J. Andreu

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Synthetic developmental regulator MciZ targets FtsZ across Bacillus species and inhibits bacterial division

D. Andreu, Javier Valle, L. Araújo-Bazán, 2019, Molecular microbiology.

Interaction of tubulin with octyl glucoside and deoxycholate. 1. Binding and hydrodynamic studies.

J. Andreu, J. A. Muñoz, 1986, Biochemistry.

Interaction of bacterial F1-ATPase with octyl glucoside and deoxycholate

F. Mollinedo, J. Andreu, E. Muñoz, 1986 .

Self-Organization of FtsZ Polymers in Solution Reveals Spacer Role of the Disordered C-Terminal Tail.

J. F. Díaz, R. Núnez-Ramírez, O. Llorca, 2017, Biophysical journal.

Bacterial cell division proteins as antibiotic targets.

T. den Blaauwen, O. Monasterio, J. Andreu, 2014, Bioorganic chemistry.

Stoichiometric and substoichiometric inhibition of tubulin self-assembly by colchicine analogues.

S. N. Timasheff, M. J. Gorbunoff, B. Perez-Ramirez, 1996, Biochemistry.

Conformational states of tubulin liganded to colchicine, tropolone methyl ether, and podophyllotoxin.

S. N. Timasheff, J. Andreu, 1982, Biochemistry.

The interactions of tropolone with magnesium ions and tubulin.

S. N. Timasheff, J. Andreu, 1982, Biochimica et biophysica acta.

Structure of bacterial tubulin BtubA/B: evidence for horizontal gene transfer.

Jan Löwe, J. Löwe, J. Andreu, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Purification and assembly of bacterial tubulin BtubA/B and constructs bearing eukaryotic tubulin sequences.

J. Andreu, M. A. Oliva, 2013, Methods in cell biology.

The Interactions of Cell Division Protein FtsZ with Guanine Nucleotides*

J. Díaz, W. Garcia, M. Menéndez, 2007, Journal of Biological Chemistry.

Large scale purification of brain tubulin with the modified Weisenberg procedure.

J. Andreu, 2007, Methods in molecular medicine.

The nucleotide switch of tubulin and microtubule assembly: a polymerization-driven structural change.

R. Buey, J. F. Díaz, J. Andreu, 2006, Biochemistry.

A purple acidophilic di-ferric DNA ligase from Ferroplasma

K. Timmis, M. Ferrer, P. Golyshin, 2008, Proceedings of the National Academy of Sciences.

Nucleotide‐induced folding of cell division protein FtsZ from Staphylococcus aureus

D. Laurents, C. Fernández‐Tornero, L. Araújo-Bazán, 2020, The FEBS journal.

Thermal transitions in the structure of tubulin

A. Mozo-Villarías, A. Morros, J. Andreu, 1991, European Biophysics Journal.

Mechanism of colchicine binding to tubulin. Tolerance of substituents in ring C' of biphenyl analogues.

S. N. Timasheff, M. J. Gorbunoff, F. Medrano, 1991, Biochemistry.

Roles of colchicine rings B and C in the binding process to tubulin.

S. N. Timasheff, M. J. Gorbunoff, F. Medrano, 1989, Biochemistry.

Polymerization of nucleotide‐free, GDP‐ and GTP‐bound cell division protein FtsZ: GDP makes the difference

S. Huecas, J. Andreu, 2004, FEBS letters.

Solution structure of Taxotere-induced microtubules to 3-nm resolution. The change in protofilament number is linked to the binding of the taxol side chain.

J. M. de Pereda, J. F. Díaz, V. Peyrot, 1994, The Journal of biological chemistry.

Possible binding site for paclitaxel at microtubule pores

M. Botta, J. F. Díaz, G. Maccari, 2009, The FEBS journal.

Protein shape and assembly studied with X ray solution scattering: Fundaments and practice

P. Chacón, R. Buey, J. Díaz, 2009 .

Tubulin bound to colchicine forms polymers different from microtubules.

S. N. Timasheff, J. Andreu, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Chirality and Spectroscopic Changes Induced by the Recognition of Ethyl 5‐Amino‐2‐methyl‐1,2‐dihydro‐3‐phenylpyrido[3,4‐b]pyrazin‐7‐yl Carbamate Analogs by Tubulin

P. Barbier, V. Peyrot, C. Briand, 1999 .

New interfacial microtubule inhibitors of marine origin, PM050489/PM060184, with potent antitumor activity and a distinct mechanism.

I. Barasoain, C. Galmarini, M. Peñalva, 2013, ACS chemical biology.

Effect of 2'-OH acetylation on the bioactivity and conformation of 7-O-[N-(4'-fluoresceincarbonyl)-L-alanyl]taxol. A NMR-fluorescence microscopy study.

I. Barasoain, M. Abal, F. Amat-Guerri, 1998, Bioorganic & medicinal chemistry.

The Antibacterial Cell Division Inhibitor PC190723 Is an FtsZ Polymer-stabilizing Agent That Induces Filament Assembly and Condensation*

A. J. Martin-Galiano, R. Núnez-Ramírez, O. Llorca, 2010, The Journal of Biological Chemistry.

A Polymerization-Associated Structural Switch in FtsZ That Enables Treadmilling of Model Filaments

J. Löwe, J. Andreu, M. A. Oliva, 2017, mBio.

A polymerisation-associated conformational switch in FtsZ that enables treadmilling

J. Löwe, J. Andreu, M. A. Oliva, 2016, bioRxiv.

Interaction of epothilone analogs with the paclitaxel binding site: relationship between binding affinity, microtubule stabilization, and cytotoxicity.

A. Ritzén, K. Nicolaou, P. Giannakakou, 2004, Chemistry & biology.

Farnesyltransferase inhibitors reverse taxane resistance.

A. Marcus, F. Khuri, Jun Zhou, 2006, Cancer research.

FtsZ filament structures in different nucleotide states reveal the mechanism of assembly dynamics

C. Fernández‐Tornero, S. Huecas, J. Andreu, 2022, PLoS biology.

Targeting the FtsZ Allosteric Binding Site with a Novel Fluorescence Polarization Screen, Cytological and Structural Approaches for Antibacterial Discovery

M. Artola, M. López-Rodríguez, C. Fernández‐Tornero, 2021, Journal of medicinal chemistry.

Mechanism of FtsZ assembly dynamics revealed by filament structures in different nucleotide states

C. Fernández‐Tornero, S. Huecas, J. Andreu, 2021, bioRxiv.

Drug–tubulin interactions interrogated by transient absorption spectroscopy

G. Sastre, M. Miranda, D. Jornet, 2015 .

A new tubulin-binding site and pharmacophore for microtubule-destabilizing anticancer drugs

M. Steinmetz, K. Altmann, A. Prota, 2014, Proceedings of the National Academy of Sciences.

Cyclostreptin binds covalently to microtubule pores and lumenal taxoid binding sites.

I. Barasoain, E. Calvo, R. Buey, 2007, Nature chemical biology.

Comparative study of the colchicine binding site and the assembly of fish and mammalian microtubule proteins.

J. M. de Pereda, M. Wallin, J. Andreu, 1995, Cell motility and the cytoskeleton.

Tubulin assembly probed with antibodies to synthetic peptides.

D. Andreu, M. Arevalo, J. Andreu, 1990, Journal of molecular biology.

Low resolution structure of microtubules in solution. Synchrotron X-ray scattering and electron microscopy of taxol-induced microtubules assembled from purified tubulin in comparison with glycerol and MAP-induced microtubules.

E. Nogales, J. Díaz, J. Díaz, 1992, Journal of molecular biology.

The Search for Antibacterial Inhibitors Targeting Cell Division Protein FtsZ at Its Nucleotide and Allosteric Binding Sites

S. Huecas, J. Andreu, Henar Vázquez-Villa, 2022, Biomedicines.

New Fluorescent Water‐Soluble Taxol Derivatives

I. Barasoain, M. Abal, F. Amat-Guerri, 1996 .

Glycoprotein nature of energy‐transducing ATPases

J. Andreu, E. Muñoz, Rudolf Warth, 1978, FEBS letters.

Understanding nucleotide-regulated FtsZ filament dynamics and the monomer assembly switch with large-scale atomistic simulations.

P. Chacón, J. López-Blanco, E. Ramírez-Aportela, 2014, Biophysical journal.

Peloruside A Does Not Bind to the Taxoid Site on β-Tubulin and Retains Its Activity in Multidrug-Resistant Cell Lines

P. Teesdale-Spittle, J. Miller, R. Buey, 2004, Cancer Research.

Retains Its Activity in Multidrug-Resistant Cell Lines-Tubulin β Peloruside A Does Not Bind to the Taxoid Site on

P. Teesdale-Spittle, J. Miller, R. Buey, 2004 .

Advances in Brief Peloruside A Does Not Bind to the Taxoid Site on-Tubulin and Retains Its Activity in Multidrug-Resistant Cell Lines

P. Teesdale-Spittle, J. Miller, R. Buey, 2004 .

Fast mixing device for time-resolved synchrotron x-ray scattering studies of radiation sensitive proteins

P. Chacón, J. Díaz, G. Diakun, 1998 .

PM060184, a new tubulin binding agent with potent antitumor activity including P-glycoprotein over-expressing tumors.

I. Barasoain, B. Bouchet, C. Galmarini, 2014, Biochemical pharmacology.

Polymerization of the tubulin-colchicine complex: relation to microtubule assembly.

T. Wagenknecht, S. N. Timasheff, J. Andreu, 1983, Biochemistry.

Fluorescent taxoid probes for microtubule research.

I. Barasoain, J. Andreu, J. Díaz, 2010, Methods in cell biology.

Binding of gossypol to purified tubulin and inhibition of its assembly into microtubules.

F. Medrano, J. Andreu, 1986, European journal of biochemistry.

The ligand- and microtubule assembly-induced GTPase activity of purified calf brain tubulin.

S. N. Timasheff, J. Andreu, 1981, Archives of biochemistry and biophysics.

Membrane adenosine triphosphatase of Micrococcus lysodeikticus. Molecular properties of the purified enzyme unstimulated by trypsin.

J. Andreu, E. Muñoz, J. A. Albendea, 1973, European journal of biochemistry.

Molecular properties of random coil and refolded forms of alpha and beta subunits of an energy transducing ATPase from bacterial membranes.

J. Andreu, E. Muñoz, 1979, Biochemistry.

Identification of betaIII- and betaIV-tubulin isotypes in cold-adapted microtubules from Atlantic cod (Gadus morhua): antibody mapping and cDNA sequencing.

I. Barasoain, R. Luduena, M. Wallin, 1999, Cell motility and the cytoskeleton.

The measurement of cooperative protein self-assembly by turbidity and other techniques.

S. N. Timasheff, J. Andreu, 1986, Methods in enzymology.

Tubulin binding properties of two chiral isomers with 1-deaza-7,8-dihydropteridine structure.

V. Peyrot, C. Briand, J. Andreu, 1993, Advances in experimental medicine and biology.

Mechanism of binding of the new antimitotic drug MDL 27048 to the colchicine site of tubulin: equilibrium studies.

M. Menéndez, V. Peyrot, C. Briand, 1992, Biochemistry.

Interaction of tubulin with bifunctional colchicine analogues: an equilibrium study.

J. Lee, S. N. Timasheff, M. J. Gorbunoff, 1984, Biochemistry.

Differential sensitivity to trypsin digestion of purified forms of Micrococcus lysodeikticus ATPase (BFI). A study of their structural and conformational differences and mechanism of conversion.

J. Andreu, E. Muñoz, J. Carreira, 1977, Biochimica et biophysica acta.

Isolation and partial characterization of the two major subunits of the BF1 factor (ATPase) from Micrococcus lysodeikticus and evidence for their glycoprotein nature

J. Andreu, E. Muñoz, J. Carreira, 1976, FEBS letters.

Micrococcus lysodeikticus ATPase. Purification by preparative gel electrophoresis and subunit structure studied by urea and sodium dodecylsulfate gel electrophoresis.

J. Andreu, E. Muñoz, 1975, Biochimica et biophysica acta.

Thermodynamics of ligand-induced assembly of tubulin.

M. Menéndez, J. Andreu, J. Díaz, 1993, Biochemistry.

Leghemoglobin in Lupin Plants (Lupinus albus cv Multolupa).

M. D. de Felipe, J. Andreu, S. de la Viña, 1989, Plant physiology.

Leghemoglobin inLupinPlants (Lupinus albus cvMultolupa)

J. Andreu, Consejo Superior, 1989 .

Leghemoglobin in Lupin Plants

J. Andreu, M. R. Felipe, A. Vivo, 2022 .

Tubulin homolog TubZ in a phage-encoded partition system

Y. Sakaguchi, J. Andreu, M. A. Oliva, 2012, Proceedings of the National Academy of Sciences.

Cytological Profile of Antibacterial FtsZ Inhibitors and Synthetic Peptide MciZ

D. Andreu, S. Huecas, J. Andreu, 2016, Front. Microbiol..

Interactions of bacterial cell division protein FtsZ with C8-substituted guanine nucleotide inhibitors. A combined NMR, biochemical and molecular modeling perspective.

A. Morreale, F. Cañada, A. Perona, 2013, Journal of the American Chemical Society.

Chrysophaentins are competitive inhibitors of FtsZ and inhibit Z-ring formation in live bacteria.

C. Bewley, P. Wipf, Jared T. Hammill, 2013, Bioorganic & medicinal chemistry.

Probing FtsZ and tubulin with C8-substituted GTP analogs reveals differences in their nucleotide binding sites.

J. Löwe, T. den Blaauwen, G. Koomen, 2008, Chemistry & biology.

The interaction of microtubules with stabilizers characterized at biochemical and structural levels.

J. Andreu, J. Jiménez‐Barbero, J. Díaz, 2009, Topics in current chemistry.

Chemical synthesis and biological evaluation of novel epothilone B and trans-12,13-cyclopropyl epothilone B analogues

A. Ritzén, K. Nicolaou, K. Altmann, 2002 .

Cyclostreptin derivatives specifically target cellular tubulin and further map the paclitaxel site.

I. Barasoain, J. Díaz, E. Calvo, 2012, Biochemistry.

Role of the colchicine ring A and its methoxy groups in the binding to tubulin and microtubule inhibition.

S. N. Timasheff, M. J. Gorbunoff, B. Perez-Ramirez, 1998, Biochemistry.

Beyond a Fluorescent Probe: Inhibition of Cell Division Protein FtsZ by mant-GTP Elucidated by NMR and Biochemical Approaches.

A. Morreale, F. Cañada, A. Perona, 2015, ACS chemical biology.

Tubulin structure probed with antibodies to synthetic peptides. Mapping of three major types of limited proteolysis fragments.

D. Andreu, F. Medrano, J. Andreu, 1988, Biochemistry.

Endowing indole-based tubulin inhibitors with an anchor for derivatization: highly potent 3-substituted indolephenstatins and indoleisocombretastatins.

F. Mollinedo, J. Andreu, M. Medarde, 2013, Journal of medicinal chemistry.

Control of the Structural Stability of the Tubulin Dimer by One High Affinity Bound Magnesium Ion at Nucleotide N-site*

G. Rivas, M. Menéndez, J. Andreu, 1998, The Journal of Biological Chemistry.

Assembly of purified GDP-tubulin into microtubules induced by taxol and taxotere: reversibility, ligand stoichiometry, and competition.

J. Díaz, J. Andreu, J M Andreu, 1993, Biochemistry.

Tubulin‐Colchicine Interactions and Polymerization of the Complex a

S. N. Timasheff, J. Andreu, SERGE N. TIMASHEFF, 1986, Annals of the New York Academy of Sciences.

Interaction of tubulin with single ring analogues of colchicine.

S. N. Timasheff, J. Andreu, 1982, Biochemistry.

Optimization of taxane binding to microtubules: binding affinity dissection and incremental construction of a high-affinity analog of paclitaxel.

Federico Gago, F. Gago, I. Barasoain, 2008, Chemistry & biology.

Structural stability of the PsbQ protein of higher plant photosystem II.

M. Menéndez, J. B. Arellano, M. Balsera, 2004, Biochemistry.

Inter‐conversion of catalytic abilities in a bifunctional carboxyl/feruloyl‐esterase from earthworm gut metagenome

T. Nechitaylo, M. Ferrer, P. Golyshin, 2009, Microbial Biotechnology.

Tau Induces Ring and Microtubule Formation from R‚-Tubulin Dimers under Nonassembly Conditions †

P. Barbier, V. Peyrot, O. Monasterio, 2004 .

Essential Cell Division Protein FtsZ Assembles into One Monomer-thick Ribbons under Conditions Resembling the Crowded Intracellular Environment*

G. Rivas, J. Mingorance, J. Andreu, 2003, Journal of Biological Chemistry.

Chemically synthesized 182–235 segment of tau protein and analogue peptides are efficient in vitro microtubule assembly inducers of low apparent sequence specificity

D. Andreu, I. Novella, J. Andreu, 1992, FEBS letters.

Effective GTP-replacing FtsZ inhibitors and antibacterial mechanism of action.

P. Chacón, M. Artola, S. Sieber, 2015, ACS chemical biology.

Tubulin binding of two 1-deaza-7,8-dihydropteridines with different biological properties: enantiomers NSC 613862 (S)-(-) and NSC 613863 (R)-(+).

V. Peyrot, C. Briand, C Briand, 1993, Biochemistry.

Protein domains and conformational changes in the activation of RepA, a DNA replication initiator

R. Giraldo, J. Andreu, Ramón Díaz‐Orejas, 1998, The EMBO journal.

Design, synthesis and cytotoxic activities of naphthyl analogues of combretastatin A-4.

I. Barasoain, J. Andreu, A. B. Maya, 2000, Bioorganic & medicinal chemistry letters.

Different kinetic pathways of the binding of two biphenyl analogues of colchicine to tubulin.

Y. Engelborghs, M. J. Gorbunoff, J. Andreu, 1996, Biochemistry.

Taxanes: microtubule and centrosome targets, and cell cycle dependent mechanisms of action.

I. Barasoain, M. Abal, J. Andreu, 2003, Current cancer drug targets.

The bound conformation of microtubule-stabilizing agents: NMR insights into the bioactive 3D structure of discodermolide and dictyostatin.

Jesús Jiménez-Barbero, Ian Paterson, I. Paterson, 2008, Chemistry.

Microtubule interactions with chemically diverse stabilizing agents: thermodynamics of binding to the paclitaxel site predicts cytotoxicity.

I. Barasoain, P. Giannakakou, R. Buey, 2005, Chemistry & biology.

Probing the pore drug binding site of microtubules with fluorescent taxanes: evidence of two binding poses.

Maurizio Botta, Mattia Mori, Giorgio Maccari, 2010, Chemistry & biology.

Synthesis and antimitotic and tubulin interaction profiles of novel pinacol derivatives of podophyllotoxins.

I. Barasoain, C. Trigili, J. Andreu, 2012, Journal of medicinal chemistry.

Macromolecular Accessibility of Fluorescent Taxoids Bound at a Paclitaxel Binding Site in the Microtubule Surface*

I. Barasoain, J. Díaz, F. Amat-Guerri, 2005, Journal of Biological Chemistry.

Assembly of Archaeal Cell Division Protein FtsZ and a GTPase-inactive Mutant into Double-stranded Filaments*

J. Valpuesta, J. Martín-Benito, S. Huecas, 2003, Journal of Biological Chemistry.

Mapping Flexibility and the Assembly Switch of Cell Division Protein FtsZ by Computational and Mutational Approaches*♦

R. Buey, J. Andreu, José M Andreu, 2010, The Journal of Biological Chemistry.

Energetics and geometry of FtsZ polymers: nucleated self-assembly of single protofilaments.

J. Valpuesta, J. Martín-Benito, O. Llorca, 2008, Biophysical journal.

Chemical synthesis of five tubulin antigenic sequences. Production and characterization of their corresponding anti-tubulin monospecific antibodies.

D. Andreu, J. Andreu, S. de la Viña, 2009, International journal of peptide and protein research.

Micrococcus lysodeikticus membrane ATPase. Effect of trypsin on stimulation of a purified form of the enzyme and idenfification of its natural inhibitor.

J. Andreu, E. Muñoz, J. Carreira, 1976, Biochimica et biophysica acta.

Zampanolide Binding to Tubulin Indicates Cross-Talk of Taxane Site with Colchicine and Nucleotide Sites.

K. Altmann, J. Miller, A. Prota, 2017, Journal of natural products.

Changes in Microtubule Protofilament Number Induced by Taxol Binding to an Easily Accessible Site

P. Chacón, G. Diakun, J. Valpuesta, 1998, The Journal of Biological Chemistry.

Fluorescent taxoids as probes of the microtubule cytoskeleton.

I. Barasoain, M. Lillo, M. Abal, 1998, Cell motility and the cytoskeleton.

Novel Polyphenol Oxidase Mined from a Metagenome Expression Library of Bovine Rumen

K. Timmis, M. Pita, M. Ferrer, 2006, Journal of Biological Chemistry.

Magnesium-induced Linear Self-association of the FtsZ Bacterial Cell Division Protein Monomer

G. Rivas, A. Minton, A. López, 2000, The Journal of Biological Chemistry.

Induction of apoptosis in leukemic cells by the reversible microtubule-disrupting agent 2-methoxy-5-(2',3',4'-trimethoxyphenyl)-2,4,6-cycloheptatrien-1 -one: protection by Bcl-2 and Bcl-X(L) and cell cycle arrest.

I. Barasoain, F. Mollinedo, C. Gajate, 2000, Cancer research.

Analysis of mebendazole binding to its target biomolecule by laser flash photolysis.

L. Domingo, M. Miranda, J. Andreu, 2016, Journal of photochemistry and photobiology. B, Biology.

Structural features of the plasmid pMV158‐encoded transcriptional repressor CopG, a protein sharing similarities with both helix‐turn‐helix and β‐sheet DNA binding proteins

G. Rivas, P. Acebo, M. Espinosa, 1998 .

Centrosome and spindle pole microtubules are main targets of a fluorescent taxoid inducing cell death.

I. Barasoain, M. Abal, F. Amat-Guerri, 2001, Cell motility and the cytoskeleton.

Interaction of tubulin with octyl glucoside and deoxycholate. 2. Protein conformation, binding of colchicine ligands, and microtubule assembly.

J. Carrascosa, J. Andreu, J. de la Torre, 1986, Biochemistry.

The microtubule stabilizing agent laulimalide does not bind in the taxoid site, kills cells resistant to paclitaxel and epothilones, and may not require its epoxide moiety for activity.

Arun K. Ghosh, P. Giannakakou, A. O'brate, 2002, Biochemistry.

The interaction of baccatin III with the taxol binding site of microtubules determined by a homogeneous assay with fluorescent taxoid.

I. Barasoain, J. Andreu, 2001, Biochemistry.

Energetics of the Cooperative Assembly of Cell Division Protein FtsZ and the Nucleotide Hydrolysis Switch*

S. Huecas, J. Andreu, 2003, Journal of Biological Chemistry.

Tubulin secondary structure analysis, limited proteolysis sites, and homology to FtsZ.

P. Chacón, J. M. de Pereda, J. Andreu, 1996, Biochemistry.

Insights into the interaction of discodermolide and docetaxel with tubulin. Mapping the binding sites of microtubule-stabilizing agents by using an integrated NMR and computational approach.

I. Paterson, C. Trigili, Á. Canales, 2011, ACS chemical biology.

Septin C-Terminal Domain Interactions: Implications for Filament Stability and Assembly

W. Garcia, R. Garratt, J. Andreu, 2012, Cell Biochemistry and Biophysics.

Site-directed antibodies to tubulin.

J. M. de Pereda, J. Andreu, 1993, Cell motility and the cytoskeleton.

Triazolopyrimidines Are Microtubule-Stabilizing Agents that Bind the Vinca Inhibitor Site of Tubulin.

M. Steinmetz, S. Wendeborn, I. Barasoain, 2017, Cell chemical biology.

Activation of Cell Division Protein FtsZ

J. Díaz, A. Kralicek, J. Mingorance, 2001, The Journal of Biological Chemistry.

Fast Kinetics of Taxol Binding to Microtubules

I. Barasoain, J. Díaz, J. Andreu, 2003, The Journal of Biological Chemistry.

Insights into nucleotide recognition by cell division protein FtsZ from a mant-GTP competition assay and molecular dynamics.

Antonio Morreale, A. Morreale, R. Gil-Redondo, 2010, Biochemistry.

Molecular recognition of epothilones by microtubules and tubulin dimers revealed by biochemical and NMR approaches.

K. Altmann, F. Gago, T. Carlomagno, 2014, ACS chemical biology.

Non-cytotoxic variants of the Kid protein that retain their auto-regulatory activity.

J. Rafferty, D. Hargreaves, M. Lemonnier, 2003, Plasmid.

Reversible Unfolding of FtsZ Cell Division Proteins from Archaea and Bacteria

O. Monasterio, J. Andreu, M. A. Oliva, 2002, The Journal of Biological Chemistry.

Folding, stability and polymerization properties of FtsZ chimeras with inserted tubulin loops involved in the interaction with the cytosolic chaperonin CCT and in microtubule formation.

J. Carrascosa, J. Valpuesta, I. Barthelemy, 2005, Journal of molecular biology.

Targeting the assembly of bacterial cell division protein FtsZ with small molecules.

P. Chacón, J. Andreu, M. Martín-Fontecha, 2012, ACS chemical biology.

FtsZ folding, self-association, activation and assembly

S. Huecas, J. Andreu, M. A. Oliva, 2004 .

Self assembly of human septin 2 into amyloid filaments.

W. Garcia, R. Garratt, R. Giraldo, 2012, Biochimie.

Urea-induced unfolding studies of free- and ligand-bound tetrameric ATP-dependent Saccharomyces cerevisiae phosphoenolpyruvate carboxykinase. Influence of quaternary structure on protein conformational stability.

F. González-Nilo, C. Alfonso, J. Andreu, 2002, The international journal of biochemistry & cell biology.

Circular dichroism and Fourier transform infrared spectroscopic studies on the secondary structure of Saccharomyces cerevisiae and Escherichia coli phospho enolpyruvate carboxykinases.

H. Goldie, L. R. Olsen, J. Andreu, 1995, Biochimica et biophysica acta.

Stability of Escherichia coli phosphoenolpyruvate carboxykinase against urea-induced unfolding and ligand effects.

H. Goldie, J. Andreu, E. Cardemil, 1998, European journal of biochemistry.

Low-resolution structures of proteins in solution retrieved from X-ray scattering with a genetic algorithm.

E Pantos, P Chacón, P. Chacón, 1998, Biophysical journal.

How Protein Filaments Treadmill.

J. Andreu, 2020, Biophysical journal.

Stathmin and Interfacial Microtubule Inhibitors Recognize a Naturally Curved Conformation of Tubulin Dimers*

Carlos Alfonso, C. Alfonso, P. Barbier, 2010, The Journal of Biological Chemistry.

Structural intermediates in the assembly of taxoid-induced microtubules and GDP-tubulin double rings: time-resolved X-ray scattering.

G. Diakun, J. Bordas, J. Andreu, 1996, Biophysical journal.

Synthetic inhibitors of bacterial cell division targeting the GTP-binding site of FtsZ.

P. Chacón, M. Artola, I. Barasoain, 2013, ACS chemical biology.

Reconstruction of protein form with X-ray solution scattering and a genetic algorithm.

P Chacón, P. Chacón, F. Morán, 2000, Journal of molecular biology.

Physical and spectroscopic methods for the evaluation of the interactions of antimitotic agents with tubulin.

S. N. Timasheff, G. Na, J. Andreu, 1991, Pharmacology & therapeutics.

Hydrophobic Interactions of Tubulin

J. Andreu, 1986, Annals of the New York Academy of Sciences.

Bacterial Tubulin Distinct Loop Sequences and Primitive Assembly Properties Support Its Origin from a Eukaryotic Tubulin Ancestor*

A. Bhattacharyya, J. Valpuesta, J. Andreu, 2011, The Journal of Biological Chemistry.

Tubulin and FtsZ Superfamily of Protein Assembly Machines

J. Andreu, M. A. Oliva, 2014 .

Molecular Recognition of Taxol by Microtubules

Y. Engelborghs, A. A. Souto, J. Andreu, 2000, The Journal of Biological Chemistry.

Roles of ring C oxygens in the binding of colchicine to tubulin.

S. N. Timasheff, M. J. Gorbunoff, F. Medrano, 1991, Biochemistry.

Mapping surface sequences of the tubulin dimer and taxol-induced microtubules with limited proteolysis.

J. M. de Pereda, J. Andreu, 1996, Biochemistry.

Physicochemical characterization of the heat-stable microtubule-associated protein MAP2.

J. Ávila, J. Andreu, M. A. Hernández, 1986, European journal of biochemistry.

Cytoplasmic microtubules in human neutrophil degranulation: reversible inhibition by the colchicine analogue 2-methoxy-5-(2',3',4'-trimethoxyphenyl)-2,4,6-cycloheptatrien-1- one.

F. Mollinedo, J. Andreu, J. Nieto, 1989, Molecular pharmacology.

Kinetics of dissociation of the tubulin-colchicine complex. Complete reaction scheme and comparison to thermodynamic measurements.

J. Fernando Díaz, J. Andreu, 1991, The Journal of biological chemistry.

Crystal structures of taxane-tubulin complexes: Implications for the mechanism of microtubule stabilization by Taxol

M. Steinmetz, K. Altmann, D. Lucena‐Agell, 2021 .

Reversible inhibition of microtubules and cell growth by the bicyclic colchicine analogue MTC.

J. Avila, J. Andreu, J. C. Diez, 1987, Cell motility and the cytoskeleton.

Interaction of tubulin and cellular microtubules with the new antitumor drug MDL 27048. A powerful and reversible microtubule inhibitor.

V. Peyrot, C. Briand, J. Andreu, 1989, The Journal of biological chemistry.

Action of a deazapteridine on microtubular system effect of chirality

I. Barasoain, V. Peyrot, C. Briand, 1992 .

C-terminal cleavage of tubulin by subtilisin enhances ring formation.

V. Peyrot, C. Briand, J. Andreu, 1990, Archives of biochemistry and biophysics.

The active GTP- and ground GDP-liganded states of tubulin are distinguished by the binding of chiral isomers of ethyl 5-amino-2-methyl-1,2-dihydro-3-phenylpyrido[3,4-b]pyrazin-7-yl carbamate.

P. Barbier, V. Peyrot, J. Andreu, 1998, Biochemistry.

Solution structure of GDP-tubulin double rings to 3 nm resolution and comparison with microtubules.

J. Bordas, J. Andreu, E. Pantos, 1994, Journal of molecular biology.

NMR determination of the bioactive conformation of peloruside A bound to microtubules.

Jesús Jiménez-Barbero, R. Buey, P. Northcote, 2006, Journal of the American Chemical Society.

Conformation and self-association of a hybrid peptide of cecropin A and melittin with improved antibiotic activity

M. Fuxreiter, M. Pons, D. Andreu, 1996 .

Phage phi29 protein p6 is in a monomer-dimer equilibrium that shifts to higher association states at the millimolar concentrations found in vivo.

M. Salas, J. Andreu, J. Hermoso, 1997, Biochemistry.

Modulation of microtubule interprotofilament interactions by modified taxanes.

A. Nogales, J. Díaz, W. Bras, 2011, Biophysical journal.

Confomational and molecular responses to pH variation of the purified membrane adenosine triphospate of Micrococcus lysodeikticus

J. Andreu, J. Carreira, M. Nieto, 1975 .

3-Hydroxyphenylpropionate and Phenylpropionate Are Synergistic Activators of the MhpR Transcriptional Regulator from Escherichia coli*

J. García, B. Galán, G. Rivas, 2009, The Journal of Biological Chemistry.

Membrane adenosine triphosphatase of Micrococcus lysodeikticus. Isolation of two forms of the enzyme complex and correlation between enzymatic stability, latency and activity.

J. Andreu, E. Muñoz, J. Carreira, 1976, Molecular and Cellular Biochemistry.

Helicity of α(404–451) and β(394–445) tubulin C‐terminal recombinant peptides

D. Andreu, M. Jiménez, M. Rico, 1999, Protein science : a publication of the Protein Society.

Conserved GTPase mechanism in bacterial FtsZ and archaeal tubulin filaments

C. Fernández‐Tornero, J. Andreu, F. M. Ruiz, 2022, The FEBS journal.

Tau induces ring and microtubule formation from alphabeta-tubulin dimers under nonassembly conditions.

P. Barbier, V. Peyrot, O. Monasterio, 2004, Biochemistry.