Gallivan J-P, McGarvey Michael J
Department of Medicine, Faculty of Medicine, Imperial College London, St Mary's Hospital Campus, London W2 1NY, UK.
FEBS Lett. 2003 Nov 20;554(3):485-8. doi: 10.1016/s0014-5793(03)01229-8.
NS3 proteins of flaviviruses contain motifs which indicate that they possess protease and helicase activities. The helicases are members of the DExD/H box helicase superfamily and NS3 proteins from some flaviviruses have been shown to possess ATPase and helicase activities in vitro. The Q motif is a recently recognised cluster of nine amino acids common to most DExD/H box helicases which is proposed to regulate ATP binding and hydrolysis. In addition a conserved residue occurs 17 amino acids upstream of the Q motif ('+17'). We have analysed full-length and truncated NS3 proteins from Powassan virus (a tick-borne flavivirus) to investigate the role that the Q motif plays in the hydrolysis of ATP by a viral helicase. The Q motif appears to be essential for the activity of Powassan virus NS3 ATPase, however NS3 deletion mutants that contain the Q motif but lack the '+17' amino acid have ATPase activity albeit at a reduced level.
黄病毒的NS3蛋白含有一些基序,表明它们具有蛋白酶和解旋酶活性。这些解旋酶属于DExD/H盒解旋酶超家族,并且已证明一些黄病毒的NS3蛋白在体外具有ATP酶和解旋酶活性。Q基序是最近在大多数DExD/H盒解旋酶中发现的由九个氨基酸组成的保守簇,它被认为可调节ATP的结合和水解。此外,在Q基序上游17个氨基酸处(“+17”)存在一个保守残基。我们分析了波瓦桑病毒(一种蜱传黄病毒)的全长和截短的NS3蛋白,以研究Q基序在病毒解旋酶ATP水解中所起的作用。Q基序似乎对波瓦桑病毒NS3 ATP酶的活性至关重要,然而,含有Q基序但缺少“+17”氨基酸的NS3缺失突变体仍具有ATP酶活性,尽管活性水平有所降低。