pI: 10.3078 |
Length (AA): 328 |
MW (Da): 39170 |
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 |
---|---|---|---|---|---|---|---|---|---|
123 | 212 | 2cxh (A) | 15 | 107 | 23.00 | 0.000000000016 | 0.38 | 0.53 | -1.13 |
2 | 163 | 4uos (A) | 2 | 176 | 14.00 | 0.063 | 0 | 0.584002 | -0.45 |
119 | 312 | 5a53 (C) | 25 | 250 | 16.00 | 0 | 0.31 | 0.635563 | 0.02 |
2 | 175 | 4uos (A) | 2 | 184 | 13.00 | 0.16 | 0.01 | 0.672188 | -0.72 |
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 - 8 hs, intra-erythrocytic - 16 hs, intra-erythrocytic - 24 hs, Ring. | Otto TD Zanghi G |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intra-erythrocytic - 0 hs, intra-erythrocytic - 32 hs, gametocyte, merozoite, sporozoite, early ring, early trophozoite, late ring, late trophozoite. | Otto TD PlasmoDB |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 48 hs, early schizont, Oocyst, Female Gametocyte. | Otto TD PlasmoDB Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | intra-erythrocytic - 40 hs, Sporozoite, Male Gametocyte. | Otto TD Zanghi G Lasonder E |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
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. |
PlasmoDB | Data on upregulation of P. falciparum genes in different life cycle stages, combined from several microarray experiments available in PlasmoDB |
Ortholog group members (OG5_128253)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G01560 | protein MATERNAL EFFECT EMBRYO ARREST 49 |
Babesia bovis | BBOV_IV002520 | RNA processing factor 1, putative |
Brugia malayi | Bm1_43415 | Brix domain containing protein |
Candida albicans | CaO19.2667 | brix domain protein similar to S. cerevisiae RPF1 (YHR088W) nucleolar protein involved in 60S ribosomal subunit biogenesis |
Candida albicans | CaO19.10184 | brix domain protein similar to S. cerevisiae RPF1 (YHR088W) nucleolar protein involved in 60S ribosomal subunit biogenesis |
Caenorhabditis elegans | CELE_F44G4.1 | Protein F44G4.1 |
Cryptosporidium hominis | Chro.20022 | hypothetical protein |
Cryptosporidium parvum | cgd2_160 | IMP4-like U3 small nucleolar ribonucleoprotein (snoRNP) |
Dictyostelium discoideum | DDB_G0285829 | brix domain-containing protein |
Drosophila melanogaster | Dmel_CG6712 | CG6712 gene product from transcript CG6712-RA |
Echinococcus granulosus | EgrG_000592900 | ribosome production factor 1 |
Entamoeba histolytica | EHI_126010 | ribosome biogenesis protein, putative |
Echinococcus multilocularis | EmuJ_000592900 | ribosome production factor 1 |
Giardia lamblia | GL50803_17112 | U3 small nucleolar ribonucleoprotein protein IMP4, putative |
Homo sapiens | 80135 | ribosome production factor 1 homolog (S. cerevisiae) |
Leishmania braziliensis | LbrM.27.0540 | RNA processing factor 1, putative,ribosome biogenesis protein |
Leishmania donovani | LdBPK_270460.1 | ribosome production factor 1, putative |
Leishmania infantum | LinJ.27.0460 | RNA processing factor 1, putative,ribosome biogenesis protein |
Leishmania major | LmjF.27.0450 | RNA processing factor 1, putative,ribosome biogenesis protein |
Leishmania mexicana | LmxM.27.0450 | RNA processing factor 1, putative,ribosome biogenesis protein |
Loa Loa (eye worm) | LOAG_06925 | brix domain-containing protein |
Mus musculus | ensembl-mmu:ENSMUSG00000028187 | ribosome production factor 1 homolog (S. cerevisiae) |
Neospora caninum | NCLIV_066680 | hypothetical protein |
Oryza sativa | 4340048 | Os06g0137500 |
Onchocerca volvulus | OVOC10541 | Putative ribosome production factor 1 |
Plasmodium berghei | PBANKA_0822700 | ribosome production factor 1, putative |
Plasmodium falciparum | PF3D7_0921800 | ribosome production factor 1, putative |
Plasmodium knowlesi | PKNH_0719800 | ribosome production factor 1, putative |
Plasmodium vivax | PVX_099507 | hypothetical protein, conserved |
Saccharomyces cerevisiae | YHR088W | Rpf1p |
Schistosoma japonicum | Sjp_0212760 | Ribosome production factor 1, putative |
Schistosoma mansoni | Smp_145800 | U3 small nucleolar ribonucleoprotein protein imp4 |
Schmidtea mediterranea | mk4.011562.00 | Probable ribosome production factor 1 |
Schmidtea mediterranea | mk4.007152.00 | Probable ribosome production factor 1 |
Trypanosoma brucei gambiense | Tbg972.11.1130 | RNA processing factor 1, putative,ribosome biogenesis protein |
Trypanosoma brucei | Tb927.11.1050 | ribosome production factor 1, putative |
Trypanosoma congolense | TcIL3000.11.990 | ribosome production factor 1, putative |
Trypanosoma cruzi | TcCLB.506925.510 | ribosome production factor 1, putative |
Toxoplasma gondii | TGME49_251600 | IMP4 family U3 small nucleolar ribonucleoprotein (snoRNP), putative |
Theileria parva | TP03_0398 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_495410 | U3 small nucleolar ribonucleoprotein imp4, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb11.03.0050 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb11.03.0050 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb11.03.0050 | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb11.03.0050 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F44G4.1 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_F44G4.1 | Caenorhabditis elegans | slow growth | wormbase |
YHR088W | Saccharomyces cerevisiae | inviable | yeastgenome |
TGME49_251600 | 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 |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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.