pI: 9.1793 |
Length (AA): 133 |
MW (Da): 15178 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
42 | 118 | 1ryq (A) | 0 | 60 | 27.00 | 0 | 0.7 | 0.46 | 0.3 |
34 | 131 | 3h7h (A) | 4 | 103 | 41.00 | 0 | 1 | 1.27604 | -0.57 |
42 | 133 | 2exu (A) | 3 | 93 | 32.00 | 0 | 1 | 0.932129 | -0.6 |
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, intra-erythrocytic - 32 hs, intra-erythrocytic - 40 hs, intra-erythrocytic - 48 hs, merozoite, sporozoite, Oocyst, Ring, Sporozoite, Female Gametocyte, Male Gametocyte. | Otto TD PlasmoDB Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | early ring, early trophozoite, late ring. | PlasmoDB |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | early schizont, late trophozoite. | PlasmoDB |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | late schizont. | PlasmoDB |
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. |
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. |
Ortholog group members (OG5_128605)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G08565 | transcription elongation factor SPT4-1 |
Arabidopsis thaliana | AT5G63670 | transcription elongation factor SPT4-2 |
Babesia bovis | BBOV_I002950 | transcription factor, putative |
Brugia malayi | Bm1_28880 | Transcription initiation protein SPT4 homolog 1, putative |
Candida albicans | CaO19.3947 | Zn-finger protein |
Candida albicans | CaO19.11429 | Zn-finger protein |
Caenorhabditis elegans | CELE_F54C4.2 | Protein SPT-4 |
Cryptosporidium parvum | cgd2_2820 | transcription factor, putative |
Dictyostelium discoideum | DDB_G0285293 | transcription initiation factor Spt4 |
Drosophila melanogaster | Dmel_CG12372 | CG12372 gene product from transcript CG12372-RA |
Echinococcus granulosus | EgrG_000232500 | transcription elongation factor spt4 |
Entamoeba histolytica | EHI_148350 | transcription initiation protein SPT4, putative |
Echinococcus multilocularis | EmuJ_000232500 | transcription elongation factor spt4 |
Homo sapiens | ENSG00000213246 | suppressor of Ty 4 homolog 1 (S. cerevisiae) |
Loa Loa (eye worm) | LOAG_04253 | transcription elongation factor SPT4 |
Mus musculus | ENSMUSG00000020485 | suppressor of Ty 4A |
Mus musculus | 100041294 | predicted gene 3258 |
Neospora caninum | NCLIV_026170 | hypothetical protein |
Oryza sativa | 4343956 | Os07g0623400 |
Plasmodium berghei | PBANKA_0514000 | transcription elongation factor SPT4, putative |
Plasmodium falciparum | PF3D7_1030000 | transcription elongation factor SPT4, putative |
Plasmodium knowlesi | PKNH_0614700 | transcription elongation factor SPT4, putative |
Plasmodium vivax | PVX_111225 | transcription elongation factor SPT4, putative |
Plasmodium yoelii | PY04106 | transcription initiation protein spt4 homolog 1-related |
Saccharomyces cerevisiae | YGR063C | transcription elongation factor SPT4 |
Schistosoma japonicum | Sjp_0208960 | Transcription elongation factor SPT4, putative |
Schistosoma mansoni | Smp_012530.2 | transcription elongation factor SPT4-like protein |
Schmidtea mediterranea | mk4.011221.00 | Transcription elongation factor SPT4 |
Schmidtea mediterranea | mk4.011101.00 | Transcription elongation factor SPT4 |
Toxoplasma gondii | TGME49_261220 | transcription elongation factor SPT4 |
Theileria parva | TP01_0543 | transcription factor, putative |
Trichomonas vaginalis | TVAG_107370 | suppressor of ty, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_F54C4.2 | Caenorhabditis elegans | embryonic arrest | wormbase |
PBANKA_0514000 | Plasmodium berghei | Essential | plasmo |
TGME49_261220 | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
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 |
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.