pI: 6.4404 |
Length (AA): 1366 |
MW (Da): 154703 |
Paralog Number:
2
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:
PDB Structures:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | Procyclic, 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_127440)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G48600 | structural maintenance of chromosomes protein 4 |
Babesia bovis | BBOV_III010300 | SMC family, C-terminal domain containing protein |
Brugia malayi | Bm1_07830 | SMC family, C-terminal domain containing protein |
Candida albicans | CaO19.8579 | potential SMC chromosomal ATPase similar to S. cerevisiae SMC4 (YLR086W) nuclear condensin complex ATPase |
Candida albicans | CaO19.964 | potential SMC chromosomal ATPase similar to S. cerevisiae SMC4 (YLR086W) nuclear condensin complex ATPase |
Caenorhabditis elegans | CELE_F35G12.8 | Protein SMC-4 |
Caenorhabditis elegans | CELE_R13G10.1 | Protein DPY-27 |
Cryptosporidium hominis | Chro.70215 | stable maintenance of chromosomes; Smc4p |
Cryptosporidium parvum | cgd7_1850 | SMC4SMC4, chromosomal ATpase with giant coiled coil regions |
Dictyostelium discoideum | DDB_G0286403 | structural maintenance of chromosome protein |
Drosophila melanogaster | Dmel_CG11397 | gluon |
Echinococcus granulosus | EgrG_000517500 | structural maintenance of chromosomes protein |
Entamoeba histolytica | EHI_199700 | SMC4 protein, putative |
Echinococcus multilocularis | EmuJ_000517500 | structural maintenance of chromosomes protein |
Giardia lamblia | GL50803_17465 | SMC4-like protein |
Homo sapiens | ENSG00000113810 | structural maintenance of chromosomes 4 |
Leishmania braziliensis | LbrM.21.1570 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_211580.1 | RecF/RecN/SMC N terminal domain/SMC proteins Flexible Hinge Domain, putative |
Leishmania infantum | LinJ.21.1580 | hypothetical protein, conserved |
Leishmania major | LmjF.21.1330 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.21.1330partial | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_02100 | hypothetical protein |
Loa Loa (eye worm) | LOAG_10473 | hypothetical protein |
Loa Loa (eye worm) | LOAG_10474 | Smc4l1 protein |
Mycobacterium leprae | ML1629c | PROBABLE CHROMOSOME PARTITION PROTEIN SMC |
Mus musculus | ENSMUSG00000034349 | structural maintenance of chromosomes 4 |
Neospora caninum | NCLIV_031540 | chromosome condensation protein, putative |
Oryza sativa | 9267154 | Os05g0497100 |
Onchocerca volvulus | OVOC2348 |
|
Plasmodium berghei | PBANKA_1108700 | structural maintenance of chromosomes protein 4, putative |
Plasmodium falciparum | PF3D7_0509100 | structural maintenance of chromosomes protein 4, putative |
Plasmodium knowlesi | PKNH_1024500 | structural maintenance of chromosomes protein 4, putative |
Plasmodium vivax | PVX_098020 | chromosome condensation protein, putative |
Plasmodium yoelii | PY03258 | chromosome assembly protein xcap-c |
Saccharomyces cerevisiae | YLR086W | condensin subunit SMC4 |
Schistosoma japonicum | Sjp_0302410 | ko:K06675 structural maintenance of chromosome 4, putative |
Schistosoma japonicum | Sjp_0084840 | ko:K06675 structural maintenance of chromosome 4, putative |
Schistosoma mansoni | Smp_173700 | chondroitin sulfate proteoglycan |
Schmidtea mediterranea | mk4.000285.04 | Structural maintenance of chromosomes protein 4 |
Schmidtea mediterranea | mk4.000285.05 | |
Trypanosoma brucei gambiense | Tbg972.10.760 | structural maintenance of chromosome 4, putative |
Trypanosoma brucei | Tb927.10.740 | structural maintenance of chromosome 4, putative |
Trypanosoma brucei | Tb11.v5.0750 | dual specificity protein phosphatase, putative |
Trypanosoma brucei | Tb11.v5.0749 | structural maintenance of chromosome 4, putative |
Trypanosoma congolense | TcIL3000_10_600 | structural maintenance of chromosome 4, putative |
Trypanosoma cruzi | TcCLB.506855.90 | structural maintenance of chromosome protein 4, putative |
Trypanosoma cruzi | TcCLB.508779.90 | structural maintenance of chromosome protein 4, putative |
Toxoplasma gondii | TGME49_231170 | RecF/RecN/SMC N terminal domain-containing protein |
Treponema pallidum | TP0367 | chromosome segregation protein |
Theileria parva | TP02_0117 | hypothetical protein |
Trichomonas vaginalis | TVAG_160280 | condensin subunit Smc4 |
Trichomonas vaginalis | TVAG_434480 | condensin subunit Smc4 |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.740 this record | Trypanosoma brucei | significant gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.740 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.740 this record | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.740 this record | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_R13G10.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_R13G10.1 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_R13G10.1 | Caenorhabditis elegans | slow growth | wormbase |
CELE_F35G12.8 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_F35G12.8 | Caenorhabditis elegans | larval arrest | wormbase |
YLR086W | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_231170 | Toxoplasma gondii | Probably essential | sidik |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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 |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
Affected Entity | Phenotypic quality | Occurs in | Occurs at | Evidence | Observed in | Drugs/Inhibitors |
---|---|---|---|---|---|---|
cell proliferation (GO:0008283) | increased (PATO:0000470) | 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: | increased cell proliferation (significant gain of fitness) in bloodstream forms (stage 3 days). | References: | 21363968 | |
cell proliferation (GO:0008283) | normal (PATO:0000461) | 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: | normal cell proliferation (no significant loss or gain of fitness) in bloodstream forms (stage 6 days). | 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.
Druggability index (range: 0 to 1): 0.4
1 literature reference was collected for this gene.