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    • 9. 发明授权
    • PCNA binding substance
    • PCNA结合物质
    • US06613878B1
    • 2003-09-02
    • US08945645
    • 1998-07-31
    • Lynne S. CoxDavid P. LaneEmma WarbrickDavid M. Glover
    • Lynne S. CoxDavid P. LaneEmma WarbrickDavid M. Glover
    • A61K3808
    • C12N9/22A61K38/00C07K14/4738
    • Fragments of Fen1 that interact with PCNA are disclosed, together with the use of such fragments or mimetics of Fen1 in methods of screening for compounds useful in treating disorders in which PCNA is implicated. In particular, substances which have the property of binding to PCNA are disclosed, said substances comprising: (i) a fragment of the Fen1 protein containing a peptide of 89 amino acids from the C-terminal region or an active portion thereof; or, (ii) a fragment of the Fen1 protein containing the sequence motif QGRLDxFF; or, (iii) a functional mimetic of said protein fragments; where “x” is preferably the selected form the amino acids S, D or G.
    • 公开了与PCNA相互作用的Fen1片段,以及在筛选可用于治疗PCNA所涉及的疾病的化合物的方法中使用Fen1的这种片段或模拟物。 特别地,公开了具有与PCNA结合的性质的物质,所述物质包括:(i)含有C末端区域或其活性部分的89个氨基酸的肽的Fen1蛋白的片段; 或(ii)含有序列基序QGRLDxFF的Fen1蛋白的片段; 或(iii)所述蛋白质片段的功能模拟物;其中“x”优选为所选形式的氨基酸S,D或G.