Functional analysis of disease-causing mutations in human galactokinase

Keyphrases

• Catabolism 20%
• Clinical Manifestations 20%
• Disease-causing mutations 100%
• Early-onset Cataract 20%
• Escherichia Coli 40%
• Functional Analysis 100%
• Functional Change 20%
• Galactokinase 100%
• Galactose 20%
• Galactosemia 60%
• GALK1 20%
• Inherited Disease 20%
• Inhibition Studies 20%
• Kinetic Mechanism 20%
• Kinetic Properties 20%
• Product Inhibition 20%
• Proton Transfer 20%
• Rate-determining Step 20%
• Recombinant Enzyme 20%
• Solvent Kinetic Isotope Effect 20%
• Structure Function 20%
• Ternary Complex 20%

Biochemistry, Genetics and Molecular Biology

• Adenosine Triphosphate 40%
• Enzyme 60%
• Escherichia coli 40%
• Galactokinase 100%
• Galactose 20%
• Genetic Disorder 20%
• Kinetic Isotope Effect 20%
• Kinetics 20%
• Product Inhibition 20%
• Proton Transport 20%
• Structure Activity Relation 20%
• Ternary Complex 20%
• Wild Type 40%