Depletion of Plasmodium berghei plasmoredoxin reveals a non-essential role for life cycle progression of the malaria parasite

scientific article

Depletion of Plasmodium berghei plasmoredoxin reveals a non-essential role for life cycle progression of the malaria parasite is …
instance of (P31):
scholarly articleQ13442814

External links are
P819ADS bibcode2008PLoSO...3.2474B
P356DOI10.1371/JOURNAL.PONE.0002474
P932PMC publication ID2429964
P698PubMed publication ID18575607
P5875ResearchGate publication ID5279926

P50authorKatja BeckerQ1711972
Kai MatuschewskiQ32416278
P2093author name stringKathrin Buchholz
R Heiner Schirmer
Stefan Rahlfs
P2860cites workInteractions of methylene blue with human disulfide reductases and their orthologues from Plasmodium falciparumQ24657634
A new mathematical model for relative quantification in real-time RT-PCRQ27860781
The yeast Saccharomyces cerevisiae contains two glutaredoxin genes that are required for protection against reactive oxygen species.Q27933841
Thioredoxin deficiency in yeast prolongs S phase and shortens the G1 interval of the cell cycleQ27934271
The yeast glutaredoxins are active as glutathione peroxidasesQ27938891
Thioredoxin networks in the malarial parasite Plasmodium falciparumQ27972980
Substitution of the thioredoxin system for glutathione reductase in Drosophila melanogasterQ28142820
Thioredoxin--a fold for all reasonsQ29618984
Structural and biochemical characterization of a mitochondrial peroxiredoxin from Plasmodium falciparumQ30042256
Plasmoredoxin, a novel redox-active protein unique for malarial parasitesQ30046719
High efficiency transfection of Plasmodium berghei facilitates novel selection proceduresQ30080002
Construction and characterization of glutaredoxin-negative mutants of Escherichia coliQ33552014
Early embryonic lethality caused by targeted disruption of the mouse thioredoxin gene.Q52521278
The role of the thioredoxin and glutaredoxin pathways in reducing protein disulfide bonds in the Escherichia coli cytoplasm.Q54563918
A single glutaredoxin or thioredoxin gene is essential for viability in the yeast Saccharomyces cerevisiaeQ73874034
The genetics of disulfide bond metabolismQ77936221
Plasmodium falciparum 2-Cys peroxiredoxin reacts with plasmoredoxin and peroxynitriteQ81529503
Disulfide bond formation in the Escherichia coli cytoplasm: an in vivo role reversal for the thioredoxinsQ33889552
Interactions of glutaredoxins, ribonucleotide reductase, and components of the DNA replication system of Escherichia coli.Q33905769
Plasmodium berghei resists killing by reactive oxygen speciesQ34033550
Roles of the glutathione- and thioredoxin-dependent reduction systems in the Escherichia coli and saccharomyces cerevisiae responses to oxidative stress.Q34052736
The absence of mitochondrial thioredoxin 2 causes massive apoptosis, exencephaly, and early embryonic lethality in homozygous miceQ34463545
The thioredoxin system of Plasmodium falciparum and other parasitesQ34777950
Plasmodium falciparum thioredoxins and glutaredoxins as central players in redox metabolismQ35666792
Thioredoxin reductase and glutathione synthesis in Plasmodium falciparumQ35666796
Oxidative stress in malaria parasite-infected erythrocytes: host-parasite interactionsQ35704960
Redox and antioxidant systems of the malaria parasite Plasmodium falciparumQ35896735
Dithiol proteins as guardians of the intracellular redox milieu in parasites: old and new drug targets in trypanosomes and malaria-causing plasmodiaQ36013371
Monovalent fragments (Fab) of monoclonal antibodies to a sporozoite surface antigen (Pb44) protect mice against malarial infectionQ36343693
Interference with redox-active enzymes as a basis for the design of antimalarial drugsQ36393707
Thioredoxin reductase is essential for the survival of Plasmodium falciparum erythrocytic stagesQ39148737
Inhibition of glutathione-dependent degradation of heme by chloroquine and amodiaquine as a possible basis for their antimalarial mode of actionQ41925134
Gene targeting in Plasmodium bergheiQ47908495
Comparison of in vivo and in vitro antimalarial activity of artemisinin, dihydroartemisinin and sodium artesunate in the Plasmodium berghei-rodent modelQ48013465
Demonstration of heat-shock protein 70 in the sporozoite stage of malaria parasitesQ48015403
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectmalariaQ12156
Plasmodium bergheiQ65021
plasmoredoxinQ59907914
plasmoredoxin, putativeQ59952724
plasmoredoxinQ59972419
P304page(s)e2474
P577publication date2008-06-25
P1433published inPLOS OneQ564954
P1476titleDepletion of Plasmodium berghei plasmoredoxin reveals a non-essential role for life cycle progression of the malaria parasite
P478volume3

Reverse relations

cites work (P2860)
Q37070139Glutathione-deficient Plasmodium berghei parasites exhibit growth delay and nuclear DNA damage.
Q28475176Identification of proteins targeted by the thioredoxin superfamily in Plasmodium falciparum
Q41714322Molecular genetics evidence for the in vivo roles of the two major NADPH-dependent disulfide reductases in the malaria parasite
Q27663706Redox Regulation of Plasmodium falciparum Ornithine δ-Aminotransferase
Q38956970The Architecture of Thiol Antioxidant Systems among Invertebrate Parasites.
Q28474756The glutathione biosynthetic pathway of Plasmodium is essential for mosquito transmission

Q59907914plasmoredoxindescribed by sourceP1343

Search more.