pI: 9.9824 |
Length (AA): 762 |
MW (Da): 89160 |
Paralog Number:
3
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:
PDB Structures:
Ortholog group members (OG5_127895)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G42400 | histone methyltransferase SDG25 |
Babesia bovis | BBOV_III006000 | SET domain containing protein |
Brugia malayi | Bm1_45235 | SET domain containing protein |
Candida albicans | CaO19.6009 | potential histone lysine methyltransferase, similar to S. cerevisiae SET1 (YHR119W) subunit of the COMPASS histone methyltransfe |
Candida albicans | CaO19.13430 | potential histone lysine methyltransferase, similar to S. cerevisiae SET1 (YHR119W) subunit of the COMPASS histone methyltransfe |
Caenorhabditis elegans | CELE_C26E6.9 | Protein SET-2, isoform B |
Cryptosporidium hominis | Chro.80318 | SET-domain protein |
Cryptosporidium parvum | cgd8_2730 | multidomain chromatinic protein with the following architecture: 3x PHD-bromo-3xPHD-SET domain and associated cysteine cluster a |
Dictyostelium discoideum | DDB_G0289257 | SET domain-containing protein |
Drosophila melanogaster | Dmel_CG40351 | CG40351 gene product from transcript CG40351-RF |
Giardia lamblia | GL50803_13838 | Hypothetical protein |
Homo sapiens | ENSG00000139718 | SET domain containing 1B |
Homo sapiens | ENSG00000099381 | SET domain containing 1A |
Loa Loa (eye worm) | LOAG_01475 | hypothetical protein |
Loa Loa (eye worm) | LOAG_11302 | histone methyltransferase |
Mus musculus | ENSMUSG00000042308 | SET domain containing 1A |
Mus musculus | ENSMUSG00000038384 | SET domain containing 1B |
Oryza sativa | 4352779 | Os12g0613200 |
Plasmodium berghei | PBANKA_1128500 | SET domain protein, putative |
Plasmodium falciparum | PF3D7_0629700 | SET domain protein, putative |
Plasmodium knowlesi | PKNH_1119800 | SET domain protein, putative |
Plasmodium vivax | PVX_114585 | SET domain containing protein |
Plasmodium yoelii | PY00684 | Bromodomain, putative |
Plasmodium yoelii | PY02230 | similar to KIAA0304 gene product-related |
Saccharomyces cerevisiae | YHR119W | Set1p |
Schmidtea mediterranea | mk4.001072.06 | Probable histone-lysine N-methyltransferase set-2 |
Theileria parva | TP04_0805 | SET-domain protein, putative |
Theileria parva | TP04_0804 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_127920 | mixed-lineage leukemia protein, mll, putative |
Trichomonas vaginalis | TVAG_185780 | mixed-lineage leukemia protein, mll, putative |
Trichomonas vaginalis | TVAG_440830 | PHD finger protein, putative |
Trichomonas vaginalis | TVAG_162900 | mixed-lineage leukemia protein, mll, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_C26E6.9 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_1128500 | Plasmodium berghei | Essential | plasmo |
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 |
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 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
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.