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Crystal Structure of the Herpes Simplex Virus 1 DNA Polymerase

The Journal of biological chemistry, 2006-06, Vol.281 (26), p.18193-18200

2006

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Crystal Structure of Type II Peptide Deformylase from Staphylococcus aureus

The Journal of biological chemistry, 2002-08, Vol.277 (34), p.31163-31171

2002

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Immobilization of a Novel Antibacterial Agent on Solid Phase and Subsequent Isolation of EF-Tu

Bioconjugate chemistry, 2004-03, Vol.15 (2), p.333-343

2004

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The Cyclosporin A-binding Immunophilin CyP-40 and the FK506-binding Immunophilin hsp56 Bind to a Common Site on hsp90 and Exist in Independent Cytosolic Heterocomplexes with the Untransformed Glucocorticoid Receptor (∗)

The Journal of biological chemistry, 1995-09, Vol.270 (35), p.20479-20484

1995

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Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E

Biochemistry (Easton), 1993-07, Vol.32 (26), p.6548-6554

1993

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Co-crystallization of Staphylococcus aureus peptide deformylase (PDF) with potent inhibitors

Acta crystallographica. Section D, Biological crystallography., 2002-12, Vol.58 (12), p.2153-2156

2002

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Crystal structure of the catalytic subunit of Cdc25B required for G2/M phase transition of the cell cycle

Journal of molecular biology, 1999-10, Vol.293 (3), p.559-568

1999

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Crystal structure of the catalytic subunit of Cdc25B required for G 2 /M phase transition of the cell cycle 1 1Edited by I. A. Wilson

Journal of molecular biology, 1999-10, Vol.293 (3), p.559-568

1999

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An active FK506-binding domain of 17,000 daltons is isolated following limited proteolysis of chicken thymus HSP56

Biochemistry (Easton), 1993-11, Vol.32 (47), p.12571-12576

1993

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Secondary structure and topology of interleukin-1 receptor antagonist protein determined by heteronuclear three-dimensional NMR spectroscopy

Biochemistry (Easton), 1992-06, Vol.31 (23), p.5237-5245

1992

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Identification of a C-terminal cdc25 sequence required for promotion of germinal vesicle breakdown

Biochemical journal, 2000-05, Vol.347 Pt 3 (3), p.653-660

2000

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The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase

The Journal of biological chemistry, 1993-07, Vol.268 (20), p.14875-14880

1993

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Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E

The Journal of biological chemistry, 1993-03, Vol.268 (9), p.6119-6124

1993

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Characterization of the protein-protein interactions determining the heat shock protein (hsp90.hsp70.hsp56) heterocomplex

The Journal of biological chemistry, 1994-04, Vol.269 (15), p.11155-11161

1994

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Tryptophan fluorescence of terminal deoxynucleotidyl transferase: effects of quenchers on time-resolved emission spectra

Biochemistry (Easton), 1985-12, Vol.24 (25), p.7250-7257

1985

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The hsp56 immunophilin component of untransformed steroid receptor complexes is localized both to microtubules in the cytoplasm and to the same nonrandom regions within the nucleus as the steroid receptor

Molecular endocrinology (Baltimore, Md.), 1994-12, Vol.8 (12), p.1731-1741

1994

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The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase

Biochemical pharmacology, 1996-03, Vol.51 (6), p.743-750

1996

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FKBP54, a novel FK506-binding protein in avian progesterone receptor complexes and HeLa extracts

The Journal of biological chemistry, 1993-11, Vol.268 (32), p.24270-24273

1993

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Tissue distribution and cellular localization of hsp56, an FK506-binding protein. Characterization using a highly specific polyclonal antibody

The Journal of biological chemistry, 1992-10, Vol.267 (30), p.21285-21288

1992

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Actin, troponin C, Alzheimer amyloid precursor protein and pro-interleukin 1 beta as substrates of the protease from human immunodeficiency virus

The Journal of biological chemistry, 1991-08, Vol.266 (22), p.14548-14553

1991

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The binding of a novel bisheteroarylpiperazine mediates inhibition of human immunodeficiency virus type 1 reverse transcriptase

The Journal of biological chemistry, 1992-01, Vol.267 (1), p.27-30

1992

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Kinetic studies with the non-nucleoside human immunodeficiency virus type-1 reverse transcriptase inhibitor U-90152E

Biochemical pharmacology, 1994-06, Vol.47 (11), p.2017-2028

1994

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A recombinant ribonuclease H domain of HIV-1 reverse transcriptase that is enzymatically active

The Journal of biological chemistry, 1991-11, Vol.266 (31), p.20583-20585

1991

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Purification and characterization of heterodimeric human immunodeficiency virus type 1 (HIV-1) reverse transcriptase produced by in vitro processing of p66 with recombinant HIV-1 protease

The Journal of biological chemistry, 1992-07, Vol.267 (20), p.14227-14232

1992

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The native v-Raf/hsp90/p50 heterocomplex contains a novel immunophilin of the FK506 binding class

The Journal of biological chemistry, 1994-09, Vol.269 (35), p.22157-22161

1994

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Crystal Structure of the Herpes Simplex Virus 1 DNA Polymerase

Crystal Structure of Type II Peptide Deformylase from Staphylococcus aureus

Immobilization of a Novel Antibacterial Agent on Solid Phase and Subsequent Isolation of EF-Tu

The Cyclosporin A-binding Immunophilin CyP-40 and the FK506-binding Immunophilin hsp56 Bind to a Common Site on hsp90 and Exist in Independent Cytosolic Heterocomplexes with the Untransformed Glucocorticoid Receptor (∗)

Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E

Co-crystallization of Staphylococcus aureus peptide deformylase (PDF) with potent inhibitors

Crystal structure of the catalytic subunit of Cdc25B required for G2/M phase transition of the cell cycle

Crystal structure of the catalytic subunit of Cdc25B required for G 2 /M phase transition of the cell cycle 1 1Edited by I. A. Wilson

An active FK506-binding domain of 17,000 daltons is isolated following limited proteolysis of chicken thymus HSP56

Secondary structure and topology of interleukin-1 receptor antagonist protein determined by heteronuclear three-dimensional NMR spectroscopy

Identification of a C-terminal cdc25 sequence required for promotion of germinal vesicle breakdown

The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase

Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E

Characterization of the protein-protein interactions determining the heat shock protein (hsp90.hsp70.hsp56) heterocomplex

Tryptophan fluorescence of terminal deoxynucleotidyl transferase: effects of quenchers on time-resolved emission spectra

The hsp56 immunophilin component of untransformed steroid receptor complexes is localized both to microtubules in the cytoplasm and to the same nonrandom regions within the nucleus as the steroid receptor

The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase

FKBP54, a novel FK506-binding protein in avian progesterone receptor complexes and HeLa extracts

Tissue distribution and cellular localization of hsp56, an FK506-binding protein. Characterization using a highly specific polyclonal antibody

Actin, troponin C, Alzheimer amyloid precursor protein and pro-interleukin 1 beta as substrates of the protease from human immunodeficiency virus

The binding of a novel bisheteroarylpiperazine mediates inhibition of human immunodeficiency virus type 1 reverse transcriptase

Kinetic studies with the non-nucleoside human immunodeficiency virus type-1 reverse transcriptase inhibitor U-90152E

A recombinant ribonuclease H domain of HIV-1 reverse transcriptase that is enzymatically active

Purification and characterization of heterodimeric human immunodeficiency virus type 1 (HIV-1) reverse transcriptase produced by in vitro processing of p66 with recombinant HIV-1 protease

The native v-Raf/hsp90/p50 heterocomplex contains a novel immunophilin of the FK506 binding class

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