Rv0597c ATPase

Summary
Product Feature Type Start End Strand Length AA Length is TF
Rv0597c ATPase CDS 695668 696903 - 1 236 411 FALSE

Rv0597c (ATPase) is predicted to be co-regulated in modules bicluster_0156 with residual 0.52 and bicluster_0517 with residual 0.45.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 180.00 and 890.00 for bicluster_0156 and 770.00 and 2,600.00 for bicluster_0517 respectively.

These modules are enriched for following go terms: .

This gene is found to be for growth on cholesterol.

Mutant available?:

Displaying 1 - 1 of 1
Gene Target Differential Expression Distance Expression pvalue Type
No results were found
Displaying 1 - 3 of 3
ChipSeq TF Differential Expression Distance Expression pvalue Type
Repressed 22 -0.72 0.0165959 CDS
Transcriptional regulator, PadR family
No 31 -0.12 0.962221 CDS
HTH-type transcriptional regulator
No 51 0.05 0.896467 CDS
Motif 1 Motif 2 Residual
bicluster_0156
e.value: 
180
Motif Bicluster: 
e.value: 
890
Motif Bicluster: 
0.52
bicluster_0517
e.value: 
770
Motif Bicluster: 
e.value: 
2600
Motif Bicluster: 
0.45
Product (LegacyBRC) Product (RefSeq)
Putative uncharacterized protein
Operon # Operon
399
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
15607737 NP_215111.1 Run
Description:Expression data from transcription factor over expression experiments. TFOE are matched to the ChIP-seq experiment done simultaneously. This dataset is described in Rustad et al. 2014, Genome Biology.
Quantitative Proteomics Data
t-test p-value Cholesterol/Glycerol Ratio
0.750000 0.79

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: