Structure-function analysis of human immunodeficiency virus type 1 gp120 amino acid mutations associated with resistance to the CCR5 coreceptor antagonist vicriviroc.
第一作者:
Robert A,Ogert
第一单位:
Department of Biological Sciences-Virology, Schering-Plough Research Institute, Kenilworth, New Jersey 07033, USA.
作者:
医学主题词
氨基酸取代(Amino Acid Substitution);抗HIV药(Anti-HIV Agents);DNA突变分析(DNA Mutational Analysis);抗药性, 病毒(Drug Resistance, Viral);HIV包膜蛋白质gp120(HIV Envelope Protein gp120);HIV-1(HIV-1);人类(Humans);模型, 分子(Models, Molecular);突变, 误义(Mutation, Missense);哌嗪类(Piperazines);蛋白质结合(Protein Binding);蛋白质结构, 三级(Protein Structure, Tertiary);嘧啶类(Pyrimidines);受体, CCR5(Receptors, CCR5);受体, HIV(Receptors, HIV);病毒内化(Virus Internalization)
DOI
10.1128/JVI.01351-09
PMID
19776131
发布时间
2021-10-20
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Journal of virology
12151-63页
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