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人类免疫缺陷病毒1型蛋白酶及其底物结合位点的分子建模

Molecular modeling of the HIV-1 protease and its substrate binding site.

作者信息

Weber I T, Miller M, Jaskólski M, Leis J, Skalka A M, Wlodawer A

机构信息

Crystallography Laboratory, NCI-Frederick Cancer Research Facility, MD 21701.

出版信息

Science. 1989 Feb 17;243(4893):928-31. doi: 10.1126/science.2537531.

Abstract

The human immunodeficiency virus (HIV-1) encodes a protease that is essential for viral replication and is a member of the aspartic protease family. The recently determined three-dimensional structure of the related protease from Rous sarcoma virus has been used to model the smaller HIV-1 dimer. The active site has been analyzed by comparison to the structure of the aspartic protease, rhizopuspepsin, complexed with a peptide inhibitor. The HIV-1 protease is predicted to interact with seven residues of the protein substrate. This information can be used to design protease inhibitors and possible antiviral drugs.

摘要

人类免疫缺陷病毒(HIV-1)编码一种蛋白酶,它对病毒复制至关重要,是天冬氨酸蛋白酶家族的成员。最近确定的劳斯肉瘤病毒相关蛋白酶的三维结构已被用于构建较小的HIV-1二聚体模型。通过与与肽抑制剂复合的天冬氨酸蛋白酶根霉胃蛋白酶的结构进行比较,对活性位点进行了分析。预计HIV-1蛋白酶与蛋白质底物的七个残基相互作用。这些信息可用于设计蛋白酶抑制剂和可能的抗病毒药物。

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