Skip navigation
Veuillez utiliser cette adresse pour citer ce document : http://repositorio2.unb.br/jspui/handle/10482/44692
Fichier(s) constituant ce document :
Fichier Description TailleFormat 
ARTIGO_DynamicConformationalLandscape.pdf14,76 MBAdobe PDFVoir/Ouvrir
Titre: The dynamic conformational landscape of the protein methyltransferase SETD8
Auteur(s): Shi Chen
Wiewiora, Rafal P.
Fanwang Meng
Babault, Nicolas
Anqi Ma
Wenyu Yu
Kun Qian
Hao Hu
Hua Zou
Junyi Wang
Shijie Fan
Blum, Gil
Pittella-Silva, Fabio
Beauchamp, Kyle A.
Tempel, Wolfram
Hualiang Jiang
Kaixian Chen
Skene, Robert J.
Yujun George Zheng
Brown, Peter J.
Jian Jin Cheng Luo
Chodera, John D.
Minkui Luo
Assunto:: Proteínas
Câncer
Date de publication: 13-mai-2019
Editeur: eLife Sciences Publications Ltd.
Référence bibliographique: SHI CHEN et al. The dynamic conformational landscape of the protein methyltransferase SETD8. eLife, v.19, n.8, e45403, 2019. DOI: https://doi.org/10.7554/eLife.45403. Disponível em: https://elifesciences.org/articles/45403. Acesso em: 05 set. 2022.
Abstract: Elucidating the conformational heterogeneity of proteins is essential for understanding protein function and developing exogenous ligands. With the rapid development of experimental and computational methods, it is of great interest to integrate these approaches to illuminate the conformational landscapes of target proteins. SETD8 is a protein lysine methyltransferase (PKMT), which functions in vivo via the methylation of histone and nonhistone targets. Utilizing covalent inhibitors and depleting native ligands to trap hidden conformational states, we obtained diverse X-ray structures of SETD8. These structures were used to seed distributed atomistic molecular dynamics simulations that generated a total of six milliseconds of trajectory data. Markov state models, built via an automated machine learning approach and corroborated experimentally, reveal how slow conformational motions and conformational states are relevant to catalysis. These findings provide molecular insight on enzymatic catalysis and allosteric mechanisms of a PKMT via its detailed conformational landscape.
Licença:: Copyright Chen et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
DOI: https://doi.org/10.7554/eLife.45403
Collection(s) :Artigos publicados em periódicos e afins

Affichage détaillé " class="statisticsLink btn btn-primary" href="/jspui/handle/10482/44692/statistics">



Tous les documents dans DSpace sont protégés par copyright, avec tous droits réservés.