Rv1178 N-succinyl-L,L-diaminopimelate aminotransferase alternative (EC

Product Feature Type Start End Strand Length AA Length is TF
Rv1178 N-succinyl-L,L-diaminopimelate aminotransferase alternative (EC CDS 1309364 1310452 + 1 089 362 FALSE

Rv1178 (N-succinyl-L,L-diaminopimelate aminotransferase alternative (EC is predicted to be co-regulated in modules bicluster_0236 with residual 0.53 and bicluster_0470 with residual 0.49.

This regulation is possibly mediated by two de-novo identified cis-regulatory motifs in each module with e-values , 1,500.00 and 1,800.00 for bicluster_0236 and 150.00 and 8,000.00 for bicluster_0470 respectively.

These modules are enriched for following go terms: cellular macromolecule catabolic process, tetrapyrrole metabolic process, tetrapyrrole biosynthetic process, porphyrin-containing compound metabolic ..., porphyrin-containing compound biosynthet... .

This gene is found to be for growth on cholesterol.

Mutant available?: Yes

Last update: 10/16/2017 - 11:09
BEI Mutant Available BEI Mutant ID BEI MT Number BEI Target ID Order from BEI
Yes NR-14927 MT1215 279
Product (LegacyBRC) Product (RefSeq)
PROBABLE AMINOTRANSFERASE N-succinyldiaminopimelate aminotransferase
Operon # Operon
799 -
PATRIC Locus Tag Enzyme Name PATRIC Pathways Transcriptomics


Succinyldiaminopimelate transaminase Lysine biosynthesis
Locus Tuberculist Genome View


Locus Tag KEGG Pathways


not assigned to any KEGG Pathway.
BioCyc Gene Page Cellular Overview Map
Link to STRING STRING Network


GI Number Protein ID Blast Conserved Domains
15608318 NP_215694.1 Run

succinyldiaminopimelate transaminase activity

succinyldiaminopimelate transaminase activity

Catalysis of the reaction: 2-oxoglutarate + N-succinyl-LL-2,6-diaminopimelate = L-2-succinylamino-6-oxopimelate + L-glutamate.
GO Category: 
Total items in this category:  

plasma membrane

plasma membrane

The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.
GO Category: 
Total items in this category:  
No TFOE experiment results were found
Quantitative Proteomics Data
t-test p-value Cholesterol/Glycerol Ratio
0.560000 2.18

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: