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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3390/molecules19010672</dc:identifier><dc:language>eng</dc:language><dc:creator>Antonini, L. V.</dc:creator><dc:creator>Peregrina, J. R.</dc:creator><dc:creator>Angulo, J.</dc:creator><dc:creator>Medina Trullenque, María Milagros</dc:creator><dc:creator>Nieto, P. M.</dc:creator><dc:title>A STD-NMR study of the interaction of the Anabaena Ferredoxin-NAD P+ reductase with the Coenzyme</dc:title><dc:identifier>ART-2014-85181</dc:identifier><dc:description>Ferredoxin-NADP+ reductase (FNR) catalyzes the electron transfer from ferredoxin to NADP+ via its flavin FAD cofactor. To get further insights in the architecture of the transient complexes produced during the hydride transfer event between the enzyme and the NADP+ coenzyme we have applied NMR spectroscopy using Saturation Transfer Difference (STD) techniques to analyze the interaction between FNRox and the oxidized state of its NADP+ coenzyme. We have found that STD NMR, together with the use of selected mutations on FNR and of the non-FNR reacting coenzyme analogue NAD+, are appropriate tools to provide further information about the the interaction epitope.</dc:description><dc:date>2014</dc:date><dc:source>http://zaguan.unizar.es/record/32460</dc:source><dc:doi>10.3390/molecules19010672</dc:doi><dc:identifier>http://zaguan.unizar.es/record/32460</dc:identifier><dc:identifier>oai:zaguan.unizar.es:32460</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/BIO2010-14983</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/CTQ2012-32605</dc:relation><dc:identifier.citation>MOLECULES 19, 1 (2014), 672-685</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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