管道(软件)
古细菌
计算生物学
基因组
小桶
计算机科学
比例(比率)
生物合成
代谢途径
克莱德
生物
系统发育学
基因
遗传学
程序设计语言
转录组
物理
基因表达
量子力学
作者
José P. Faria,Filipe Liu,Janaka N. Edirisinghe,Nidhi Gupta,Samuel M. D. Seaver,Andrew Freiburger,Qizhi Zhang,Pamela Weisenhorn,Neal Conrad,Raphy Zarecki,Hyun‐Seob Song,Matthew DeJongh,Aaron A. Best,Robert W. Cottingham,Adam P. Arkin,Christopher S. Henry
标识
DOI:10.1101/2023.10.04.556561
摘要
Abstract Since the release of ModelSEED in 2010, the systems biology research community has used the ModelSEED genome-scale metabolic model reconstruction pipeline to build over 200,000 draft metabolic reconstructions that support hundreds of publications. Here we describe the first comprehensive update to this reconstruction tool, with new features such as (i) a dramatically improved representation of energy metabolism, which ensures that models produce accurate amounts of ATP per mol of nutrient consumed; (ii) a new template for Archaea model reconstruction; and (iii) a significantly improved curation of all metabolic pathways with mappings to RAST subsystems annotations. We applied the improved pipeline to build and analyze core and genome-scale models for Archaea and Bacteria genomes in KEGG. The new ModelSEED pipeline generates larger models that possess more reactions and genes and require fewer gap-filled reactions. In addition, we see conserved patterns in the ATP biosynthesis mechanism across phylogeny, and identify clades where our understanding of energy biosynthesis is still poor. The ModelSEED v2 pipeline is currently available only as new reconstruction and gap-filling Apps in the KBase platform.
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