NS3型
登革热
丝氨酸蛋白酶
登革热病毒
病毒学
蛋白酵素
蛋白酶
生物
MASP1公司
丝氨酸
病毒
酶
生物化学
丙型肝炎病毒
作者
H. M. Krishna Murthy,Stephen Clum,R. Padmanabhan
标识
DOI:10.1074/jbc.274.9.5573
摘要
The mosquito-borne dengue viruses are widespread human pathogens causing dengue fever, dengue hemorrhagic fever, and dengue shock syndrome, placing 40% of the world's population at risk with no effective treatment. The viral genome is a positive strand RNA that encodes a single polyprotein precursor. Processing of the polyprotein precursor into mature proteins is carried out by the host signal peptidase and by NS3 serine protease, which requires NS2B as a cofactor. We report here the crystal structure of the NS3 serine protease domain at 2.1 A resolution. This structure of the protease combined with modeling of peptide substrates into the active site suggests identities of residues involved in substrate recognition as well as providing a structural basis for several mutational effects on enzyme activity. This structure will be useful for development of specific inhibitors as therapeutics against dengue and other flaviviral proteases.
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