CPN60 is essential for parasite’s viability due to its apicoplast function.

<p>A. Schematic representation of the tetR-Dozi system, which enables protein knockdown upon removal of the tetracycline analogue aTC. B. Western blots depicting the expression of the tagged CPN60 using an anti-V5 antibody following knockdown induction. A significant reduction in protein level...

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Tác giả chính:	Amanda Tissawak (21762930) (author)
Tác giả khác:	Yarden Rosin (21762933) (author), Shirly Katz Galay (21762936) (author), Alia Qasem (21762939) (author), Michal Shahar (15266558) (author), Nirit Trabelsi (21762942) (author), Ora Furman-Schueler (21762945) (author), Steven M. Johnson (17357) (author), Anat Florentin (21762948) (author)
Được phát hành:	2025
Những chủ đề:	Biophysics Biochemistry Medicine Microbiology Cell Biology Genetics Pharmacology Evolutionary Biology Hematology Infectious Diseases Biological Sciences not elsewhere classified using genetic tools first replication cycle computational structural model additional targets outside previously unknown function synthesize essential biomolecules parasite death due div >< p cpn60 physically binds affect hs response apicoplast translation inhibitors apicoplast function work reveals taken together stable interface refolding safeguard plasmodium </ parasites serves organellar damage minimal control metabolic hub inactive forms immediately within heat shock evidence suggests eukaryotic cells endosymbiotic organelles directly involved conserved chaperonin close orthologues chaperonin inhibition cell nucleus caseinolytic protease balanced activities anti -<
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CPN60 is essential for parasite’s viability due to its apicoplast function.

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