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环磷酸腺苷受体:环磷酸腺苷类似物对DNA结合及蛋白水解失活的影响

Cyclic adenosine monophosphate receptor: effect of cyclic AMP analogues on DNA binding and proteolytic inactivation.

作者信息

Krakow J S

出版信息

Biochim Biophys Acta. 1975 Apr 2;383(4):345-50. doi: 10.1016/0005-2787(75)90303-2.

Abstract

The cyclic AMP receptor protein of Escherichia coli in the presence of cyclic AMP undergoes a conformational change resulting in an increased affinity for DNA and an increased susceptibility to attack by proteolytic enzymes resulting in loss of DNA binding capacity. Of several cyclic nucleotides tested only cyclic AMP and cyclic tubercidin monophosphate are able to effect the conformational transition in cyclic AMP receptor protein, prerequisite to proteolytic inactivation or DNA binding. Other analogues such as cyclic GMP or cyclic IMP which are competitive inhibitors of cyclic AMP do not support DNA binding or proteolytic inactivation.

摘要

大肠杆菌的环磷酸腺苷受体蛋白在环磷酸腺苷存在的情况下会发生构象变化,导致对DNA的亲和力增加,并且对蛋白水解酶的攻击更敏感,从而导致DNA结合能力丧失。在测试的几种环核苷酸中,只有环磷酸腺苷和环结核菌素单磷酸能够影响环磷酸腺苷受体蛋白的构象转变,这是蛋白水解失活或DNA结合的前提条件。其他类似物,如环磷酸鸟苷或环磷酸肌苷,它们是环磷酸腺苷的竞争性抑制剂,不支持DNA结合或蛋白水解失活。

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