Detailed view for CaO19.1619

Basic information

TDR Targets ID: 653852
Candida albicans, Rpo21 C-terminus domain kinase
Source Database / ID:  KEGG  

pI: 9.6864 | Length (AA): 586 | MW (Da): 67187 | Paralog Number: 1

Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 0

Druggability Group : DG

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

PF00069   Protein kinase domain

Gene Ontology

Mouse over links to read term descriptions.
GO:0005524   ATP binding  
GO:0004672   protein kinase activity  
GO:0006468   protein amino acid phosphorylation  

Metabolic Pathways

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

Structural information

Modbase 3D models:

No model available for this protein in Modbase.

PDB Structures:

No structure availble in the PDB for this protein

Expression

No expression data available for this gene

Orthologs

Ortholog group members (OG5_128263)

Species Accession Gene Product
Arabidopsis thaliana AT5G10270   1
Arabidopsis thaliana AT5G64960   cyclin-dependent kinase C-2
Brugia malayi Bm1_46210   Protein kinase domain containing protein
Candida albicans CaO19.1619   Rpo21 C-terminus domain kinase
Candida albicans CaO19.9187   Rpo21 C-terminus domain kinase
Caenorhabditis elegans CELE_B0285.1   Protein CDK-12, isoform B
Dictyostelium discoideum DDB_G0273207   CDK family protein kinase
Dictyostelium discoideum DDB_G0273721   CDK family protein kinase
Drosophila melanogaster Dmel_CG7597   CG7597 gene product from transcript CG7597-RB
Echinococcus granulosus EgrG_001041300   Cell division cycle 2 protein kinase
Echinococcus multilocularis EmuJ_001041300   Cell division cycle 2 protein kinase
Homo sapiens ENSG00000065883   cyclin-dependent kinase 13
Homo sapiens ENSG00000167258   cyclin-dependent kinase 12
Loa Loa (eye worm) LOAG_03355   hypothetical protein
Loa Loa (eye worm) LOAG_04967   CMGC/CDK/CRK7 protein kinase
Mus musculus ENSMUSG00000041297   cyclin-dependent kinase 13
Mus musculus ENSMUSG00000003119   cyclin-dependent kinase 12
Neospora caninum NCLIV_023400   hypothetical protein
Oryza sativa 9268645   Os08g0453800
Oryza sativa 4338674   Os05g0389700
Oryza sativa 4325386   Os01g0958000
Saccharomyces cerevisiae YKL139W   Ctk1p
Schistosoma japonicum Sjp_0094410   Cell division cycle 2-like protein kinase 5, putative
Schistosoma japonicum Sjp_0094420   ko:K08819 Cdc2-related kinase, arginine/serine-rich, putative
Schistosoma mansoni Smp_007510   protein kinase
Schmidtea mediterranea mk4.000235.06   Cyclin-dependent kinase 12
Schmidtea mediterranea mk4.004836.01  
Schmidtea mediterranea mk4.012172.00   Cyclin-dependent kinase 12
Toxoplasma gondii TGME49_281450   cell-cycle-associated protein kinase, putative
Trichomonas vaginalis TVAG_359930   CMGC family protein kinase
Trichomonas vaginalis TVAG_249190   CMGC family protein kinase
Trichomonas vaginalis TVAG_265810   CMGC family protein kinase
Trichomonas vaginalis TVAG_235250   CMGC family protein kinase

Essentiality

CaO19.1619 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
CELE_B0285.1 Caenorhabditis elegans embryonic lethal wormbase
CELE_B0285.1 Caenorhabditis elegans larval arrest wormbase
CELE_B0285.1 Caenorhabditis elegans larval lethal wormbase
CELE_B0285.1 Caenorhabditis elegans slow growth wormbase
CELE_B0285.1 Caenorhabditis elegans sterile wormbase
YKL139W Saccharomyces cerevisiae inviable yeastgenome
TGME49_281450 Toxoplasma gondii Essentiality uncertain sidik
Show/Hide essentiality data references
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • 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.
  • 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.
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • 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
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection
  • 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.

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

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
Homo sapiens cyclin-dependent kinase 12 Compounds References
Homo sapiens cyclin-dependent kinase 13 Compounds References
By sequence similarity to non orthologous druggable targets
Species Target Length Identity Alignment span Linked Drugs Reference
Rattus norvegicus Mitogen-activated protein kinase 1 358 aa 32.3% 325 aa Compounds References
Rattus norvegicus MAP kinase p38 alpha 360 aa 34.1% 323 aa Compounds References
Homo sapiens Cyclin-dependent kinase 1/cyclin B1 297 aa 40.3% 290 aa Compounds References
Rattus norvegicus Cell division protein kinase 5 292 aa 37.6% 295 aa Compounds References
Rattus norvegicus Serine/threonine-protein kinase pim-3 326 aa 26.5% 298 aa Compounds References
Plasmodium falciparum (isolate 3D7) Cell division control protein 2 homolog 288 aa 40.1% 292 aa Compounds References
Oryctolagus cuniculus Cyclin-dependent kinase 4 189 aa 35.4% 192 aa Compounds References
Schizosaccharomyces pombe 972h- Casein kinase II subunit alpha 332 aa 28.1% 302 aa Compounds References
Patiria pectinifera Cdc2 300 aa 39.5% 296 aa Compounds References
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 CaO19.1619 (Candida albicans), Rpo21 C-terminus domain kinase
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