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virulence, detoxification, adaptation
information pathways
cell wall and cell processes
stable RNAs
insertion seqs and phages
PE/PPE
intermediary metabolism and respiration
unknown
regulatory proteins
conserved hypotheticals
lipid metabolism
pseudogenes
General annotation
TypeCDS
FunctionInvolved in phthiocerol dimycocerosate (PDIM) and phenolic glycolipid (PGL) biosynthesis. In M. tuberculosis H37Rv TesA interacts with the PpsE protein. PpsE is part of the phenolphthiocerol synthase PKS cluster.
Productthioesterase TesA
Comments-
Functional categoryLipid metabolism
MutantM. marinum tesA|MMAR_1778 transposon mutant lacks PDIM A, PDIM B, and PGLs, defect corrected by complemetation; mutant is more susceptible to some antibiotics (partially complemented by tesA expression) but not isoniazid (See Alibaud et al., 2011). M. marinum tesA|MMAR_1778 deletion mutant produces only trace amounts of PDIMs and PGLs, defect corrected by complementation with tesA but not tesA-S92A; mutant is more susceptible to several antibiotics (complemented by tesA expression) but not streptomycin (See Chavadi et al., 2011).
Check for mutants available at TARGET website
Coordinates
TypeStartEndOrientation
CDS21723212173070-
Genomic sequence
Feature type Upstream flanking region (bp) Downstream flanking region (bp) Update
       
Protein sequence
>Mycobacterium marinum M|MMAR_1778|tesA
VNGRSSNSKSDEKLTAPTLYIFPHAGGTAKDYVPFAKEFSGEVKRVAVQYPGQQDGYGLPPLESIPGLAEEIFAIMKPAARIDTPVALFGHSMGGMLAFEVALRFEAAGYRVLALFLSACSAPGHIKYKQLKGYSDNEMLDLVARATGTDPEFFNDEEFRVGVLPTLRAVRAIAGYSCPPENKLSCPIYTFIGSKDWIATREDMEPWRERTTGDFSLREFPGDHFYLNKNLPELVSDIEIGTLQQFDQI