Rv2393 Sirohydrochlorin ferrochelatase (EC 4.99.1.4)

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv2393 che1 Sirohydrochlorin ferrochelatase (EC 4.99.1.4) CDS 2687128 2687973 + 846 281 FALSE

Rv2393 (Sirohydrochlorin ferrochelatase (EC 4.99.1.4)) is predicted to be co-regulated in modules bicluster_0119 with residual 0.32 and bicluster_0325 with residual 0.54.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 2,300.00 and 5,600.00 for bicluster_0119 and 0.00 and 72.00 for bicluster_0325 respectively.

These modules are enriched for following go terms: gene expression, macromolecule metabolic process, cellular macromolecule biosynthetic proc..., macromolecule biosynthetic process, ribosome, ribonucleoprotein complex, non-membrane-bounded organelle, intracellular non-membrane-bounded organ..., nucleotidyltransferase activity.

This gene is found to be for growth on cholesterol.

Mutant available?:

Product (LegacyBRC) Product (RefSeq)
Putative uncharacterized protein
Operon # Operon
1578 - - -
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

Sirohydrochlorin ferrochelatase Porphyrin and chlorophyll metabolism
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
15609530 NP_216909.1 Run
GO:0051266

sirohydrochlorin ferrochelatase activity

sirohydrochlorin ferrochelatase activity

Details: 
Catalysis of the reaction: siroheme + 2 H+ = Fe(2+) + sirohydrochlorin.
GO Category: 
molecular_function
2
Total items in this category:  
GO:0051266

sirohydrochlorin ferrochelatase activity

sirohydrochlorin ferrochelatase activity

Details: 
Catalysis of the reaction: siroheme + 2 H+ = Fe(2+) + sirohydrochlorin.
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
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: