pI: 5.6945 |
Length (AA): 540 |
MW (Da): 59956 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
272 | 444 | 5fwj (A) | 11 | 471 | 30.00 | 0.26 | 0.14 | 0.28107 | 1.24 |
368 | 427 | 2nax (A) | 549 | 608 | 23.00 | 0.00000038 | 0.18 | 0.269811 | 0.63 |
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:
Ortholog group members (OG5_129507)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G04885 | PCF11P-similar protein 4 |
Brugia malayi | Bm1_44480 | hypothetical protein |
Candida albicans | CaO19.8302 | similar to S. cerevisiae PCF11 (YDR228C) subunit of pre-mRNA cleavage factor CFI involved in polyadenylation |
Candida albicans | CaO19.684 | similar to S. cerevisiae PCF11 (YDR228C) subunit of pre-mRNA cleavage factor CFI involved in polyadenylation |
Caenorhabditis elegans | CELE_R144.2 | Protein PCF-11, isoform B |
Dictyostelium discoideum | DDB_G0279559 | ENTH domain-containing protein |
Drosophila melanogaster | Dmel_CG10228 | Inverse regulator a |
Echinococcus granulosus | EgrG_001068800 | ENTH VHS domain containing protein |
Echinococcus multilocularis | EmuJ_001068800 | ENTH (VHS) domain containing protein |
Homo sapiens | 51585 | PCF11 cleavage and polyadenylation factor subunit |
Loa Loa (eye worm) | LOAG_06367 | hypothetical protein |
Mus musculus | ENSMUSG00000041328 | cleavage and polyadenylation factor subunit homolog (S. cerevisiae) |
Oryza sativa | 4344833 | Os08g0187700 |
Saccharomyces cerevisiae | YDR228C | Pcf11p |
Schistosoma japonicum | Sjp_0027180 | Pre-mRNA cleavage complex 2 protein Pcf11, putative |
Schistosoma mansoni | Smp_168190 | hypothetical protein |
Schistosoma mansoni | Smp_084870 | hypothetical protein |
Schmidtea mediterranea | mk4.001275.05 | |
Schmidtea mediterranea | mk4.006105.01 | Polyadenylation and cleavage factor homolog 11 |
Schmidtea mediterranea | mk4.006659.00 | Polyadenylation and cleavage factor homolog 11 |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_R144.2 | Caenorhabditis elegans | adult lethal | wormbase |
CELE_R144.2 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_R144.2 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_R144.2 | Caenorhabditis elegans | sterile | wormbase |
YDR228C | Saccharomyces cerevisiae | inviable | yeastgenome |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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.