首页> The FEBS journal> Targeting the histone-fold dimerization interface of oocyst rupture proteins from Plasmodium berghei for antimalarial inhibitor discovery.

Targeting the histone-fold dimerization interface of oocyst rupture proteins from Plasmodium berghei for antimalarial inhibitor discovery.

导出 LinkOut

翻译打印收藏纠错

第一作者： Federico,Ballabio

第一单位： Department of Biosciences, University of Milano, Italy.;National Research Council of Italy, Biophysics Institute (CNR-IBF), Milan, Italy.

作者： Federico,Ballabio ^[1] ; Chiara,Bertaso ^[2] ; Marta,Villa ^[2] ; Ophelia,Livero ^[2] ; Alessandro,Del Cont Bernard ^[2] ; Rosaria,Russo ^[3] ; Renate,Gessmann ^[4] ; Inga,Siden-Kiamos ^[4] ; Claude Marie Francois,Preira ^[5] ; Amit,Kumawat ^[2] ; Paolo,Gabrieli ^[2] ; Carlo,Camilloni ^[2] ; Chiara,Currà ^[6] ; Simona,Masiero ^[2] ; Marco,Nardini ^[2] ; Louise J,Gourlay ^[2]

作者单位： Department of Biosciences, University of Milano, Italy.;National Research Council of Italy, Biophysics Institute (CNR-IBF), Milan, Italy. ^[1] Department of Biosciences, University of Milano, Italy. ^[2] Department of Pathophysiology and Transplantation, L.I.T.A. Segrate, Italy. ^[3] Foundation for Research and Technology Hellas, Institute of Molecular biology and Biotechnology, Heraklion, Crete, Greece. ^[4] Department of Biology, Voutes University Campus, University of Crete, Heraklion, Crete, Greece. ^[5] Foundation for Research and Technology Hellas, Institute of Molecular biology and Biotechnology, Heraklion, Crete, Greece.;Department of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy. ^[6]

关键词 Plasmodium spp.cyclic peptide inhibitors histone‐fold domain in silico molecular docking oocyst rupture proteins