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Title: Structures of EccB 1 and EccD 1 from the core complex of the mycobacterial ESX-1 type VII secretion system

Abstract

The ESX-1 type VII secretion system is an important determinant of virulence in pathogenic mycobacteria, including Mycobacterium tuberculosis. This complicated molecular machine secretes folded proteins through the mycobacterial cell envelope to subvert the host immune response. Despite its important role in disease very little is known about the molecular architecture of the ESX-1 secretion system. This study characterizes the structures of the soluble domains of two conserved core ESX-1 components – EccB 1 and EccD 1. The periplasmic domain of EccB 1 consists of 4 repeat domains and a central domain, which together form a quasi 2-fold symmetrical structure. The repeat domains of EccB 1 are structurally similar to a known peptidoglycan binding protein suggesting a role in anchoring the ESX-1 system within the periplasmic space. The cytoplasmic domain of EccD 1 has a ubiquitin-like fold and forms a dimer with a negatively charged groove. In conclusion, these structures represent a major step towards resolving the molecular architecture of the entire ESX-1 assembly and may contribute to ESX-1 targeted tuberculosis intervention strategies.

Authors:
 [1];  [2];  [3];  [2];  [2];  [2];  [2];  [3]
  1. Univ. of Kentucky, Lexington, KY (United States); Univ. of Virginia, Charlottesville, VA (United States)
  2. Univ. of California, Los Angeles, CA (United States)
  3. Univ. of Kentucky, Lexington, KY (United States)
Publication Date:
Research Org.:
Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS); Univ. of Kentucky, Lexington, KY (United States); Carnegie Inst. of Washington, Washington, DC (United States); Univ. of California, Los Angeles, CA (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22); US National Institutes of Health (NIH/NIGMS); USDOE Office of Science (SC), Biological and Environmental Research (BER) (SC-23)
OSTI Identifier:
1249240
Alternate Identifier(s):
OSTI ID: 1364020; OSTI ID: 1466594
Grant/Contract Number:  
FC02-02ER63421; W-31-109-Eng-38.; 23616-002-06 F3:02; P30GM110787; P20GM103486
Resource Type:
Journal Article: Accepted Manuscript
Journal Name:
BMC Structural Biology (Online)
Additional Journal Information:
Journal Name: BMC Structural Biology (Online); Journal Volume: 16; Journal Issue: 1; Journal ID: ISSN 1472-6807
Publisher:
BioMed Central
Country of Publication:
United States
Language:
ENGLISH
Subject:
59 BASIC BIOLOGICAL SCIENCES; 60 APPLIED LIFE SCIENCES; EccB; EccD; Mycobacterium tuberculosis; Type VII secretion system; ESX

Citation Formats

Wagner, Jonathan M., Chan, Sum, Evans, Timothy J., Kahng, Sara, Kim, Jennifer, Arbing, Mark A., Eisenberg, David, and Korotkov, Konstantin V. Structures of EccB1 and EccD1 from the core complex of the mycobacterial ESX-1 type VII secretion system. United States: N. p., 2016. Web. doi:10.1186/s12900-016-0056-6.
Wagner, Jonathan M., Chan, Sum, Evans, Timothy J., Kahng, Sara, Kim, Jennifer, Arbing, Mark A., Eisenberg, David, & Korotkov, Konstantin V. Structures of EccB1 and EccD1 from the core complex of the mycobacterial ESX-1 type VII secretion system. United States. doi:10.1186/s12900-016-0056-6.
Wagner, Jonathan M., Chan, Sum, Evans, Timothy J., Kahng, Sara, Kim, Jennifer, Arbing, Mark A., Eisenberg, David, and Korotkov, Konstantin V. Sat . "Structures of EccB1 and EccD1 from the core complex of the mycobacterial ESX-1 type VII secretion system". United States. doi:10.1186/s12900-016-0056-6. https://www.osti.gov/servlets/purl/1249240.
@article{osti_1249240,
title = {Structures of EccB1 and EccD1 from the core complex of the mycobacterial ESX-1 type VII secretion system},
author = {Wagner, Jonathan M. and Chan, Sum and Evans, Timothy J. and Kahng, Sara and Kim, Jennifer and Arbing, Mark A. and Eisenberg, David and Korotkov, Konstantin V.},
abstractNote = {The ESX-1 type VII secretion system is an important determinant of virulence in pathogenic mycobacteria, including Mycobacterium tuberculosis. This complicated molecular machine secretes folded proteins through the mycobacterial cell envelope to subvert the host immune response. Despite its important role in disease very little is known about the molecular architecture of the ESX-1 secretion system. This study characterizes the structures of the soluble domains of two conserved core ESX-1 components – EccB1 and EccD1. The periplasmic domain of EccB1 consists of 4 repeat domains and a central domain, which together form a quasi 2-fold symmetrical structure. The repeat domains of EccB1 are structurally similar to a known peptidoglycan binding protein suggesting a role in anchoring the ESX-1 system within the periplasmic space. The cytoplasmic domain of EccD1 has a ubiquitin-like fold and forms a dimer with a negatively charged groove. In conclusion, these structures represent a major step towards resolving the molecular architecture of the entire ESX-1 assembly and may contribute to ESX-1 targeted tuberculosis intervention strategies.},
doi = {10.1186/s12900-016-0056-6},
journal = {BMC Structural Biology (Online)},
number = 1,
volume = 16,
place = {United States},
year = {Sat Feb 27 00:00:00 EST 2016},
month = {Sat Feb 27 00:00:00 EST 2016}
}

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