pI: 7.0781 |
Length (AA): 181 |
MW (Da): 19124 |
Paralog Number:
0
Signal peptide: Y | GPI Anchor: N | Predicted trans-membrane segments: 4
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 |
---|---|---|---|---|---|---|---|---|---|
7 | 178 | 2bl2 (A) | 4 | 156 | 16.00 | 0 | 0.05 | 1.11 | -1.3 |
117 | 173 | 4bem (A) | 11 | 74 | 39.00 | 0.17 | 0.04 | 0.406517 | 0.97 |
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 80-100% percentile | intra-erythrocytic - 0 hs, intra-erythrocytic - 8 hs, intra-erythrocytic - 16 hs, intra-erythrocytic - 24 hs, intra-erythrocytic - 40 hs, intra-erythrocytic - 48 hs, gametocyte, merozoite, sporozoite, early ring, early schizont, early trophozoite, late ring, late schizont, late trophozoite, Ring, Sporozoite. | Otto TD PlasmoDB Zanghi G |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intra-erythrocytic - 32 hs, Oocyst, Female Gametocyte, Male Gametocyte. | Otto TD Zanghi G Lasonder E |
Otto TD | New insights into the blood-stage transcriptome of Plasmodium falciparum using RNA-Seq. |
Lasonder E | Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes. Molecular insight into sex-specific processes and translational repression. |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
PlasmoDB | Data on upregulation of P. falciparum genes in different life cycle stages, combined from several microarray experiments available in PlasmoDB |
Ortholog group members (OG5_127898)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G25610 | ATPase, F0/V0 complex, subunit C protein |
Arabidopsis thaliana | AT4G32530 | ATPase, F0/V0 complex, subunit C protein |
Babesia bovis | BBOV_III009220 | ATP synthase subunit C domain containing protein |
Brugia malayi | Bm1_43140 | Vacuolar ATP synthase 21 kDa proteolipid subunit, putative |
Candida albicans | CaO19.4954 | Proteolipid - vacuolar ATPase V0 domain subunit c'' |
Candida albicans | CaO19.12419 | c subunit of V0 domain of V-ATPase |
Caenorhabditis elegans | CELE_T01H3.1 | Protein VHA-4 |
Cryptosporidium hominis | Chro.80551 | V-ATPase subunit c proteolipid |
Cryptosporidium parvum | cgd8_4790 | proteolipid subunit of the vacuolar ATpase |
Dictyostelium discoideum | DDB_G0274141 | hypothetical protein |
Drosophila melanogaster | Dmel_CG7026 | Vacuolar H[+] ATPase PPA1 subunit 2 |
Drosophila melanogaster | Dmel_CG7007 | Vacuolar H[+] ATPase PPA1 subunit 1 |
Echinococcus granulosus | EgrG_001145000 | V type proton ATPase 21 kDa proteolipid subunit |
Entamoeba histolytica | EHI_029370 | Vacuolar ATP synthase proteolipid subunit, putative |
Echinococcus multilocularis | EmuJ_001145000 | V type proton ATPase 21 kDa proteolipid subunit |
Giardia lamblia | GL50803_15598 | Vacuolar ATP synthase 16 kDa proteolipid subunit |
Homo sapiens | ENSG00000117410 | ATPase, H+ transporting, lysosomal 21kDa, V0 subunit b |
Leishmania braziliensis | LbrM.30.3690 | V-type ATPase, C subunit, putative |
Leishmania donovani | LdBPK_303720.1 | V-type ATPase, C subunit, putative |
Leishmania infantum | LinJ.30.3720 | V-type ATPase, C subunit, putative |
Leishmania major | LmjF.30.3660 | V-type ATPase, C subunit, putative |
Leishmania mexicana | LmxM.29.3660 | V-type ATPase, C subunit, putative |
Loa Loa (eye worm) | LOAG_05327 | vacuolar ATP synthase proteolipid subunit |
Mus musculus | ENSMUSG00000033379 | ATPase, H+ transporting, lysosomal V0 subunit B |
Neospora caninum | NCLIV_043040 | GE13384, related |
Oryza sativa | 4327731 | Os01g0610100 |
Plasmodium berghei | PBANKA_1131000 | V-type proton ATPase 21 kDa proteolipid subunit, putative |
Plasmodium falciparum | PF3D7_1354400 | V-type proton ATPase 21 kDa proteolipid subunit, putative |
Plasmodium knowlesi | PKNH_1117400 | V-type proton ATPase 21 kDa proteolipid subunit, putative |
Plasmodium vivax | PVX_114705 | V-type proton ATPase 21 kDa proteolipid subunit, putative |
Plasmodium yoelii | PY05899 | ATP synthase subunit C, putative |
Saccharomyces cerevisiae | YHR026W | H(+)-transporting V0 sector ATPase subunit c'' |
Schistosoma japonicum | Sjp_0036000 | ko:K03661 V-type H+-transporting ATPase 21kDa proteolipid subunit, putative |
Schistosoma mansoni | Smp_064350 | vacuolar ATP synthase proteolipid subunit |
Schmidtea mediterranea | mk4.001760.02 | V-type proton ATPase 21 kDa proteolipid subunit |
Trypanosoma brucei gambiense | Tbg972.6.4850 | V-type ATPase, C subunit, putative |
Trypanosoma brucei | Tb927.6.5050 | V-type ATPase, C subunit, putative |
Trypanosoma congolense | TcIL3000_6_4480 | V-type ATPase, C subunit, putative |
Trypanosoma cruzi | TcCLB.506945.300 | V-type ATPase, C subunit, putative |
Toxoplasma gondii | TGME49_291310 | V-ATPase subunit c' proteolipid, putative |
Theileria parva | TP04_0832 | vacuolar ATP synthase subunit C, putative |
Trichomonas vaginalis | TVAG_371960 | vacuolar ATP synthase proteolipid subunit 1, 2, 3, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.6.5050 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.6.5050 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.6.5050 | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb927.6.5050 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_T01H3.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_T01H3.1 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_T01H3.1 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_1131000 | Plasmodium berghei | Essential | plasmo |
TGME49_291310 | Toxoplasma gondii | Probably essential | sidik |
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 |
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 |
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 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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.