Rv0253 Nitrite reductase [NAD(P)H] small subunit (EC 1.7.1.4)

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv0253 nirD Nitrite reductase [NAD(P)H] small subunit (EC 1.7.1.4) CDS 305453 305809 + 357 118 FALSE

Rv0253 (Nitrite reductase [NAD(P)H] small subunit (EC 1.7.1.4)) is predicted to be co-regulated in modules bicluster_0134 with residual 0.52 and bicluster_0380 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 9.50 for bicluster_0134 and 0.07 and 0.10 for bicluster_0380 respectively.

These modules are enriched for following go terms: oxidoreductase activity, acting on other... .

This gene is found to be for growth on cholesterol.

Mutant available?:

Product (LegacyBRC) Product (RefSeq)
PROBABLE NITRITE REDUCTASE [NAD[P]H] SMALL SUBUNIT NIRD nitrite reductase [NAD(P)H] small subunit NirD
Operon # Operon
176 -
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

Nitrite reductase (NAD(P)H) Nitrogen metabolism
Locus Tuberculist Genome View

Tuberculist

Quickview
Locus Tag KEGG Pathways

KEGG

Nitrogen metabolism

24
Total items in this category:  

KEGG

Microbial metabolism in diverse environments

296
Total items in this category:  
BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network

STRING

GI Number Protein ID Blast Conserved Domains
15607394 NP_214767.1 Run
GO:0008942

nitrite reductase [NAD(P)H] activity

nitrite reductase [NAD(P)H] activity

Details: 
Catalysis of the reaction: ammonium hydroxide + 3 NAD(P)+ + H2O = nitrite + 3 NAD(P)H + 3 H+.
GO Category: 
molecular_function
2
Total items in this category:  
No TFOE experiment results were found

Quantitative Proteomics Data

t-test p-value Cholesterol/Glycerol Ratio
0.480000 0.83

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: