Jinek Martin, Chen Ya-Wen, Clausen Henrik, Cohen Stephen M, Conti Elena
European Molecular Biology Laboratory, Meyerhofstrasse 1, D-69117 Heidelberg, Germany.
Nat Struct Mol Biol. 2006 Oct;13(10):945-6. doi: 10.1038/nsmb1144. Epub 2006 Sep 10.
Fringe proteins are beta1,3-N-acetylglucosaminyltransferases that modify Notch receptors, altering their ligand-binding specificity to regulate Notch signaling in development. We present the crystal structure of mouse Manic Fringe bound to UDP and manganese. The structure reveals amino acid residues involved in recognition of donor substrates and catalysis, and a putative binding pocket for acceptor substrates. Mutations of several invariant residues in this pocket impair Fringe activity in vivo.
边缘蛋白是β1,3-N-乙酰葡糖胺基转移酶,可修饰Notch受体,改变其配体结合特异性,从而在发育过程中调节Notch信号通路。我们展示了与UDP和锰结合的小鼠躁狂边缘蛋白的晶体结构。该结构揭示了参与识别供体底物和催化的氨基酸残基,以及一个假定的受体底物结合口袋。该口袋中几个不变残基的突变会损害体内边缘蛋白的活性。