pI: 8.4515 |
Length (AA): 567 |
MW (Da): 63533 |
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 |
---|---|---|---|---|---|---|---|---|---|
123 | 295 | 1zt2 (B) | 29 | 201 | 11.00 | 0.000000026 | 0.18 | 0.16 | -0.1 |
28 | 534 | 4rr2 (D) | 22 | 456 | 29.00 | 0 | 1 | 0.99228 | 0.45 |
133 | 289 | 4rr2 (B) | 76 | 234 | 22.00 | 0 | 0.87 | 0.491196 | 0.15 |
331 | 533 | 3lgb (A) | 316 | 511 | 33.00 | 0 | 1 | 0.676125 | -0.75 |
339 | 510 | 5dqo (A) | 276 | 432 | 47.00 | 0 | 1 | 0.453051 | 0.41 |
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 |
---|---|---|---|
Mid 40-60% percentile | amastigotes. | Fernandes MC |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_127945)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G67320 | probable DNA primase large subunit |
Babesia bovis | BBOV_IV002300 | DNA primase, large subunit |
Brugia malayi | Bm1_51365 | Eukaryotic-type DNA primase, large subunit family protein |
Candida albicans | CaO19.10403 | DNA primase large subunit |
Candida albicans | CaO19.2885 | DNA primase large subunit |
Caenorhabditis elegans | CELE_W02D9.1 | Protein PRI-2, isoform B |
Cryptosporidium hominis | Chro.80166 | hypothetical protein |
Cryptosporidium parvum | cgd8_1410 | DNA primase large subunit |
Dictyostelium discoideum | DDB_G0270442 | DNA polymerase alpha primase subunit |
Drosophila melanogaster | Dmel_CG5553 | DNA polymerase alpha 60kD |
Echinococcus granulosus | EgrG_000487100 | DNA primase large subunit |
Entamoeba histolytica | EHI_147530 | DNA primase large subunit, putative |
Echinococcus multilocularis | EmuJ_000487100 | DNA primase large subunit |
Giardia lamblia | GL50803_6980 | DNA pol/primase, large sub |
Homo sapiens | 101930420 | DNA primase large subunit-like |
Homo sapiens | ENSG00000146143 | primase, DNA, polypeptide 2 (58kDa) |
Leishmania braziliensis | LbrM.03.0100 | DNA primase large subunit, putative |
Leishmania donovani | LdBPK_030080.1 | DNA primase large subunit, putative |
Leishmania infantum | LinJ.03.0080 | DNA primase large subunit, putative |
Leishmania major | LmjF.03.0090 | DNA primase large subunit, putative |
Leishmania mexicana | LmxM.03.0090 | DNA primase large subunit, putative |
Loa Loa (eye worm) | LOAG_07121 | hypothetical protein |
Loa Loa (eye worm) | LOAG_12771 | hypothetical protein |
Mus musculus | ENSMUSG00000026134 | DNA primase, p58 subunit |
Neospora caninum | NCLIV_006750 | DNA primase, large subunit, putative |
Oryza sativa | 4342990 | Os07g0406800 |
Plasmodium berghei | PBANKA_0812000 | DNA primase large subunit, putative |
Plasmodium falciparum | PF3D7_0910900 | DNA primase large subunit, putative |
Plasmodium knowlesi | PKNH_0708900 | DNA primase large subunit, putative |
Plasmodium vivax | PVX_098985 | DNA primase large subunit, putative |
Plasmodium yoelii | PY00851 | DNA primase large subunit |
Saccharomyces cerevisiae | YKL045W | DNA primase subunit PRI2 |
Schistosoma japonicum | Sjp_0022440 | ko:K02685 DNA primase large subunit, putative |
Schistosoma japonicum | Sjp_0132960 | ko:K02685 DNA primase large subunit, putative |
Schistosoma mansoni | Smp_079050.1 | DNA primase large subunit |
Schmidtea mediterranea | mk4.004339.00 | DNA primase large subunit |
Schmidtea mediterranea | mk4.012252.05 | |
Schmidtea mediterranea | mk4.012252.03 | DNA primase large subunit |
Schmidtea mediterranea | mk4.011200.00 | DNA primase large subunit |
Schmidtea mediterranea | mk4.012252.02 | DNA primase large subunit |
Schmidtea mediterranea | mk4.034123.00 | DNA primase large subunit |
Schmidtea mediterranea | mk4.044580.00 | DNA primase large subunit |
Schmidtea mediterranea | mk4.019229.01 | DNA primase large subunit |
Schmidtea mediterranea | mk4.006282.00 | DNA primase large subunit |
Trypanosoma brucei gambiense | Tbg972.10.3940 | DNA primase large subunit, putative |
Trypanosoma brucei | Tb927.10.3110 | DNA primase large subunit, putative |
Trypanosoma cruzi | TcCLB.510943.140 | DNA primase large subunit, putative |
Trypanosoma cruzi | TcCLB.504867.80 | DNA primase large subunit, putative |
Toxoplasma gondii | TGME49_297840 | DNA primase, large subunit |
Theileria parva | TP03_0424 | DNA primase large subunit, putative |
Trichomonas vaginalis | TVAG_091480 | DNA primase large subunit, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.3110 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.3110 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.3110 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.10.3110 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_W02D9.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_W02D9.1 | Caenorhabditis elegans | sterile | wormbase |
YKL045W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0812000 | Plasmodium berghei | Essential | plasmo |
TGME49_297840 | Toxoplasma gondii | Probably essential | sidik |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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.