Property | Value | Creator | Evidence | PMID | Comment |
Interaction | PhysicalInteraction Rv2525c | kandarpbioinfo | IPI | | 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 |
Interaction | PhysicalInteraction Rv2525c | kandarpbioinfo | IPI | | ChIP (Physical interaction) JA. McDonough, JR. McCann et al. Identification of functional Tat signal sequences in Mycobacterium tuberculosis proteins. J. Bacteriol. 2008 |
Citation | Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis. JE. Posey, TM. Shinnick et al. J. Bacteriol. 2006 | priti.priety | IDA | 16452415 | Spectrophotometric Analysis |
Interaction | PhysicalInteraction Rv2068c | priti.priety | IDA | | Spectrophotometric Analysis JE. Posey, TM. Shinnick et al. Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis. J. Bacteriol. 2006 |
Citation | The twin-arginine translocation pathway of Mycobacterium smegmatis is functional and required for the export of mycobacterial beta-lactamases. JA. McDonough, KE. Hacker et al. J. Bacteriol. 2005 | priti.priety | IDA | 16267291 | Spectrophotometric Analysis |
Interaction | PhysicalInteraction Rv2068c | priti.priety | IDA | | 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 |
Citation | Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis. JE. Posey, TM. Shinnick et al. J. Bacteriol. 2006 | ashwinigbhat | IDA | 16452415 | Spectrophotometric Analysis |
Interaction | PhysicalInteraction Rv2068c | ashwinigbhat | IDA | | Spectrophotometric Analysis JE. Posey, TM. Shinnick et al. Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis. J. Bacteriol. 2006 |
Citation | The twin-arginine translocation pathway of Mycobacterium smegmatis is functional and required for the export of mycobacterial beta-lactamases. JA. McDonough, KE. Hacker et al. J. Bacteriol. 2005 | ashwinigbhat | IDA | 16267291 | Spectrophotometric Analysis |
Interaction | PhysicalInteraction Rv2068c | ashwinigbhat | IDA | | 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 |
Interaction | Operon Rv1224 | gaat3s | NAS | | Gene Neighbourhood(Functional Linkage) JE. Posey, TM. Shinnick et al. Characterization of the twin-arginine translocase secretion system of Mycobacterium smegmatis. J. Bacteriol. 2006 |
Interaction | Operon Rv1224 | gaat3s | NAS | | Gene Neighbourhood(Functional Linkage) authors,BC. Berks,F. Sargent,T. Palmer The Tat protein export pathway. Mol. Microbiol. 2000 |
Interaction | Operon Rv1224 | gaat3s | NAS | | 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 |
Interaction | RegulatedBy Rv1221 | yamir.moreno | IEP | | 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. Fontn, V. Aris et al. Mycobacterium tuberculosis Sigma Factor E Regulon Modulates the Host Inflammatory Response. J. Infect. Dis. 2008 |
Interaction | RegulatedBy Rv1221 | yamir.moreno | IEP | | 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. Fontn, V. Aris et al. Mycobacterium tuberculosis Sigma Factor E Regulon Modulates the Host Inflammatory Response. J. Infect. Dis. 2008 |
Citation | The twin-arginine translocation pathway of Mycobacterium smegmatis is functional and required for the export of mycobacterial beta-lactamases. JA. McDonough, KE. Hacker et al. J. Bacteriol. 2005 | jlew | | 16267291 | MS deletion mutant. We describe phenotypic analyses of tatA and tatC deletion mutants of M. smegmatis, which demonstrated that tatA and tatC encode components of a functional Tat system. |
Citation | Inactivation of Rv2525c, a substrate of the twin arginine translocation (Tat) system of Mycobacterium tuberculosis, increases beta-lactam susceptibility and virulence. B. Saint-Joanis, C. Demangel et al. J. Bacteriol. 2006 | jlew | | 16952959 | essential in Mtb. Saint-Joanis B, Demangel C, Jackson M, Brodin P, Marsollier L, Boshoff H, Cole ST. |