pI: 4.7652 |
Length (AA): 869 |
MW (Da): 98189 |
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 3 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 |
---|---|---|---|---|---|---|---|---|---|
11 | 868 | 1qbk (B) | 4 | 871 | 63.00 | 0 | 1 | 1.70594 | -0.16 |
35 | 762 | 3w5k (A) | 16 | 749 | 17.00 | 0 | 1 | 0.971745 | 0.08 |
134 | 285 | 3sl9 (A) | 150 | 299 | 11.00 | 0 | 0.85 | 0.483914 | -1.73 |
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_127643)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G16950 | transportin 1 |
Babesia bovis | BBOV_II003640 | transportin, putative |
Brugia malayi | Bm1_44175 | Importin-beta N-terminal domain containing protein |
Candida albicans | CaO19.3556 | Karyopherin/transportin |
Caenorhabditis elegans | CELE_R06A4.4 | Protein IMB-2, isoform A |
Cryptosporidium hominis | Chro.80396 | karyopherin (importin) beta 2 |
Cryptosporidium parvum | cgd8_3440 | importin beta like ARM repeat alpha superhelix |
Dictyostelium discoideum | DDB_G0269948 | hypothetical protein |
Drosophila melanogaster | Dmel_CG8219 | CG8219 gene product from transcript CG8219-RA |
Drosophila melanogaster | Dmel_CG7398 | Transportin |
Echinococcus granulosus | EgrG_000427400 | transportin 1 |
Entamoeba histolytica | EHI_060990 | HEAT repeat domain containing protein |
Echinococcus multilocularis | EmuJ_000427400 | transportin 1 |
Homo sapiens | 3842 | transportin 1 |
Homo sapiens | ENSG00000105576 | transportin 2 |
Leishmania braziliensis | LbrM.34.2280 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_352380.1 | Importin 1 |
Leishmania infantum | LinJ.35.2380 | hypothetical protein, conserved |
Leishmania major | LmjF.35.2330 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.34.2330 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_12124 | importin-beta domain-containing protein |
Loa Loa (eye worm) | LOAG_13613 | Tnpo1 protein |
Mus musculus | ENSMUSG00000031691 | transportin 2 (importin 3, karyopherin beta 2b) |
Mus musculus | ENSMUSG00000009470 | transportin 1 |
Neospora caninum | NCLIV_059680 | CBR-IMB-2 protein, related |
Oryza sativa | 4337505 | Os04g0691500 |
Plasmodium berghei | PBANKA_1126400 | transportin, putative |
Plasmodium falciparum | PF3D7_0627700 | transportin |
Plasmodium knowlesi | PKNH_1122100 | transportin, putative |
Plasmodium vivax | PVX_114490 | transportin, putative |
Plasmodium yoelii | PY02706 | transportin-related |
Saccharomyces cerevisiae | YBR017C | Kap104p |
Schistosoma japonicum | Sjp_0214200 | Transportin-1, putative |
Schistosoma mansoni | Smp_142770 | importin-beta 2 |
Schmidtea mediterranea | mk4.001891.03 | |
Schmidtea mediterranea | mk4.001891.02 | |
Schmidtea mediterranea | mk4.001891.00 | |
Schmidtea mediterranea | mk4.001891.04 | |
Trypanosoma brucei gambiense | Tbg972.9.8490 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.9.13520 | Importin 1 |
Trypanosoma cruzi | TcCLB.510655.90 | Importin 1 |
Toxoplasma gondii | TGME49_216590 | HEAT repeat-containing protein |
Theileria parva | TP04_0218 | transportin, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.4360 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.4360 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.4360 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb09.211.4360 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_R06A4.4 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_R06A4.4 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_R06A4.4 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_R06A4.4 | Caenorhabditis elegans | slow growth | wormbase |
PBANKA_1126400 | Plasmodium berghei | Essential | plasmo |
TGME49_216590 | Toxoplasma gondii | Probably essential | sidik |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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.