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Sequence Hiberarchy Evolution Measurement Method and its Application
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作者 Jian Ding QIU Ru Ping LIANG +1 位作者 Jin Yuan MO Xiao Yong ZOU 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第12期1645-1648,共4页
A novel method based on discrete wavelet transform (DWT) and cross-covariance for revealing the evolution of species at different spatial resolutions is presented. The trypsin proteins of different species are chose... A novel method based on discrete wavelet transform (DWT) and cross-covariance for revealing the evolution of species at different spatial resolutions is presented. The trypsin proteins of different species are chosen as an example to describe the evolution relationship according to the evolution vectors by using this method. The results indicated that this method is a promising approach to reveal species evolution at different spatial resolutions. 展开更多
关键词 Sequence hiberarchy evolution measurement protein evolution hydrophobicity
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分子水平的非随机进化——相互作用蛋白质间的达尔文选择
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作者 贺福初 吴祖泽 《科技通报》 1993年第6期353-358,共6页
通过分析13种生物120余种蛋白质的分子进化,首次揭示:配基-受体、蛋白酶-酶抑制剂、亚基-亚基等相互作用蛋白质间在纵向进化(物种间)、横向进化(不同功能蛋白质间)中均存在协同进化的规律.此结果表明,相互作用蛋白质其分子进化普遍为非... 通过分析13种生物120余种蛋白质的分子进化,首次揭示:配基-受体、蛋白酶-酶抑制剂、亚基-亚基等相互作用蛋白质间在纵向进化(物种间)、横向进化(不同功能蛋白质间)中均存在协同进化的规律.此结果表明,相互作用蛋白质其分子进化普遍为非随机过程,由于其相互作用为功能发挥所必需,因而彼此间以典型的达尔文选择方式进化.本文结果既弥补了中性理论中分子进化与功能方式无关的不足,亦指出达尔文选择适用于分子进化。 展开更多
关键词 蛋白 达尔文选择 分子进化
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Evolution and protein interactions of AP2 proteins in Brassicaceae: Evidence linking development and environmental responses 被引量:3
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作者 Liping Zeng Yue Yin +5 位作者 Chenjiang You Qianli Pan Duo Xu Taijie Jin Bailong Zhang Hong Ma 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2016年第6期549-563,共15页
Plants have evolved a large number of transcription factors(TF), which are enriched among duplicate genes,highlighting their roles in complex regulatory networks. The APETALA2/EREBP-like genes constitute a large pla... Plants have evolved a large number of transcription factors(TF), which are enriched among duplicate genes,highlighting their roles in complex regulatory networks. The APETALA2/EREBP-like genes constitute a large plant TF family and participate in development and stress responses. To probe the conservation and divergence of AP2/EREBP genes,we analyzed the duplication patterns of this family in Brassicaceae and identified interacting proteins of representative Arabidopsis AP2/EREBP proteins. We found that many AP2/EREBP duplicates generated early in Brassicaceae history were quickly lost, but many others were retained in all tested Brassicaceae species, suggesting early functional divergence followed by persistent conservation. In addition,the sequences of the AP2 domain and exon numbers were highly conserved in rosids. Furthermore, we used 16 A.thaliana AP2/EREBP proteins as baits in yeast screens and identified 1,970 potential AP2/EREBP-interacting proteins,with a small subset of interactions verified in planta. Many AP2 genes also exhibit reduced expression in an antherdefective mutant, providing a possible link to developmental regulation. The putative AP2-interacting proteins participate in many functions in development and stress responses,including photomorphogenesis, flower development, pathogenesis, drought and cold responses, abscisic acid and auxin signaling. Our results present the AP2/EREBP evolution patterns in Brassicaceae, and support a proposed interaction network of AP2/EREBP proteins and their putative interacting proteins for further study. 展开更多
关键词 APETALA2 EREBP evolution Brassicaceae protein interaction
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A topology framework for macromolecular complexes and condensates
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作者 Maziar Heidari Duane Moes +2 位作者 Otto Schullian Barbara Scalvini Alireza Mashaghi 《Nano Research》 SCIE EI CSCD 2022年第11期9809-9817,共9页
Macromolecular assemblies such as protein complexes and protein/RNA condensates are involved in most fundamental cellular processes.The arrangement of subunits within these nano-assemblies is critical for their biolog... Macromolecular assemblies such as protein complexes and protein/RNA condensates are involved in most fundamental cellular processes.The arrangement of subunits within these nano-assemblies is critical for their biological function and is determined by the topology of physical contacts within and between the subunits forming the complex.Describing the spatial arrangement of these interactions is of central importance to understand their functional and stability consequences.In this concept article,we propose a circuit topology-based formalism to define the topology of a complex consisting of linear polymeric chains with interand intrachain interactions.We apply our method to a system of model polymer chains as well as protein assemblies.We show that circuit topology can categorize different forms of chain assemblies.Our multi-chain circuit topology should aid analysis and predictions of mechanistic and evolutionary principles in the design of macromolecular assemblies. 展开更多
关键词 TOPOLOGY macromolecular complex protein evolution FOLDING
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