Analysis of drug resistance in HIV protease

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منابع مشابه

Molecular Basis for Drug Resistance in HIV-1 Protease

HIV-1 protease is one of the major antiviral targets in the treatment of patients infected with HIV-1. The nine FDA approved HIV-1 protease inhibitors were developed with extensive use of structure-based drug design, thus the atomic details of how the inhibitors bind are well characterized. From this structural understanding the molecular basis for drug resistance in HIV-1 protease can be eluci...

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In silico analysis of drug resistance in wild type and mutant HIV-1 subtype d protease

Methods The mutation frequency of subtype d in untreated persons was obtained from Stanford DR database, http://hivdb. stanford.edu/. Based on the database the wild type PTD sequence was generated. Crystal structure 3LZS showed more similarity based on BLASTp program. The protein structure 3LZS was used as a template to build wild type, major (L10V, N37D, K69Y), minor (K20I, L33I, P39T, Q61N), ...

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Analysis of drug resistance to HIV-1 protease using fitness function in genetic algorithm

Methods Drug resistance is predicted for all FDA approved HIV-1 protease inhibitors and organic leads synthesized by Dr. Deeb and Dr. Godzari with wild type and mutant strains of subtype B. Initially the structural feature of HIV-1 protease with the inhibitor complex has been anlysed on the basis of “Binding Energies”. Finally the fitness function in Genetic Algorithm was used for optimizing th...

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HIV-1 Protease: Structural Perspectives on Drug Resistance

Antiviral inhibitors of HIV-1 protease are a notable success of structure-based drug design and have dramatically improved AIDS therapy. Analysis of the structures and activities of drug resistant protease variants has revealed novel molecular mechanisms of drug resistance and guided the design of tight-binding inhibitors for resistant variants. The plethora of structures reveals distinct molec...

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Rapid enzymatic test for phenotypic HIV protease drug resistance.

A phenotypic resistance test based on recombinant expression of the active HIV protease in E. coli from patient blood samples was developed. The protease is purified in a rapid one-step procedure as active enzyme and tested for inhibition by five selected synthetic inhibitors (amprenavir, indinavir, nelfinavir, ritonavir, and saquinavir) used presently for chemotherapy of HIV-infected patients....

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ژورنال

عنوان ژورنال: BMC Bioinformatics

سال: 2018

ISSN: 1471-2105

DOI: 10.1186/s12859-018-2331-y