Beatriz Aguirre-López

发表

The importance of arginine codons AGA and AGG for the expression in E. coli of triosephosphate isomerase from seven different species

R. Pérez-Montfort, A. Gómez-Puyou, Beatriz Aguirre-López, 2017, Biotechnology reports.

In Kluyveromyces lactis a Pair of Paralogous Isozymes Catalyze the First Committed Step of Leucine Biosynthesis in Either the Mitochondria or the Cytosol

C. Scazzocchio, Erendira Rojas-Ortega, James González, 2020, Frontiers in Microbiology.

Novel and Selective Rhipicephalus microplus Triosephosphate Isomerase Inhibitors with Acaricidal Activity

R. Pérez-Montfort, Rodrigo Nunes da Fonseca, J. Moraes, 2018, Veterinary sciences.

Alanine Represses γ-Aminobutyric Acid Utilization and Induces Alanine Transaminase Required for Mitochondrial Function in Saccharomyces cerevisiae

Beatriz Aguirre-López, Alicia González, L. Riego-Ruiz, 2021, Frontiers in Microbiology.

Selective inactivation of triosephosphate isomerase from Trypanosoma cruzi by brevifolin carboxylate derivatives isolated from Geranium bellum Rose.

J. Salas-Pacheco, A. Téllez-Valencia, Beatriz Aguirre-López, 2009, Bioorganic & medicinal chemistry letters.

Potent and Selective Inhibitors of Trypanosoma cruzi Triosephosphate Isomerase with Concomitant Inhibition of Cruzipain: Inhibition of Parasite Growth through Multitarget Activity

R. Pérez-Montfort, A. Gómez-Puyou, A. Merlino, 2016, ChemMedChem.

Massive screening yields novel and selective Trypanosoma cruzi triosephosphate isomerase dimer-interface-irreversible inhibitors with anti-trypanosomal activity.

R. Pérez-Montfort, A. Gómez-Puyou, A. Merlino, 2010, European journal of medicinal chemistry.

Structural Basis of Human Triosephosphate Isomerase Deficiency

Miguel Costas, A. Torres-Larios, David Rodriguez-Larrea, 2008, Journal of Biological Chemistry.

New chemotypes as Trypanosoma cruzi triosephosphate isomerase inhibitors: a deeper insight into the mechanism of inhibition

Leticia Pérez-Díaz, Beatriz Garat, Hugo Cerecetto, 2014, Journal of enzyme inhibition and medicinal chemistry.

1,2,4-thiadiazol-5(4H)-ones: a new class of selective inhibitors of Trypanosoma cruzi triosephosphate isomerase. Study of the mechanism of inhibition

R. Pérez-Montfort, C. Batthyány, Beatriz Aguirre-López, 2013, Journal of enzyme inhibition and medicinal chemistry.

3-H-[1,2]Dithiole as a New Anti-Trypanosoma cruzi Chemotype: Biological and Mechanism of Action Studies

R. Pérez-Montfort, A. Gómez-Puyou, Beatriz Aguirre-López, 2015, Molecules.

Development of bis-thiazoles as inhibitors of triosephosphate isomerase from Trypanosoma cruzi. Identification of new non-mutagenic agents that are active in vivo.

R. Pérez-Montfort, Beatriz Aguirre-López, N. Cabrera, 2015, European journal of medicinal chemistry.

Crosstalk between the subunits of the homodimeric enzyme triosephosphate isomerase

R. Pérez-Montfort, A. Gómez-Puyou, G. Hernández-Alcántara, 2007, Proteins.

Saccharomyces cerevisiae Differential Functionalization of Presumed ScALT1 and ScALT2 Alanine Transaminases Has Been Driven by Diversification of Pyridoxal Phosphate Interactions

Erendira Rojas-Ortega, J. P. Pardo, H. Reyes-Vivas, 2018, Front. Microbiol..

Development of bis-thiazoles as inhibitors of triosephosphate isomerase from Trypanosoma cruzi. Identification of new non-mutagenic agents that are active in vivo.

R. Pérez-Montfort, Beatriz Aguirre-López, N. Cabrera, 2015, European journal of medicinal chemistry.