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Critical differences in HIV‐1 and HIV‐2 protease specificity for clinical inhibitors

Protein science, 2012-03, Vol.21 (3), p.339-350

2012

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Structural and Kinetic Analysis of Caspase-3 Reveals Role for S5 Binding Site in Substrate Recognition

Journal of molecular biology, 2006-07, Vol.360 (3), p.654-666

2006

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A Novel Bis-Tetrahydrofuranylurethane-Containing Nonpeptidic Protease Inhibitor (PI), GRL-98065, Is Potent against Multiple-PI-Resistant Human Immunodeficiency Virus In Vitro

Antimicrobial Agents and Chemotherapy, 2007-06, Vol.51 (6), p.2143-2155

2007

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High Resolution Crystal Structures of HIV-1 Protease with a Potent Non-peptide Inhibitor (UIC-94017) Active Against Multi-drug-resistant Clinical Strains

Journal of molecular biology, 2004-04, Vol.338 (2), p.341-352

2004

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Effectiveness of Nonpeptide Clinical Inhibitor TMC-114 on HIV-1 Protease with Highly Drug Resistant Mutations D30N, I50V, and L90M

Journal of medicinal chemistry, 2006-02, Vol.49 (4), p.1379-1387

2006

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Crystal structures of HIV protease V82A and L90M mutants reveal changes in the indinavir‐binding site

European journal of biochemistry, 2004-04, Vol.271 (8), p.1516-1524

2004

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Kinetic, Stability, and Structural Changes in High-resolution Crystal Structures of HIV-1 Protease with Drug-resistant Mutations L24I, I50V, and G73S

Journal of molecular biology, 2005-12, Vol.354 (4), p.789-800

2005

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Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 Å resolution crystal structures of HIV‐1 protease mutants with substrate analogs

The FEBS journal, 2005-10, Vol.272 (20), p.5265-5277

2005

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Potent New Antiviral Compound Shows Similar Inhibition and Structural Interactions with Drug Resistant Mutants and Wild Type HIV-1 Protease

Journal of medicinal chemistry, 2007-09, Vol.50 (18), p.4509-4515

2007

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Mechanism of Drug Resistance Revealed by the Crystal Structure of the Unliganded HIV-1 Protease with F53L Mutation

Journal of molecular biology, 2006-05, Vol.358 (5), p.1191-1199

2006

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HIV-1 Protease Dimer Interface Mutations that Compensate for Viral Reverse Transcriptase Instability in Infectious Virions

Journal of molecular biology, 2007-09, Vol.372 (2), p.369-381

2007

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Susceptibility of Potent Antiviral Inhibitor to Highly Drug Resistant Mutations D30N, I50V and L90M of HIV-1 Protease

Journal of medicinal chemistry, 2006-02, Vol.49 (4), p.1379-1387

2006

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Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 Aa resolution crystal structures of HIV-1 protease mutants with substrate analogs

The FEBS journal, 2005-10, Vol.272 (20), p.5265-5277

2005

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Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 angstroms resolution crystal structures of HIV-1 protease mutants with substrate analogs

The FEBS journal, 2005-10, Vol.272 (20), p.5265-5277

2005

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Anti-PEG antibodies compromise the integrity of PEGylated lipid-based nanoparticles via complement

Journal of controlled release, 2022-01, Vol.341, p.475-486

2022

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A unified theory of spin-relaxation due to spin-orbit coupling in metals and semiconductors

Scientific reports, 2013-11, Vol.3 (1), p.3233-3233, Article 3233

2013

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Braiding-based quantum control of a Majorana qubit built from quantum dots

Physical review. B, 2024-03, Vol.109 (12), Article 125410

2024

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Editorial: Effector functions of therapeutic antibodies

Frontiers in immunology, 2023-01, Vol.13, p.1126966-1126966

2023

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Valley-enhanced fast relaxation of gate-controlled donor qubits in silicon

Nanotechnology, 2016-08, Vol.27 (31), p.314002-314002

2016

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Testing the Applicability of MALDI-TOF MS as an Alternative Stock Identification Method in a Cryptic Species Complex

Molecules (Basel, Switzerland), 2020-07, Vol.25 (14), p.3214

2020

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Hsp70-associated chaperones have a critical role in buffering protein production costs

eLife, 2018-01, Vol.7

2018

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Dephasing of Majorana qubits due to quasistatic disorder

Physical review. B, 2022-01, Vol.105 (3), Article 035413

2022

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The effect of computerized cognitive training and transcranial direct current stimulation on working memory among post-stroke individuals: a systematic review with meta-analysis and meta-regression

BMC neurology, 2024-09, Vol.24 (1), p.314-14, Article 314

2024

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Infirm effect of phylogeny on morphometric features in a cryptic Gobio species complex

Contributions to zoology (Amsterdam, Netherlands : 1995), 2022-02, Vol.91 (2), p.79-96

2022

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Control of valley dynamics in silicon quantum dots in the presence of an interface step

Physical review. B, 2016-07, Vol.94 (3), Article 035438

2016

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Critical differences in HIV‐1 and HIV‐2 protease specificity for clinical inhibitors

Structural and Kinetic Analysis of Caspase-3 Reveals Role for S5 Binding Site in Substrate Recognition

A Novel Bis-Tetrahydrofuranylurethane-Containing Nonpeptidic Protease Inhibitor (PI), GRL-98065, Is Potent against Multiple-PI-Resistant Human Immunodeficiency Virus In Vitro

High Resolution Crystal Structures of HIV-1 Protease with a Potent Non-peptide Inhibitor (UIC-94017) Active Against Multi-drug-resistant Clinical Strains

Effectiveness of Nonpeptide Clinical Inhibitor TMC-114 on HIV-1 Protease with Highly Drug Resistant Mutations D30N, I50V, and L90M

Crystal structures of HIV protease V82A and L90M mutants reveal changes in the indinavir‐binding site

Kinetic, Stability, and Structural Changes in High-resolution Crystal Structures of HIV-1 Protease with Drug-resistant Mutations L24I, I50V, and G73S

Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 Å resolution crystal structures of HIV‐1 protease mutants with substrate analogs

Potent New Antiviral Compound Shows Similar Inhibition and Structural Interactions with Drug Resistant Mutants and Wild Type HIV-1 Protease

Mechanism of Drug Resistance Revealed by the Crystal Structure of the Unliganded HIV-1 Protease with F53L Mutation

HIV-1 Protease Dimer Interface Mutations that Compensate for Viral Reverse Transcriptase Instability in Infectious Virions

Susceptibility of Potent Antiviral Inhibitor to Highly Drug Resistant Mutations D30N, I50V and L90M of HIV-1 Protease

Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 Aa resolution crystal structures of HIV-1 protease mutants with substrate analogs

Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 angstroms resolution crystal structures of HIV-1 protease mutants with substrate analogs

Anti-PEG antibodies compromise the integrity of PEGylated lipid-based nanoparticles via complement

A unified theory of spin-relaxation due to spin-orbit coupling in metals and semiconductors

Braiding-based quantum control of a Majorana qubit built from quantum dots

Editorial: Effector functions of therapeutic antibodies

Valley-enhanced fast relaxation of gate-controlled donor qubits in silicon

Testing the Applicability of MALDI-TOF MS as an Alternative Stock Identification Method in a Cryptic Species Complex

Hsp70-associated chaperones have a critical role in buffering protein production costs

Dephasing of Majorana qubits due to quasistatic disorder

The effect of computerized cognitive training and transcranial direct current stimulation on working memory among post-stroke individuals: a systematic review with meta-analysis and meta-regression

Infirm effect of phylogeny on morphometric features in a cryptic Gobio species complex

Control of valley dynamics in silicon quantum dots in the presence of an interface step

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