Oncoprotein protein kinase
    12.
    发明授权
    Oncoprotein protein kinase 失效
    癌蛋白蛋白激酶

    公开(公告)号:US06706509B2

    公开(公告)日:2004-03-16

    申请号:US09861012

    申请日:2001-05-18

    IPC分类号: C12N912

    摘要: An isolated polypeptide (JNK) characterized by having a molecular weight of 46 kD as determined by reducing SDS-PAGE, having serine and threonine kinase activity, phosphorylating the c-Jun N-terminal activation domain and polynucleotide sequences and method of detection of JNK are provided herein. JNK phosphorylates c-Jun N-terminal activation domain which affects gene expression from AP-1 sites.

    摘要翻译: 分离的多肽(JNK),其分子量为46kD,通过还原SDS-PAGE测定,具有丝氨酸和苏氨酸激酶活性,磷酸化c-Jun N-末端激活域和多核苷酸序列和检测JNK的方法是 本文提供。 JNK磷酸化影响AP-1位点基因表达的c-Jun N末端激活结构域。

    Oncoprotein protein kinase
    14.
    发明授权
    Oncoprotein protein kinase 失效
    癌蛋白蛋白激酶

    公开(公告)号:US06342595B1

    公开(公告)日:2002-01-29

    申请号:US09461649

    申请日:1999-12-14

    IPC分类号: C12N1563

    摘要: The present invention provides an isolated polynucleotide encoding a c-Jun peptide consisting of about amino acid residues 33 to 79 as set fort in SEQ ID NO: 10 or conservative variations thereof. The invention also provides a method for producing a peptide of SEQ ID NO:1 comprising (a) culturing a host cell containing a polynucleotide encoding a c-Jun peptide consisting of about amino acid residues 33 to 79 as set forth in SEQ ID NO: 10 under conditions which allow expression of the polynucleotide; and (b) obtaining the peptide of SEQ ID NO:1.

    摘要翻译: 本发明提供了编码由SEQ ID NO:10所设置的约氨基酸残基33至79或其保守变体组成的c-Jun肽的分离的多核苷酸。 本发明还提供了生产SEQ ID NO:1的肽的方法,其包含(a)培养含有编码由SEQ ID NO:1所示的约氨基酸残基33至79组成的c-Jun肽的多核苷酸的宿主细胞。 10,在允许多核苷酸表达的条件下; 和(b)获得SEQ ID NO:1的肽。

    Oncoprotein kinase
    15.
    发明授权
    Oncoprotein kinase 失效
    癌蛋白激酶

    公开(公告)号:US06193965B1

    公开(公告)日:2001-02-27

    申请号:US09452370

    申请日:1999-11-30

    IPC分类号: A61K3816

    CPC分类号: C12N9/12 A61K38/00 C07K16/40

    摘要: An isolated polypeptide (JNK) characterized by having a molecular weight of 46 kD or 55 kD as determined by reducing SDS-PAGE, having serine and theonine kinase activity, phosphorylating the c-Jun N-terminal activation domain and polynucleotide sequences and method of detection of JNK are provided herein. JNK phosphorylates c-Jun N-terminal activation domain which affects gene expression from AP-1 sites.

    摘要翻译: 分离的多肽(JNK),其特征在于通过还原SDS-PAGE测定分子量为46kD或55kD,具有丝氨酸和腺嘌呤激酶活性,磷酸化c-Jun N-末端激活结构域和多核苷酸序列和检测方法 的JNK。 JNK磷酸化影响AP-1位点基因表达的c-Jun N末端激活结构域。