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A comparison between internal protein nanoenvironments of α-helices and ß-sheets.
Mazoni, Ivan; Salim, Jose Augusto; de Moraes, Fabio Rogerio; Borro, Luiz; Neshich, Goran.
Afiliação
  • Mazoni I; Computational Biology Research Group, Embrapa Agricultural Informatics, Campinas, SP, Brazil.
  • Salim JA; Research Center on Biodiversity and Computing (BIOCOMP), Polytechnic School of the University of São Paulo (USP), São Paulo, Brazil.
  • de Moraes FR; Physics Department, Institute of Biosciences, Languages, and Exact Sciences (IBILCE), São Paulo State University (Unesp), Ribeirão Preto, SP, Brazil.
  • Borro L; IoT & AI Solutions, CPqD Foundation, Campinas, SP, Brazil.
  • Neshich G; Computational Biology Research Group, Embrapa Agricultural Informatics, Campinas, SP, Brazil.
PLoS One ; 15(12): e0244315, 2020.
Article em En | MEDLINE | ID: mdl-33378364
ABSTRACT
Secondary structure elements are generally found in almost all protein structures revealed so far. In general, there are more ß-sheets than α helices found inside the protein structures. For example, considering the PDB, DSSP and Stride definitions for secondary structure elements and by using the consensus among those, we found 60,727 helices in 4,376 chains identified in all-α structures and 129,440 helices in 7,898 chains identified in all-α and α + ß structures. For ß-sheets, we identified 837,345 strands in 184,925 ß-sheets located within 50,803 chains of all-ß structures and 1,541,961 strands in 355,431 ß-sheets located within 86,939 chains in all-ß and α + ß structures (data extracted on February 1, 2019). In this paper we would first like to address a full characterization of the nanoenvironment found at beta sheet locations and then compare those characteristics with the ones we already published for alpha helical secondary structure elements. For such characterization, we use here, as in our previous work about alpha helical nanoenvironments, set of STING protein structure descriptors. As in the previous work, we assume that we will be able to prove that there is a set of protein structure parameters/attributes/descriptors, which could fully describe the nanoenvironment around beta sheets and that appropriate statistically analysis will point out to significant changes in values for those parameters when compared for loci considered inside and outside defined secondary structure element. Clearly, while the univariate analysis is straightforward and intuitively understood, it is severely limited in coverage it could be successfully applied at best in up to 25% of studied cases. The indication of the main descriptors for the specific secondary structure element (SSE) by means of the multivariate MANOVA test is the strong statistical tool for complete discrimination among the SSEs, and it revealed itself as the one with the highest coverage. The complete description of the nanoenvironment, by analogy, might be understood in terms of describing a key lock system, where all lock mini cylinders need to combine their elevation (controlled by a matching key) to open the lock. The main idea is as follows a set of descriptors (cylinders in the key-lock example) must precisely combine their values (elevation) to form and maintain a specific secondary structure element nanoenvironment (a required condition for a key being able to open a lock).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estrutura Secundária de Proteína / Conformação Proteica em alfa-Hélice / Conformação Proteica em Folha beta Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estrutura Secundária de Proteína / Conformação Proteica em alfa-Hélice / Conformação Proteica em Folha beta Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Brasil