首页> Molecular pharmacology> Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors.

Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors.

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第一作者： Pelemans H

作者： Pelemans H ^[1] ; Esnouf R ; De Clercq-E ; Balzarini J

作者单位： Rega Institute for Medical Research, Katholieke Universiteit Leuven, Leuven, Belgium. ^[1]

关键词 HIV-1 Reverse Transcriptase Reverse Transcriptase Inhibitors Tryptophan HIV-1逆转录酶逆转录酶抑制剂色氨酸

发布时间 2013-11-20

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Molecular pharmacology

2000年57卷5期

954-960页

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Molecular pharmacology

2000年57卷5期

954-960页

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Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors.

Molecular pharmacology

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Molecular pharmacology

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Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors.

Molecular pharmacology

相似文献

同项目论文

Molecular pharmacology

相关期刊

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