Proteome-wide 3D structure prediction provides insights into the ancestral metabolism of ancient archaea and bacteria.
Proteome-wide 3D structure prediction provides insights into the ancestral metabolism of ancient archaea and bacteria.
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DOI:
10.1038/s41467-022-35523-8
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发表时间:
2022-12-21
影响因子:
16.6
通讯作者:
Xiao, Xiang
中科院分区:
文献类型:
--
作者:
Zhao, Weishu;Zhong, Bozitao;Zheng, Lirong;Tan, Pan;Wang, Yinzhao;Leng, Hao;de Souza, Nicolas;Liu, Zhuo;Hong, Liang;Xiao, Xiang
Ancestral metabolism has remained controversial due to a lack of evidence beyond sequence-based reconstructions. Although prebiotic chemists have provided hints that metabolism might originate from non-enzymatic protometabolic pathways, gaps between ancestral reconstruction and prebiotic processes mean there is much that is still unknown. Here, we apply proteome-wide 3D structure predictions and comparisons to investigate ancestorial metabolism of ancient bacteria and archaea, to provide information beyond sequence as a bridge to the prebiotic processes. We compare representative bacterial and archaeal strains, which reveal surprisingly similar physiological and metabolic characteristics via microbiological and biophysical experiments. Pairwise comparison of protein structures identify the conserved metabolic modules in bacteria and archaea, despite interference from overly variable sequences. The conserved modules (for example, middle of glycolysis, partial TCA, proton/sulfur respiration, building block biosynthesis) constitute the basic functions that possibly existed in the archaeal-bacterial common ancestor, which are remarkably consistent with the experimentally confirmed protometabolic pathways. These structure-based findings provide a new perspective to reconstructing the ancestral metabolism and understanding its origin, which suggests high-throughput protein 3D structure prediction is a promising approach, deserving broader application in future ancestral exploration. Previous studies have reconstructed ancestral metabolism using sequence-based approaches. This study uses a high-throughput version of AlphaFold2 to compare proteome-wide 3D structure predictions of two representative strains of ancient archaea and bacteria.
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影响因子:
64.8
作者:
Jumper J;Evans R;Pritzel A;Green T;Figurnov M;Ronneberger O;Tunyasuvunakool K;Bates R;Žídek A;Potapenko A;Bridgland A;Meyer C;Kohl SAA;Ballard AJ;Cowie A;Romera-Paredes B;Nikolov S;Jain R;Adler J;Back T;Petersen S;Reiman D;Clancy E;Zielinski M;Steinegger M;Pacholska M;Berghammer T;Bodenstein S;Silver D;Vinyals O;Senior AW;Kavukcuoglu K;Kohli P;Hassabis D
通讯作者:
Hassabis D
DOI:
10.1093/bioinformatics/btp163
发表时间:
2009-06-01
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Cock PJ;Antao T;Chang JT;Chapman BA;Cox CJ;Dalke A;Friedberg I;Hamelryck T;Kauff F;Wilczynski B;de Hoon MJ
通讯作者:
de Hoon MJ
影响因子:
5.7
作者:
Cisse, Aline;Schachner-Nedherer, Anna-Laurence;Peters, Judith
通讯作者:
Peters, Judith
影响因子:
64.8
作者:
Boussau, Bastien;Blanquart, Samuel;Gouy, Manolo
通讯作者:
Gouy, Manolo
影响因子:
11
作者:
Gu, Jiahao;Wang, Xiaojun;Luo, Haiwei
通讯作者:
Luo, Haiwei