Rv3279c Biotin-protein ligase (EC 6.3.4.15)

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv3279c birA Biotin-protein ligase (EC 6.3.4.15) CDS 3661212 3662012 - 801 266 FALSE

Rv3279c (Biotin-protein ligase (EC 6.3.4.15)) is predicted to be co-regulated in modules bicluster_0054 with residual 0.52 and bicluster_0171 with residual 0.49.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 0.32 and 0.27 for bicluster_0054 and 0.77 and 120.00 for bicluster_0171 respectively.

These modules are enriched for following go terms: .

This gene is found to be for growth on cholesterol.

Mutant available?:

Product (LegacyBRC) Product (RefSeq)
POSSIBLE BIFUNCTIONAL PROTEIN BIRA: BIOTIN OPERON REPRESSOR + BIOTIN--[ACETYL-COA-CARBOXYLASE] SYNTHETASE [BIOTIN--PROTEIN LIGASE] biotin--protein ligase
Operon # Operon
2145
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

Biotin--[acetyl-CoA-carboxylase] ligase Biotin metabolism
Locus Tuberculist Genome View

Tuberculist

Quickview
Locus Tag KEGG Pathways

KEGG

Biotin metabolism

13
Total items in this category:  

KEGG

Metabolic pathways

601
Total items in this category:  
BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network

STRING

GI Number Protein ID Blast Conserved Domains
15610415 NP_217796.1 Run
GO:0004077

biotin-[acetyl-CoA-carboxylase] ligase activity

biotin-[acetyl-CoA-carboxylase] ligase activity

Details: 
Catalysis of the reaction: ATP + biotin + apo-(acetyl-CoA:carbon-dioxide ligase (ADP forming)) = AMP + diphosphate + (acetyl-CoA:carbon-dioxide ligase (ADP forming)).
GO Category: 
molecular_function
1
Total items in this category:  
GO:0018271

biotin-protein ligase activity

biotin-protein ligase activity

Details: 
Catalysis of the reaction: ATP + biotin + protein = AMP + diphosphate + biotin-protein.
GO Category: 
molecular_function
1
Total items in this category:  
No TFOE experiment results were found

Quantitative Proteomics Data

t-test p-value Cholesterol/Glycerol Ratio
NA NA

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: