Influence of UDP-GlcNAc 2-epimerase/ManNAc kinase mutant proteins on hereditary inclusion body myopathy

Keyphrases

• Mutant Protein 100%
• Hereditary Myopathy 100%
• UDP-GlcNAc 2-epimerase/ManNAc Kinase 100%
• Kinase Domain 66%
• Epimerase 66%
• UDP-N-acetylglucosamine Pyrophosphorylase 66%
• Enzymatic Activity 33%
• Escherichia Coli 33%
• 3D Structure 33%
• Functional Domain 33%
• Structural Change 33%
• Disease Phenotype 33%
• Point mutant 33%
• Gel Filtration 33%
• Protein Surface 33%
• Glucokinase 33%
• Insect Cells 33%
• CD Spectroscopy 33%
• Enzymatic Function 33%
• Disease Mechanisms 33%
• Sialic Acid Biosynthesis 33%
• Neuromuscular Disease 33%
• Enzyme mutation 33%
• Extent of Reduction 33%
• GNE Gene 33%
• N-acetylglutamate Kinase 33%

Biochemistry, Genetics and Molecular Biology

• Phosphotransferase 100%
• Kinase 100%
• Mutant Protein 100%
• Uridine Diphosphate 100%
• 2-Epimerase 100%
• Enzyme 50%
• Enzyme Activity 50%
• N-Acetylglucosamine 50%
• Membrane Protein 25%
• Escherichia coli 25%
• Anabolism 25%
• Transmembrane Protein 25%
• Circular Dichroism 25%
• Gel Filtration 25%
• Sialic Acid 25%
• Glucokinase 25%
• Insect Cell 25%
• Sf9 25%
• N-Acetylmannosamine 25%
• GNE (Gene) 25%