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蛋白激酶B底物特异性的分子基础;与丝裂原活化蛋白激酶相关蛋白激酶-1和p70核糖体蛋白S6激酶的比较。

Molecular basis for the substrate specificity of protein kinase B; comparison with MAPKAP kinase-1 and p70 S6 kinase.

作者信息

Alessi D R, Caudwell F B, Andjelkovic M, Hemmings B A, Cohen P

机构信息

MRC Protein Phosphorylation Unit, Department of Biochemistry, University of Dundee, UK.

出版信息

FEBS Lett. 1996 Dec 16;399(3):333-8. doi: 10.1016/s0014-5793(96)01370-1.

Abstract

The substrate specificity of protein kinase-B alpha (PKBalpha, also known as RAC kinase or Akt) was investigated using synthetic peptide substrates related to the sequence surrounding the phosphorylation site on glycogen synthase kinase-3 (GSK3). The minimum sequence motif required for efficient phosphorylation was Arg-Xaa-Arg-Yaa-Zaa-Ser/Thr-Hyd, where Xaa is any amino acid, Yaa and Zaa are small residues other than glycine and Hyd is a bulky hydrophobic residue (Phe, Leu). The most effective substrate, Arg-Pro-Arg-Thr-Ser-Ser-Phe, was phosphorylated with a Km of 5 microM and Vmax of 260 U/mg. PKBalpha phosphorylated histone H2B (Km 5 microM, Vmax 68 U/mg) specifically at Ser-36 which also lies in an Arg-Xaa-Arg-Xaa-Xaa-Ser-Hyd motif. The peptide Arg-Pro-Arg-Ala-Ala-Thr-Phe may be a relatively specific substrate for PKBalpha because, unlike other substrates, it is not phosphorylated by p70 S6 kinase or MAP kinase activated protein (MAPKAP) kinase-1.

摘要

利用与糖原合酶激酶-3(GSK3)磷酸化位点周围序列相关的合成肽底物,研究了蛋白激酶Bα(PKBα,也称为RAC激酶或Akt)的底物特异性。有效磷酸化所需的最小序列基序为Arg-Xaa-Arg-Yaa-Zaa-Ser/Thr-Hyd,其中Xaa为任何氨基酸,Yaa和Zaa为除甘氨酸外的小残基,Hyd为大的疏水残基(苯丙氨酸、亮氨酸)。最有效的底物Arg-Pro-Arg-Thr-Ser-Ser-Phe被磷酸化,其米氏常数(Km)为5微摩尔,最大反应速度(Vmax)为260单位/毫克。PKBα特异性地在同样位于Arg-Xaa-Arg-Xaa-Xaa-Ser-Hyd基序中的Ser-36位点磷酸化组蛋白H2B(Km 5微摩尔,Vmax 68单位/毫克)。肽Arg-Pro-Arg-Ala-Ala-Thr-Phe可能是PKBα相对特异的底物,因为与其他底物不同,它不会被p70 S6激酶或丝裂原活化蛋白激酶激活蛋白(MAPKAP)激酶-1磷酸化。

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