Rv3685c Probable cytochrome P450 137 cyp137 (EC 1.14.-.-)


Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv3685c cyp137 Probable cytochrome P450 137 cyp137 (EC 1.14.-.-) CDS 4127295 4128725 - 1 431 476 FALSE

Rv3685c (Probable cytochrome P450 137 cyp137 (EC 1.14.-.-)) is predicted to be co-regulated in modules bicluster_0104 with residual 0.59 and bicluster_0592 with residual 0.49.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 3,600.00 and 3,500.00 for bicluster_0104 and 900.00 and 6,300.00 for bicluster_0592 respectively.

These modules are enriched for following go terms: pyrimidine nucleobase biosynthetic proce..., pyrimidine nucleobase metabolic process, nucleobase biosynthetic process .

This gene is found to be for growth on cholesterol.

Mutant available?:

BASS Score Distance to Tuberculist Start Codon Internal TSS New Internal UTR Re-Annotated Start Tuberculist Annotated Start
-0.092 69 4128656 42 4128614 4128725
Product (LegacyBRC) Product (RefSeq)
Putative cytochrome P450 137 cytochrome P450 137
Operon # Operon
2401 -
Locus Tuberculist Genome View


Locus Tag KEGG Pathways


Bisphenol degradation

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Polycyclic aromatic hydrocarbon degradation

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Aminobenzoate degradation

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Limonene and pinene degradation

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Metabolic pathways

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Biosynthesis of secondary metabolites

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Microbial metabolism in diverse environments

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BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network


GI Number Protein ID Blast Conserved Domains
15610821 NP_218202.1 Run

plasma membrane

plasma membrane

The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.
GO Category: 
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No TFOE experiment results were found

Quantitative Proteomics Data

t-test p-value Cholesterol/Glycerol Ratio
0.780000 1.69

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: