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Maximization of non-idle enzymes improves the coverage of the estimated maximal in vivo enzyme catalytic rates in Escherichia coli
Author(s) -
Rudan Xu,
Zahra RazaghiMoghadam,
Zoran Nikoloski
Publication year - 2021
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btab575
Subject(s) - flux (metallurgy) , in vivo , proteomics , escherichia coli , enzyme , computational biology , biology , biological system , computer science , chemistry , biochemistry , genetics , gene , organic chemistry
Constraint-based modeling approaches allow the estimation of maximal in vivo enzyme catalytic rates that can serve as proxies for enzyme turnover numbers. Yet, genome-scale flux profiling remains a challenge in deploying these approaches to catalogue proxies for enzyme catalytic rates across organisms.

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