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dc.contributor.authorShi Chen-
dc.contributor.authorWiewiora, Rafal P.-
dc.contributor.authorFanwang Meng-
dc.contributor.authorBabault, Nicolas-
dc.contributor.authorAnqi Ma-
dc.contributor.authorWenyu Yu-
dc.contributor.authorKun Qian-
dc.contributor.authorHao Hu-
dc.contributor.authorHua Zou-
dc.contributor.authorJunyi Wang-
dc.contributor.authorShijie Fan-
dc.contributor.authorBlum, Gil-
dc.contributor.authorPittella-Silva, Fabio-
dc.contributor.authorBeauchamp, Kyle A.-
dc.contributor.authorTempel, Wolfram-
dc.contributor.authorHualiang Jiang-
dc.contributor.authorKaixian Chen-
dc.contributor.authorSkene, Robert J.-
dc.contributor.authorYujun George Zheng-
dc.contributor.authorBrown, Peter J.-
dc.contributor.authorJian Jin Cheng Luo-
dc.contributor.authorChodera, John D.-
dc.contributor.authorMinkui Luo-
dc.date.accessioned2022-09-05T15:22:23Z-
dc.date.available2022-09-05T15:22:23Z-
dc.date.issued2019-05-13-
dc.identifier.citationSHI 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.pt_BR
dc.identifier.urihttps://repositorio.unb.br/handle/10482/44692-
dc.language.isoInglêspt_BR
dc.publishereLife Sciences Publications Ltd.pt_BR
dc.rightsAcesso Abertopt_BR
dc.titleThe dynamic conformational landscape of the protein methyltransferase SETD8pt_BR
dc.typeArtigopt_BR
dc.subject.keywordProteínaspt_BR
dc.subject.keywordCâncerpt_BR
dc.rights.licenseCopyright 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.pt_BR
dc.identifier.doihttps://doi.org/10.7554/eLife.45403pt_BR
dc.description.abstract1Elucidating 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.pt_BR
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