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Cell redox homeostasis
Stable Identifier
R-HSA-1222541
Type
Pathway
Species
Homo sapiens
Related Species
Mycobacterium tuberculosis
ReviewStatus
5/5
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Disease (Homo sapiens)
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Bacterial Infection Pathways (Homo sapiens)
Infection with Mycobacterium tuberculosis (Homo sapiens)
Latent infection - Other responses of Mtb to phagocytosis (Homo sapiens)
Cell redox homeostasis (Homo sapiens)
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The most important response of
Mtb
to oxidative stress is provided by catalase and peroxiredoxins, both of which get their reducing equivalents through a network of disulfide proteins and, finally, from NAD(P)H. Multiple redundancies make choosing a good drug target difficult (Koul et al. 2011). Optimum efficacy can only be expected from inhibitors of the most upstream components of the redox cascades, i.e. the NAD(P)H-dependent reductases TrxB and Lpd (Jaeger & Flohe 2006).
Literature References
PubMed ID
Title
Journal
Year
17012768
The thiol-based redox networks of pathogens: unexploited targets in the search for new drugs
Flohé, L
,
Jaeger, T
Biofactors
2006
21270886
The challenge of new drug discovery for tuberculosis
Lounis, N
,
Guillemont, J
,
Andries, K
,
Arnoult, E
,
Koul, A
Nature
2011
Participants
Events
AhpD reactivates AhpC
(Homo sapiens)
DlaT reactivates AhpD
(Homo sapiens)
LpdC dimer reactivates DlaT
(Homo sapiens)
TrxA reactivates AhpC
(Homo sapiens)
TrxB reactivates TrxA
(Homo sapiens)
TrxA/B1 reactivates Tpx
(Homo sapiens)
Fgd1 reactivates F420
(Homo sapiens)
Participates
as an event of
Latent infection - Other responses of Mtb to phagocytosis (Homo sapiens)
Event Information
Go Biological Process
cell redox homeostasis (0045454)
Disease
Name
Identifier
Synonyms
tuberculosis
DOID:399
tuberculous abscess, Tuberculoma (finding), tuberculoma
Authored
Stephan, R (2011-01-10)
Reviewed
Warner, D (2012-04-30)
Created
Jassal, B (2011-02-28)
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