Christian ROUMESTAND

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Professor (PU-CLEX2)

University of Montpellier

France

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About

Christian Roumestand is a Professor at the University of Montpellier, France. His research focuses on structural and functional characterizations of proteins, with recent work exploring fungal effectors, protein folding pathways, and adaptation mechanisms under high pressure. He has published articles that contribute to a greater understanding of protein dynamics and interactions in both pathogenic fungi and tumor biology.

Recent Grants

Grant: Close

DELTAV

Open Date: 2009-01-01

Close Date: 2013-01-01

Grant: Close

TOXOCELLJONCTION

Open Date: 2009-01-01

Close Date: 2013-01-01

Grant: Close

NMR@CBS : 700 MHz NMR upgrade for the CBS RIO platform for structural biology

Open Date: 2007-01-01

Close Date: 2007-01-01

Grant: Close

Recherche et caractérisation d’inhibiteurs spécifiques de la protéine de signalistion cellulaire PKB (Akt), une enzyme majeure intervenant dans les processus d’apoptose

Open Date: 2005-01-01

Close Date: 2008-01-01

Grant: Close

Les protéines oncogènes TCL1 : plus que des co-activateurs d’Akt

Open Date: 2004-01-01

Close Date: 2008-01-01

Articles (13)

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2025

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2020

Collaborators (10)

Pierre Gladieux

University of Montpellier

FRANCE

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ANDRE PADILLA

CNRS Délégation Languedoc-Roussillon

FRANCE

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Assia Mouhand

Assistant professor (Biochemistry/Structural biology)

University of Montpellier

FRANCE

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Robert Noble

Lecturer

City, University of London

UNITED KINGDOM

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Philippe M. Oger

Université Claude Bernard Lyon 1

FRANCE

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Stephane Delbecq

Prof

University of Montpellier

FRANCE

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Philippe Barthe

University of Montpellier

FRANCE

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Judith Peters

Professor

Université Grenoble Alpes

FRANCE

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Virginie Ropars

Researcher

CEA Saclay

FRANCE

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Karine de Guillen

FRANCE

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Christian ROUMESTAND

Research Interests

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About

Recent Grants

Articles (13)

Structural and Functional Characterization of the 28 kDa Structured Core of BmSA1, the Major Surface Antigen of Babesia Microti

Structure‐guided insights into the biology of fungal effectors

A molten globule ensemble primes Arf1–GDP for the nucleotide switch

The structural landscape and diversity of Pyricularia oryzae MAX effectors revisited

Does a Similar 3D Structure Mean a Similar Folding Pathway? The Presence of a C-Terminal α-Helical Extension in the 3D Structure of MAX60 Drastically Changes the Folding Pathway Described for Other MAX-Effectors from Magnaporthe oryzae

Combining High-Pressure NMR and Geometrical Sampling to Obtain a Full Topological Description of Protein Folding Landscapes: Application to the Folding of Two MAX Effectors from <i>Magnaporthe oryzae</i>

Unravelling the Adaptation Mechanisms to High Pressure in Proteins

1H, 13C, 15 N backbone and side-chain NMR assignments for three MAX effectors from Magnaporthe oryzae

Paracrine Behaviors Arbitrate Parasite-Like Interactions Between Tumor Subclones

Comparative Assessment of NMR Probes for the Experimental Description of Protein Folding Pathways with High-Pressure NMR

Protein-Ligand Binding Volume Determined from a Single 2D NMR Spectrum with Increasing Pressure.

Pressure and Chemical Unfolding of an α-Helical Bundle Protein: The GH2 Domain of the Protein Adaptor GIPC1

Combining High-Pressure Perturbation with NMR Spectroscopy for a Structural and Dynamical Characterization of Protein Folding Pathways

Collaborators (10)

Pierre Gladieux

ANDRE PADILLA

Assia Mouhand

Robert Noble

Philippe M. Oger

Stephane Delbecq

Philippe Barthe

Judith Peters

Virginie Ropars

Karine de Guillen

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