Backbone 1H, 13C, and 15N Chemical Shift Assignments for the Multi-Drug Resistant HIV-1 Protease Variant, MDR 769

Backbone ¹H, ¹³C, and ¹⁵N chemical shift assignment for HIV-1 protease subtypes and multi-drug resistant variant MDR 769.

Crystal Structures Of A Multidrug-Resistant Hiv-1 Protease Reveal An Expanded Active Site Cavity

Wide Open 1.3a Structure Of A Multi-Drug Resistant Hiv-1 Protease Represents A Novel Drug Target

Crystal Structures Of Multidrug-resistant Clinical Isolate 769 Hiv-1 Protease Variants

Mdr769 Hiv-1 Protease Complexed With MaCA HEPTA-Peptide

Mdr769 Hiv-1 Protease Complexed With RtRH HEPTA-Peptide

Mdr769 Hiv-1 Protease Complexed With RhIN HEPTA-Peptide

Mdr769 Hiv-1 Protease Complexed With PrRT HEPTA-Peptide

Mdr769 Hiv-1 Protease Complexed With TfPR HEPTA-Peptide

Mdr769 Hiv-1 Protease Complexed With P1P6 HEPTA-Peptide

Mdr769 Hiv-1 Protease Complexed With NcP1 HEPTA-Peptide

Mdr769 Hiv-1 Protease Complexed With P2NC HEPTA-Peptide

Mdr769 Hiv-1 Protease Complexed With CaP2 HEPTA-Peptide

Crystal Structures Of Multidrug-Resistant Hiv-1 Protease In Complex With Mechanism-Based Aspartyl Protease Inhibitors.

Crystal Structure Of Multidrug-resistant Clinical Isolate 769 Hiv-1 Protease In Complex With Ritonavir

Substrate P2NC IN COMPLEX WITH A HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 Protease Variant

Substrate CaP2 IN COMPLEX WITH A HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 Protease Variant

Crystallographic Study Of Multi-drug Resistant Hiv-1 Protease Lopinavir Complex: Mechanism Of Drug Recognition And Resistance

Crystal Structure Of A Multi-drug Resistant Clinical Isolate-769 Hiv-1 Protease Variant That Is Resistant To The Dimerization I

Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax