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Insights into Enzymatic Catalysis from Binding and Hydrolysis of Diadenosine Tetraphosphate by E. coli Adenylate Kinase
Department of Chemistry, Konstanz Research School Chemical Biology, University of Konstanz, Konstanz, Germany.
Umeå University, Faculty of Science and Technology, Department of Chemistry.ORCID iD: 0000-0001-7301-8445
Umeå University, Faculty of Science and Technology, Department of Chemistry.
Umeå University, Faculty of Science and Technology, Department of Chemistry. Umeå University, Faculty of Medicine, Umeå Centre for Microbial Research (UCMR).ORCID iD: 0000-0003-0124-0199
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2023 (English)In: Biochemistry, ISSN 0006-2960, E-ISSN 1520-4995, Vol. 62, no 15, p. 2238-2243Article in journal (Refereed) Published
Abstract [en]

Adenylate kinases play a crucial role in cellular energy homeostasis through the interconversion of ATP, AMP, and ADP in all living organisms. Here, we explore how adenylate kinase (AdK) from Escherichia coli interacts with diadenosine tetraphosphate (AP4A), a putative alarmone associated with transcriptional regulation, stress, and DNA damage response. From a combination of EPR and NMR spectroscopy together with X-ray crystallography, we found that AdK interacts with AP4A with two distinct modes that occur on disparate time scales. First, AdK dynamically interconverts between open and closed states with equal weights in the presence of AP4A. On a much slower time scale, AdK hydrolyses AP4A, and we suggest that the dynamically accessed substrate-bound open AdK conformation enables this hydrolytic activity. The partitioning of the enzyme into open and closed states is discussed in relation to a recently proposed linkage between active site dynamics and collective conformational dynamics.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2023. Vol. 62, no 15, p. 2238-2243
National Category
Biochemistry and Molecular Biology
Identifiers
URN: urn:nbn:se:umu:diva-212552DOI: 10.1021/acs.biochem.3c00189ISI: 001022362500001PubMedID: 37418448Scopus ID: 2-s2.0-85165636090OAI: oai:DiVA.org:umu-212552DiVA, id: diva2:1786375
Funder
EU, Horizon 2020, 772027─SPICE-ERC-2017-COGEU, European Research CouncilSwedish Research Council, 2019-03771Swedish Research Council, 2021-04513Available from: 2023-08-08 Created: 2023-08-08 Last updated: 2023-08-08Bibliographically approved

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Oelker, MelanieRogne, PerSauer-Eriksson, A. ElisabethWolf-Watz, Magnus

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