pI: 5.6158 |
Length (AA): 610 |
MW (Da): 67750 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: | 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:
PDB Structures:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 80-100% percentile | Procyclic, Bloodstream Form. | Siegel TN |
Siegel TN | Genome-wide analysis of mRNA abundance in two life-cycle stages of Trypanosoma brucei and identification of splicing and polyadenylation sites. |
Ortholog group members (OG5_127237)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G78900 | V-type proton ATPase catalytic subunit A |
Babesia bovis | BBOV_III008150 | vacuolar ATP synthase catalytic subunit A |
Brugia malayi | Bm1_50960 | vacuolar ATP synthase catalytic subunit A, osteoclast isoform |
Candida albicans | CaO19.9249 | likely vacuolar ATPase V1 complex subunit A similar to S. cerevisiae TFP1 (YDL185W) |
Caenorhabditis elegans | CELE_Y49A3A.2 | Protein VHA-13 |
Cryptosporidium hominis | Chro.70559 | vacuolar ATP synthase catalytic subunit a |
Cryptosporidium parvum | cgd7_5000 | vacuolar ATP synthase subunit A |
Chlamydia trachomatis | CT_308 | V-type ATP synthase subunit A |
Dictyostelium discoideum | DDB_G0287127 | vacuolar H+-ATPase A subunit |
Drosophila melanogaster | Dmel_CG5075 | Vacuolar H[+] ATPase 68kD subunit 3 |
Drosophila melanogaster | Dmel_CG12403 | Vacuolar H[+] ATPase 68kD subunit 1 |
Drosophila melanogaster | Dmel_CG3762 | Vacuolar H[+] ATPase 68 kDa subunit 2 |
Echinococcus granulosus | EgrG_000183100 | vacuolar H ATPase v1 sector subunit A |
Entamoeba histolytica | EHI_043010 | V-type ATPase, A subunit, putative |
Echinococcus multilocularis | EmuJ_000183100 | vacuolar H+ ATPase v1 sector subunit A |
Giardia lamblia | GL50803_7532 | Vacuolar ATP synthase catalytic subunit A |
Homo sapiens | ENSG00000114573 | ATPase, H+ transporting, lysosomal 70kDa, V1 subunit A |
Leishmania braziliensis | LbrM.20.3260 | vacuolar ATP synthase catalytic subunit A, putative |
Leishmania donovani | LdBPK_343460.1 | vacuolar ATP synthase catalytic subunit A, putative |
Leishmania infantum | LinJ.34.3460 | vacuolar ATP synthase catalytic subunit A, putative |
Leishmania major | LmjF.34.3670 | vacuolar ATP synthase catalytic subunit A, putative |
Leishmania mexicana | LmxM.33.3670 | vacuolar ATP synthase catalytic subunit A, putative |
Loa Loa (eye worm) | LOAG_08611 | hypothetical protein |
Loa Loa (eye worm) | LOAG_01530 | vacuolar H ATPase family member |
Mus musculus | ENSMUSG00000052459 | ATPase, H+ transporting, lysosomal V1 subunit A |
Neospora caninum | NCLIV_029990 | vacuolar ATP synthase catalytic subunit A, putative |
Oryza sativa | 4341751 | Os06g0662000 |
Oryza sativa | 4328470 | Os02g0175400 |
Onchocerca volvulus | OVOC4417 |
|
Plasmodium berghei | PBANKA_1410400 | V-type proton ATPase catalytic subunit A, putative |
Plasmodium falciparum | PF3D7_1311900 | V-type proton ATPase catalytic subunit A |
Plasmodium knowlesi | PKNH_1412600 | V-type proton ATPase catalytic subunit A, putative |
Plasmodium vivax | PVX_122430 | vacuolar ATP synthase catalytic subunit A, putative |
Plasmodium yoelii | PY01556 | V-type ATPase, A subunit |
Saccharomyces cerevisiae | YDL185W | H(+)-transporting V1 sector ATPase subunit A |
Schistosoma japonicum | Sjp_0213820 | ko:K02145 V-type H+-transporting ATPase subunit A, putative |
Schistosoma mansoni | Smp_147050 | ATP synthase alpha subunit vacuolar |
Schmidtea mediterranea | mk4.042236.00 | |
Schmidtea mediterranea | mk4.012972.00 | |
Trypanosoma brucei gambiense | Tbg972.4.910 | V-type ATPase, A subunit, putative |
Trypanosoma brucei | Tb927.4.1080 | V-type ATPase, A subunit, putative |
Trypanosoma congolense | TcIL3000_4_700 | V-type ATPase, A subunit, putative |
Trypanosoma cruzi | TcCLB.506405.120 | V-type ATPase, A subunit, putative |
Trypanosoma cruzi | TcCLB.503929.10 | V-type ATPase, A subunit, putative |
Toxoplasma gondii | TGME49_256970 | vacuolar ATP synthase subunit A, putative |
Treponema pallidum | TP0529 | V-type ATP synthase subunit A |
Treponema pallidum | TP0426 | V-type ATP synthase subunit A |
Theileria parva | TP04_0714 | vacuolar ATP synthase catalytic subunit A, putative |
Trichomonas vaginalis | TVAG_420260 | ATP synthase beta subunit, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.4.1080 this record | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.4.1080 this record | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.4.1080 this record | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb927.4.1080 this record | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_Y49A3A.2 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_Y49A3A.2 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_Y49A3A.2 | Caenorhabditis elegans | slow growth | wormbase |
CELE_Y49A3A.2 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_1410400 | Plasmodium berghei | Essential | plasmo |
TGME49_256970 | Toxoplasma gondii | Probably essential | sidik |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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 |
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 |
Affected Entity | Phenotypic quality | Occurs in | Occurs at | Evidence | Observed in | Drugs/Inhibitors |
---|---|---|---|---|---|---|
cell proliferation (GO:0008283) | decreased (PATO:0000468) | bloodstream stage trypomastigotes (PLO:0027) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | decreased cell proliferation (significant loss of fitness) in bloodstream forms (stage 6 days). | References: | 21363968 | |
cell proliferation (GO:0008283) | increased (PATO:0000470) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | increased cell proliferation (significant gain of fitness) in procyclic forms . | References: | 21363968 | |
cell proliferation (GO:0008283) | normal (PATO:0000461) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | normal cell proliferation (no significant loss or gain of fitness) in differentiation of procyclic to bloodstream forms . | References: | 21363968 |
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.
Druggability index (range: 0 to 1): 1
38 literature references were collected for this gene.