Foot-and-mouth disease virus 3C protease: recent structural and functional insights into an antiviral target.

Foot-and-mouth disease virus 3C protease: recent structural and functional insights into an antiviral target.
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DOI:
10.1016/j.biocel.2006.07.006
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发表时间:
2007
期刊:
The international journal of biochemistry & cell biology
影响因子:
--
通讯作者:
Leatherbarrow RJ
Leatherbarrow RJ
中科院分区:
其他
文献类型:
--
作者:
Curry S;Roqué-Rosell N;Zunszain PA;Leatherbarrow RJ

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来自口蹄疫病毒的3C蛋白酶(FMDV 3Cpro)在病毒致病过程中起关键作用,在多聚蛋白前体的加工和RNA复制中起重要作用。尽管最近的结构和功能研究揭示了对酶的机制和功能的新见解,但在实现FMDV 3Cpro作为抗病毒药物靶点的潜力之前,必须解决关键问题。
The 3C protease from foot-and-mouth disease virus (FMDV 3Cpro) is critical for viral pathogenesis, having vital roles in both the processing of the polyprotein precursor and RNA replication. Although recent structural and functional studies have revealed new insights into the mechanism and function of the enzyme, key questions remain that must be addressed before the potential of FMDV 3Cpro as an antiviral drug target can be realised.
冠状病毒主蛋白酶的结构揭示了甲over依蛋白酶折叠与额外的α-螺旋结构域的组合。
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