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X-ray coordinates defining the human papillomavirus E2 transactivation domain / inhibitor co-crystal and the inhibitor binding pocket

机译:定义人乳头瘤病毒E2反式激活域/抑制剂共晶体和抑制剂结合口袋的X射线坐标

摘要

A crystallizable composition, comprising an PV E2 TAD-like polypeptide of SEQ ID NO.2 complexed with an inhibitor L. The invention also provides a method for producing the crystallized HPV E2 TAD-inhibitor complex (HPV E2 TAD-L) comprising: a) mixing purified HPV E2 TAD, contained in a purification buffer, with solublized inhibitor L to generate a complex solution containing the HPV E2 TAD-L complex; and b) crystallizing the complex from a) in a crystallization buffer. The invention also provides a method for producing crystallized apo HPV E2 TAD, comprising: a) mixing apo HPV E2 TAD, contained in a purification buffer, with a crystallization buffer. X-ray crystal structure coordinates the HPV E2 TAD-L complex, are also provided, which define an inhibitor binding pocket. The inhibitor binding pocket is useful for screening potential small molecule inhibitors that bind to the pocket.
机译:一种可结晶的组合物,其包含与抑制剂L复合的SEQ ID NO.2的PV E2 TAD-样多肽。本发明还提供了一种生产结晶的HPV E2 TAD-抑制剂复合物(HPV E2 TAD-L)的方法,该方法包括: )将纯化缓冲液中包含的纯化的HPV E2 TAD与增溶的抑制剂L混合以产生包含HPV E2 TAD-L复合物的复合物溶液; b)由a)在结晶缓冲液中结晶该配合物。本发明还提供了一种生产结晶的载脂蛋白HPV E2 TAD的方法,该方法包括:a)将纯化缓冲液中所含的载脂蛋白HPV E2 TAD与结晶缓冲液混合。还提供了X射线晶体结构与HPV E2 TAD-L配合物的坐标,它们定义了抑制剂的结合口袋。抑制剂结合口袋可用于筛选与口袋结合的潜在小分子抑制剂。

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