NEW INSIGHTS INTO ENZYME STRUCTURE AND FUNCTION
NEW INSIGHTS INTO ENZYME STRUCTURE AND FUNCTION
批准号:
3301744
负责人:
EVAN R KANTROWITZ
金额:
$12.77万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-07-01 至 1993-06-30
关键词:
Escherichia coli X ray crystallography alkaline phosphatase chemical binding circular dichroism enzyme mechanism enzyme model enzyme structure metalloenzyme mutant nuclear magnetic resonance spectroscopy protein folding protein sequence protein structure function site directed mutagenesis stop flow technique zinc
中文摘要
点击翻译按钮获取中文摘要
英文摘要
A variety of diseases including sickle cell anemia, beta-
thalassemia, Tay-Sachs and phenylketonuria are the result of a
single amino acid alteration in the structure of a particular
protein or enzyme. Although we can determine the structure of a
protein to atomic resolution, we still do not understand how, in
detail, this structure is related to the function of the particular
protein of enzyme. In order to understand the molecular basis of
diseases, we need to elucidate at the molecular level the
relationship between protein structure and function. Therefore,
the long term goals of this project are to acquire a deeper
understanding of the relationship between protein structure and
function by using E. coli alkaline phosphatase as a model system.
This enzyme catalyzes the nonspecific hydrolysis of phosphate
esters, and is the model for the study of all alkaline
phosphatases.
The specific aims of this proposal are to answer fundamental
questions concerning the relationship between structure and
function of alkaline phosphatase. We will concentrate on the
molecular details of the catalytic mechanism, the mode by which
information is passed between the subunits of the enzyme, and the
function of the metals in this enzyme. We will use a variety of
molecular biology techniques to create altered versions of the
enzyme with single amino acid substitutions. Initially, work will
concentrate on the analysis of mutants that have been already
created. Selection of additional sites for amino acid
substitutions will be based on all the biochemical and structural
data currently available. Kinetic and biophysical methods such as
stopped-flow kinetics, circular dichroism, NMR spectroscopy, and
X-ray crystallography will be used to analyze the results of the
amino acid substitutions. Correlations will be made between the
functional changes induced by the amino acid substitution and the
three-dimensional structure of the mutant enzymes. This work will
not only be important for the understanding of this particular
system, but more importantly for formulating general concepts about
enzyme catalysis, cooperativity and the function of metals in
proteins.
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DIRECT OBSERVATION OF THE QUATERNARY CONFORMATIONAL CHANGES INDUCED BY SUBSTRATE
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批准号:8362170
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项目类别:
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资助金额:$0.27万
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财政年份:2011
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负责人:EVAN R KANTROWITZ
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依托单位:
DIRECT OBSERVATION OF THE QUATERNARY CONFORMATIONAL CHANGES INDUCED BY SUBSTRATE
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批准号:8170121
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项目类别:
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资助金额:$0.78万
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财政年份:2010
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负责人:EVAN R KANTROWITZ
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依托单位:
DIRECT OBSERVATION OF THE QUATERNARY CONFORMATIONAL CHANGES INDUCED BY SUBSTRATE
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批准号:7954451
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项目类别:
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资助金额:$0.21万
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财政年份:2009
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负责人:EVAN R KANTROWITZ
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依托单位:
DIRECT OBSERVATION OF THE QUATERNARY CONFORMATIONAL CHANGES INDUCED BY SUBSTRATE
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批准号:7722147
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项目类别:
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资助金额:$0.02万
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财政年份:2008
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负责人:EVAN R KANTROWITZ
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依托单位:
TIME EVOLUTION OF THE ALLOSTERIC TRANSITION OF ASPARTATE TRANSCARBAMOYLASE
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批准号:7597962
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项目类别:
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资助金额:$0.3万
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财政年份:2007
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负责人:EVAN R KANTROWITZ
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依托单位:
TIME EVOLUTION OF THE ALLOSTERIC TRANSITION OF ASPARTATE TRANSCARBAMOYLASE
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批准号:7370443
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项目类别:
-
资助金额:$0.32万
-
财政年份:2006
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负责人:EVAN R KANTROWITZ
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依托单位:
TIME EVOLUTION OF THE ALLOSTERIC TRANSITION OF ASPARTATE TRANSCARBAMOYLASE
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批准号:7180422
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项目类别:
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资助金额:$0.71万
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财政年份:2005
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负责人:EVAN R KANTROWITZ
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依托单位:
STRUCTURE OF A COBALT-SUBSTITUTED MUTANT OF ALKALINE PHOSPHASE
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批准号:6972664
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项目类别:
-
资助金额:$0.19万
-
财政年份:2004
-
负责人:EVAN R KANTROWITZ
-
依托单位:
TIME EVOLUTION OF ALLOSTERIC TRANSITION OF ASPARTATE TRANSCARBAMOYLASE
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批准号:6976330
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项目类别:
-
资助金额:$0.15万
-
财政年份:2004
-
负责人:EVAN R KANTROWITZ
-
依托单位:
STRUCT & FUNCT OF MUTANT VERSIONS OF ALKALINE PHOSPHATASE FROM ESCHERICHIA COLI
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批准号:6221083
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项目类别:
-
资助金额:$0.13万
-
财政年份:1999
-
负责人:EVAN R KANTROWITZ
-
依托单位:
STRUCTURE REFINEMENT OF MUTANT VERSIONS OF E COLI ASPARTATE TRANSCARBAMOYLASE
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批准号:6221094
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项目类别:
-
资助金额:$0.13万
-
财政年份:1999
-
负责人:EVAN R KANTROWITZ
-
依托单位:
STRUCT & FUNCT OF MUTANT VERSIONS OF ALKALINE PHOSPHATASE FROM ECOLI
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批准号:6295156
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项目类别:
-
资助金额:$1.19万
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财政年份:1998
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负责人:EVAN R KANTROWITZ
-
依托单位:
STRUCT & FUNCT OF MUTANT VERSIONS OF ALKALINE PHOSPHATASE FROM ECOLI
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批准号:6122466
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项目类别:
-
资助金额:$0.0万
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财政年份:1998
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负责人:EVAN R KANTROWITZ
-
依托单位:
STRUCT & FUNCT OF MUTANT VERSIONS OF ALKALINE PHOSPHATASE FROM ECOLI
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批准号:6282501
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项目类别:
-
资助金额:$1.19万
-
财政年份:1998
-
负责人:EVAN R KANTROWITZ
-
依托单位:
STRUCT & FUNCT RELATIONSHIP OF MUTANT VERSIONS OF ALKALINE PHOSPHATASE OF E COLI
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批准号:6253447
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项目类别:
-
资助金额:$0.61万
-
财政年份:1997
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负责人:EVAN R KANTROWITZ
-
依托单位:
STRUCTURE REFINEMENT OF MUTANT VERSIONS OF E COLI ASPARTATE TRANSCARBAMOYLASE
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批准号:6253455
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项目类别:
-
资助金额:$0.61万
-
财政年份:1997
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负责人:EVAN R KANTROWITZ
-
依托单位:
The Molecular Basis of Cellular Control Mechanisms
-
批准号:7369649
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项目类别:
-
资助金额:$29.54万
-
财政年份:1996
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负责人:EVAN R KANTROWITZ
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依托单位:
THE MOLECULAR BASIS OF CELLULAR CONTROL MECHANISMS
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批准号:7176839
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项目类别:
-
资助金额:$27.19万
-
财政年份:1996
-
负责人:EVAN R KANTROWITZ
-
依托单位:
THE MOLECULAR BASIS OF CELLULAR CONTROL MECHANISMS
-
批准号:6720562
-
项目类别:
-
资助金额:$30.67万
-
财政年份:1996
-
负责人:EVAN R KANTROWITZ
-
依托单位:
The Molecular Basis of Cellular Control Mechanisms
-
批准号:7752494
-
项目类别:
-
资助金额:$25.62万
-
财政年份:1996
-
负责人:EVAN R KANTROWITZ
-
依托单位:
海外基金