Rv2094c - SEC-independent protein translocase membrane-bound protein tatA


Protein Domains

Gene Information
LocusRv2094c
SymboltatA
Gene NameSEC-independent protein translocase membrane-bound protein tatA
Location2353046 - 2353297 (-)
SpeciesMycobacterium tuberculosis H37Rv complete genome.
LengthGene:252 bp
Protein:84 aa
External LinksTuberculist
Target Gene Information
String Protein-Protein Interactions
STITCH Chemical-Protein Interactions
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Orthologs
Orthogroup Number22099
Related GenesCE1620 cg1685 DIP1242 jk0942 MAP1830c MAV_2409 Mkms_2519 ML1331 Mmcs_2474 MSMEG_3887 MT2155 MUL_2326 Mvan_3442 nfa31640
Transcriptional Regulation
Operons View gene in operon browser
Regulatory Network
Search for regulators of Rv2094c
Expression Correlation Genes with Correlated Expression
Scatterplot of Gene Expression

Sequence
Proteins
Genomic Sequence
Community Annotations Pending Curatorial Review
FieldValueStatusCreatorDate
InteractionPhysicalInteraction Rv2525cactivekandarpbioinfo2012-10-05
ChIP (Physical interaction)
JA. McDonough, JR. McCann et al. Identification of functional Tat signal sequences in Mycobacterium tuberculosis proteins. J. Bacteriol. 2008
InteractionPhysicalInteraction Rv2525cactivekandarpbioinfo2012-10-05
ChIP (Physical interaction)
B. Saint-Joanis, C. Demangel et al. Inactivation of Rv2525c, a substrate of the twin arginine translocation (Tat) system of Mycobacterium tuberculosis, increases beta-lactam susceptibility and virulence. J. Bacteriol. 2006
InteractionPhysicalInteraction Rv2068cactiveashwinigbhat2012-10-05
Spectrophotometric Analysis
JA. McDonough, KE. Hacker et al. The twin-arginine translocation pathway of Mycobacterium smegmatis is functional and required for the export of mycobacterial beta-lactamases. J. Bacteriol. 2005
InteractionPhysicalInteraction Rv2068cactiveashwinigbhat2012-10-05
Spectrophotometric Analysis
JE. Posey, TM. Shinnick et al. Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis. J. Bacteriol. 2006
InteractionPhysicalInteraction Rv2068cactivepriti.priety2012-10-05
Spectrophotometric Analysis
JA. McDonough, KE. Hacker et al. The twin-arginine translocation pathway of Mycobacterium smegmatis is functional and required for the export of mycobacterial beta-lactamases. J. Bacteriol. 2005
InteractionPhysicalInteraction Rv2068cactivepriti.priety2012-10-05
Spectrophotometric Analysis
JE. Posey, TM. Shinnick et al. Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis. J. Bacteriol. 2006
InteractionOperon Rv1224activegaat3s2012-10-05
Gene Neighbourhood(Functional Linkage)
JA. McDonough, KE. Hacker et al. The twin-arginine translocation pathway of Mycobacterium smegmatis is functional and required for the export of mycobacterial beta-lactamases. J. Bacteriol. 2005
InteractionOperon Rv1224activegaat3s2012-10-05
Gene Neighbourhood(Functional Linkage)
authors,BC. Berks,F. Sargent,T. Palmer The Tat protein export pathway. Mol. Microbiol. 2000
InteractionOperon Rv1224activegaat3s2012-10-05
Gene Neighbourhood(Functional Linkage)
JE. Posey, TM. Shinnick et al. Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis. J. Bacteriol. 2006
InteractionRegulatedBy Rv1221activeyamir.moreno2012-10-05
Microarrays. mRNA levels of regulated element measured and compared between wild-type and trans-element mutation (knockout, over expression etc.) performed by using microarray (or macroarray) experiments.. qRT-PCR. mRNA expression levels of regulated element measured and compared between wild-type and trans-element mutation (knockout, over expression etc.) performed by using qRT-PCR technique.
PA. Fontán, V. Aris et al. Mycobacterium tuberculosis Sigma Factor E Regulon Modulates the Host Inflammatory Response. J. Infect. Dis. 2008
InteractionRegulatedBy Rv1221activeyamir.moreno2012-10-05
Microarrays. mRNA levels of regulated element measured and compared between wild-type and trans-element mutation (knockout, over expression etc.) performed by using microarray (or macroarray) experiments.. qRT-PCR. mRNA expression levels of regulated element measured and compared between wild-type and trans-element mutation (knockout, over expression etc.) performed by using qRT-PCR technique.
PA. Fontán, V. Aris et al. Mycobacterium tuberculosis Sigma Factor E Regulon Modulates the Host Inflammatory Response. J. Infect. Dis. 2008