pI: 5.7165 |
Length (AA): 876 |
MW (Da): 100508 |
Paralog Number:
2
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 7 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 |
---|---|---|---|---|---|---|---|---|---|
396 | 647 | 1fch (A) | 285 | 574 | 19.00 | 0.0000000000063 | 1 | 0.56 | -0.57 |
495 | 591 | 1na0 (A) | 8 | 104 | 25.00 | 0.000011 | 0.94 | 0.63 | -1.85 |
204 | 314 | 4s3l (A) | 136 | 249 | 28.00 | 0.6 | 0.02 | 0.105212 | 1.95 |
421 | 725 | 4i1a (B) | 14 | 363 | 15.00 | 0 | 1 | 0.411274 | 0.3 |
532 | 605 | 3cv0 (A) | 351 | 424 | 20.00 | 0 | 1 | 0.479575 | -1.22 |
532 | 609 | 1fch (A) | 300 | 377 | 14.00 | 0 | 0.51 | 0.380141 | -1.27 |
711 | 835 | 2fo7 (A) | 4 | 131 | 10.00 | 0.000031 | 0.03 | 0.222994 | -0.3 |
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 |
---|---|---|---|
Mid 40-60% percentile | epimastigote. | Smircich P |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | metacyclic. | Smircich P |
Smircich P | Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi. |
Ortholog group members (OG5_128247)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G37130 | tetratricopeptide repeat domain-containing protein |
Arabidopsis thaliana | AT5G17270 | tetratricopeptide repeat-containing protein |
Babesia bovis | BBOV_IV006090 | tetratricopeptide repeat containing domain protein |
Brugia malayi | Bm1_46435 | Transcription initiation factor TFIID subunit A family protein |
Candida albicans | CaO19.12816 | similar to S. cerevisiae YNL313C |
Candida albicans | CaO19.5356 | similar to S. cerevisiae YNL313C |
Caenorhabditis elegans | CELE_T20B12.1 | Protein T20B12.1 |
Cryptosporidium hominis | Chro.20342 | hypothetical protein |
Cryptosporidium parvum | cgd2_3250 | 3x TPR domain-containing protein |
Dictyostelium discoideum | DDB_G0293372 | tetratricopeptide repeat domain 27 |
Drosophila melanogaster | Dmel_CG5290 | CG5290 gene product from transcript CG5290-RA |
Echinococcus granulosus | EgrG_000240000 | tetratricopeptide repeat protein 27 |
Entamoeba histolytica | EHI_122710 | hypothetical protein, conserved |
Echinococcus multilocularis | EmuJ_000240000 | tetratricopeptide repeat protein 27 |
Homo sapiens | ENSG00000018699 | tetratricopeptide repeat domain 27 |
Leishmania braziliensis | LbrM.17.1400 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_171340.1 | hypothetical protein, conserved |
Leishmania infantum | LinJ.17.1340 | hypothetical protein, conserved |
Leishmania major | LmjF.17.1240 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.17.1240 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_01905 | hypothetical protein |
Mus musculus | ENSMUSG00000024078 | tetratricopeptide repeat domain 27 |
Neospora caninum | NCLIV_041560 | hypothetical protein |
Oryza sativa | 4343142 | Os07g0455100 |
Onchocerca volvulus | OVOC8858 | Tetratricopeptide repeat protein 27 homolog |
Plasmodium berghei | PBANKA_1409300 | conserved Plasmodium protein, unknown function |
Plasmodium falciparum | PF3D7_1310800 | conserved Plasmodium protein, unknown function |
Plasmodium knowlesi | PKNH_1411200 | conserved Plasmodium protein, unknown function |
Plasmodium vivax | PVX_122370 | hypothetical protein, conserved |
Plasmodium yoelii | PY02799 | unnamed protein product |
Saccharomyces cerevisiae | YNL313C | Emw1p |
Schistosoma japonicum | Sjp_0121070 | Tetratricopeptide repeat protein 27, putative |
Schistosoma mansoni | Smp_152860 | hypothetical protein |
Schmidtea mediterranea | mk4.001454.04 | |
Trypanosoma brucei gambiense | Tbg972.5.3560 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.5.2520 | TPR repeat, putative |
Trypanosoma congolense | TcIL3000_5_2410 | Tetratricopeptide repeat/TPR repeat, putative |
Trypanosoma cruzi | TcCLB.509177.10 | TPR repeat, putative |
Trypanosoma cruzi | TcCLB.511303.110 | TPR repeat, putative |
Trypanosoma cruzi | TcCLB.509175.18 | TPR repeat, putative |
Toxoplasma gondii | TGME49_289190 | tetratricopeptide repeat-containing protein |
Theileria parva | TP01_0417 | hypothetical protein, conserved |
Theileria parva | TP01_0415 | hypothetical protein |
Trichomonas vaginalis | TVAG_208660 | TPR repeat-containing protein T20B12.1, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.5.2520 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.5.2520 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.5.2520 | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb927.5.2520 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_T20B12.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_T20B12.1 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_T20B12.1 | Caenorhabditis elegans | slow growth | wormbase |
CELE_T20B12.1 | Caenorhabditis elegans | sterile | wormbase |
YNL313C | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_289190 | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
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 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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.