pI: 10.2335 |
Length (AA): 153 |
MW (Da): 18141 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
1 | 129 | 2rtx (A) | 1 | 119 | 25.00 | 0 | 0.68 | 1.01034 | 0.29 |
14 | 106 | 1j26 (A) | 17 | 109 | 35.00 | 0.000000000017 | 1 | 1.15944 | -1.1 |
1 | 122 | 2rtx (A) | 1 | 117 | 25.00 | 0 | 0.5 | 1.17456 | 0.01 |
10 | 107 | 1j26 (A) | 13 | 110 | 35.00 | 0 | 1 | 1.26195 | -0.78 |
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 | intra-erythrocytic - 32 hs. | Otto TD |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intra-erythrocytic - 24 hs, intra-erythrocytic - 40 hs, intra-erythrocytic - 48 hs, Oocyst. | Otto TD Zanghi G |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 8 hs, intra-erythrocytic - 16 hs, Sporozoite, Female Gametocyte. | Otto TD Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | intra-erythrocytic - 0 hs, Ring, Male Gametocyte. | Otto TD Zanghi G Lasonder E |
Otto TD | New insights into the blood-stage transcriptome of Plasmodium falciparum using RNA-Seq. |
Lasonder E | Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes. Molecular insight into sex-specific processes and translational repression. |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
Ortholog group members (OG5_128349)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G62850 | Class I peptide chain release factor |
Brugia malayi | Bm1_53040 | Hypothetical 23.2 kDa protein in SKM1-TRF4 intergenic region |
Candida albicans | CaO19.8055 | similar to S. cerevisiae YOL114C |
Candida albicans | CaO19.425 | similar to S. cerevisiae YOL114C |
Caenorhabditis elegans | CELE_R02F2.9 | Protein R02F2.9 |
Dictyostelium discoideum | DDB_G0272142 | hypothetical protein |
Drosophila melanogaster | Dmel_CG6094 | CG6094 gene product from transcript CG6094-RB |
Escherichia coli | b0191 | alternative stalled-ribosome rescue factor B |
Echinococcus granulosus | EgrG_001118500 | Class I peptide chain release factor |
Echinococcus multilocularis | EmuJ_001118500 | Class I peptide chain release factor |
Homo sapiens | ENSG00000167862 | immature colon carcinoma transcript 1 |
Leishmania braziliensis | LbrM.30.1180 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_301120.1 | RF-1 domain containing protein, putative |
Leishmania infantum | LinJ.30.1120 | hypothetical protein, conserved |
Leishmania major | LmjF.30.1060 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.29.1060 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_06021 | hypothetical protein |
Mus musculus | ENSMUSG00000018858 | immature colon carcinoma transcript 1 |
Oryza sativa | 4332255 | Os03g0249200 |
Plasmodium berghei | PBANKA_0930400 | peptidyl-tRNA hydrolase ICT1, putative |
Plasmodium falciparum | PF3D7_1117600 | peptidyl-tRNA hydrolase ICT1, peptidyl-tRNA hydrolase ICT1, putative |
Plasmodium knowlesi | PKNH_0915300 | peptidyl-tRNA hydrolase ICT1, putative |
Plasmodium vivax | PVX_091510 | Immature colon carcinoma transcript 1, putative |
Saccharomyces cerevisiae | YOL114C | hypothetical protein |
Schistosoma japonicum | Sjp_0213280 | Immature colon carcinoma transcript 1 protein precursor, putative |
Schistosoma mansoni | Smp_086710 | hypothetical protein |
Schmidtea mediterranea | mk4.000718.03 | Peptidyl-tRNA hydrolase ICT1, mitochondrial |
Trypanosoma brucei gambiense | Tbg972.6.2260 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.6.2500 | RF-1 domain containing protein, putative |
Trypanosoma congolense | TcIL3000_6_2000 | RF-1 domain containing protein, putative |
Trypanosoma cruzi | TcCLB.509965.210 | RF-1 domain containing protein, putative |
Trypanosoma cruzi | TcCLB.509053.150 | RF-1 domain containing protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.6.2500 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.6.2500 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.6.2500 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.6.2500 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b0191 | Escherichia coli | non-essential | goodall |
PBANKA_0930400 | Plasmodium berghei | Dispensable | plasmo |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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.