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Human Immunodeficiency Virus Type 1 Protease Inhibitors: Evaluation of Resistance Engendered by Amino Acid Substitutions in the Enzyme's Substrate Binding Site

Biochemistry (Easton), 1994-03, Vol.33 (8), p.2004-2010

1994

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5-Chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of HIV-1 reverse transcriptase

Journal of medicinal chemistry, 1993-04, Vol.36 (9), p.1291-1294

1993

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Substrate requirements of human rhinovirus 3C protease for peptide cleavage in vitro

The Journal of biological chemistry, 1990-06, Vol.265 (16), p.9062-9065

1990

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Sequence-Specific Interaction of Tat Protein and Tat Peptides with the Transactivation-Responsive Sequence Element of Human Immunodeficiency Virus Type 1 in vitro

Proceedings of the National Academy of Sciences - PNAS, 1990-11, Vol.87 (22), p.8985-8989

1990

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Functional analysis of HIV-1 reverse transcriptase amino acids involved in resistance to multiple nonnucleoside inhibitors

The Journal of biological chemistry, 1992-09, Vol.267 (25), p.17526-17530

1992

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Peptide substrate cleavage specificity of the human cytomegalovirus protease

The Journal of biological chemistry, 1994-05, Vol.269 (20), p.14337-14340

1994

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Human Immunodeficiency Virus 1 (HIV-1)-Specific Reverse Transcriptase (RT) Inhibitors may Suppress the Replication of Specific Drug-Resistant (E138K)RT HIV-1 Mutants or Select for Highly Resistant (Y181C → C181I)RT HIV-1 Mutants

Proceedings of the National Academy of Sciences - PNAS, 1994-07, Vol.91 (14), p.6599-6603

1994

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An Uniquely Purified HCV NS3 Protease and NS4A21–34 Peptide Form a Highly Active Serine Protease Complex in Peptide Hydrolysis

Protein expression and purification, 1999-08, Vol.16 (3), p.440-447

1999

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Human immunodeficiency virus 1 (HIV-1)-specific reverse transcriptase (RT) inhibitors may suppress the replication of specific drug-resistant (E138K)RT HIV-1 mutants or select for highly resistant (Y181C()C181I)RT HIV-1 mutants

Proceedings of the National Academy of Sciences - PNAS, 1994-07, Vol.91 (14), p.6599

1994

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Bacterial expression of antibody fragments that block human rhinovirus infection of cultured cells

The Journal of biological chemistry, 1990-02, Vol.265 (4), p.2292-2295

1990

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Purification, solution properties and crystallization of SIV integrase containing a continuous core and C-terminal domain

Acta crystallographica. Section D, Biological crystallography., 1999-11, Vol.55 (11), p.1906-1910

1999

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[21] Qualitative study of drug resistance in retroviral protease using structural modeling and site-directed mutagenesis

Methods in Enzymology, 1994, Vol.241, p.385,IN17,393-392,IN19,394

1994

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Attempted prophylaxis of human immunodeficiency virus type 1 infection in chimpanzees with a nonnucleoside reverse transcriptase inhibitor

AIDS research and human retroviruses, 1994, Vol.10 (1), p.107-110

1994

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Genomic characterization and epidemiology of an emerging SARS-CoV-2 variant in Delhi, India

Science (American Association for the Advancement of Science), 2021-11, Vol.374 (6570), p.995-999

2021

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Complex of NS3 protease and NS4A peptide of BK strain hepatitis C virus: A 2.2 Å resolution structure in a hexagonal crystal form

Protein science, 1998-04, Vol.7 (4), p.837-847

1998

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Handbook of Metamaterial-Derived Frequency Selective Surfaces

Volltextzugriff (PDF)

Identification of a Small Molecule Nonpeptide Active Site β-Secretase Inhibitor That Displays a Nontraditional Binding Mode for Aspartyl Proteases

Journal of medicinal chemistry, 2004-12, Vol.47 (25), p.6117-6119

2004

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X-ray structure of simian immunodeficiency virus integrase containing the core and C-terminal domain (residues 50-293)--an initial glance of the viral DNA binding platform

Journal of molecular biology, 2000-02, Vol.296 (2), p.521-533

2000

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Only a Small Fraction of Purified Hepatitis C RNA-Dependent RNA Polymerase Is Catalytically Competent: Implications for Viral Replication and in Vitro Assays

Biochemistry (Easton), 2000-07, Vol.39 (28), p.8243-8249

2000

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[1] Purification of viral polymerases: General considerations

Methods in Enzymology, 1996, Vol.275, p.3-16

1996

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Determination of disulfide bond pairs and stability in recombinant tick anticoagulant peptide

The Journal of biological chemistry, 1991-07, Vol.266 (21), p.13560-13563

1991

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NMR Behavior of the Aromatic Protons of Bovine Neurophysin-I and Its Peptide Complexes: Implications for Solution Structure and for Function

Biochemistry (Easton), 1995-02, Vol.34 (7), p.2137-2147

1995

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Isolation and characterization of a resistant core peptide of recombinant human granulocyte‐macrophage colony‐stimulating factor (gm‐csf); confirmation of the gm‐csf amino acid sequence by mass spectrometry

Protein science, 1993-11, Vol.2 (11), p.1948-1958

1993

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Application of peptide-mediated ring current shifts to the study of neurophysin-peptide interactions: a partial model of the neurophysin-peptide complex

Biochemistry (Easton), 1987-03, Vol.26 (6), p.1518-1525

1987

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Dimerization of native and proteolytically modified neurophysins as monitored by proton magnetic resonance spectroscopy: proximity of tyrosine-49 to the subunit interface

Biochemistry (Easton), 1986-10, Vol.25 (21), p.6579-6586

1986

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Human Immunodeficiency Virus Type 1 Protease Inhibitors: Evaluation of Resistance Engendered by Amino Acid Substitutions in the Enzyme's Substrate Binding Site

5-Chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of HIV-1 reverse transcriptase

Substrate requirements of human rhinovirus 3C protease for peptide cleavage in vitro

Sequence-Specific Interaction of Tat Protein and Tat Peptides with the Transactivation-Responsive Sequence Element of Human Immunodeficiency Virus Type 1 in vitro

Functional analysis of HIV-1 reverse transcriptase amino acids involved in resistance to multiple nonnucleoside inhibitors

Peptide substrate cleavage specificity of the human cytomegalovirus protease

Human Immunodeficiency Virus 1 (HIV-1)-Specific Reverse Transcriptase (RT) Inhibitors may Suppress the Replication of Specific Drug-Resistant (E138K)RT HIV-1 Mutants or Select for Highly Resistant (Y181C → C181I)RT HIV-1 Mutants

An Uniquely Purified HCV NS3 Protease and NS4A21–34 Peptide Form a Highly Active Serine Protease Complex in Peptide Hydrolysis

Human immunodeficiency virus 1 (HIV-1)-specific reverse transcriptase (RT) inhibitors may suppress the replication of specific drug-resistant (E138K)RT HIV-1 mutants or select for highly resistant (Y181C()C181I)RT HIV-1 mutants

Bacterial expression of antibody fragments that block human rhinovirus infection of cultured cells

Purification, solution properties and crystallization of SIV integrase containing a continuous core and C-terminal domain

[21] Qualitative study of drug resistance in retroviral protease using structural modeling and site-directed mutagenesis

Attempted prophylaxis of human immunodeficiency virus type 1 infection in chimpanzees with a nonnucleoside reverse transcriptase inhibitor

Genomic characterization and epidemiology of an emerging SARS-CoV-2 variant in Delhi, India

Complex of NS3 protease and NS4A peptide of BK strain hepatitis C virus: A 2.2 Å resolution structure in a hexagonal crystal form

Handbook of Metamaterial-Derived Frequency Selective Surfaces

Identification of a Small Molecule Nonpeptide Active Site β-Secretase Inhibitor That Displays a Nontraditional Binding Mode for Aspartyl Proteases

X-ray structure of simian immunodeficiency virus integrase containing the core and C-terminal domain (residues 50-293)--an initial glance of the viral DNA binding platform

Only a Small Fraction of Purified Hepatitis C RNA-Dependent RNA Polymerase Is Catalytically Competent: Implications for Viral Replication and in Vitro Assays

[1] Purification of viral polymerases: General considerations

Determination of disulfide bond pairs and stability in recombinant tick anticoagulant peptide

NMR Behavior of the Aromatic Protons of Bovine Neurophysin-I and Its Peptide Complexes: Implications for Solution Structure and for Function

Isolation and characterization of a resistant core peptide of recombinant human granulocyte‐macrophage colony‐stimulating factor (gm‐csf); confirmation of the gm‐csf amino acid sequence by mass spectrometry

Application of peptide-mediated ring current shifts to the study of neurophysin-peptide interactions: a partial model of the neurophysin-peptide complex

Dimerization of native and proteolytically modified neurophysins as monitored by proton magnetic resonance spectroscopy: proximity of tyrosine-49 to the subunit interface

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