Detailed view for TcCLB.510575.5

Basic information

TDR Targets ID: 37994
Trypanosoma cruzi, proton motive ATPase, putative
Source Database / ID:  TriTrypDB  GeneDB

pI: 7.6393 | Length (AA): 251 | MW (Da): 28607 | Paralog Number: 4

Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 3

Druggability Group : DG1

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

Pfam domains

No Pfam domain information for this protein.

Gene Ontology

Mouse over links to read term descriptions.
No GO information for this protein.

Metabolic Pathways

This gene is not mapped to any metabolic pathway in KEGG.

Structural information

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
2 217 1m56 (A) 23 262 15.00 0 0.02 0.86 -0.58
18 199 5ksd (A) 669 838 29.00 0 0.32 0.8918 0.3

Help me make sense of these data.

Target Beg: first modeled residue
Target End: last modeled residue
Template: template structure used for modelling (PDB accession and chain)
Template Beg: first template residue in target-template alignment
Template End: last template residue in target-template alignment
Identity: sequence identity
Evalue: E value for target-template hit
Model Score: GA341 score (>0.7 for reliable model)
MPQS: ModPipe Quality Score (>1.1 for reliable model)
zDope: zDope Score (negative for reliable model)

A more detailed description of these scores is available at the Modbase Model Evaluation Help Pages, and in the papers referenced therein.

PDB Structures:

No structure availble in the PDB for this protein

Expression

No expression data available for this gene

Orthologs

Ortholog group members (OG5_127253)

Species Accession Gene Product
Arabidopsis thaliana AT4G11730   putative plasma membrane-type ATPase
Arabidopsis thaliana AT2G18960   H(+)-ATPase 1
Arabidopsis thaliana AT2G24520   H(+)-ATPase 5
Arabidopsis thaliana AT3G47950   H(+)-ATPase 4
Arabidopsis thaliana AT5G57350   H(+)-ATPase 3
Arabidopsis thaliana AT1G17260   autoinhibited H(+)-ATPase isoform 10
Arabidopsis thaliana AT5G62670   H(+)-ATPase 11
Arabidopsis thaliana AT3G60330   H(+)-ATPase 7
Arabidopsis thaliana AT3G42640   H(+)-ATPase 8
Arabidopsis thaliana AT2G07560   H(+)-ATPase 6
Arabidopsis thaliana AT4G30190   H(+)-ATPase 2
Arabidopsis thaliana AT1G80660   H(+)-ATPase 9
Candida albicans CaO19.12838   adenosine triphosphatase
Candida albicans CaO19.5383   adenosine triphosphatase
Dictyostelium discoideum DDB_G0268810   magnesium-translocating P-type ATPase
Dictyostelium discoideum DDB_G0282817   P-type ATPase
Escherichia coli b4242   magnesium transporter
Leishmania braziliensis LbrM.18.1740   P-type H -ATPase, putative
Leishmania braziliensis LbrM.18.1550   P-type H -ATPase, putative
Leishmania donovani LdBPK_181510.1   P-type H+-ATPase 1B, putative
Leishmania infantum LinJ.18.1490   P-type H -ATPase, putative
Leishmania infantum LinJ.18.1500   P-type H -ATPase, putative
Leishmania infantum LinJ.18.1510   P-type H -ATPase, putative
Leishmania major LmjF.18.1510   P-type H -ATPase, putative
Leishmania major LmjF.18.1520   P-type H -ATPase, putative
Leishmania mexicana LmxM.18.1510   P-type H -ATPase, putative
Leishmania mexicana LmxM.18.1520   P-type H -ATPase, putative
Neospora caninum NCLIV_022240   ATPase, related
Oryza sativa 4331853   Os03g0183900
Oryza sativa 4337257   Os04g0656100
Oryza sativa 4342621   Os07g0191200
Oryza sativa 4331015   Os02g0797300
Oryza sativa 4331281   Os03g0100800
Oryza sativa 4333770   Os03g0689300
Oryza sativa 4340312   Os06g0181500
Oryza sativa 4352910   Os12g0638700
Oryza sativa 4338405   Os05g0319800
Saccharomyces cerevisiae YPL036W   H(+)-exporting P2-type ATPase PMA2
Saccharomyces cerevisiae YGL008C   H(+)-exporting P2-type ATPase PMA1
Trypanosoma brucei gambiense Tbg972.10.15070   P-type H -ATPase, putative
Trypanosoma brucei Tb927.10.12510   P-type H+-ATPase, putative
Trypanosoma brucei Tb927.10.12500   P-type H+-ATPase, putative
Trypanosoma congolense TcIL3000_10_10700   P-type H+-ATPase, putative
Trypanosoma cruzi TcCLB.506333.10   plasma-membrane proton-efflux P-type ATPase, putative
Trypanosoma cruzi TcCLB.510575.5   proton motive ATPase, putative
Trypanosoma cruzi TcCLB.505763.19   P-type H+-ATPase, putative
Trypanosoma cruzi TcCLB.505763.10   proton motive ATPase 1, putative
Trypanosoma cruzi TcCLB.506649.20   P-type H+-ATPase, putative
Toxoplasma gondii TGME49_252640   P-type ATPase PMA1
Toxoplasma gondii TGME49_284602   E1-E2 ATPase subfamily protein

Essentiality

TcCLB.510575.5 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.10.12510 Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb927.10.12510 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.10.12510 Trypanosoma brucei significant loss of fitness in procyclic forms alsford
Tb927.10.12510 Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
Tb927.10.12500 Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb927.10.12500 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.10.12500 Trypanosoma brucei significant loss of fitness in procyclic forms alsford
Tb927.10.12500 Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
b4242 Escherichia coli non-essential goodall
YGL008C Saccharomyces cerevisiae inviable yeastgenome
TGME49_284602 Toxoplasma gondii Probably non-essential sidik
TGME49_252640 Toxoplasma gondii Probably non-essential sidik
TGME49_284602 Toxoplasma gondii Essentiality uncertain sidik
TGME49_252640 Toxoplasma gondii Essentiality uncertain sidik
Show/Hide essentiality data references
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • neb C. elegans RNAi phenotypes Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • 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
  • 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
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • goodall The Essential Genome of Escherichia coli K-12 (Transposon directed high-throughput mutagenesis) Goodall, Emily CA, et al. "The essential genome of Escherichia coli K-12." mBio 9.1 (2018): e02096-17.
  • sidik A Genome-wide CRISPR Screen in Toxoplasma Identifies Essential Apicomplexan Genes. Sidik, Saima M., et al. "A genome-wide CRISPR screen in toxoplasma identifies essential apicomplexan genes." Cell 166.6 (2016): 1423-1435.
  • plasmo Functional Profiling of a Plasmodium Genome Reveals an Abundance of Essential Genes. Bushell, Ellen, et al. "Functional profiling of a Plasmodium genome reveals an abundance of essential genes." Cell 170.2 (2017): 260-272.
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan

Phenotypes and Validation (curated)

We have no manually annotated phenotypes for this target. What does this mean? / Care to help?

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.

Annotated validation

No validation data for this target

Associated compounds / Druggability

Druggability index (range: 0 to 1): 0.1

Known modulators for this target

No chemical compounds associated to this gene

Predicted associations

By orthology with druggable targets
Species Known druggable target Linked compounds Reference
Trypanosoma cruzi P-type H+-ATPase, putative Compounds References
Trypanosoma cruzi P-type H+-ATPase, putative Compounds References
By sequence similarity to non orthologous druggable targets
No additional associated druggable targets
Obtained from network model
No druggable targets predicted through repurposing network model

Assayability

Assay information

No assay information for this target.

Reagent availability

No reagent availability information for this target.

Bibliographic References

No literature references available for this target.

If you have references for this gene, please enter them in a user comment (below) or Contact us.

User comments

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Gene identifier TcCLB.510575.5 (Trypanosoma cruzi), proton motive ATPase, putative
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