2020
DOI: 10.1016/j.actatropica.2019.105217
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Functional insight into the glycosomal peroxiredoxin of Leishmania

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Cited by 7 publications
(9 citation statements)
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“…Retention of cPRX2-coding genes is a generalized feature of all Leishmania species with complete sequence annotation of the cPRX loci ( L. aethiopica , L. braziliensis , L. donovani , L. enriettii , L. mexicana , L. panamensis , and L. tarentolae ). Interestingly, Leishmaniinae are also unique in harboring a glycosomal PRX (gPRX) isoform [ 47 ], whose coding sequence falls within the same genetic locus as cPRX1 and cPRX2 . Based on the highly repetitive character of cPRX loci , e.g.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Retention of cPRX2-coding genes is a generalized feature of all Leishmania species with complete sequence annotation of the cPRX loci ( L. aethiopica , L. braziliensis , L. donovani , L. enriettii , L. mexicana , L. panamensis , and L. tarentolae ). Interestingly, Leishmaniinae are also unique in harboring a glycosomal PRX (gPRX) isoform [ 47 ], whose coding sequence falls within the same genetic locus as cPRX1 and cPRX2 . Based on the highly repetitive character of cPRX loci , e.g.…”
Section: Resultsmentioning
confidence: 99%
“…The construct to target LicPRX1 was built from a pTEX- HYG R -based plasmid previously used to disrupt LimTXNPx [ 17 ], by sequential cloning of the LicPRX1 5’UTR (primers P11/P12) and 3’UTR (primers P13/P14) into Bam HI/ Eco RV and Kpn I sites, respectively. The DNA cassette to target LicPRX2 was assembled from the pGL-HYG R -(5′UTRLicPRX1)-LiDRP-(3′UTRLigPRX) [ 47 ], by sequentially cloning the LicPRX2 5’UTR (primers P15/P16) and the LicPRX2 3’UTR (primers P17/P18) into Hin dIII/ Xma I and Bam HI/ Bgl II restriction sites, respectively. Prior to transfection, integration cassettes were separated from plasmid backbones by digestion with Bam HI ( LicPRX1 cassette) or Hin dIII/ Bgl II ( LicPRX2 cassette).…”
Section: Methodsmentioning
confidence: 99%
“…This protein family has been described in a wide variety of organisms and several biological functions have been reported for Leishmania parasites, such as virulence factor and protection against reactive oxygen and nitrogen species [88]. In this manner, they are directly associated with cell proliferation, senescence, apoptosis, and circadian rhythms [89]. These proteins have been described in the secretome of L. braziliensis and the antigenicity of tryparedoxin peroxidase has also been evaluated for both human and canine VL-diagnosis [90][91][92].…”
Section: Plos Onementioning
confidence: 99%
“…Previous work identified the loss of peroxisomes in other free living related species 51 . Members of the peroxisomal proteins are studied as a drug target for the development of novel therapies against diseases caused by parasites [52][53][54][55] . We propose that the peroxisomal protein set, absent specifically in metazoan parasites, can be considered as targets for drugs against human parasites.…”
Section: Trait Lossmentioning
confidence: 99%