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      The EcoCyc Database in 2021

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          Abstract

          The EcoCyc model-organism database collects and summarizes experimental data for Escherichia coli K-12. EcoCyc is regularly updated by the manual curation of individual database entries, such as genes, proteins, and metabolic pathways, and by the programmatic addition of results from select high-throughput analyses. Updates to the Pathway Tools software that supports EcoCyc and to the web interface that enables user access have continuously improved its usability and expanded its functionality. This article highlights recent improvements to the curated data in the areas of metabolism, transport, DNA repair, and regulation of gene expression. New and revised data analysis and visualization tools include an interactive metabolic network explorer, a circular genome viewer, and various improvements to the speed and usability of existing tools.

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          Genetic regulatory mechanisms in the synthesis of proteins.

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            The EcoCyc database: reflecting new knowledge about Escherichia coli K-12

            EcoCyc (EcoCyc.org) is a freely accessible, comprehensive database that collects and summarizes experimental data for Escherichia coli K-12, the best-studied bacterial model organism. New experimental discoveries about gene products, their function and regulation, new metabolic pathways, enzymes and cofactors are regularly added to EcoCyc. New SmartTable tools allow users to browse collections of related EcoCyc content. SmartTables can also serve as repositories for user- or curator-generated lists. EcoCyc now supports running and modifying E. coli metabolic models directly on the EcoCyc website.
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              Acetyl-phosphate is a critical determinant of lysine acetylation in E. coli.

              Lysine acetylation is a frequently occurring posttranslational modification in bacteria; however, little is known about its origin and regulation. Using the model bacterium Escherichia coli (E. coli), we found that most acetylation occurred at a low level and accumulated in growth-arrested cells in a manner that depended on the formation of acetyl-phosphate (AcP) through glycolysis. Mutant cells unable to produce AcP had significantly reduced acetylation levels, while mutant cells unable to convert AcP to acetate had significantly elevated acetylation levels. We showed that AcP can chemically acetylate lysine residues in vitro and that AcP levels are correlated with acetylation levels in vivo, suggesting that AcP may acetylate proteins nonenzymatically in cells. These results uncover a critical role for AcP in bacterial acetylation and indicate that most acetylation in E. coli occurs at a low level and is dynamically affected by metabolism and cell proliferation in a global, uniform manner. Copyright © 2013 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                28 July 2021
                2021
                : 12
                : 711077
                Affiliations
                [1] 1Bioinformatics Research Group, Artificial Intelligence Center, SRI International , Menlo Park, CA, United States
                [2] 2Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México , Cuernavaca, México
                [3] 3Department of Molecular Sciences, Macquarie University , Sydney, NSW, Australia
                [4] 4Instituto de Energías Renovables, Universidad Nacional Autónoma de México , Temixco, México
                [5] 5Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago , Maywood, IL, United States
                [6] 6Department of Biomedical Engineering, Boston University , Boston, MA, United States
                Author notes

                Edited by: Jörg Stülke, University of Göttingen, Germany

                Reviewed by: Jürgen Lassak, Ludwig Maximilian University of Munich, Germany; Michael Y. Galperin, National Center for Biotechnology Information (NLM), United States; Deborah A. Siegele, Texas A&M University, United States

                *Correspondence: Peter D. Karp, pkarp@ 123456ai.sri.com

                Present address: Wai Kit Ong, X, The Moonshot Factory, Mountain View, CA, United States

                This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2021.711077
                8357350
                34394059
                55d75d55-5de6-4eba-acee-14c2b43eb3a1
                Copyright © 2021 Keseler, Gama-Castro, Mackie, Billington, Bonavides-Martínez, Caspi, Kothari, Krummenacker, Midford, Muñiz-Rascado, Ong, Paley, Santos-Zavaleta, Subhraveti, Tierrafría, Wolfe, Collado-Vides, Paulsen and Karp.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 17 May 2021
                : 02 July 2021
                Page count
                Figures: 6, Tables: 3, Equations: 0, References: 53, Pages: 10, Words: 6086
                Funding
                Funded by: National Institute of General Medical Sciences of the National Institutes of Health
                Award ID: GM077678
                Award ID: RO1GM110597
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                escherichia coli,ecocyc,model-organism database,drug efflux transporters,metabolism,gene regulation

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