2022
DOI: 10.1128/mbio.00134-22
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The Antibacterial Type VII Secretion System of Bacillus subtilis: Structure and Interactions of the Pseudokinase YukC/EssB

Abstract: Type VII secretion systems mediate protein extrusion from Gram-positive bacteria and are classified as T7SSa and T7SSb in Actinobacteria and in Firmicutes , respectively. Despite the genetic divergence of T7SSa and T7SSb, the high degree of structural similarity of their WXG100 substrates suggests similar secretion mechanisms.

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Cited by 26 publications
(34 citation statements)
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References 106 publications
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“…EssB, which also has a single transmembrane helix, has an N-terminal cytoplasmic pseudokinase-like domain and a C-terminal extracellular domain through which the protein dimerises. The extracellular domain is hypothesised to interact with other components, substrates or possibly the cell wall [43,49]. The pseudokinase domain of EssB, while lacking catalytic residues, retains structural similarity to the substrate-binding region of protein kinases [49].…”
Section: T7ssb-specific Core Components: Esaa Essa and Essbmentioning
confidence: 99%
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“…EssB, which also has a single transmembrane helix, has an N-terminal cytoplasmic pseudokinase-like domain and a C-terminal extracellular domain through which the protein dimerises. The extracellular domain is hypothesised to interact with other components, substrates or possibly the cell wall [43,49]. The pseudokinase domain of EssB, while lacking catalytic residues, retains structural similarity to the substrate-binding region of protein kinases [49].…”
Section: T7ssb-specific Core Components: Esaa Essa and Essbmentioning
confidence: 99%
“…EsaA, EssB EsaA interaction with EssB transmembrane domain, by BACTH. [43,120] EssA, EssB EssA -EssB direct interaction by BACTH. [43] EssA, EsaB EsaB -EssA direct interaction by BACTH.…”
Section: The T7ssb As a Bacterial Weapon Variable Contribution Of The...mentioning
confidence: 99%
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“…Bacillus subtilis) species (7,8). The primary role of the T7SSb is inhibition of competitor bacteria via secretion of antibacterial toxins (9)(10)(11)(12)(13)(14)(15). These toxin substrates usually have a transport-associated N-terminal LXG domain (IPR006829), and a highly polymorphic Cterminal toxin domain.…”
Section: Introductionmentioning
confidence: 99%