putative |
Trichomonas vaginalis | TVAG_226350 | clathrin coat assembly protein ap-1, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_R160.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_R160.1 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_R160.1 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_R160.1 | Caenorhabditis elegans | slow growth | wormbase |
TGME49_230920 | Toxoplasma gondii | Essentiality uncertain | sidik |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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.