pI: 5.587 |
Length (AA): 610 |
MW (Da): 67986 |
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 4 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 |
---|---|---|---|---|---|---|---|---|---|
13 | 579 | 1sky (E) | 2 | 470 | 26.00 | 0 | 1 | 0.87 | -0.07 |
70 | 607 | 1vdz (A) | 60 | 588 | 49.00 | 0 | 1 | 1.36 | -0.69 |
13 | 610 | 3vr4 (A) | 2 | 586 | 49.00 | 0 | 1 | 1.60653 | -0.81 |
13 | 607 | 5d80 (A) | 24 | 614 | 61.00 | 0 | 1 | 1.67681 | -0.08 |
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_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 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.4.1080 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.4.1080 | Trypanosoma brucei | significant gain of fitness in procyclic forms | alsford |
Tb927.4.1080 | 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 |
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 |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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.
Druggability index (range: 0 to 1): 0.8