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dc.contributor.authorBustos, Daniel
dc.contributor.authorPalma, Jonathan M.
dc.contributor.authorVidal, Maira
dc.contributor.authorGonzález, Wendy
dc.contributor.authorHernández, Erix W.
dc.date.accessioned2022-08-02T15:25:55Z
dc.date.available2022-08-02T15:25:55Z
dc.date.issued2021
dc.identifier.urihttp://repositorio.ucm.cl/handle/ucm/3954
dc.description.abstractIn structural bioinformatics, computational biology, or any other field where is important to assess cavities, clefts, pores, or grooves in a macromolecular system, it is imperative to perform this evaluation over a trajectory or an ensemble of structures to measure all possible structural changes produced by the atomic movements, especially in the constriction regions. This is mainly true in membrane proteins such as ions channels or transporters where the movements of the amino acid residue side chains that form the pore can significantly alter their dimensions and thus affect the protein function. In this work, we present a brief tutorial to measure the radius of the pore within macromolecules in large structural ensembles using non-commercial software widely reported in the literature.es_CL
dc.language.isoenes_CL
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
dc.source2021 IEEE International Conference on Automation/XXIV Congress of the Chilean Association of Automatic Control (ICA-ACCA)es_CL
dc.subjectFenestrationses_CL
dc.subjectHomology modelinges_CL
dc.subjectHOLEes_CL
dc.subjectK2P channelses_CL
dc.titleBrief tutorial to evaluate molecular cavities in large conformational ensembles: a K2P channel study casees_CL
dc.typeArticlees_CL
dc.ucm.indexacionScopuses_CL
dc.ucm.uriieeexplore.ieee.org/document/9465239es_CL
dc.ucm.doidoi.org/10.1109/ICAACCA51523.2021.9465239es_CL


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Atribución-NoComercial-SinDerivadas 3.0 Chile
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