A. Lecoq

发表

Modifications of the amide bond and conformational constraints in pseudopeptide analogues

A. Aubry, J. Vidal, G. Boussard, 1993 .

Seismic Vulnerability Analysis of a Coupled Tank-Piping System by Means of Hybrid Simulation and Acoustic Emission

O. Bursi, R. di Filippo, O. Sayginer, 2020, Experimental Techniques.

Identification and functional characterization of a novel α-conotoxin (EIIA) from Conus ermineus

D. Servent, E. Girard, C. Malosse, 2013, Analytical and Bioanalytical Chemistry.

X‐Ray conformational study of hydrazino peptide analogues

A. Aubry, J. Vidal, M. Marraud, 1991, Biopolymers.

Increasing the humoral immunogenic properties of the HIV-1 Tat protein using a ligand-stabilizing strategy.

A. Ménez, E. Lajeunesse, L. Bellanger, 2008, Vaccine.

Beta-Folding in N-Hydroxy and N-Amino Peptides,

A. Aubry, G. Boussard, M. Marraud, 1992 .

Hydrazino and N-Amino peptides. Chemical and structural aspects

A. Aubry, M. Marraud, A. Lecoq, 1991 .

Hydroxamide, N-amino amide and hydrazide peptidomimetic groups. A synthetic and conformational approach

A. Aubry, M. Marraud, V. Dupont, 1991 .

Antigen DIMERIC state and its applications for anti-HIV vaccine

A. Ménez, E. Lajeunesse, P. Drevet, 2004 .

Mapping the Functional Anatomy of BgK on Kv1.1, Kv1.2, and Kv1.3

A. Ménez, A. Harvey, S. Gasparini, 1999, The Journal of Biological Chemistry.

SYNTHESIS OF 1-(N-BENZYLOXYCARBONYLAMINO)-5-(N-TERBUTYLOXYCARBONYLAMINO)PENTYLPHOSPHINIC ACID

V. Dive, A. Lecoq, Athanasis Yiotakis, 1994 .

Phosphinic peptide analogues as potent inhibitors of Corynebacterium rathayii bacterial collagenase.

V. Dive, A. Nicolaou, A. Yiotakis, 1994, The Biochemical journal.

Development of Highly Potent and Selective Phosphinic Peptide Inhibitors of Zinc Endopeptidase 24-15 Using Combinatorial Chemistry (*)

F. Checler, V. Dive, A. Nicolaou, 1995, The Journal of Biological Chemistry.

Cyclic peptides with a phosphinic bond as potent inhibitors of a zinc bacterial collagenase.

V. Dive, P. Cuniasse, I. Raynal, 1994, Journal of medicinal chemistry.

Cyclodipeptide synthases are a family of tRNA-dependent peptide bond-forming enzymes.

R. Amouroux, S. Lautru, J. Pernodet, 2009, Nature chemical biology.

The couple Pro/AzaPro : a means of β-turn formation control synthesis and conformation of two AzaPro-containing dipeptides

A. Aubry, G. Boussard, M. Marraud, 1992 .

Conformational perturbations induced by N-amination and N-hydroxylation of peptides

A. Aubry, G. Boussard, M. Marraud, 1993 .

Substrate and Reaction Specificity of Mycobacterium tuberculosis Cytochrome P450 CYP121

O. Lequin, M. Le Du, P. Belin, 2013, The Journal of Biological Chemistry.

Identification and structural basis of the reaction catalyzed by CYP121, an essential cytochrome P450 in Mycobacterium tuberculosis

O. Lequin, J. Charbonnier, J. Pernodet, 2009, Proceedings of the National Academy of Sciences.

HIV-1 Tat Raises an Adjuvant-free Humoral Immune Response Controlled by Its Core Region and Its Ability to Form Cysteine-mediated Oligomers*

A. Ménez, C. Vidaud, E. Lajeunesse, 2006, Journal of Biological Chemistry.

On the Convergent Evolution of Animal Toxins

C. Roumestand, C. Vita, A. Ménez, 1997, The Journal of Biological Chemistry.

Immunoprevalence of the CD4+ T‐cell response to HIV Tat and Vpr proteins is provided by clustered and disperse epitopes, respectively

D. Houitte, S. Muller, B. Maillère, 2008, European journal of immunology.

Isolation of a Tarantula Toxin Specific for a Class of Proton-gated Na+ Channels*

Alain Lecoq, Rainer Waldmann, Pierre Escoubas, 2000, The Journal of Biological Chemistry.

Analysis of 51 cyclodipeptide synthases reveals the basis for substrate specificity.

J. Seguin, J. Pernodet, M. Moutiez, 2015, Nature chemical biology.

Conformational and functional variability supported by the BPTI fold: Solution structure of the Ca2+ channel blocker calcicludine

S. Zinn-Justin, A. Ménez, B. Gilquin, 1999, Proteins.

Nonribosomal peptide synthesis in animals: the cyclodipeptide synthase of Nematostella.

J. Charbonnier, J. Seguin, J. Pernodet, 2011, Chemistry & biology.

Structure of the BgK-Kv1.1 Complex Based on Distance Restraints Identified by Double Mutant Cycles

S. Grissmer, A. Ménez, B. Gilquin, 2002, The Journal of Biological Chemistry.

Delineation of the functional site of alpha-dendrotoxin. The functional topographies of dendrotoxins are different but share a conserved core with those of other Kv1 potassium channel-blocking toxins.

S. Zinn-Justin, A. Ménez, J. Danse, 1998, The Journal of biological chemistry.

Structure-based secondary structure-independent approach to design protein ligands: Application to the design of Kv1.2 potassium channel blockers.

A Joly, P Cuniasse, M. Lefranc, 2006, Journal of the American Chemical Society.

Crystal state conformation of three azapeptides containing the Azaproline residue, a β‐turn regulator

Alain Lecoq, Michel Marraud, A. Aubry, 1993 .

Delineation of the Functional Site of α-Dendrotoxin

S. Zinn-Justin, A. Ménez, J. Danse, 1998, Journal of Biological Chemistry.

Identification and structural basis of the reaction catalyzed by CYP121, an essential cytochrome P450 in Mycobacterium tuberculosis

O. Lequin, J. Charbonnier, J. Pernodet, 2009, Proceedings of the National Academy of Sciences.