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Results: 1-9 |
Results: 9
AN NMR-BASED IDENTIFICATION OF PEPTIDE-FRAGMENTS MIMICKING THE INTERACTIONS OF THE CATHEPSIN-B PROPEPTIDE
Authors: YU YL VRANKEN W GOUDREAU N DEMIGUEL E MAGNY MC MORT JS DUPRAS R STORER AC NI F
Citation: Yl. Yu et al., AN NMR-BASED IDENTIFICATION OF PEPTIDE-FRAGMENTS MIMICKING THE INTERACTIONS OF THE CATHEPSIN-B PROPEPTIDE, FEBS letters, 429(1), 1998, pp. 9-16
STRUCTURE-BASED DESIGN OF NEW CONSTRAINED CYCLIC AGONISTS OF THE CHOLECYSTOKININ CCK-B RECEPTOR
Authors: BLOMMAERT AGS DHOTEL H DUCOS B DURIEUX C GOUDREAU N BADO A GARBAY C ROGUES BP
Citation: Ags. Blommaert et al., STRUCTURE-BASED DESIGN OF NEW CONSTRAINED CYCLIC AGONISTS OF THE CHOLECYSTOKININ CCK-B RECEPTOR, Journal of medicinal chemistry, 40(5), 1997, pp. 647-658
COMPARATIVE CONFORMATIONAL-ANALYSIS OF CCK-B AGONIST BOC-TRP-PHG-ASP-(1-NAL)-NH2 AND CCK-B ANTAGONIST BOC-TRP-PHG-ASP-(1-NAL)-N(ME)(2) USING H-1-NMR SPECTROSCOPY AND RESTRAINED MOLECULAR-DYNAMICS
Authors: GOUDREAU N WENG JH ROQUES BP
Citation: N. Goudreau et al., COMPARATIVE CONFORMATIONAL-ANALYSIS OF CCK-B AGONIST BOC-TRP-PHG-ASP-(1-NAL)-NH2 AND CCK-B ANTAGONIST BOC-TRP-PHG-ASP-(1-NAL)-N(ME)(2) USING H-1-NMR SPECTROSCOPY AND RESTRAINED MOLECULAR-DYNAMICS, Archiv der pharmazie, 329(4), 1996, pp. 197-204
HIS(381) OF THE RAT CCKB RECEPTOR IS ESSENTIAL FOR CCKB VERSUS CCKA RECEPTOR ANTAGONIST SELECTIVITY
Authors: JAGERSCHMIDT A GUILLAUMEROUSSELET N VIKLAND ML GOUDREAU N MAIGRET B ROQUES BP
Citation: A. Jagerschmidt et al., HIS(381) OF THE RAT CCKB RECEPTOR IS ESSENTIAL FOR CCKB VERSUS CCKA RECEPTOR ANTAGONIST SELECTIVITY, European journal of pharmacology, 296(1), 1996, pp. 97-106
MUTATION OF ASP(100) IN THE 2ND TRANSMEMBRANE DOMAIN OF THE CHOLECYSTOKININ-B RECEPTOR INCREASES ANTAGONIST BINDING AND REDUCES SIGNAL-TRANSDUCTION
Authors: JAGERSCHMIDT A GUILLAUME N GOUDREAU N MAIGRET B ROQUES BP
Citation: A. Jagerschmidt et al., MUTATION OF ASP(100) IN THE 2ND TRANSMEMBRANE DOMAIN OF THE CHOLECYSTOKININ-B RECEPTOR INCREASES ANTAGONIST BINDING AND REDUCES SIGNAL-TRANSDUCTION, Molecular pharmacology, 48(5), 1995, pp. 783-789
NMR STRUCTURE OF THE N-TERMINAL SH3 DOMAIN OF GRB2 AND ITS COMPLEX WITH A PROLINE-RICH PEPTIDE FROM SOS
Authors: GOUDREAU N CORNILLE F DUCHESNE M PARKER F TOCQUE B GARBAY C ROGUES BP
Citation: N. Goudreau et al., NMR STRUCTURE OF THE N-TERMINAL SH3 DOMAIN OF GRB2 AND ITS COMPLEX WITH A PROLINE-RICH PEPTIDE FROM SOS, Nature structural biology, 1(12), 1994, pp. 898-907
SOLID-PHASE SYNTHESIS, CONFORMATIONAL-ANALYSIS AND IN-VITRO CLEAVAGE OF SYNTHETIC HUMAN SYNAPTOBREVIN-II-1-93 BY TETANUS TOXIN-L CHAIN
Authors: CORNILLE F GOUDREAU N FICHEUX D NIEMANN H ROQUES BP
Citation: F. Cornille et al., SOLID-PHASE SYNTHESIS, CONFORMATIONAL-ANALYSIS AND IN-VITRO CLEAVAGE OF SYNTHETIC HUMAN SYNAPTOBREVIN-II-1-93 BY TETANUS TOXIN-L CHAIN, European journal of biochemistry, 222(1), 1994, pp. 173-181
CONFORMATIONAL-ANALYSIS OF CCK-B AGONISTS USING H-1-NMR AND RESTRAINED MOLECULAR-DYNAMICS - COMPARISON OF BIOLOGICALLY-ACTIVE BOC-TRP-(N-ME)NLE-ASP-PHE-NH2 AND INACTIVE BOC-TRP-(N-ME)PHE-ASP-PHE-NH2
Authors: GOUDREAU N WENG JH ROQUES BP
Citation: N. Goudreau et al., CONFORMATIONAL-ANALYSIS OF CCK-B AGONISTS USING H-1-NMR AND RESTRAINED MOLECULAR-DYNAMICS - COMPARISON OF BIOLOGICALLY-ACTIVE BOC-TRP-(N-ME)NLE-ASP-PHE-NH2 AND INACTIVE BOC-TRP-(N-ME)PHE-ASP-PHE-NH2, Biopolymers, 34(2), 1994, pp. 155-169
DNS-GLY-(P-NO2)PHE-BETA-ALA, A SPECIFIC FLUOROGENIC SUBSTRATE FOR NEUTRAL ENDOPEPTIDASE-24.11
Authors: GOUDREAU N GUIS C SOLEILHAC JM ROQUES BP
Citation: N. Goudreau et al., DNS-GLY-(P-NO2)PHE-BETA-ALA, A SPECIFIC FLUOROGENIC SUBSTRATE FOR NEUTRAL ENDOPEPTIDASE-24.11, Analytical biochemistry, 219(1), 1994, pp. 87-95
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