Complex Molecules Flashcards
These are proteins to which oligosaccharides are attached.
Glycoproteins
Underlying mechanism by which GAGs allow for the formation of gel-like substance
Hydrogen bonding between gag chains
I-cell disease is an autosomal recessive disorder caused by a deficiency of ______, which phosphorylates mannose residues to mannose-6-phosphate on N-linked glycoproteins in the Golgi apparatus within cells.
GlcNac phosphotransferase
What is the only significant sphingophospholipid in humans?
Sphingomyelin
Which glycerolphospholipids flips from the inner leaflet to the outer leaflet and is important in apoptosis?
Phosphatidylserine
Which glycerophospholipids flips from inner leaflet to outer leaflet and is important in apoptosis?
Phosphatidylserine
N-acetylgalactosamine + Glucuronic acid = ___________
Chondroitin sulfate
What is the most abundant GAG?
Chondroitin sulfate
What is the main GAG for the skin?
Dermatan Sulfate
_____________ is a phospholipid , which is exclusively located in mitochondria , and has unique structure that consist of 2 phosphate residues and 4 kinds of fatty acyl chains.
Cardiolipin
What refers to a large family of naturally occuring organic compounds characterized by multiples of phenol units?
Polyphenols
Glucosamine + Iduronic acid= ______________
Heparin
N-acetylgalactosamine + Iduronic acid= ______________
Dermatan sulfate
Cause of mucopolysaccharidoses which are inherited lysosomal storage disease.
Defects in the degradation of GAGs in the proteoglycans
In what organs heme is biosynthesized?
Liver and Bone marrow