pI: 8.3571 |
Length (AA): 426 |
MW (Da): 48030 |
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 5 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 | 152 | 4p6z (S) | 1 | 147 | 15.00 | 0 | 0.92 | 0.685508 | -1.39 |
1 | 425 | 2jkr (M) | 1 | 434 | 23.00 | 0 | 1 | 1.15535 | -0.06 |
1 | 134 | 2vgl (S) | 1 | 129 | 14.00 | 0.00000000027 | 0.32 | 0.455054 | -0.93 |
2 | 425 | 1w63 (M) | 3 | 421 | 22.00 | 0 | 1 | 1.15601 | 0.31 |
171 | 425 | 4ikn (A) | 165 | 417 | 38.00 | 0 | 1 | 0.955492 | -0.17 |
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 |
---|---|---|---|
Upper 80-100% percentile | Trophozoite, Rahman HM-1 IMSS Trophozoite. | Hon CC |
Hon CC | Transcriptomics of virulent and avirulent strains |
Ortholog group members (OG5_129247)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G56590 | protein ZIG SUPPRESSOR 4 |
Brugia malayi | Bm1_30830 | Adaptin or adaptin-related protein protein 7 |
Caenorhabditis elegans | CELE_F53H8.1 | Protein APM-3 |
Dictyostelium discoideum | DDB_G0277901 | clathrin-adaptor medium chain AP-3 |
Drosophila melanogaster | Dmel_CG3035 | carmine |
Echinococcus granulosus | EgrG_000610600 | AP 3 complex subunit mu 1 |
Entamoeba histolytica | EHI_099240 | clathrin-adaptor medium chain, putative |
Echinococcus multilocularis | EmuJ_000610600 | AP 3 complex subunit mu 1 |
Homo sapiens | ENSG00000185009 | adaptor-related protein complex 3, mu 1 subunit |
Homo sapiens | ENSG00000070718 | adaptor-related protein complex 3, mu 2 subunit |
Leishmania braziliensis | LbrM.20.2150 | adaptor complex subunit medium chain 3, putative |
Leishmania donovani | LdBPK_342420.1 | AP-3 complex subunit mu, putative |
Leishmania infantum | LinJ.34.2420 | adaptor complex subunit medium chain 3, putative |
Leishmania major | LmjF.34.2590 | adaptor complex subunit medium chain 3, putative |
Leishmania mexicana | LmxM.33.2590 | adaptor complex subunit medium chain 3, putative |
Loa Loa (eye worm) | LOAG_13462 | hypothetical protein |
Loa Loa (eye worm) | LOAG_02604 | hypothetical protein |
Loa Loa (eye worm) | LOAG_02605 | hypothetical protein |
Mus musculus | 55946 | adaptor-related protein complex 3, mu 1 subunit |
Mus musculus | ENSMUSG00000031539 | adaptor-related protein complex 3, mu 2 subunit |
Oryza sativa | 4338648 | Os05g0383100 |
Schistosoma japonicum | Sjp_0049390 | AP-3 complex subunit mu-1, putative |
Schistosoma mansoni | Smp_027010.2 | clathrin coat adaptor ap3 medium chain |
Schistosoma mansoni | Smp_027010.1 | clathrin coat adaptor ap3 medium chain |
Schmidtea mediterranea | mk4.000685.06 | |
Schmidtea mediterranea | mk4.001966.01 | |
Trypanosoma brucei gambiense | Tbg972.4.1940 | mu-adaptin 3, putative,adaptor complex AP-3 medium subunit, putative |
Trypanosoma brucei | Tb927.4.2020 | AP-3 complex subunit mu, putative |
Trypanosoma congolense | TcIL3000_4_1760 | AP-3 complex subunit mu, putative |
Trypanosoma cruzi | TcCLB.510877.50 | AP-3 complex subunit mu, putative |
Trichomonas vaginalis | TVAG_476310 | clathrin coat adaptor ap3 medium chain, putative |
Trichomonas vaginalis | TVAG_136750 | clathrin coat adaptor ap3 medium chain, putative |
Trichomonas vaginalis | TVAG_450230 | clathrin coat associated protein ap-50, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.4.2020 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.4.2020 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.4.2020 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.4.2020 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F53H8.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_F53H8.1 | Caenorhabditis elegans | larval arrest | wormbase |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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.