pI: 6.3437 |
Length (AA): 492 |
MW (Da): 55017 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
40 | 488 | 5ejj (A) | 132 | 572 | 32.00 | 0 | 1 | 1.0286 | 0.98 |
193 | 485 | 5ejj (A) | 294 | 569 | 41.00 | 0 | 1 | 0.896528 | 0.11 |
267 | 486 | 2z84 (A) | 8 | 216 | 33.00 | 0 | 1 | 0.851154 | -0.4 |
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 |
---|---|---|---|
NA% percentile | Procyclic. | Siegel TN |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% 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_129023)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G48380 | putative Ufm1-specific protease |
Babesia bovis | BBOV_III009030 | protein of unknown function (DUF1671) protein family |
Brugia malayi | Bm1_39095 | hypothetical protein |
Caenorhabditis elegans | CELE_F38A5.1 | Protein F38A5.1, isoform B |
Cryptosporidium hominis | Chro.60116 | CG16979 protein |
Cryptosporidium parvum | cgd6_900 | SPAC25H1.04/CG16979-cterm -like; cysteine protease |
Dictyostelium discoideum | DDB_G0282953 | hypothetical protein |
Drosophila melanogaster | Dmel_CG16979 | CG16979 gene product from transcript CG16979-RA |
Drosophila melanogaster | Dmel_CG30157 | CG30157 gene product from transcript CG30157-RA |
Echinococcus granulosus | EgrG_000627900 | E3 ubiquitin protein ligase listerin |
Echinococcus granulosus | EgrG_000799700 | ufm1 specific protease 1 |
Echinococcus granulosus | EgrG_000586500 | Ufm1 specific protease 2 |
Echinococcus multilocularis | EmuJ_000799700 | ufm1 specific protease 1 |
Echinococcus multilocularis | EmuJ_000627900 | E3 ubiquitin protein ligase listerin |
Echinococcus multilocularis | EmuJ_000586500 | Ufm1 specific protease 2 |
Homo sapiens | 55325 | UFM1-specific peptidase 2 |
Homo sapiens | ENSG00000176125 | UFM1-specific peptidase 1 (non-functional) |
Leishmania braziliensis | LbrM.20.3630 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_343830.1 | Peptidase family C78, putative |
Leishmania infantum | LinJ.34.3830 | hypothetical protein, conserved |
Leishmania major | LmjF.34.4000 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.33.4000 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_03930 | Ufm1-specific protease 2 |
Mus musculus | ENSMUSG00000051502 | UFM1-specific peptidase 1 |
Mus musculus | ENSMUSG00000031634 | UFM1-specific peptidase 2 |
Neospora caninum | NCLIV_060120 | hypothetical protein, conserved |
Oryza sativa | 4351994 | Os12g0285500 |
Schistosoma japonicum | Sjp_0213530 | expressed protein |
Schistosoma japonicum | Sjp_0082310 | Probable Ufm1-specific protease 2, putative |
Schistosoma japonicum | Sjp_0213520 | Zinc finger protein 294, putative |
Schistosoma japonicum | Sjp_0213540 | expressed protein |
Schistosoma japonicum | Sjp_0308760 | IPR012462,Peptidase, ubiquitin fold modifier-specific,domain-containing |
Schistosoma japonicum | Sjp_0215670 | ko:K01376 Peptidase, ubiquitin fold modifier-specific [EC:3.4.22.-], putative |
Schistosoma japonicum | Sjp_0317800 | Ufm1-specific protease 2, putative |
Schistosoma japonicum | Sjp_0116050 | expressed protein |
Schistosoma mansoni | Smp_179040 | UfSP2 peptidase (C78 family) |
Schmidtea mediterranea | mk4.006398.01 | Probable Ufm1-specific protease |
Trypanosoma brucei gambiense | Tbg972.4.500 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.4.730 | Peptidase family C78, putative |
Trypanosoma congolense | TcIL3000_0_00270 | Peptidase family C78, putative |
Trypanosoma cruzi | TcCLB.507053.30 | Peptidase family C78, putative |
Toxoplasma gondii | TGME49_216020 | peptidase family c78 protein |
Theileria parva | TP04_0807 | hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.4.730 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.4.730 this record | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.4.730 this record | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.4.730 this record | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
TGME49_216020 | Toxoplasma gondii | Essentiality uncertain | 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 |
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 |
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 |
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) | 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 3 days). | References: | 21363968 | |
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 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.
1 literature reference was collected for this gene.