pI: 5.4265 |
Length (AA): 669 |
MW (Da): 75894 |
Paralog Number:
5
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 |
---|---|---|---|---|---|---|---|---|---|
26 | 669 | 2x19 (B) | 312 | 949 | 11.00 | 0 | 0.93 | 0.987231 | 0.45 |
509 | 669 | 3hr0 (A) | 536 | 698 | 27.00 | 0 | 0.92 | 0.609058 | -0.46 |
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_129076)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G01400 | hypothetical protein |
Brugia malayi | Bm1_01690 | Conserved oligomeric Golgi complex component 4, putative |
Candida albicans | CaO19.6880 | similar to S. cerevisiae COG4 (YPR105C) intra-Golgi transport complex subunit |
Candida albicans | CaO19.14169 | similar to S. cerevisiae COG4 (YPR105C) intra-Golgi transport complex component |
Caenorhabditis elegans | CELE_Y51H7C.6 | Protein COGC-4, isoform A |
Cryptosporidium parvum | cgd7_3750 | oligomeric golgi complex protein 4 |
Dictyostelium discoideum | DDB_G0267960 | oligomeric Golgi complex component |
Drosophila melanogaster | Dmel_CG7456 | CG7456 gene product from transcript CG7456-RA |
Echinococcus granulosus | EgrG_000481000 | oligomeric Golgi complex subunit |
Echinococcus multilocularis | EmuJ_000481000 | oligomeric Golgi complex subunit |
Homo sapiens | ENSG00000103051 | component of oligomeric golgi complex 4 |
Loa Loa (eye worm) | LOAG_00872 | hypothetical protein |
Mus musculus | ENSMUSG00000031753 | component of oligomeric golgi complex 4 |
Oryza sativa | 9267023 | Os02g0456000 |
Saccharomyces cerevisiae | YPR105C | Cog4p |
Schistosoma japonicum | Sjp_0010360 | Conserved oligomeric Golgi complex component 4, putative |
Schistosoma japonicum | Sjp_0010340 | Conserved oligomeric Golgi complex component 4, putative |
Schistosoma mansoni | Smp_192100 | hypothetical protein |
Schistosoma mansoni | Smp_118480 | hypothetical protein |
Schistosoma mansoni | Smp_166460 | oligomeric golgi complex component |
Schistosoma mansoni | Smp_180640 | hypothetical protein |
Schistosoma mansoni | Smp_121530 | hypothetical protein |
Schistosoma mansoni | Smp_080070 | hypothetical protein |
Schmidtea mediterranea | mk4.001556.10 | |
Schmidtea mediterranea | mk4.001556.07 | Conserved oligomeric Golgi complex subunit 4 |
Schmidtea mediterranea | mk4.001556.08 | Conserved oligomeric Golgi complex subunit 4 |
Trichomonas vaginalis | TVAG_476340 | hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_Y51H7C.6 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_Y51H7C.6 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_Y51H7C.6 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_Y51H7C.6 | Caenorhabditis elegans | slow growth | wormbase |
CELE_Y51H7C.6 | Caenorhabditis elegans | sterile | wormbase |
YPR105C | Saccharomyces cerevisiae | inviable | yeastgenome |
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 |
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 |
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 |
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.