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Structural characterization of cassava linamarase-linamarin enzyme complex: an integrated computational approach

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dc.creator Paul, Lucas
dc.creator Shadrack, Daniel
dc.creator Mudogo, Celestin
dc.creator Mtei, Kelvin
dc.creator Machunda, Revocatus
dc.creator Ntie‐Kang, Fidele
dc.date 2022-09-22T11:12:40Z
dc.date 2022-09-22T11:12:40Z
dc.date 2021-05-21
dc.date.accessioned 2022-10-25T09:24:49Z
dc.date.available 2022-10-25T09:24:49Z
dc.identifier https://doi.org/10.1080/07391102.2021.1925156
dc.identifier https://dspace.nm-aist.ac.tz/handle/20.500.12479/1675
dc.identifier.uri http://hdl.handle.net/123456789/95792
dc.description This research article was published by Taylor & Francis Group., 2021
dc.description Cassava linamarase is a hydrolyzing enzyme that belongs to a glycoside hydrolase family 1 (GH1). It is responsible for breaking down linamarin to toxic cyanide. The enzyme provides a defensive mechanism for plants against herbivores and has various applications in many fields. Understanding the structure of linamarase at the molecular level is a key to avail its reaction mechanism. In this study, the three-dimensional (3D) structure of linamarase was built for the first time using homology modelling and used to study its interaction with linamarin. Molecular docking calculations established the binding and orientation nature of linamarin, while molecular dynamics (MD) simulation established protein-ligand complexes' stability. Binding-free energy based on MM/PBSA was further used to rescore the docking results. An ensemble structure was found to be relatively stable compared to the modelled structure. This study sheds light on the exploration of linamarase towards understanding its reaction mechanisms. Communicated by Ramaswamy H. Sarma
dc.format application/pdf
dc.language en
dc.publisher Taylor & Francis Group
dc.subject Linamarase
dc.subject Linamarin
dc.subject Molecular dynamics simulation
dc.subject Molecular docking
dc.subject Cassava
dc.title Structural characterization of cassava linamarase-linamarin enzyme complex: an integrated computational approach
dc.type Article


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