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HIV-1 Vaccine Development: Constrained Peptide Immunogens Show Improved Binding to the Anti-HIV-1 gp41 MAb

Biochemistry (Easton), 2003-03, Vol.42 (11), p.3214-3223

2003

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Characterization of a solid state reaction product from a lyophilized formulation of a cyclic heptapeptide. A novel example of an excipient-induced oxidation

Pharmaceutical research, 1996-12, Vol.13 (12), p.1811-1814

1996

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Conformational Restriction of Flexible Ligands Guided by the Transferred NOE Experiment: Potent Macrocyclic Inhibitors of Farnesyltransferase

Journal of the American Chemical Society, 2001-03, Vol.123 (9), p.2107-2108

2001

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Cyclopsychotride A, a Biologically Active, 31-Residue Cyclic Peptide Isolated from Psychotria longipes

Journal of natural products (Washington, D.C.), 1994-12, Vol.57 (12), p.1619-1625

1994

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NMR studies of novel inhibitors bound to farnesyl‐protein transferase

Protein science, 1995-04, Vol.4 (4), p.681-688

1995

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3,8-Diazabicyclo[3.2.1]octan-2-one Peptide Mimetics: Synthesis of a Conformationally Restricted Inhibitor of Farnesyltransferase

Organic letters, 2001-03, Vol.3 (6), p.865-868

2001

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Structure and dynamics of the Pf1 filamentous bacteriophage coat protein in micelles

Biochemistry (Easton), 1987-03, Vol.26 (5), p.1373-1381

1987

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NMR and molecular modeling characterization of RGD containing peptides

International Journal of Peptide and Protein Research, 1992-01, Vol.39 (1), p.63-76

1992

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Dynamics of the multidomain fibrinolytic protein urokinase from two-dimensional NMR

Nature (London), 1989-02, Vol.337 (6207), p.579-582

1989

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Two Tarantula Peptides Inhibit Activation of Multiple Sodium Channels

Biochemistry (Easton), 2002-12, Vol.41 (50), p.14734-14747

2002

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Comparison of the dynamics of the membrane-bound form of fd coat protein in micelles and in bilayers by solution and solid-state nitrogen-15 nuclear magnetic resonance spectroscopy

Proteins, structure, function, and bioinformatics, 1988, Vol.4 (2), p.123-130

1988

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Secondary structure of filamentous bacteriophage coat protein is preserved in lipid environments

Journal of molecular biology, 1988-04, Vol.200 (4), p.741-743

1988

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The solution conformation Ac-Pen-Arg-Gly-Asp-Cys-OH, a potent fibrinogen receptor antagonist

Biopolymers, 1993-08, Vol.33 (8), p.1287-1297

1993

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Structure of synthetic peptide analogues of an eggshell protein of Schistosoma mansoni

Protein science, 1993-06, Vol.2 (6), p.900-914

1993

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Enhancement of alpha -helicity in the HIV-1 inhibitory peptide DP178 leads to an increased affinity for human monoclonal antibody 2F5 but does not elicit neutralizing responses in vitro. Implications for vaccine design

The Journal of biological chemistry, 2002-11, Vol.277 (48), p.45811-45820

2002

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Amide and α-keto carbonyl inhibitors of thrombin based on arginine and lysine: Synthesis, stability and biological characterization

Bioorganic & medicinal chemistry, 1995-08, Vol.3 (8), p.1063-1078

1995

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Synthesis and solution conformation of c(D-Trp-D-Cys(SO3-Na+)-Pro-D-Val-Leu), a potent endothelin-A receptor antagonist

International Journal of Peptide and Protein Research, 1993-08, Vol.42 (2), p.194-203

1993

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Synthesis and biological evaluation of unnatural canthine alkaloids

Tetrahedron letters, 2005-04, Vol.46 (16), p.2779-2782

2005

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Conformation of a novel tetrapeptide inhibitor NH2-d-Trp-d-Met-Phe(pCl)-Gla-NH2 bound to farnesyl-protein transferase

The journal of peptide research, 1999-07, Vol.54 (1), p.66-73

1999

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Progress towards the development of a HIV-1 gp41-directed vaccine

Current HIV research, 2004-04, Vol.2 (2), p.193-204

2004

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One- and two- dimensional 15N/ 1H NMR of filamentous phage coat proteins in solution

Biochemical and biophysical research communications, 1985-03, Vol.127 (2), p.540-545

1985

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Enhancement of α-helicity in the HIV-1 inhibitory peptide DP178 leads to an increased affinity for human monoclonal antibody 2F5 but does not elicit neutralizing responses in vitro. Implications for vaccine design

The Journal of biological chemistry, 2003-02, Vol.278 (7), p.5492

2003

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Enhancement of [alpha]-Helicity in the HIV-1 Inhibitory Peptide DP178 Leads to an Increased Affinity for Human Monoclonal Antibody 2F5 but Does Not Elicit Neutralizing Responses in Vitro. Implications for Vaccine Design

The Journal of biological chemistry, 2002-11, Vol.277 (48), p.45811-45820

2002

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HIV-1 Vaccine Development: Constrained Peptide Immunogens Show Improved Binding to the Anti-HIV-1 gp41 MAb

Characterization of a solid state reaction product from a lyophilized formulation of a cyclic heptapeptide. A novel example of an excipient-induced oxidation

Conformational Restriction of Flexible Ligands Guided by the Transferred NOE Experiment: Potent Macrocyclic Inhibitors of Farnesyltransferase

Cyclopsychotride A, a Biologically Active, 31-Residue Cyclic Peptide Isolated from Psychotria longipes

NMR studies of novel inhibitors bound to farnesyl‐protein transferase

N-Arylpiperazinone Inhibitors of Farnesyltransferase: Discovery and Biological Activity

3,8-Diazabicyclo[3.2.1]octan-2-one Peptide Mimetics: Synthesis of a Conformationally Restricted Inhibitor of Farnesyltransferase

Structure and dynamics of the Pf1 filamentous bacteriophage coat protein in micelles

NMR and molecular modeling characterization of RGD containing peptides

Dynamics of the multidomain fibrinolytic protein urokinase from two-dimensional NMR

Two Tarantula Peptides Inhibit Activation of Multiple Sodium Channels

Comparison of the dynamics of the membrane-bound form of fd coat protein in micelles and in bilayers by solution and solid-state nitrogen-15 nuclear magnetic resonance spectroscopy

Secondary structure of filamentous bacteriophage coat protein is preserved in lipid environments

The solution conformation Ac-Pen-Arg-Gly-Asp-Cys-OH, a potent fibrinogen receptor antagonist

Structure of synthetic peptide analogues of an eggshell protein of Schistosoma mansoni

Enhancement of alpha -helicity in the HIV-1 inhibitory peptide DP178 leads to an increased affinity for human monoclonal antibody 2F5 but does not elicit neutralizing responses in vitro. Implications for vaccine design

Amide and α-keto carbonyl inhibitors of thrombin based on arginine and lysine: Synthesis, stability and biological characterization

Synthesis and solution conformation of c(D-Trp-D-Cys(SO3-Na+)-Pro-D-Val-Leu), a potent endothelin-A receptor antagonist

3-Aminopyrrolidinone Farnesyltransferase Inhibitors: Design of Macrocyclic Compounds with Improved Pharmacokinetics and Excellent Cell Potency

Synthesis and biological evaluation of unnatural canthine alkaloids

Conformation of a novel tetrapeptide inhibitor NH2-d-Trp-d-Met-Phe(pCl)-Gla-NH2 bound to farnesyl-protein transferase

Progress towards the development of a HIV-1 gp41-directed vaccine

One- and two- dimensional 15N/ 1H NMR of filamentous phage coat proteins in solution

Enhancement of α-helicity in the HIV-1 inhibitory peptide DP178 leads to an increased affinity for human monoclonal antibody 2F5 but does not elicit neutralizing responses in vitro. Implications for vaccine design

Enhancement of [alpha]-Helicity in the HIV-1 Inhibitory Peptide DP178 Leads to an Increased Affinity for Human Monoclonal Antibody 2F5 but Does Not Elicit Neutralizing Responses in Vitro. Implications for Vaccine Design

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