Rv0153c Protein tyrosine phosphatase (EC 3.1.3.48)

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv0153c ptbB Protein tyrosine phosphatase (EC 3.1.3.48) CDS 181155 181985 - 831 276 FALSE

Rv0153c (Protein tyrosine phosphatase (EC 3.1.3.48)) is predicted to be co-regulated in modules bicluster_0098 with residual 0.64 and bicluster_0314 with residual 0.57.

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_0098 and 0.00 and 0.00 for bicluster_0314 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)
PHOSPHOTYROSINE PROTEIN PHOSPHATASE PTPB [PROTEIN-TYROSINE-PHOSPHATASE] [PTPase] phosphotyrosine protein phosphatase PTPB (protein-tyrosine-phosphatase) (PTPase)
Operon # Operon
110 -
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics

PATRIC

Not assigned Not assigned
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
15607295 NP_214667.1 Run
GO:0004437

inositol or phosphatidylinositol phosphatase activity

inositol or phosphatidylinositol phosphatase activity

Details: 
OBSOLETE. Catalysis of the removal of a phosphate group from phosphorylated myo-inositol (1,2,3,5/4,6-cyclohexanehexol) or a phosphatidylinositol.
GO Category: 
molecular_function
1
Total items in this category:  
GO:0004722

protein serine/threonine phosphatase activity

protein serine/threonine phosphatase activity

Details: 
Catalysis of the reaction: protein serine phosphate + H2O = protein serine + phosphate, and protein threonine phosphate + H2O = protein threonine + phosphate.
GO Category: 
molecular_function
1
Total items in this category:  
GO:0004725

protein tyrosine phosphatase activity

protein tyrosine phosphatase activity

Details: 
Catalysis of the reaction: protein tyrosine phosphate + H2O = protein tyrosine + phosphate.
GO Category: 
molecular_function
2
Total items in this category:  
GO:0005576

extracellular region

extracellular region

Details: 
The space external to the outermost structure of a cell. For cells without external protective or external encapsulating structures this refers to space outside of the plasma membrane. This term covers the host cell environment outside an intracellular parasite.
GO Category: 
cellular_component
272
Total items in this category:  
GO:0006470

protein dephosphorylation

protein dephosphorylation

Details: 
The process of removing one or more phosphoric residues from a protein.
GO Category: 
biological_process
3
Total items in this category:  
GO:0009405

pathogenesis

pathogenesis

Details: 
The set of specific processes that generate the ability of an organism to cause disease in another.
GO Category: 
biological_process
65
Total items in this category:  
GO:0004438

phosphatidylinositol-3-phosphatase activity

phosphatidylinositol-3-phosphatase activity

Details: 
Catalysis of the reaction: 1-phosphatidyl-1D-myo-inositol 3-phosphate + H2O = 1-phosphatidyl-1D-myo-inositol + phosphate.
GO Category: 
molecular_function
3
Total items in this category:  
No TFOE experiment results were found

Quantitative Proteomics Data

t-test p-value Cholesterol/Glycerol Ratio
0.050000 0.02

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: