pI: 5.6649 |
Length (AA): 860 |
MW (Da): 97841 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: | 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 4 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 |
---|---|---|---|---|---|---|---|---|---|
9 | 849 | 1tr2 (A) | 22 | 913 | 12.00 | 0 | 0.7 | 0.907107 | 0.99 |
612 | 730 | 5h7u (A) | 38 | 159 | 30.00 | 0.51 | 0.3 | 0.109372 | 1.43 |
613 | 798 | 3f57 (A) | 1698 | 1896 | 11.00 | 0 | 0.6 | 0.285479 | -0.45 |
767 | 833 | 5wst (A) | 866 | 932 | 7.00 | 0.65 | 0 | 0.269307 | -1.45 |
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 |
---|---|---|---|
Upper 80-100% percentile | Procyclic. | Siegel TN |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | Bloodstream Form. | Siegel TN |
Siegel TN | Genome-wide analysis of mRNA abundance in two life-cycle stages of Trypanosoma brucei and identification of splicing and polyadenylation sites. |
Ortholog group members (OG5_128086)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G31520 | SDA1 family protein |
Arabidopsis thaliana | AT1G13160 | NUC130/3NT and SDA1 domain-containing protein |
Babesia bovis | BBOV_I002170 | conserved hypothetical protein |
Brugia malayi | Bm1_52515 | SDA1 family protein |
Candida albicans | CaO19.13969 | similar to S. cerevisiae YGR245C |
Candida albicans | CaO19.6648 | similar to S. cerevisiae YGR245C |
Caenorhabditis elegans | CELE_Y39B6A.14 | Protein PRO-3 |
Cryptosporidium hominis | Chro.20363 | severe depolymerization of actin; Sda1p |
Cryptosporidium parvum | cgd2_3430 | SDA1-like protein |
Dictyostelium discoideum | DDB_G0269688 | SDA1 domain-containing protein |
Drosophila melanogaster | Dmel_CG8070 | Mystery 45A |
Echinococcus granulosus | EgrG_001056400 | protein sda1 |
Entamoeba histolytica | EHI_009540 | hypothetical protein, conserved |
Echinococcus multilocularis | EmuJ_001056400 | protein sda1 |
Giardia lamblia | GL50803_16299 | Sda1, severe depolymerization of actin |
Homo sapiens | ENSG00000198301 | SDA1 domain containing 1 |
Leishmania braziliensis | LbrM.17.1500 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_171480.1 | NUC130/3NT domain/SDA1, putative |
Leishmania infantum | LinJ.17.1480 | hypothetical protein, conserved |
Leishmania major | LmjF.17.1370 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.17.1370 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_00368 | hypothetical protein |
Mus musculus | ENSMUSG00000029415 | SDA1 domain containing 1 |
Neospora caninum | NCLIV_001430 | F3F19.18, related |
Oryza sativa | 4337094 | Os04g0630000 |
Plasmodium berghei | PBANKA_0613800 | protein SDA1, putative |
Plasmodium falciparum | PF3D7_0716100 | protein SDA1, putative |
Plasmodium knowlesi | PKNH_0310700 | protein SDA1, putative |
Plasmodium vivax | PVX_000620 | protein SDA1, putative |
Plasmodium yoelii | PY01027 | Drosophila melanogaster LD33051p |
Saccharomyces cerevisiae | YGR245C | Sda1p |
Schistosoma japonicum | Sjp_0032450 | Protein SDA1 homolog, putative |
Schistosoma mansoni | Smp_176520 | hsda/sda1 |
Schmidtea mediterranea | mk4.015334.01 | Protein SDA1 homolog |
Schmidtea mediterranea | mk4.007293.00 | Protein SDA1 homolog |
Trypanosoma brucei gambiense | Tbg972.5.3740 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.5.2660 | NUC130/3NT domain/SDA1, putative |
Trypanosoma congolense | TcIL3000_5_2710 | NUC130/3NT domain/SDA1, putative |
Trypanosoma congolense | TcIL3000_0_09530 | NUC130/3NT domain/SDA1, putative |
Trypanosoma cruzi | TcCLB.509179.110 | NUC130/3NT domain/SDA1, putative |
Trypanosoma cruzi | TcCLB.507047.140 | NUC130/3NT domain/SDA1, putative |
Toxoplasma gondii | TGME49_294430 | hypothetical protein |
Theileria parva | TP03_0112 | hypothetical protein |
Trichomonas vaginalis | TVAG_349040 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.5.2660 this record | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.5.2660 this record | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.5.2660 this record | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.5.2660 this record | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_Y39B6A.14 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_Y39B6A.14 | Caenorhabditis elegans | slow growth | wormbase |
YGR245C | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0613800 | Plasmodium berghei | Essential | plasmo |
TGME49_294430 | Toxoplasma gondii | Probably essential | sidik |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
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 |
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 |
Affected Entity | Phenotypic quality | Occurs in | Occurs at | Evidence | Observed in | Drugs/Inhibitors |
---|---|---|---|---|---|---|
cell proliferation (GO:0008283) | decreased (PATO:0000468) | bloodstream stage trypomastigotes (PLO:0027) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | decreased cell proliferation (significant loss of fitness) in bloodstream forms (stage 6 days). | References: | 21363968 | |
cell proliferation (GO:0008283) | decreased (PATO:0000468) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | decreased cell proliferation (significant loss of fitness) in procyclic forms . | References: | 21363968 | |
cell proliferation (GO:0008283) | normal (PATO:0000461) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | normal cell proliferation (no significant loss or gain of fitness) in differentiation of procyclic to bloodstream forms . | References: | 21363968 |
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.
1 literature reference was collected for this gene.