Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene

Keyphrases

• Congenital Disorders of Glycosylation 100%
• Conserved Oligomeric Golgi Complex 100%
• N-glycosylation Defects 100%
• COG4 100%
• Surface Proteins 50%
• Exocyst 50%
• Missense mutation 50%
• Membrane Targeting 50%
• Transport Vesicles 50%
• Salt-bridge Network 50%
• Structural Resemblance 50%
• C-terminal Fragments 50%

Biochemistry, Genetics and Molecular Biology

• Golgi Apparatus 100%
• Congenital Disorder of Glycosylation 66%
• Exocyst 33%
• Missense Mutation 33%
• Protein Targeting 33%
• Vesicular Transporter 33%
• Cell Surface Protein 33%