PuSH - Publikationsserver des Helmholtz Zentrums München

Banasik, M.* ; Napolitano, V.* ; Blat, A.* ; Abdulkarim, K.* ; Plewka, J.* ; Czaplewski, C.* ; Gieldon, A.* ; Kozak, M.* ; Wladyka, B.* ; Popowicz, G.M. ; Dubin, G.*

Structural dynamics of the TPR domain of the peroxisomal cargo receptor Pex5 in Trypanosoma.

Int. J. Biol. Macromol. 280:135510 (2024)
Verlagsversion DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Peroxisomal protein import has been identified as a valid target in trypanosomiases, an important health threat in Central and South America. The importomer is built of multiple peroxins (Pex) and structural characterization of these proteins facilitates rational inhibitor development. We report crystal structures of the Trypanosoma brucei and T. cruzi tetratricopeptide repeat domain (TPR) of the cytoplasmic peroxisomal targeting signal 1 (PTS1) receptor Pex5. The structure of the TPR domain of TbPex5 represents an apo-form of the receptor which, together with the previously determined structure of the complex of TbPex5 TPR and PTS1 demonstrate significant receptor dynamics associated with signal peptide recognition. The structure of the complex of TPR domain of TcPex5 with PTS1 provided in this study details the molecular interactions that guide signal peptide recognition at the atomic level in the pathogenic species currently perceived as the most relevant among Trypanosoma. Small - angle X - ray scattering (SAXS) data obtained in solution supports the crystallographic findings on the compaction of the TPR domains of TbPex5 and TcPex5 upon interaction with the cargo.
Altmetric
Weitere Metriken?
[➜Einloggen]
Zusatzinfos bearbeiten [➜Einloggen]
Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Chagas Disease ; Pex5 ; Peroxin ; Structural Dynamics ; Tpr Domain ; Trypanosoma; Protein Import; Chagas-disease; Recognition; Inhibitors; Insights
ISSN (print) / ISBN 0141-8130
e-ISSN 1879-0003
Zeitschrift International Journal of Biological Macromolecules
Quellenangaben Band: 280, Heft: , Seiten: , Artikelnummer: 135510 Supplement: ,
Verlag Elsevier
Verlagsort Radarweg 29, 1043 Nx Amsterdam, Netherlands
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Structural Biology (STB)
Förderungen Polish Ministry of Science and Higher Education
Foundation for Polish Science
National Science Centre, Poland
Polish National Science Centre