Detailed view for cgd1_1530

Basic information

TDR Targets ID: 376519
Cryptosporidium parvum, Rpn5 like 26S proteasomal regulatory subunit 12, PINT domain containing protein
Source Database / ID: 

pI: 6.505 | Length (AA): 559 | MW (Da): 65614 | Paralog Number: 0

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

PF01399   PCI domain

Gene Ontology

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

Metabolic Pathways

Proteasome (KEGG)

Structural information

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
1 558 4fgv (A) 458 1011 9.00 0 0.97 1.03501 0.02
3 444 4a3t (A) 17 464 14.00 0 0.99 0.751498 0.45
34 185 5cwh (A) 3 160 13.00 0.12 0.82 0.446614 -1
371 549 4d10 (C) 205 397 30.00 0.00044 0.89 0.489215 0.64

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_127889)

Species Accession Gene Product
Arabidopsis thaliana AT5G64760   26S proteasome regulatory particle non-ATPase subunit 5B
Arabidopsis thaliana AT5G09900   26S proteasome regulatory particle non-ATPase subunit 5A
Babesia bovis BBOV_III011560   PCI domain containing protein
Brugia malayi Bm1_12660   PCI domain containing protein
Candida albicans CaO19.11515   similar to N terminus of S. cerevisiae RPN5 (YDL147W) subunit of the 19S regulatory particle of the 26S proteasome
Candida albicans CaO19.4034   frameshift
Candida albicans CaO19.11517   frameshift
Candida albicans CaO19.4032   similar to N terminus of S. cerevisiae RPN5 (YDL147W) subunit of the 19S regulatory particle of the 26S proteasome
Caenorhabditis elegans CELE_F10G7.8   Protein RPN-5
Cryptosporidium hominis Chro.10177   hypothetical protein
Cryptosporidium parvum cgd1_1530   Rpn5 like 26S proteasomal regulatory subunit 12, PINT domain containing protein
Dictyostelium discoideum DDB_G0281051   26S proteasome non-ATPase regulatory subunit 12
Drosophila melanogaster Dmel_CG1100   Regulatory particle non-ATPase 5
Echinococcus granulosus EgrG_000421800   26S proteasome non ATPase regulatory subunit 12
Entamoeba histolytica EHI_136180   proteasome regulatory subunit, putative
Echinococcus multilocularis EmuJ_000421800   26S proteasome non ATPase regulatory subunit 12
Homo sapiens 5718   proteasome (prosome, macropain) 26S subunit, non-ATPase, 12
Leishmania braziliensis LbrM.21.0840   proteasome regulatory non-ATP-ase subunit 5, putative,19S proteasome regulatory subunit
Leishmania donovani LdBPK_210840.1   proteasome regulatory non-ATP-ase subunit 5, putative
Leishmania infantum LinJ.21.0840   proteasome regulatory non-ATP-ase subunit 5, putative,19S proteasome regulatory subunit
Leishmania major LmjF.21.0760   proteasome regulatory non-ATP-ase subunit 5, putative,19S proteasome regulatory subunit
Leishmania mexicana LmxM.21.0760   proteasome regulatory non-ATP-ase subunit 5, putative,19S proteasome regulatory subunit
Loa Loa (eye worm) LOAG_05097   PCI domain-containing protein
Mus musculus ENSMUSG00000020720   proteasome (prosome, macropain) 26S subunit, non-ATPase, 12
Neospora caninum NCLIV_026180   hypothetical protein
Oryza sativa 4334802   Os03g0851300
Plasmodium berghei PBANKA_0502200   26S proteasome regulatory subunit p55, putative
Plasmodium falciparum PF3D7_1017900   26S proteasome regulatory subunit p55, putative
Plasmodium knowlesi PKNH_0602100   26S proteasome regulatory subunit p55, putative
Plasmodium vivax PVX_001760   26S proteasome regulatory subunit p55, putative
Plasmodium yoelii PY02643   hypothetical protein
Saccharomyces cerevisiae YDL147W   proteasome regulatory particle lid subunit RPN5
Schistosoma japonicum Sjp_0092210   26S proteasome non-ATPase regulatory subunit 12, putative
Schistosoma japonicum Sjp_0078790   ko:K03035 26S proteasome regulatory subunit N5, putative
Schistosoma mansoni Smp_058650   proteasome regulatory subunit-related
Schmidtea mediterranea mk4.002954.00  
Trypanosoma brucei gambiense Tbg972.10.1830   proteasome regulatory non-ATP-ase subunit 5,19S proteasome regulatory subunit
Trypanosoma brucei Tb927.10.1550   proteasome regulatory non-ATP-ase subunit 5
Trypanosoma congolense TcIL3000_10_1350   proteasome regulatory non-ATP-ase subunit 5, putative
Trypanosoma cruzi TcCLB.506977.90   proteasome regulatory non-ATP-ase subunit 5, putative
Toxoplasma gondii TGME49_261210   26s proteasome subunit p55, putative
Theileria parva TP02_0768   26S proteasome subunit p55, putative
Trichomonas vaginalis TVAG_438030   proteasome regulatory subunits, putative

Essentiality

cgd1_1530 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.10.1550 Trypanosoma brucei significant loss of fitness in bloodstream forms (3 days) alsford
Tb927.10.1550 Trypanosoma brucei significant loss of fitness in bloodstream forms (6 days) alsford
Tb927.10.1550 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.10.1550 Trypanosoma brucei significant loss of fitness in differentiation of procyclic to bloodstream forms alsford
CELE_F10G7.8 Caenorhabditis elegans embryonic lethal wormbase
CELE_F10G7.8 Caenorhabditis elegans sterile wormbase
YDL147W Saccharomyces cerevisiae inviable yeastgenome
PBANKA_0502200 Plasmodium berghei Essential plasmo
TGME49_261210 Toxoplasma gondii Probably essential sidik
Show/Hide essentiality data references
  • 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.
  • 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
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • 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.
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • neb C. elegans RNAi phenotypes Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs
  • 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.
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection

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 proteasome (prosome, macropain) 26S subunit, non-ATPase, 12 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 cgd1_1530 (Cryptosporidium parvum), Rpn5 like 26S proteasomal regulatory subunit 12, PINT domain containing protein
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