pI: 9.5288 |
Length (AA): 286 |
MW (Da): 32301 |
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 |
---|---|---|---|---|---|---|---|---|---|
15 | 206 | 4qtu (B) | 12 | 202 | 53.00 | 0 | 1 | 1.40883 | -1.44 |
38 | 271 | 3kr9 (A) | 2 | 217 | 16.00 | 0 | 1 | 0.850082 | 0.31 |
56 | 129 | 3cc8 (A) | 35 | 107 | 36.00 | 0.006 | 0.58 | 0.595241 | 0.05 |
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_128094)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G57280 | methyltransferase-like protein |
Babesia bovis | BBOV_III004000 | conserved hypothetical protein |
Brugia malayi | Bm1_15635 | hypothetical protein |
Candida albicans | CaO19.9522 | similar to rat methylglycine transferase |
Candida albicans | CaO19.1966 | similar to rat methylglycine transferase |
Caenorhabditis elegans | CELE_C27F2.4 | Protein C27F2.4 |
Cryptosporidium hominis | Chro.10303 | S-adenosylmethionine-dependentmethyltransferase |
Cryptosporidium parvum | cgd1_2680 | HUSSY-3 like methyltransferase |
Dictyostelium discoideum | DDB_G0269722 | hypothetical protein |
Drosophila melanogaster | Dmel_CG10903 | CG10903 gene product from transcript CG10903-RB |
Echinococcus granulosus | EgrG_000721700 | williams beuren syndrome chromosome region 22 |
Entamoeba histolytica | EHI_029570 | methyltransferase, putative |
Echinococcus multilocularis | EmuJ_000721700 | williams beuren syndrome chromosome region 22 |
Giardia lamblia | GL50803_21512 | S-adenosylmethionine-dependent methyltransferase, putative |
Homo sapiens | ENSG00000071462 | Williams Beuren syndrome chromosome region 22 |
Leishmania braziliensis | LbrM.20.2300 | methyltransferase-like protein |
Leishmania donovani | LdBPK_342580.1 | methyltransferase-like protein |
Leishmania infantum | LinJ.34.2580 | methyltransferase-like protein |
Leishmania major | LmjF.34.2750 | methyltransferase-like protein |
Leishmania mexicana | LmxM.33.2750 | methyltransferase-like protein |
Loa Loa (eye worm) | LOAG_05054 | methyltransferase |
Mus musculus | ENSMUSG00000005378 | Williams Beuren syndrome chromosome region 22 |
Neospora caninum | NCLIV_026450 | hypothetical protein, conserved |
Oryza sativa | 4331056 | Os02g0804300 |
Onchocerca volvulus | OVOC9165 | Ribosome biogenesis methyltransferase WBSCR22 homolog |
Plasmodium berghei | PBANKA_1237000 | 18S rRNA (guanine-N(7))-methyltransferase, putative |
Plasmodium falciparum | PF3D7_0522300 | 18S rRNA (guanine-N(7))-methyltransferase, putative |
Plasmodium knowlesi | PKNH_1010600 | 18S rRNA (guanine-N(7))-methyltransferase, putative |
Plasmodium vivax | PVX_080135 | S-adenosylmethionine-dependent methyltransferase, putative |
Saccharomyces cerevisiae | YCR047C | Bud23p |
Schistosoma japonicum | Sjp_0035040 | ko:K00599 Williams Beuren syndrome chromosome region 22 [EC:2.1.1.-], putative |
Schistosoma mansoni | Smp_166830 | methyltransferase-related |
Trypanosoma brucei gambiense | Tbg972.4.1810 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.4.1900 | Methyltransferase domain/Methyltransferase involved in Williams-Beuren syndrome, putative |
Trypanosoma congolense | TcIL3000_0_39410 | Methyltransferase domain/Methyltransferase involved in Williams-Beuren syndrome, putative |
Trypanosoma congolense | TcIL3000_4_1580 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.503923.30 | Methyltransferase domain/Methyltransferase involved in Williams-Beuren syndrome, putative |
Trypanosoma cruzi | TcCLB.508583.10 | Methyltransferase domain/Methyltransferase involved in Williams-Beuren syndrome, putative |
Toxoplasma gondii | TGME49_260610 | methyltransferase |
Theileria parva | TP03_0020 | methyltransferase, putative |
Trichomonas vaginalis | TVAG_021330 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.4.1900 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.4.1900 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.4.1900 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.4.1900 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_C27F2.4 | Caenorhabditis elegans | slow growth | wormbase |
TGME49_260610 | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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.