Detailed view for Rv3777

Basic information

TDR Targets ID: 980378
Mycobacterium tuberculosis, Probable oxidoreductase

Source Database / ID:  Tuberculist 

pI: 6.6413 | Length (AA): 328 | MW (Da): 33931 | Paralog Number: 0

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

Druggability Group : DG2

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

Gene Ontology

Mouse over links to read term descriptions.
GO:0016491   oxidoreductase activity  
GO:0008270   zinc ion binding  
GO:0055114   oxidation reduction  

Metabolic Pathways

This gene is not mapped to any metabolic pathway in 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
2 328 2c0c (A) 22 360 30.00 0 1 1.29505 -0.3
4 328 4dup (A) 7 331 46.00 0 1 1.53325 -0.54
136 238 2zb3 (A) 149 254 29.00 0.043 1 0.784924 -1.34
140 204 5xtf (A) 4 72 26.00 0 1 0.548571 -0.99

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_129009)

Species Accession Gene Product
Arabidopsis thaliana AT4G21580   oxidoreductase, zinc-binding dehydrogenase family protein
Dictyostelium discoideum DDB_G0272440   alcohol dehydrogenase
Homo sapiens ENSG00000115129   tumor protein p53 inducible protein 3
Leishmania braziliensis LbrM.29.1090   hypothetical protein, conserved
Leishmania donovani LdBPK_291100.1   putative NAD(P)H quinone oxidoreductase, PIG3 family, putative
Leishmania infantum LinJ.29.1100   hypothetical protein, conserved
Leishmania major LmjF.29.1010   hypothetical protein, conserved
Leishmania mexicana LmxM.08_29.1010   hypothetical protein, conserved
Mycobacterium leprae ML0118c   Probable oxidireductase
Mycobacterium tuberculosis Rv3777   Probable oxidoreductase
Mycobacterium ulcerans MUL_0096   oxidoreductase
Neospora caninum NCLIV_019330   NADPH:quinone reductase and related Zn-dependent oxidoreductases, related
Oryza sativa 4331066   Os02g0805600
Plasmodium berghei PBANKA_0708600   quinone oxidoreductase, putative
Plasmodium yoelii PY04242   quinone oxidoreductase, putative
Trypanosoma brucei gambiense Tbg972.3.5590   oxidoreductase, putative
Trypanosoma brucei Tb927.3.4990   oxidoreductase, putative
Trypanosoma congolense TcIL3000_3_3020   oxidoreductase, putative
Trypanosoma cruzi TcCLB.506485.80   oxidoreductase, putative
Toxoplasma gondii TGME49_244870   quinone oxidoreductase, putative

Essentiality

Rv3777 has one or more orthologs with essentiality data
Gene/Ortholog Organism Phenotype Source Study
Tb927.3.4990 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (3 days) alsford
Tb927.3.4990 Trypanosoma brucei no significant loss or gain of fitness in bloodstream forms (6 days) alsford
Tb927.3.4990 Trypanosoma brucei no significant loss or gain of fitness in procyclic forms alsford
Tb927.3.4990 Trypanosoma brucei no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms alsford
TGME49_244870 Toxoplasma gondii Probably non-essential sidik
Show/Hide essentiality data references
  • keio Systematic single-gene knock-out mutants of E. coli K12 The Keio Collection
  • 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.
  • shigen Profiling of E. coli Chromosome (PEC) National Institute of Genetics, Japan
  • gerdes Experimental determination and system-level analysis of essential genes in E. coli MG1655 Gerdes et al., J Bacteriol. 2003 185:5673-84
  • neb C. elegans RNAi phenotypes Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs
  • yeastgenome Systematic deletion of yeast genes Saccharomyces Genome Database
  • blattner Systematic mutagenesis of the E. coli (MG1655) genome J Bacteriol 2004, 186:4921-4930
  • alsford High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome Genome Res 2011, 21:915-924
  • 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.
  • nmpdr Genome-scale essentiality datasets from published studies (M. tuberculosis) National Microbial Pathogen Data Resource
  • wormbase C. elegans RNAi experiments WormBase web site, http://www.wormbase.org, release WS170

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
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

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 Rv3777 (Mycobacterium tuberculosis), Probable oxidoreductase
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