pI: 8.4612 |
Length (AA): 245 |
MW (Da): 27562 |
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 |
---|---|---|---|---|---|---|---|---|---|
3 | 245 | 1sxj (C) | 14 | 261 | 46.00 | 0 | 1 | 1.60284 | -0.78 |
3 | 245 | 1sxj (B) | 10 | 250 | 41.00 | 0 | 1 | 1.56784 | -0.83 |
5 | 245 | 1iqp (A) | 16 | 256 | 45.00 | 0 | 1 | 1.60057 | -0.91 |
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_127045)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G02480 | protein STICHEL |
Arabidopsis thaliana | AT1G77470 | replication factor C subunit 3 |
Arabidopsis thaliana | AT1G14460 | AAA-type ATPase family protein |
Babesia bovis | BBOV_II002510 | replication factor C3 protein, putative |
Brugia malayi | Bm1_41025 | Putative activator 1 36 kDa subunit |
Candida albicans | CaO19.10723 | Replication factor C subunit 3 |
Candida albicans | CaO19.3211 | Replication factor C subunit 3 |
Caenorhabditis elegans | CELE_F44B9.8 | Protein F44B9.8 |
Cryptosporidium hominis | Chro.30359 | replication factor C3 |
Cryptosporidium parvum | cgd3_3170 | replication factor RFC3 AAA+ ATpase |
Chlamydia trachomatis | CT_334 | DNA polymerase III subunit gamma and tau |
Dictyostelium discoideum | DDB_G0282235 | replication factor C subunit |
Drosophila melanogaster | Dmel_CG5313 | Replication factor C subunit 3 |
Escherichia coli | b0470 | DNA polymerase III/DNA elongation factor III, tau and gamma subunits |
Echinococcus granulosus | EgrG_000570600 | replication factor C subunit 5 |
Entamoeba histolytica | EHI_099850 | replication factor C familiy protein |
Echinococcus multilocularis | EmuJ_000570600 | replication factor C subunit 5 |
Giardia lamblia | GL50803_24636 | Replication factor C, subunit 3 |
Homo sapiens | ENSG00000111445 | replication factor C (activator 1) 5, 36.5kDa |
Leishmania braziliensis | LbrM.34.3160 | replication factor C, subunit 3, putative |
Leishmania donovani | LdBPK_353300.1 | replication factor C, subunit 3, putative |
Leishmania infantum | LinJ.35.3300 | replication factor C, subunit 3, putative |
Leishmania major | LmjF.35.3250 | replication factor C, subunit 3, putative |
Leishmania mexicana | LmxM.34.3250 | replication factor C, subunit 3, putative |
Loa Loa (eye worm) | LOAG_02279 | replication factor C subunit 3 |
Mycobacterium leprae | ML2335c | DNA POLYMERASE III (SUBUNIT GAMMA/TAU) DNAZ/X |
Mus musculus | 72151 | replication factor C (activator 1) 5 |
Mycobacterium tuberculosis | Rv3721c | DNA polymerase III (subunit gamma/tau) DnaZ/X |
Mycobacterium ulcerans | MUL_4315 | DNA polymerase III subunits gamma and tau |
Neospora caninum | NCLIV_013120 | activator 1 36 kDa, putative |
Oryza sativa | 9270748 | Os11g0244300 |
Oryza sativa | 4330895 | Os02g0775200 |
Oryza sativa | 4351770 | Os12g0209300 |
Onchocerca volvulus | OVOC9422 | Putative replication factor C subunit 5 |
Plasmodium berghei | PBANKA_1326800 | replication factor C subunit 3, putative |
Plasmodium falciparum | PF3D7_1463200 | replication factor C subunit 3, putative |
Plasmodium knowlesi | PKNH_1218300 | replication factor C subunit 3, putative |
Plasmodium vivax | PVX_117300 | replication factor C3, putative |
Plasmodium yoelii | PY04255 | replication factor C3 |
Saccharomyces cerevisiae | YNL290W | replication factor C subunit 3 |
Schistosoma japonicum | Sjp_0046720 | ko:K10756 replication factor C subunit 3/5, putative |
Schistosoma mansoni | Smp_178880 | replication factor C / DNA polymerase III gamma-tau subunit |
Schistosoma mansoni | Smp_066260 | replication factor C / DNA polymerase III gamma-tau subunit |
Schmidtea mediterranea | mk4.056823.00 | Replication factor C subunit 4 |
Schmidtea mediterranea | mk4.001716.00 | Probable replication factor C subunit 5 |
Trypanosoma brucei gambiense | Tbg972.9.7480 | replication factor C, subunit 3, putative |
Trypanosoma brucei | Tb927.9.12300 | replication factor C, subunit 3, putative |
Trypanosoma cruzi | TcCLB.510737.110 | replication factor C, subunit 3, putative |
Trypanosoma cruzi | TcCLB.510661.270 | replication factor C, subunit 3, putative |
Toxoplasma gondii | TGME49_213000 | replication factor C, subunit 5, putative |
Treponema pallidum | TP1005 | DNA polymerase III subunits gamma and tau |
Theileria parva | TP04_0380 | replication factor C subunit 3, putative |
Trichomonas vaginalis | TVAG_447650 | werner helicase interacting protein, putative |
Wolbachia endosymbiont of Brugia malayi | Wbm0434 | DNA polymerase III, gamma/tau subunit |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.3310 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.3310 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.3310 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb09.211.3310 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
b0470 | Escherichia coli | essential | goodall |
CELE_F44B9.8 | Caenorhabditis elegans | embryonic lethal | wormbase |
YNL290W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_1326800 | Plasmodium berghei | Essential | plasmo |
TGME49_213000 | Toxoplasma gondii | Probably essential | sidik |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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.