Publicaciones (252) Publicaciones de Federico Gago Badenas

2024

  1. A distinctive family of L,D-transpeptidases catalyzing L-Ala-mDAP crosslinks in Alpha- and Betaproteobacteria

    Nature Communications, Vol. 15, Núm. 1

  2. Flexible structural arrangement and DNA-binding properties of protein p6 from Bacillus subtillis phage ϕ29

    Nucleic Acids Research, Vol. 52, Núm. 4, pp. 2045-2065

2023

  1. Chemical modulation of microtubule structure through the laulimalide/peloruside site

    Structure, Vol. 31, Núm. 1, pp. 88-99.e5

  2. Computational Approaches to Enzyme Inhibition by Marine Natural Products in the Search for New Drugs

    Marine Drugs, Vol. 21, Núm. 2

  3. Insertion of an Amphipathic Linker in a Tetrapodal Tryptophan Derivative Leads to a Novel and Highly Potent Entry Inhibitor of Enterovirus A71 Clinical Isolates

    International Journal of Molecular Sciences, Vol. 24, Núm. 4

  4. Modulation of taxane binding to tubulin curved and straight conformations by systematic 3′N modification provides for improved microtubule binding, persistent cytotoxicity and in vivo potency

    European Journal of Medicinal Chemistry, Vol. 259

  5. Molecular basis of the final step of cell division in Streptococcus pneumoniae

    Cell Reports, Vol. 42, Núm. 7

  6. Structural insight into the stabilization of microtubules by taxanes

    eLife, Vol. 12

2022

  1. A Versatile Class of 1,4,4-Trisubstituted Piperidines Block Coronavirus Replication In Vitro

    Pharmaceuticals, Vol. 15, Núm. 8

  2. Alternative Approaches to Understand Microtubule Cap Morphology and Function

    ACS Omega

  3. Identification of 1,2,3-triazolium salt-based inhibitors of Leishmania infantum trypanothione disulfide reductase with enhanced antileishmanial potency in cellulo and increased selectivity

    European Journal of Medicinal Chemistry, Vol. 244

  4. Identification of L. infantum trypanothione synthetase inhibitors with leishmanicidal activity from a (non-biased) in-house chemical library

    European Journal of Medicinal Chemistry, Vol. 243

  5. Organotropic dendrons with high potency as HIV-1, HIV-2 and EV-A71 cell entry inhibitors

    European Journal of Medicinal Chemistry, Vol. 237

  6. Pyridazino-pyrrolo-quinoxalinium salts as highly potent and selective leishmanicidal agents targeting trypanothione reductase

    European Journal of Medicinal Chemistry, Vol. 227

2021

  1. Double Arylation of the Indole Side Chain of Tri- And Tetrapodal Tryptophan Derivatives Renders Highly Potent HIV-1 and EV-A71 Entry Inhibitors

    Journal of Medicinal Chemistry, Vol. 64, Núm. 14, pp. 10027-10046

  2. Efficient Dimerization Disruption of Leishmania infantum Trypanothione Reductase by Triazole-phenyl-thiazoles

    Journal of Medicinal Chemistry, Vol. 64, Núm. 9, pp. 6137-6160

  3. Insight into the sequence-specific elements leading to increased DNA bending and ligase-mediated circularization propensity by antitumor trabectedin

    Journal of Computer-Aided Molecular Design, Vol. 35, Núm. 6, pp. 707-719

  4. Multivalent Tryptophan- and Tyrosine-Containing [60]Fullerene Hexa-Adducts as Dual HIV and Enterovirus A71 Entry Inhibitors

    Chemistry - A European Journal, Vol. 27, Núm. 41, pp. 10700-10710

  5. On the need to tell apart fraternal twins eef1a1 and eef1a2, and their respective outfits

    International Journal of Molecular Sciences, Vol. 22, Núm. 13

  6. Small molecule–peptide conjugates as dimerization inhibitors of leishmania infantum trypanothione disulfide reductase

    Pharmaceuticals, Vol. 14, Núm. 7