Rv1210 DNA-3-methyladenine glycosylase (EC 3.2.2.20)

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv1210 tagA DNA-3-methyladenine glycosylase (EC 3.2.2.20) CDS 1353522 1354136 + 615 204 FALSE

Rv1210 (DNA-3-methyladenine glycosylase (EC 3.2.2.20)) is predicted to be co-regulated in modules bicluster_0072 with residual 0.54 and bicluster_0357 with residual 0.54.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 0.00 and 0.32 for bicluster_0072 and 94.00 and 1,300.00 for bicluster_0357 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)
PROBABLE DNA-3-METHYLADENINE GLYCOSYLASE I TAGA [TAG I] [3-methyladenine-DNA glycosylase I constitutive] [DNA-3-methyladenine glycosidase I ] DNA-3-methyladenine glycosylase I
Operon # Operon
824 - - -
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

Not assigned Not assigned
Locus Tuberculist Genome View

Tuberculist

Quickview
Locus Tag KEGG Pathways

KEGG

Base excision repair

17
Total items in this category:  
BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network

STRING

GI Number Protein ID Blast Conserved Domains
15608350 NP_215726.1 Run
GO:0008725

DNA-3-methyladenine glycosylase activity

DNA-3-methyladenine glycosylase activity

Details: 
Catalysis of the reaction: DNA containing 3-methyladenine + H2O = DNA with abasic site + 3-methyladenine. This reaction is the hydrolysis of DNA by cleavage of the N-C1' glycosidic bond between the damaged DNA 3-methyladenine and the deoxyribose sugar to remove the 3-methyladenine, leaving an abasic site.
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
0.660000 1.30

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: