(PDF) Chemical Synthesis and Enzymatic Activity of a

Chemical Synthesis and Enzymatic Activity of a 99-Residue Peptide With a Sequence Proposed for the Human Immunodeficiency Virus Protease.

Proceedings of the National Academy of Sciences of the United States of America - United States

doi 10.1073/pnas.85.19.7129

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October 1, 1988

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Proceedings of the National Academy of Sciences

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Chemical Synthesis and Enzymatic Activity of a 99-Residue Peptide With a Sequence Proposed for the Human Immunodeficiency Virus Protease.

Proceedings of the National Academy of Sciences of the United States of America - United States

doi 10.1073/pnas.85.19.7129

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Modular Total Chemical Synthesis of a Human Immunodeficiency Virus Type 1 Protease

Synthesis and Biological Evaluation of Novel Isopropanolamine Derivatives as Non-Peptide Human Immunodeficiency Virus Protease Inhibitors

Synthesis of a 42 Residue Peptide Corresponding to the Entire Amino Acid Sequence of Human GIP.

Synthesis and Anti-Human Immunodeficiency Virus Activity of 4-Branched (+/-)-4-Thiostavudines

Comparative Properties of Feline Immunodeficiency Virus (FIV) and Human Immunodeficiency Virus Type 1 (HIV-1) Proteinases Prepared by Total Chemical Synthesis

Anti-Human Immunodeficiency Virus-1 Protease Activity of New Lanostane-Type Triterpenoids From Ganoderma Sinense

FR901724, a Novel Anti-Human Immunodeficiency Virus (HIV) Peptide Produced by Streptomyces, Shows Synergistic Antiviral Activities With HIV Protease Inhibitor and 2',3'-Dideoxynucleosides.

Activity of Tethered Human Immunodeficiency Virus 1 Protease Containing Mutations in the Flap Region of One Subunit

Crystal Structure of Human Immunodeficiency Virus (HIV) Type 2 Protease in Complex With a Reduced Amide Inhibitor and Comparison With HIV-1 Protease Structures.