MOLECULAR PROPERTIES OF PEP CARBOXYLASE REVELANT TO ITS ALLOSTERIC REGULATION
PEP羧化酶的分子特性与其变构调节相关
基本信息
- 批准号:3734247
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
Phosphoenolpyruvate (PEP) carboxylase is of interest because of its central
role in the photosynthetic metabolism of CAM and C4 plants. As would be
expected for a key enzyme in a major metabolic pathway, the activity of the
enzyme is highly regulated, and a fundamental regulatory element appears to
be the interplay of the activation caused by phosphorylated activators such
as glucose 6-phosphate and AMP and the inhibition caused by malate and ATP.
The overall goal of this research is to elucidate various molecular aspects
of the process by which effectors, particularly activators such as AMP and
glucose 6-phosphate, regulate PEP carboxylase from Crassula argentea and
other sources. The research will probe the binding site(s) of activators
and inhibitors through the use of photoaffinity labels. The proposed
research will also test the molecular mechanism of activation, in light of
a novel hypothesis that has recently been proposed. The specific aims
include estimating the number of activator binding sites and the
dissociation constants for the activators, determining whether all
activators share a common binding site, comparing the AMP and ATP binding
sites, identifying the peptide sequence at the activator binding site, and
testing the role of activator dephosphorylation in the activation process.
The results are expected to provide molecular information on how and where
activators exert their influence on the enzyme. This information will
provide greater insight into the structure-function relationships of this
specific enzyme and, more generally, into the process of metabolic
regulation at the enzyme level.
磷酸烯醇式丙酮酸(PEP)羧基酶因其核心功能而备受关注。
在CAM和C4植物光合代谢中的作用就像是
对于主要代谢途径中的一个关键酶来说,
酶是高度受调节的,一个基本的调节元件似乎是
是由磷酸化激活剂引起的激活的相互作用
葡萄糖、6-磷酸和AMP以及苹果酸和三磷酸腺苷的抑制作用。
这项研究的总体目标是阐明分子的各个方面。
效应器,特别是AMP和AMP等激活剂的过程
葡萄糖6-磷酸,调节青海牡蛎PEP羧化酶和
其他消息来源。这项研究将探索激活剂的结合部位(S)
以及通过使用光亲和标记的抑制剂。建议数
研究还将测试激活的分子机制,鉴于
最近提出了一个新的假说。具体目标
包括估计激活剂结合位点的数量和
激活剂的离解常数,决定所有
激活剂共享一个共同的结合部位,比较AMP和ATP结合
位点,识别激活剂结合位点上的肽序列,以及
检测激活剂去磷酸化在激活过程中的作用。
预计结果将提供有关如何以及在哪里进行的分子信息。
激活剂对酶产生影响。此信息将
更深入地了解以下内容的结构-功能关系
特定的酶,更广泛地说,进入新陈代谢过程
在酶水平上的调节。
项目成果
期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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{{ truncateString('SCOTT D GROVER', 18)}}的其他基金
STRUCTURE/REGULATION RELATIONSHIPS IN PEP CARBOXYLASE
PEP 羧化酶的结构/调控关系
- 批准号:
6481216 - 财政年份:2001
- 资助金额:
-- - 项目类别:
STRUCTURE/REGULATION RELATIONSHIPS IN PEP CARBOXYLASE
PEP 羧化酶的结构/调控关系
- 批准号:
6325836 - 财政年份:2000
- 资助金额:
-- - 项目类别:
EFFECTOR BINDING SITES AND REGULATORY MECHNISIMS IN PEP CARBOXYLASE
PEP 羧化酶中的效应子结合位点和调控机制
- 批准号:
6107119 - 财政年份:1999
- 资助金额:
-- - 项目类别:
EFFECTOR BINDING SITES AND REGULATORY MECHNISIMS IN PEP CARBOXYLASE
PEP 羧化酶中的效应子结合位点和调控机制
- 批准号:
6296632 - 财政年份:1998
- 资助金额:
-- - 项目类别:
EFFECTOR BINDING SITES AND REGULATORY MECHNISIMS IN PEP CARBOXYLASE
PEP 羧化酶中的效应子结合位点和调控机制
- 批准号:
6271532 - 财政年份:1998
- 资助金额:
-- - 项目类别:
EFFECTOR BINDING SITES AND REGULATORY MECHNISIMS IN PEP CARBOXYLASE
PEP 羧化酶中的效应子结合位点和调控机制
- 批准号:
6240010 - 财政年份:1997
- 资助金额:
-- - 项目类别:
MOLECULAR PROPERTIES OF PEP CARBOXYLASE REVELANT TO ITS ALLOSTERIC REGULATION
PEP羧化酶的分子特性与其变构调节相关
- 批准号:
3777848 - 财政年份:
- 资助金额:
-- - 项目类别:
EFFECT OF REGULATORY LIGANDS AND THEIR BINDING SITES ON PEP CARBOXYLASES
调节配体及其结合位点对 PEP 羧化酶的影响
- 批准号:
3915698 - 财政年份:
- 资助金额:
-- - 项目类别:
EFFECT OF REGULATORY LIGANDS AND THEIR BINDING SITES ON PEP CARBOXYLASES
调节配体及其结合位点对 PEP 羧化酶的影响
- 批准号:
3936807 - 财政年份:
- 资助金额:
-- - 项目类别:
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