pI: 9.7357 |
Length (AA): 257 |
MW (Da): 27525 |
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 5 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 |
---|---|---|---|---|---|---|---|---|---|
32 | 163 | 1quq (A) | 46 | 171 | 33.00 | 0.00000022 | 0.99 | 0.88 | -0.76 |
192 | 256 | 1dpu (A) | 202 | 265 | 19.00 | 0.0000000096 | 0.57 | 0.59 | -1.69 |
28 | 168 | 2pi2 (A) | 42 | 176 | 30.00 | 0 | 1 | 0.836538 | -0.28 |
30 | 163 | 4gnx (B) | 46 | 175 | 34.00 | 0 | 1 | 0.807401 | 0.01 |
198 | 256 | 4ou0 (A) | 209 | 265 | 21.00 | 0.0000016 | 1 | 0.586472 | -1.47 |
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 60-80% percentile | metacyclic. | Fernandes MC |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | amastigotes. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_128774)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G24490 | replicon protein A2 |
Arabidopsis thaliana | AT3G02920 | replication protein RPA32B |
Brugia malayi | Bm1_13550 | hypothetical protein |
Candida albicans | CaO19.9807 | subunit 2 of replication factor RF-A |
Candida albicans | CaO19.2267 | subunit 2 of replication factor RF-A |
Caenorhabditis elegans | CELE_M04F3.1 | Protein RPA-2 |
Drosophila melanogaster | Dmel_CG9273 | Replication protein A2 |
Echinococcus granulosus | EgrG_000604700 | replication protein A 32 kDa subunit |
Echinococcus multilocularis | EmuJ_000604700 | replication protein A 32 kDa subunit |
Homo sapiens | ENSG00000117748 | replication protein A2, 32kDa |
Leishmania braziliensis | LbrM.15.0300 | replication Factor A 28 kDa subunit, putative |
Leishmania donovani | LdBPK_150310.1 | replication Factor A 28 kDa subunit, putative |
Leishmania infantum | LinJ.15.0310 | replication Factor A 28 kDa subunit, putative |
Leishmania major | LmjF.15.0270 | replication Factor A 28 kDa subunit, putative |
Leishmania mexicana | LmxM.15.0270 | replication Factor A 28 kDa subunit, putative |
Loa Loa (eye worm) | LOAG_08766 | hypothetical protein |
Mus musculus | ENSMUSG00000028884 | replication protein A2 |
Oryza sativa | 4331236 | Os02g0829100 |
Oryza sativa | 4330068 | Os02g0633400 |
Onchocerca volvulus | OVOC9765 |
|
Saccharomyces cerevisiae | YNL312W | Rfa2p |
Schistosoma japonicum | Sjp_0216400 | ko:K10739 replication factor A2, putative |
Schistosoma mansoni | Smp_080530 | replication protein A |
Schmidtea mediterranea | mk4.001983.01 | |
Trypanosoma brucei gambiense | Tbg972.5.2360 | replication Factor A 28 kDa subunit, putative |
Trypanosoma brucei | Tb927.5.1700 | replication Factor A 28 kDa subunit, putative |
Trypanosoma congolense | TcIL3000_0_38740 | replication Factor A 28 kDa subunit, putative |
Trypanosoma congolense | TcIL3000_5_1640 | replication Factor A 28 kDa subunit, putative |
Trypanosoma cruzi | TcCLB.510821.50 | replication Factor A 28 kDa subunit, putative |
Trichomonas vaginalis | TVAG_005990 | Replication protein A 30 kDa subunit, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.5.1700 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.5.1700 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.5.1700 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.5.1700 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_M04F3.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_M04F3.1 | Caenorhabditis elegans | slow growth | wormbase |
CELE_M04F3.1 | Caenorhabditis elegans | sterile | wormbase |
YNL312W | Saccharomyces cerevisiae | inviable | yeastgenome |
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 |
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 |
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 |
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.