pI: 7.6656 |
Length (AA): 99 |
MW (Da): 10495 |
Paralog Number:
1
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 |
---|---|---|---|---|---|---|---|---|---|
1 | 88 | 3mxh (P) | 12 | 89 | 12.00 | 0.000000000012 | 0.37 | 0.935689 | -0.23 |
1 | 93 | 2cpi (A) | 111 | 198 | 32.00 | 0 | 0.99 | 1.21219 | 0.83 |
31 | 89 | 1oo0 (B) | 94 | 152 | 20.00 | 0 | 0.1 | 0.68326 | 1 |
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 |
---|---|---|---|
NA% percentile | VEG Tachyzoite, ME49 merozoite, ME49 Oocyst, ME49 Bradyzoite. | Gregory Hehl AB Fritz HM Sibley/Greg |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | ME49 Tachyzoite. | Gregory |
Sibley/Greg | ToxoDB |
Fritz HM | Transcriptomic analysis of toxoplasma development reveals many novel functions and structures specific to sporozoites and oocysts. |
Hehl AB | Asexual expansion of Toxoplasma gondii merozoites is distinct from tachyzoites and entails expression of non-overlapping gene families to attach, invade, and replicate within feline enterocytes. |
Gregory | ToxoDB |
Ortholog group members (OG5_127674)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G45630 | RNA binding (RRM/RBD/RNP motifs) family protein |
Arabidopsis thaliana | AT2G28540 | RNA recognition motif-containing protein |
Arabidopsis thaliana | AT5G60170 | RNA binding (RRM/RBD/RNP motifs) family protein |
Babesia bovis | BBOV_IV004110 | conserved hypothetical protein |
Brugia malayi | Bm1_39595 | Not-like |
Candida albicans | CaO19.2379 | potential RRM domain protein similar to MOT2 (YER068W) component of the cytoplasmic mRNA deadenylase and CCR4-NOT transcription |
Candida albicans | CaO19.9915 | potential RRM domain protein similar to MOT2 (YER068W) component of the cytoplasmic mRNA deadenylase and CCR4-NOT transcription |
Caenorhabditis elegans | CELE_C49H3.5 | Protein NTL-4, isoform B |
Cryptosporidium hominis | Chro.70553 | protein potential transcriptional repressor Not4hp |
Cryptosporidium parvum | cgd7_4960 | Not4hp/Mot2p, RING finger+RRM domains |
Dictyostelium discoideum | DDB_G0275005 | RING zinc finger-containing protein |
Drosophila melanogaster | Dmel_CG31716 | Cnot 4 homologue |
Echinococcus granulosus | EgrG_001028400 | CCR4 NOT transcription complex subunit 4 |
Entamoeba histolytica | EHI_080710 | hypothetical protein, conserved |
Echinococcus multilocularis | EmuJ_001028400 | CCR4 NOT transcription complex subunit 4 |
Giardia lamblia | GL50803_8427 | Transcriptional repressor NOT4Hp, putative |
Homo sapiens | ENSG00000080802 | CCR4-NOT transcription complex, subunit 4 |
Loa Loa (eye worm) | LOAG_11511 | CCR4-NOT transcription complex component |
Loa Loa (eye worm) | LOAG_14798 | hypothetical protein |
Mus musculus | ENSMUSG00000038784 | CCR4-NOT transcription complex, subunit 4 |
Neospora caninum | NCLIV_016050 | hypothetical protein |
Oryza sativa | 4351244 | Os12g0102400 |
Oryza sativa | 4349535 | Os11g0102800 |
Plasmodium berghei | PBANKA_1449900 | CCR4-NOT transcription complex subunit 4, putative |
Plasmodium falciparum | PF3D7_1235300 | CCR4-NOT transcription complex subunit 4, putative |
Plasmodium knowlesi | PKNH_1455000 | CCR4-NOT transcription complex subunit 4, putative |
Plasmodium vivax | PVX_100715 | hypothetical protein, conserved |
Plasmodium yoelii | PY00512 | putative protein potential transcriptional repressor Not4hp |
Saccharomyces cerevisiae | YER068W | CCR4-NOT core ubiquitin-protein ligase subunit MOT2 |
Schistosoma japonicum | Sjp_0037100 | ko:K10643 CCR4-NOT transcription complex, subunit 4, putative |
Schmidtea mediterranea | mk4.000299.11 | |
Toxoplasma gondii | TGME49_328300 | hypothetical protein |
Toxoplasma gondii | TGME49_239410 | hypothetical protein |
Theileria parva | TP01_0345 | hypothetical protein |
Trichomonas vaginalis | TVAG_450320 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_415730 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_407280 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_C49H3.5 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_C49H3.5 | Caenorhabditis elegans | slow growth | wormbase |
TGME49_239410 | Toxoplasma gondii | Probably essential | sidik |
TGME49_328300 this record | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
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.