Rv0535 5'-methylthioadenosine phosphorylase (EC 2.4.2.28)

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv0535 pnp 5'-methylthioadenosine phosphorylase (EC 2.4.2.28) CDS 626457 627251 + 795 264 FALSE

Rv0535 (5'-methylthioadenosine phosphorylase (EC 2.4.2.28)) is predicted to be co-regulated in modules bicluster_0099 with residual 0.60 and bicluster_0344 with residual 0.49.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 5.70 and 470.00 for bicluster_0099 and 0.10 and 8.00 for bicluster_0344 respectively.

These modules are enriched for following go terms: .

This gene is found to be for growth on cholesterol.

Mutant available?: Yes

Last update: 10/16/2017 - 02:57
BEI Mutant Available BEI Mutant ID BEI MT Number BEI Target ID Order from BEI
Yes NR-18021 MT0559 1136
Product (LegacyBRC) Product (RefSeq)
PROBABLE 5&apos-METHYLTHIOADENOSINE PHOSPHORYLASE PNP [MTA PHOSPHORYLASE] 5'-methylthioadenosine phosphorylase
Operon # Operon
361 -
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

S-methyl-5'-thioadenosine phosphorylase 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:  
BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network

STRING

GI Number Protein ID Blast Conserved Domains
15607675 NP_215049.1 Run
GO:0017061

S-methyl-5-thioadenosine phosphorylase activity

S-methyl-5-thioadenosine phosphorylase activity

Details: 
Catalysis of the reaction: 5'-methylthioadenosine + phosphate = adenine + 5-methylthio-D-ribose 1-phosphate.
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
0.340000 2.27

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: