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In vitro selection and characterization of human immunodeficiency virus type 1 (HIV-1) isolates with reduced sensitivity to hydroxyethylamino sulfonamide inhibitors of HIV-1 aspartyl protease

Journal of Virology, 1995-09, Vol.69 (9), p.5228-5235

1995

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Pim-1 Ligand-bound Structures Reveal the Mechanism of Serine/Threonine Kinase Inhibition by LY294002

The Journal of biological chemistry, 2005-04, Vol.280 (14), p.13728-13734

2005

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FK506 binding protein mutational analysis. Defining the surface residue contributions to stability of the calcineurin co-complex

The Journal of biological chemistry, 1995-08, Vol.270 (32), p.18935-18940

1995

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Charged surface residues of FKBP12 participate in formation of the FKBP12-FK506-calcineurin complex

The Journal of biological chemistry, 1992-08, Vol.267 (23), p.16029-16032

1992

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PPIase catalysis by human FK506-binding protein proceeds through a conformational twist mechanism

The Journal of biological chemistry, 1992-02, Vol.267 (5), p.3316-3324

1992

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Structure and Mechanism of Inosine Monophosphate Dehydrogenase in Complex with the Immunosuppressant Mycophenolic Acid

Cell, 1996-06, Vol.85 (6), p.921-930

1996

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Design, synthesis and structure of non-macrocyclic inhibitors of FKBP12, the major binding protein for the immunosuppressant FK506

Acta crystallographica. Section D, Biological crystallography., 1995-07, Vol.51 (4), p.522-528

1995

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Biochemical Analysis of the Modular Enzyme Inosine 5′-Monophosphate Dehydrogenase

Protein expression and purification, 1999-11, Vol.17 (2), p.282-289

1999

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FK506-binding protein mutational analysis: defining the active-site residue contributions to catalysis and the stability of ligand complexes

Protein engineering, 1996-02, Vol.9 (2), p.173-180

1996

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A mutational analysis of the active site of human type II inosine 5′-monophosphate dehydrogenase

Biochimica et biophysica acta, 2002-01, Vol.1594 (1), p.27-39

2002

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Comparison of three classes of human liver alcohol dehydrogenase : emphasis on different substrate binding pockets

European journal of biochemistry, 1990-10, Vol.193 (2), p.303-310

1990

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Practical applications of time-averaged restrained molecular dynamics to ligand-receptor systems: FK506 bound to the Q50R,A95H,K98I triple mutant of FKBP-13

Journal of biomolecular NMR, 1996-07, Vol.8 (1), p.67-76

1996

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Charged surface residues of FKBP12 participate in formation of the FKLBP12-FK506-calcineurin complex

The Journal of biological chemistry, 1992-01, Vol.267 (23), p.16029-16032

1992

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The dog heartworm

Schweizerische medizinische Wochenschrift, 1997-11, Vol.127 (48), p.2014

1997

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In vitro selection and characterization of human immunodeficiency virus type 1 (HIV-1) isolates with reduced sensitivity to hydroxyethylamino sulfonamide inhibitors of HIV-1 aspartyl protease

Pim-1 Ligand-bound Structures Reveal the Mechanism of Serine/Threonine Kinase Inhibition by LY294002

FK506 binding protein mutational analysis. Defining the surface residue contributions to stability of the calcineurin co-complex

Charged surface residues of FKBP12 participate in formation of the FKBP12-FK506-calcineurin complex

PPIase catalysis by human FK506-binding protein proceeds through a conformational twist mechanism

Structure and Mechanism of Inosine Monophosphate Dehydrogenase in Complex with the Immunosuppressant Mycophenolic Acid

Design, synthesis and structure of non-macrocyclic inhibitors of FKBP12, the major binding protein for the immunosuppressant FK506

Biochemical Analysis of the Modular Enzyme Inosine 5′-Monophosphate Dehydrogenase

FK506-binding protein mutational analysis: defining the active-site residue contributions to catalysis and the stability of ligand complexes

A mutational analysis of the active site of human type II inosine 5′-monophosphate dehydrogenase

Comparison of three classes of human liver alcohol dehydrogenase : emphasis on different substrate binding pockets

Practical applications of time-averaged restrained molecular dynamics to ligand-receptor systems: FK506 bound to the Q50R,A95H,K98I triple mutant of FKBP-13

Charged surface residues of FKBP12 participate in formation of the FKLBP12-FK506-calcineurin complex

The dog heartworm

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