Philippe Roche

Dr. Philippe Roche

Laboratory of integrative Structural and Chemical Biology (iSCB), Centre de Recherche en Cancérologie de Marseille (CRCM); CNRS UMR 7258, INSERM U 1068, Institut Paoli-Calmettes; and Aix-Marseille Universités, Marseille 13009, France
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Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 1990 in Nature
Verified
Journal Article
Closed access
PLPatrice Lerouge
Patrice Lerouge
PRPhilippe Roche
Philippe Roche
CFCatherine Faucher
Catherine Faucher
FMFabienne Maillet
Fabienne Maillet
GTGeorges Truchet
Georges Truchet
JDJean Dénarié
Jean Dénarié

1 June 1991 in Nature
Verified
Journal Article
Closed access
GTGeorges Truchet
Georges Truchet
PRPhilippe Roche
Philippe Roche
PLPatrice Lerouge
Patrice Lerouge
JVJacques Vasse
Jacques Vasse
SCSylvie Camut
Sylvie Camut
JPJean-Claude Promé
Jean-Claude Promé

1 December 1991 in Cell
Verified
Journal Article
Closed access
PRPhilippe Roche
Philippe Roche
FDFrédéric Debellé
Frédéric Debellé
FMFabienne Maillet
Fabienne Maillet
PLPatrice Lerouge
Patrice Lerouge
CFCatherine Faucher
Catherine Faucher
JPJean-Claude Promé
Jean-Claude Promé

1 August 2011 in Current Opinion in Chemical Biology
Verified
Journal Article
Closed access
XMXavier Morelli
Xavier Morelli
RBRaphaël Bourgeas
Raphaël Bourgeas
PRPhilippe Roche
Philippe Roche

30 November 2012 in Nucleic Acids Research
Verified
Journal Article
Open access
PDF file
MBMarie Jeanne Basse
Marie Jeanne Basse
SBStephane Betzi
Stephane Betzi
RBRaphaël Bourgeas
Raphaël Bourgeas
SBSofia Bouzidi
Sofia Bouzidi
BCBernard Chetrit
Bernard Chetrit
PRPhilippe Roche
Philippe Roche
Protein–protein interactions are considered as one of the next generation of therapeutic targets. Specific tools thus need to be developed to tackle this challenging chemical space. In an effort to derive some common principles from recent successes, we have built 2P2Idb (freely accessible at http://2p2idb.cnrs-mrs.fr), a hand-curated structural database dedicated to protein–protein interactions with known orthosteric modulators. It includes all interactions for which both the protein–protein and protein–ligand complexes have been structurally characterized. A web server provides links to related sites of interest, binding affinity data, pre-calculated structural information about protein–protein interfaces and 3D interactive views through java applets. Comparison of interfaces in 2P2Idb to those of representative datasets of heterodimeric complexes has led to the identification of geometrical parameters and residue properties to assess the druggability of protein–protein complexes. A tool is proposed to calculate a series of biophysical and geometrical parameters that characterize protein–protein interfaces. A large range of descriptors are computed including, buried accessible surface area, gap volume, non-bonded contacts, hydrogen-bonds, atom and residue composition, number of segments and secondary structure contribution. All together the 2P2I database represents a structural source of information for scientists from academic institutions or pharmaceutical industries.

24 December 1996 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
PDF file
PRPhilippe Roche
Philippe Roche
FMFabienne Maillet
Fabienne Maillet
CPClaire Plazanet
Claire Plazanet
FDFrédéric Debellé
Frédéric Debellé
MFMyriam Ferro
Myriam Ferro
JDJean Dénarié
Jean Dénarié
Symbiotic bacteria of the genus Rhizobium synthesize lipo-chitooligosaccharides, called Nod factors (NFs), which act as morphogenic signal molecules on legume hosts. The common nodABC genes, present in all Rhizobium species, are required for the synthesis of the core structure of NFs. NodC is an N -acetylglucosaminyltransferase, and NodB is a chitooligosaccharide deacetylase; NodA is involved in N-acylation of the aminosugar backbone. Specific nod genes are involved in diverse NF substitutions that confer plant specificity. We transferred to R. tropici , a broad host-range tropical symbiont, the ability to nodulate alfalfa, by introducing nod genes of R. meliloti . In addition to the specific nodL and nodFE genes, the common nodABC genes of R. meliloti were required for infection and nodulation of alfalfa. Purified NFs of the R. tropici hybrid strain, which contained chitin tetramers and were partly N-acylated with unsaturated C16 fatty acids, were able to elicit nodule formation on alfalfa. Inactivation of the R. meliloti nodABC genes suppressed the ability of the NFs to nodulate alfalfa. Studies of NFs from nodA , nodB , nodC , and nodI mutants indicate that ( i ) NodA of R. meliloti , in contrast to NodA of R. tropici , is able to transfer unsaturated C16 fatty acids onto the chitin backbone and ( ii ) NodC of R. meliloti specifies the synthesis of chitin tetramers. These results show that allelic variation of the common nodABC genes is a genetic mechanism that plays an important role in signaling variation and in the control of host range.