Rv1030 Potassium-transporting ATPase B chain (EC 3.6.3.12) (TC 3.A.3.7.1)

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv1030 kdpB Potassium-transporting ATPase B chain (EC 3.6.3.12) (TC 3.A.3.7.1) CDS 1153724 1155853 + 2 130 709 FALSE

Rv1030 (Potassium-transporting ATPase B chain (EC 3.6.3.12) (TC 3.A.3.7.1)) is predicted to be co-regulated in modules bicluster_0547 with residual 0.53 and bicluster_0563 with residual 0.52.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 0.00 and 19.00 for bicluster_0547 and 0.00 and 1,400.00 for bicluster_0563 respectively.

These modules are enriched for following go terms: .

This gene is found to be for growth on cholesterol.

Mutant available?: Yes

BASS Score Distance to Tuberculist Start Codon Internal TSS Re-Annotated Start Tuberculist Annotated Start
-1.21 2100 1155824 1153727 1153724
Last update: 10/16/2017 - 11:08
BEI Mutant Available BEI Mutant ID BEI MT Number BEI Target ID Order from BEI
Yes NR-15645 MT1059 1511
Product (LegacyBRC) Product (RefSeq)
Potassium-transporting ATPase B chain potassium-transporting ATPase subunit B
Operon # Operon
690 - - -
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

Not assigned Not assigned
Locus Tuberculist Genome View

Tuberculist

Quickview
Locus Tag KEGG Pathways

KEGG

Two-component system

53
Total items in this category:  
BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network

STRING

GI Number Protein ID Blast Conserved Domains
15608170 NP_215546.1 Run
GO:0008556

potassium-transporting ATPase activity

potassium-transporting ATPase activity

Details: 
Catalysis of the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + K+(out) = ADP + phosphate + K+(in).
GO Category: 
molecular_function
3
Total items in this category:  
No TFOE experiment results were found

Quantitative Proteomics Data

t-test p-value Cholesterol/Glycerol Ratio
0.280000 1.01

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: