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p34cdc2调控机制。

Mechanisms of p34cdc2 regulation.

作者信息

Atherton-Fessler S, Parker L L, Geahlen R L, Piwnica-Worms H

机构信息

Department of Physiology, Tufts University School of Medicine, Boston, Massachusetts 02111.

出版信息

Mol Cell Biol. 1993 Mar;13(3):1675-85. doi: 10.1128/mcb.13.3.1675-1685.1993.

Abstract

The kinase activity of human p34cdc2 is negatively regulated by phosphorylation at Thr-14 and Tyr-15. These residues lie within the putative nucleotide binding domain of p34cdc2. It has been proposed that phosphorylation within this motif ablates the binding of ATP to the active site of p34cdc2, thereby inhibiting p34cdc2 kinase activity (K. Gould and P. Nurse, Nature [London] 342:39-44, 1989). To understand the mechanism of this inactivation, various forms of p34cdc2 were tested for the ability to bind nucleotide. The active site of p34cdc2 was specifically modified by the MgATP analog 5'-p-fluorosulfonylbenzoyladenosine (FSBA). The apparent Km for modification of wild-type, monomeric p34cdc2 was 148 microM FSBA and was not significantly affected by association with cyclin B. Tyrosine-phosphorylated p34cdc2 was modified by FSBA with a slightly higher Km (241 microM FSBA). FSBA modification of both tyrosine-phosphorylated and unphosphorylated p34cdc2 was competitively inhibited by ATP, and half-maximal inhibition in each case occurred at approximately 250 microM ATP. In addition to being negatively regulated by phosphorylation, the kinase activity of p34cdc2 was positively regulated by the cyclin-dependent phosphorylation of Thr-161. Mutation of p34cdc2 at Thr-161 resulted in the formation of an enzymatically inactive p34cdc2/cyclin B complex both in vivo and in vitro. However, mutation of Thr-161 did not significantly affect the ability of p34cdc2 to bind nucleotide (FSBA). Taken together, these results indicate that inhibition of p34cdc2 kinase activity by phosphorylation of Tyr-15 (within the putative ATP binding domain) or by mutation of Thr-161 involves a mechanism other than inhibition of nucleotide binding. We propose instead that the defect resides at the level of catalysis.

摘要

人p34cdc2的激酶活性受到苏氨酸-14和酪氨酸-15磷酸化的负调控。这些残基位于p34cdc2假定的核苷酸结合结构域内。有人提出,该基序内的磷酸化消除了ATP与p34cdc2活性位点的结合,从而抑制p34cdc2激酶活性(K. 古尔德和P. 纳斯,《自然》[伦敦] 342:39 - 44,1989年)。为了解这种失活机制,对各种形式的p34cdc2进行了核苷酸结合能力测试。p34cdc2的活性位点被MgATP类似物5'-对氟磺酰苯甲酰腺苷(FSBA)特异性修饰。野生型单体p34cdc2修饰的表观Km为148μM FSBA,与细胞周期蛋白B结合对此没有显著影响。酪氨酸磷酸化的p34cdc2被FSBA修饰,Km略高(241μM FSBA)。酪氨酸磷酸化和未磷酸化的p34cdc2的FSBA修饰均受到ATP的竞争性抑制,每种情况下半最大抑制浓度约为250μM ATP。除了受到磷酸化的负调控外,p34cdc2的激酶活性还受到苏氨酸-161的细胞周期蛋白依赖性磷酸化的正调控。p34cdc2苏氨酸-161位点的突变在体内和体外均导致形成无酶活性的p34cdc2/细胞周期蛋白B复合物。然而,苏氨酸-161位点的突变并未显著影响p34cdc2结合核苷酸(FSBA)的能力。综上所述,这些结果表明,酪氨酸-15磷酸化(在假定的ATP结合结构域内)或苏氨酸-161位点突变对p34cdc2激酶活性的抑制涉及一种不同于抑制核苷酸结合的机制。我们反而认为缺陷存在于催化水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ac/359480/23d1e1fa5c34/molcellb00015-0375-a.jpg

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