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Basic Characteristics of Mutations
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Mutation Site
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L325F |
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Mutation Site Sentence
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Table 6. Amino acid positions with evidence of diversifying selection and the mutations with evidence of directional selection in HIV-1 gp41 within the protease inhibitor (PI) and nonnucleoside RT inhibitor (NNRTI)-treatment groups. |
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Mutation Level
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Amino acid level |
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Mutation Type
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Nonsynonymous substitution |
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Gene/Protein/Region
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gp41 |
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Standardized Encoding Gene
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Env
|
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Genotype/Subtype
|
HIV-1 |
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Viral Reference
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-
|
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Functional Impact and Mechanisms
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Disease
|
HIV Infections
|
|
Immune
|
- |
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Target Gene
|
-
|
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Clinical and Epidemiological Correlations
|
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Clinical Information
|
Y |
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Treatment
|
PIs |
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Location
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America |
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Literature Information
|
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PMID
|
30040081
|
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Title
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Selection analyses of paired HIV-1 gag and gp41 sequences obtained before and after antiretroviral therapy
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Author
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Tzou PL,Rhee SY,Pond SLK,Manasa J,Shafer RW
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Journal
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Scientific data
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Journal Info
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2018 Jul 24;5:180147
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Abstract
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Most HIV-1-infected individuals with virological failure on a pharmacologically-boosted protease inhibitor (PI) regimen do not develop PI-resistance protease mutations. One proposed explanation is that HIV-1 gag or gp41 cytoplasmic domain mutations might also reduce PI susceptibility. In a recent study of paired gag and gp41 sequences from individuals with virological failure on a PI regimen, we did not identify PI-selected mutations and concluded that if such mutations existed, larger numbers of paired sequences from multiple studies would be needed for their identification. In this study, we generated site-specific amino acid profiles using gag and gp41 published sequences from 5,338 and 4,242 ART-naive individuals, respectively, to assist researchers identify unusual mutations arising during therapy and to provide scripts for performing established and novel maximal likelihood estimates of dN/dS substitution rates in paired sequences. The pipelines used to generate the curated sequences, amino acid profiles, and dN/dS analyses will facilitate the application of consistent methods to paired gag and gp41 sequence datasets and expedite the identification of potential sites under PI-selection pressure.
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Sequence Data
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Table 1
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