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A conserved membrane protein negatively regulates Mce1 complexes in mycobacteria
by
Wang, Yuchun
, Chng, Shu-Sin
, Chen, Yushu
in
45/70
/ 631/326/1320
/ 631/45/287/1183
/ 631/45/612/1237
/ 82/16
/ 82/83
/ Assemblies
/ Binding
/ Fatty acids
/ Global health
/ Humanities and Social Sciences
/ Lipid metabolism
/ Lipids
/ Membrane proteins
/ Membranes
/ multidisciplinary
/ Proteins
/ Public health
/ Science
/ Science (multidisciplinary)
/ Substrates
/ Tuberculosis
/ Virulence factors
2023
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A conserved membrane protein negatively regulates Mce1 complexes in mycobacteria
by
Wang, Yuchun
, Chng, Shu-Sin
, Chen, Yushu
in
45/70
/ 631/326/1320
/ 631/45/287/1183
/ 631/45/612/1237
/ 82/16
/ 82/83
/ Assemblies
/ Binding
/ Fatty acids
/ Global health
/ Humanities and Social Sciences
/ Lipid metabolism
/ Lipids
/ Membrane proteins
/ Membranes
/ multidisciplinary
/ Proteins
/ Public health
/ Science
/ Science (multidisciplinary)
/ Substrates
/ Tuberculosis
/ Virulence factors
2023
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Do you wish to request the book?
A conserved membrane protein negatively regulates Mce1 complexes in mycobacteria
by
Wang, Yuchun
, Chng, Shu-Sin
, Chen, Yushu
in
45/70
/ 631/326/1320
/ 631/45/287/1183
/ 631/45/612/1237
/ 82/16
/ 82/83
/ Assemblies
/ Binding
/ Fatty acids
/ Global health
/ Humanities and Social Sciences
/ Lipid metabolism
/ Lipids
/ Membrane proteins
/ Membranes
/ multidisciplinary
/ Proteins
/ Public health
/ Science
/ Science (multidisciplinary)
/ Substrates
/ Tuberculosis
/ Virulence factors
2023
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A conserved membrane protein negatively regulates Mce1 complexes in mycobacteria
Journal Article
A conserved membrane protein negatively regulates Mce1 complexes in mycobacteria
2023
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Overview
Tuberculosis continues to pose a serious threat to global health.
Mycobacterium tuberculosis
, the causative agent of tuberculosis, is an intracellular pathogen that relies on various mechanisms to survive and persist within the host. Among their many virulence factors, mycobacteria encode Mce systems. Some of these systems are implicated in lipid uptake, but the molecular basis for Mce function(s) is poorly understood. To gain insights into the composition and architecture of Mce systems, we characterized the putative Mce1 complex involved in fatty acid transport. We show that the Mce1 system in
Mycobacterium smegmatis
comprises a canonical ATP-binding cassette transporter associated with distinct heterohexameric assemblies of substrate-binding proteins. Furthermore, we establish that the conserved membrane protein Mce1N negatively regulates Mce1 function via a unique mechanism involving blocking transporter assembly. Our work offers a molecular understanding of Mce complexes, sheds light on mycobacterial lipid metabolism and its regulation, and informs future anti-mycobacterial strategies.
Mycobacterial Mce systems are putative ABC transporters for lipids. Here, the authors revealed two distinct Mce1 complexes comprising different heterohexameric substrate binding assemblies that are negatively regulated via a novel mechanism.
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