Detailed view for Rv2115c

Basic information

TDR Targets ID: 8355
Mycobacterium tuberculosis, Mycobacterial proteasome ATPase Mpa

Source Database / ID:  Tuberculist 

pI: 4.6304 | Length (AA): 609 | MW (Da): 67401 | Paralog Number: 0

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

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

PF00004   ATPase family associated with various cellular activities (AAA)
PF16450   Proteasomal ATPase OB/ID domain

Gene Ontology

Mouse over links to read term descriptions.
GO:0019941   modification-dependent protein catabolic process  
GO:0010498   proteasomal protein catabolic process  
GO:0000502   proteasome complex  
GO:0000166   nucleotide binding  
GO:0017111   nucleoside-triphosphatase activity  
GO:0016887   ATPase activity  
GO:0005524   ATP binding  

Metabolic Pathways

Proteasome (KEGG)

Structural information

Modbase 3D models:

There are 8 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
24 96 3k29 (A) 43 112 19.00 0 0.18 0.375769 -1.2
25 96 2fxo (A) 848 910 25.00 0 0.05 0.229127 -0.25
26 94 3i00 (A) 377 440 34.00 0.39 0.07 0.3776 -0.02
52 234 3m9b (A) 52 234 99.99 0 1 1.39929 -0.09
53 528 5e7p (A) 286 744 25.00 0 1 0.960909 0.56
82 151 3h43 (A) 75 146 30.00 0 1 0.522843 -0.66
97 601 5kwa (A) 97 601 99.99 0 1 1.86503 -0.56
438 507 3kw6 (A) 0 68 17.00 0.028 0.33 0.423243 -1.2

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:

  • 3FP9:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date
  • 3M91:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date
  • 3M9B:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date
  • 3M9D:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date
  • 3M9H:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date
  • 5KWA:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date
  • 5KZF:
  • Resolution Method # Atoms # Residues Dep. Date Pub. Date Mod. Date

Expression

Upregulation Percent Ranking Stage Dataset
Upper 80-100% percentile Dormant phase, Dormant phase. hasan murphy
Show/Hide expression data references
  • murphy Identification of gene targets against dormant phase Mycobacterium tuberculosis infections.
  • hasan Prioritizing genomic drug targets in pathogens: application to Mycobacterium tuberculosis.

Orthologs

Ortholog group members (OG5_237684)

Species Accession Gene Product
Mycobacterium leprae ML1316   Probable mycobacterium proteasome ATPase Mpa
Mycobacterium tuberculosis Rv2115c   Mycobacterial proteasome ATPase Mpa
Mycobacterium ulcerans MUL_2337   ATPase

Essentiality

Rv2115c has direct evidence of essentiality
Gene/Ortholog Organism Phenotype Source Study
mtu2148 this record Mycobacterium tuberculosis non-essential nmpdr
Show/Hide essentiality data references
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • 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.
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • 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.
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection
  • 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
  • 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)

Annotated phenotypes:

Affected Entity Phenotypic quality Occurs in Occurs at Evidence Observed in Drugs/Inhibitors
growth (GO:0040007) decreased (PATO:0000468) inferred from animal model system (ECO:0000179) Mycobacterium tuberculosis No drug identifiers listed for this gene.
Annotator: crowther@u.washington.edu. Comment: 2007-12-28. References: 14671303 15659170

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
Non orthologous druggable targets
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

232 literature references were collected for this gene.

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

User comments

No user comments are available for this gene. Log in to add comments, or register.

Enter your comment

User ()
Gene identifier Rv2115c (Mycobacterium tuberculosis), Mycobacterial proteasome ATPase Mpa
Title for this comment
Comment