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Sequence dependence of protein isoprenylation

The Journal of biological chemistry, 1991-08, Vol.266 (22), p.14603-14610

1991

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Selective Inhibition of ras-Dependent Transformation by a Farnesyltransferase Inhibitor

Science (American Association for the Advancement of Science), 1993-06, Vol.260 (5116), p.1934-1937

1993

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Selective inhibition of farnesyl-protein transferase blocks ras processing in vivo

The Journal of biological chemistry, 1993-04, Vol.268 (11), p.7617-7620

1993

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Steady-state kinetic mechanism of ras farnesyl:protein transferase

Biochemistry (Easton), 1992-04, Vol.31 (15), p.3800-3807

1992

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Stabilization of a reaction intermediate as a catalytic device: definition of the functional role of the flexible loop in triosephosphate isomerase

Biochemistry (Easton), 1990-04, Vol.29 (13), p.3186-3194

1990

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Synthesis and SAR of thioester and thiol inhibitors of IMP-1 Metallo-β-Lactamase

Bioorganic & medicinal chemistry letters, 1999-09, Vol.9 (17), p.2549-2554

1999

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Engineering a Cell-Free Murein Biosynthetic Pathway: Combinatorial Enzymology in Drug Discovery

Journal of the American Chemical Society, 1998-12, Vol.120 (51), p.13527-13528

1998

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An array of target-specific screening strains for antibacterial discovery

Nature biotechnology, 2002-05, Vol.20 (5), p.478-483

2002

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Structural homology among mammalian and Saccharomyces cerevisiae isoprenyl-protein transferases

The Journal of biological chemistry, 1991-10, Vol.266 (28), p.18884-18888

1991

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Isoprenoid diphosphate utilization by recombinant human farnesyl:protein transferase: Interactive binding between substrates and a preferred kinetic pathway

Biochemistry (Easton), 1993-08, Vol.32 (32), p.8341-8347

1993

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Drug–target residence time and its implications for lead optimization

Nature reviews. Drug discovery, 2006-08, Vol.5 (9), p.730-739

2006

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2-Substituted Piperazines as Constrained Amino Acids. Application to the Synthesis of Potent, Non Carboxylic Acid Inhibitors of Farnesyltransferase

Journal of medicinal chemistry, 1996-03, Vol.39 (7), p.1345-1348

1996

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Potent, non-thiol inhibitors of farnesyltransferase

Bioorganic & medicinal chemistry letters, 1998-12, Vol.8 (23), p.3311-3316

1998

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Biocatalytic synthesis of aromatics from D-glucose: the role of transketolase

Journal of the American Chemical Society, 1992-05, Vol.114 (10), p.3956-3962

1992

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Catalytic Properties of Mutant 23 S Ribosomes Resistant to Oxazolidinones

The Journal of biological chemistry, 2003-03, Vol.278 (11), p.9802-9807

2003

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Development of a Whole-Cell Assay for Peptidoglycan Biosynthesis Inhibitors

Antimicrobial Agents and Chemotherapy, 2002-04, Vol.46 (4), p.943-946

2002

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Conditionally Lethal Escherichia coli Murein Mutants Contain Point Defects That Map to Regions Conserved among Murein and Folyl Poly-γ-glutamate Ligases: Identification of a Ligase Superfamily

Biochemistry (Easton), 1997-05, Vol.36 (20), p.6223-6229

1997

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N-Arylalkyl Pseudopeptide Inhibitors of Farnesyltransferase

Journal of medicinal chemistry, 1998-07, Vol.41 (14), p.2651-2656

1998

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Inhibition of IMP-1 metallo-β-lactamase and sensitization of IMP-1-producing bacteria by thioester derivatives

FEMS microbiology letters, 1999-10, Vol.179 (2), p.289-296

1999

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Oxazolidinones Mechanism of Action: Inhibition of the First Peptide Bond Formation

The Journal of biological chemistry, 2001-10, Vol.276 (40), p.37199-37205

2001

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Pseudodipeptide Inhibitors of Protein Farnesyltransferase

Journal of medicinal chemistry, 1995-09, Vol.38 (20), p.3967-3971

1995

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Phosphonate biosynthesis: molecular cloning of the gene for phosphoenolpyruvate mutase from Tetrahymena pyriformis and overexpression of the gene product in Escherichia coli

Biochemistry (Easton), 1992-03, Vol.31 (9), p.2598-2608

1992

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Degradation and detoxification of organophosphonates. Cleavage of the carbon-phosphorus bond

Journal of the American Chemical Society, 1986, Vol.108 (2), p.332-334

1986

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Kinetic Mechanism of the Escherichia coli UDPMurNAc-Tripeptide d-Alanyl-d-alanine-Adding Enzyme: Use of a Glutathione S-Transferase Fusion

Biochemistry (Easton), 1996-12, Vol.35 (50), p.16264-16269

1996

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Homogenous Assays for Escherichia coli DnaB-Stimulated DnaG Primase and DnaB Helicase and Their Use in Screening for Chemical Inhibitors

Analytical biochemistry, 2002-05, Vol.304 (2), p.174-179

2002

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Sequence dependence of protein isoprenylation

Selective Inhibition of ras-Dependent Transformation by a Farnesyltransferase Inhibitor

Selective inhibition of farnesyl-protein transferase blocks ras processing in vivo

Steady-state kinetic mechanism of ras farnesyl:protein transferase

Stabilization of a reaction intermediate as a catalytic device: definition of the functional role of the flexible loop in triosephosphate isomerase

Synthesis and SAR of thioester and thiol inhibitors of IMP-1 Metallo-β-Lactamase

Engineering a Cell-Free Murein Biosynthetic Pathway: Combinatorial Enzymology in Drug Discovery

An array of target-specific screening strains for antibacterial discovery

Structural homology among mammalian and Saccharomyces cerevisiae isoprenyl-protein transferases

Isoprenoid diphosphate utilization by recombinant human farnesyl:protein transferase: Interactive binding between substrates and a preferred kinetic pathway

Drug–target residence time and its implications for lead optimization

2-Substituted Piperazines as Constrained Amino Acids. Application to the Synthesis of Potent, Non Carboxylic Acid Inhibitors of Farnesyltransferase

Potent, non-thiol inhibitors of farnesyltransferase

Biocatalytic synthesis of aromatics from D-glucose: the role of transketolase

Catalytic Properties of Mutant 23 S Ribosomes Resistant to Oxazolidinones

Development of a Whole-Cell Assay for Peptidoglycan Biosynthesis Inhibitors

Conditionally Lethal Escherichia coli Murein Mutants Contain Point Defects That Map to Regions Conserved among Murein and Folyl Poly-γ-glutamate Ligases: Identification of a Ligase Superfamily

N-Arylalkyl Pseudopeptide Inhibitors of Farnesyltransferase

Inhibition of IMP-1 metallo-β-lactamase and sensitization of IMP-1-producing bacteria by thioester derivatives

Oxazolidinones Mechanism of Action: Inhibition of the First Peptide Bond Formation

Pseudodipeptide Inhibitors of Protein Farnesyltransferase

Phosphonate biosynthesis: molecular cloning of the gene for phosphoenolpyruvate mutase from Tetrahymena pyriformis and overexpression of the gene product in Escherichia coli

Degradation and detoxification of organophosphonates. Cleavage of the carbon-phosphorus bond

Kinetic Mechanism of the Escherichia coli UDPMurNAc-Tripeptide d-Alanyl-d-alanine-Adding Enzyme: Use of a Glutathione S-Transferase Fusion

Homogenous Assays for Escherichia coli DnaB-Stimulated DnaG Primase and DnaB Helicase and Their Use in Screening for Chemical Inhibitors

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