Identifying and Evaluating Anomalous Structural Change-based Nodes in Generalized Dynamic Social Networks

2021 ◽  
Vol 15 (4) ◽  
pp. 1-22
Author(s):  
Huan Wang ◽  
Chunming Qiao ◽  
Xuan Guo ◽  
Lei Fang ◽  
Ying Sha ◽  
...  

Recently, dynamic social network research has attracted a great amount of attention, especially in the area of anomaly analysis that analyzes the anomalous change in the evolution of dynamic social networks. However, most of the current research focused on anomaly analysis of the macro representation of dynamic social networks and failed to analyze the nodes that have anomalous structural changes at a micro level. To identify and evaluate anomalous structural change-based nodes in generalized dynamic social networks that only have limited structural information, this research considers undirected and unweighted graphs and develops a multiple-neighbor superposition similarity method ( ), which mainly consists of a multiple-neighbor range algorithm ( ) and a superposition similarity fluctuation algorithm ( ). introduces observation nodes, characterizes the structural similarities of nodes within multiple-neighbor ranges, and proposes a new multiple-neighbor similarity index on the basis of extensional similarity indices. Subsequently, maximally reflects the structural change of each node, using a new superposition similarity fluctuation index from the perspective of diverse multiple-neighbor similarities. As a result, based on and , not only identifies anomalous structural change-based nodes by detecting the anomalous structural changes of nodes but also evaluates their anomalous degrees by quantifying these changes. Results obtained by comparing with state-of-the-art methods via extensive experiments show that can accurately identify anomalous structural change-based nodes and evaluate their anomalous degrees well.

2016 ◽  
Vol 6 (1) ◽  
pp. 72-95
Author(s):  
Nahuel Oddone ◽  
Ramón Padilla-Pérez

Economic and social development requires major structural changes to transform the composition of output, employment and international trade (ECLAC, 2012). Through rising productivity in existing activities and by moving towards more complex and technology-intensive sectors and processes, structural change is expected to lead to higher long-term economic growth, increased export competitiveness and well-paid jobs. In the past two decades, the conceptual framework of value chains has been widely disseminated as a tool to study structural change at the micro-level (Gereffi and Korzeniewicz, 1994; Gereffi et al., 2005; Humphrey and Schmitz, 2012; OCDE, 2013; Padilla-Pérez, 2014; Stumpo and Rivas, 2013).


2019 ◽  
Vol 26 (6) ◽  
pp. 449-457
Author(s):  
Ting Song ◽  
Keke Cao ◽  
Yu dan Fan ◽  
Zhichao Zhang ◽  
Zong W. Guo ◽  
...  

Background: The significance of multi-site phosphorylation of BCL-2 protein in the flexible loop domain remains controversial, in part due to the lack of structural biology studies of phosphorylated BCL-2. Objective: The purpose of the study is to explore the phosphorylation induced structural changes of BCL-2 protein. Methods: We constructed a phosphomietic mutant BCL-2(62-206) (t69e, s70e and s87e) (EEEBCL- 2-EK (62-206)), in which the BH4 domain and the part of loop region was truncated (residues 2-61) to enable a backbone resonance assignment. The phosphorylation-induced structural change was visualized by overlapping a well dispersed 15N-1H heteronuclear single quantum coherence (HSQC) NMR spectroscopy between EEE-BCL-2-EK (62-206) and BCL-2. Results: The EEE-BCL-2-EK (62-206) protein reproduced the biochemical and cellular activity of the native phosphorylated BCL-2 (pBCL-2), which was distinct from non-phosphorylated BCL-2 (npBCL-2) protein. Some residues in BH3 binding groove occurred chemical shift in the EEEBCL- 2-EK (62-206) spectrum, indicating that the phosphorylation in the loop region induces a structural change of active site. Conclusion: The phosphorylation of BCL-2 induced structural change in BH3 binding groove.


1986 ◽  
Vol 18 (9) ◽  
pp. 1189-1207
Author(s):  
B Ó Huallacháin

The conventional approach to assessing structural change in regional input – output tables is to measure the impact of coefficient change on the estimation of outputs and multipliers. The methods developed and tested in this paper focus exclusively on the coefficients. Univariate and multivariate statistical analyses can be used to identify and measure various types of changes ranging from coefficient instability to changes in interindustry relationships as a system. A distinction is made between structural changes in input relationships and those in output relationships. The methods are tested by using Washington State data for the years 1963 and 1967. The results are compared with previous analyses of change in these data.


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Truong Khanh Linh Dang ◽  
Thach Nguyen ◽  
Michael Habeck ◽  
Mehmet Gültas ◽  
Stephan Waack

Abstract Background Conformational transitions are implicated in the biological function of many proteins. Structural changes in proteins can be described approximately as the relative movement of rigid domains against each other. Despite previous efforts, there is a need to develop new domain segmentation algorithms that are capable of analysing the entire structure database efficiently and do not require the choice of protein-dependent tuning parameters such as the number of rigid domains. Results We develop a graph-based method for detecting rigid domains in proteins. Structural information from multiple conformational states is represented by a graph whose nodes correspond to amino acids. Graph clustering algorithms allow us to reduce the graph and run the Viterbi algorithm on the associated line graph to obtain a segmentation of the input structures into rigid domains. In contrast to many alternative methods, our approach does not require knowledge about the number of rigid domains. Moreover, we identified default values for the algorithmic parameters that are suitable for a large number of conformational ensembles. We test our algorithm on examples from the DynDom database and illustrate our method on various challenging systems whose structural transitions have been studied extensively. Conclusions The results strongly suggest that our graph-based algorithm forms a novel framework to characterize structural transitions in proteins via detecting their rigid domains. The web server is available at http://azifi.tz.agrar.uni-goettingen.de/webservice/.


MethodsX ◽  
2020 ◽  
Vol 7 ◽  
pp. 101030
Author(s):  
Leonardo López ◽  
Maximiliano Fernández ◽  
Leonardo Giovanini

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