pI: 6.0063 |
Length (AA): 430 |
MW (Da): 48327 |
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 is 1 model calculated for this protein. More info on
this model, including the
model itself is available at:
Modbase
Target Beg | Target End | Template | Template Beg | Template End | Identity | Evalue | Model Score | MPQS | zDope |
---|---|---|---|---|---|---|---|---|---|
62 | 216 | 4uos (A) | 19 | 172 | 16.00 | 0.033 | 0.05 | 0.625965 | -1.27 |
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 |
---|---|---|---|
Mid 40-60% percentile | amastigotes, metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_129228)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G28560 | protein shoot redifferentiation defective 2 |
Babesia bovis | BBOV_III010690 | hypothetical protein |
Brugia malayi | Bm1_46635 | hypothetical protein |
Caenorhabditis elegans | CELE_B0273.3 | Protein B0273.3 |
Caenorhabditis elegans | CELE_Y48G1BM.1 | Protein Y48G1BM.1 |
Caenorhabditis elegans | CELE_T02C12.2 | Protein T02C12.2 |
Cryptosporidium hominis | Chro.70130 | hypothetical protein |
Cryptosporidium parvum | cgd7_1050 | hypothetical protein |
Dictyostelium discoideum | DDB_G0274687 | hypothetical protein |
Drosophila melanogaster | Dmel_CG42515 | PSEA-binding protein 49kD |
Drosophila melanogaster | Dmel_CG42516 | CG42516 gene product from transcript CG42516-RB |
Echinococcus granulosus | EgrG_000128600 | expressed conserved protein |
Echinococcus granulosus | EgrG_000128500 | snRNA activating protein complex subunit 3 |
Entamoeba histolytica | EHI_197110 | snRNA activating protein complex subunit, putative |
Echinococcus multilocularis | EmuJ_000128500 | snRNA activating protein complex subunit 3 |
Echinococcus multilocularis | EmuJ_000128600 | expressed conserved protein |
Homo sapiens | 6619 | small nuclear RNA activating complex, polypeptide 3, 50kDa |
Leishmania braziliensis | LbrM.34.4640 | small nuclear RNA gene activation protein (SNAP) 50, putative |
Leishmania donovani | LdBPK_354730.1 | small nuclear RNA gene activation protein (SNAP) 50, putative |
Leishmania infantum | LinJ.35.4730 | small nuclear RNA gene activation protein (SNAP) 50, putative |
Leishmania major | LmjF.35.4660 | small nuclear RNA gene activation protein (SNAP) 50, putative |
Leishmania mexicana | LmxM.34.4660 | small nuclear RNA gene activation protein (SNAP) 50, putative |
Loa Loa (eye worm) | LOAG_10462 | hypothetical protein |
Mus musculus | ENSMUSG00000028483 | small nuclear RNA activating complex, polypeptide 3 |
Oryza sativa | 4324317 | Os01g0912600 |
Plasmodium berghei | PBANKA_1324500 | snRNA-activating protein complex subunit 3, putative |
Plasmodium falciparum | PF3D7_1460800 | snRNA-activating protein complex subunit 3, putative |
Plasmodium knowlesi | PKNH_1220900 | snRNA-activating protein complex subunit 3, putative |
Plasmodium vivax | PVX_117415 | snRNA-activating protein complex subunit 3, putative |
Plasmodium yoelii | PY05165 | hypothetical protein |
Schistosoma japonicum | Sjp_0214600 | snRNA-activating protein complex subunit 3, putative |
Schistosoma mansoni | Smp_092780.1 | hypothetical protein |
Schistosoma mansoni | Smp_092780.2 | hypothetical protein |
Schmidtea mediterranea | mk4.010426.00 | snRNA-activating protein complex subunit 3 |
Trypanosoma brucei gambiense | Tbg972.9.5750 | small nuclear RNA gene activation protein (SNAP) 50, putative |
Trypanosoma brucei | Tb927.9.9970 | Small nuclear RNA gene activation protein (SNAP) 50 |
Trypanosoma congolense | TcIL3000_9_3640 | small nuclear RNA gene activation protein 50 (EMBL:AJ581666) |
Trypanosoma cruzi | TcCLB.510731.50 | small nuclear RNA gene activation protein (SNAP) 50, putative |
Trypanosoma cruzi | TcCLB.506887.60 | small nuclear RNA gene activation protein (SNAP) 50, putative |
Theileria parva | TP02_0077 | hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.1510 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.1510 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.1510 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb09.211.1510 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_T02C12.2 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_T02C12.2 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_T02C12.2 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_T02C12.2 | Caenorhabditis elegans | slow growth | wormbase |
CELE_T02C12.2 | Caenorhabditis elegans | sterile | wormbase |
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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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.