pI: 6.4982 |
Length (AA): 449 |
MW (Da): 48311 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
90 | 171 | 5eyo (A) | 23 | 104 | 48.00 | 0 | 0.77 | 0.870228 | -1.44 |
90 | 141 | 4h10 (A) | 72 | 125 | 27.00 | 0 | 0.74 | 0.480513 | -1.26 |
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_132718)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G38860 | transcription factor BIM3 |
Brugia malayi | Bm1_19765 | Helix-loop-helix DNA-binding domain containing protein |
Caenorhabditis elegans | CELE_F46G10.6 | Protein MXL-3 |
Drosophila melanogaster | Dmel_CG9648 | CG9648 gene product from transcript CG9648-RD |
Echinococcus granulosus | EgrG_000451950 | bhlhzip transcription factor max:bigmax |
Echinococcus multilocularis | EmuJ_000451950 | bhlhzip transcription factor max:bigmax |
Homo sapiens | ENSG00000125952 | MYC associated factor X |
Loa Loa (eye worm) | LOAG_06802 | helix-loop-helix DNA-binding domain-containing protein |
Mus musculus | ENSMUSG00000059436 | Max protein |
Schistosoma japonicum | Sjp_0217460 | ko:K04453 Max protein, putative |
Schistosoma mansoni | Smp_068220 | bhlhzip transcription factor max/bigmax |
Schmidtea mediterranea | mk4.000488.03 | Putative bhlhzip transcription factor max/bigmax |
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.