Rv2458 Homocysteine S-methyltransferase (EC 2.1.1.10)

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv2458 mmuM Homocysteine S-methyltransferase (EC 2.1.1.10) CDS 2759779 2760687 + 909 302 FALSE

Rv2458 (Homocysteine S-methyltransferase (EC 2.1.1.10)) is predicted to be co-regulated in modules bicluster_0172 with residual 0.58 and bicluster_0459 with residual 0.37.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 0.00 and 0.00 for bicluster_0172 and 2,300.00 and 2,800.00 for bicluster_0459 respectively.

These modules are enriched for following go terms: GTPase activity.

This gene is found to be for growth on cholesterol.

Mutant available?:

Product (LegacyBRC) Product (RefSeq)
PROBABLE HOMOCYSTEINE S-METHYLTRANSFERASE MMUM [S-METHYLMETHIONINE:HOMOCYSTEINE METHYLTRANSFERASE] [CYSTEINE METHYLTRANSFERASE] homocysteine methyltransferase
Operon # Operon
1620
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

Homocysteine S-methyltransferase Cysteine and methionine metabolism
Locus Tuberculist Genome View

Tuberculist

Quickview
Locus Tag KEGG Pathways

KEGG

Cysteine and methionine metabolism

28
Total items in this category:  

KEGG

Metabolic pathways

601
Total items in this category:  

KEGG

Biosynthesis of secondary metabolites

326
Total items in this category:  
BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network

STRING

GI Number Protein ID Blast Conserved Domains
15609595 NP_216974.1 Run
GO:0008898

homocysteine S-methyltransferase activity

homocysteine S-methyltransferase activity

Details: 
Catalysis of the reaction: S-adenosyl-L-methionine + L-homocysteine = S-adenosyl-L-homocysteine + L-methionine.
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
0.020000 0.76

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: