The Hypertrophic Cardiomyopathy Myosin Mutation R453C Alters ATP Binding and Hydrolysis of Human Cardiac β- Myosin*
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            Overview
            
                    
                
             
            
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                    has subject area   
                
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          Adenosine Triphosphatases - Cardiac Myosins
    
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          Adenosine Triphosphatases - Myosin Heavy Chains
    
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          Aortic Valve Disease - Cardiomyopathy, Hypertrophic
    
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          Biochemical Phenomena - Kinetics
    
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          Biochemical Phenomena - Protein Binding
    
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          Cardiomyopathies - Cardiomyopathy, Hypertrophic
    
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          Crystallography, X-Ray
    
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          Cytoskeletal Proteins - Actins
    
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          Cytoskeletal Proteins - Cardiac Myosins
    
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          Cytoskeletal Proteins - Myosin Heavy Chains
    
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          Humans
    
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          Hydrolysis
    
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          Macromolecular Substances - Actins
    
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          Macromolecular Substances - Cardiac Myosins
    
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          Macromolecular Substances - Myosin Heavy Chains
    
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          Mechanical Phenomena - Kinetics
    
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          Metabolism - Protein Binding
    
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          Models, Molecular
    
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          Muscle Proteins - Actins
    
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          Muscle Proteins - Cardiac Myosins
    
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          Muscle Proteins - Myosin Heavy Chains
    
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          Mutagenesis - Amino Acid Substitution
    
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          Mutation
    
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          Nucleic Acids, Nucleotides, and Nucleosides - Adenosine Diphosphate
    
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          Nucleic Acids, Nucleotides, and Nucleosides - Adenosine Triphosphate
    
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          Protein Engineering - Amino Acid Substitution
    
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          Protein Structure, Secondary
    
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          Protein Structure, Tertiary
    
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          Purines - Adenosine Diphosphate
    
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          Purines - Adenosine Triphosphate
    
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          Ribonucleotides - Adenosine Diphosphate
    
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          Ribonucleotides - Adenosine Triphosphate
    
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                    Date in CU Experts   
                
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			February 1, 2018 12:30 PM
    
Full Author List   
                
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    	Bloemink M; Deacon J; Langer S; Vera C; Combs A; Leinwand L; Geeves MA   
    
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