pI: 10.4197 |
Length (AA): 300 |
MW (Da): 36075 |
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 2 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 |
---|---|---|---|---|---|---|---|---|---|
51 | 223 | 1tua (A) | 7 | 184 | 15.00 | 0 | 1 | 0.87 | -0.98 |
46 | 219 | 4qmf (D) | 38 | 211 | 61.00 | 0 | 1 | 1.3723 | -0.92 |
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 - 0 hs, intra-erythrocytic - 8 hs, intra-erythrocytic - 16 hs, intra-erythrocytic - 24 hs, merozoite, sporozoite, early ring, early trophozoite, late ring, late trophozoite, Oocyst, Ring. | Otto TD PlasmoDB Zanghi G |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intra-erythrocytic - 32 hs, intra-erythrocytic - 40 hs, gametocyte, early schizont, Female Gametocyte. | Otto TD PlasmoDB Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 48 hs, late schizont, Sporozoite, Male Gametocyte. | Otto TD PlasmoDB Zanghi G Lasonder E |
Otto TD | New insights into the blood-stage transcriptome of Plasmodium falciparum using RNA-Seq. |
PlasmoDB | Data on upregulation of P. falciparum genes in different life cycle stages, combined from several microarray experiments available in PlasmoDB |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
Lasonder E | Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes. Molecular insight into sex-specific processes and translational repression. |
Ortholog group members (OG5_127855)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G08420 | RNA-binding KH domain-containing protein |
Babesia bovis | BBOV_II006650 | Ribosomal RNA assembly protein mis3, putative |
Brugia malayi | Bm1_51375 | Hypothetical 37.2 kDa protein in CHA1-PRD1 intergenic region |
Candida albicans | CaO19.8277 | similar to S. cerevisiae KRR1 (YCL059C) part of nucleolar complex required for 40S ribosome biogenesis |
Candida albicans | CaO19.661 | similar to S. cerevisiae KRR1 (YCL059C) part of nucleolar complex required for 40S ribosome biogenesis |
Caenorhabditis elegans | CELE_C05C8.2 | Protein C05C8.2 |
Cryptosporidium hominis | Chro.30334 | hypothetical protein |
Cryptosporidium parvum | cgd3_2950 | ribosomal RNA assembly protein mis3/dribble/Krr1p. KH domain |
Dictyostelium discoideum | DDB_G0280805 | hypothetical protein |
Drosophila melanogaster | Dmel_CG4258 | dribble |
Echinococcus granulosus | EgrG_000930900 | krr1 small subunit processome component |
Entamoeba histolytica | EHI_142020 | RNA-binding protein, putative |
Echinococcus multilocularis | EmuJ_000930900 | krr1 small subunit processome component |
Giardia lamblia | GL50803_12598 | KRR1 |
Homo sapiens | 11103 | KRR1, small subunit (SSU) processome component, homolog (yeast) |
Leishmania braziliensis | LbrM.30.3000 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_303050.1 | hypothetical protein, conserved |
Leishmania infantum | LinJ.30.3050 | hypothetical protein, conserved |
Leishmania major | LmjF.30.3020 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.29.3020 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_07118 | dribble-PA |
Mus musculus | ENSMUSG00000063334 | KRR1, small subunit (SSU) processome component, homolog (yeast) |
Neospora caninum | NCLIV_025560 | ribosomal RNA assembly protein, putative |
Oryza sativa | 9270811 | Os01g0713700 |
Oryza sativa | 4348775 | Os10g0452800 |
Onchocerca volvulus | OVOC6918 | KRR1 small subunit processome component homolog |
Plasmodium berghei | PBANKA_0305300 | KRR1 small subunit processome component, putative |
Plasmodium falciparum | PF3D7_0208200 | KRR1 small subunit processome component, putative |
Plasmodium knowlesi | PKNH_0412900 | KRR1 small subunit processome component, putative |
Plasmodium vivax | PVX_003860 | KRR1 small subunit processome component, putative |
Plasmodium yoelii | PY03494 | RNA-binding protein |
Saccharomyces cerevisiae | YCL059C | Krr1p |
Schistosoma japonicum | Sjp_0083680 | ko:K06961 KRR1, small subunit (SSU) processome component, homolog (yeast), putative |
Schistosoma mansoni | Smp_115060 | hypothetical protein |
Schistosoma mansoni | Smp_009340 | hypothetical protein |
Schmidtea mediterranea | mk4.000000.36 | KRR1 small subunit processome component homolog |
Schmidtea mediterranea | mk4.000158.06 | KRR1 small subunit processome component homolog |
Trypanosoma brucei gambiense | Tbg972.6.4160 | ribosomal RNA assembly protein, putative |
Trypanosoma brucei | Tb927.6.4350 | ribosomal RNA assembly protein, putative |
Trypanosoma congolense | TcIL3000_6_3770 | ribosomal RNA assembly protein, putative |
Trypanosoma cruzi | TcCLB.509065.130 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.506943.120 | hypothetical protein, conserved |
Toxoplasma gondii | TGME49_262070 | ribosomal rna assembly protein mis3, putative |
Theileria parva | TP02_0631 | hypothetical protein, conserved |
Trichomonas vaginalis | TVAG_171780 | HIV-1 rev binding protein, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.6.4350 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.6.4350 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.6.4350 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.6.4350 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_C05C8.2 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_C05C8.2 | Caenorhabditis elegans | slow growth | wormbase |
YCL059C | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0305300 | Plasmodium berghei | Essential | plasmo |
TGME49_262070 | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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.