Rv1928c Probable short-chain type dehydrogenase/reductase (EC 1.-.-.-)

Summary
Product Feature Type Start End Strand Length AA Length is TF
Rv1928c Probable short-chain type dehydrogenase/reductase (EC 1.-.-.-) CDS 2180450 2181217 - 768 255 FALSE

Rv1928c (Probable short-chain type dehydrogenase/reductase (EC 1.-.-.-)) is predicted to be co-regulated in modules bicluster_0069 with residual 0.54 and bicluster_0573 with residual 0.50.

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_0069 and 49.00 and 180.00 for bicluster_0573 respectively.

These modules are enriched for following go terms: cellular component biogenesis.

This gene is found to be for growth on cholesterol.

Mutant available?: Yes

Last update: 10/16/2017 - 11:45
BEI Mutant Available BEI Mutant ID BEI MT Number BEI Target ID Order from BEI
Yes NR-18583 MT1980 2613
Displaying 1 - 1 of 1
Gene Target Differential Expression Distance Expression pvalue Type
No results were found
Displaying 1 - 1 of 1
ChipSeq TF Differential Expression Distance Expression pvalue Type
No results were found
Motif 1 Motif 2 Residual
bicluster_0069
e.value: 
0.0000000000000036
Motif Bicluster: 
e.value: 
0.0000025
Motif Bicluster: 
0.54
bicluster_0573
e.value: 
49
Motif Bicluster: 
e.value: 
180
Motif Bicluster: 
0.50
Product (LegacyBRC) Product (RefSeq)
PROBABLE SHORT-CHAIN TYPE DEHYDROGENASE_REDUCTASE short chain dehydrogenase
Operon # Operon
1268
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
15609065 NP_216444.1 Run
Description:Expression data from transcription factor over expression experiments. TFOE are matched to the ChIP-seq experiment done simultaneously. This dataset is described in Rustad et al. 2014, Genome Biology.
Quantitative Proteomics Data
t-test p-value Cholesterol/Glycerol Ratio
0.780000 1.83

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: