Rv3824c Polyketide synthase associated protein PapA1

Summary

Symbol Product Feature Type Start End Strand Length AA Length is TF
Rv3824c papA1 Polyketide synthase associated protein PapA1 CDS 4291639 4293174 - 1 536 511 FALSE

Rv3824c (Polyketide synthase associated protein PapA1) is predicted to be co-regulated in modules bicluster_0122 with residual 0.57 and bicluster_0244 with residual 0.55.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 1.10 and 6.50 for bicluster_0122 and 0.00 and 0.00 for bicluster_0244 respectively.

These modules are enriched for following go terms: cellular protein modification process, protein modification process, phosphorylation, protein kinase activity .

This gene is found to be for growth on cholesterol.

Mutant available?: Yes

Last update: 10/16/2017 - 16:54
BEI Mutant Available BEI Mutant ID BEI MT Number BEI Target ID Order from BEI
Yes NR-18163 MT3932 1626
Product (LegacyBRC) Product (RefSeq)
SL659 acyltransferase papA1 polyketide synthase associated protein
Operon # Operon
2501
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
15610960 NP_218341.1 Run
GO:0008415

NA

NA

Details: 
NA
GO Category: 
NA
6
Total items in this category:  
GO:0046506

sulfolipid biosynthetic process

sulfolipid biosynthetic process

Details: 
The chemical reactions and pathways resulting in the formation of sulfolipid, a compound containing a sulfonic acid residue joined by a carbon-sulfur bond to a lipid.
GO Category: 
biological_process
5
Total items in this category:  
No TFOE experiment results were found

Quantitative Proteomics Data

t-test p-value Cholesterol/Glycerol Ratio
0.000000 0.43

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: