Rv2260 Putative hydrolase in cluster with formaldehyde/S-nitrosomycothiol reductase MscR

Summary

Product Feature Type Start End Strand Length AA Length is TF
Rv2260 Putative hydrolase in cluster with formaldehyde/S-nitrosomycothiol reductase MscR CDS 2533330 2533965 + 636 211 FALSE

Rv2260 (Putative hydrolase in cluster with formaldehyde/S-nitrosomycothiol reductase MscR) is predicted to be co-regulated in modules bicluster_0496 with residual 0.57 and bicluster_0585 with residual 0.58.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 0.00 and 0.00 for bicluster_0496 and 0.06 and 350.00 for bicluster_0585 respectively.

These modules are enriched for following go terms: sulfur compound metabolic process cofactor biosynthetic process, coenzyme metabolic process, cofactor metabolic process.

This gene is found to be for growth on cholesterol.

Mutant available?:

BASS Score Re-Annotated Start Tuberculist Annotated Start
-0.297 2533327 2533330
Product (LegacyBRC) Product (RefSeq)
Putative uncharacterized protein
Operon # Operon
1484 -
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

Not assigned Not assigned
Locus Tuberculist Genome View

Tuberculist

Quickview
Locus Tag KEGG Pathways

KEGG

not assigned to any KEGG Pathway.
BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network

STRING

GI Number Protein ID Blast Conserved Domains
15609397 NP_216776.1 Run
GO:0004416

hydroxyacylglutathione hydrolase activity

hydroxyacylglutathione hydrolase activity

Details: 
Catalysis of the reaction: (S)-(2-hydroxyacyl)glutathione + H2O = glutathione + a 2-hydroxy carboxylate.
GO Category: 
molecular_function
3
Total items in this category:  
GO:0040007

growth

growth

Details: 
The increase in size or mass of an entire organism, a part of an organism or a cell.
GO Category: 
biological_process
621
Total items in this category:  
No TFOE experiment results were found

Quantitative Proteomics Data

t-test p-value Cholesterol/Glycerol Ratio
0.540000 0.55

How essentiality calculations were done?

The relative representation of each mutant was determined by calculating the fold change (sequence reads/insertion in cholesterol divided by sequence reads/insertion in glycerol) for each gene. Statistical significance was determined by t-test. Each insertion site in each replicate sample was treated as a separate data point. The hyperbola used for defining genes specifically required for growth in cholesterol was defined by the formula, y = 3.8/x+0.7. Genes above this line are annotated as required for growth on cholesterol.

TRIP log2 fold abundance change

reports the log2 abundance fold change of each TFI strain, relative to no induction, in absence or presence of drug, averaged across experimental replicates. Also reported are the accompanying z-scores and two-sided t-test p-values for each TFI strain under each condition. Please refer to Ma et al., 2020, Nature Microbiology for more information.

p-value Untreated:
p-value INH: